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Tytuł:
Linking a European cohort of children born with congenital anomalies to vital statistics and mortality records: A EUROlinkCAT study.
Autorzy:
Loane M; Faculty of Life and Health Sciences, Ulster University, Northern Ireland, United Kingdom.
Given JE; Faculty of Life and Health Sciences, Ulster University, Northern Ireland, United Kingdom.
Tan J; Population Health Research Institute, St George's, University of London, London, United Kingdom.
Reid A; Population Health Research Institute, St George's, University of London, London, United Kingdom.
Akhmedzhanova D; OMNI-Net for Children International Charitable Fund, Rivne Regional Medical Diagnostic Center, Rivne, Ukraine.
Astolfi G; Emilia Romagna Registry of Birth Defects, University Hospital of Ferrara, Ferrara, Italy.
Barišić I; Klinika za dječje bolesti, Zagreb, Croatia.
Bertille N; Institut National de la Santé et de la Recherche Médicale, Paris, France.
Bonet LB; Rare Diseases Research Unit, Foundation for the Promotion of Health and Biomedical Research in the Valencian Region, Valencia, Spain.
Carbonell CC; Rare Diseases Research Unit, Foundation for the Promotion of Health and Biomedical Research in the Valencian Region, Valencia, Spain.
Carollo OM; Departamento de Salud Gobierno Vasco, Basque Country, Spain.
Coi A; Unit of Epidemiology of Rare Diseases and Congenital Anomalies, Institute of Clinical Physiology, National Research Council, Pisa, Italy.
Densem J; Biomedical Computing Limited, Battle, United Kingdom.
Draper E; East Midlands & South Yorkshire Congenital Anomaly Registry, University of Leicester, Leicester, United Kingdom.
Garne E; Hospital Lillebaelt, Region Syddanmark, Denmark.
Gatt M; Directorate for Health Information and Research, G'Mangia, Malta.
Glinianaia SV; Faculty of Medical Sciences, Population Health Sciences Institute, Newcastle University, Newcastle upon Tyne, United Kingdom.
Heino A; Finnish Institute for Health and Welfare, Helsinki, Finland.
Hond ED; Provinciaal Instituut voor Hygiëne (PIH), Antwerpen, Belgium.
Jordan S; Swansea University, Wales, United Kingdom.
Khoshnood B; Institut National de la Santé et de la Recherche Médicale, Paris, France.
Kiuru-Kuhlefelt S; Finnish Institute for Health and Welfare, Helsinki, Finland.
Klungsøyr K; Division of Mental and Physical Health, Department of Global Public Health and Primary Care, Norwegian Institute of Public Health, University of Bergen, Bergen, Norway.
Lelong N; Institut National de la Santé et de la Recherche Médicale, Paris, France.
Lutke LR; Department of Genetics, University Medical Center, University of Groningen, Groningen, The Netherlands.
Neville AJ; Emilia Romagna Registry of Birth Defects, University Hospital of Ferrara, Ferrara, Italy.
Ostapchuk L; OMNI-Net for Children International Charitable Fund, Rivne Regional Medical Diagnostic Center, Rivne, Ukraine.
Puccini A; Territorial Care Service, Emilia Romagna Health Authority, Bologna, Italy.
Rissmann A; Medical Faculty Otto-von-Guericke, Malformation Monitoring Centre Saxony-Anhalt, University Magdeburg, Magdeburg, Germany.
Santoro M; Unit of Epidemiology of Rare Diseases and Congenital Anomalies, Institute of Clinical Physiology, National Research Council, Pisa, Italy.
Scanlon I; Swansea University, Wales, United Kingdom.
Thys G; Provinciaal Instituut voor Hygiëne (PIH), Antwerpen, Belgium.
Tucker D; Public Health Wales, Wales, United Kingdom.
Urhoj SK; Section of Epidemiology, University of Copenhagen, Copenhagen, Denmark.
de Walle HEK; Department of Genetics, University Medical Center, University of Groningen, Groningen, The Netherlands.
Wellesley D; Wessex Clinical Genetics Service, Princess Anne Hospital, Southampton, United Kingdom.
Zurriaga O; Rare Diseases Research Unit, Foundation for the Promotion of Health and Biomedical Research in the Valencian Region, Valencia, Spain.
Morris JK; Population Health Research Institute, St George's, University of London, London, United Kingdom.
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Źródło:
PloS one [PLoS One] 2021 Aug 27; Vol. 16 (8), pp. e0256535. Date of Electronic Publication: 2021 Aug 27 (Print Publication: 2021).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Birth Certificates*
Vital Statistics*
Congenital Abnormalities/*epidemiology
Congenital Abnormalities/pathology ; Europe/epidemiology ; Female ; Humans ; Infant, Newborn ; Male ; Pregnancy ; Registries
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Observed birth prevalence of congenital anomalies among live births at a regional facility in KwaZulu Natal Province, South Africa.
Autorzy:
Saib MZ; KwaZulu Natal Department of Health, Paediatrics and Child Health, Grey's Hospital, Pietermaritzburg, South Africa.; Paediatrics & Child Health, Nelson R Mandela School of Clinical Medicine, College of Health Sciences, University of KwaZulu Natal, Durban, South Africa.
