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

I Hausser

Showing results (21-30 of 65) with videos related to

Pageof 7
Sort By:
The British Journal of Dermatology|May 10, 2002
Persistent erythematous eyelid swelling due to metastatic lobular carcinoma of the breastT Zimmermann, U Jappe, I Hausser, et al.
Klinische Padiatrie|May 10, 2014
White sponge nevus - a rare autosomal dominant keratinopathyS Benoit, N Schlipf, I Hausser, et al.
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|July 24, 1998
[Comèl-Netherton syndrome]S Blaschke, R Möller, I Hausser, et al.
European Journal of Dermatology : EJD|November 1, 2000
Preclinical diagnosis of pseudoxanthoma elasticum - methodological restrictions and ethical problemsB Hermes, A Grützkau, I Hausser, et al.
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|February 1, 1994
[Hyalinosis cutis et mucosae and Ehlers-Danlos syndrome. A rare combination of syndromes]I König, I Hausser, I Anton-Lamprecht, et al.
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|June 1, 1993
[Olmsted syndrome. Successful therapy by treatment with etretinate]I Hausser, Y Frantzmann, I Anton-Lamprecht, et al.
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|January 1, 1991
[Hyalinosis cutis et mucosae (Urbach-Wiethe disease)--ultrastructural and immunological characteristics]I Hausser, S Biltz, E Rauterberg, et al.
Klinische Padiatrie|May 17, 2000
[Neonatal progeroid syndrome (Wiedemann-Rautenstrauch syndrome): case report and review of the literature]T Hoppen, I Hausser, U Theile, et al.
Acta Dermato-Venereologica|July 1, 1996
Autosomal recessive cutis laxa syndrome. A case reportK Jung, U Ueberham, I Hausser, et al.
American Journal of Human Genetics|March 1, 1997
Mutations in the COL5A1 gene are causal in the Ehlers-Danlos syndromes I and IIA De Paepe, L Nuytinck, I Hausser, et al.
Pageof 7

Showing results (21-30 of 65) with videos related to

Sort By:
Pageof 7
The British Journal of Dermatology|May 10, 2002
Persistent erythematous eyelid swelling due to metastatic lobular carcinoma of the breastT Zimmermann, U Jappe, I Hausser, et al.
Klinische Padiatrie|May 10, 2014
White sponge nevus - a rare autosomal dominant keratinopathyS Benoit, N Schlipf, I Hausser, et al.
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|July 24, 1998
[Comèl-Netherton syndrome]S Blaschke, R Möller, I Hausser, et al.
European Journal of Dermatology : EJD|November 1, 2000
Preclinical diagnosis of pseudoxanthoma elasticum - methodological restrictions and ethical problemsB Hermes, A Grützkau, I Hausser, et al.
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|February 1, 1994
[Hyalinosis cutis et mucosae and Ehlers-Danlos syndrome. A rare combination of syndromes]I König, I Hausser, I Anton-Lamprecht, et al.
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|June 1, 1993
[Olmsted syndrome. Successful therapy by treatment with etretinate]I Hausser, Y Frantzmann, I Anton-Lamprecht, et al.
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|January 1, 1991
[Hyalinosis cutis et mucosae (Urbach-Wiethe disease)--ultrastructural and immunological characteristics]I Hausser, S Biltz, E Rauterberg, et al.
Klinische Padiatrie|May 17, 2000
[Neonatal progeroid syndrome (Wiedemann-Rautenstrauch syndrome): case report and review of the literature]T Hoppen, I Hausser, U Theile, et al.
Acta Dermato-Venereologica|July 1, 1996
Autosomal recessive cutis laxa syndrome. A case reportK Jung, U Ueberham, I Hausser, et al.
American Journal of Human Genetics|March 1, 1997
Mutations in the COL5A1 gene are causal in the Ehlers-Danlos syndromes I and IIA De Paepe, L Nuytinck, I Hausser, et al.
Pageof 7