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Wyszukujesz frazę ""Syndrome"" wg kryterium: Temat


Starter badań:

Tytuł:
An improved deep convolutional neural network architecture for chromosome abnormality detection using hybrid optimization model.
Autorzy:
Nimitha N; Department of ECE, RMK College of Engineering and Technology, Puduvoyal, India.
Ezhumalai P; Department of Computer Science and Engineering, RMD Engineering College, Chennai, India.
Chokkalingam A; Department of ECE, RMK College of Engineering and Technology, Puduvoyal, India.
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Źródło:
Microscopy research and technique [Microsc Res Tech] 2022 Sep; Vol. 85 (9), pp. 3115-3129. Date of Electronic Publication: 2022 Jun 16.
Typ publikacji:
Journal Article
MeSH Terms:
Down Syndrome*
Klinefelter Syndrome*
Turner Syndrome*
Chromosome Aberrations ; Humans ; Neural Networks, Computer ; Trisomy/genetics ; Trisomy 13 Syndrome ; Trisomy 18 Syndrome
Czasopismo naukowe
Tytuł:
Noninvasive Prenatal Screening for Trisomy 21 in Patients with a Vanishing Twin.
Autorzy:
Kleinfinger P; Laboratory CERBA, 7/11 Rue de l'Équerre, 95310 Saint-Ouen-l'Aumône, France.
Luscan A; Laboratory CERBA, 7/11 Rue de l'Équerre, 95310 Saint-Ouen-l'Aumône, France.
Descourvieres L; Obstetrics Center, Jeanne de Flandre Hospital, CHRU Lille, 59000 Lille, France.
Buzas D; Department of Obstetrics and Gynecology, René Dubos Hospital, 95300 Pontoise, France.
Boughalem A; Laboratory CERBA, 7/11 Rue de l'Équerre, 95310 Saint-Ouen-l'Aumône, France.
Serero S; Laboratory CERBA, 7/11 Rue de l'Équerre, 95310 Saint-Ouen-l'Aumône, France.
Valduga M; Laboratory CERBA, 7/11 Rue de l'Équerre, 95310 Saint-Ouen-l'Aumône, France.
Trost D; Laboratory CERBA, 7/11 Rue de l'Équerre, 95310 Saint-Ouen-l'Aumône, France.
Costa JM; Laboratory CERBA, 7/11 Rue de l'Équerre, 95310 Saint-Ouen-l'Aumône, France.
Vivanti AJ; Department of Obstetrics and Gynecology, DMU Santé des Femmes et des Nouveau-nés, Antoine Béclère Hospital, AP-HP, Université Paris Saclay, 92140 Clamart, France.
Lohmann L; Laboratory CERBA, 7/11 Rue de l'Équerre, 95310 Saint-Ouen-l'Aumône, France.
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Źródło:
Genes [Genes (Basel)] 2022 Nov 03; Vol. 13 (11). Date of Electronic Publication: 2022 Nov 03.
Typ publikacji:
Journal Article
MeSH Terms:
Down Syndrome*/diagnosis
Down Syndrome*/genetics
Noninvasive Prenatal Testing*
Pregnancy ; Female ; Humans ; Trisomy/diagnosis ; Trisomy/genetics ; Trisomy 18 Syndrome/diagnosis ; Trisomy 18 Syndrome/genetics ; Prenatal Diagnosis/methods ; Trisomy 13 Syndrome/diagnosis ; Trisomy 13 Syndrome/genetics
Czasopismo naukowe
Tytuł:
Circulating Endothelial Cells: A New Possible Marker of Endothelial Damage in Kawasaki Disease, Multisystem Inflammatory Syndrome in Children and Acute SARS-CoV-2 Infection.
Autorzy:
Fabi M; Pediatric Emergency Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, 40138 Bologna, Italy.
Petrovic B; Department of Medical and Surgical Sciences (DIMEC), University of Bologna, 40138 Bologna, Italy.; Center for Applied Biomedical Research (CRBA), University of Bologna, 40138 Bologna, Italy.
Andreozzi L; Pediatric Emergency Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, 40138 Bologna, Italy.
Corinaldesi E; Pediatric Unit, Ramazzini Hospital, 41012 Carpi, Italy.
