Hypomyelination versus delayed myelination

Annals of Neurology

Volumn 68, Issue 1, 2010, Pages 115-

  Van Der Knaap, Marjo S ^a   Wolf, Nicole I ^a  

^a VU UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

MYELIN;

CHILD CARE; DISEASE COURSE; GENE; GENE MUTATION; HUMAN; LETTER; MCT8 GENE; MYELINATION; NUCLEAR MAGNETIC RESONANCE IMAGING; PELIZAEUS MERZBACHER DISEASE; PRIORITY JOURNAL;

AGE FACTORS; BRAIN DISEASES; DISEASE PROGRESSION; HUMANS; INFANT; MAGNETIC RESONANCE IMAGING; MALE; MONOCARBOXYLIC ACID TRANSPORTERS; MYELIN SHEATH;

EID: 77954045409     PISSN: 03645134     EISSN: 15318249     Source Type: Journal    
DOI: 10.1002/ana.21751     Document Type: Letter

References (5)

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2. Namba N, Etani Y, Kitaoka T, et al. Clinical phenotype and endocrinological investigations in a patient with a mutation in the MCT8 thyroid hormone transporter. Eur J Pediatr 2008;167:785-791. (Pubitemid 351733513)
3. Schiffmann R, van der Knaap MS. An MRI-based approach to the diagnosis of white matter disorders. Neurology 2009;72:750-759.
4. Van der Knaap MS, Valk J, Bakker CJ, et al. Myelination as an expression of the functional maturity of the brain. Dev Med Child Neurol 1991;33:849-857.
5. Pujol J, López-Sala A, Sebastián-Gallés N, et al. Delayed myelination in children with developmental delay detected by volumetric MRI. Neuroimage 2004;22:897-903. (Pubitemid 38759454)