Cerebellar and brainstem involvement in familial juvenile nephronophthisis type I

Pediatric Neurology

Volumn 28, Issue 2, 2003, Pages 142-144

  Takano, Kyoko ^a   Nakamoto, Tetsu ^b   Okajima, Maki ^a   Sudo, Akira ^a   Uetake, Kimiaki ^b   Saitoh, Shinji ^a  

^a HOKKAIDO UNIVERSITY   (Japan)

^b Obihiro Kosei Hospital   (Japan)

Author keywords

Cerebellar ataxia; Nephronophthisis; NPHP1; Ocular motor apraxia

Indexed keywords

APRAXIA; ARTICLE; BRAIN DISEASE; BRAIN FOURTH VENTRICLE; BRAIN STEM; BRAIN VENTRICLE DILATATION; CASE REPORT; CEREBELLAR ATAXIA; CEREBELLUM; CEREBELLUM VERMIS; DISEASE ASSOCIATION; FAMILIAL DISEASE; GENE; GENE DELETION; HUMAN; HUMAN CELL; HYPOPLASIA; MALE; MOLECULAR GENETICS; NEPHRONOPHTHISIS; NERVOUS SYSTEM DEVELOPMENT; NPHP1 GENE; NUCLEAR MAGNETIC RESONANCE IMAGING; NYSTAGMUS; OCULAR MOTOR APRAXIA; PRIORITY JOURNAL; SCHOOL CHILD;

EID: 0344837861     PISSN: 08878994     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0887-8994(02)00619-7     Document Type: Article

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