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H B Wessel

Showing results (11-20 of 18) with videos related to

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The Journal of Pediatrics|December 1, 1992
Tardive dyskinesia associated with use of metoclopramide in a childP E Putnam, S R Orenstein, H B Wessel, et al.
Journal of Computer Assisted Tomography|February 1, 1979
Multiple cystic encephalomalacia of infancy: computed tomographic findings in two cases with associated intracerebral calcificationP J Dubois, E R Heinz, H B Wessel, et al.
American Journal of Medical Genetics|August 1, 1992
X inactivation and dystrophin studies in a t(X;12) female: evidence for biochemical normalization in Duchenne muscular dystrophy carriersS L Wenger, M W Steele, E P Hoffman, et al.
Neurology|September 1, 1978
Imipramine in absence and myoclonic-astatic seizuresG H Fromm, H B Wessel, J D Glass, et al.
American Journal of Human Genetics|June 1, 1993
Molecular genetic and genetic correlations in sodium channelopathies: lack of founder effect and evidence for a second geneJ Wang, J Zhou, S M Todorovic, et al.
Journal of Medical Genetics|March 3, 2009
Mutations in LAMB2 causing a severe form of synaptic congenital myasthenic syndromeR A Maselli, J J Ng, J A Anderson, et al.
American Journal of Human Genetics|June 1, 1994
Detection of new paternal dystrophin gene mutations in isolated cases of dystrophinopathy in femalesE Pegoraro, R N Schimke, K Arahata, et al.
Neurology|April 1, 1995
Genetic and biochemical normalization in female carriers of Duchenne muscular dystrophy: evidence for failure of dystrophin production in dystrophin-competent myonucleiE Pegoraro, R N Schimke, C Garcia, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
The Journal of Pediatrics|December 1, 1992
Tardive dyskinesia associated with use of metoclopramide in a childP E Putnam, S R Orenstein, H B Wessel, et al.
Journal of Computer Assisted Tomography|February 1, 1979
Multiple cystic encephalomalacia of infancy: computed tomographic findings in two cases with associated intracerebral calcificationP J Dubois, E R Heinz, H B Wessel, et al.
American Journal of Medical Genetics|August 1, 1992
X inactivation and dystrophin studies in a t(X;12) female: evidence for biochemical normalization in Duchenne muscular dystrophy carriersS L Wenger, M W Steele, E P Hoffman, et al.
Neurology|September 1, 1978
Imipramine in absence and myoclonic-astatic seizuresG H Fromm, H B Wessel, J D Glass, et al.
American Journal of Human Genetics|June 1, 1993
Molecular genetic and genetic correlations in sodium channelopathies: lack of founder effect and evidence for a second geneJ Wang, J Zhou, S M Todorovic, et al.
Journal of Medical Genetics|March 3, 2009
Mutations in LAMB2 causing a severe form of synaptic congenital myasthenic syndromeR A Maselli, J J Ng, J A Anderson, et al.
American Journal of Human Genetics|June 1, 1994
Detection of new paternal dystrophin gene mutations in isolated cases of dystrophinopathy in femalesE Pegoraro, R N Schimke, K Arahata, et al.
Neurology|April 1, 1995
Genetic and biochemical normalization in female carriers of Duchenne muscular dystrophy: evidence for failure of dystrophin production in dystrophin-competent myonucleiE Pegoraro, R N Schimke, C Garcia, et al.
Pageof 2