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6 in total

Review 1. The proton-coupled folate transporter (PCFT-SLC46A1) and the syndrome of systemic and cerebral folate deficiency of infancy: Hereditary folate malabsorption.

Authors: Rongbao Zhao; Srinivas Aluri; I David Goldman
Journal: Mol Aspects Med Date: 2016-09-21

2. Mutation of the proton-coupled folate transporter gene (PCFT-SLC46A1) in Turkish siblings with hereditary folate malabsorption.

Authors: Berna Atabay; Meral Turker; Esra Arun Ozer; Kris Mahadeo; Ndeye Diop-Bove; I David Goldman
Journal: Pediatr Hematol Oncol Date: 2010-11 Impact factor: 1.969

Review 3. Membrane transporters and folate homeostasis: intestinal absorption and transport into systemic compartments and tissues.

Authors: Rongbao Zhao; Larry H Matherly; I David Goldman
Journal: Expert Rev Mol Med Date: 2009-01-28 Impact factor: 5.600

4. The spectrum of mutations in the PCFT gene, coding for an intestinal folate transporter, that are the basis for hereditary folate malabsorption.

Authors: Rongbao Zhao; Sang Hee Min; Andong Qiu; Antoinette Sakaris; Gary L Goldberg; Claudio Sandoval; J Jeffrey Malatack; David S Rosenblatt; I David Goldman
Journal: Blood Date: 2007-04-19 Impact factor: 22.113

5. The clinical course and genetic defect in the PCFT gene in a 27-year-old woman with hereditary folate malabsorption.

Authors: Sang Hee Min; Sun Young Oh; George I Karp; Mortimer Poncz; Rongbao Zhao; I David Goldman
Journal: J Pediatr Date: 2008-09 Impact factor: 4.406

Review 6. Drug treatment of inborn errors of metabolism: a systematic review.

Authors: Majid Alfadhel; Khalid Al-Thihli; Hiba Moubayed; Wafaa Eyaid; Majed Al-Jeraisy
Journal: Arch Dis Child Date: 2013-03-26 Impact factor: 3.791

6 in total