Molecular mechanisms and neuroimaging criteria for severe L1 syndrome with X-linked hydrocephalus

Journal of Neurosurgery

Volumn 105 PEDIATRICS, Issue SUPPL. 5, 2006, Pages 403-412

  Kanemura, Yonehiro ^b   Okamoto, Nobuhiko ^b   Sakamoto, Hiroaki ^b   Shofuda, Tomoko ^b   Kamiguchi, Hiroyuki ^b   Yamasaki, Mami ^a  

^a NATIONAL HOSPITAL ORGANIZATION   (Japan)

^b NONE

Author keywords

L1 syndrome; L1CAM; Molecular mechanism; Pediatric neurosurgery; X linked hydrocephalus

Indexed keywords

ARTICLE; BRAIN VENTRICLE; CEREBELLUM VERMIS; CEREBELLUM VERMIS HYPOPLASIA; CEREBROSPINAL FLUID SHUNTING; CORPUS CALLOSUM; CORPUS CALLOSUM HYPOPLASIA; DISEASE SEVERITY; DNA SEQUENCE; FEMALE; GENE MUTATION; GENETIC ANALYSIS; GENETIC DISORDER; HUMAN; HYDROCEPHALUS; HYPOPLASIA; INFANT; L1 SYNDROME; MAJOR CLINICAL STUDY; MALE; MENTAL DEFICIENCY; NEUROIMAGING; NEWBORN; OPTIC LOBE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SPASTIC PARAPLEGIA; X CHROMOSOME LINKED DISORDER; X LINKED HYDROCEPHALUS;

EID: 33845602716     PISSN: 00223085     EISSN: 00223085     Source Type: Journal    
DOI: 10.3171/ped.2006.105.5.403     Document Type: Article

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