These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
104 related articles for article (PubMed ID: 8006671)
1. Methylenetetrahydrofolate reductase deficiency revealed by a neuropathy in a psychotic adult. Pasquier F; Lebert F; Petit H; Zittoun J; Marquet J J Neurol Neurosurg Psychiatry; 1994 Jun; 57(6):765-6. PubMed ID: 8006671 [No Abstract] [Full Text] [Related]
2. [An adult case of homocystinuria probably due to methylenetetrahydrofolate-reductase deficiency--treatment with folic acid and the course of coagulation-fibrinolysis parameters]. Hamano H; Nanba A; Nagayama M; Takizawa S; Shinohara Y Rinsho Shinkeigaku; 1996 Feb; 36(2):330-5. PubMed ID: 8752689 [TBL] [Abstract][Full Text] [Related]
3. Homocystinuria (methylenetetrahydrofolate reductase deficiency) and mutation of factor V gene. Goyette P; Rosenblatt D; Rozen R J Inherit Metab Dis; 1998 Aug; 21(6):690-1. PubMed ID: 9762613 [No Abstract] [Full Text] [Related]
4. Intermittent encephalopathy, reversible nerve conduction slowing, and MRI evidence of cerebral white matter disease in methylenetetrahydrofolate reductase deficiency. Walk D; Kang SS; Horwitz A Neurology; 1994 Feb; 44(2):344-7. PubMed ID: 8309589 [TBL] [Abstract][Full Text] [Related]
5. Rapid diagnosis and methionine administration: basis for a favourable outcome in a patient with methylene tetrahydrofolate reductase deficiency. Abeling NG; van Gennip AH; Blom H; Wevers RA; Vreken P; van Tinteren HL; Bakker HD J Inherit Metab Dis; 1999 May; 22(3):240-2. PubMed ID: 10384377 [No Abstract] [Full Text] [Related]
6. The pathogenesis of hydrocephalus in inborn errors of the single carbon transfer pathway. Rossi A; Biancheri R; Tortori-Donati P Neuropediatrics; 2001 Dec; 32(6):335-6. PubMed ID: 11870591 [No Abstract] [Full Text] [Related]
7. Methylenetetrahydrofolate reductase deficiency in a patient with phenotypic findings of Angelman syndrome. Arn PH; Williams CA; Zori RT; Driscoll DJ; Rosenblatt DS Am J Med Genet; 1998 May; 77(3):198-200. PubMed ID: 9605586 [TBL] [Abstract][Full Text] [Related]
17. Genetic predisposition to hyperhomocysteinemia: deficiency of methylenetetrahydrofolate reductase (MTHFR). Rozen R Thromb Haemost; 1997 Jul; 78(1):523-6. PubMed ID: 9198208 [No Abstract] [Full Text] [Related]
18. An early onset form of methylenetetrahydrofolate reductase deficiency: a report of a family from Kuwait. Al Tawari AA; Ramadan DG; Neubauer D; Heberle LC; Al Awadi F Brain Dev; 2002 Aug; 24(5):304-9. PubMed ID: 12142069 [TBL] [Abstract][Full Text] [Related]