Results 1 to 10 of about 893,587 (215)

Agreement of Ocular Biometry Measured by LenStar LS 900 and CASIA2 Optical Coherence Tomography [PDF]

Reviews in Clinical Medicine, 2021
Introduction:The present study aimed to compare the anterior segment measurements between optical low-coherence reflectometry (LenStar LS900) and anterior segment optical coherence tomography (CASIA2 OCT). Methods:A total of 198 right eyes of 198 healthy
Maliheh Karimpour, Nasrin Moghadas Sharif, Naser Shoeibi, Negareh Yazdani, Asieh Ehsaei   +4 more
doaj   +1 more source

Medical errors can cost lives [PDF]

Archives of Medical Science
Consolato M. Sergi
doaj   +2 more sources

Learning from medical errors [PDF]

CVIR Endovascular
Joseph J. Gemmete
doaj   +2 more sources

Ocular changes in premature infants [PDF]

Reviews in Clinical Medicine, 2017
Introduction: This article aimed to review the literatures on visual impairments and ocular changes in premature infants with low birth weight and gestational age.Methods: Five electronic databases including: PubMed, Web of Science, Science direct, Ovid,
Negareh Yazdani, Leyla Shahkarami, Javad Heravian Shandiz, Veda Vakili, Hadi Ostadimoghaddam, AbbasAli Yekta, Seyed Hosein Hoseini-Yazdi   +6 more
doaj   +1 more source

The Correlation between Glucose and Lipid Biomarkers Variations with biometric characteristics and Intraocular Pressure Changes during Ramadan Fasting [PDF]

Journal of Fasting and Health, 2018
Introduction: The aim of present study was to assess the correlation between glucose and lipid biomarkers variations with biometric characteristics and intraocular pressure changes following Ramadan fasting.
Mohammad Reza Sedaghat, Nasrin Moghadas Sharif, Farshad Asgarizadeh, Tahereh Rakhshandadi, Javad Heravian Shandiz   +4 more
doaj   +1 more source

Comprehensive evaluation of dehydration impact on ocular tissue during Ramadan fasting [PDF]

Journal of Fasting and Health, 2015
Purpose: The present study aimed to review the effect of dehydration during Ramadan fasting on the health and ocular parameters leading to changes in eye function.
Javad Heravian, Mohsen Nematy, Negare Yazdani, Abbas Azimi, Hadi Ostadimoghaddam, Abbasali Yekta, Seyed Hosein Hoseini-Yazdi   +6 more
doaj   +3 more sources

Fatal pitfalls in newborn screening for mitochondrial trifunctional protein (MTP)/long-chain 3-Hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency

Orphanet Journal of Rare Diseases, 2018
Background Mitochondrial trifunctional protein (MTP) and long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency are long-chain fatty acid oxidation disorders with particularly high morbidity and mortality.
Amelie S. Lotz-Havla, Wulf Röschinger, Katharina Schiergens, Katharina Singer, Daniela Karall, Vassiliki Konstantopoulou, Saskia B. Wortmann, Esther M. Maier   +7 more
doaj   +1 more source

Part-time versus full-time occlusion therapy for treatment of amblyopia: A meta-analysis

Journal of Current Ophthalmology, 2017
Purpose: To compare full-time occlusion (FTO) and part-time occlusion (PTO) therapy in the treatment of amblyopia, with the secondary aim of evaluating the minimum number of hours of part-time patching required for maximal effect from occlusion. Methods:
Negareh Yazdani, Ramin Sadeghi, Hamed Momeni-Moghaddam, Leili Zarifmahmoudi, Asieh Ehsaei, Brendan T. Barrett   +5 more
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

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