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Scholar Results 1 - 10 of about 101 related to Beutler: The effect of HFE genotypes on measurements of iron overload in patients attending.... (0.14 sec) 

The effect of HFE genotypes on measurements of iron overload in patients attending a health …

- annals.org [PDF] 
E Beutler, V Felitti, T Gelbart, N Ho - Annals of internal medicine, 2000 - Am Coll Physicians
Page 1. The Effect of HFE Genotypes on Measurements of Iron Overload in
Patients Attending a Health Appraisal Clinic Ernest Beutler ...
Cited by 229 - Related articles - BL Direct - All 5 versions

EASL International Consensus Conference on Haemochromatosis, Part II. Expert Document


P Adams, P Brissot, L Powell - Journal of Hepatology, 2000 - gastrojournal.org
The precise frequency of the different iron overload states due to
haemochromatosis (HC) is unknown and need to be addressed in population studies
. The appropriate terminology for different iron overload states along the ...
Cited by 184 - Related articles - Cached - All 5 versions

HFE mutations analysis in 711 hemochromatosis probands: evidence for S65C implication …

- bloodjournal.org
C Mura, O Raguenes, C Ferec - Blood, 1999 - Am Soc Hematology
Hereditary hemochromatosis (HH) is a common autosomal recessive genetic disorder
of iron metabolism. The HFE candidate gene encoding an HLA class I-like protein
involved in HH was identified in 1996. Two missense mutations have been ...
Cited by 308 - Related articles - BL Direct - All 7 versions

A population-based study of the clinical expression of the hemochromatosis gene


JK Olynyk, DJ Cullen, S Aquilia, E Rossi, L … - The New England journal of medicine, 1999 - nejm.highwire.org
Background and Methods Hereditary hemochromatosis is associated with
homozygosity for the C282Y mutation in the hemochromatosis (HFE) gene on
chromosome 6, elevated serum transferrin saturation, and excess iron ...
Cited by 549 - Related articles - BL Direct - All 5 versions

Prevalence of C282Y and H63D mutations in the hemochromatosis (HFE) gene in the United …

- soso91.com [PDF] 
KK Steinberg, ME Cogswell, JC Chang, SP … - Jama, 2001 - Am Med Assoc
You are seeing this message because your Web browser does not support basic Web
standards. Find out more about why this message is appearing and what you can do
to make your experience on this site better. ... Add to CiteULike Add to ...
Cited by 148 - Related articles - BL Direct - All 7 versions

Screening for hemochromatosis: high prevalence and low morbidity in an unselected …


A Åsberg, K Hveem, K Thorstensen, E … - Scandinavian journal of gastroenterology, 2001 - informahealthcare.com
AÊ sberg A, Hveem K, Thorstensen K, Ellekjær E, Kannelønning K, Fjøsne U,
Halvorsen TB, Smethurst H-BG, Sagen E, Bjerve KS. Screening for hemochromatosis:
high prevalence and low morbidity in an unselected population of 65,238 ...
Cited by 231 - Related articles - BL Direct - All 7 versions

Noninvasive prediction of fibrosis in C282Y homozygous hemochromatosis


D Guyader, C Jacquelinet, R Moirand, B … - Gastroenterology, 1998 - Elsevier
Liver biopsy has previously been an important step in the diagnosis of
hemochromatosis 7 because (1) it shows liver iron overload and assesses the
hepatocytic type of iron deposition with typical periportal and perilobular ...
Cited by 229 - Related articles - BL Direct - All 6 versions

Phenotypic expression of HFE mutations: a French study of 1110 unrelated iron-overloaded …


R Moirand, AM Jouanolle, P Brissot, JY Le … - Gastroenterology, 1999 - Elsevier
Hemochromatosis is an autosomal recessive disorder characterized by abnormal
intestinal iron absorption that leads to progressive increase of total body iron
stores and, ultimately, clinical complications. Until recently, the ...
Cited by 116 - Related articles - BL Direct - All 8 versions

Hemochromatosis and iron-overload screening in a racially diverse population

- hemocromatosis.es [PDF] 
PC Adams, DM Reboussin, JC Barton, CE … - The New England journal of medicine, 2005 - nejm.highwire.org
Results Of the 99,711 participants, 299 were homozygous for the C282Y mutation.
The estimated prevalence of C282Y homozygotes was higher in non-Hispanic whites
(0.44 percent) than in Native Americans (0.11 percent), Hispanics (0.027 ...
Cited by 206 - Related articles - All 15 versions

Molecular medicine and hemochromatosis: at the crossroads


BR Bacon, LW Powell, PC Adams, TF Kresina … - Gastroenterology, 1999 - Elsevier
The elucidation of the genetic basis for hereditary hemochromatosis has
stimulated renewed, vigorous interest in all aspects of this disease, from
purely clinical to the most basic research issues. The molecular tests for ...
Cited by 285 - Related articles - BL Direct - All 7 versions


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