Filice E; Specialty School of Pediatrics, Alma Mater Studiorum, University of Bologna, 40138 Bologna, Italy.
Biagi C; Pediatric Emergency Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, 40138 Bologna, Italy.
Rizzello A; Alma Mater Studiorum, University of Bologna, 40126 Bologna, Italy.
Mattesini BE; Alma Mater Studiorum, University of Bologna, 40126 Bologna, Italy.
Bugani S; Department of Medical and Surgical Sciences (DIMEC), University of Bologna, 40138 Bologna, Italy.; Center for Applied Biomedical Research (CRBA), University of Bologna, 40138 Bologna, Italy.
Lanari M; Pediatric Emergency Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, 40138 Bologna, Italy.
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Źródło:
International journal of molecular sciences [Int J Mol Sci] 2022 Sep 03; Vol. 23 (17). Date of Electronic Publication: 2022 Sep 03.
Typ publikacji:
Journal Article; Multicenter Study
MeSH Terms:
COVID-19*/complications
Mucocutaneous Lymph Node Syndrome*/complications
Mucocutaneous Lymph Node Syndrome*/diagnosis
Vascular System Injuries*
Biomarkers ; Child ; Endothelial Cells/pathology ; Humans ; Prospective Studies ; SARS-CoV-2 ; Systemic Inflammatory Response Syndrome/complications ; Systemic Inflammatory Response Syndrome/diagnosis
SCR Disease Name:
pediatric multisystem inflammatory disease, COVID-19 related
Czasopismo naukowe
Tytuł:
Impairment of cytokine production following immunological synapse formation in patients with Wiskott-Aldrich syndrome and leukocyte adhesion deficiency type 1.
Autorzy:
Sasahara Y; Department of Pediatrics, Tohoku University Graduate School of Medicine, Miyagi, Japan. Electronic address: .
Wada T; Department of Pediatrics, School of Medicine, Institute of Medical, Pharmaceutical and Health Sciences, Kanazawa University, Ishikawa, Japan.
Morio T; Department of Pediatrics and Developmental Biology, Graduate School of Medical Sciences, Tokyo Medical and Dental University, Tokyo, Japan.
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Źródło:
Clinical immunology (Orlando, Fla.) [Clin Immunol] 2022 Sep; Vol. 242, pp. 109098. Date of Electronic Publication: 2022 Aug 13.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Wiskott-Aldrich Syndrome*
Adolescent ; Cytokines ; Humans ; Immunological Synapses/metabolism ; Leukocyte-Adhesion Deficiency Syndrome ; Lymphocyte Activation ; Wiskott-Aldrich Syndrome Protein/genetics
SCR Disease Name:
Leukocyte adhesion deficiency type 1
Czasopismo naukowe
Tytuł:
Partial lipodystrophy, severe dyslipidaemia and insulin resistant diabetes as early signs of Werner syndrome.
Autorzy:
Atallah I; Division of Genetic Medicine, Lausanne University Hospital (CHUV) and University of Lausanne, Lausanne, Switzerland (Drs Atallah, Good, Superti-Furga, and Tran).
McCormick D; Centre for Cardiovascular Science, Queen's Medical Research Institute, University of Edinburgh, Edinburgh, United Kingdom of Great Britain and Northern Ireland (Drs McCormick and Semple).
Good JM; Division of Genetic Medicine, Lausanne University Hospital (CHUV) and University of Lausanne, Lausanne, Switzerland (Drs Atallah, Good, Superti-Furga, and Tran).
Barigou M; Endocrinology Diabetes and Metabolism Division, Lausanne University Hospital (CHUV), Lausanne, Switzerland (Dr Barigou).
Fraga M; Service of Gastroenterology and Hepatology, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland (Dr Fraga).
Sempoux C; Service of Clinical Pathology, Institute of Pathology, Lausanne University Hospital (CHUV) and University of Lausanne, Lausanne, Switzerland (Dr Sempoux).
Superti-Furga A; Division of Genetic Medicine, Lausanne University Hospital (CHUV) and University of Lausanne, Lausanne, Switzerland (Drs Atallah, Good, Superti-Furga, and Tran).