Dhada BL; KwaZulu Natal Department of Health, Paediatrics and Child Health, Grey's Hospital, Pietermaritzburg, South Africa.; Paediatrics & Child Health, Nelson R Mandela School of Clinical Medicine, College of Health Sciences, University of KwaZulu Natal, Durban, South Africa.
Aldous C; School of Clinical Medicine, College of Health Sciences, University of KwaZulu Natal, Durban, South Africa.
Malherbe HL; KwaZulu Natal Research Innovation and Sequencing Platform (KRISP), School of Laboratory Medicine and Medical Sciences, College of Health Sciences, University of KwaZulu Natal, Durban, South Africa.; Rare Diseases South Africa NPC, Johannesburg, South Africa.
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Źródło:
PloS one [PLoS One] 2021 Aug 03; Vol. 16 (8), pp. e0255456. Date of Electronic Publication: 2021 Aug 03 (Print Publication: 2021).
Typ publikacji:
Journal Article; Observational Study
MeSH Terms:
Congenital Abnormalities/*epidemiology
Live Birth/*epidemiology
Congenital Abnormalities/classification ; Female ; Humans ; Infant, Newborn ; Male ; Prevalence ; Registries ; Retrospective Studies ; South Africa/epidemiology
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Recommendations for neonatologists and pediatricians working in first level birthing centers on the first communication of genetic disease and malformation syndrome diagnosis: consensus issued by 6 Italian scientific societies and 4 parents' associations.
Autorzy:
Serra G; Department of Health Promotion, Mother and Child Care, Internal Medicine and Medical Specialties 'G. D'Alessandro', University of Palermo, Palermo, Italy. .
Memo L; Clinical Genetics Outpatient Service, Neonatology and Neonatal Intensive Care Unit, San Bortolo Hospital, Vicenza, Italy.
Coscia A; University Neonatology Unit, AOU Città della Salute e della Scienza, Turin, Italy.
Giuffré M; Department of Health Promotion, Mother and Child Care, Internal Medicine and Medical Specialties 'G. D'Alessandro', University of Palermo, Palermo, Italy.
Iuculano A; Unit of Prenatal and Preimplantation Diagnosis, Thalassaemic Hospital, AO Brotzu, Cagliari, Italy.
Lanna M; Unit of Obstetrics and Gynecology, Prenatal Diagnosis and Fetal Therapy 'U. Nicolini', Buzzi Hospital, ASST FBF Sacco, Milan, Italy.
Valentini D; Unit of General Pediatrics, Emergency and Acceptance Department, Bambino Gesù Pediatric Hospital, Rome, Italy.
Contardi A; Coordinator of the Italian Association of Down People, Rome, Italy.
Filippeschi S; President of the Italian National Association of Volunteers Cornelia de Lange, Pesaro, Italy.
Frusca T; President of the Italian Society of Obstetric and Gynecological Ultrasound and Biophysical Methodologies, Parma, Italy.
Mosca F; President of the Italian Society of Neonatology, Milan, Italy.
Ramenghi LA; President of the Italian Society of Perinatal Medicine, Genoa, Italy.
Romano C; Coordinator of the Clinical Genetics Study Group of the Italian Society of Human Genetics, Troina, EN, Italy.
Scopinaro A; President of Italian Federation of Rare Diseases and of Williams Syndrome People Association, Rome, Italy.
Villani A; President of the Italian Society of Pediatrics, Rome, Italy.
Zampino G; President of the Italian Society of Pediatric Genetic Diseases and Congenital Disabilities, Rome, Italy.
Corsello G; Department of Health Promotion, Mother and Child Care, Internal Medicine and Medical Specialties 'G. D'Alessandro', University of Palermo, Palermo, Italy.
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Corporate Authors:
their respective Scientific Societies and Parents’ Associations
Źródło:
Italian journal of pediatrics [Ital J Pediatr] 2021 Apr 19; Vol. 47 (1), pp. 94. Date of Electronic Publication: 2021 Apr 19.
Typ publikacji:
Journal Article
MeSH Terms:
Birthing Centers*
Genetic Counseling*
Neonatologists*
Pediatricians*
Prenatal Diagnosis*
Congenital Abnormalities/*diagnosis
Genetic Diseases, Inborn/*diagnosis
Congenital Abnormalities/psychology ; Congenital Abnormalities/therapy ; Consensus ; Female ; Genetic Diseases, Inborn/psychology ; Genetic Diseases, Inborn/therapy ; Humans ; Intensive Care Units, Neonatal ; Italy ; Parents/psychology ; Pregnancy ; Societies, Scientific ; Truth Disclosure
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
The application of late amniocentesis: a retrospective study in a tertiary fetal medicine center in China.
Autorzy:
Li Y; Department of Obstetrics and Gynecology, Department of Fetal Medicine and Prenatal Diagnosis, Key Laboratory for Major Obstetric Diseases of Guangdong Province, The Third Affiliated Hospital of Guangzhou Medical University, 63 Duobao Road, Liwan District, Guangzhou, China.
Yan H; Department of Obstetrics and Gynecology, Department of Fetal Medicine and Prenatal Diagnosis, Key Laboratory for Major Obstetric Diseases of Guangdong Province, The Third Affiliated Hospital of Guangzhou Medical University, 63 Duobao Road, Liwan District, Guangzhou, China.
