Literature DB >> 5220030

[Hepato-renal glycogenosis with complex tubulopathy. 2. Cases of a new entity].

M Odievre.   

Abstract

Entities:  

Mesh：

Year:  1966        PMID： 5220030

Source DB:  PubMed          Journal:  Rev Int Hepatol


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  9 in total

1.  A secondary respiratory chain defect in a patient with Fanconi-Bickel syndrome.

Authors:  M H Odièvre; A Lombès; P Dessemme; R Santer; M Brivet; B Chevallier; B Lagardère; M Odièvre
Journal:  J Inherit Metab Dis       Date:  2002-09       Impact factor: 4.982

2.  [Debré-De Toni-Fanconi syndrome with glycogenosis of the liver].

Authors:  B Bauer
Journal:  Klin Wochenschr       Date:  1968-03-15

3.  Normal kinetics of intestinal glucose absorption in the absence of GLUT2: evidence for a transport pathway requiring glucose phosphorylation and transfer into the endoplasmic reticulum.

Authors:  F Stümpel; R Burcelin; K Jungermann; B Thorens
Journal:  Proc Natl Acad Sci U S A       Date:  2001-09-18       Impact factor: 11.205

Review 4.  Type I glycogen storage disease: kidney involvement, pathogenesis and its treatment.

Authors:  Y T Chen
Journal:  Pediatr Nephrol       Date:  1991-01       Impact factor: 3.714

5.  Normal hepatic glucose production in the absence of GLUT2 reveals an alternative pathway for glucose release from hepatocytes.

Authors:  M T Guillam; R Burcelin; B Thorens
Journal:  Proc Natl Acad Sci U S A       Date:  1998-10-13       Impact factor: 11.205

6.  Fanconi-Bickel syndrome.

Authors:  F Manz; H Bickel; J Brodehl; D Feist; K Gellissen; B Geschöll-Bauer; G Gilli; E Harms; H Helwig; W Nützenadel
Journal:  Pediatr Nephrol       Date:  1987-07       Impact factor: 3.714

Review 7.  Glycogen storage diseases: new perspectives.

Authors:  Hasan Ozen
Journal:  World J Gastroenterol       Date:  2007-05-14       Impact factor: 5.742

8.  Diabetes-like renal glomerular disease in Fanconi-Bickel syndrome.

Authors:  G T Berry; L Baker; F S Kaplan; C L Witzleben
Journal:  Pediatr Nephrol       Date:  1995-06       Impact factor: 3.714

9.  Fanconi-Bickel syndrome versus osteogenesis imperfeeta: An Iranian case with a novel mutation in glucose transporter 2 gene, and review of literature.

Authors:  Fatemeh Hadipour; Peymaneh Sarkheil; Mehrdad Noruzinia; Zahra Hadipour; Taghi Baghdadi; Yousef Shafeghati
Journal:  Indian J Hum Genet       Date:  2013-01
  9 in total

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