Novel Mutation in the Hemojuvelin Gene (HJV) in a Patient with Juvenile Hemochromatosis Presenting with Insulin-dependent Diabetes Mellitus, Secondary Hypothyroidism and Hypogonadism-Reference-Cited by-同舟云学术

Novel Mutation in the Hemojuvelin Gene (HJV) in a Patient with Juvenile Hemochromatosis Presenting with Insulin-dependent Diabetes Mellitus, Secondary Hypothyroidism and Hypogonadism

Published:2020-04-24 Issue: Volume:21 Page:
ISSN:1941-5923
Container-title:American Journal of Case Reports
language:en
Short-container-title:Am J Case Rep

Author:

Santiago de Sousa Azulay Rossana¹,Magalhães Marcelo¹,Tavares Maria da Gloria¹,Dualibe Roberta¹,Barbosa Lívia²,Sá Gaspar Silvia²,Faria André M.³,Nascimento Gilvan Cortês¹,Damianse Sabrina Da Silva Pereira¹,Rocha Viviane Chaves de Carvalho¹,Gomes Marília B.⁴,dos Santos Faria Manuel¹

Affiliation:

1. Endocrinology Unit, University Hospital of the Federal University of Maranhão (HUUFMA), São Luís, Brazil

2. Research Group in Clinical and Molecular Endocrinology and Metabology (ENDOCLIM), São Luís, Brazil

3. Neuroendocrine Unit, Functional Neurosurgery Division, Psychiatry Institute, Hospital das Clínicas, University of São Paulo Medical School, São Paulo, Brazil

4. Diabetes Unit, State University of Rio de Janeiro (UERJ), Rio de Janeiro, Brazil

Publisher

International Scientific Information, Inc.

Subject

General Medicine

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1. Clinical evaluation of hyperferritinemia with or without iron overload;Journal of Laboratory and Precision Medicine;2024-04

2. Appropriate Clinical Genetic Testing of Hemochromatosis Type 2–4, Including Ferroportin Disease;The Application of Clinical Genetics;2021-08

3. Juvenile Hemochromatosis: A Case Report and Review of the Literature;Pharmaceuticals;2020-08-15