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Showing results (91-100 of 100) with videos related to

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European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|February 25, 2018
How do parents perceive adverse drug events of their children's anticonvulsant medication?V A Bach, M P Neininger, U P Spindler, et al.
Molecular Syndromology|October 27, 2016
Phenotypic Variability from Benign Infantile Epilepsy to Ohtahara Syndrome Associated with a Novel Mutation in <i>SCN2A</i>Steffen Syrbe, Boris S Zhorov, Astrid Bertsche, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|February 29, 2016
Hydrocephalus in aqueductal stenosis--a retrospective outcome analysis and proposal of subtype classificationImke Rodis, Cynthia Vanessa Mahr, Michael K Fehrenbach, et al.
Klinische Padiatrie|December 20, 2017
How do Parents Perceive the Initial Medical Consultation on their Child's Developmental Disorder?Lena Charlott Hotopp, Ulrike Petra Spindler, Vivien Angela Bach, et al.
Plos One|September 23, 2016
The Cerebral Surfactant System and Its Alteration in Hydrocephalic ConditionsStefan Schob, Donald Lobsien, Benjamin Friedrich, et al.
Orphanet Journal of Rare Diseases|October 17, 2015
47 patients with FLNA associated periventricular nodular heterotopiaMax Lange, Burkhard Kasper, Axel Bohring, et al.
Orphanet Journal of Rare Diseases|May 5, 2019
Safety and efficacy of mTOR inhibitor treatment in patients with tuberous sclerosis complex under 2 years of age - a multicenter retrospective studyAfshin Saffari, Ines Brösse, Adelheid Wiemer-Kruel, et al.
Cancer Research|May 12, 2011
PHLDA1 expression marks the putative epithelial stem cells and contributes to intestinal tumorigenesisAnuratha Sakthianandeswaren, Michael Christie, Carla D'Andreti, et al.
Nature|July 28, 2016
A radio-pulsing white dwarf binary starT R Marsh, B T Gänsicke, S Hümmerich, et al.
Nature Genetics|March 10, 2015
De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathySteffen Syrbe, Ulrike B S Hedrich, Erik Riesch, et al.
Pageof 10

Showing results (91-100 of 100) with videos related to

Sort By:
Pageof 10
You have reached the last page of results.This site can display upto 100 results.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|February 25, 2018
How do parents perceive adverse drug events of their children's anticonvulsant medication?V A Bach, M P Neininger, U P Spindler, et al.
Molecular Syndromology|October 27, 2016
Phenotypic Variability from Benign Infantile Epilepsy to Ohtahara Syndrome Associated with a Novel Mutation in <i>SCN2A</i>Steffen Syrbe, Boris S Zhorov, Astrid Bertsche, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|February 29, 2016
Hydrocephalus in aqueductal stenosis--a retrospective outcome analysis and proposal of subtype classificationImke Rodis, Cynthia Vanessa Mahr, Michael K Fehrenbach, et al.
Klinische Padiatrie|December 20, 2017
How do Parents Perceive the Initial Medical Consultation on their Child's Developmental Disorder?Lena Charlott Hotopp, Ulrike Petra Spindler, Vivien Angela Bach, et al.
Plos One|September 23, 2016
The Cerebral Surfactant System and Its Alteration in Hydrocephalic ConditionsStefan Schob, Donald Lobsien, Benjamin Friedrich, et al.
Orphanet Journal of Rare Diseases|October 17, 2015
47 patients with FLNA associated periventricular nodular heterotopiaMax Lange, Burkhard Kasper, Axel Bohring, et al.
Orphanet Journal of Rare Diseases|May 5, 2019
Safety and efficacy of mTOR inhibitor treatment in patients with tuberous sclerosis complex under 2 years of age - a multicenter retrospective studyAfshin Saffari, Ines Brösse, Adelheid Wiemer-Kruel, et al.
Cancer Research|May 12, 2011
PHLDA1 expression marks the putative epithelial stem cells and contributes to intestinal tumorigenesisAnuratha Sakthianandeswaren, Michael Christie, Carla D'Andreti, et al.
Nature|July 28, 2016
A radio-pulsing white dwarf binary starT R Marsh, B T Gänsicke, S Hümmerich, et al.
Nature Genetics|March 10, 2015
De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathySteffen Syrbe, Ulrike B S Hedrich, Erik Riesch, et al.
Pageof 10