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Tytuł :
[Using Trigger Tool to detect incidents and adverse events in a mutual insurance company that collaborate with the Social Security system].
Autorzy :
Ortner Sancho J; MC Mutual, Barcelona, Spain. .
Manzanera López R; MC Mutual, Barcelona, Spain.
Grau Balcells N; MC Mutual, Barcelona, Spain.
Moya Alcocer DJ; MC Mutual, Barcelona, Spain.
Farrús Esteban X; MC Mutual, Barcelona, Spain.
Martínez JM; MC Mutual, Barcelona, Spain.; Departamento de Estadística e Investigación Operativa. Universitat Politècnica de Catalunya, Barcelona, Spain.; Grupo de Investigación en Salud Pública. Universidad de Alicante, Alicante, Spain.
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Transliterated Title :
Uso del Trigger Tool para la Detección de Incidentes y Eventos Adversos en una Mutua Colaboradora con la Seguridad Social.
Źródło :
Archivos de prevencion de riesgos laborales [Arch Prev Riesgos Labor] 2020 Jul 15; Vol. 23 (3), pp. 343-356. Date of Electronic Publication: 2020 Jul 15.
Typ publikacji :
Journal Article
MeSH Terms :
Medical Errors*/prevention & control
Medical Errors*/statistics & numerical data
Patient Safety*/statistics & numerical data
Social Security*
Accidents, Occupational/prevention & control ; Accidents, Occupational/statistics & numerical data ; Diagnostic Errors/prevention & control ; Diagnostic Errors/statistics & numerical data ; Humans ; Male ; Precipitating Factors
Czasopismo naukowe
Tytuł :
Assessment of candidate variants causative of inborn metabolic diseases in SUDI cases in South Africa, and a case report.
Autorzy :
Heathfield LJ; Division of Forensic Medicine and Toxicology, Department of Pathology, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa. .; MRC/UCT Research Unit for Genomic and Precision Medicine, Division of Human Genetics, Institute of Infectious Diseases and Molecular Medicine, Department of Pathology, University of Cape Town, Cape Town, South Africa. .
Bhengu W; Division of Forensic Medicine and Toxicology, Department of Pathology, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.; MRC/UCT Research Unit for Genomic and Precision Medicine, Division of Human Genetics, Institute of Infectious Diseases and Molecular Medicine, Department of Pathology, University of Cape Town, Cape Town, South Africa.
Louw S; MRC/UCT Research Unit for Genomic and Precision Medicine, Division of Human Genetics, Institute of Infectious Diseases and Molecular Medicine, Department of Pathology, University of Cape Town, Cape Town, South Africa.
Martin LJ; Division of Forensic Medicine and Toxicology, Department of Pathology, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.
Ramesar R; MRC/UCT Research Unit for Genomic and Precision Medicine, Division of Human Genetics, Institute of Infectious Diseases and Molecular Medicine, Department of Pathology, University of Cape Town, Cape Town, South Africa.
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Źródło :
International journal of legal medicine [Int J Legal Med] 2020 Sep; Vol. 134 (5), pp. 1639-1645. Date of Electronic Publication: 2020 Jun 18.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Molecular Epidemiology*
Acyl-CoA Dehydrogenase/*genetics
Glutaryl-CoA Dehydrogenase/*genetics
Metabolism, Inborn Errors/*diagnosis
Metabolism, Inborn Errors/*epidemiology
Metabolism, Inborn Errors/*genetics
UTP-Hexose-1-Phosphate Uridylyltransferase/*genetics
Acyl-CoA Dehydrogenase/deficiency ; Adult ; DNA/isolation & purification ; Female ; Genetic Carrier Screening ; Genetic Loci ; Genotype ; Humans ; Infant ; Infant, Newborn ; Lipid Metabolism, Inborn Errors/genetics ; Male ; South Africa/epidemiology ; Sudden Infant Death/epidemiology
SCR Disease Name :
Medium chain acyl CoA dehydrogenase deficiency
Czasopismo naukowe
Tytuł :
[Treatment of common inborn errors of metabolism in the neonatal period].
Autorzy :
Mei YB; Neonatal Intensive Care Unit of Faculty of Pediatrics, Chinese People's Liberation Army (PLA) General Hospital,Neonatal Intensive Care Unit of BaYi Children's Hospital, the Seventh Medical Center of Chinese PLA General Hospital, Beijing 100700, China.
Feng ZC; Neonatal Intensive Care Unit of Faculty of Pediatrics, Chinese People's Liberation Army (PLA) General Hospital,Neonatal Intensive Care Unit of BaYi Children's Hospital, the Seventh Medical Center of Chinese PLA General Hospital, Beijing 100700, China.
