Comment on "Delayed myelination is not a constant feature of Allan-Herndon-Dudley syndrome: Report of a new case and review of the literature" by Azzolini S et al. Brain & Development 2014;36:716-720

Brain and Development

Volumn 37, Issue 10, 2015, Pages 988-989

  Yamamoto, Toshiyuki ^a   Takanashi, Jun ichi ^a   Kurosawa, Kenji ^b   Deguchi, Kimiko ^c   Osaka, Hitoshi ^d   Inoue, Ken ^e  

^a TOKYO WOMEN'S MEDICAL UNIVERSITY   (Japan)

^b KANAGAWA CHILDREN'S MEDICAL CENTER   (Japan)

^c Deguchi Pediatric Clinic   (Japan)

^d JICHI MEDICAL UNIVERSITY   (Japan)

^e NATIONAL INSTITUTE OF NEUROSCIENCE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

MONOCARBOXYLATE TRANSPORTER 8; MYELIN; NUCLEOTIDE; MONOCARBOXYLATE TRANSPORTER;

ALLAN HERNDON DUDLEY SYNDROME; CLINICAL FEATURE; DELAYED MYELINATION; DEMYELINATING DISEASE; DEVELOPMENTAL DISORDER; FREE LIOTHYRONINE INDEX; HUMAN; LETTER; MYELINATION; NEUROIMAGING; NUCLEAR MAGNETIC RESONANCE IMAGING; PELIZAEUS MERZBACHER DISEASE; PSYCHOMOTOR DISORDER; TEMPORAL LOBE; THYROID FUNCTION TEST; WHITE MATTER; FRAMESHIFT MUTATION; GENETICS; MALE; MENTAL RETARDATION, X-LINKED; MUSCLE HYPOTONIA; MUSCULAR ATROPHY; MYELIN SHEATH; PATHOLOGY;

FRAMESHIFT MUTATION; HUMANS; MALE; MENTAL RETARDATION, X-LINKED; MONOCARBOXYLIC ACID TRANSPORTERS; MUSCLE HYPOTONIA; MUSCULAR ATROPHY; MYELIN SHEATH;

EID: 84941993134     PISSN: 03877604     EISSN: 18727131     Source Type: Journal    
DOI: 10.1016/j.braindev.2015.03.007     Document Type: Letter

References (7)

1. Azzolini S., Nosadini M., Balzarin M., Sartori S., Suppiej A., Mardari R., et al. Delayed myelination is not a constant feature of Allan-Herndon-Dudley syndrome: report of a new case and review of the literature. Brain Dev 2014, 36:716-720.
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7. Schwartz C.E., May M.M., Carpenter N.J., Rogers R.C., Martin J., Bialer M.G., et al. Allan-Herndon-Dudley syndrome and the monocarboxylate transporter 8 (MCT8) gene. Am J Hum Genet 2005, 77:41-53.