'Familial alternating hemiplegia of childhood or channelopathy? A report with valuable pathophysiological implications' (multiple letters) [1]

Developmental Medicine and Child Neurology

Volumn 46, Issue 7, 2004, Pages 500-501

  Auvin, Stéphane ^a   Joriot Chekaf, Sylvie ^c   Cuvellier, Jean Christophe ^c   Vallée, Louis ^c   Kanavakis, Emmanuel ^b   Xaidara, Athina ^c   Papathanasiou Klontza, Dimitra ^c   Papadimitriou, Alexandros ^c   Velentza, Stavroula ^c   Youroukos, Sotiris ^c  

^a LILLE UNIVERSITY HOSPITAL   (France)

^b UNIVERSITY OF ATHENS   (Greece)

^c NONE

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM CHANNEL; CALCIUM ION; FLUNARIZINE;

ALTERNATING HEMIPLEGIA OF CHILDHOOD; AUTOSOMAL DOMINANT DISORDER; CHANNELOPATHY; CHILD; CLINICAL FEATURE; DISEASE ASSOCIATION; EYE MOVEMENT DISORDER; FAMILIAL DISEASE; FLUSHING; GENE LOCUS; GENE MUTATION; GENETIC PREDISPOSITION; GENETIC SUSCEPTIBILITY; HEMIPLEGIA; HUMAN; LETTER; MIGRAINE; PRIORITY JOURNAL; SEIZURE;

CALCIUM CHANNEL BLOCKERS; CALCIUM CHANNELS; CALCIUM CHANNELS, L-TYPE; CHILD; CHROMOSOMES, HUMAN, PAIR 1; HEMIPLEGIA; HUMANS; NA(+)-K(+)-EXCHANGING ATPASE; NERVE TISSUE PROTEINS;

EID: 3042854209     PISSN: 00121622     EISSN: None     Source Type: Journal    
DOI: 10.1017/S0012162204210829     Document Type: Letter

References (0)