Found: 14
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Megaloblastic Anemia and Immune Abnormalities in a Patient with Methionine Synthase Deficiency.
- Published in:
- Acta Paediatrica, 1987, v. 76, n. 6, p. 991, doi. 10.1111/j.1651-2227.1987.tb17284.x
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- Publication type:
- Article
The Three Transcobalamins in Myeloproliferative Disorders and Acute Leukaemia.
- Published in:
- British Journal of Haematology, 1975, v. 31, n. 3, p. 287, doi. 10.1111/j.1365-2141.1975.tb00860.x
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- Publication type:
- Article
Folate metabolism disorder in Kearns-Sayre syndrome.
- Published in:
- Annals of Neurology, 1983, v. 13, n. 6, p. 687, doi. 10.1002/ana.410130624
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- Publication type:
- Article
Study of folate in psoriasis: blood levels, intestinal absorption and cutaneous loss.
- Published in:
- British Journal of Dermatology, 1973, v. 89, n. 4, p. 335
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- Publication type:
- Article
Iron Supplements versus Placebo during Pregnancy: Its Effects on Iron and Folate Status on Mothers and Newborns.
- Published in:
- Annals of Nutrition & Metabolism, 1983, v. 27, n. 4, p. 320, doi. 10.1159/000176693
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- Publication type:
- Article
Effect of Folate Deficiency on Vitamin B<sub>12</sub> Absorption.
- Published in:
- Annals of Nutrition & Metabolism, 1982, v. 26, n. 6, p. 367, doi. 10.1159/000176587
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- Publication type:
- Article
Reliability of biochemical parameters used in prenatal diagnosis of combined methylmalonic aciduria and homocystinuria.
- Published in:
- 1998
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- Publication type:
- journal article
Methylenetetrahydrofolate reductase deficiency: prenatal diagnosis and family studies.
- Published in:
- 1994
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- Publication type:
- journal article
Pharmacokinetics of (−)−folinic acid after oral and intravenous administration of the racemate.
- Published in:
- British Journal of Clinical Pharmacology, 1989, v. 28, n. 3, p. 289, doi. 10.1111/j.1365-2125.1989.tb05429.x
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- Publication type:
- Article
Haemolytic uraemic syndrome and pulmonary hypertension in a patient with methionine synthase deficiency.
- Published in:
- 1999
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- Publication type:
- journal article
Insidious peripheral neuropathy occurring under treatment in infantile MTHFR deficiency.
- Published in:
- Journal of Inherited Metabolic Disease, 2009, v. 32, p. 303, doi. 10.1007/s10545-009-1240-7
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- Publication type:
- Article
Impact of new mutations in the methylenetetrahydrofolate reductase gene assessed on biochemical phenotypes: A familial study.
- Published in:
- Journal of Inherited Metabolic Disease, 2001, v. 24, n. 8, p. 833, doi. 10.1023/A:1013988123902
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- Publication type:
- Article
A family study of congenital malabsorption of folate.
- Published in:
- Journal of Inherited Metabolic Disease, 2001, v. 24, n. 7, p. 749, doi. 10.1023/A:1012905823879
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- Publication type:
- Article
Thymidylate Synthesis in a Folate Deprived Cell Line.
- Published in:
- British Journal of Haematology, 1981, v. 49, n. 1, p. 87, doi. 10.1111/j.1365-2141.1981.tb07200.x
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- Publication type:
- Article