Results 11 to 20 of about 851,257 (308)

Determining factors of the cognitive outcome in early treated PKU: A study of 39 pediatric patients

Molecular Genetics and Metabolism Reports, 2019
Phenylketonuria (PKU) is a disorder of phenylalanine metabolism, characterized by a neurotoxic phenylalanine (Phe) accumulation, and treatable with a life-long Phe-restricted diet. Though early and continuously treated PKU (ETPKU) patients exhibit normal
Yvan Herenger, Emmanuelle Maes, Laurent François, Jeremy Pasco, Juliette Bouchereau, Samia Pichard, Hélène Ogier de Baulny, Manuel Schiff   +7 more
doaj   +1 more source

Structural Factors Underlying Medical Malpractice: From the Perspective of Social Science Experts and Medical Specialists [PDF]

Journal of Qualitative Research in Health Sciences, 2021
Introduction: Medical malpractice is generally attributed to the lack of individual competence of physicians, but from a sociological point of view, it is a problem that arises in a social context influenced by external factors and variables. The purpose
simin kazemi
doaj   +1 more source

“Double Hit” Homozygous Mutations for Two Different Rare Inborn Errors of Metabolism: A Burden for Countries with High Prevalences of Consangineous Marriages

Journal of Pediatric Research, 2018
Inborn errors of metabolism comprise a broad range of genetic diseases of which most are inherited in an autosomal recessive manner. Although being rare, there is a significant increase in their rate especially in countries where consanguineous marriages
Asburçe Olgaç, Leyla Tümer, Serdar Ceylaner, Gürsel Biberoğlu, Alev Hasanoğlu   +4 more
doaj   +1 more source

Comparison of cyclopentolate versus tropicamide cycloplegia: A systematic review and meta-analysis

Journal of Optometry, 2018
Purpose: The aim of the present meta-analysis is to compare the efficacy of cyclopentolate and tropicamide in controlling accommodation during refraction. Methods: A comprehensive literature search was performed in PubMed, Scopus, Science direct and Ovid
Negareh Yazdani, Ramin Sadeghi, Hamed Momeni-Moghaddam, Leili Zarifmahmoudi, Asieh Ehsaei   +4 more
doaj   +1 more source

Evaluating the effective factors for reporting medical errors among midwives working at teaching hospitals affiliated to Isfahan University of Medical Sciences

Iranian Journal of Nursing and Midwifery Research, 2017
Background: Recently, evaluation and accreditation system of hospitals has had a special emphasis on reporting malpractices and sharing errors or lessons learnt from errors, but still due to lack of promotion of systematic approach for solving problems ...
Fahimeh Khorasani, Marjan Beigi
doaj   +1 more source

Tragedy of Errors- An Analysis of Human Factor in Medical Errors [PDF]

Journal of Clinical and Diagnostic Research, 2020
William Shakespeare wrote a play “Comedy of error”, but this is about medical error which may often result in tragic outcome. We often read about medical errors and sometimes realise in our clinical practice that an error has been committed by us or our
Manika Agarwal, Sharat Agarwal
doaj   +1 more source

Retrospective Evaluation of Common Dentistry Errors in Selected Dental Clinics of the Armed Forces, Iran [PDF]

Journal of Research in Applied and Basic Medical Sciences, 2023
Background & Aims: The occurrence of errors in dental practice is an inevitable factor resulting in a reduction in the quality of medical services. These errors can prompt adverse complications, weaken the patient's trust in the dentist, and induce ...
Elahe Tahmasebi, Mohsen Yazdanian, Mahmood Salesi, Samira Hajisadeghi, Ehsan Moghadam   +4 more
doaj  

The genetic basis of classical galactosaemia in Polish patients

Orphanet Journal of Rare Diseases, 2021
Classic galactosemia (OMIM #230400) is an autosomal recessive disorder caused by homozygous or compound heterozygous pathogenic variants in the galactose-1-phosphate uridylyltransferase gene (GALT; 606999) on chromosome 9p13. Its diagnosis is established
Aleksandra Jezela-Stanek, Anna Bauer, Katarzyna Wertheim-Tysarowska, Jerzy Bal, Agnieszka Magdalena Rygiel, Jolanta Sykut-Cegielska   +5 more
doaj   +1 more source

Fucosidosis: clinical and molecular findings of Turkish patients

The Turkish Journal of Pediatrics, 2022
Background. Fucosidosis is a rare, autosomal recessive lysosomal storage disease caused by alpha L- fucosidase enzyme deficiency in all tissues. Here, we identify a patient with a novel homozygous pathogenic variant and atypical clinical findings ...
Merve Emecen Şanlı, Serap Uysal
doaj   +1 more source

Nutritional and Behavioral Intervention for Long‐Term Childhood Acute Leukemia Survivors With Metabolic Syndrome

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Purpose Metabolic syndrome (MetS) is a common complication in survivors of childhood acute lymphoblastic and myeloid leukemia (AL), and a major risk factor for premature cardiovascular disease, type‐2‐diabetes, and metabolic dysfunction‐associated steatotic liver disease (MASLD).
Visentin Sandrine, Béliard Sophie, Renard Cécile, Caussy Cyrielle, Hamidou Zeinab, Romano David, Gacem Mélanie, Petit Arnaud, Saultier Paul, Borentain Patrick, Michel Gérard   +10 more
wiley   +1 more source