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H Doose

Showing results (61-70 of 70) with videos related to

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Neuropadiatrie|August 1, 1970
Centrencephalic myoclonic-astatic petit mal. Clinical and genetic investigationH Doose, H Gerken, R Leonhardt, et al.
European Neurology|January 1, 1978
Sinal myoclonusM Nohl, H Doose, G Gross-Selbeck, et al.
Neuropediatrics|April 21, 2001
Atypical "benign" partial epilepsy of childhood or pseudo-lennox syndrome. Part II: family studyH Doose, A Hahn, B A Neubauer, et al.
Neuropediatrics|May 1, 1984
Cerebellar atrophy following diphenylhydantoin intoxicationW K Baier, U Beck, H Doose, et al.
Neuropediatrics|August 1, 1985
Longterm follow-up of childhood epilepsy with absences. I. Epilepsy with absences at onsetE Dieterich, W K Baier, H Doose, et al.
Developmental Medicine and Child Neurology|October 1, 1988
Benign partial epilepsy--treatment with sulthiameH Doose, W K Baier, J P Ernst, et al.
Neuropadiatrie|November 1, 1977
Cranial computertomography in children with tuberous sclerosisH D Kuhlendahl, G Gross-Selbeck, H Doose, et al.
Neuropediatrics|August 1, 1993
Exclusion of linkage of genetic focal sharp waves to the HLA region on chromosome 6p in families with benign partial epilepsy with centrotemporal sharp wavesW Whitehouse, U Diebold, M Rees, et al.
Neuropediatrics|August 1, 1993
Benign childhood epilepsy with centrotemporal spikes and the focal sharp wave trait is not linked to the fragile X regionM Rees, U Diebold, K Parker, et al.
Neuropediatrics|June 10, 2005
SCN1A mutation analysis in myoclonic astatic epilepsy and severe idiopathic generalized epilepsy of infancy with generalized tonic-clonic seizuresK Ebach, H Joos, H Doose, et al.
Pageof 7

Showing results (61-70 of 70) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 70 results.
Neuropadiatrie|August 1, 1970
Centrencephalic myoclonic-astatic petit mal. Clinical and genetic investigationH Doose, H Gerken, R Leonhardt, et al.
European Neurology|January 1, 1978
Sinal myoclonusM Nohl, H Doose, G Gross-Selbeck, et al.
Neuropediatrics|April 21, 2001
Atypical "benign" partial epilepsy of childhood or pseudo-lennox syndrome. Part II: family studyH Doose, A Hahn, B A Neubauer, et al.
Neuropediatrics|May 1, 1984
Cerebellar atrophy following diphenylhydantoin intoxicationW K Baier, U Beck, H Doose, et al.
Neuropediatrics|August 1, 1985
Longterm follow-up of childhood epilepsy with absences. I. Epilepsy with absences at onsetE Dieterich, W K Baier, H Doose, et al.
Developmental Medicine and Child Neurology|October 1, 1988
Benign partial epilepsy--treatment with sulthiameH Doose, W K Baier, J P Ernst, et al.
Neuropadiatrie|November 1, 1977
Cranial computertomography in children with tuberous sclerosisH D Kuhlendahl, G Gross-Selbeck, H Doose, et al.
Neuropediatrics|August 1, 1993
Exclusion of linkage of genetic focal sharp waves to the HLA region on chromosome 6p in families with benign partial epilepsy with centrotemporal sharp wavesW Whitehouse, U Diebold, M Rees, et al.
Neuropediatrics|August 1, 1993
Benign childhood epilepsy with centrotemporal spikes and the focal sharp wave trait is not linked to the fragile X regionM Rees, U Diebold, K Parker, et al.
Neuropediatrics|June 10, 2005
SCN1A mutation analysis in myoclonic astatic epilepsy and severe idiopathic generalized epilepsy of infancy with generalized tonic-clonic seizuresK Ebach, H Joos, H Doose, et al.
Pageof 7