Chen J; Department of Obstetrics and Gynecology, Department of Fetal Medicine and Prenatal Diagnosis, Key Laboratory for Major Obstetric Diseases of Guangdong Province, The Third Affiliated Hospital of Guangzhou Medical University, 63 Duobao Road, Liwan District, Guangzhou, China.
Chen F; Department of Obstetrics and Gynecology, Department of Fetal Medicine and Prenatal Diagnosis, Key Laboratory for Major Obstetric Diseases of Guangdong Province, The Third Affiliated Hospital of Guangzhou Medical University, 63 Duobao Road, Liwan District, Guangzhou, China.
Jian W; Department of Obstetrics and Gynecology, Department of Fetal Medicine and Prenatal Diagnosis, Key Laboratory for Major Obstetric Diseases of Guangdong Province, The Third Affiliated Hospital of Guangzhou Medical University, 63 Duobao Road, Liwan District, Guangzhou, China.
Wang J; Department of Obstetrics and Gynecology, Department of Fetal Medicine and Prenatal Diagnosis, Key Laboratory for Major Obstetric Diseases of Guangdong Province, The Third Affiliated Hospital of Guangzhou Medical University, 63 Duobao Road, Liwan District, Guangzhou, China.
Ye X; Department of Obstetrics and Gynecology, Department of Fetal Medicine and Prenatal Diagnosis, Key Laboratory for Major Obstetric Diseases of Guangdong Province, The Third Affiliated Hospital of Guangzhou Medical University, 63 Duobao Road, Liwan District, Guangzhou, China.
Li Y; Department of Obstetrics and Gynecology, Department of Fetal Medicine and Prenatal Diagnosis, Key Laboratory for Major Obstetric Diseases of Guangdong Province, The Third Affiliated Hospital of Guangzhou Medical University, 63 Duobao Road, Liwan District, Guangzhou, China.
Li N; Department of Obstetrics and Gynecology, Department of Fetal Medicine and Prenatal Diagnosis, Key Laboratory for Major Obstetric Diseases of Guangdong Province, The Third Affiliated Hospital of Guangzhou Medical University, 63 Duobao Road, Liwan District, Guangzhou, China.
Chiu PCN; Department of Obstetrics and Gynecology, the University of Hong Kong, Hong Kong, China.; Shenzhen Key Laboratory of Fertility Regulation, the University of Hong Kong-Shenzhen Hospital, Shenzhen, China.
Chen M; Department of Obstetrics and Gynecology, Department of Fetal Medicine and Prenatal Diagnosis, Key Laboratory for Major Obstetric Diseases of Guangdong Province, The Third Affiliated Hospital of Guangzhou Medical University, 63 Duobao Road, Liwan District, Guangzhou, China. .
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Źródło:
BMC pregnancy and childbirth [BMC Pregnancy Childbirth] 2021 Mar 30; Vol. 21 (1), pp. 266. Date of Electronic Publication: 2021 Mar 30.
Typ publikacji:
Journal Article
MeSH Terms:
Aneuploidy*
Amniocentesis/*statistics & numerical data
Congenital Abnormalities/*diagnosis
Genetic Testing/*statistics & numerical data
Ultrasonography, Prenatal/*statistics & numerical data
Abortion, Eugenic/statistics & numerical data ; Adolescent ; Adult ; Age of Onset ; Amniocentesis/adverse effects ; China/epidemiology ; Congenital Abnormalities/epidemiology ; Congenital Abnormalities/genetics ; Female ; Genetic Counseling ; Humans ; Middle Aged ; Pregnancy ; Reproducibility of Results ; Retrospective Studies ; Tertiary Care Centers ; Time Factors ; Exome Sequencing ; Young Adult
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Predictors of congenital anomalies among newborns in Arsi zone public hospitals, Southeast Ethiopia: a case-control study.
Autorzy:
Jemal S; Department of Human Anatomy, School of Medicine, College of Medicine and Health Sciences, University of Gondar, Gondar, Amhara, Ethiopia.
Fentahun E; Department of Human Anatomy, School of Medicine, College of Medicine and Health Sciences, University of Gondar, Gondar, Amhara, Ethiopia.
Oumer M; Department of Human Anatomy, School of Medicine, College of Medicine and Health Sciences, University of Gondar, Gondar, Amhara, Ethiopia.
Muche A; Department of Human Anatomy, School of Medicine, College of Medicine and Health Sciences, University of Gondar, Gondar, Amhara, Ethiopia. .
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Źródło:
Italian journal of pediatrics [Ital J Pediatr] 2021 Jun 30; Vol. 47 (1), pp. 143. Date of Electronic Publication: 2021 Jun 30.
Typ publikacji:
Journal Article; Multicenter Study
MeSH Terms:
Congenital Abnormalities/*epidemiology
Case-Control Studies ; Congenital Abnormalities/etiology ; Ethiopia/epidemiology ; Female ; Hospitals, Public ; Humans ; Infant, Newborn ; Male ; Predictive Value of Tests ; Pregnancy ; Risk Factors
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Inherited Defects of the ASC-1 Complex in Congenital Neuromuscular Diseases.
Autorzy:
Meunier J; Basic and Translational Myology Laboratory, UMR8251, University of Paris/National Center for Scientific Research, 75013 Paris, France.
Villar-Quiles RN; Basic and Translational Myology Laboratory, UMR8251, University of Paris/National Center for Scientific Research, 75013 Paris, France.; Reference Center for Neuromuscular Disorders, Pitié-Salpêtrière Hospital, APHP, Institute of Myology, 75013 Paris, France.
