GJ Hankey, P Eikelbloom, P Dusitanond… - Stroke, 2011 - espace.library.uq.edu.au Hankey, GJ, Eikelbloom, P, Dusitanond, P, Thom, J, Loh, K, van Bockxmeer, F and Jamrozik, K (2005) Homocysteine-lowering treatment with folic acid, cobalamin, and pyridoxine does not suppress blood markers of inflammation, endothelial dysfunction, or hypercoagulability in ... Cached - All 3 versions
S Stockler, B Plecko, SM Gospe Jr… - Molecular Genetics and …, 2011 - Elsevier Antiquitin (ATQ) deficiency is the main cause of pyridoxine dependent epilepsy characterized by early onset epileptic encephalopathy responsive to large dosages of pyridoxine. Despite seizure control most patients have intellectual disability. Folinic acid responsive seizures (FARS) ... Related articles - All 2 versions
J Cui, UA Leuenberger, C Blaha… - The Journal of …, 2011 - Physiological Soc During exercise, sympathetic nervous system activity increases and this contributes to an increase in blood pressure (ie exercise pressor reflex). Although animal studies suggest that purinergic P2 receptors on thin fibre sensory nerves are stimulated and evoke this reflex, human ... Related articles - All 4 versions
JSS Kwok, SLM Fung, GCY Lui, ELK Law… - Pathology, 2011 - journals.lww.com CBS is encoded by the CBS gene. Most of the CBS mutations are missense mutations, of which the vast majority are private mutations. 2 Most affected patients are compound heterozygotes of these private mutations. To our knowledge there are more than 150 pathogenic ... All 2 versions
NS Yeghiazaryan, P Striano, L Spaccini… - European Journal of …, 2011 - Elsevier Pyridoxine-dependent seizures (PDS; OMIM 266100) is rare autosomal recessive disorder characterized by recurrent seizures in the prenatal, neonatal, or postnatal period, and often death in untreated patients. [1] and [2] Affected neonates usually show hypothermia, jitteriness, ... Related articles - All 2 versions
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