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Źródło :
Zhonghua er ke za zhi = Chinese journal of pediatrics [Zhonghua Er Ke Za Zhi] 2021 May 02; Vol. 59 (5), pp. 431-433.
Typ publikacji :
Journal Article
MeSH Terms :
Amino Acid Metabolism, Inborn Errors*
Metabolism, Inborn Errors*/therapy
Humans ; Infant, Newborn ; Neonatal Screening
Czasopismo naukowe
Tytuł :
Impact of Refractive Errors on Da Vinci SI Robotic System.
Autorzy :
Tuna MB; Department of Urology, Acibadem Maslak Hospital, Istanbul, Turkey.
Kilavuzoglu AE; Department of Ophthalmology, Acibadem Mehmet Ali Aydinlar University Medical Faculty.
Mourmouris P; 2nd Department of Urology, National and Kapodistrian University of Athens, Sismanoglio Hospital.
Argun OB; Department of Urology, Acibadem Mehmet Ali Aydinlar University School of Medicine, Istanbul, Turkey.
Doganca T; Department of Urology, Acibadem Maslak Hospital.
Obek C; Department of Urology, Acibadem Mehmet Ali Aydinlar University School of Medicine, Istanbul, Turkey.
Ozisik O; Aix Marseille University, Inserm, MMG.
Kural AR; Department of Urology, Acibadem Mehmet Ali Aydinlar University School of Medicine, Istanbul, Turkey.
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Źródło :
JSLS : Journal of the Society of Laparoendoscopic Surgeons [JSLS] 2020 Jul-Sep; Vol. 24 (3).
Typ publikacji :
Journal Article
MeSH Terms :
Clinical Competence*
Refractive Errors*/diagnosis
Refractive Errors*/psychology
Refractive Errors*/therapy
Robotic Surgical Procedures*
Surgeons*
Visual Acuity*
Medical Errors/*prevention & control
Adolescent ; Adult ; Female ; Healthy Volunteers ; Humans ; Male ; Middle Aged ; Young Adult
Czasopismo naukowe
Tytuł :
Altered Metabolic Flexibility in Inherited Metabolic Diseases of Mitochondrial Fatty Acid Metabolism.
Autorzy :
Tucci S; Department of General Pediatrics, Adolescent Medicine and Neonatology, Faculty of Medicine, Medical Center-University of Freiburg, 79106 Freiburg, Germany.
Alatibi KI; Department of General Pediatrics, Adolescent Medicine and Neonatology, Faculty of Medicine, Medical Center-University of Freiburg, 79106 Freiburg, Germany.; Faculty of Biology, University of Freiburg, Schaenzlestrasse 1, 79104 Freiburg, Germany.
Wehbe Z; Department of General Pediatrics, Adolescent Medicine and Neonatology, Faculty of Medicine, Medical Center-University of Freiburg, 79106 Freiburg, Germany.; Center of Pediatric and Adolescent Medicine-Medical Center, Department of Pediatric Hematology and Oncology, Faculty of Medicine, University of Freiburg, 79106 Freiburg, Germany.
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Źródło :
International journal of molecular sciences [Int J Mol Sci] 2021 Apr 06; Vol. 22 (7). Date of Electronic Publication: 2021 Apr 06.
Typ publikacji :
Journal Article; Review
MeSH Terms :
Lipogenesis*
Congenital Bone Marrow Failure Syndromes/*metabolism
Fatty Acids/*metabolism
Lipid Metabolism, Inborn Errors/*metabolism
Metabolic Diseases/*metabolism
Mitochondria/*metabolism
Mitochondrial Diseases/*metabolism
Muscular Diseases/*metabolism
Animals ; Bacterial Proteins/metabolism ; Coenzyme A Ligases/deficiency ; Coenzyme A Ligases/metabolism ; Congenital Bone Marrow Failure Syndromes/genetics ; Congenital Bone Marrow Failure Syndromes/pathology ; Fatty Acids/genetics ; Humans ; Lipid Metabolism, Inborn Errors/genetics ; Lipid Metabolism, Inborn Errors/pathology ; Metabolic Diseases/genetics ; Metabolic Diseases/pathology ; Mice ; Mitochondria/genetics ; Mitochondria/pathology ; Mitochondrial Diseases/genetics ; Mitochondrial Diseases/pathology ; Muscular Diseases/genetics ; Muscular Diseases/pathology
SCR Disease Name :
VLCAD deficiency
Czasopismo naukowe
Tytuł :
Cause of recurrent rhabdomyolysis, carnitine palmitoyltransferase II deficiency and novel pathogenic mutation.