Duband-Goulet I; Basic and Translational Myology Laboratory, UMR8251, University of Paris/National Center for Scientific Research, 75013 Paris, France.
Ferreiro A; Basic and Translational Myology Laboratory, UMR8251, University of Paris/National Center for Scientific Research, 75013 Paris, France.; Reference Center for Neuromuscular Disorders, Pitié-Salpêtrière Hospital, APHP, Institute of Myology, 75013 Paris, France.
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Źródło:
International journal of molecular sciences [Int J Mol Sci] 2021 Jun 03; Vol. 22 (11). Date of Electronic Publication: 2021 Jun 03.
Typ publikacji:
Journal Article; Review
MeSH Terms:
Carrier Proteins/*genetics
Congenital Abnormalities/*genetics
Neuromuscular Diseases/*genetics
Transcription Factors/*genetics
Congenital Abnormalities/pathology ; Genetic Association Studies ; Genetic Predisposition to Disease ; Humans ; Multiprotein Complexes/genetics ; Mutation ; Neuromuscular Diseases/pathology
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Pre-pregnancy obesity and risk of congenital abnormalities of the kidney and urinary tract (CAKUT)-systematic review, meta-analysis and ecological study.
Autorzy:
Jadresić L; Department of Paediatrics, Gloucestershire Hospitals NHS Foundation Trust, Gloucester, England. .
Au H; University of Hong Kong, Pok Fu Lam, Hong Kong.
Woodhouse C; University College, London, UK.
Nitsch D; Department of Non-Communicable Disease Epidemiology, Faculty of Epidemiology and Population Health, London School of Hygiene and Tropical Medicine, London, UK.
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Źródło:
Pediatric nephrology (Berlin, Germany) [Pediatr Nephrol] 2021 Jan; Vol. 36 (1), pp. 119-132. Date of Electronic Publication: 2020 Jun 28.
Typ publikacji:
Journal Article; Meta-Analysis; Systematic Review
MeSH Terms:
Congenital Abnormalities*
Obesity, Maternal*
Urinary Tract*
Urogenital Abnormalities*
Female ; Humans ; Hydronephrosis ; Kidney ; Kidney Diseases ; Pregnancy
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Bone-conduction hearing aid is effective in congenital oval window atresia.
Autorzy:
Gao M; Department of Otolaryngology Head and Neck Surgery, Beijing Tongren Hospital, Capital Medical University, Ministry of Education Key Laboratory of Otolaryngology Head and Neck Surgery, Capital Medical University, Beijing, China.
Zhao C; Department of Otolaryngology Head and Neck Surgery, Beijing Tongren Hospital, Capital Medical University, Ministry of Education Key Laboratory of Otolaryngology Head and Neck Surgery, Capital Medical University, Beijing, China.
Yang J; Department of Otolaryngology Head and Neck Surgery, Beijing Tongren Hospital, Capital Medical University, Ministry of Education Key Laboratory of Otolaryngology Head and Neck Surgery, Capital Medical University, Beijing, China.
Chen P; Department of Otolaryngology Head and Neck Surgery, Beijing Tongren Hospital, Capital Medical University, Ministry of Education Key Laboratory of Otolaryngology Head and Neck Surgery, Capital Medical University, Beijing, China.
Liu Y; Department of Otolaryngology Head and Neck Surgery, Beijing Tongren Hospital, Capital Medical University, Ministry of Education Key Laboratory of Otolaryngology Head and Neck Surgery, Capital Medical University, Beijing, China.
Wang D; Department of Otolaryngology Head and Neck Surgery, Beijing Tongren Hospital, Capital Medical University, Ministry of Education Key Laboratory of Otolaryngology Head and Neck Surgery, Capital Medical University, Beijing, China.
Zhao S; Department of Otolaryngology Head and Neck Surgery, Beijing Tongren Hospital, Capital Medical University, Ministry of Education Key Laboratory of Otolaryngology Head and Neck Surgery, Capital Medical University, Beijing, China.
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Źródło:
Acta oto-laryngologica [Acta Otolaryngol] 2021 Apr; Vol. 141 (4), pp. 321-327. Date of Electronic Publication: 2021 Jan 13.
Typ publikacji:
Journal Article
MeSH Terms:
Congenital Abnormalities*
Hearing Aids*
Hearing Loss, Conductive/*rehabilitation
Oval Window, Ear/*abnormalities
Adolescent ; Adult ; Auditory Threshold ; Bone Conduction ; Child ; China ; Ear/abnormalities ; Female ; Hearing Loss, Conductive/etiology ; Humans ; Male ; Retrospective Studies ; Young Adult
SCR Disease Name:
Aural Atresia, Congenital
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Assessing pregnancy and neonatal outcomes in Malawi, South Africa, Uganda, and Zimbabwe: Results from a systematic chart review.
Autorzy:
Balkus JE; Department of Epidemiology, University of Washington, Seattle, Washington, United States of America.; Vaccine and Infectious Diseases Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
Neradilek M; Vaccine and Infectious Diseases Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
Fairlie L; Faculty of Health Sciences, Wits Reproductive Health and HIV Institute, University of the Witwatersrand, Gauteng, South Africa.
Makanani B; College of Medicine-Johns Hopkins Research Project, Blantyre, Malawi.
