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Neuropediatrics|November 1, 1982
Familial nemaline myopathyG Scarlato, G Pellegrini, M Moggio, et al.Neuropediatrics|August 1, 1980
Estimation of monoamine and cyclic-AMP turnover and amino acid concentrations of spinal fluid in autistic childrenB G Winsberg, J Sverd, S Castells, et al.Neuropediatrics|February 12, 2021
Etiological and Clinical Profile of Acute Nonbacterial Encephalitis in Children: A Single-Center Prospective StudyAli Bülent Cengiz, Ceren Günbey, Mehmet Ceyhan, et al.Neuropediatrics|February 12, 2021
Epilepsy in Nicolaides-Baraitser Syndrome: Review of Literature and Report of 25 Patients Focusing on Treatment AspectsBenedikt Hofmeister, Celina von Stülpnagel, Cornelia Betzler, et al.Neuropediatrics|February 12, 2021
The outcome of 41 Late-Diagnosed Turkish GA-1 Patients: A Candidate for the Turkish NBSSebile Kılavuz, Derya Bulut, Deniz Kor, et al.Neuropediatrics|February 1, 1988
Arthrogryposis multiplex congenita associated with lissencephaly: a case reportG Massa, P Casaer, B Ceulemans, et al.Neuropediatrics|August 2, 2019
Static Leukoencephalopathy Associated with 17p13.3 Microdeletion Syndrome: A Case ReportAyaka Hirasawa-Inoue, Eri Takeshita, Yuko Shimizu-Motohashi, et al.Neuropediatrics|September 22, 2019
Recurrent Myalgia since Early Infancy-Misleading Clinical Course in a Child with Carnitine Palmitoyltransferase-II DeficiencyMaria Arélin, Stephan Zierz, Uta Ceglarek, et al.Neuropediatrics|September 22, 2019
Cooccurrence of Two Different Genetic Diseases: A Case of Valproic Acid Hepatotoxicity in Nicolaides-Baraitser Syndrome (SMARCA2 Mutation)-Due to a POLG1-Related Effect?Benedikt Hofmeister, Celina von Stülpnagel, Steffen Berweck, et al.Neuropediatrics|October 30, 2018
Inherited Disorders of Neurotransmitters: Classification and Practical Approaches for Diagnosis and TreatmentHeiko Brennenstuhl, Sabine Jung-Klawitter, Birgit Assmann, et al.Pageof 255