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Sibylle Eigelshoven

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Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|July 2, 2011
Immediate and delayed hypersensitivity to corticosteroidsSarah Basedow, Sibylle Eigelshoven, Bernhard Homey
Folia Histochemica Et Cytobiologica|May 8, 2009
Cytokeratin 18 expression in immature Sertoli cells: co-localization with interstitial lymphocytic infiltratesRoland Kruse, Sibylle Eigelshoven, Anna Kaiser, et al.
Archives of Dermatology|September 20, 2006
Thelalgia in man: successful treatment with botulinum toxinSibylle Eigelshoven, Roland Kruse, Lucie Rauch, et al.
Archives of Dermatological Research|June 17, 2009
Novel mutations in the P2RY5 gene in one Turkish and two Indian patients presenting with hypotrichosis and woolly hairSandra M Pasternack, Sundaram Murugusundram, Sibylle Eigelshoven, et al.
Pediatric Dermatology|June 26, 2008
Richner-Hanhart syndrome detected by expanded newborn screeningThomas Meissner, Regina Christine Betz, Sandra M Pasternack, et al.
European Journal of Cell Biology|April 3, 2007
Identification of a keratin-associated protein with a putative role in vesicle transportLaura Planko, Karsten Böhse, Jörg Höhfeld, et al.
Journal of the American Academy of Dermatology|July 28, 2010
Marie Unna hereditary hypotrichosis: identification of a U2HR mutation in the family from the original 1925 reportSilke Redler, Roland Kruse, Sibylle Eigelshoven, et al.
European Journal of Dermatology : EJD|August 29, 2006
Investigation of the HLA-DRB1 locus in alopecia areataPatricia Entz, Bettina Blaumeiser, Regina C Betz, et al.
Pediatric Dermatology|March 5, 2010
Waardenburg syndrome type I with heterochromia iridis and circumscribed hypopigmentation of the skinSibylle Eigelshoven, Gitta Kameda, Anne-Katrin Kortüm, et al.
American Journal of Human Genetics|February 9, 2006
Loss-of-function mutations in the keratin 5 gene lead to Dowling-Degos diseaseRegina C Betz, Laura Planko, Sibylle Eigelshoven, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|July 2, 2011
Immediate and delayed hypersensitivity to corticosteroidsSarah Basedow, Sibylle Eigelshoven, Bernhard Homey
Folia Histochemica Et Cytobiologica|May 8, 2009
Cytokeratin 18 expression in immature Sertoli cells: co-localization with interstitial lymphocytic infiltratesRoland Kruse, Sibylle Eigelshoven, Anna Kaiser, et al.
Archives of Dermatology|September 20, 2006
Thelalgia in man: successful treatment with botulinum toxinSibylle Eigelshoven, Roland Kruse, Lucie Rauch, et al.
Archives of Dermatological Research|June 17, 2009
Novel mutations in the P2RY5 gene in one Turkish and two Indian patients presenting with hypotrichosis and woolly hairSandra M Pasternack, Sundaram Murugusundram, Sibylle Eigelshoven, et al.
Pediatric Dermatology|June 26, 2008
Richner-Hanhart syndrome detected by expanded newborn screeningThomas Meissner, Regina Christine Betz, Sandra M Pasternack, et al.
European Journal of Cell Biology|April 3, 2007
Identification of a keratin-associated protein with a putative role in vesicle transportLaura Planko, Karsten Böhse, Jörg Höhfeld, et al.
Journal of the American Academy of Dermatology|July 28, 2010
Marie Unna hereditary hypotrichosis: identification of a U2HR mutation in the family from the original 1925 reportSilke Redler, Roland Kruse, Sibylle Eigelshoven, et al.
European Journal of Dermatology : EJD|August 29, 2006
Investigation of the HLA-DRB1 locus in alopecia areataPatricia Entz, Bettina Blaumeiser, Regina C Betz, et al.
Pediatric Dermatology|March 5, 2010
Waardenburg syndrome type I with heterochromia iridis and circumscribed hypopigmentation of the skinSibylle Eigelshoven, Gitta Kameda, Anne-Katrin Kortüm, et al.
American Journal of Human Genetics|February 9, 2006
Loss-of-function mutations in the keratin 5 gene lead to Dowling-Degos diseaseRegina C Betz, Laura Planko, Sibylle Eigelshoven, et al.
Pageof 2