Diagnosis and therapy of genetic haemochromatosis (review and 2017 update).

Fitzsimons, Edward J; Cullis, Jonathan O; Thomas, Derrick W; Tsochatzis, Emmanouil; Griffiths, William J H

Fitzsimons, Edward J; Cullis, Jonathan O; Thomas, Derrick W; Tsochatzis, Emmanouil; Griffiths, William J H.

Afiliação

Fitzsimons EJ; Department of Haematology, Gartnavel General Hospital, Glasgow, UK.
Cullis JO; Department of Haematology, Salisbury NHS Foundation Trust, Salisbury, UK.
Thomas DW; Department of Haematology, Plymouth Hospitals NHS Trust, Plymouth, UK.
Tsochatzis E; UCL Institute for Liver and Digestive Health, Royal Free London NHS Foundation Trust and UCL, London, UK.
Griffiths WJH; Department of Hepatology, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.

Br J Haematol ; 181(3): 293-303, 2018 05.

Article em En | MEDLINE | ID: mdl-29663319

Assuntos

Hemocromatose/diagnóstico; Hemocromatose/genética; Hemocromatose/terapia; Hemocromatose/patologia; Humanos

Palavras-chave

haemochromatosis; iron biochemistry; iron overload

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hemocromatose Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Revista: Br J Haematol Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Reino Unido

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