Semple RK; Centre for Cardiovascular Science, Queen's Medical Research Institute, University of Edinburgh, Edinburgh, United Kingdom of Great Britain and Northern Ireland (Drs McCormick and Semple). Electronic address: .
Tran C; Division of Genetic Medicine, Lausanne University Hospital (CHUV) and University of Lausanne, Lausanne, Switzerland (Drs Atallah, Good, Superti-Furga, and Tran). Electronic address: .
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Źródło:
Journal of clinical lipidology [J Clin Lipidol] 2022 Sep-Oct; Vol. 16 (5), pp. 583-590. Date of Electronic Publication: 2022 Jun 19.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Werner Syndrome*/diagnosis
Werner Syndrome*/genetics
Werner Syndrome*/complications
Lipodystrophy*
Diabetes Mellitus*/diagnosis
Diabetes Mellitus*/genetics
Insulin Resistance*/genetics
Dyslipidemias*/complications
Dyslipidemias*/diagnosis
Dyslipidemias*/genetics
Insulins*/metabolism
Female ; Humans ; Adult ; Werner Syndrome Helicase/genetics ; Werner Syndrome Helicase/metabolism ; RecQ Helicases/genetics ; RecQ Helicases/metabolism ; Exodeoxyribonucleases/genetics ; Exodeoxyribonucleases/metabolism
SCR Disease Name:
Lipodystrophy, Partial, Acquired
Czasopismo naukowe
Tytuł:
Coronavirus disease 2019-related Kawasaki syndrome: a case report.
Autorzy:
Aelami MH; Department of Pediatrics, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Malek A; Department of Pediatrics, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Saeidinia A; Department of Pediatrics, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran. .; Pharmaceutical Research Center, Fakouri Boulevard, Booali Research Center, Mashhad University of Medical Sciences, Mashhad, Iran. .
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Źródło:
Journal of medical case reports [J Med Case Rep] 2022 Nov 09; Vol. 16 (1), pp. 432. Date of Electronic Publication: 2022 Nov 09.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
COVID-19*/complications
Mucocutaneous Lymph Node Syndrome*/complications
Mucocutaneous Lymph Node Syndrome*/diagnosis
Coronary Aneurysm*/diagnostic imaging
Coronary Aneurysm*/etiology
Female ; Child ; Humans ; Iran ; Fever/etiology ; Abdominal Pain/etiology ; Systemic Inflammatory Response Syndrome
Czasopismo naukowe
Tytuł:
Congenital adrenal calcifications as the first clinical indication of sphingosine lyase insufficiency syndrome: A case report and review of the literature.
Autorzy:
Ron HA; Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Scobell R; Division of Nephrology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.; Department of Pediatrics, The Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Strong A; Division of Nephrology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Salazar EG; Division of Neonatalogy, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Ganetzky R; Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.; Department of Pediatrics, The Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
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Źródło:
American journal of medical genetics. Part A [Am J Med Genet A] 2022 Nov; Vol. 188 (11), pp. 3312-3317. Date of Electronic Publication: 2022 Aug 16.
Typ publikacji:
Case Reports; Review
MeSH Terms:
Adrenal Gland Diseases*
Adrenal Insufficiency*/diagnosis
Adrenal Insufficiency*/genetics
Calcinosis*/diagnosis
Calcinosis*/genetics
Lyases*
Nephrotic Syndrome*/pathology
Aldehyde-Lyases/genetics ; Child ; Female ; Humans ; Infant, Newborn ; Pregnancy ; Sphingosine ; Steroids ; Syndrome
Recenzja
Tytuł:
The Unique Experience of a New Multidisciplinary Program for 22q Deletion and Duplication Syndromes in a Community Hospital in Florida: A Reaffirmation That Multidisciplinary Care Is Essential for Best Outcomes in These Patients.
Autorzy:
Meneses Z; Charles E. Schmidt College of Medicine, Florida Atlantic University, Boca Raton, FL 33431, USA.
Durant J; Charles E. Schmidt College of Medicine, Florida Atlantic University, Boca Raton, FL 33431, USA.
Ale H; Department of Allergy and Immunology, Joe DiMaggio Children's Hospital, Hollywood, FL 33021, USA.