Autorzy :
Çakar NE; Department of Pediatric Metabolism, Okmeydanı Training and Research Hospital Istanbul, Turkey.
Gör Z; Department of Pediatric Metabolism, Okmeydanı Training and Research Hospital Istanbul, Turkey.
Yeşil G; Department of Medical Genetics, Bezmialem Vakif University Istanbul, Turkey.
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Transliterated Title :
Új patogén mutáció következtében kialakuló karnitin-palmitoil-transzferáz II-hiánnyal magyarázható ismétlődő rhabdomyolysis.
Źródło :
Ideggyogyaszati szemle [Ideggyogy Sz] 2021 Mar 30; Vol. 74 (3-4), pp. 135-138.
Typ publikacji :
Case Reports
MeSH Terms :
Metabolism, Inborn Errors*/complications
Metabolism, Inborn Errors*/genetics
Rhabdomyolysis*/genetics
Adolescent ; Carnitine O-Palmitoyltransferase/deficiency ; Carnitine O-Palmitoyltransferase/genetics ; Humans ; Male ; Mutation
SCR Disease Name :
Carnitine palmitoyl transferase 2 deficiency
Raport
Tytuł :
Sitosterolemia: Twenty Years of Discovery of the Function of ABCG5 ABCG8 .
Autorzy :
Williams K; Department of Pharmaceutical Sciences, College of Pharmacy, University of Kentucky, Lexington, KY 40536, USA.
Segard A; Department of Pharmaceutical Sciences, College of Pharmacy, University of Kentucky, Lexington, KY 40536, USA.
Graf GA; Department of Pharmaceutical Sciences, College of Pharmacy, University of Kentucky, Lexington, KY 40536, USA.; Saha Cardiovascular Research Center, Lexington, KY 40536, USA.; Barnstable Brown Diabetes and Obesity Center, Lexington, KY 40536, USA.
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Źródło :
International journal of molecular sciences [Int J Mol Sci] 2021 Mar 05; Vol. 22 (5). Date of Electronic Publication: 2021 Mar 05.
Typ publikacji :
Historical Article; Journal Article; Review
MeSH Terms :
ATP Binding Cassette Transporter, Subfamily G, Member 5*/genetics
ATP Binding Cassette Transporter, Subfamily G, Member 5*/history
ATP Binding Cassette Transporter, Subfamily G, Member 5*/metabolism
ATP Binding Cassette Transporter, Subfamily G, Member 8*/genetics
ATP Binding Cassette Transporter, Subfamily G, Member 8*/history
ATP Binding Cassette Transporter, Subfamily G, Member 8*/metabolism
Hypercholesterolemia*/genetics
Hypercholesterolemia*/history
Hypercholesterolemia*/metabolism
Hypercholesterolemia*/pathology
Intestinal Diseases*/genetics
Intestinal Diseases*/history
Intestinal Diseases*/metabolism
Intestinal Diseases*/pathology
Lipid Metabolism, Inborn Errors*/genetics
Lipid Metabolism, Inborn Errors*/history
Lipid Metabolism, Inborn Errors*/metabolism
Lipid Metabolism, Inborn Errors*/pathology
Lipoproteins*/genetics
Lipoproteins*/history
Lipoproteins*/metabolism
Mutation*
Cholesterol/*metabolism
Phytosterols/*adverse effects
Animals ; Enterocytes/metabolism ; Enterocytes/pathology ; Hepatocytes/metabolism ; Hepatocytes/pathology ; History, 21st Century ; Humans ; Phytosterols/genetics ; Phytosterols/history ; Phytosterols/metabolism
SCR Disease Name :
Sitosterolemia
Czasopismo naukowe
Tytuł :
The effects of pharmacological accommodation and cycloplegia on axial length and choroidal thickness.
Autorzy :
Bahar A; Ophthalmology Department, Pamukkale University, Denizli, Turkey.
Pekel G; Ophthalmology Department, Pamukkale University, Denizli, Turkey.
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Źródło :
Arquivos brasileiros de oftalmologia [Arq Bras Oftalmol] 2021 Mar-Apr; Vol. 84 (2), pp. 107-112.
Typ publikacji :
Journal Article
MeSH Terms :
Eye Color*
Refractive Errors*/chemically induced
Refractive Errors*/drug therapy
Accommodation, Ocular ; Adult ; Cyclopentolate/pharmacology ; Eye ; Humans ; Mydriatics/pharmacology ; Refraction, Ocular
Czasopismo naukowe
Tytuł :
Twenty common errors in the diagnosis and treatment of periprosthetic joint infection.
