نتایج جستجو برای: alport syndrorme
تعداد نتایج: 843 فیلتر نتایج به سال:
Glomerulopathies due to defective known genes are partially or completely reversed at 24 months without becoming a central source of information in the field clear change in creatinine clearance. Other reports deof mechanisms of progression of renal disease. Among scribed no effects of ACE inhibitor in few sporadic cases. hereditary diseases, Alport syndrome of glomerulopathy In this issue of K...
Alport posttransplantation anti-glomerular basement membrane (GBM) nephritis is mediated by alloantibodies against the noncollagenous (NC1) domains of the alpha3alpha4alpha5(IV) collagen network, which is present in the GBM of the allograft but absent from Alport kidneys. The specificity of kidney-bound anti-GBM alloantibodies from a patient who had autosomal recessive Alport syndrome (ARAS) an...
Families with 3 different syndromes characterized by autosomal dominant inheritance of low platelet count and giant platelets were studied. Fechtner syndrome is an autosomal-dominant variant of Alport syndrome manifested by nephritis, sensorineural hearing loss, and cataract formation in addition to macrothrombocytopenia and polymorphonuclear inclusion bodies. Sebastian platelet syndrome is an ...
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