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Scholar Results 1 - 10 of about 101 related to Bacon: HFE genotype in patients with hemochromatosis and other liver diseases. (0.09 sec) 

HFE genotype in patients with hemochromatosis and other liver diseases

- annals.org [PDF] 
BR Bacon, JK Olynyk, EM Brunt, RS Britton, … - Annals of internal medicine, 1999 - Am Coll Physicians
Bruce R. Bacon, MD; John K. Olynyk, MD; Elizabeth M. Brunt, MD; Robert S.
Britton, PhD; and Roger K. Wolff, PhD ... Background: Hereditary
hemochromatosis is a common inherited disorder of iron metabolism. The gene ...
Cited by 176 - Related articles - BL Direct - All 4 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

[PDF] Evolution of untreated hereditary hemochromatosis in the Busselton population: a 17-year …


JK Olynyk, SE Hagan, DJ Cullen, J Beilby, DE … - Mayo Clinic Proceedings, 2004 - mayoclinicproceedings.com
309 © 2004 Mayo Foundation for Medical Education and Research ... Evolution of
Untreated Hereditary Hemochromatosis in the Busselton Population: A 17-Year
Study ... J OHN K. O LYNYK , MD; S IMONE E. H AGAN , MBBS; D IGBY J. C ...
Cited by 74 - Related articles - View as HTML - BL Direct - All 11 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

Distribution of transferrin saturation in an Australian population: relevance to the early …

- uq.edu.au [PDF] 
CE McLaren, GJ McLachlan, JW Halliday, SI … - Gastroenterology, 1998 - Elsevier
Hereditary hemochromatosis (HC) is the most common autosomal recessively
inherited disorder in white populations. 1 , 2 , 3 , 4 , 5 , 6 , 7 , 8 and 9
Past surveys have estimated the gene frequency of HC by identifying ...
Cited by 130 - Related articles - BL Direct - All 8 versions

Hereditary hemochromatosis: Presentation and diagnosis in the 1990 s


BR Bacon, SA Sadiq - The American journal of gastroenterology, 1997 - cat.inist.fr
Objectives: In the past, patients with hereditary hemochromatosis have been
identified predominantly from symptomatic presentation or from family studies.
In the 1990 s, iron studies on routine screening chemistry panels have ...
Cited by 93 - Related articles - BL Direct - All 2 versions

[PDF] Hemochromatosis: diagnosis and management


BR Bacon - Gastroenterology, 2001 - usagiedu.com
Hereditary hemochromatosis (HH) is a common in- herited disorder of iron
metabolism that affects between 1 in 200 and 1 in 400 persons of northern
European descent and is characterized by increased gastrointestinal iron ...
Cited by 142 - Related articles - View as HTML - BL Direct - All 18 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

A population-based study of the biochemical and clinical expression of the H63D …


PA Gochee, LW Powell, DJ Cullen, D Du Sart, … - Gastroenterology, 2002 - Elsevier
Sixty-two subjects (2.1%) were homozygous for the H63D mutation, 711 (23.6%)
were heterozygous, and 1758 (58.4%) were wild-type for the H63D mutation. Serum
transferrin saturation was significantly increased in male and female H63D ...
Cited by 156 - Related articles - BL Direct - All 11 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


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