Autorzy :
Li C; Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Center for Musculoskeletal Surgery (CMSC), Charitéplatz 1, 10117, Berlin, Germany.
Renz N; Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Center for Musculoskeletal Surgery (CMSC), Charitéplatz 1, 10117, Berlin, Germany.
Trampuz A; Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Center for Musculoskeletal Surgery (CMSC), Charitéplatz 1, 10117, Berlin, Germany. .
Ojeda-Thies C; Department of Traumatology and Orthopedic Surgery, Hospital Universitario 12 de Octubre, Madrid, Spain.
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Źródło :
International orthopaedics [Int Orthop] 2020 Jan; Vol. 44 (1), pp. 3-14. Date of Electronic Publication: 2019 Oct 22.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't; Review
MeSH Terms :
Medical Errors*
Prosthesis-Related Infections/*diagnosis
Prosthesis-Related Infections/*therapy
Aged ; Anti-Bacterial Agents/administration & dosage ; Biomarkers/blood ; Blood Sedimentation ; C-Reactive Protein/analysis ; Debridement ; Diagnostic Errors ; Female ; Humans ; Male ; Middle Aged ; Prosthesis-Related Infections/blood ; Prosthesis-Related Infections/microbiology ; Reoperation ; Synovial Fluid/microbiology ; Therapeutic Irrigation ; Treatment Outcome
Czasopismo naukowe
Tytuł :
Twenty Common Mistakes Made in Daily Clinical Practice.
Autorzy :
Frishman WH; Department of Medicine, New York Medical College, Valhalla, NY; Westchester Medical Center Health Care System, Valhalla, NY.
Alpert JS; Professor of Medicine, University of Arizona Department of Medicine, Tucson; Editor in Chief, The American Journal of Medicine. Electronic address: .
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Źródło :
The American journal of medicine [Am J Med] 2020 Jan; Vol. 133 (1), pp. 1-3. Date of Electronic Publication: 2019 Jul 23.
Typ publikacji :
Editorial
MeSH Terms :
Medical Errors*
Practice Patterns, Physicians'*
Diagnostic Errors ; Humans
Opinia redakcyjna
Tytuł :
[Newborn Screening Program in the Community of Madrid: evaluation of positive cases.]
Autorzy :
Cambra Conejero A; Laboratorio de Cribado Neonatal de la Comunidad de Madrid. Servicio de Bioquímica Clínica. Hospital General Universitario Gregorio Marañón. Madrid. España.
Martínez Figueras L; Laboratorio de Cribado Neonatal de la Comunidad de Madrid. Servicio de Bioquímica Clínica. Hospital General Universitario Gregorio Marañón. Madrid. España.
Ortiz Temprado A; Laboratorio de Cribado Neonatal de la Comunidad de Madrid. Servicio de Bioquímica Clínica. Hospital General Universitario Gregorio Marañón. Madrid. España.
Blanco Soto P; Laboratorio de Cribado Neonatal de la Comunidad de Madrid. Servicio de Bioquímica Clínica. Hospital General Universitario Gregorio Marañón. Madrid. España.
Martín Rivada Á; Sección de Gastroenterología y Nutrición. Hospital Infantil Universitario Niño Jesús. Madrid. España.
Palomino Pérez L; Sección de Gastroenterología y Nutrición. Hospital Infantil Universitario Niño Jesús. Madrid. España.
Cañedo Villarroya E; Sección de Gastroenterología y Nutrición. Hospital Infantil Universitario Niño Jesús. Madrid. España.
Pedrón Giner C; Sección de Gastroenterología y Nutrición. Hospital Infantil Universitario Niño Jesús. Madrid. España.
Quijada Fraile P; Unidad de Enfermedades Mitocondriales-Metabólicas Hereditarias. Centro de Referencia Nacional (CSUR) y Europeo (MetabERN) en Enfermedades Metabólicas. Hospital Universitario 12 de Octubre. Madrid. España.
Martín-Hernández E; Unidad de Enfermedades Mitocondriales-Metabólicas Hereditarias. Centro de Referencia Nacional (CSUR) y Europeo (MetabERN) en Enfermedades Metabólicas. Hospital Universitario 12 de Octubre. Madrid. España.
García Silva MT; Unidad de Enfermedades Mitocondriales-Metabólicas Hereditarias. Centro de Referencia Nacional (CSUR) y Europeo (MetabERN) en Enfermedades Metabólicas. Hospital Universitario 12 de Octubre. Madrid. España.
Chumillas Calzada S; Unidad de Enfermedades Mitocondriales-Metabólicas Hereditarias. Centro de Referencia Nacional (CSUR) y Europeo (MetabERN) en Enfermedades Metabólicas. Hospital Universitario 12 de Octubre. Madrid. España.
