Congenital isolated defect of folic acid absorption-Reference-Cited by-同舟云学术

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Congenital isolated defect of folic acid absorption

Published:1973-03 Issue:3 Volume:82 Page:450-455
ISSN:0022-3476
Container-title:The Journal of Pediatrics
language:en
Short-container-title:The Journal of Pediatrics

Author:

Santiago-Borrero Pedro J.,Santini Rafael,Pérez-Santiago Enrique,Maldonado Norman,Millán Sara,Coll-Camález Graciela

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology, and Child Health

Reference24 articles.

1. The metabolic effects of intestinal resection in man;Booth;Postgrad. Med. J.,1961

2. The urinary excretion of orally administered tritium-labeled folic acid as a test of folic acid absorption;Klipstein;Blood,1963

3. The absorption and malabsorption of folic acid and its polyglutamates;Bernstein;Am. J. Med.,1970

4. Progress in gastroenterology: The digestion and absorption of dietary folate;Rosenberg;Gastroenterology,1971

5. Absorption of folic acid from the small intestine of the rat;Burgen;Br. J. Pharmacol.,1962

Cited by 45 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. The proton-coupled folate transporter (PCFT-SLC46A1) and the syndrome of systemic and cerebral folate deficiency of infancy: Hereditary folate malabsorption;Molecular Aspects of Medicine;2017-02

2. Molecular Genetics of Hereditary Folate Malabsorption;eLS;2016-01-15

3. CSF 5-Methyltetrahydrofolate Serial Monitoring to Guide Treatment of Congenital Folate Malabsorption Due to Proton-Coupled Folate Transporter (PCFT) Deficiency;JIMD Reports;2015

4. Prevalence of a Loss-of-Function Mutation in the Proton-Coupled Folate Transporter Gene (PCFT-SLC46A1) Causing Hereditary Folate Malabsorption in Puerto Rico;The Journal of Pediatrics;2011-10

5. Membrane transporters and folate homeostasis: intestinal absorption and transport into systemic compartments and tissues;Expert Reviews in Molecular Medicine;2009-01

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