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Der Nervenarzt
|
January 13, 2018
[Genetics of tremor]
G Kuhlenbäumer, F Hopfner
Fortschritte Der Neurologie-Psychiatrie
|
May 12, 2004
[Spontaneous dissection of brain providing neck artery]
G Kuhlenbäumer, E B Ringelstein, F Stögbauer
Recent Results in Cancer Research. Fortschritte Der Krebsforschung. Progres Dans Les Recherches Sur Le Cancer
|
January 1, 1993
Mutations in the regulatory domains of bcr/abl-positive leukemias detected by solid-phase automated DNA sequencing
J Maurer, R Reinhardt, G Kuhlenbäumer, et al.
Neuromuscular Disorders : NMD
|
September 21, 2000
Diagnostic guidelines for hereditary neuralgic amyotrophy or heredofamilial neuritis with brachial plexus predilection. On behalf of the European CMT Consortium
G Kuhlenbäumer, F Stögbauer, V Timmerman, et al.
Journal of Neurology
|
March 27, 2001
Thirty-seven CAG repeats in the androgen receptor gene in two healthy individuals
G Kuhlenbäumer, W Kress, E B Ringelstein, et al.
Transplantation Proceedings
|
May 1, 1997
Transcription of the gene for the rat T cell differentiation marker RT6 is mainly mediated by a promoter 5' of exon 2
G Kuhlenbäumer, F Haag, F Koch-Nolte, et al.
Der Nervenarzt
|
October 3, 1998
[X-chromosomal recessive spinobulbar muscular atrophy (Kennedy type). Description of a family, clinical aspects, molecular genetics, differential diagnosis and therapy]
G Kuhlenbäumer, M Bocchicchio, W Kress, et al.
Neurology
|
February 19, 2000
Hereditary recurrent focal neuropathies: clinical and molecular features
F Stögbauer, P Young, G Kuhlenbäumer, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
September 1, 1996
Structure of the gene encoding the rat T cell ecto-ADP-ribosyltransferase RT6
F A Haag, G Kuhlenbäumer, F Koch-Nolte, et al.
Cephalalgia : an International Journal of Headache
|
January 24, 2006
Genetic variants of the NOTCH3 gene in migraine--a mutation analysis and association study
S Schwaag, S Evers, A Schirmacher, et al.
Page
of 5
Search research articles
Search
Showing results (1-10 of 44) with videos related to
Sort By:
Page
of 5
Der Nervenarzt
|
January 13, 2018
[Genetics of tremor]
G Kuhlenbäumer, F Hopfner
Fortschritte Der Neurologie-Psychiatrie
|
May 12, 2004
[Spontaneous dissection of brain providing neck artery]
G Kuhlenbäumer, E B Ringelstein, F Stögbauer
Recent Results in Cancer Research. Fortschritte Der Krebsforschung. Progres Dans Les Recherches Sur Le Cancer
|
January 1, 1993
Mutations in the regulatory domains of bcr/abl-positive leukemias detected by solid-phase automated DNA sequencing
J Maurer, R Reinhardt, G Kuhlenbäumer, et al.
Neuromuscular Disorders : NMD
|
September 21, 2000
Diagnostic guidelines for hereditary neuralgic amyotrophy or heredofamilial neuritis with brachial plexus predilection. On behalf of the European CMT Consortium
G Kuhlenbäumer, F Stögbauer, V Timmerman, et al.
Journal of Neurology
|
March 27, 2001
Thirty-seven CAG repeats in the androgen receptor gene in two healthy individuals
G Kuhlenbäumer, W Kress, E B Ringelstein, et al.
Transplantation Proceedings
|
May 1, 1997
Transcription of the gene for the rat T cell differentiation marker RT6 is mainly mediated by a promoter 5' of exon 2
G Kuhlenbäumer, F Haag, F Koch-Nolte, et al.
Der Nervenarzt
|
October 3, 1998
[X-chromosomal recessive spinobulbar muscular atrophy (Kennedy type). Description of a family, clinical aspects, molecular genetics, differential diagnosis and therapy]
G Kuhlenbäumer, M Bocchicchio, W Kress, et al.
Neurology
|
February 19, 2000
Hereditary recurrent focal neuropathies: clinical and molecular features
F Stögbauer, P Young, G Kuhlenbäumer, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
September 1, 1996
Structure of the gene encoding the rat T cell ecto-ADP-ribosyltransferase RT6
F A Haag, G Kuhlenbäumer, F Koch-Nolte, et al.
Cephalalgia : an International Journal of Headache
|
January 24, 2006
Genetic variants of the NOTCH3 gene in migraine--a mutation analysis and association study
S Schwaag, S Evers, A Schirmacher, et al.
Page
of 5