نتایج جستجو برای: clinical type

تعداد نتایج: 2362523  

Journal: : 2022

Glutaric aciduria type 1 (glutaryl-CoA dehydrogenase deficiency, glutaric acidemia 1) (OMIM 231670) is an autosomal recessive disease caused by mutations in the gene encoding enzyme glutaryl-CoA (GCDH). Glutaryl-CoA (GCDH) plays important role degradation metabolism of L-lysine, L-hydroxylysine and L-tryptophan. The insufficiency or absence leads to accumulation by-products such amino acids as ...

Journal: :Point of Care: The Journal of Near-Patient Testing & Technology 2017

Journal: :Biomedical Journal of Scientific & Technical Research 2017

Journal: :Gastroenterology 1980

F GHALAMKARPOUR, P TOOSI,

In a prospective clinical trial, the incidence of scrotal tongue in psoriatic patients was studied. One hundred psoriatics and the same number of non-psoriatic individuals were evaluated for the incidence of fissured tongue, age, duration of illness, and clinical types of psoriasis. In this study 49 psoriatic patients (49%) and 28 non-psoriatic persons (28%) had fissured tongue. The most c...

Journal: :medical journal of islamic republic of iran 0
alireza monajemi philosophy of science department, institute for humanities and cultural studies, tehran, iran. minoo yaghmaei medical school, shahid beheshti university of medical sciences & school of medical education sciences, shahid beheshti univer-sity of medical sciences, tehran, iran.

most contemporary clinical reasoning tests typically assess non-automatic thinking. therefore, a test is needed to measure automatic reasoning or pattern recognition, which has been largely neglected in clinical reasoning tests. the puzzle test (pt) is dedicated to assess automatic clinical reasoning in routine situations. this test has been introduced first in 2009 by monajemi et al in the oly...

Journal: :future of medical education journal 0
mani mirfeizi department of midwifery, karaj branch, islamic azad university, karaj, iran zahra mehdizadeh tourzani department of midwifery, karaj branch, islamic azad university, karaj, iran touran bahrami babaheydari department of nursing, albourz university of medical sciences, karaj, iran seyedeh zahra mirfeizi rheumatic diseases research center, department of rheumatology, mashhad university of medical sciences, mashhad, iran mohammad asghari jafarabadi medical education research center, department of statistics and epidemiology, tabriz university of medical sciences, tabriz, iran mahyar mirheidar research management, mashhad university of medical sciences, mashhad, iran

background: objective structured clinical examination (osce) is one of the best methods of evaluating the achievement of domains such as educational objectives and cognitive, emotional, and psycho-motor aspects of medical students. according to available evidences, no study has been conducted  on the evaluating of osce in midwifery students. the main purpose of this study was the evaluation of ...

رشیدی قادر , فریبا, طالع , علی, علایی , عبدالرسول, مجتهدزاده , فریدون,

Mucopolysaccharidosis type maroteaux-lamy is a very rare hereditary disease. The disease is marked by the deficiency of the lysosomal enzyme N-Acetyl galactosamine-a-4-sulfate sulfatase (arylsulfatase B). It is inherited as an autosomal recessive trait. The most clinical manifestations are: corneal clouding, organomegaly, hernias, coarse facial features, cardiac insufficiency and skeletal abn...

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