نتایج جستجو برای: deficiency syndrome

تعداد نتایج: 738061  

Journal: :acta medica iranica 0
m. pourissa s. refahi n. garaaghagi

the robert/sc (pseudothalidomide) syndrome is a rare autosomal recessive disorder, associated with phocomelia and craniofacial abnormalities. an anomalous fetus with lower limb phocomelia and micromelia, lumbar myeloschisis, upper limb and ribs defects and craniofacial abnormalities is reported whose diabetic mother took mebendazole and glibenclamide in early pregnancy. ultrasonographic finding...

Journal: :Mechanisms of Ageing and Development 2013

Journal: :Journal of Nepal Medical Association 2003

Journal: :Egyptian Journal of Chest Diseases and Tuberculosis 2014

Journal: :World of Irish nursing 1986
C Taafee

2012
Abdoljalal Marjani Sedigheh Moghasemi

In this study, we aimed to assess levels of serum 25-hydroxyvitamin D in relation to metabolic syndrome among postmenopausal women in Gorgan. The study group included 100 postmenopausal women who were referred to the different Health Centers in Gorgan. Body mass index, waist circumference, Hip, waist to hip ratio, diastolic blood pressure, triglyceride, fasting blood glucose and 25-hydroxyvitam...

Journal: :iranian red crescent medical journal 0
peyman petramfar department of neurology, school of medicine, shiraz university of medical sciences, shiraz, ir iran farideh hosseinzadeh student research committee, shiraz university of medical sciences, shiraz, ir iran s. saeed mohammadi student research committee, shiraz university of medical sciences, shiraz, ir iran; student research committee, shiraz university of medical sciences, shiraz, ir iran. tel: +98-9364402630, fax: +98-7733444844

conclusions demyelinating disease, anterior ischemic optic neuropathy, non-arteritic anterior ischemic optic neuropathy, autoimmune disease, and hereditary optic neuropathy could cause optic neuropathy. normal cbc parameters and the absence of clinical manifestations of vitamin b12 deficiency could not rule out its diagnosis. careful physical examinations and history-taking with a classical app...

Journal: :Proceedings of the Royal Society of Medicine 1946

2017

1. Children with proven growth hormone deficiency (GHD) 2. Children with height less than 3rd percentile for chronologic age with chronic renal insufficiency 3. Patients with AIDS wasting 4. Adults with proven GHD 5. Patients with Turner’s syndrome 6. Children with growth failure due to Prader-Willi syndrome 7. Patients with short stature due to Noonan syndrome 8. Promotion of wound healing in ...

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