Osteoporosis in Klinefelter's syndrome
Ferlin, A., Schipilliti, M., Di Mambro, A., Vinanzi, C., Foresta, C.
Published in Molecular human reproduction (01.06.2010)
Published in Molecular human reproduction (01.06.2010)
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Detailed functional studies on androgen receptor mild mutations demonstrate their association with male infertility
Zuccarello, D., Ferlin, A., Vinanzi, C., Prana, E., Garolla, A., Callewaert, L., Claessens, F., Brinkmann, A. O., Foresta, C.
Published in Clinical endocrinology (Oxford) (01.04.2008)
Published in Clinical endocrinology (Oxford) (01.04.2008)
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Circulating endothelial progenitor cells and endothelial function after chronic Tadalafil treatment in subjects with erectile dysfunction
FORESTA, C, FERLIN, A, DE TONI, L, LANA, A, VINANZI, C, GALAN, A, CARETTA, N
Published in International journal of impotence research (01.09.2006)
Published in International journal of impotence research (01.09.2006)
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Journal Article
Molecular analysis of the androgen receptor gene in testicular cancer
Garolla, A, Ferlin, A, Vinanzi, C, Roverato, A, Sotti, G, Artibani, W, Foresta, C
Published in Endocrine-related cancer (01.09.2005)
Published in Endocrine-related cancer (01.09.2005)
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Journal Article
Somatic mosaicism in von Hippel-Lindau disease
Murgia, Alessandra, Martella, Maddalena, Vinanzi, Cinzia, Polli, Roberta, Perilongo, Giorgio, Opocher, Giuseppe
Published in Human mutation (01.01.2000)
Published in Human mutation (01.01.2000)
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Journal Article
Molecular diagnosis of inherited diseases
Murigia, A, Polli, R, Martella, M, Vinanzi, C, Opocher, G
Published in Clinica chimica acta (01.02.1999)
Published in Clinica chimica acta (01.02.1999)
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Journal Article
Conference Proceeding
Molecular Genetics Applied to Clinical Practice: The Cx26 Hearing Impairment
Orzan, E., Polli, R., Martella, M., Vinanzi, C., Leonardi, M., Murgia, A.
Published in British Journal of Audiology (01.10.1999)
Published in British Journal of Audiology (01.10.1999)
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Journal Article
Conference Proceeding
The guanine triphosphatase (GTPase) activating protein (GAP)-related domain of the neurofibromatosis type 1 gene is not mutated in neural crest-derived sporadic tumours
MURGIA, A, ANGLANI, F, VINANZI, C, POLLI, R, BASSO, G, PERILONGO, G, GIANGASPERO, F, ZACCHELLO, F
Published in European journal of cancer (1990) (01.03.1998)
Published in European journal of cancer (1990) (01.03.1998)
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Journal Article
Insulin-Like Factor 3: A Novel Circulating Hormone of Testis Origin in Humans
Foresta, Carlo, Bettella, Andrea, Vinanzi, Cinzia, Dabrilli, Paolo, Meriggiola, Maria Cristina, Garolla, Andrea, Ferlin, Alberto
Published in The journal of clinical endocrinology and metabolism (01.12.2004)
Published in The journal of clinical endocrinology and metabolism (01.12.2004)
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Journal Article
Osteoporosis in Klinefelter's syndrome : Klinefelter's syndrome: basic science to clinic
FERLIN, A, SCHIPILLITI, M, DI MAMBRO, A, VINANZI, C, FORESTA, C
Published in Molecular human reproduction (2010)
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Published in Molecular human reproduction (2010)
Journal Article
FRAXA and FRAXE: new tools for the diagnosis of mental retardation
Murgia, A, Vinanzi, C, Polli, R, Artifoni, L, Zacchello, F
Published in Acta geneticae medicae et gemellologiae (1996)
Published in Acta geneticae medicae et gemellologiae (1996)
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Journal Article
Cx26 deafness: mutation analysis and clinical variability
Murgia, A, Orzan, E, Polli, R, Martella, M, Vinanzi, C, Leonardi, E, Arslan, E, Zacchello, F
Published in Journal of medical genetics (01.11.1999)
Published in Journal of medical genetics (01.11.1999)
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Journal Article
Androgen receptor gene CAG and GGC repeat lengths in cryptorchidism
Ferlin, Alberto, Garolla, Andrea, Bettella, Andrea, Bartoloni, Lucia, Vinanzi, Cinzia, Roverato, Alberto, Foresta, Carlo
Published in European journal of endocrinology (01.03.2005)
Published in European journal of endocrinology (01.03.2005)
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Journal Article
Amplification of the Xq28 FRAXE repeats: extreme phenotype variability?
Murgia, A, Polli, R, Vinanzi, C, Salis, M, Drigo, P, Artifoni, L, Zacchello, F
Published in American journal of medical genetics (09.08.1996)
Published in American journal of medical genetics (09.08.1996)
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