Mgodi N; University of Zimbabwe College of Health Sciences Clinical Trials Research Centre, Harare, Zimbabwe.
Mhlanga F; University of Zimbabwe College of Health Sciences Clinical Trials Research Centre, Harare, Zimbabwe.
Nakabiito C; Makerere University-Johns Hopkins University Research Collaboration, Kampala, Uganda.
Mayo A; FHI 360, Durham, North Carolina, United Stated of America.
Harrell T; Vaccine and Infectious Diseases Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
Piper J; US National Institutes of Health, Bethesda, Maryland, United States of America.
Bunge KE; Department of Obstetrics and Gynecology, University of Pittsburgh, Pittsburgh, Pennsylvania, United Stated of America.
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Corporate Authors:
MTN-042B Study Team
Źródło:
PloS one [PLoS One] 2021 Mar 31; Vol. 16 (3), pp. e0248423. Date of Electronic Publication: 2021 Mar 31 (Print Publication: 2021).
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Systematic Review
MeSH Terms:
Congenital Abnormalities*/epidemiology
HIV*
HIV Infections*/epidemiology
HIV Infections*/virology
Hypertension, Pregnancy-Induced*/epidemiology
Hypertension, Pregnancy-Induced*/mortality
Perinatal Mortality*
Premature Birth*/epidemiology
Stillbirth*/epidemiology
Adolescent ; Adult ; Child ; Female ; Humans ; Infant, Newborn ; Middle Aged ; Pregnancy ; Young Adult ; Cross-Sectional Studies ; Infant, Low Birth Weight ; Malawi/epidemiology ; Maternal Mortality ; Prevalence ; South Africa/epidemiology ; Uganda/epidemiology ; Zimbabwe/epidemiology
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
An outbreak of abortions, stillbirths and malformations in a Spanish sheep flock associated with a bovine viral diarrhoea virus 2-contaminated orf vaccine.
Autorzy:
Asín J; Department of Animal Pathology, University of Zaragoza, Zaragoza, Spain.
Hilbe M; Institute of Veterinary Pathology, Vetsuisse Faculty, University of Zurich, Zurich, Switzerland.
de Miguel R; Department of Animal Pathology, University of Zaragoza, Zaragoza, Spain.
Rodríguez-Largo A; Department of Animal Pathology, University of Zaragoza, Zaragoza, Spain.
Lanau A; Sociedad Cooperativa Limitada Agropecuaria del Sobrarbe (SCLAS) Veterinary Service, Huesca, Spain.
Akerman A; Sociedad Cooperativa Limitada Agropecuaria del Sobrarbe (SCLAS) Veterinary Service, Huesca, Spain.
Stalder H; Institute of Virology and Immunology, Bern, Switzerland.; Department of Infectious Diseases and Pathobiology, Vetsuisse Faculty, University of Bern, Switzerland.
Schweizer M; Institute of Virology and Immunology, Bern, Switzerland.; Department of Infectious Diseases and Pathobiology, Vetsuisse Faculty, University of Bern, Switzerland.
Luján L; Department of Animal Pathology, University of Zaragoza, Zaragoza, Spain.; Instituto Universitario de Investigación Mixto Agroalimentario de Aragón (IA2), Universidad de Zaragoza, Zaragoza, Spain.
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Źródło:
Transboundary and emerging diseases [Transbound Emerg Dis] 2021 Mar; Vol. 68 (2), pp. 233-239. Date of Electronic Publication: 2020 May 20.
Typ publikacji:
Journal Article
MeSH Terms:
Abortion, Veterinary/*epidemiology
Congenital Abnormalities/*veterinary
Disease Outbreaks/*veterinary
Sheep Diseases/*epidemiology
Stillbirth/*veterinary
Viral Vaccines/*adverse effects
Animals ; Congenital Abnormalities/epidemiology ; Diarrhea Virus 2, Bovine Viral/immunology ; Sheep ; Sheep, Domestic ; Spain/epidemiology ; Stillbirth/epidemiology
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Application of retrosigmoid sinus approach in Bonebridge implantation.
Autorzy:
Wang D; Department of Otolaryngology - Head and Neck Surgery, Beijing Tongren Hospital, Key Laboratory of Otolaryngology - Head and Neck Surgery, Capital Medical University, Beijing, China.; Beijing Institute of Otolaryngology, Beijing, China.
Ren R; Department of Otolaryngology - Head and Neck Surgery, Beijing Tongren Hospital, Key Laboratory of Otolaryngology - Head and Neck Surgery, Capital Medical University, Beijing, China.; Beijing Institute of Otolaryngology, Beijing, China.
Chen P; Department of Otolaryngology - Head and Neck Surgery, Beijing Tongren Hospital, Key Laboratory of Otolaryngology - Head and Neck Surgery, Capital Medical University, Beijing, China.; Beijing Institute of Otolaryngology, Beijing, China.
Yang J; Department of Otolaryngology - Head and Neck Surgery, Beijing Tongren Hospital, Key Laboratory of Otolaryngology - Head and Neck Surgery, Capital Medical University, Beijing, China.; Beijing Institute of Otolaryngology, Beijing, China.
Gao M; Department of Otolaryngology - Head and Neck Surgery, Beijing Tongren Hospital, Key Laboratory of Otolaryngology - Head and Neck Surgery, Capital Medical University, Beijing, China.; Beijing Institute of Otolaryngology, Beijing, China.
