Pages that link to "Q67687685"
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The following pages link to Idiopathic hemochromatosis. Demonstration of recessive transmission and early detection by family HLA typing (Q67687685):
Displaying 50 items.
- Human ferritin gene is assigned to chromosome 19 (Q24602041) (← links)
- Recent advances in understanding haemochromatosis: a transition state (Q24676226) (← links)
- HLA frequencies and haplotypes in children with idiopathic thrombocytopenic purpura (ITP). (Q33472709) (← links)
- Familial screening for genetic haemochromatosis by means of DNA markers (Q33594012) (← links)
- Neurofibromatosis type 1 (NF1): knowledge, experience, and reproductive decisions of affected patients and families (Q33595557) (← links)
- Screening for hemochromatosis. A public health perspective (Q33644877) (← links)
- Should all patients with diabetes mellitus be screened for hemochromatosis? (Q33729647) (← links)
- Pathogenesis of liver fibrosis: role of oxidative stress (Q34025940) (← links)
- Hepatology in the new millennium. Advances in viral hepatitis, hepatic disorders, and liver transplantation (Q34057526) (← links)
- EMQN best practice guidelines for the molecular genetic diagnosis of hereditary hemochromatosis (HH). (Q34483947) (← links)
- Idiopathic hemochromotosis and alpha-1-antitrypsin deficiency: coexistence in a family with progressive liver disease in the proband (Q34549247) (← links)
- Duodenal iron proteins in idiopathic hemochromatosis (Q34564684) (← links)
- Iron overload disorders (Q34746229) (← links)
- Erythrocyte ferritin content in idiopathic haemochromatosis and alcoholic liver disease with iron overload. (Q34991137) (← links)
- Occult celiac disease prevents penetrance of hemochromatosis (Q35045685) (← links)
- Hereditary hemochromatosis: update for 2003. (Q35068027) (← links)
- Segregation of genetic hemochromatosis indexed by latent capacity of transferrin (Q35197396) (← links)
- Combined segregation and linkage analysis of genetic hemochromatosis using affection status, serum iron, and HLA. (Q35198463) (← links)
- The use of association data to identify family members at high risk for marker-linked diseases. (Q35199679) (← links)
- Genetic distances between the Utah Mormons and related populations (Q35199964) (← links)
- Genetic analysis of idiopathic hemochromatosis using both qualitative (disease status) and quantitative (serum iron) information (Q35200364) (← links)
- Mapping the locus for hereditary hemochromatosis: localization between HLA-B and HLA-A. (Q35201032) (← links)
- Association of certain human leukocyte antigens with nephropathic cystinosis in the absence of linkage between these loci (Q35201231) (← links)
- Chromosome 3q (22-ter) encodes the human transferrin receptor (Q35203100) (← links)
- Genetic linkage between hereditary hemochromatosis and HLA (Q35203482) (← links)
- When and how should we screen for hereditary hemochromatosis? (Q35209877) (← links)
- Haplotype analysis of hemochromatosis: evaluation of different linkage-disequilibrium approaches and evolution of disease chromosomes (Q35250515) (← links)
- Spur cell anaemia and hepatic iron stores in patients with alcoholic liver disease undergoing orthotopic liver transplantation (Q35356303) (← links)
- Screening for hemochromatosis: patients with liver disease, families, and populations. (Q35628117) (← links)
- Plasma ferritin concentrations: their clinical significance and relevance to patient care. (Q35645729) (← links)
- Histocompatibility antigens as markers of abnormal iron metabolism in idiopathic hemochromatosis (Q35674291) (← links)
- Anonymous marker loci within 400 kb of HLA-A generate haplotypes in linkage disequilibrium with the hemochromatosis gene (HFE) (Q35889091) (← links)
- Adult liver transplantation for metabolic liver disease (Q35960858) (← links)
- The iron-loaded cell--the cytopathology of iron storage. A review (Q36058544) (← links)
- Hereditary and nutritional iron overload (Q36167860) (← links)
- Articular manifestations of systemic diseases (Q36299511) (← links)
- Defective iron homeostasis in beta 2-microglobulin knockout mice recapitulates hereditary hemochromatosis in man. (Q36367618) (← links)
- A cosmid library specific for human chromosome regions 6p21.3 and 6q27. (Q36743344) (← links)
- Rheumatic manifestations of haemochromatosis (Q36848359) (← links)
- Phenotypic expression of hereditary hemochromatosis: what have we learned from the population studies? (Q37738631) (← links)
- The pathology of hepatic iron overload: a free radical--mediated process? (Q37870467) (← links)
- Proteins of iron storage and transport (Q37940648) (← links)
- Hereditary (primary) haemochromatosis (Q37952696) (← links)
- Diagnosis and clinical evaluation of iron overload (Q38648376) (← links)
- The clinical manifestations of chronic iron overload (Q38648389) (← links)
- HLA-DRW4 in 91% of Jewish pemphigus vulgaris patients (Q39560394) (← links)
- HLA Determinants in Idiopathic Hemochromatosis (Q39570598) (← links)
- The genetics of haemochromatosis (Q39631713) (← links)
- Serum Ferritin (Q39798842) (← links)
- Typing for Human Alloantigens with the Primed Lymphocyte Typing Technique (Q40104185) (← links)