P. Adams

发表

The relationship between iron overload, clinical symptoms, and age in 410 patients with genetic hemochromatosis

P. Brissot, R. Moirand, Y. Deugnier, 1997, Hepatology.

Quantifying Brain Iron in Hereditary Hemochromatosis Using R2* and Susceptibility Mapping

E. Haacke, M. Jog, S. Sethi, 2022, American Journal of Neuroradiology.

Alcoholism in hereditary hemochromatosis revisited: Prevalence and clinical consequences among homozygous siblings

P. Adams, S. Agnew, 1996, Hepatology.

Epidemiology and diagnostic testing for hemochromatosis and iron overload

P. Adams, P. Adams, 2015, International journal of laboratory hematology.

Clinical and family studies in genetic hemochromatosis: Microsatellite and HFE studies in five atypical families

V. David, J. Legall, P. Adams, 1997, Hepatology.

Prevalence of the C282Y mutation of the hemochromatosis gene in liver transplant recipients and donors

S. Chakrabarti, W. Howson, G. Jeffrey, 1999, Hepatology.

Review article: the modern diagnosis and management of haemochromatosis

P. Adams, Paul C. Adams, 2006, Alimentary pharmacology & therapeutics.

Alternate splicing produces a soluble form of the hereditary hemochromatosis protein HFE.

S. Chakrabarti, G. Jeffrey, P. Adams, 1999, Blood cells, molecules & diseases.

A genome‐wide linkage scan for iron phenotype quantitative trait loci: the HEIRS Family Study

B. Snively, S. Rich, M. Speechley, 2007, Clinical genetics.

Initial screening transferrin saturation values, serum ferritin concentrations, and HFE genotypes in Native Americans and whites in the Hemochromatosis and Iron Overload Screening Study

M. Speechley, L. Lovato, P. Adams, 2005, Clinical genetics.

Hereditary hemochromatosis screening: effect of mutation penetrance and prevalence on cost‐effectiveness of testing algorithms

F. Rousseau, D. Reinharz, G Gagné, 2006, Clinical genetics.

Blood from patients with hereditary hemochromatosis—a wasted resource?

G. Jeffrey, P. Adams, P. Adams, 1999, Transfusion.