Liu Y; Department of Otolaryngology - Head and Neck Surgery, Beijing Tongren Hospital, Key Laboratory of Otolaryngology - Head and Neck Surgery, Capital Medical University, Beijing, China.; Beijing Institute of Otolaryngology, Beijing, China.
Zhao S; Department of Otolaryngology - Head and Neck Surgery, Beijing Tongren Hospital, Key Laboratory of Otolaryngology - Head and Neck Surgery, Capital Medical University, Beijing, China.; Beijing Institute of Otolaryngology, Beijing, China.
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Źródło:
Acta oto-laryngologica [Acta Otolaryngol] 2021 Feb; Vol. 141 (2), pp. 129-134. Date of Electronic Publication: 2020 Nov 03.
Typ publikacji:
Journal Article
MeSH Terms:
Congenital Abnormalities*
Hearing Aids*
Ear/*abnormalities
Hearing Loss, Conductive/*surgery
Mastoidectomy/*adverse effects
Otologic Surgical Procedures/*methods
Adolescent ; Adult ; Audiometry, Pure-Tone ; Bone Conduction ; Child ; Female ; Hearing Loss, Conductive/etiology ; Humans ; Male ; Middle Aged ; Paranasal Sinuses ; Retrospective Studies ; Speech Reception Threshold Test ; Temporal Bone/diagnostic imaging ; Tomography, X-Ray Computed
SCR Disease Name:
Aural Atresia, Congenital
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Increasing serum alkaline phosphatase is associated with bone deformity progression for patients with polyostotic fibrous dysplasia.
Autorzy:
Wang J; Musculoskeletal Tumor Center, Peking University People's Hospital, No. 11 Xizhimen South Street, Beijing, 100044, China.
Du Z; Musculoskeletal Tumor Center, Peking University People's Hospital, No. 11 Xizhimen South Street, Beijing, 100044, China.
Li D; Musculoskeletal Tumor Center, Peking University People's Hospital, No. 11 Xizhimen South Street, Beijing, 100044, China.
Yang R; Musculoskeletal Tumor Center, Peking University People's Hospital, No. 11 Xizhimen South Street, Beijing, 100044, China.
XiaodongTang; Musculoskeletal Tumor Center, Peking University People's Hospital, No. 11 Xizhimen South Street, Beijing, 100044, China.
Yan T; Musculoskeletal Tumor Center, Peking University People's Hospital, No. 11 Xizhimen South Street, Beijing, 100044, China.
Guo W; Musculoskeletal Tumor Center, Peking University People's Hospital, No. 11 Xizhimen South Street, Beijing, 100044, China. .
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Źródło:
Journal of orthopaedic surgery and research [J Orthop Surg Res] 2020 Dec 03; Vol. 15 (1), pp. 583. Date of Electronic Publication: 2020 Dec 03.
Typ publikacji:
Journal Article
MeSH Terms:
Alkaline Phosphatase/*blood
Bone and Bones/*abnormalities
Bone and Bones/*pathology
Congenital Abnormalities/*etiology
Congenital Abnormalities/*pathology
Fibrous Dysplasia, Polyostotic/*diagnosis
Fibrous Dysplasia, Polyostotic/*pathology
Adolescent ; Biomarkers/blood ; Bone Remodeling ; Bone and Bones/metabolism ; Bone and Bones/surgery ; Calcium/metabolism ; Congenital Abnormalities/surgery ; Disease Progression ; Female ; Fibrous Dysplasia, Polyostotic/complications ; Fibrous Dysplasia, Polyostotic/surgery ; Humans ; Male ; Phosphates/metabolism ; Retrospective Studies ; Risk Factors ; Severity of Illness Index
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Evaluation and Management of Unexpected Functional Rudimentary Uteri in Mayer-Rokitansky-Küster-Hauser Syndrome of Chinese Women.
Autorzy:
Deng S; Department of Obstetrics and Gynecology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, National Clinical Research Center for Obstetrical and Gynecological Diseases, Beijing, China.
Zhu L; Department of Obstetrics and Gynecology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, National Clinical Research Center for Obstetrical and Gynecological Diseases, Beijing, China.
Tian Q; Department of Obstetrics and Gynecology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, National Clinical Research Center for Obstetrical and Gynecological Diseases, Beijing, China.
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Źródło:
BioMed research international [Biomed Res Int] 2020 Nov 24; Vol. 2020, pp. 6808409. Date of Electronic Publication: 2020 Nov 24 (Print Publication: 2020).
Typ publikacji:
Evaluation Study; Journal Article
MeSH Terms:
Asian People*
46, XX Disorders of Sex Development/*pathology
Congenital Abnormalities/*pathology
Mullerian Ducts/*abnormalities
Uterus/*abnormalities
46, XX Disorders of Sex Development/diagnostic imaging ; 46, XX Disorders of Sex Development/surgery ; Adolescent ; Adult ; Child ; Congenital Abnormalities/diagnostic imaging ; Congenital Abnormalities/surgery ; Female ; Humans ; Magnetic Resonance Imaging ; Mullerian Ducts/diagnostic imaging ; Mullerian Ducts/pathology ; Mullerian Ducts/surgery ; Preoperative Care ; Ultrasonography ; Uterus/diagnostic imaging ; Uterus/surgery ; Young Adult
SCR Disease Name:
Mullerian aplasia
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Role of prenatal imaging in the diagnosis and management of fetal facio-cervical masses.
