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Imerslund-Gräsbeck syndrome (selective vitamin B12 malabsorption with proteinuria)
Ralph Gräsbeck
Orphanet J Rare Dis. 2006; 1: 17. Published online 2006 May 19. doi: 10.1186/1750-1172-1-17
PMCID:
PMC1513194
Abstract Full Text PDF–260K
 Is Cited by the Following 5 Articles in this Archive:
Ancient founder mutation is responsible for Imerslund-Gräsbeck Syndrome among diverse ethnicities
Cameron M Beech, Sandya Liyanarachchi, Nidhi P Shah, Amy C Sturm, May F Sadiq, Albert de la Chapelle, Stephan M Tanner
Orphanet J Rare Dis. 2011; 6: 74. Published online 2011 November 13. doi: 10.1186/1750-1172-6-74
PMCID:
PMC3226546
Abstract Full Text PDF–339K Supplementary Material
Luminal expression of cubilin is impaired in Imerslund-Gräsbeck syndrome with compound AMN mutations in intron 3 and exon 7
Fares Namour, Gabriele Dobrovoljski, Celine Chery, Sandra Audonnet, François Feillet, Wolfgang Sperl, Jean-Louis Gueant
Haematologica. 2011 November; 96(11): 1715–1719. doi: 10.3324/haematol.2011.043984
PMCID:
PMC3208692
Abstract Full Text PDF–835K
Unusual Cause of Childhood Anemia: Imerslund Grasbeck Syndrome
Kishan Prasad Hosapatna Laxminarayana, Sunil Kumar Yeshvanth, Jayaprakash K Shetty, Harish S Permi, Chandrika Rao
J Lab Physicians. 2011 Jul-Dec; 3(2): 113–115. doi: 10.4103/0974-2727.86845
PMCID:
PMC3249707
Abstract Full Text
Vitamin B12 deficiency in a 15-year old boy due to mutations in the intrinsic factor gene
Ulrik M. Overgaard, Stephan M. Tanner, Henrik S. Birgens
Br J Haematol. Author manuscript; available in PMC 2011 August 1.
Published in final edited form as: Br J Haematol. 2010 August; 150(3): 369–371. Published online 2010 April 12. doi: 10.1111/j.1365-2141.2010.08198.x
PMCID:
PMC2914612
Full Text PDF–45K
Juvenile cobalamin deficiency in individuals of African ancestry is caused by a founder mutation in the intrinsic factor gene GIF
Andrea E. Ament, Zhongyuan Li, Amy C. Sturm, James D. Perko, Sarah Lawson, Margaret Masterson, Edward V. Quadros, Stephan M. Tanner
Br J Haematol. Author manuscript; available in PMC 2010 February 1.
Published in final edited form as: Br J Haematol. 2009 February; 144(4): 622–624. Published online 2008 November 19. doi: 10.1111/j.1365-2141.2008.07496.x
PMCID:
PMC2636683
Full Text PDF–163K Supplementary Material
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