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I Hausser

Showing results (41-50 of 65) with videos related to

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Neurology|April 10, 2002
Sequence analysis of the COL5A2 gene in patients with spontaneous cervical artery dissectionsC Grond-Ginsbach, F Wigger, M Morcher, et al.
Stroke|August 6, 2000
Mutations in the tropoelastin gene (ELN) were not found in patients with spontaneous cervical artery dissectionsC Grond-Ginsbach, C Thomas-Feles, I Werner, et al.
The British Journal of Dermatology|August 1, 2014
A mouse organotypic tissue culture model for autosomal recessive congenital ichthyosisS Rosenberger, A Dick, S Latzko, et al.
VASA. Zeitschrift Fur Gefasskrankheiten|May 14, 2010
Treatment of an asymptomatic penetrating aortic ulcer in a young patientM Hakimi, P Geisbüsch, M-L Gross, et al.
The British Journal of Dermatology|April 16, 2002
Genetic analysis of a severe case of Netherton syndrome and application for prenatal testingF B Müller, I Hausser, D Berg, et al.
Clinical and Experimental Dermatology|March 22, 2008
Effective treatment of severe thermodysregulation by oral retinoids in a patient with recessive congenital lamellar ichthyosisH A Haenssle, A Finkenrath, I Hausser, et al.
Stroke|September 2, 1999
Mutations in the COL5A1 coding sequence are not common in patients with spontaneous cervical artery dissectionsC Grond-Ginsbach, R Weber, J Haas, et al.
Der Pathologe|December 11, 1999
[Restrictive dermopathy]C Gross, I Hausser, A von der Wense, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|March 26, 2017
At first sight or second glance: clinical presentation of mosaic manifestations of autosomal dominant skin disorders - a case seriesF Toberer, R Happle, R Schneiderbauer, et al.
The British Journal of Dermatology|September 18, 2008
Novel and recurrent mutations in the 1B domain of keratin 1 in palmoplantar keratoderma with tonotubulesG Grimberg, I Hausser, F B Müller, et al.
Pageof 7

Showing results (41-50 of 65) with videos related to

Sort By:
Pageof 7
Neurology|April 10, 2002
Sequence analysis of the COL5A2 gene in patients with spontaneous cervical artery dissectionsC Grond-Ginsbach, F Wigger, M Morcher, et al.
Stroke|August 6, 2000
Mutations in the tropoelastin gene (ELN) were not found in patients with spontaneous cervical artery dissectionsC Grond-Ginsbach, C Thomas-Feles, I Werner, et al.
The British Journal of Dermatology|August 1, 2014
A mouse organotypic tissue culture model for autosomal recessive congenital ichthyosisS Rosenberger, A Dick, S Latzko, et al.
VASA. Zeitschrift Fur Gefasskrankheiten|May 14, 2010
Treatment of an asymptomatic penetrating aortic ulcer in a young patientM Hakimi, P Geisbüsch, M-L Gross, et al.
The British Journal of Dermatology|April 16, 2002
Genetic analysis of a severe case of Netherton syndrome and application for prenatal testingF B Müller, I Hausser, D Berg, et al.
Clinical and Experimental Dermatology|March 22, 2008
Effective treatment of severe thermodysregulation by oral retinoids in a patient with recessive congenital lamellar ichthyosisH A Haenssle, A Finkenrath, I Hausser, et al.
Stroke|September 2, 1999
Mutations in the COL5A1 coding sequence are not common in patients with spontaneous cervical artery dissectionsC Grond-Ginsbach, R Weber, J Haas, et al.
Der Pathologe|December 11, 1999
[Restrictive dermopathy]C Gross, I Hausser, A von der Wense, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|March 26, 2017
At first sight or second glance: clinical presentation of mosaic manifestations of autosomal dominant skin disorders - a case seriesF Toberer, R Happle, R Schneiderbauer, et al.
The British Journal of Dermatology|September 18, 2008
Novel and recurrent mutations in the 1B domain of keratin 1 in palmoplantar keratoderma with tonotubulesG Grimberg, I Hausser, F B Müller, et al.
Pageof 7