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

Ingrid Hausser

Showing results (61-70 of 112) with videos related to

Pageof 12
Sort By:
Clinical and Experimental Dermatology|May 20, 2024
Skin fragility and wound management in Ehlers-Danlos syndromes: a report by the International Consortium on Ehlers-Danlos Syndromes and Hypermobility Spectrum Disorders Skin Working GroupChloe Angwin, Brent J Doolan, Ingrid Hausser, et al.
Clinical Journal of the American Society of Nephrology : CJASN|April 4, 2008
Ultrastructural evidence of dermal gadolinium deposits in a patient with nephrogenic systemic fibrosis and end-stage renal diseaseJosef A Schroeder, Christian Weingart, Brigitte Coras, et al.
Stroke|October 21, 2006
Familial cervical artery dissections: clinical, morphologic, and genetic studiesJuan Jose Martin, Ingrid Hausser, Philippe Lyrer, et al.
American Journal of Medical Genetics. Part A|February 4, 2005
Ullrich congenital muscular dystrophy: connective tissue abnormalities in the skin support overlap with Ehlers-Danlos syndromesJanbernd Kirschner, Ingrid Hausser, Yaqun Zou, et al.
Redox Biology|April 21, 2025
Endogenous acrolein accumulation in akr7a3 mutants causes microvascular dysfunction due to increased arachidonic acid metabolismXin Zhang, Johannes Gschwind, Vanessa Erben, et al.
Journal of Clinical Medicine|June 24, 2022
Multiple Arterial Dissections and Connective Tissue AbnormalitiesPhilipp Erhart, Daniel Körfer, Susanne Dihlmann, et al.
The Journal of Investigative Dermatology|April 20, 2024
Autosomal Dominant Lamellar Ichthyosis Due to a Missense Variant in the Gene NKPD1Katalin Komlosi, Cristina Glocker, Hao-Hsiang Hsu-Rehder, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|July 2, 2009
Mechanisms of fibroblast cell therapy for dystrophic epidermolysis bullosa: high stability of collagen VII favors long-term skin integrityJohannes S Kern, Stefan Loeckermann, Anja Fritsch, et al.
Human Molecular Genetics|September 14, 2006
Bathing suit ichthyosis is caused by transglutaminase-1 deficiency: evidence for a temperature-sensitive phenotypeVinzenz Oji, Juliette Mazereeuw Hautier, Bijan Ahvazi, et al.
Molecular Therapy. Nucleic Acids|June 3, 2018
Deletion of a Pathogenic Mutation-Containing Exon of COL7A1 Allows Clonal Gene Editing Correction of RDEB Patient Epidermal Stem CellsÁngeles Mencía, Cristina Chamorro, Jose Bonafont, et al.
Pageof 12

Showing results (61-70 of 112) with videos related to

Sort By:
Pageof 12
Clinical and Experimental Dermatology|May 20, 2024
Skin fragility and wound management in Ehlers-Danlos syndromes: a report by the International Consortium on Ehlers-Danlos Syndromes and Hypermobility Spectrum Disorders Skin Working GroupChloe Angwin, Brent J Doolan, Ingrid Hausser, et al.
Clinical Journal of the American Society of Nephrology : CJASN|April 4, 2008
Ultrastructural evidence of dermal gadolinium deposits in a patient with nephrogenic systemic fibrosis and end-stage renal diseaseJosef A Schroeder, Christian Weingart, Brigitte Coras, et al.
Stroke|October 21, 2006
Familial cervical artery dissections: clinical, morphologic, and genetic studiesJuan Jose Martin, Ingrid Hausser, Philippe Lyrer, et al.
American Journal of Medical Genetics. Part A|February 4, 2005
Ullrich congenital muscular dystrophy: connective tissue abnormalities in the skin support overlap with Ehlers-Danlos syndromesJanbernd Kirschner, Ingrid Hausser, Yaqun Zou, et al.
Redox Biology|April 21, 2025
Endogenous acrolein accumulation in akr7a3 mutants causes microvascular dysfunction due to increased arachidonic acid metabolismXin Zhang, Johannes Gschwind, Vanessa Erben, et al.
Journal of Clinical Medicine|June 24, 2022
Multiple Arterial Dissections and Connective Tissue AbnormalitiesPhilipp Erhart, Daniel Körfer, Susanne Dihlmann, et al.
The Journal of Investigative Dermatology|April 20, 2024
Autosomal Dominant Lamellar Ichthyosis Due to a Missense Variant in the Gene NKPD1Katalin Komlosi, Cristina Glocker, Hao-Hsiang Hsu-Rehder, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|July 2, 2009
Mechanisms of fibroblast cell therapy for dystrophic epidermolysis bullosa: high stability of collagen VII favors long-term skin integrityJohannes S Kern, Stefan Loeckermann, Anja Fritsch, et al.
Human Molecular Genetics|September 14, 2006
Bathing suit ichthyosis is caused by transglutaminase-1 deficiency: evidence for a temperature-sensitive phenotypeVinzenz Oji, Juliette Mazereeuw Hautier, Bijan Ahvazi, et al.
Molecular Therapy. Nucleic Acids|June 3, 2018
Deletion of a Pathogenic Mutation-Containing Exon of COL7A1 Allows Clonal Gene Editing Correction of RDEB Patient Epidermal Stem CellsÁngeles Mencía, Cristina Chamorro, Jose Bonafont, et al.
Pageof 12