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C Bodemer

Showing results (111-120 of 214) with videos related to

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Human Molecular Genetics|November 2, 2001
Genetic bases of severe junctional epidermolysis bullosa presenting spontaneous amelioration with agingY Gache, M Allegra, C Bodemer, et al.
Human Immunology|September 1, 1994
Microchimerism frequency two to thirty years after cadaveric kidney transplantationS Caillat-Zucman, C Legendre, C Suberbielle, et al.
Annales De Dermatologie Et De Venereologie|June 23, 2012
[Eruptive naevi in epidermolysis bullosa hereditaria patients]J Miquel, J Chevrant-Breton, A Dupuy, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|January 16, 2022
Skin biopsy is helpful in the diagnosis of hereditary fibrosing POIKiloderma with tendon contractures, myopathy and pulmonary fibrosis, due to FAM111B mutationS Leclerc-Mercier, S Mercier, N Bellon, et al.
Clinical Genetics|April 24, 2010
Germline mosaicism in keratitis-ichthyosis-deafness syndrome: pre-natal diagnosis in a familial lethal formE Sbidian, D Feldmann, J Bengoa, et al.
Blood|February 27, 2001
Differentiation of Langerhans cells in Langerhans cell histiocytosisF Geissmann, Y Lepelletier, S Fraitag, et al.
Annales De Dermatologie Et De Venereologie|January 1, 1993
[Cutaneous manifestations disclosing T-cell gamma/delta lymphoma in a 13-year-old-girl]J C Amoric, C Bodemer, J Donadieu, et al.
Annales De Dermatologie Et De Venereologie|December 22, 1999
[Scleroderma in children: a retrospective study of 70 cases]C Bodemer, M Belon, D Hamel-Teillac, et al.
The Journal of Biological Chemistry|March 30, 2001
Reduced expression of the epithelial adhesion ligand laminin 5 in the skin causes intradermal tissue separationF Spirito, S Chavanas, C Prost-Squarcioni, et al.
The British Journal of Dermatology|September 8, 2011
Nutritional outcome in children with severe generalized recessive dystrophic epidermolysis bullosa: a short- and long-term evaluation of gastrostomy and enteral feedingV Colomb, E Bourdon-Lannoy, C Lambe, et al.
Pageof 22

Showing results (111-120 of 214) with videos related to

Sort By:
Pageof 22
Human Molecular Genetics|November 2, 2001
Genetic bases of severe junctional epidermolysis bullosa presenting spontaneous amelioration with agingY Gache, M Allegra, C Bodemer, et al.
Human Immunology|September 1, 1994
Microchimerism frequency two to thirty years after cadaveric kidney transplantationS Caillat-Zucman, C Legendre, C Suberbielle, et al.
Annales De Dermatologie Et De Venereologie|June 23, 2012
[Eruptive naevi in epidermolysis bullosa hereditaria patients]J Miquel, J Chevrant-Breton, A Dupuy, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|January 16, 2022
Skin biopsy is helpful in the diagnosis of hereditary fibrosing POIKiloderma with tendon contractures, myopathy and pulmonary fibrosis, due to FAM111B mutationS Leclerc-Mercier, S Mercier, N Bellon, et al.
Clinical Genetics|April 24, 2010
Germline mosaicism in keratitis-ichthyosis-deafness syndrome: pre-natal diagnosis in a familial lethal formE Sbidian, D Feldmann, J Bengoa, et al.
Blood|February 27, 2001
Differentiation of Langerhans cells in Langerhans cell histiocytosisF Geissmann, Y Lepelletier, S Fraitag, et al.
Annales De Dermatologie Et De Venereologie|January 1, 1993
[Cutaneous manifestations disclosing T-cell gamma/delta lymphoma in a 13-year-old-girl]J C Amoric, C Bodemer, J Donadieu, et al.
Annales De Dermatologie Et De Venereologie|December 22, 1999
[Scleroderma in children: a retrospective study of 70 cases]C Bodemer, M Belon, D Hamel-Teillac, et al.
The Journal of Biological Chemistry|March 30, 2001
Reduced expression of the epithelial adhesion ligand laminin 5 in the skin causes intradermal tissue separationF Spirito, S Chavanas, C Prost-Squarcioni, et al.
The British Journal of Dermatology|September 8, 2011
Nutritional outcome in children with severe generalized recessive dystrophic epidermolysis bullosa: a short- and long-term evaluation of gastrostomy and enteral feedingV Colomb, E Bourdon-Lannoy, C Lambe, et al.
Pageof 22