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10 in total

1. Hyperhomocysteinemia from trimethylation of hepatic phosphatidylethanolamine during cholesterol cholelithogenesis in inbred mice.

Authors: Ji Zhang; Diane E Handy; Yufang Wang; Guylaine Bouchard; Jacob Selhub; Joseph Loscalzo; Martin C Carey
Journal: Hepatology Date: 2011-06-23 Impact factor: 17.425

Review 2. The skin in genetically-controlled metabolic disorders.

Authors: P C Newbold
Journal: J Med Genet Date: 1973-06 Impact factor: 6.318

3. The pathogenesis of folic acid deficiency in man.

Authors: D G Weir
Journal: Ir J Med Sci Date: 1974-01 Impact factor: 1.568

4. Homocystinuria. Reduced folate levels during pyridoxine treatment.

Authors: B Wilcken; B Turner
Journal: Arch Dis Child Date: 1973-01 Impact factor: 3.791

5. Homocystinuria.

Authors: N A Carson
Journal: Proc R Soc Med Date: 1970-01

6. Homocystinuria. Report of two cases in siblings.

Authors: I C Verma; S Sinclair
Journal: Indian J Pediatr Date: 1970-06 Impact factor: 1.967

7. Homocystinuria.

Authors: D C Cusworth; C E Dent
Journal: Biochem J Date: 1969-02 Impact factor: 3.857

Review 8. The role of vitamins in the pathogenesis and treatment of hyperhomocyst(e)inaemia.

Authors: J B Ubbink
Journal: J Inherit Metab Dis Date: 1997-06 Impact factor: 4.982

9. Homocystinuria due to cystathionine synthase deficiency. Studies of nitrogen balance and sulfur excretion.

Authors: J R Poole; S H Mudd; E B Conerly; W A Edwards
Journal: J Clin Invest Date: 1975-05 Impact factor: 14.808

10. Inborn errors of metabolism. Vitamin-responsive genetic disease.

Authors: S H Mudd
Journal: J Clin Pathol Suppl (R Coll Pathol) Date: 1974

10 in total