نتایج جستجو برای: hereditary enzymopathy

تعداد نتایج: 84335  

Journal: :iranian journal of blood and cancer 0
nazemi a molavi ma raeisi e

background: neonates affected by hereditary spherocytosis may suffer from significant jaundice. this study was conducted on neonates with jaundice hospitalized at the children’s hospital in bandar abbas, south iran, to determine the frequency of hereditary spherocytosis among them. patients and methods: in this cross-sectional study, 814 neonates with jaundice hospitalized at the children’s hos...

محمدی, شباهنگ, امام جمعه, حسام‌الدین, حسین‌نژاد یزدی, مریم, دانشی, احمد, فرهادی, محمد, یداله زاده, مهدی,

    Background & Aim: When inner ear is disturbed, both hearing sensitivity and selective property decrease. Early rehabilitation for proper progression of speech and language appropriate to age is mandatory. Several studies were performed to compare factors that affect the results of cochlear implantations to select the best candidates on the basis of different criteria. This study was underta...

Journal: :iranian red crescent medical journal 0
heidar sharafi baqiyatallah research center for gastroenterology and liver diseases, baqiyatallah university of medical sciences, tehran, ir iran; middle east liver diseases (meld) center, tehran, ir iran seyed moayed alavian baqiyatallah research center for gastroenterology and liver diseases, baqiyatallah university of medical sciences, tehran, ir iran; middle east liver diseases (meld) center, tehran, ir iran; middle east liver diseases (meld) center, p.o. box 14155/3651, tehran, ir iran. tel: +98-2188945186, fax: +98-2188945188

Journal: :genetics in the 3rd millennium 0
غلام علی شهیدی gholam ali shahidi assist prof of neurology, rasul akram hospital, iran university of medical sciences, tehran, iran محمد روحانی mohammad rohani

the hereditary ataxias comprise a wide spectrum of heterogeneous disorders that share three features: ataxia, involvement of cerebellum or its connections, and heritability. in many hereditary ataxias, the underlying gene mutations have been identified. knowledge of the causative mutations allows a rational classification of hereditary ataxias as autosomal recessive, autosomal dominant or mater...

Journal: :medical journal of islamic republic of iran 0
h pour-jafari from the departments o.f*genetics sciences. hamadan. i.r. iran. a sarihi

congenital cutis laxa is an exceptional condition. no large scale pedigree has been reported from iran. we report a family with 106 members with two members affected with cutis laxa. our cases were two patients (male and female) with pre- and postnatal growth retardation, cutis laxa, characteristic facies and other manifestations which proved that they were affected with cutis laxa. their famil...

Journal: :بینا 0
محمدحسین دهقان mh dehghan پاسداران- بوستان نهم- بیمارستان لبافی نژاد- مرکز تحقیقات چشم رضا سلیمانی زاد r soleimanzad پاسداران- بوستان نهم- بیمارستان لبافی نژاد- مرکز تحقیقات چشم حمید احمدیه h ahmadieh پاسداران- بوستان نهم- بیمارستان لبافی نژاد- مرکز تحقیقات چشم محسن آذرمینا m azarmina پاسداران- بوستان نهم- بیمارستان لبافی نژاد- مرکز تحقیقات چشم مسعود سهیلیان m soheilian پاسداران- بوستان نهم- بیمارستان لبافی نژاد- مرکز تحقیقات چشم سیامک مرادیان s moradian پاسداران- بوستان نهم- بیمارستان لبافی نژاد- مرکز تحقیقات چشم معصومه ثناگو

purpose: to evaluate the clinical manifestations and results of lensectomy in patients with hereditary lens subluxation at labbafinejad medical center, tehran-iran from 1996 t 2003. method: in an interventional case series, records of patients with hereditary lens subluxation who had undergone lensectomy were reviewed. patients with at least 6 months of follow up were included. background disea...

Journal: :iranian journal of public health 0
d.d. farhud; t.rezaie jami; m.r. khosh-sorour; m. islami; b.broumand

alport syndrome is a progressive hereditary nephritis leading to renal failure. nearly all of the documents declare that alport syndrome is inherited as x-linked dominant trait and reports of autosomal inheritance form is very rare. this paper presents an iranian large alport family with autosomal recessive inheritance. in our patients alport disease was confirmed with electron microscopic stud...

Journal: :journal of algebraic systems 2014
tayyebeh amouzegar

let $m$ be a right module over a ring $r$, $tau_m$ a preradical on $sigma[m]$, and$ninsigma[m]$. in this note we show that if $n_1, n_2in sigma[m]$ are two$tau_m$-lifting modules such that $n_i$ is $n_j$-projective ($i,j=1,2$), then $n=n_1oplusn_2$ is $tau_m$-lifting. we investigate when homomorphic image of a $tau_m$-lifting moduleis $tau_m$-lifting.

Journal: :iranian journal of otorhinolaryngology 0
bijan khademi department of otorhinolaryngology, shiraz institute for cancer research, shiraz university of medical sciences, shiraz, iran venon asefi otorhinolaryngologist, shiraz, iran mehdi tarzi otorhinolaryngologist, shiraz, iran

introduction: maxillary osteomyelitis is a rare phenomenon. if it occurs, evaluation for underlying disease especially osteopetrosis must be considered. osteomyelitis occurs as a complication in 10% of the cases of osteopetrosis. case report: this is a case report of maxillary osteomyelitis presented in a 15-year old boy with osteopetrosis.  in this case, the disease represented mainly with fac...

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