Literature DB >> 6969796

Therapy of congenital folate malabsorption.

M Poncz, N Colman, V Herbert, E Schwartz, A R Cohen.   

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Year:  1981        PMID: 6969796     DOI: 10.1016/s0022-3476(81)80541-0

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


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  15 in total

1.  A family study of congenital malabsorption of folate.

Authors:  S Jebnoun; S Kacem; C H Mokrani; A Chabchoub; N Khrouf; J Zittoun
Journal:  J Inherit Metab Dis       Date:  2001-12       Impact factor: 4.982

2.  CSF 5-Methyltetrahydrofolate Serial Monitoring to Guide Treatment of Congenital Folate Malabsorption Due to Proton-Coupled Folate Transporter (PCFT) Deficiency.

Authors:  A Torres; S A Newton; B Crompton; A Borzutzky; E J Neufeld; L Notarangelo; G T Berry
Journal:  JIMD Rep       Date:  2015-05-26

3.  Temporal expression of genes involved in folate metabolism and transport during placental development, preeclampsia and neural tube defects.

Authors:  Palani Selvam Mohanraj; Beenish Rahat; Aatish Mahajan; Rashmi Bagga; Jyotdeep Kaur
Journal:  Mol Biol Rep       Date:  2019-04-02       Impact factor: 2.316

Review 4.  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

5.  Congenital isolated folic acid malabsorption.

Authors:  J Urbach; A Abrahamov; N Grossowicz
Journal:  Arch Dis Child       Date:  1987-01       Impact factor: 3.791

Review 6.  Megaloblastic anemia--etiology and management.

Authors:  A K Saraya; M K Gupta
Journal:  Indian J Pediatr       Date:  1987 May-Jun       Impact factor: 1.967

Review 7.  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

8.  The inability of oral leucovorin to elevate CSF 5-methyl-tetrahydrofolate following high dose intravenous methotrexate therapy.

Authors:  J Allen; G Rosen; H Juergens; B Mehta
Journal:  J Neurooncol       Date:  1983       Impact factor: 4.130

9.  A novel deletion mutation in the proton-coupled folate transporter (PCFT; SLC46A1) in a Nicaraguan child with hereditary folate malabsorption.

Authors:  N Diop-Bove; M Jain; F Scaglia; I D Goldman
Journal:  Gene       Date:  2013-06-28       Impact factor: 3.688

10.  Congenital folate malabsorption.

Authors:  L Corbeel; G Van den Berghe; J Jaeken; J Van Tornout; R Eeckels
Journal:  Eur J Pediatr       Date:  1985-03       Impact factor: 3.183

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