نتایج جستجو برای: 4 hydroxybutyric aciduria

تعداد نتایج: 1305100  

Journal: :Journal of Inherited Metabolic Disease 2008

Journal: :Journal of Clinical Investigation 1979

Journal: :Toxicology 2013
Noreen Yaqoob Andrew R Evans Edward A Lock

The industrial solvent trichloroethylene (TCE) has been reported to increase the excretion of formic acid in the urine of male Fischer 344 (F-344) rats following large oral doses. We have examined the dose-response relationship for formic aciduria in male and female Fischer 344 rats, the effect of some known metabolites of TCE and examined the response in male Wistar rats to help understand its...

Journal: :Acta Crystallographica Section E Structure Reports Online 2008

Journal: :Turk pediatri arsivi 2014
Osman Baştuğ Fatih Kardaş Mehmet Adnan Öztürk Hülya Halis Şeyma Memur Levent Korkmaz Zuhal Tağ Tamer Güneş

Fumaric aciduria is a rare autosomal recessive metabolic disease which is characterized with excessive fumaric acid exretion in urine. In the prenatal period, polyhydramniosis, intrauterine growth retardation, enlarged brain ventricles and brain anomalies are observed. Growth and development failure, hypotonia, seizures and brain atrophy are the common characteristics of patients with fumarase ...

Journal: :iranian journal of child neurology 0
zahra pirzadeh assistant professor of pediatric neurology, qazvin medical university of medical sciences, qazvin, iran

objectiveglutaric aciduria type 1 (gal 1) is a cerebral organic academia, which manifests as encephalopathy with long-term neurological handicap. in this study, clinical presentation, neuroimaging, molecular finding of cgdh mutation of our patients were reviewed.materials and methodsthis was a descriptive and cross-sectional study. patients in whom gla1 were suspected by clinical manifestation,...

Journal: :Anais da Academia Brasileira de Ciências 2015

Journal: :Diabetes care 2008
Robert M Cohen Tamara J LeCaire Christopher J Lindsell Eric P Smith Donn J D'Alessio

When estimating long-term glycemic control, A1C is considered the gold standard (1–3), but patients with seemingly equivalent A1C differ in their risk for microvascular complications (4,5). Recently, the “glycation gap,” defined as the difference between the measured A1C and that which would be predicted from another measure of glycemic control, fructosamine, has been proposed as a means of ide...

Journal: :Addiction 2013
Cornelis A J de Jong Rama Kamal Martijn van Noorden Barbara Broers

How do we formulate low‐risk drinking guidelines if zero consumption is lowest risk?

Journal: :The Journal of biological chemistry 1992
B L Schafer R W Bishop V J Kratunis S S Kalinowski S T Mosley K M Gibson R D Tanaka

Mevalonic aciduria is the first proposed inherited disorder of the cholesterol/isoprene biosynthetic pathway in humans, and it is presumed to be caused by a mutation in the gene coding for mevalonate kinase. To elucidate the molecular basis of this inherited disorder, a 2.0-kilobase human mevalonate kinase cDNA clone was isolated and sequenced. The 1188-base pair open reading frame coded for a ...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید