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 Fimiani

Showing results (161-170 of 171) with videos related to

Pageof 18
Sort By:
Human Mutation|July 5, 2001
Pseudoxanthoma elasticum: Point mutations in the ABCC6 gene and a large deletion including also ABCC1 and MYH11I Meloni, P Rubegni, G De Aloe, et al.
British Journal of Haematology|July 21, 2005
Role of extracorporeal photochemotherapy in patients with refractory chronic graft-versus-host diseaseP Rubegni, A Cuccia, P Sbano, et al.
The British Journal of Dermatology|February 8, 2019
Dermoscopy for the diagnosis of eyelid margin tumoursE Cinotti, A La Rocca, B Labeille, et al.
Scandinavian Journal of Rheumatology|October 10, 2012
Expression of RXFP1 in skin of scleroderma patients and control subjectsN Giordano, N Volpi, D Franci, et al.
American Journal of Medical Genetics|November 29, 2002
Cortical periventricular heterotopia with ectodermal dysplasiaR Zannolli, E Conversano, L Serracca, et al.
American Journal of Medical Genetics. Part A|December 21, 2002
Novel CNS syndrome and ectodermal dysplasiaR Zannolli, F Macucci, R M Di Bartolo, et al.
Transplantation Proceedings|March 27, 2001
Photopheresis immunomodulation after heart transplantationM Maccherini, F Diciolla, F Laghi Pasini, et al.
American Journal of Medical Genetics. Part A|April 27, 2004
Hypertelorism, ptosis, and myopia associated with drug-resistant epilepsy, mental delay, growth deficiency, ectodermal defects, and osteopeniaR Zannolli, S Buoni, F Macucci, et al.
American Journal of Medical Genetics. Part A|December 21, 2002
18q-syndrome and ectodermal dysplasia syndrome: description of a child and his familyR Zannolli, M Pierluigi, L Pucci, et al.
Journal of Medical Genetics|November 25, 2003
Hereditary xanthinuria type II associated with mental delay, autism, cortical renal cysts, nephrocalcinosis, osteopenia, and hair and teeth defectsR Zannolli, V Micheli, M A Mazzei, et al.
Pageof 18

Showing results (161-170 of 171) with videos related to

Sort By:
Pageof 18
Human Mutation|July 5, 2001
Pseudoxanthoma elasticum: Point mutations in the ABCC6 gene and a large deletion including also ABCC1 and MYH11I Meloni, P Rubegni, G De Aloe, et al.
British Journal of Haematology|July 21, 2005
Role of extracorporeal photochemotherapy in patients with refractory chronic graft-versus-host diseaseP Rubegni, A Cuccia, P Sbano, et al.
The British Journal of Dermatology|February 8, 2019
Dermoscopy for the diagnosis of eyelid margin tumoursE Cinotti, A La Rocca, B Labeille, et al.
Scandinavian Journal of Rheumatology|October 10, 2012
Expression of RXFP1 in skin of scleroderma patients and control subjectsN Giordano, N Volpi, D Franci, et al.
American Journal of Medical Genetics|November 29, 2002
Cortical periventricular heterotopia with ectodermal dysplasiaR Zannolli, E Conversano, L Serracca, et al.
American Journal of Medical Genetics. Part A|December 21, 2002
Novel CNS syndrome and ectodermal dysplasiaR Zannolli, F Macucci, R M Di Bartolo, et al.
Transplantation Proceedings|March 27, 2001
Photopheresis immunomodulation after heart transplantationM Maccherini, F Diciolla, F Laghi Pasini, et al.
American Journal of Medical Genetics. Part A|April 27, 2004
Hypertelorism, ptosis, and myopia associated with drug-resistant epilepsy, mental delay, growth deficiency, ectodermal defects, and osteopeniaR Zannolli, S Buoni, F Macucci, et al.
American Journal of Medical Genetics. Part A|December 21, 2002
18q-syndrome and ectodermal dysplasia syndrome: description of a child and his familyR Zannolli, M Pierluigi, L Pucci, et al.
Journal of Medical Genetics|November 25, 2003
Hereditary xanthinuria type II associated with mental delay, autism, cortical renal cysts, nephrocalcinosis, osteopenia, and hair and teeth defectsR Zannolli, V Micheli, M A Mazzei, et al.
Pageof 18