Bellusci M; Unidad de Enfermedades Mitocondriales-Metabólicas Hereditarias. Centro de Referencia Nacional (CSUR) y Europeo (MetabERN) en Enfermedades Metabólicas. Hospital Universitario 12 de Octubre. Madrid. España.
Belanger-Quintana A; Centro de Referencia Nacional (CSUR) en Enfermedades Metabólicas. Hospital Universitario Ramón y Cajal. Madrid. España.
Stanescu S; Centro de Referencia Nacional (CSUR) en Enfermedades Metabólicas. Hospital Universitario Ramón y Cajal. Madrid. España.
Martínez-Pardo Casanova M; Centro de Referencia Nacional (CSUR) en Enfermedades Metabólicas. Hospital Universitario Ramón y Cajal. Madrid. España.
Moráis López A; Unidad de Nutrición Infantil y Enfermedades Metabólicas. Hospital Universitario La Paz. Madrid. España.
Bergua Martínez A; Unidad de Nutrición Infantil y Enfermedades Metabólicas. Hospital Universitario La Paz. Madrid. España.
Ruiz-Salas P; Centro de Diagnóstico de Enfermedades Moleculares. Universidad Autónoma de Madrid. IdiPAZ. CIBERER. Madrid. España.
Pérez González B; Centro de Diagnóstico de Enfermedades Moleculares. Universidad Autónoma de Madrid. IdiPAZ. CIBERER. Madrid. España.
Ugarte M; Centro de Diagnóstico de Enfermedades Moleculares. Universidad Autónoma de Madrid. IdiPAZ. CIBERER. Madrid. España.
Ruano MLF; Laboratorio de Cribado Neonatal de la Comunidad de Madrid. Servicio de Bioquímica Clínica. Hospital General Universitario Gregorio Marañón. Madrid. España.
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Transliterated Title :
Análisis de casos positivos de cribado neonatal de errores congénitos del metabolismo en la Comunidad de Madrid.
Źródło :
Revista espanola de salud publica [Rev Esp Salud Publica] 2020 Dec 16; Vol. 94. Date of Electronic Publication: 2020 Dec 16.
Typ publikacji :
Journal Article
MeSH Terms :
Acyl-CoA Dehydrogenase/*deficiency
Amino Acid Metabolism, Inborn Errors/*diagnosis
Lipid Metabolism, Inborn Errors/*diagnosis
Neonatal Screening/*methods
Tandem Mass Spectrometry/*methods
Amino Acid Metabolism, Inborn Errors/epidemiology ; Carnitine/analogs & derivatives ; Carnitine/blood ; Cities ; Female ; Humans ; Infant, Newborn ; Lipid Metabolism, Inborn Errors/epidemiology ; Male ; Predictive Value of Tests ; Prevalence ; Spain
SCR Disease Name :
Medium chain acyl CoA dehydrogenase deficiency
Czasopismo naukowe
Tytuł :
Critical Incidents Involving the Medical Emergency Team: A 5-Year Retrospective Assessment for Healthcare Improvement.
Autorzy :
Danielis M
Destrebecq A
Terzoni S
Palese A
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Źródło :
Dimensions of critical care nursing : DCCN [Dimens Crit Care Nurs] 2021 May-Jun 01; Vol. 40 (3), pp. 186-191.
Typ publikacji :
Journal Article
MeSH Terms :
Medical Errors*
Risk Management*
Delivery of Health Care ; Emergency Service, Hospital ; Humans ; Retrospective Studies
Czasopismo naukowe
Tytuł :
Re: Re: Surviving clinical errors in practice.
Autorzy :
Gartrell B; Wildbase, Tāwharau Ora, School of Veterinary Science, Massey University, Palmerston North, New Zealand.
White B; Wildbase, Tāwharau Ora, School of Veterinary Science, Massey University, Palmerston North, New Zealand.
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Źródło :
New Zealand veterinary journal [N Z Vet J] 2021 May; Vol. 69 (3), pp. 190-191. Date of Electronic Publication: 2021 Mar 10.
Typ publikacji :
Journal Article; Comment
MeSH Terms :
Medical Errors*/veterinary
Animals
Czasopismo naukowe
Tytuł :
Clinical Implication of Diagnostic and Histopathologic Discrepancies in Sinonasal Malignancies.
Autorzy :
Choi KY; Department of Otolaryngology Head and Neck Surgery, The Pennsylvania State University, College of Medicine, Hershey, Pennsylvania, U.S.A.
Amit M; Department of Head and Neck Surgery, University of Texas MD Anderson Cancer Center, Houston, Texas, U.S.A.
