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Pediatric Neurology|October 2, 2007
Albinism and developmental delay: the need to test for 15q11-q13 deletionReem Saadeh, Emily C Lisi, Denise A S Batista, et al.Pediatric Neurology|October 2, 2007
Novel de novo mutation of a conserved SCN1A amino-acid residue (R1596)Dennis J Dlugos, Thomas N Ferraro, Russell J BuonoPediatric Neurology|August 30, 2008
Infant botulism type Ba: first culture-confirmed case in the United Arab EmiratesWaseem M Fathalla, Khalid A Mohammed, Elamin AhmedPediatric Neurology|August 30, 2008
Sleep-disordered breathing in Chiari malformation type 1Jayaprakash A GosalakkalPediatric Neurology|September 23, 2008
Leigh and Leigh-like syndrome in children and adultsJosef FinstererPediatric Neurology|September 23, 2008
Anxiety and depressive symptoms in children presenting with a first seizureJulia C Loney, Elaine C Wirrell, Elisabeth M S Sherman, et al.Pediatric Neurology|September 23, 2008
Prospective study examining remote effects of botulinum toxin a in children with cerebral palsyBeth E Crowner, Brad A RacettePediatric Neurology|September 23, 2008
Evaluation of bone turnover in epileptic children using oxcarbazepineAli Cansu, Ediz Yesilkaya, Ayşe Serdaroğlu, et al.Pediatric Neurology|September 23, 2008
Epidermal nevus syndrome with azygos anterior cerebral arteryBülent Kara, Nagehan Inan, Dilek Bayramgürler, et al.Pediatric Neurology|November 21, 2007
Novel mutation confirms seizure locus SCN1A is also familial hemiplegic migraine locus FHM3J Jay Gargus, Anne TournayPageof 597