Autorzy:
Zheng W; Department of Radiology, Women's Hospital, Zhejiang University School of Medicine, Xueshi Rd No. 1, Hangzhou, Zhejiang, People's Republic of China.
Gai S; Department of Ultrasound, Women's Hospital, Zhejiang University School of Medicine, Xueshi Rd No. 1, Hangzhou, Zhejiang, People's Republic of China.
Qin J; Department of Ultrasound, Women's Hospital, Zhejiang University School of Medicine, Xueshi Rd No. 1, Hangzhou, Zhejiang, People's Republic of China.
Qiu F; Department of Otolaryngology, Children's Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, Binsheng Rd No. 3333, Hangzhou, Zhejiang, People's Republic of China.
Li B; Department of Obstetrics, Women's Hospital, Zhejiang University School of Medicine, Xueshi Rd No. 1, Hangzhou, Zhejiang, People's Republic of China.
Zou Y; Department of Radiology, Women's Hospital, Zhejiang University School of Medicine, Xueshi Rd No. 1, Hangzhou, Zhejiang, People's Republic of China. .
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Źródło:
Scientific reports [Sci Rep] 2021 Jan 14; Vol. 11 (1), pp. 1385. Date of Electronic Publication: 2021 Jan 14.
Typ publikacji:
Journal Article; Randomized Controlled Trial; Research Support, Non-U.S. Gov't
MeSH Terms:
Magnetic Resonance Imaging*
Prenatal Diagnosis*
Ultrasonography, Prenatal*
Congenital Abnormalities/*diagnostic imaging
Fetal Diseases/*diagnostic imaging
Adult ; Congenital Abnormalities/mortality ; Cross-Sectional Studies ; Female ; Fetal Diseases/mortality ; Humans ; Pregnancy ; Retrospective Studies
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Influence of indications on perinatal outcomes after radio frequency ablation in complicated monochorionic pregnancies: a retrospective cohort study.
Autorzy:
Wang H; Department of Obstetrics, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, Shandong, China.
Zhou Q; Department of Obstetrics, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, Shandong, China.
Wang X; Department of Obstetrics, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, Shandong, China.; Department of Obstetrics, Maternal Child Health Care Hospital of Shandong Province, Jinan, Shandong, China.; Key Laboratory of Birth Regulation and Control Technology of National Health Commission of China, Maternal Child Health Care Hospital of Shandong Province, Jinan, Shandong, China.
Song J; Department of Neonatology, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, Shandong, China.
Chen P; Department of Obstetrics, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, Shandong, China.
Wang Y; Department of Obstetrics, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, Shandong, China.
Li L; Department of Obstetrics, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, Shandong, China.
Li H; Department of Obstetrics, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, Shandong, China. .
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Źródło:
BMC pregnancy and childbirth [BMC Pregnancy Childbirth] 2021 Jan 09; Vol. 21 (1), pp. 41. Date of Electronic Publication: 2021 Jan 09.
Typ publikacji:
Journal Article
MeSH Terms:
Twins, Monozygotic*
Congenital Abnormalities/*surgery
Fetal Growth Retardation/*surgery
Fetofetal Transfusion/*surgery
Pregnancy Reduction, Multifetal/*methods
Radiofrequency Ablation/*statistics & numerical data
Adult ; Congenital Abnormalities/mortality ; Epidemiologic Methods ; Female ; Fetal Growth Retardation/mortality ; Fetal Membranes, Premature Rupture/epidemiology ; Fetofetal Transfusion/mortality ; Gestational Age ; Humans ; Pregnancy ; Pregnancy Complications/surgery ; Pregnancy Outcome ; Pregnancy Reduction, Multifetal/mortality ; Pregnancy, Twin
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
[Congenital high airway obstruction syndrome (CHAOS): a case report].
Autorzy:
Moussaoui KE; Département de Gynécologie Obstétrique, Maternité Souissi, CHU Ibn Sina, Rabat, Maroc.
Slaoui A; Département de Gynécologie Obstétrique, Maternité Souissi, CHU Ibn Sina, Rabat, Maroc.
Baidada A; Département de Gynécologie Obstétrique, Maternité Souissi, CHU Ibn Sina, Rabat, Maroc.
Kharabch A; Département de Gynécologie Obstétrique, Maternité Souissi, CHU Ibn Sina, Rabat, Maroc.
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Transliterated Title:
Syndrome congénital d´obstruction des voies aériennes supérieures (syndrome du CHAOS): à propos d’un cas.
Źródło:
The Pan African medical journal [Pan Afr Med J] 2021 Jan 01; Vol. 38, pp. 1. Date of Electronic Publication: 2021 Jan 01 (Print Publication: 2021).
Typ publikacji:
Case Reports
MeSH Terms:
Airway Obstruction/*diagnostic imaging
Congenital Abnormalities/*diagnostic imaging
Hydrops Fetalis/*diagnostic imaging
Airway Obstruction/complications ; Airway Obstruction/congenital ; Congenital Abnormalities/physiopathology ; Fatal Outcome ; Female ; Humans ; Hydrops Fetalis/etiology ; Infant, Newborn ; Karyotyping ; Pregnancy ; Pregnancy Outcome ; Syndrome ; Ultrasonography, Prenatal ; Young Adult
Raport
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Active middle ear implant (vibrant soundbridge) in children with unilateral congenital aural atresia.