Tam S; Department of Head and Neck Surgery, University of Texas MD Anderson Cancer Center, Houston, Texas, U.S.A.
Bell D; Department of Head and Neck Surgery, University of Texas MD Anderson Cancer Center, Houston, Texas, U.S.A.
Phan J; Department of Radiation Oncology, University of Texas MD Anderson Cancer Center, Houston, Texas, U.S.A.
Garden AS; Department of Head and Neck Surgery, University of Texas MD Anderson Cancer Center, Houston, Texas, U.S.A.
Williams MD; Department of Pathology, University of Texas MD Anderson Cancer Center, Houston, Texas, U.S.A.
Ferrarotto R; Department of Thoracic, Head and Neck Medical Oncology, University of Texas MD Anderson Cancer Center, Houston, Texas, U.S.A.
El-Naggar AK; Department of Pathology, University of Texas MD Anderson Cancer Center, Houston, Texas, U.S.A.
Raza SM; Department of Head and Neck Surgery, University of Texas MD Anderson Cancer Center, Houston, Texas, U.S.A.
DeMonte F; Department of Neurosurgery, University of Texas MD Anderson Cancer Center, Houston, Texas, U.S.A.
Kupferman ME; Department of Head and Neck Surgery, University of Texas MD Anderson Cancer Center, Houston, Texas, U.S.A.
Hanna EY; Department of Head and Neck Surgery, University of Texas MD Anderson Cancer Center, Houston, Texas, U.S.A.
Su SY; Department of Head and Neck Surgery, University of Texas MD Anderson Cancer Center, Houston, Texas, U.S.A.
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Źródło :
The Laryngoscope [Laryngoscope] 2021 May; Vol. 131 (5), pp. E1468-E1475. Date of Electronic Publication: 2020 Sep 18.
Typ publikacji :
Journal Article
MeSH Terms :
Carcinoma/*diagnosis
Carcinoma, Neuroendocrine/*diagnosis
Diagnostic Errors/*statistics & numerical data
Maxillary Sinus Neoplasms/*diagnosis
Paranasal Sinus Neoplasms/*diagnosis
Paranasal Sinuses/*pathology
Sarcoma/*diagnosis
Adolescent ; Adult ; Aged ; Aged, 80 and over ; Carcinoma/epidemiology ; Carcinoma/pathology ; Carcinoma/therapy ; Carcinoma, Neuroendocrine/epidemiology ; Carcinoma, Neuroendocrine/pathology ; Carcinoma, Neuroendocrine/therapy ; Child ; Child, Preschool ; Diagnostic Errors/prevention & control ; Female ; Humans ; Incidence ; Kaplan-Meier Estimate ; Male ; Maxillary Sinus Neoplasms/epidemiology ; Maxillary Sinus Neoplasms/pathology ; Maxillary Sinus Neoplasms/therapy ; Middle Aged ; Neoplasm Staging ; Paranasal Sinus Neoplasms/epidemiology ; Paranasal Sinus Neoplasms/pathology ; Paranasal Sinus Neoplasms/therapy ; Referral and Consultation/statistics & numerical data ; Retrospective Studies ; Sarcoma/epidemiology ; Sarcoma/pathology ; Sarcoma/therapy ; Young Adult
SCR Disease Name :
Sinonasal undifferentiated carcinoma
Czasopismo naukowe
Tytuł :
Gerstmann-Sträussler-Scheinker syndrome misdiagnosed as cervical spondylotic myelopathy: A case report with 5-year follow-up.
Autorzy :
Cao L; Department of Neurology, The First Affiliated Hospital of Shenzhen University.; Department of Neurology, The Third Affiliated Hospital of Shenzhen University.
Feng H; Department of Neurology, The First Affiliated Hospital of Shenzhen University.; Department of Neurology, Shenzhen Second People's Hospital.
Huang X; Department of Gastroenterology, Shiyan People's Hospital, Shenzhen, China.
Yi J; Department of Neurology, The Third Affiliated Hospital of Shenzhen University.
Zhou Y; Department of Neurology, The First Affiliated Hospital of Shenzhen University.
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Źródło :
Medicine [Medicine (Baltimore)] 2021 Apr 23; Vol. 100 (16), pp. e25687.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Diagnostic Errors*
Gerstmann-Straussler-Scheinker Disease/*diagnosis
Spinal Cord Diseases/*diagnosis
Spondylosis/*diagnosis
Brain/pathology ; Cervical Vertebrae/pathology ; Follow-Up Studies ; Gerstmann-Straussler-Scheinker Disease/genetics ; Humans ; Male ; Middle Aged ; Mutation ; Prion Proteins/genetics ; Syndrome
Czasopismo naukowe
Tytuł :
Update on the Diagnostic Pitfalls of Autopsy and Post-Mortem Genetic Testing in Cardiomyopathies.