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Źródło:
Genes [Genes (Basel)] 2022 Oct 26; Vol. 13 (11). Date of Electronic Publication: 2022 Oct 26.
Typ publikacji:
Journal Article
MeSH Terms:
Hospitals, Community*
DiGeorge Syndrome*/genetics
Adult ; Child ; Male ; Female ; Humans ; Infant, Newborn ; Infant ; Child, Preschool ; Adolescent ; Young Adult ; Syndrome ; Florida ; Chromosome Duplication
Czasopismo naukowe
Tytuł:
Research on Werner Syndrome: Trends from Past to Present and Future Prospects.
Autorzy:
Tsuge K; Department of Regenerative Medicine Research, Faculty of Pharmaceutical Sciences, Sanyo-Onoda City University, 1-1-1 Daigaku-Street, Sanyo-Onoda Yamaguchi 756-0884, Japan.
Shimamoto A; Department of Regenerative Medicine Research, Faculty of Pharmaceutical Sciences, Sanyo-Onoda City University, 1-1-1 Daigaku-Street, Sanyo-Onoda Yamaguchi 756-0884, Japan.
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Źródło:
Genes [Genes (Basel)] 2022 Oct 06; Vol. 13 (10). Date of Electronic Publication: 2022 Oct 06.
Typ publikacji:
Journal Article; Review; Research Support, Non-U.S. Gov't
MeSH Terms:
Werner Syndrome*/genetics
Werner Syndrome*/therapy
Humans ; Werner Syndrome Helicase/genetics ; Werner Syndrome Helicase/metabolism ; RecQ Helicases/genetics ; Exodeoxyribonucleases/genetics ; Epigenesis, Genetic ; Phosphodiesterase I/genetics ; Phosphodiesterase I/metabolism ; DNA ; Chromosomal Instability ; Telomere-Binding Proteins/genetics
Czasopismo naukowe
Tytuł:
WT1 complete gonadal dysgenesis with membranoproliferative glomerulonephritis: case series and literature review.
Autorzy:
Anderson E; Queensland Fertility Group, Virtus Genetics, Brisbane, Australia.
Aldridge M; Department of Nephrology, The Queensland Children's Hospital, Brisbane, Australia.
Turner R; Monash IVF, The Wesley Hospital, Brisbane, Australia.
Harraway J; Mater Pathology, The Mater Hospital, Brisbane, Australia.
McManus S; Mater Pathology, The Mater Hospital, Brisbane, Australia.
Stewart A; Department of Anatomical Pathology, The Royal Brisbane and Women's Hospital, Brisbane, Australia.
Borzi P; Department of Paediatric Surgery and Urology, The Queensland Children's Hospital, Brisbane, Australia.; Department of Paediatrics, The Wesley Hospital, Brisbane, Australia.; The School of Medicine, The University of Queensland, Brisbane, Australia.
Trnka P; Department of Nephrology, The Queensland Children's Hospital, Brisbane, Australia.; The School of Medicine, The University of Queensland, Brisbane, Australia.
Burke J; Department of Nephrology, The Queensland Children's Hospital, Brisbane, Australia.; The School of Medicine, The University of Queensland, Brisbane, Australia.
Coman D; Queensland Fertility Group, Virtus Genetics, Brisbane, Australia. .; Department of Paediatrics, The Wesley Hospital, Brisbane, Australia. .; The School of Medicine, The University of Queensland, Brisbane, Australia. .; Department of Metabolic Medicine, The Queensland Children's Hospital, 501 Stanley Street, South Brisbane, QLD, 4101, Australia. .; The School of Medicine, Griffith University, Gold Coast, Australia. .
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Źródło:
Pediatric nephrology (Berlin, Germany) [Pediatr Nephrol] 2022 Oct; Vol. 37 (10), pp. 2369-2374. Date of Electronic Publication: 2022 Feb 24.
Typ publikacji:
Journal Article; Review
MeSH Terms:
Denys-Drash Syndrome*/genetics
Denys-Drash Syndrome*/pathology
Glomerulonephritis, Membranoproliferative*/genetics
Gonadal Dysgenesis*/genetics
Kidney Neoplasms*/genetics
Wilms Tumor*/genetics
Frasier Syndrome/genetics ; Genes, Wilms Tumor ; Humans ; Mutation ; WT1 Proteins/genetics
Czasopismo naukowe
Tytuł:
Amniotic band sequence in vascular Ehlers-Danlos Syndrome (EDS): Experience of the EDS National Diagnostic Services in the UK.
