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Steffen Syrbe

Showing results (1-10 of 135) with videos related to

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Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 5, 2024
Developmental and epileptic encephalopathies - therapeutic consequences of genetic testingSteffen Syrbe
Seminars in Neurology|June 11, 2015
Epileptic Encephalopathies in Childhood: The Role of Genetic TestingJohannes R Lemke, Steffen Syrbe
Pediatric Dermatology|September 5, 2018
Sweaty feet in adolescents-Early use of botulinum type A toxin in juvenile plantar hyperhidrosisMatthias K Bernhard, Matthias Krause, Steffen Syrbe
Orphanet Journal of Rare Diseases|January 6, 2025
Long-term neuropsychologic outcome of pre-emptive mTOR inhibitor treatment in children with tuberous sclerosis complex (TSC) under 4 months of age (PROTECT), a two-arm, randomized, observer-blind, controlled phase IIb national multicentre clinical trial: study protocolJan H Driedger, Julian Schröter, , et al.
Clinical Case Reports|December 22, 2025
Diagnostic Challenges and Consideration of Landau-Kleffner Syndrome as a Differential Diagnosis for Language Disorders: A Case ReportDilara Tomal, Sibylle Hodecker, Konstantin Mechler, et al.
Springerplus|June 20, 2015
Pronounced reversible hyperammonemic encephalopathy associated with combined valproate-topiramate therapy in a 7-year-old girlSebastian Weise, Steffen Syrbe, Matthias Preuss, et al.
Frontiers in Neurology|April 12, 2021
Voltage Gated Sodium Channel Genes in Epilepsy: Mutations, Functional Studies, and Treatment DimensionsIbitayo Abigail Ademuwagun, Solomon Oladapo Rotimi, Steffen Syrbe, et al.
Progress in Retinal and Eye Research|April 3, 2018
The primate fovea: Structure, function and developmentAndreas Bringmann, Steffen Syrbe, Katja Görner, et al.
Experimental Eye Research|December 16, 2017
Müller glial cells of the primate foveola: An electron microscopical studySteffen Syrbe, Heidrun Kuhrt, Ulrich Gärtner, et al.
Molecular and Cellular Pediatrics|June 22, 2026
Cardiomyopathy and mitochondrial encephalomyopathy in a female child associated with a heterozygous X-linked AIFM1 variantChristoph Sandmann, Swathi Gudapati, Johannes A Mayr, et al.
Pageof 14

Showing results (1-10 of 135) with videos related to

Sort By:
Pageof 14
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 5, 2024
Developmental and epileptic encephalopathies - therapeutic consequences of genetic testingSteffen Syrbe
Seminars in Neurology|June 11, 2015
Epileptic Encephalopathies in Childhood: The Role of Genetic TestingJohannes R Lemke, Steffen Syrbe
Pediatric Dermatology|September 5, 2018
Sweaty feet in adolescents-Early use of botulinum type A toxin in juvenile plantar hyperhidrosisMatthias K Bernhard, Matthias Krause, Steffen Syrbe
Orphanet Journal of Rare Diseases|January 6, 2025
Long-term neuropsychologic outcome of pre-emptive mTOR inhibitor treatment in children with tuberous sclerosis complex (TSC) under 4 months of age (PROTECT), a two-arm, randomized, observer-blind, controlled phase IIb national multicentre clinical trial: study protocolJan H Driedger, Julian Schröter, , et al.
Clinical Case Reports|December 22, 2025
Diagnostic Challenges and Consideration of Landau-Kleffner Syndrome as a Differential Diagnosis for Language Disorders: A Case ReportDilara Tomal, Sibylle Hodecker, Konstantin Mechler, et al.
Springerplus|June 20, 2015
Pronounced reversible hyperammonemic encephalopathy associated with combined valproate-topiramate therapy in a 7-year-old girlSebastian Weise, Steffen Syrbe, Matthias Preuss, et al.
Frontiers in Neurology|April 12, 2021
Voltage Gated Sodium Channel Genes in Epilepsy: Mutations, Functional Studies, and Treatment DimensionsIbitayo Abigail Ademuwagun, Solomon Oladapo Rotimi, Steffen Syrbe, et al.
Progress in Retinal and Eye Research|April 3, 2018
The primate fovea: Structure, function and developmentAndreas Bringmann, Steffen Syrbe, Katja Görner, et al.
Experimental Eye Research|December 16, 2017
Müller glial cells of the primate foveola: An electron microscopical studySteffen Syrbe, Heidrun Kuhrt, Ulrich Gärtner, et al.
Molecular and Cellular Pediatrics|June 22, 2026
Cardiomyopathy and mitochondrial encephalomyopathy in a female child associated with a heterozygous X-linked AIFM1 variantChristoph Sandmann, Swathi Gudapati, Johannes A Mayr, et al.
Pageof 14