Autorzy :
Grassi S; Department of Health Surveillance and Bioethics, Section of Legal Medicine, Fondazione Policlinico A. Gemelli IRCCS, Università Cattolica del Sacro Cuore, 00168 Rome, Italy.
Campuzano O; Centro de Investigación Biomédica en Red de Enfermedades Cardiovasculares (CIBERCV), 28029 Madrid, Spain.; Cardiovascular Genetics Center, Institut d'Investigació Biomèdica Girona (IDIBGI), University of Girona, 17190 Girona, Spain.; Medical Science Department, School of Medicine, University of Girona, 17003 Girona, Spain.
Coll M; Centro de Investigación Biomédica en Red de Enfermedades Cardiovasculares (CIBERCV), 28029 Madrid, Spain.; Cardiovascular Genetics Center, Institut d'Investigació Biomèdica Girona (IDIBGI), University of Girona, 17190 Girona, Spain.; Medical Science Department, School of Medicine, University of Girona, 17003 Girona, Spain.
Cazzato F; Department of Health Surveillance and Bioethics, Section of Legal Medicine, Fondazione Policlinico A. Gemelli IRCCS, Università Cattolica del Sacro Cuore, 00168 Rome, Italy.
Sarquella-Brugada G; Medical Science Department, School of Medicine, University of Girona, 17003 Girona, Spain.; Arrhythmias Unit, Hospital Sant Joan de Déu, University of Barcelona, 08950 Barcelona, Spain.
Rossi R; Department of Health Surveillance and Bioethics, Section of Legal Medicine, Fondazione Policlinico A. Gemelli IRCCS, Università Cattolica del Sacro Cuore, 00168 Rome, Italy.
Arena V; Area of Pathology, Department of Woman and Child Health and Public Health, Fondazione Policlinico Universitario A. Gemelli IRCCS, 00147 Rome, Italy.; Istituto di Anatomia Patologica, Università Cattolica del Sacro Cuore, 00168 Rome, Italy.
Brugada J; Centro de Investigación Biomédica en Red de Enfermedades Cardiovasculares (CIBERCV), 28029 Madrid, Spain.; Arrhythmias Unit, Hospital Sant Joan de Déu, University of Barcelona, 08950 Barcelona, Spain.; Institut Clínic Cardiovascular (ICCV), Hospital Clínic, Universitat de Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), 08036 Barcelona, Spain.
Brugada R; Centro de Investigación Biomédica en Red de Enfermedades Cardiovasculares (CIBERCV), 28029 Madrid, Spain.; Cardiovascular Genetics Center, Institut d'Investigació Biomèdica Girona (IDIBGI), University of Girona, 17190 Girona, Spain.; Medical Science Department, School of Medicine, University of Girona, 17003 Girona, Spain.
Oliva A; Department of Health Surveillance and Bioethics, Section of Legal Medicine, Fondazione Policlinico A. Gemelli IRCCS, Università Cattolica del Sacro Cuore, 00168 Rome, Italy.
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Źródło :
International journal of molecular sciences [Int J Mol Sci] 2021 Apr 16; Vol. 22 (8). Date of Electronic Publication: 2021 Apr 16.
Typ publikacji :
Journal Article; Review
MeSH Terms :
Diagnostic Errors*
Cardiomyopathies/*genetics
Death, Sudden, Cardiac/*pathology
Genetic Testing/*methods
Biopsy/methods ; Biopsy/standards ; Cardiomyopathies/pathology ; Forensic Medicine/methods ; Forensic Medicine/standards ; Genetic Testing/standards ; Humans
Czasopismo naukowe
Tytuł :
Misinterpretation of viral load in COVID-19 clinical outcomes.
Autorzy :
Miranda RL; Neuropathology and Molecular Genetics Laboratory, Instituto Estadual do Cérebro Paulo Niemeyer, Rio de Janeiro, RJ, Brazil.
Guterres A; Neuropathology and Molecular Genetics Laboratory, Instituto Estadual do Cérebro Paulo Niemeyer, Rio de Janeiro, RJ, Brazil. Electronic address: .
de Azeredo Lima CH; Neuropathology and Molecular Genetics Laboratory, Instituto Estadual do Cérebro Paulo Niemeyer, Rio de Janeiro, RJ, Brazil.
Filho PN; Instituto Estadual do Cérebro Paulo Niemeyer, Rio de Janeiro, RJ, Brazil.
