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Results: 1-8 |
Results: 8
Identification of key mutations in HIV reverse transcriptase gene can influence the clinical outcome of HAART
Authors: Setti, M Bruzzone, B Ansaldi, F Borrelli, P Indiveri, F Icardi, G
Citation: M. Setti et al., Identification of key mutations in HIV reverse transcriptase gene can influence the clinical outcome of HAART, J MED VIROL, 64(3), 2001, pp. 199-206
Etiology and age incidence of precocious puberty in girls: A multicentric study
Authors: Cisternino, M Arrigo, T Pasquino, AM Tinelli, C Antoniazzi, F Beduschi, L Bindi, G Borrelli, P De Sanctis, V Farello, G Galluzzi, F Gargantini, L Lo Presti, D Sposito, M Tato, L
Citation: M. Cisternino et al., Etiology and age incidence of precocious puberty in girls: A multicentric study, J PED END M, 13, 2000, pp. 695-701
When to stop GnRH analog therapy: The experience of the Italian Study Group for Physiopathology of Puberty
Authors: Arrigo, T Cisternino, M Galluzzi, F Bertelloni, S Pasquino, AM Antoniazzi, F Borrelli, P Crisafulli, G Wasniewska, M De Luca, F
Citation: T. Arrigo et al., When to stop GnRH analog therapy: The experience of the Italian Study Group for Physiopathology of Puberty, J PED END M, 13, 2000, pp. 759-764
End results in central precocious puberty with GnRH analog treatment: The data of the Italian Study Group for Physiopathology of Puberty
Authors: Antoniazzi, F Arrigo, T Cisternino, M Galluzzi, F Bertelloni, S Pasquino, AM Borrelli, P Osio, D Mengarda, F De Luca, F Tato, L
Citation: F. Antoniazzi et al., End results in central precocious puberty with GnRH analog treatment: The data of the Italian Study Group for Physiopathology of Puberty, J PED END M, 13, 2000, pp. 773-780
Novel 7-DHCR mutation in a child with Smith-Lemli-Opitz syndrome
Authors: Patrono, C Rizzo, C Tessa, A Giannotti, A Borrelli, P Carrozzo, R Piemonte, F Bertini, E Dionisi-Vici, C Santorelli, FM
Citation: C. Patrono et al., Novel 7-DHCR mutation in a child with Smith-Lemli-Opitz syndrome, AM J MED G, 91(2), 2000, pp. 138-140
Short arm rearrangements of sex chromosomes with haploinsufficiency of theSHOX gene are associated with Leri-Weill dyschondrosteosis
Authors: Palka, G Stuppia, L Franchi, PG Chiarelli, F Fischetto, R Borrelli, P Giannotti, A Fioretti, G Rinaldi, MM Mingarelli, R Rappold, GA Calabrese, G
Citation: G. Palka et al., Short arm rearrangements of sex chromosomes with haploinsufficiency of theSHOX gene are associated with Leri-Weill dyschondrosteosis, CLIN GENET, 57(6), 2000, pp. 449-453
Analysis of the factors affecting anxological response to GnRH agonist treatment and final height outcome in girls with idiopathic central precociouspuberty
Authors: Arrigo, T Cisternino, M Galluzzi, F Bertelloni, S Pasquino, AM Antoniazzi, F Borrelli, P Crisafulli, G Wasniewska, M De Luca, F
Citation: T. Arrigo et al., Analysis of the factors affecting anxological response to GnRH agonist treatment and final height outcome in girls with idiopathic central precociouspuberty, EUR J ENDOC, 141(2), 1999, pp. 140-144
Loss of the SHOX gene associated with Leri-Weill dyschondrosteosis in a 45,X male
Authors: Stuppia, L Calabrese, G Borrelli, P Gatta, V Morizio, E Mingarelli, R Di Gilio, MC Crino, A Giannotti, A Rappold, GA Palka, G
Citation: L. Stuppia et al., Loss of the SHOX gene associated with Leri-Weill dyschondrosteosis in a 45,X male, J MED GENET, 36(9), 1999, pp. 711-713
Risultati: 1-8 |