Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

M Weissert

Showing results (11-20 of 22) with videos related to

Pageof 3
Sort By:
Journal of Inherited Metabolic Disease|January 1, 1992
Mitochondrial DNA deletion in an 8-year-old boy with Pearson syndromeK E Baerlocher, A Feldges, M Weissert, et al.
Neuropediatrics|December 1, 1994
Childhood stroke at three years of age with transient protein C deficiency, familial antiphospholipid antibodies and F. XII deficiency--a family studyW Korte, H Otremba, S Lutz, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|January 3, 2001
Microsomal epoxide hydrolase expression as a predictor of tamoxifen response in primary breast cancer: a retrospective exploratory study with long-term follow-upP Fritz, T E Mürdter, M Eichelbaum, et al.
Neuropediatrics|December 1, 1994
Follow-up of optic pathway gliomas in children with neurofibromatosis type 1C Kuenzle, M Weissert, E Roulet, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 17, 2003
Ictal bradycardia in a young child with focal cortical dysplasia in the right insular cortexM Seeck, S Zaim, V Chaves-Vischer, et al.
Clinical Genetics|April 25, 2006
Clinical profiles of four patients with Rett syndrome carrying a novel exon 1 mutation or genomic rearrangement in the MECP2 geneD Bartholdi, A Klein, M Weissert, et al.
Elife|December 21, 2016
Transcriptional signatures of somatic neoblasts and germline cells in <i>Macrostomum lignano</i>Magda Grudniewska, Stijn Mouton, Daniil Simanov, et al.
Annals of Neurology|October 20, 1998
Progressive myoclonus epilepsy and mitochondrial myopathy associated with mutations in the tRNA(Ser(UCN)) geneM Jaksch, T Klopstock, G Kurlemann, et al.
Developmental Cell|March 29, 2017
Serum Proteases Potentiate BMP-Induced Cell Cycle Re-entry of Dedifferentiating Muscle Cells during Newt Limb RegenerationInes Wagner, Heng Wang, Philipp M Weissert, et al.
Neuropediatrics|April 12, 2005
The first three years of the Swiss Neuropaediatric Stroke Registry (SNPSR): a population-based study of incidence, symptoms and risk factorsM Steinlin, I Pfister, J Pavlovic, et al.
Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
Journal of Inherited Metabolic Disease|January 1, 1992
Mitochondrial DNA deletion in an 8-year-old boy with Pearson syndromeK E Baerlocher, A Feldges, M Weissert, et al.
Neuropediatrics|December 1, 1994
Childhood stroke at three years of age with transient protein C deficiency, familial antiphospholipid antibodies and F. XII deficiency--a family studyW Korte, H Otremba, S Lutz, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|January 3, 2001
Microsomal epoxide hydrolase expression as a predictor of tamoxifen response in primary breast cancer: a retrospective exploratory study with long-term follow-upP Fritz, T E Mürdter, M Eichelbaum, et al.
Neuropediatrics|December 1, 1994
Follow-up of optic pathway gliomas in children with neurofibromatosis type 1C Kuenzle, M Weissert, E Roulet, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 17, 2003
Ictal bradycardia in a young child with focal cortical dysplasia in the right insular cortexM Seeck, S Zaim, V Chaves-Vischer, et al.
Clinical Genetics|April 25, 2006
Clinical profiles of four patients with Rett syndrome carrying a novel exon 1 mutation or genomic rearrangement in the MECP2 geneD Bartholdi, A Klein, M Weissert, et al.
Elife|December 21, 2016
Transcriptional signatures of somatic neoblasts and germline cells in <i>Macrostomum lignano</i>Magda Grudniewska, Stijn Mouton, Daniil Simanov, et al.
Annals of Neurology|October 20, 1998
Progressive myoclonus epilepsy and mitochondrial myopathy associated with mutations in the tRNA(Ser(UCN)) geneM Jaksch, T Klopstock, G Kurlemann, et al.
Developmental Cell|March 29, 2017
Serum Proteases Potentiate BMP-Induced Cell Cycle Re-entry of Dedifferentiating Muscle Cells during Newt Limb RegenerationInes Wagner, Heng Wang, Philipp M Weissert, et al.
Neuropediatrics|April 12, 2005
The first three years of the Swiss Neuropaediatric Stroke Registry (SNPSR): a population-based study of incidence, symptoms and risk factorsM Steinlin, I Pfister, J Pavlovic, et al.
Pageof 3