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D Steinberger

Showing results (31-40 of 45) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|June 1, 2011
Milestones in magnetic resonance imaging and transcranial sonography of movement disordersDaniela Berg, Jonathan D Steinberger, C Warren Olanow, et al.
Human Genetics|August 1, 1997
Evidence of a third locus in X-linked recessive spastic paraplegiaR Steinmüller, A Lantigua-Cruz, R Garcia-Garcia, et al.
Annals of Neurology|May 19, 1998
High penetrance and pronounced variation in expressivity of GCH1 mutations in five families with dopa-responsive dystoniaD Steinberger, Y Weber, R Korinthenberg, et al.
Techniques in Vascular and Interventional Radiology|July 5, 2017
Needs-Based Innovation in Interventional Radiology: The Biodesign ProcessJonathan D Steinberger, Lyn Denend, Dan E Azagury, et al.
Journal of Cranio-Maxillo-Facial Surgery : Official Publication of the European Association for Cranio-Maxillo-Facial Surgery|July 27, 2001
Standardized evaluation and documentation of findings in patients with craniosynostosisT H Jünger, M Reicherts, D Steinberger, et al.
Clinical and Laboratory Haematology|September 24, 2005
Mutation screening for the prothrombin variant G20210A by melting point analysis with the Light Cycler system: atypical results, detection of the variant C20209T and possible clinical implicationsC Wylenzek, J Trübenbach, P Gohl, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 28, 2007
Frequency of GCH1 deletions in Dopa-responsive dystoniaB Zirn, D Steinberger, C Troidl, et al.
Journal of Medical Genetics|July 7, 2009
Enhancer deletions of the SHOX gene as a frequent cause of short stature: the essential role of a 250 kb downstream regulatory domainJ Chen, G Wildhardt, Z Zhong, et al.
AJNR. American Journal of Neuroradiology|October 20, 2000
Prominent basal emissary foramina in syndromic craniosynostosis: correlation with phenotypic and molecular diagnosesC D Robson, J B Mulliken, R L Robertson, et al.
Oncogenesis|April 5, 2013
Selection of a highly invasive neuroblastoma cell population through long-term human cytomegalovirus infectionM Michaelis, S Barth, R Breitling, et al.
Pageof 5

Showing results (31-40 of 45) with videos related to

Sort By:
Pageof 5
Movement Disorders : Official Journal of the Movement Disorder Society|June 1, 2011
Milestones in magnetic resonance imaging and transcranial sonography of movement disordersDaniela Berg, Jonathan D Steinberger, C Warren Olanow, et al.
Human Genetics|August 1, 1997
Evidence of a third locus in X-linked recessive spastic paraplegiaR Steinmüller, A Lantigua-Cruz, R Garcia-Garcia, et al.
Annals of Neurology|May 19, 1998
High penetrance and pronounced variation in expressivity of GCH1 mutations in five families with dopa-responsive dystoniaD Steinberger, Y Weber, R Korinthenberg, et al.
Techniques in Vascular and Interventional Radiology|July 5, 2017
Needs-Based Innovation in Interventional Radiology: The Biodesign ProcessJonathan D Steinberger, Lyn Denend, Dan E Azagury, et al.
Journal of Cranio-Maxillo-Facial Surgery : Official Publication of the European Association for Cranio-Maxillo-Facial Surgery|July 27, 2001
Standardized evaluation and documentation of findings in patients with craniosynostosisT H Jünger, M Reicherts, D Steinberger, et al.
Clinical and Laboratory Haematology|September 24, 2005
Mutation screening for the prothrombin variant G20210A by melting point analysis with the Light Cycler system: atypical results, detection of the variant C20209T and possible clinical implicationsC Wylenzek, J Trübenbach, P Gohl, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 28, 2007
Frequency of GCH1 deletions in Dopa-responsive dystoniaB Zirn, D Steinberger, C Troidl, et al.
Journal of Medical Genetics|July 7, 2009
Enhancer deletions of the SHOX gene as a frequent cause of short stature: the essential role of a 250 kb downstream regulatory domainJ Chen, G Wildhardt, Z Zhong, et al.
AJNR. American Journal of Neuroradiology|October 20, 2000
Prominent basal emissary foramina in syndromic craniosynostosis: correlation with phenotypic and molecular diagnosesC D Robson, J B Mulliken, R L Robertson, et al.
Oncogenesis|April 5, 2013
Selection of a highly invasive neuroblastoma cell population through long-term human cytomegalovirus infectionM Michaelis, S Barth, R Breitling, et al.
Pageof 5