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Pediatric Transplantation
|
November 25, 2011
Variable disease progression after successful stem cell transplantation: prospective follow-up investigations in eight patients with Hurler syndrome
Lorenz Grigull, Karl-Walter Sykora, Andreas Tenger, et al.
Journal of Inherited Metabolic Disease
|
June 26, 2016
The value of plasma vitamin B6 profiles in early onset epileptic encephalopathies
Déborah Mathis, Lucia Abela, Monique Albersen, et al.
Human Mutation
|
October 28, 2006
Biochemical and molecular characterization of 18 patients with pyridoxine-dependent epilepsy and mutations of the antiquitin (ALDH7A1) gene
Barbara Plecko, Karl Paul, Eduard Paschke, et al.
Pediatric Nephrology (Berlin, Germany)
|
March 26, 2014
Neurological involvement in children with E. coli O104:H4-induced hemolytic uremic syndrome
Angela Bauer, Sebastian Loos, Carola Wehrmann, et al.
Molecular Genetics and Metabolism
|
June 28, 2011
Pyridoxine dependent epilepsy and antiquitin deficiency: clinical and molecular characteristics and recommendations for diagnosis, treatment and follow-up
Sylvia Stockler, Barbara Plecko, Sidney M Gospe, et al.
Pediatric Neurology
|
March 21, 2016
Pyridoxine-Dependent Epilepsy: An Expanding Clinical Spectrum
Clara D M van Karnebeek, Sylvia A Tiebout, Jikkemien Niermeijer, et al.
Journal of Child Neurology
|
January 19, 2013
Pediatric herpes simplex virus encephalitis: a retrospective multicenter experience
Lena Schleede, Wolfgang Bueter, Sara Baumgartner-Sigl, et al.
Epilepsia Open
|
November 14, 2024
Defining neonatal status epilepticus: A scoping review from the ILAE neonatal task force
Magda L Nunes, Elissa G Yozawitz, Courtney J Wusthoff, et al.
Epilepsia
|
September 5, 2018
Systematic review of the screening, diagnosis, and management of ADHD in children with epilepsy. Consensus paper of the Task Force on Comorbidities of the ILAE Pediatric Commission
Stéphane Auvin, Elaine Wirrell, Kirsten A Donald, et al.
Molecular Genetics and Metabolism
|
March 13, 2022
Timing of therapy and neurodevelopmental outcomes in 18 families with pyridoxine-dependent epilepsy
Laura A Tseng, Jose E Abdenur, Ashley Andrews, et al.
Page
of 9
Search research articles
Search
Showing results (51-60 of 83) with videos related to
Sort By:
Page
of 9
Pediatric Transplantation
|
November 25, 2011
Variable disease progression after successful stem cell transplantation: prospective follow-up investigations in eight patients with Hurler syndrome
Lorenz Grigull, Karl-Walter Sykora, Andreas Tenger, et al.
Journal of Inherited Metabolic Disease
|
June 26, 2016
The value of plasma vitamin B6 profiles in early onset epileptic encephalopathies
Déborah Mathis, Lucia Abela, Monique Albersen, et al.
Human Mutation
|
October 28, 2006
Biochemical and molecular characterization of 18 patients with pyridoxine-dependent epilepsy and mutations of the antiquitin (ALDH7A1) gene
Barbara Plecko, Karl Paul, Eduard Paschke, et al.
Pediatric Nephrology (Berlin, Germany)
|
March 26, 2014
Neurological involvement in children with E. coli O104:H4-induced hemolytic uremic syndrome
Angela Bauer, Sebastian Loos, Carola Wehrmann, et al.
Molecular Genetics and Metabolism
|
June 28, 2011
Pyridoxine dependent epilepsy and antiquitin deficiency: clinical and molecular characteristics and recommendations for diagnosis, treatment and follow-up
Sylvia Stockler, Barbara Plecko, Sidney M Gospe, et al.
Pediatric Neurology
|
March 21, 2016
Pyridoxine-Dependent Epilepsy: An Expanding Clinical Spectrum
Clara D M van Karnebeek, Sylvia A Tiebout, Jikkemien Niermeijer, et al.
Journal of Child Neurology
|
January 19, 2013
Pediatric herpes simplex virus encephalitis: a retrospective multicenter experience
Lena Schleede, Wolfgang Bueter, Sara Baumgartner-Sigl, et al.
Epilepsia Open
|
November 14, 2024
Defining neonatal status epilepticus: A scoping review from the ILAE neonatal task force
Magda L Nunes, Elissa G Yozawitz, Courtney J Wusthoff, et al.
Epilepsia
|
September 5, 2018
Systematic review of the screening, diagnosis, and management of ADHD in children with epilepsy. Consensus paper of the Task Force on Comorbidities of the ILAE Pediatric Commission
Stéphane Auvin, Elaine Wirrell, Kirsten A Donald, et al.
Molecular Genetics and Metabolism
|
March 13, 2022
Timing of therapy and neurodevelopmental outcomes in 18 families with pyridoxine-dependent epilepsy
Laura A Tseng, Jose E Abdenur, Ashley Andrews, et al.
Page
of 9