نتایج جستجو برای: mitochondrial disorders

تعداد نتایج: 792831  

Journal: :Biochimica et Biophysica Acta (BBA) - Bioenergetics 2010

Journal: :British Journal of Pharmacology 2014

Journal: :Frontiers in Cell and Developmental Biology 2020

Journal: :Middle East African Journal of Ophthalmology 2008

Journal: :JIMD reports 2012
Gloria P Duran A Martinez-Aguayo H Poggi M Lagos D Gutierrez P R Harris

BACKGROUND Mitochondrial diseases are a group of disorders caused by mutations in nuclear DNA or mitochondrial DNA, usually involving multiple organ systems. Primary adrenal insufficiency due to mitochondrial disease is extremely infrequent and has been reported in association with mitochondrial DNA deletion syndromes such as Kearns-Sayre syndrome. AIM To report a 3-year-old boy with Addison ...

Journal: :cell journal 0

introduction: a number of maternally inherited mitochondrial diseases with distinct clinical phenotypes have been associated with point mutations in mtdna, all of which result in neurologic or neuromuscular disorders. several studies showed that mutations in the trna genes of mtdna could cause mitochondrial disease due to the decreased synthesis of mitochondrial dna coded proteins. materials an...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید