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

Knut Brockmann

Showing results (31-40 of 125) with videos related to

Pageof 13
Sort By:
Journal of Pediatric Hematology/Oncology|August 13, 2005
Moyamoya syndrome associated with hemolytic anemia due to Hb AleshaKnut Brockmann, Stephan Stolpe, Carsten Fels, et al.
The Journal of Pediatrics|July 25, 2006
Pediatric multiple sclerosis: detection of clinically silent lesions by multimodal evoked potentialsDaniela Pohl, Kevin Rostasy, Stephanie Treiber-Held, et al.
Neuroradiology|October 3, 2006
Cerebral metabolic and structural alterations in hereditary spastic paraplegia with thin corpus callosum assessed by MRS and DTISteffi Dreha-Kulaczewski, Peter Dechent, Gunther Helms, et al.
American Journal of Human Genetics|December 9, 2003
A novel syndrome combining thyroid and neurological abnormalities is associated with mutations in a monocarboxylate transporter geneAlexandra M Dumitrescu, Xiao-Hui Liao, Thomas B Best, et al.
Human Mutation|March 19, 2005
Identification of ten novel mutations in patients with eIF2B-related disordersAndreas Ohlenbusch, Marco Henneke, Knut Brockmann, et al.
Neuropediatrics|February 26, 2013
Microduplication of 3p26.3 in nonsyndromic intellectual disability indicates an important role of CHL1 for normal cognitive functionMoneef Shoukier, Sigrid Fuchs, Eva Schwaibold, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 29, 2010
Identification of a de novo mutation in SPG11Paola S Denora, Knut Brockmann, Marianna Ciccolella, et al.
Journal of Medical Genetics|July 2, 2013
West syndrome, microcephaly, grey matter heterotopia and hypoplasia of corpus callosum due to a novel ARFGEF2 mutationEhud Banne, Osama Atawneh, Marco Henneke, et al.
European Journal of Human Genetics : EJHG|July 17, 2008
Axonal neuropathy with unusual pattern of amyotrophy and alacrima associated with a novel AAAS mutation p.Leu430PheKatrin Koehler, Knut Brockmann, Manuela Krumbholz, et al.
Brain & Development|January 22, 2003
Cerebral proton magnetic resonance spectroscopy of a patient with giant axonal neuropathyKnut Brockmann, Petra J W Pouwels, Peter Dechent, et al.
Pageof 13

Showing results (31-40 of 125) with videos related to

Sort By:
Pageof 13
Journal of Pediatric Hematology/Oncology|August 13, 2005
Moyamoya syndrome associated with hemolytic anemia due to Hb AleshaKnut Brockmann, Stephan Stolpe, Carsten Fels, et al.
The Journal of Pediatrics|July 25, 2006
Pediatric multiple sclerosis: detection of clinically silent lesions by multimodal evoked potentialsDaniela Pohl, Kevin Rostasy, Stephanie Treiber-Held, et al.
Neuroradiology|October 3, 2006
Cerebral metabolic and structural alterations in hereditary spastic paraplegia with thin corpus callosum assessed by MRS and DTISteffi Dreha-Kulaczewski, Peter Dechent, Gunther Helms, et al.
American Journal of Human Genetics|December 9, 2003
A novel syndrome combining thyroid and neurological abnormalities is associated with mutations in a monocarboxylate transporter geneAlexandra M Dumitrescu, Xiao-Hui Liao, Thomas B Best, et al.
Human Mutation|March 19, 2005
Identification of ten novel mutations in patients with eIF2B-related disordersAndreas Ohlenbusch, Marco Henneke, Knut Brockmann, et al.
Neuropediatrics|February 26, 2013
Microduplication of 3p26.3 in nonsyndromic intellectual disability indicates an important role of CHL1 for normal cognitive functionMoneef Shoukier, Sigrid Fuchs, Eva Schwaibold, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 29, 2010
Identification of a de novo mutation in SPG11Paola S Denora, Knut Brockmann, Marianna Ciccolella, et al.
Journal of Medical Genetics|July 2, 2013
West syndrome, microcephaly, grey matter heterotopia and hypoplasia of corpus callosum due to a novel ARFGEF2 mutationEhud Banne, Osama Atawneh, Marco Henneke, et al.
European Journal of Human Genetics : EJHG|July 17, 2008
Axonal neuropathy with unusual pattern of amyotrophy and alacrima associated with a novel AAAS mutation p.Leu430PheKatrin Koehler, Knut Brockmann, Manuela Krumbholz, et al.
Brain & Development|January 22, 2003
Cerebral proton magnetic resonance spectroscopy of a patient with giant axonal neuropathyKnut Brockmann, Petra J W Pouwels, Peter Dechent, et al.
Pageof 13