A Pediatric Patient with a CYP24A1 Mutation: Four Years of Clinical, Biochemical, and Imaging Follow-Up

Publisher： Karger

E-ISSN： 1663-2826|87|3|196-204

ISSN： 1663-2818

Source： Hormone Research in Paediatrics, Vol.87, Iss.3, 2016-11, pp. : 196-204

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Leydig-Cell Tumour in Children: Variable Clinical Presentation, Diagnostic Features, Follow-Up and Genetic Analysis of Four Cases

By  

Hormone Research in Paediatrics, Vol. 67, Iss. 2, 2006-10 ,pp. : 89-95

Karger

Access to resources Recommend Favorite

Long-Term Follow-Up of Childhood-Onset Hypopituitarism in Patients with the PROP-1 Gene Mutation

By  

Hormone Research in Paediatrics, Vol. 60, Iss. 4, 2003-10 ,pp. : 168-173

Karger

Access to resources Recommend Favorite

Long-Term (7 Years) Follow-Up of Roux-en-Y Gastric Bypass on Obese Adolescent Patients (<18 Years)

By  

Obesity Facts, Vol. 9, Iss. 2, 2016-04 ,pp. : 91-100

Karger

Access to resources Recommend Favorite

Long-Term Follow-Up of an Infant with Thyrotoxicosis due to Germline Mutation of the TSH Receptor Gene (Met453Thr)

By  

Hormone Research in Paediatrics, Vol. 51, Iss. 1, 1999-03 ,pp. : 43-46

Karger

Access to resources Recommend Favorite

Long-Term Follow-Up and Mutation Analysis of 27 Chinese Cases of Congenital Hyperinsulinism

By  

Hormone Research in Paediatrics, Vol. 81, Iss. 3, 2014-01 ,pp. : 169-176

Karger

Access to resources Recommend Favorite