Autorzy:
Schirwani S; EDS National Diagnostic Service, Sheffield Children's NHS Foundation Trust, Sheffield, UK; Sheffield Clinical Genetics Service, Sheffield Children's NHS Foundation Trust, Sheffield, UK. Electronic address: .
van Dijk FS; National EDS Service London, London North West Healthcare NHS Trust, Harrow, London, UK.
Cauldwell M; Department of Obstetrics, St George's University Hospital, London, UK.
Harrison RE; Department of Clinical Genetics, Nottingham University Hospitals NHS Trust, Nottingham, UK.
Kraus A; Yorkshire Regional Genetic Service, Leeds Teaching Hospitals NHS Trust, Leeds, UK.
Brennan P; Northern Genetics Service, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
Ghali N; National EDS Service London, London North West Healthcare NHS Trust, Harrow, London, UK.
Lahiri N; Department Clinical Genetics, St George's University Hospital & St. George's University, London, UK.
Johnson D; EDS National Diagnostic Service, Sheffield Children's NHS Foundation Trust, Sheffield, UK; Sheffield Clinical Genetics Service, Sheffield Children's NHS Foundation Trust, Sheffield, UK.
Sobey G; EDS National Diagnostic Service, Sheffield Children's NHS Foundation Trust, Sheffield, UK; Sheffield Clinical Genetics Service, Sheffield Children's NHS Foundation Trust, Sheffield, UK.
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Źródło:
European journal of medical genetics [Eur J Med Genet] 2022 Oct; Vol. 65 (10), pp. 104592. Date of Electronic Publication: 2022 Aug 12.
Typ publikacji:
Journal Article; Review
MeSH Terms:
Ehlers-Danlos Syndrome*/diagnosis
Ehlers-Danlos Syndrome*/genetics
Amniotic Band Syndrome ; Collagen Type III/genetics ; Diagnostic Services ; Humans ; United Kingdom
SCR Disease Name:
Amniotic Band Sequence
Czasopismo naukowe
Tytuł:
Public awareness for "classic" childhood diseases and inflammatory syndromes in children during the COVID-19 pandemic.
Autorzy:
Zieger M; SRH Wald-Klinikum Gera GmbH, Gera, Germany.
Strzelecki A; University of Economics in Katowice, Department of Informatics, Katowice, Poland. Electronic address: .
Springer S; SRH Wald-Klinikum Gera GmbH, Gera, Germany.
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Źródło:
Journal of pediatric nursing [J Pediatr Nurs] 2022 Sep-Oct; Vol. 66, pp. 191-195. Date of Electronic Publication: 2022 Jul 11.
Typ publikacji:
Comparative Study; Journal Article
MeSH Terms:
COVID-19*/epidemiology
Mucocutaneous Lymph Node Syndrome*
Pandemics*
Systemic Inflammatory Response Syndrome*
Child ; Humans ; Syndrome
SCR Disease Name:
pediatric multisystem inflammatory disease, COVID-19 related
Czasopismo naukowe
Tytuł:
Nitazoxanide and COVID-19: A review.
Autorzy:
Al-Kuraishy HM; Department of Pharmacology, Toxicology and Medicine, College of Medicine, Al-Mustansiriyah University, Baghdad, 14132, Iraq.
Al-Gareeb AI; Department of Pharmacology, Toxicology and Medicine, College of Medicine, Al-Mustansiriyah University, Baghdad, 14132, Iraq.
Elekhnawy E; Pharmaceutical Microbiology Department, Faculty of Pharmacy, Tanta University, Tanta, 31527, Egypt. .
Batiha GE; Department of Pharmacology and Therapeutics, Faculty of Veterinary Medicine, Damanhour University, Damanhour, 22511, AlBeheira, Egypt.
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Źródło:
Molecular biology reports [Mol Biol Rep] 2022 Nov; Vol. 49 (11), pp. 11169-11176. Date of Electronic Publication: 2022 Sep 12.
