Literature DB >> 5450108

Congenital malabsorption of folate.

P Lanzkowsky.   

Abstract

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Year:  1970        PMID： 5450108     DOI： 10.1016/0002-9343(70)90007-0

Source DB:  PubMed          Journal:  Am J Med        ISSN： 0002-9343            Impact factor:   4.965


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  10 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.  The pathogenesis of folic acid deficiency in man.

Authors:  D G Weir
Journal:  Ir J Med Sci       Date:  1974-01       Impact factor: 1.568

3.  Folate deficiency in cerebrospinal fluid associated with a defect in folate binding protein in the central nervous system.

Authors:  R A Wevers; S I Hansen; J L van Hellenberg Hubar; J Holm; M Høier-Madsen; P J Jongen
Journal:  J Neurol Neurosurg Psychiatry       Date:  1994-02       Impact factor: 10.154

Review 4.  Folate deficiency in acutely ill patients.

Authors:  E Lawlor; A Watson; J A Keogh
Journal:  Ir J Med Sci       Date:  1983-02       Impact factor: 1.568

5.  Intracranial calcification mimicking the Sturge-Weber syndrome: a consequence of cerebral folic acid deficiency?

Authors:  S Garwicz; W Mortensson
Journal:  Pediatr Radiol       Date:  1976-10-26

6.  Bilateral occipital calcification, epilepsy and coeliac disease: clinical and neuroimaging features of a new syndrome.

Authors:  A Magaudda; B Dalla Bernardina; P De Marco; Z Sfaello; M Longo; V Colamaria; O Daniele; G Tortorella; M A Tata; R Di Perri
Journal:  J Neurol Neurosurg Psychiatry       Date:  1993-08       Impact factor: 10.154

7.  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

8.  Inborn errors of metabolism. Vitamin-responsive genetic disease.

Authors:  S H Mudd
Journal:  J Clin Pathol Suppl (R Coll Pathol)       Date:  1974

9.  Reversible severe combined immunodeficiency phenotype secondary to a mutation of the proton-coupled folate transporter.

Authors:  Arturo Borzutzky; Brian Crompton; Anke K Bergmann; Silvia Giliani; Sachin Baxi; Madelena Martin; Ellis J Neufeld; Luigi D Notarangelo
Journal:  Clin Immunol       Date:  2009-09-09       Impact factor: 3.969

Review 10.  Cerebral Folate Deficiency Syndrome: Early Diagnosis, Intervention and Treatment Strategies.

Authors:  Vincent Th Ramaekers; Edward V Quadros
Journal:  Nutrients       Date:  2022-07-28       Impact factor: 6.706
  10 in total

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