Gadelha MR; Neuropathology and Molecular Genetics Laboratory, Instituto Estadual do Cérebro Paulo Niemeyer, Rio de Janeiro, RJ, Brazil; Neuroendocrinology Research Center, Endocrinology Division, - Medical School and Hospital Universitário Clementino Fraga Filho - Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
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Źródło :
Virus research [Virus Res] 2021 Apr 15; Vol. 296, pp. 198340. Date of Electronic Publication: 2021 Feb 13.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Diagnostic Errors*
Viral Load*
COVID-19/*virology
Nasopharynx/*virology
SARS-CoV-2/*isolation & purification
COVID-19/diagnosis ; Humans ; RNA, Viral/analysis ; Real-Time Polymerase Chain Reaction
Czasopismo naukowe
Tytuł :
[Clinical features and gene mutations of 6 patients with carnitine palmitoyltransferase 1A deficiency].
Autorzy :
Yu Y; Department of Pediatric Endocrinology and Genetic Metabolism, Shanghai Xinhua Children's Hospital, Shanghai Institute for Pediatric Research, Xinhua Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200092, China.
Shen LH; Department of Pediatric Endocrinology and Genetic Metabolism, Henan Children's Hospital, Zhengzhou 450000, China.
Qiu WJ; Department of Pediatric Endocrinology and Genetic Metabolism, Shanghai Xinhua Children's Hospital, Shanghai Institute for Pediatric Research, Xinhua Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200092, China.
Zhang HW; Department of Pediatric Endocrinology and Genetic Metabolism, Shanghai Xinhua Children's Hospital, Shanghai Institute for Pediatric Research, Xinhua Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200092, China.
Ye J; Department of Pediatric Endocrinology and Genetic Metabolism, Shanghai Xinhua Children's Hospital, Shanghai Institute for Pediatric Research, Xinhua Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200092, China.
Liang LL; Department of Pediatric Endocrinology and Genetic Metabolism, Shanghai Xinhua Children's Hospital, Shanghai Institute for Pediatric Research, Xinhua Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200092, China.
Wang Y; Department of Pediatric Endocrinology and Genetic Metabolism, Shanghai Xinhua Children's Hospital, Shanghai Institute for Pediatric Research, Xinhua Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200092, China.
Ji WJ; Department of Pediatric Endocrinology and Genetic Metabolism, Shanghai Xinhua Children's Hospital, Shanghai Institute for Pediatric Research, Xinhua Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200092, China.
Gu XF; Department of Pediatric Endocrinology and Genetic Metabolism, Shanghai Xinhua Children's Hospital, Shanghai Institute for Pediatric Research, Xinhua Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200092, China.
Han LS; Department of Pediatric Endocrinology and Genetic Metabolism, Shanghai Xinhua Children's Hospital, Shanghai Institute for Pediatric Research, Xinhua Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200092, China.
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Źródło :
Zhonghua yi xue za zhi [Zhonghua Yi Xue Za Zhi] 2021 Apr 13; Vol. 101 (14), pp. 1041-1044.
Typ publikacji :
Journal Article
MeSH Terms :
Hypoglycemia*
Lipid Metabolism, Inborn Errors*/genetics
Aged ; Carnitine ; Carnitine O-Palmitoyltransferase/genetics ; Child ; Child, Preschool ; Female ; Humans ; Infant ; Infant, Newborn ; Male ; Mutation ; Neonatal Screening
Czasopismo naukowe
Tytuł :
Establishing Prediction Intervals for the SpeedWheel Acuity Test in Adults and Children.
Autorzy :
Luethy ML; Department of Strabismus, Neuroophthalmology and Pediatric Ophthalmology, Universitätsspital Basel Augenklinik, Basel, Switzerland.
Schötzau A; Ophthalmology, Universitätsspital Basel Augenklinik, Basel, Switzerland.
Palmowski-Wolfe A; Ophthalmology, Universitätsspital Basel Augenklinik, Basel, Switzerland.
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Transliterated Title :
Erhebung von Vorhersageintervallen für den SpeedWheel-Sehtest für Erwachsene und Kinder.
Źródło :
Klinische Monatsblatter fur Augenheilkunde [Klin Monbl Augenheilkd] 2021 Apr; Vol. 238 (4), pp. 488-492. Date of Electronic Publication: 2021 Apr 14.
Typ publikacji :
Journal Article
MeSH Terms :
Amblyopia*/diagnosis
Refractive Errors*
Adolescent ; Adult ; Aged ; Aged, 80 and over ; Child ; Child, Preschool ; Female ; Humans ; Male ; Middle Aged ; Prospective Studies ; Vision Tests ; Visual Acuity ; Young Adult
Czasopismo naukowe

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