Typ publikacji:
Journal Article; Review
MeSH Terms:
COVID-19*/drug therapy
Respiratory Distress Syndrome*
Acute Lung Injury*/drug therapy
Humans ; Cytokine Release Syndrome ; SARS-CoV-2 ; Antiviral Agents/pharmacology ; Antiviral Agents/therapeutic use ; Cytokines/metabolism
Czasopismo naukowe
Tytuł:
Fragile X-associated tremor or ataxia syndrome in a patient with difficulty walking, falls, a tremor, and erectile dysfunction.
Autorzy:
de Oliveira DS; Neurology Service, Hospital Universitário da Universidade Federal de Juiz de Fora, Juiz de Fora, Minas Gerais, Brazil.
Brandão AI; Neurology Service, Hospital Universitário da Universidade Federal de Juiz de Fora, Juiz de Fora, Minas Gerais, Brazil.
Vale TC; Neurology Service, Hospital Universitário da Universidade Federal de Juiz de Fora, Juiz de Fora, Minas Gerais, Brazil; Department of Internal Medicine, Universidade Federal de Juiz de Fora, Juiz de Fora, Minas Gerais, Brazil. Electronic address: .
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Źródło:
Lancet (London, England) [Lancet] 2022 Oct 01; Vol. 400 (10358), pp. 1144.
Typ publikacji:
Journal Article
MeSH Terms:
Erectile Dysfunction*/complications
Fragile X Syndrome*/complications
Fragile X Syndrome*/diagnosis
Ataxia/complications ; Humans ; Male ; Mobility Limitation ; Syndrome ; Tremor/complications
Czasopismo naukowe
Tytuł:
Humoral cross-coronavirus responses against the S2 region in children with Kawasaki disease.
Autorzy:
Monteiro A; Department of Pediatrics, University at Buffalo, Buffalo, NY, USA.
Chang AJ; Department of Pediatrics, University at Buffalo, Buffalo, NY, USA.
Welliver RR; Department of Pediatrics, University at Buffalo, Buffalo, NY, USA.
Baron S; Department of Pediatrics, University at Buffalo, Buffalo, NY, USA.
Hicar MD; Department of Pediatrics, University at Buffalo, Buffalo, NY, USA. Electronic address: .
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Źródło:
Virology [Virology] 2022 Oct; Vol. 575, pp. 83-90. Date of Electronic Publication: 2022 Sep 02.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't; Research Support, N.I.H., Extramural
MeSH Terms:
COVID-19*/complications
Mucocutaneous Lymph Node Syndrome*/pathology
Antibodies, Viral ; Child ; Humans ; SARS-CoV-2 ; Spike Glycoprotein, Coronavirus ; Systemic Inflammatory Response Syndrome
SCR Disease Name:
pediatric multisystem inflammatory disease, COVID-19 related
Czasopismo naukowe
Tytuł:
Effects of tocilizumab and dexamethasone on the downregulation of proinflammatory cytokines and upregulation of antioxidants in the lungs in oleic acid-induced ARDS.
Autorzy:
Terzi F; Department of Pathology, Faculty of Veterinary Medicine, Kastamonu University, Kuzeykent Campus, 37150, Kastamonu, Turkey. .
Demirci B; Department of Anatomy, Faculty of Veterinary Medicine, Kastamonu University, 37150, Kastamonu, Turkey.
Çınar İ; Department of Medicinal Pharmacology, Faculty of Medicine, Kastamonu University, 37150, Kastamonu, Turkey.
Alhilal M; Department of Nursing, Faculty of Health Sciences, Mardin Artuklu University, 47200, Mardin, Turkey.
Erol HS; Department of Biochemistry, Faculty of Veterinary Medicine, Kastamonu University, 37150, Kastamonu, Turkey.
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Źródło:
Respiratory research [Respir Res] 2022 Sep 17; Vol. 23 (1), pp. 249. Date of Electronic Publication: 2022 Sep 17.
