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Results: 1-16 |
Results: 16
Pubertal disorders in inv dup(15) syndrome
Authors: Grosso, S Balestri, P Anichini, C Bartalini, G Pucci, L Morgese, G Berardi, R
Citation: S. Grosso et al., Pubertal disorders in inv dup(15) syndrome, GYNECOL END, 15(3), 2001, pp. 165-169
Multiple neuroendocrine disorder in Salla disease
Authors: Grosso, S Berardi, R Farnetani, MA Margollicci, M Mancini, MG Morgese, G Balestri, P
Citation: S. Grosso et al., Multiple neuroendocrine disorder in Salla disease, J CHILD NEU, 16(10), 2001, pp. 775-777
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
Severe metabolic abnormalities in the white matter of patients with vacuolating megalencephalic leukoencephalopathy with subcortical cysts. A proton MR spectroscopic imaging study
Authors: De Stefano, N Balestri, P Dotti, MT Grosso, S Mortilla, M Morgese, G Federico, A
Citation: N. De Stefano et al., Severe metabolic abnormalities in the white matter of patients with vacuolating megalencephalic leukoencephalopathy with subcortical cysts. A proton MR spectroscopic imaging study, J NEUROL, 248(5), 2001, pp. 403-409
MR brain imaging of fucosidosis type I
Authors: Galluzzi, P Rufa, A Balestri, P Cerase, A Federico, A
Citation: P. Galluzzi et al., MR brain imaging of fucosidosis type I, AM J NEUROR, 22(4), 2001, pp. 777-780
Association of Chiari I malformation, mental retardation, speech delay, and epilepsy: A specific disorder?
Authors: Grosso, S Scattolini, R Paolo, G Di Bartolo, RM Morgese, G Balestri, P
Citation: S. Grosso et al., Association of Chiari I malformation, mental retardation, speech delay, and epilepsy: A specific disorder?, NEUROSURGER, 49(5), 2001, pp. 1099-1103
Dexfenfluramine effective in drug-resistant temporal lobe epilepsy
Authors: Grosso, S Farnetani, MA Berardi, R Di Bartolo, R Magi, L Morgese, G Balestri, P
Citation: S. Grosso et al., Dexfenfluramine effective in drug-resistant temporal lobe epilepsy, NEUROLOGY, 57(6), 2001, pp. 1139-1140
Central precocious puberty and abnormal chromosomal patterns
Authors: Grosso, S Anichini, C Berardi, R Balestri, P Pucci, L Morgese, G
Citation: S. Grosso et al., Central precocious puberty and abnormal chromosomal patterns, ENDOCR PATH, 11(1), 2000, pp. 69-75
Vagal and hypoglossal Bell's palsy
Authors: Zannolli, R Acquaviva, A D'Ambrosio, A Pucci, L Balestri, P Morgese, G
Citation: R. Zannolli et al., Vagal and hypoglossal Bell's palsy, J CHILD NEU, 15(2), 2000, pp. 130-132
Endocrine disorders in two sisters affected by MELAS syndrome
Authors: Balestri, P Grosso, S
Citation: P. Balestri et S. Grosso, Endocrine disorders in two sisters affected by MELAS syndrome, J CHILD NEU, 15(11), 2000, pp. 755-758
Plasmapheresis in a child affected by acute disseminated encephalomyelitis
Authors: Balestri, P Grosso, S Acquaviva, A Bernini, M
Citation: P. Balestri et al., Plasmapheresis in a child affected by acute disseminated encephalomyelitis, BRAIN DEVEL, 22(2), 2000, pp. 123-126
Neurofibromatosis type 2 attributable to gonosomal mosaicism in a clinically normal mother, and identification of seven novel mutations in the NF2 gene
Authors: Sestini, R Vivarelli, R Balestri, P Ammannati, F Montali, E Papi, L
Citation: R. Sestini et al., Neurofibromatosis type 2 attributable to gonosomal mosaicism in a clinically normal mother, and identification of seven novel mutations in the NF2 gene, HUM GENET, 107(4), 2000, pp. 366-371
An unbalanced submicroscopic translocation t(8;16)(q24.3;p13.3)pat associated with tuberous sclerosis complex, adult polycystic kidney disease, and hypomelanosis of Ito
Authors: Eussen, BHJ Bartalini, G Bakker, L Balestri, P Di Lucca, C Van Hemel, JO Dauwerse, H van den Ouweland, AMW Ris-Stalpers, C Verhoef, S Halley, DJJ Fois, A
Citation: Bhj. Eussen et al., An unbalanced submicroscopic translocation t(8;16)(q24.3;p13.3)pat associated with tuberous sclerosis complex, adult polycystic kidney disease, and hypomelanosis of Ito, J MED GENET, 37(4), 2000, pp. 287-291
Precocious puberty with trisomy x syndrome
Authors: Grosso, S Berardi, R Pucci, L Balestri, P
Citation: S. Grosso et al., Precocious puberty with trisomy x syndrome, OBSTET GYN, 94(5), 1999, pp. 861-861
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
Alternating hemiplegia of childhood or Hashimoto's encephalopathy?
Authors: Balestri, P Grosso, S Garibaldi, G
Citation: P. Balestri et al., Alternating hemiplegia of childhood or Hashimoto's encephalopathy?, J NE NE PSY, 66(4), 1999, pp. 548-549
Risultati: 1-16 |