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 Valli

Showing results (151-160 of 177) with videos related to

Pageof 18
Sort By:
European Journal of Biochemistry|February 1, 1993
Osteogenesis imperfecta and type-I collagen mutations. A lethal variant caused by a Gly910-->Ala substitution in the alpha 1 (I) chainM Valli, A Sangalli, A Rossi, et al.
European Journal of Gynaecological Oncology|January 1, 1988
Hormonal and surgical treatment of endometrial adenocarcinomaF D'Addato, A Lanza, A Re, et al.
European Journal of Gynaecological Oncology|January 1, 1988
Techniques of pelvic and para-aortic lymphadenectomy in the surgical treatment of cervix carcinomaG Ferraris, A Lanza, F D'Addato, et al.
European Journal of Gynaecological Oncology|January 1, 1988
Complications of axillary, inguinal, pelvic and para-aortic lymphadenectomyG Ferraris, A Lanza, F D'Addato, et al.
The Italian Journal of Biochemistry|July 1, 1989
Marfan syndrome: a collagen disorder?G Zanaboni, M P De Agostini, M Valli, et al.
Pathology, Research and Practice|May 1, 1996
Quantitative study of ductal breast cancer progression. A progression index (P.I.) for premalignant lesions and in situ carcinomaG M Mariuzzi, L Mariuzzi, A Mombello, et al.
American Journal of Human Genetics|April 1, 1990
Unilateral microfibrillar abnormalities in a case of asymmetric Marfan syndromeM Godfrey, S Olson, R G Burgio, et al.
Pathology, Research and Practice|November 1, 1994
Quantitative study of ductal breast cancer progression. Morphometric evaluation of phenotypical changes occurring in benign and preinvasive epithelial lesionsG M Mariuzzi, L Mariuzzi, A Mombello, et al.
Therapie|July 27, 2001
[Pharmacologic dependence on nefopam (Acupan): a case report]M Spadari, H Tissot-Dupont, L Tichadou, et al.
Biochemical and Molecular Medicine|February 12, 1998
Phenotypic comparison of an osteogenesis imperfecta type IV proband with a de novo alpha2(I) Gly922 --> Ser substitution in type I collagen and an unrelated patient with an identical mutationA Forlino, E D'amato, M Valli, et al.
Pageof 18

Showing results (151-160 of 177) with videos related to

Sort By:
Pageof 18
European Journal of Biochemistry|February 1, 1993
Osteogenesis imperfecta and type-I collagen mutations. A lethal variant caused by a Gly910-->Ala substitution in the alpha 1 (I) chainM Valli, A Sangalli, A Rossi, et al.
European Journal of Gynaecological Oncology|January 1, 1988
Hormonal and surgical treatment of endometrial adenocarcinomaF D'Addato, A Lanza, A Re, et al.
European Journal of Gynaecological Oncology|January 1, 1988
Techniques of pelvic and para-aortic lymphadenectomy in the surgical treatment of cervix carcinomaG Ferraris, A Lanza, F D'Addato, et al.
European Journal of Gynaecological Oncology|January 1, 1988
Complications of axillary, inguinal, pelvic and para-aortic lymphadenectomyG Ferraris, A Lanza, F D'Addato, et al.
The Italian Journal of Biochemistry|July 1, 1989
Marfan syndrome: a collagen disorder?G Zanaboni, M P De Agostini, M Valli, et al.
Pathology, Research and Practice|May 1, 1996
Quantitative study of ductal breast cancer progression. A progression index (P.I.) for premalignant lesions and in situ carcinomaG M Mariuzzi, L Mariuzzi, A Mombello, et al.
American Journal of Human Genetics|April 1, 1990
Unilateral microfibrillar abnormalities in a case of asymmetric Marfan syndromeM Godfrey, S Olson, R G Burgio, et al.
Pathology, Research and Practice|November 1, 1994
Quantitative study of ductal breast cancer progression. Morphometric evaluation of phenotypical changes occurring in benign and preinvasive epithelial lesionsG M Mariuzzi, L Mariuzzi, A Mombello, et al.
Therapie|July 27, 2001
[Pharmacologic dependence on nefopam (Acupan): a case report]M Spadari, H Tissot-Dupont, L Tichadou, et al.
Biochemical and Molecular Medicine|February 12, 1998
Phenotypic comparison of an osteogenesis imperfecta type IV proband with a de novo alpha2(I) Gly922 --> Ser substitution in type I collagen and an unrelated patient with an identical mutationA Forlino, E D'amato, M Valli, et al.
Pageof 18