Autorzy:
Takahashi M; Department of Otorhinolaryngology, International University of Health and Welfare Mita Hospital, Tokyo, Japan.
Iwasaki S; Department of Otorhinolaryngology, International University of Health and Welfare Mita Hospital, Tokyo, Japan.
Furutate S; Department of Otorhinolaryngology, International University of Health and Welfare Mita Hospital, Tokyo, Japan.
Oka S; Department of Otorhinolaryngology, International University of Health and Welfare Mita Hospital, Tokyo, Japan.
Oyamada S; Department of Otorhinolaryngology, International University of Health and Welfare Mita Hospital, Tokyo, Japan.
Yasumura K; Department of Plastic and Reconstructive Surgery, Kanagawa Children's Medical Center, Kanagawa, Japan.
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Źródło:
Acta oto-laryngologica [Acta Otolaryngol] 2021 Jan; Vol. 141 (1), pp. 34-38. Date of Electronic Publication: 2020 Oct 12.
Typ publikacji:
Journal Article
MeSH Terms:
Ossicular Prosthesis*
Congenital Abnormalities/*surgery
Ear/*abnormalities
Hearing Loss, Conductive/*surgery
Speech Perception/*physiology
Audiometry, Pure-Tone ; Child ; Child, Preschool ; Congenital Abnormalities/physiopathology ; Ear/physiopathology ; Ear/surgery ; Female ; Hearing Loss, Conductive/physiopathology ; Humans ; Male ; Prosthesis Design ; Retrospective Studies
SCR Disease Name:
Aural Atresia, Congenital
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Agenesis of female internal reproductive organs, the Mayer- Rokitansky-Küster-Hauser syndrome.
Autorzy:
Sysak R
Bluska P
Stencl P
Klein M
Varga I
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Źródło:
Bratislavske lekarske listy [Bratisl Lek Listy] 2021; Vol. 122 (12), pp. 839-845.
Typ publikacji:
Journal Article
MeSH Terms:
46, XX Disorders of Sex Development*/diagnosis
46, XX Disorders of Sex Development*/surgery
Congenital Abnormalities*/diagnosis
Adolescent ; Female ; Humans ; Mullerian Ducts/abnormalities ; Mullerian Ducts/diagnostic imaging ; Ultrasonography ; Vagina/surgery
SCR Disease Name:
Mullerian aplasia
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Frequent recurrence of pregnancy-triggered congenital thrombotic thrombocytopenic purpura: A rare case report.
Autorzy:
Xu J; Department of Hematology, Affiliated Nanhai Hospital of Southern Medical University, Foshan, China.
Yu S; Department of Hematology, Affiliated Nanhai Hospital of Southern Medical University, Foshan, China.
Zhang F; Department of Hematology, Affiliated Nanhai Hospital of Southern Medical University, Foshan, China.
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Źródło:
Clinical hemorheology and microcirculation [Clin Hemorheol Microcirc] 2021; Vol. 77 (2), pp. 195-200.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Congenital Abnormalities/*diagnosis
Purpura, Thrombotic Thrombocytopenic/*diagnosis
Adult ; Congenital Abnormalities/genetics ; Female ; Humans ; Mutation ; Pregnancy ; Purpura, Thrombotic Thrombocytopenic/genetics ; Recurrence ; Young Adult
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Genetic analysis of children with congenital ocular anomalies in three ecological regions of Nepal: a phase II of Nepal pediatric ocular diseases study.
Autorzy:
Adhikari S; Tilganga Institute of Ophthalmology, PO Box 561, Kathmandu, Nepal. srij_.
Thakur N; National Academy of Medical Sciences NAMS, Bir Hospital, Kathmandu, Nepal.
Shrestha U; Sudrishti Eye Clinic, Kathmandu, Nepal.
Shrestha MK; Tilganga Institute of Ophthalmology, PO Box 561, Kathmandu, Nepal.
Manshrestha M; Tilganga Institute of Ophthalmology, PO Box 561, Kathmandu, Nepal.
Thapa B; Patan Academy of Health Sciences, Patan, Nepal.
Poudel M; Tilganga Institute of Ophthalmology, PO Box 561, Kathmandu, Nepal.
Kunwar A; The Kathmandu Centre for Genomics and Research Laboratory, Kathmandu, Nepal.
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Źródło:
BMC medical genetics [BMC Med Genet] 2020 Sep 22; Vol. 21 (1), pp. 185. Date of Electronic Publication: 2020 Sep 22.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Mutation, Missense*
Blindness/*genetics
Congenital Abnormalities/*genetics
Eye Diseases/*genetics
Genetic Predisposition to Disease/*genetics
Adolescent ; Altitude ; Blindness/diagnosis ; Blindness/epidemiology ; Child ; Child, Preschool ; Congenital Abnormalities/diagnosis ; Congenital Abnormalities/epidemiology ; Cross-Sectional Studies ; Eye Diseases/diagnosis ; Eye Diseases/epidemiology ; Female ; Homeodomain Proteins/genetics ; Humans ; Infant ; Infant, Newborn ; Male ; Membrane Proteins/genetics ; Nepal/epidemiology ; Prevalence ; Transcription Factors/genetics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Wyświetlanie 41-60 z 5892

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