Typ publikacji:
Journal Article
MeSH Terms:
Acute Lung Injury*/chemically induced
Acute Lung Injury*/drug therapy
Acute Lung Injury*/prevention & control
Respiratory Distress Syndrome*/chemically induced
Respiratory Distress Syndrome*/drug therapy
Animals ; Antibodies, Monoclonal, Humanized ; Antioxidants/adverse effects ; Cytokine Release Syndrome ; Cytokines/pharmacology ; Dexamethasone/pharmacology ; Down-Regulation ; Interleukin-6 ; Interleukin-8 ; Lung ; Male ; Oleic Acid/toxicity ; Rats ; Superoxide Dismutase ; Tumor Necrosis Factor-alpha/pharmacology ; Up-Regulation
Czasopismo naukowe
Tytuł:
WRN promotes bone development and growth by unwinding SHOX-G-quadruplexes via its helicase activity in Werner Syndrome.
Autorzy:
Tian Y; School of Biomedical Sciences, Faculty of Medicine, the Chinese University of Hong Kong, Shatin, N.T., Hong Kong SAR.
Wang W; School of Biomedical Sciences, Faculty of Medicine, the Chinese University of Hong Kong, Shatin, N.T., Hong Kong SAR.; CUHK-SDU University Joint Laboratory on Reproductive Genetics, the Chinese University of Hong Kong, Shatin, N.T., Hong Kong SAR.
Lautrup S; Department of Clinical Molecular Biology, University of Oslo and Akershus University Hospital, 1478, Lørenskog, Norway.
Zhao H; School of Biomedical Sciences, Faculty of Medicine, the Chinese University of Hong Kong, Shatin, N.T., Hong Kong SAR.; Hong Kong Branch CAS Center of Excellence for Animal Evolution and Genetics, the Chinese University of Hong Kong, Shatin, N.T., Hong Kong SAR.
Li X; CAS Key Laboratory of Tissue Microenvironment and Tumor, Shanghai Institute of Nutrition and Health, University of Chinese Academy of Sciences, Chinese Academy of Sciences, Shanghai, China.
Law PWN; School of Biomedical Sciences, Faculty of Medicine, the Chinese University of Hong Kong, Shatin, N.T., Hong Kong SAR.
Dinh ND; Department of Biomedical Engineering, the Chinese University of Hong Kong, Shatin, N.T., Hong Kong SAR.
Fang EF; Department of Clinical Molecular Biology, University of Oslo and Akershus University Hospital, 1478, Lørenskog, Norway.
Cheung HH; School of Biomedical Sciences, Faculty of Medicine, the Chinese University of Hong Kong, Shatin, N.T., Hong Kong SAR.
Chan WY; School of Biomedical Sciences, Faculty of Medicine, the Chinese University of Hong Kong, Shatin, N.T., Hong Kong SAR. .; CUHK-SDU University Joint Laboratory on Reproductive Genetics, the Chinese University of Hong Kong, Shatin, N.T., Hong Kong SAR. .; Hong Kong Branch CAS Center of Excellence for Animal Evolution and Genetics, the Chinese University of Hong Kong, Shatin, N.T., Hong Kong SAR. .
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Źródło:
Nature communications [Nat Commun] 2022 Sep 16; Vol. 13 (1), pp. 5456. Date of Electronic Publication: 2022 Sep 16.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
G-Quadruplexes*
Werner Syndrome*/genetics
Animals ; Bone Development ; DNA-Binding Proteins/metabolism ; Genes, Homeobox ; RecQ Helicases/genetics ; RecQ Helicases/metabolism ; Werner Syndrome Helicase/genetics ; Werner Syndrome Helicase/metabolism ; Zebrafish/genetics
Czasopismo naukowe
Tytuł:
Isolated Dysphagia Caused by Lateral Medullary Infarction: A Case of Atypical Avellis Syndrome.
Autorzy:
Zhu Q; Department of Neurology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Liang H; Department of Neurology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Zhu H; Department of Neurology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
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Źródło:
Neurology India [Neurol India] 2022 Sep-Oct; Vol. 70 (5), pp. 2258-2259.
