Zobrazeno 1 - 10
of 121
pro vyhledávání: '"S. CAVANI"'
Publikováno v:
Polímeros, Vol 20, Iss 3, Pp 194-200 (2010)
Neste trabalho foi avaliada a influência do tratamento de fibras de bagaço de cana-de-açúcar nas propriedades mecânicas e dinâmico-mecânicas, na estabilidade térmica, na densidade e absorção de água, quando utilizadas na preparação de co
Externí odkaz:
https://doaj.org/article/e61cd01b700443c0b09c9a27c1f1c707
Akademický článek
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Autor:
S Cavani, Claire Mulligan, Suzanne McElwaine, Franca Dagna-Bricarelli, Jürgen Groet, Afua Adjeiwaa Mensah, Andrea Rinaldi, Gareth Denyer, Finbarr E. Cotter, Giuseppe Basso, Ian Hann, Dean Nizetic, C. Baldo, Monica Spinelli
Publikováno v:
British Journal of Haematology. 125:729-742
Transient myeloproliferative disorder (TMD) is a unique, spontaneously regressing neoplasia specific to Down's syndrome (DS), affecting up to 10% of DS neonates. In 20-30% of cases, it reoccurs as progressive acute megakaryoblastic leukaemia (AMKL) a
Publikováno v:
Journal of Endocrinological Investigation. 24:217-223
Varicocele is the most common clini- cal finding in infertile men but controversy con- tinues to surround the utility of its treatment. An increased response of FSH to gonadotrophin-re- leasing hormone testing has been described in pa- tients with va
Autor:
Nicola Ragni, D. Fortini, Pier Luigi Venturini, G. Gaggero, C Magli, L. Bernardini, Luca Gianaroli, C Tindiglia, S Cavani, N. Conte
Publikováno v:
Human Reproduction. 15:2165-2172
The hypothesis that sperm aneuploidy and diploidy increase as a function of spermatogenesis impairment was addressed. Ejaculated semen samples from a series of men (n = 22) with very low total normal motile count (1 x 10(6)) was analysed in terms of
Autor:
STRIANO, PASQUALE, STRIANO, SALVATORE, M. Malacarne, S. Cavani, M. Pierluigi, R. Rinaldi, M. L. Cavaliere, M. M. Rinaldi, C. D. Bernardo, A. Coppola, M. Pintaudi, R. Gaggero, P. Grammatico, B. Dallapiccola, F. Zara, F. Faravelli, COPPOLA, ANTONIETTA
Mental retardation, facial dysmorphisms, seizures, and brain abnormalities are features of 6q terminal deletions. We have ascertained five patients with 6q subtelomere deletions (four de novo, one as a result of an unbalanced translocation) and deter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0288f269bc5cec6e5637199b082770dc
http://hdl.handle.net/11588/480221
http://hdl.handle.net/11588/480221
Autor:
S. CAVANI, M. MALACARNE, G. ZEREGA, L. STAGNI, CM CAVALLINI, M. MOGNI, M. CASTAGNETTA, F. ZUNINO, A. CAPPUCCI, A. BARBONCINI, G. PIOMBO, F. DAGNA BRICARELLI, M. PIERLUIGI, PICCIONE, Maria, CORSELLO, Giovanni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3658::cd7ede41636b61f998d826769b15a4a9
http://hdl.handle.net/10447/12039
http://hdl.handle.net/10447/12039
Autor:
S Cavani, Petersen Mb, Dean Nizetic, Perfumo C, Franca Dagna-Bricarelli, Strigini P, Pierluigi M, Perroni L, Schmiegelow K, Finbarr E. Cotter, Argusti A
Publikováno v:
British Journal of Haematology. 103:213-216
Down syndrome (DS) children have a 10-20-fold increased risk of developing ALL or AML compared to non-DS children. An increased disomic homozygosity of the polymorphic DNA markers in the pericentromeric region of chromosome 21q (21q11) has repeatedly