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Results: 1-8 |
Results: 8
Analysis of ankle kinetics during walking in individuals with Down syndrome
Authors: Cioni, M Cocilovo, A Rossi, F Paci, D Valle, MS
Citation: M. Cioni et al., Analysis of ankle kinetics during walking in individuals with Down syndrome, AM J MENT R, 106(5), 2001, pp. 470-478
Pseudo-TORCH syndrome or Baraitser-Reardon syndrome: diagnostic criteria
Authors: Vivarelli, R Grosso, S Cioni, M Galluzzi, P Monti, L Morgese, G Balestri, P
Citation: R. Vivarelli et al., Pseudo-TORCH syndrome or Baraitser-Reardon syndrome: diagnostic criteria, BRAIN DEVEL, 23(1), 2001, pp. 18-23
Sarcoma botryoides of the uterine cervix in a young woman: a case report
Authors: Atlante, M Dionisi, B Cioni, M Di Ruzza, D Sedati, P Mariani, L
Citation: M. Atlante et al., Sarcoma botryoides of the uterine cervix in a young woman: a case report, EUR J GYN O, 21(5), 2000, pp. 504-506
EEG in assessing hydroxycobalamin therapy in neonatal methylmalonic aciduria with homocystinuria
Authors: Bellieni, CV Ferrari, F De Felice, C Bagnoli, F Cioni, M Farnetani, M Gatti, MG Buonocore, G
Citation: Cv. Bellieni et al., EEG in assessing hydroxycobalamin therapy in neonatal methylmalonic aciduria with homocystinuria, BIOL NEONAT, 78(4), 2000, pp. 327-330
Intracellular levels of the LIS1 protein correlate with clinical and neuroradiological findings in patients with classical lissencephaly.
Authors: Fogli, A Guerrini, R Moro, F Fernandez-Alvarez, E Livet, MO Renieri, A Cioni, M Pilz, DT Veggiotti, P Rossi, E Ballabio, A Carrozzo, R
Citation: A. Fogli et al., Intracellular levels of the LIS1 protein correlate with clinical and neuroradiological findings in patients with classical lissencephaly., ANN NEUROL, 45(2), 1999, pp. 154-161
Selective mutism, speech delay, dysmorphisms, and deletion of the short arm of chromosome 18: a distinct entity?
Authors: Grosso, S Cioni, M Pucci, L Morgese, G Balestri, P
Citation: S. Grosso et al., Selective mutism, speech delay, dysmorphisms, and deletion of the short arm of chromosome 18: a distinct entity?, J NE NE PSY, 67(6), 1999, pp. 830-831
Screening and diagnosis of congenital adrenal hyperplasia caused by 21-hydroxylase deficiency
Authors: Balsamo, A Baserga, M Burroni, M Cacciari, E Cardillo, A Cassio, A Cerone, R Ciatti, R Cioni, M Cotugno, G Forgione, F Impellizzeri, A Lelli, A Lilliu, F Meli, C Pagliardini, S Palillo, L Parlato, G Piazzi, S Pugliese, G Romano, C Salardi, S Torelli, G Zammarchi, E
Citation: A. Balsamo et al., Screening and diagnosis of congenital adrenal hyperplasia caused by 21-hydroxylase deficiency, RIV ITAL P, 24(5), 1998, pp. 861-869
Transient neonatal hypothyroidism after gestational exposure to amiodarone: A follow-up of two cases
Authors: Grosso, S Berardi, R Cioni, M Morgese, G
Citation: S. Grosso et al., Transient neonatal hypothyroidism after gestational exposure to amiodarone: A follow-up of two cases, J ENDOC INV, 21(10), 1998, pp. 699-702
Risultati: 1-8 |