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U Stephani

Showing results (41-50 of 62) with videos related to

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Neurology|November 5, 2010
Prospective memory in patients with juvenile myoclonic epilepsy and their healthy siblingsB Wandschneider, U A Kopp, M Kliegel, et al.
Neuropediatrics|August 1, 1983
Cranial computed tomography of 64 children in continuous complete remission of leukemia II: relations to patient data and neurological complicationsU Stephani, G Harten, H J Langermann, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|March 3, 2001
Holoprosencephaly and low molecular weight proteinuria: the human homologue of murine megalin deficiencyD Müller, T Ankermann, U Stephani, et al.
Advances in Neurology|October 29, 2004
Photosensitivity: genetics and clinical significanceB A Neubauer, St Waltz, M Grothe, et al.
Neuropediatrics|November 9, 2000
Nonconvulsive status epilepticus--a possible cause of mental retardation in patients with Lennox-Gastaut syndromeM Hoffmann-Riem, W Diener, C Benninger, et al.
Developmental Medicine and Child Neurology|March 22, 2003
Grip force parameters in precision grip of individuals with myelomeningoceleM Gölge, C Schütz, M Dreesmann, et al.
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|January 9, 2015
Validating the effect of muscle artifact suppression in localizing focal epilepsyK G Mideksa, A Santillan-Guzman, N Japaridze, et al.
Acta Neurologica Scandinavica|June 18, 2002
Guidelines for the use of EEG methodology in the diagnosis of epilepsy. International League Against Epilepsy: commission report. Commission on European Affairs: Subcommission on European GuidelinesR Flink, B Pedersen, A B Guekht, et al.
Molecular Genetics and Metabolism|July 12, 2003
Partial response to biotin therapy in a patient with holocarboxylase synthetase deficiency: clinical, biochemical, and molecular genetic aspectsR Santer, H Muhle, T Suormala, et al.
Cephalalgia : an International Journal of Headache|August 8, 2007
Central mechanisms of controlled-release metoprolol in migraine: a double-blind, placebo-controlled studyM Siniatchkin, F Andrasik, P Kropp, et al.
Pageof 7

Showing results (41-50 of 62) with videos related to

Sort By:
Pageof 7
Neurology|November 5, 2010
Prospective memory in patients with juvenile myoclonic epilepsy and their healthy siblingsB Wandschneider, U A Kopp, M Kliegel, et al.
Neuropediatrics|August 1, 1983
Cranial computed tomography of 64 children in continuous complete remission of leukemia II: relations to patient data and neurological complicationsU Stephani, G Harten, H J Langermann, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|March 3, 2001
Holoprosencephaly and low molecular weight proteinuria: the human homologue of murine megalin deficiencyD Müller, T Ankermann, U Stephani, et al.
Advances in Neurology|October 29, 2004
Photosensitivity: genetics and clinical significanceB A Neubauer, St Waltz, M Grothe, et al.
Neuropediatrics|November 9, 2000
Nonconvulsive status epilepticus--a possible cause of mental retardation in patients with Lennox-Gastaut syndromeM Hoffmann-Riem, W Diener, C Benninger, et al.
Developmental Medicine and Child Neurology|March 22, 2003
Grip force parameters in precision grip of individuals with myelomeningoceleM Gölge, C Schütz, M Dreesmann, et al.
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|January 9, 2015
Validating the effect of muscle artifact suppression in localizing focal epilepsyK G Mideksa, A Santillan-Guzman, N Japaridze, et al.
Acta Neurologica Scandinavica|June 18, 2002
Guidelines for the use of EEG methodology in the diagnosis of epilepsy. International League Against Epilepsy: commission report. Commission on European Affairs: Subcommission on European GuidelinesR Flink, B Pedersen, A B Guekht, et al.
Molecular Genetics and Metabolism|July 12, 2003
Partial response to biotin therapy in a patient with holocarboxylase synthetase deficiency: clinical, biochemical, and molecular genetic aspectsR Santer, H Muhle, T Suormala, et al.
Cephalalgia : an International Journal of Headache|August 8, 2007
Central mechanisms of controlled-release metoprolol in migraine: a double-blind, placebo-controlled studyM Siniatchkin, F Andrasik, P Kropp, et al.
Pageof 7