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

M Mascaro

Showing results (111-120 of 141) with videos related to

Pageof 15
Sort By:
Annales De Dermatologie Et De Venereologie|January 1, 1991
[Bullous pemphigoid and multiple sclerosis]D Tomasini, V Bonfacini, E Martin-Ortega, et al.
Archives of Dermatology|June 20, 2002
Description of a new mutation in hepatoerythropoietic porphyria and prenatal exclusion of a homozygous fetusCécile Ged, D Ozalla, C Herrero, et al.
The Journal of Dermatological Treatment|May 31, 2003
Radiotherapy for in situ extramammary Paget disease of the vulvaG A Moreno-Arias, C Conill, M A Sola-Casas, et al.
Annales De Dermatologie Et De Venereologie|January 1, 1982
[Neonatal lupus erythematosus]V Lecha, C Herrero, X Bordas, et al.
The Journal of Investigative Dermatology|April 1, 1995
A mutation (G281E) of the human uroporphyrinogen decarboxylase gene causes both hepatoerythropoietic porphyria and overt familial porphyria cutanea tarda: biochemical and genetic studies on Spanish patientsA G Roberts, G H Elder, R E De Salamanca, et al.
Archives of Dermatological Research|May 1, 1997
T-cell population of primary and secondary cutaneous B-cell lymphomas does not express the cutaneous lymphocyte-associated antigen (CLA)R M Marti, G Hausmann, T Estrach, et al.
The British Journal of Dermatology|February 1, 1982
Specific cutaneous manifestations of Waldenström's macroglobulinaemia. A report of two casesJ M Mascaro, E Montserrat, T Estrach, et al.
Archives of Dermatology|June 1, 1993
Fanconi's anemia with cutaneous amyloidosisS Puig, J Ferrando, F Cervantes, et al.
Human Genetics|January 24, 1998
Inherited susceptibility to several cancers but absence of linkage between dysplastic nevus syndrome and CDKN2A in a melanoma family with a mutation in the CDKN2A (P16INK4A) geneS Puig, A Ruiz, T Castel, et al.
Annales De Dermatologie Et De Venereologie|January 1, 1988
[Umbilical metastasis of a carcinoid tumor of the digestive tract]A Lopez-Soto, E Martin-Ortega, P Peris, et al.
Pageof 15

Showing results (111-120 of 141) with videos related to

Sort By:
Pageof 15
Annales De Dermatologie Et De Venereologie|January 1, 1991
[Bullous pemphigoid and multiple sclerosis]D Tomasini, V Bonfacini, E Martin-Ortega, et al.
Archives of Dermatology|June 20, 2002
Description of a new mutation in hepatoerythropoietic porphyria and prenatal exclusion of a homozygous fetusCécile Ged, D Ozalla, C Herrero, et al.
The Journal of Dermatological Treatment|May 31, 2003
Radiotherapy for in situ extramammary Paget disease of the vulvaG A Moreno-Arias, C Conill, M A Sola-Casas, et al.
Annales De Dermatologie Et De Venereologie|January 1, 1982
[Neonatal lupus erythematosus]V Lecha, C Herrero, X Bordas, et al.
The Journal of Investigative Dermatology|April 1, 1995
A mutation (G281E) of the human uroporphyrinogen decarboxylase gene causes both hepatoerythropoietic porphyria and overt familial porphyria cutanea tarda: biochemical and genetic studies on Spanish patientsA G Roberts, G H Elder, R E De Salamanca, et al.
Archives of Dermatological Research|May 1, 1997
T-cell population of primary and secondary cutaneous B-cell lymphomas does not express the cutaneous lymphocyte-associated antigen (CLA)R M Marti, G Hausmann, T Estrach, et al.
The British Journal of Dermatology|February 1, 1982
Specific cutaneous manifestations of Waldenström's macroglobulinaemia. A report of two casesJ M Mascaro, E Montserrat, T Estrach, et al.
Archives of Dermatology|June 1, 1993
Fanconi's anemia with cutaneous amyloidosisS Puig, J Ferrando, F Cervantes, et al.
Human Genetics|January 24, 1998
Inherited susceptibility to several cancers but absence of linkage between dysplastic nevus syndrome and CDKN2A in a melanoma family with a mutation in the CDKN2A (P16INK4A) geneS Puig, A Ruiz, T Castel, et al.
Annales De Dermatologie Et De Venereologie|January 1, 1988
[Umbilical metastasis of a carcinoid tumor of the digestive tract]A Lopez-Soto, E Martin-Ortega, P Peris, et al.
Pageof 15