نتایج جستجو برای: iranian families
تعداد نتایج: 162129 فیلتر نتایج به سال:
Background: Pontocerebellar hypoplasia is an autosomal recessive and neurodegenerative disorder divided into sixteen subtypes. type 2B (PCH2B) shows microcephaly combined with epilepsy extrapyramidal dyskinesia chorea due to different homozygous or compound heterozygous pathogenic mutations in the TSEN2 gene. Objectives: This study was aimed find mutation responsible for pontocerebellar two fam...
A phytochemical screening of fifty five Iranian plants belonging to 21 families was carried out. A qualitative phytochemical analysis was performed for the presence of alkaloids, tannins, saponins and flavonoids. The medicinal uses of these plants are also reported.
A phytochemical screening of fifty five Iranian plants belonging to 21 families was carried out. A qualitative phytochemical analysis was performed for the presence of alkaloids, tannins, saponins and flavonoids. The medicinal uses of these plants are also reported.
Autosomal dominant polycystic kidney disease (ADPKD) is the most common genetic nephropathy, which is characterized by replacement of renal parenchyma with multiple cysts. In Iran, the disease prevalence within the chronic hemodialysis patient population is approximately 8-10%. So far, three genetic loci have been identified to be responsible for ADPKD. Little information is available concernin...
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