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Results: 1-17 |
Results: 17
Auxological evaluation in patients with DiGeorge/velocardiofacial syndrome(deletion 22q11.2 syndrome)
Authors: Digilio, MC Marino, B Cappa, M Cambiaso, P Giannotti, A Dallapiccola, B
Citation: Mc. Digilio et al., Auxological evaluation in patients with DiGeorge/velocardiofacial syndrome(deletion 22q11.2 syndrome), GENET MED, 3(1), 2001, pp. 30-33
Unresolved problems concerning optimal therapy of puberty in children withchronic renal diseases
Authors: Hokken-Koelega, ACS Saenger, P Cappa, M Greggio, N
Citation: Acs. Hokken-koelega et al., Unresolved problems concerning optimal therapy of puberty in children withchronic renal diseases, J PED END M, 14, 2001, pp. 945-952
Current concepts in tall stature and overgrowth syndromes
Authors: Drop, SLS Greggio, N Cappa, M Bernasconi, S
Citation: Sls. Drop et al., Current concepts in tall stature and overgrowth syndromes, J PED END M, 14, 2001, pp. 975-984
Th 1 cytokine production by peripheral blood mononuclear cells in X-linkedadrenoleukodystrophy
Authors: Di Biase, A Merendino, N Avellino, C Cappa, M Salvati, S
Citation: A. Di Biase et al., Th 1 cytokine production by peripheral blood mononuclear cells in X-linkedadrenoleukodystrophy, J NEUR SCI, 182(2), 2001, pp. 161-165
Susceptibility to oxidation of plasma low-density lipoprotein in X-linked adrenoleukodystrophy: Effects of simvastatin treatment
Authors: Di Biase, A Salvati, S Vari, R Avellino, C Sforza, F Cappa, M Masella, R
Citation: A. Di Biase et al., Susceptibility to oxidation of plasma low-density lipoprotein in X-linked adrenoleukodystrophy: Effects of simvastatin treatment, MOL GEN MET, 71(4), 2000, pp. 651-655
Consensus statement - Prader-Willi syndrome: Growth hormone (GH)/insulin-like growth factor axis deficiency and GH treatment
Authors: Lee, PDK Allen, DB Angulo, MA Cappa, M Carrel, AL Castro-Magana, M Chiumello, G Davies, PSW Eiholzer, U Grugni, G Hauffa, BP Hintz, RL Lammer, C Mogul, HR Myers, SE Partsch, CJ Pescovitz, OH Ritzen, EM Rosenfeld, RG Sipila, I Wilson, DM
Citation: Pdk. Lee et al., Consensus statement - Prader-Willi syndrome: Growth hormone (GH)/insulin-like growth factor axis deficiency and GH treatment, ENDOCRINOLO, 10(4), 2000, pp. 71S-73S
Two novel mutations confirm FGD1 is responsible for the Aarskog syndrome
Authors: Schwartz, CE Gillessen-Kaesbach, G May, M Cappa, M Gorski, J Steindl, K Neri, G
Citation: Ce. Schwartz et al., Two novel mutations confirm FGD1 is responsible for the Aarskog syndrome, EUR J HUM G, 8(11), 2000, pp. 869-874
Hyperparathyroidism during growth hormone treatment: a role for puberty?
Authors: Picca, S Cappa, M Rizzoni, G
Citation: S. Picca et al., Hyperparathyroidism during growth hormone treatment: a role for puberty?, PED NEPHROL, 14(1), 2000, pp. 56-58
Sequential administration of arginine and arginine plus GHRH to test somatotroph function in short children
Authors: Bellone, J Aimaretti, G Bellone, S Baffoni, C Corneli, G Origlia, C Cappa, M Ghigo, E
Citation: J. Bellone et al., Sequential administration of arginine and arginine plus GHRH to test somatotroph function in short children, J ENDOC INV, 23(2), 2000, pp. 97-101
Neuroregulation of growth hormone during exercise in children
Authors: Cappa, M Bizzarri, C Martinez, C Porzio, O Giannone, G Turchetta, A Calzolari, A
Citation: M. Cappa et al., Neuroregulation of growth hormone during exercise in children, INT J SP M, 21, 2000, pp. S125-S128
Novel point mutation in the splice donor site of exon-intron junction 6 ofthe androgen receptor gene in a patient with partial androgen insensitivity syndrome
Authors: Sammarco, I Grimaldi, P Rossi, P Cappa, M Moretti, C Frajese, G Geremia, R
Citation: I. Sammarco et al., Novel point mutation in the splice donor site of exon-intron junction 6 ofthe androgen receptor gene in a patient with partial androgen insensitivity syndrome, J CLIN END, 85(9), 2000, pp. 3256-3261
Two novel missense mutations causing adrenoleukodystrophy in Italian patients
Authors: Perusi, C Gomez-Lira, M Mottes, M Pignatti, PF Bertini, E Cappa, M Vigliani, MC Schiffer, D Rizzuto, N Salviati, A
Citation: C. Perusi et al., Two novel missense mutations causing adrenoleukodystrophy in Italian patients, MOL CELL PR, 13(3), 1999, pp. 179-182
McCune-Albright syndrome: A longitudinal clinical study of 32 patients
Authors: de Sanctis, C Lala, R Matarazzo, P Balsamo, A Bergamaschi, R Cappa, M Cisternino, M de Sanctis, V Lucci, M Franzese, A Ghizzoni, L Pasquino, AM Segni, M Rigon, F Saggese, G Bertelloni, S Buzi, F
Citation: C. De Sanctis et al., McCune-Albright syndrome: A longitudinal clinical study of 32 patients, J PED END M, 12(6), 1999, pp. 817-826
Neurophysiologic follow-up of long-term dietary treatment in adult-onset adrenoleukodystrophy
Authors: Restuccia, D Di Lazzaro, V Valeriani, M Oliviero, A Le Pera, D Barba, C Cappa, M Bertini, E Di Capua, M Tonali, P
Citation: D. Restuccia et al., Neurophysiologic follow-up of long-term dietary treatment in adult-onset adrenoleukodystrophy, NEUROLOGY, 52(4), 1999, pp. 810-816
Commentary - Somatostatin infusion withdrawal: Studies in normal children and in children with growth hormone deficiency
Authors: Cappa, M Rigamonti, AE Bizzarri, C Porzio, O Civolani, P Cella, SG Loche, S Muller, EE
Citation: M. Cappa et al., Commentary - Somatostatin infusion withdrawal: Studies in normal children and in children with growth hormone deficiency, J CLIN END, 84(12), 1999, pp. 4426-4430
X-linked adrenoleukodystrophy: first report of the Italian Study Group
Authors: Di Biase, A Salvati, S Avellino, C Cappa, M Bertini, E Moroni, I Rimoldi, M Uziel, G
Citation: A. Di Biase et al., X-linked adrenoleukodystrophy: first report of the Italian Study Group, ITAL J NEUR, 19(5), 1998, pp. 315-319
Altered bone mineral density in patients with complete androgen insensitivity syndrome
Authors: Bertelloni, S Baroncelli, GI Federico, G Cappa, M Lala, R Saggese, G
Citation: S. Bertelloni et al., Altered bone mineral density in patients with complete androgen insensitivity syndrome, HORMONE RES, 50(6), 1998, pp. 309-314
Risultati: 1-17 |