Literature DB >> 5796281

Selective vitamin B 12 malabsorption with proteinuria in Israel: clinical and genetic aspects.

I Ben-Bassat, A Feinstein, B Ramot.   

Abstract

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Year:  1969        PMID： 5796281

Source DB:  PubMed          Journal:  Isr J Med Sci        ISSN： 0021-2180


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  11 in total

1.  Genetic markers in Libyan Jews.

Authors:  B Bonné-Tamir; S Ashbel; J Modai
Journal:  Hum Genet       Date:  1977-07-26       Impact factor: 4.132

2.  [Selective malabsorption of vitamin B12, proteinuria and hypogammaglobulinaemia -- a genetic defect (author's transl)].

Authors:  H Goebell; K Havemann
Journal:  Klin Wochenschr       Date:  1974-09-15

3.  Selective vitamin B12 malabsorption in two siblings.

Authors:  S Khakee; A Stachewitsch; M Katz
Journal:  Can Med Assoc J       Date:  1974-01-05       Impact factor: 8.262

Review 4.  Diseases of Jews.

Authors:  D M Krikler
Journal:  Postgrad Med J       Date:  1970-12       Impact factor: 2.401

5.  Familial selective malabsorption of vitamin B12.

Authors:  M Bell; J T Harries; O H Wolff; A M Dawson; A H Waters
Journal:  Arch Dis Child       Date:  1973-11       Impact factor: 3.791

6.  Selective intestinal malabsorption of vitamin B12 displays recessive mendelian inheritance: assignment of a locus to chromosome 10 by linkage.

Authors:  M Aminoff; E Tahvanainen; R Gräsbeck; J Weissenbach; H Broch; A de la Chapelle
Journal:  Am J Hum Genet       Date:  1995-10       Impact factor: 11.025

7.  Congenital B12-malabsorption without proteinuria.

Authors:  C Urban; I D Mutz; W Kaulfersch
Journal:  Blut       Date:  1981-08

8.  Selective vitamin B12 malabsorption (Imerslund-Gräsbeck syndrome). Studies on gastroenterological and nephrological problems.

Authors:  M Becker; H W Rotthauwe; H P Weber; H Fischbach
Journal:  Eur J Pediatr       Date:  1977-01-26       Impact factor: 3.183

9.  Canine Imerslund-Gräsbeck syndrome maps to a region orthologous to HSA14q.

Authors:  Qianchuan He; John C Fyfe; Alejandro A Schäffer; Adam Kilkenney; Petra Werner; Ewen F Kirkness; Paula S Henthorn
Journal:  Mamm Genome       Date:  2003-11       Impact factor: 2.957

10.  Imerslund-Gräsbeck syndrome in a 15-year-old German girl caused by compound heterozygous mutations in CUBN.

Authors:  Fabian H Hauck; Stephan M Tanner; Jobst Henker; Martin W Laass
Journal:  Eur J Pediatr       Date:  2007-08-01       Impact factor: 3.183
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