Clinical and Endocrine Features of Two Allan-Herndon-Dudley Syndrome Patients with Monocarboxylate Transporter 8 Mutations-Reference-Cited by-同舟云学术

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Clinical and Endocrine Features of Two Allan-Herndon-Dudley Syndrome Patients with Monocarboxylate Transporter 8 Mutations

Published:2015 Issue:4 Volume:83 Page:288-292
ISSN:1663-2818
Container-title:Hormone Research in Paediatrics
language:en
Short-container-title:Horm Res Paediatr

Author:

Kim Ja Hye,Kim Yoo-Mi,Yum Mi-Sun,Choi Jin-Ho,Lee Beom Hee,Kim Gu-Hwan,Yoo Han-Wook

Publisher

S. Karger AG

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology and Child Health

Cited by 15 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Late-onset drug resistant epilepsy in an adolescent with Allan-Herndon-Dudley syndrome;Journal of Genetic Medicine;2024-06-30

2. Nomenclature of Genetic Movement Disorders: Recommendations of the International Parkinson and Movement Disorder Society Task Force – An Update;Movement Disorders;2022-04-28

3. Subclinical hypothyroidism and Pelizaeus-Merzbacher Disease in same-sex twins: Case report;Journal of Clinical and Translational Endocrinology: Case Reports;2021-12

4. Monocarboxylate Transporter 8 Deficiency: From Pathophysiological Understanding to Therapy Development;Frontiers in Endocrinology;2021-09-01

5. Biochemical and molecular evaluation of thyroid gland disorders in children;Biochemical and Molecular Basis of Pediatric Disease;2021

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