Typ publikacji:
Case Reports; Letter
MeSH Terms:
Deglutition Disorders*/etiology
Lateral Medullary Syndrome*/complications
Lateral Medullary Syndrome*/diagnostic imaging
Humans ; Medulla Oblongata/diagnostic imaging ; Syndrome ; Infarction/complications
Raport
Tytuł:
Multisystem inflammatory syndrome in a young adult successfully treated with plasmapheresis, immunoglobulins, and corticosteroids: a case report.
Autorzy:
Sreckovic M; Department of Internal Medicine, Faculty of Medical Sciences, University of Kragujevac, Serbia; Clinic for Cardiology, University Clinical Center Kragujevac, Kragujevac, Serbia.
Marjanovic RR; Clinic for Infectious Diseases, University Clinical Center Kragujevac, Kragujevac, Serbia.
Jovicic BP; Clinic for Infectious Diseases, University Clinical Center Kragujevac, Kragujevac, Serbia; Department of Infectious Diseases, Faculty of Medical Sciences, University of Kragujevac, Kragujevac, Serbia.
Jankovic S; Department of Pharmacology, Faculty of Medical Sciences, University of Kragujevac, Kragujevac, Serbia; Department of Pharmacology, University Clinical Center Kragujevac, Kragujevac, Serbia.
Medovic R; Department of Pediatrics, Faculty of Medical Sciences, University of Kragujevac, Kragujevac, Serbia; Department of Pediatrics, University Clinical Center Kragujevac, Kragujevac, Serbia.
Cvetkovic MB; Department for Rheumatology, Clinic for Internal Medicine, University Clinical Center Kragujevac, Kragujevac, Serbia.
Lazarevic T; Department of Internal Medicine, Faculty of Medical Sciences, University of Kragujevac, Serbia; Department of Emergency Medicine, University Clinical Center Kragujevac, Kragujevac, Serbia.
Milosavljevic M; Department of Pathology, Faculty of Medical Sciences, University of Kragujevac, Kragujevac, Serbia; Department of Pathology, University Clinical Center Kragujevac, Kragujevac, Serbia.
Simovic S; Department of Internal Medicine, Faculty of Medical Sciences, University of Kragujevac, Serbia; Clinic for Cardiology, University Clinical Center Kragujevac, Kragujevac, Serbia. Electronic address: .
Vucic R; Department of Internal Medicine, Faculty of Medical Sciences, University of Kragujevac, Serbia; Clinic for Cardiology, University Clinical Center Kragujevac, Kragujevac, Serbia.
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Źródło:
International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases [Int J Infect Dis] 2022 Sep; Vol. 122, pp. 1052-1055. Date of Electronic Publication: 2022 Jul 28.
Typ publikacji:
Case Reports
MeSH Terms:
COVID-19*/therapy
Mucocutaneous Lymph Node Syndrome*
Adrenal Cortex Hormones/therapeutic use ; Adult ; Humans ; Immunoglobulins, Intravenous/therapeutic use ; Male ; Plasmapheresis ; Systemic Inflammatory Response Syndrome/complications ; Young Adult
Raport
Tytuł:
Efficacy of MSC in Patients with Severe COVID-19: Analysis of the Literature and a Case Study.
Autorzy:
Grumet M; W. M. Keck Center for Collaborative Neuroscience, Rutgers Stem Cell Research Center, Department of Cell Biology & Neuroscience, Rutgers University, Piscataway, NJ, USA.
Sherman J; W. M. Keck Center for Collaborative Neuroscience, Rutgers Stem Cell Research Center, Department of Cell Biology & Neuroscience, Rutgers University, Piscataway, NJ, USA.
Dorf BS; W. M. Keck Center for Collaborative Neuroscience, Rutgers Stem Cell Research Center, Department of Cell Biology & Neuroscience, Rutgers University, Piscataway, NJ, USA.; Department of Medicine, North Shore University Hospital, Manhasset, NY, USA.
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Źródło:
Stem cells translational medicine [Stem Cells Transl Med] 2022 Nov 18; Vol. 11 (11), pp. 1103-1112.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
COVID-19*
Mesenchymal Stem Cell Transplantation*/methods
Mesenchymal Stem Cells*
Respiratory Distress Syndrome*/therapy
Male ; Humans ; Aged, 80 and over ; SARS-CoV-2 ; Cytokine Release Syndrome ; Cytokines
Czasopismo naukowe

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