Related references
Note: Only part of the references are listed.MCT8 Deficiency: Extrapyramidal Symptoms and Delayed Myelination as Prominent Features
Davide Tonduti et al.
JOURNAL OF CHILD NEUROLOGY (2013)
Hypomyelination Versus Delayed Myelination
Marjo S. van der Knaap et al.
ANNALS OF NEUROLOGY (2010)
White matter abnormalities and dystonic motor disorder associated with mutations in the SLC16A2 gene
Artemis D. Gika et al.
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY (2010)
Pelizaeus-Merzbacher-Like Disease Presentation of MCT8 Mutated Male Subjects
Catherine Vaurs-Barriere et al.
ANNALS OF NEUROLOGY (2009)
Invited Article: An MRI-based approach to the diagnosis of white matter disorders
Raphael Schiffmann et al.
NEUROLOGY (2009)
MCT8 mutation analysis and identification of the first female with Allan-Herndon-Dudley syndrome due to loss of MCT8 expression
Suzanna Gerarda Maria Frints et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2008)
A novel monocarboxylate transporter 8 gene mutation as a cause of severe neonatal hypotonia and developmental delay
Anastasios Papadimitriou et al.
PEDIATRICS (2008)
Clinical phenotype and endocrinological investigations in a patient with a mutation in the MCT8 thyroid hormone transporter
Noriyuki Namba et al.
EUROPEAN JOURNAL OF PEDIATRICS (2008)
Syndromes of reduced sensitivity to thyroid hormone: genetic defects in hormone receptors, cell transporters and deiodination
Samuel Refetoff et al.
BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM (2007)
Abnormal thyroid hormone metabolism in mice lacking the monocarboxylate transporter 8
Marija Trajkovic et al.
JOURNAL OF CLINICAL INVESTIGATION (2007)
Thyroid hormone deficiency changes the distribution of oligodendrocyte/myelin markers during oligodendroglial differentiation in vitro
V. Younes-Rapozo et al.
INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE (2006)
X-linked MCT8 gene mutations:: Characterization of the pediatric neurologic phenotype
KR Holden et al.
JOURNAL OF CHILD NEUROLOGY (2005)
Allan-Herndon-Dudley syndrome and the monocarboxylate transporter 8 (MCT8) gene
CE Schwartz et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2005)
A novel syndrome combining thyroid and neurological abnormalities is associated with mutations in a monocarboxylate transporter gene
AM Dumitrescu et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2004)
Association between mutations in a thyroid hormone transporter and severe X-linked psychomotor retardation
ECH Friesema et al.
LANCET (2004)