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Results:
1-24
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Results: 24
Authors:
Lore, F
Talidis, F
Di Cairano, G
Renieri, A
Citation: F. Lore et al., Multiple endocrine neoplasia type 2 syndromes may be associated with renalmalformations, J INTERN M, 250(1), 2001, pp. 37-42
Authors:
Vacca, M
Filippini, F
Budillon, A
Rossi, V
Mercadante, G
Manzati, E
Gualandi, F
Bigoni, S
Trabanelli, C
Pini, G
Calzolari, E
Ferlini, A
Meloni, I
Hayek, G
Zappella, M
Renieri, A
D'Urso, M
D'Esposito, M
MacDonald, F
Kerr, A
Dhanjal, S
Hulten, M
Citation: M. Vacca et al., Mutation analysis of the MECP2 gene in British and Italian Rett syndrome females, J MOL MED-J, 78(11), 2001, pp. 648
Authors:
Dattoli, G
Mezi, L
Migliorati, M
Renieri, A
Couprie, ME
Garzella, D
Nutarelli, D
Thomas, C
De Ninno, G
Walker, R
Citation: G. Dattoli et al., Electron beam properties and impedance characterization for storage rings used for free electron lasers, NUCL INST A, 471(3), 2001, pp. 403-411
Authors:
Zappella, M
Meloni, I
Longo, I
Hayek, G
Renieri, A
Citation: M. Zappella et al., Preserved speech variants of the Rett syndrome: Molecular and clinical analysis, AM J MED G, 104(1), 2001, pp. 14-22
Authors:
Bartolini, R
Dattoli, G
Mezi, L
Renieri, A
Migliorati, M
Couprie, ME
De Ninno, G
Roux, R
Citation: R. Bartolini et al., Suppression of the sawtooth instability in a storage ring by free-electronlaser: An example of nonlinear stabilization by noise - art. no. 134801, PHYS REV L, 8713(13), 2001, pp. 4801
Authors:
Malandrini, A
Mari, F
Palmeri, S
Gambelli, S
Berti, G
Bruttini, M
Bardelli, AM
Williamson, K
van Heyningen, V
Renieri, A
Citation: A. Malandrini et al., PAX6 mutation in a family with aniridia, congenital ptosis, and mental retardation, CLIN GENET, 60(2), 2001, pp. 151-154
Authors:
Frasca, GM
Onetti-Muda, A
Renieri, A
Citation: Gm. Frasca et al., Thin glomerular basement membrane disease, J NEPHROL, 13(1), 2000, pp. 15-19
Authors:
Jais, JP
Knebelmann, B
Giatras, I
De Marchi, M
Rizzoni, G
Renieri, A
Weber, M
Gross, O
Netzer, KO
Flinter, F
Pirson, Y
Verellen, C
Wieslander, J
Persson, U
Tryggvason, K
Martin, P
Hertz, JM
Schroder, C
Sanak, M
Krejcova, S
Carvalho, MF
Saus, J
Antignac, C
Smeets, H
Gubler, MC
Citation: Jp. Jais et al., X-linked Alport syndrome: Natural history in 195 families and genotype-phenotype correlations in males, J AM S NEPH, 11(4), 2000, pp. 649-657
Authors:
De Bona, C
Zappella, M
Hayek, G
Meloni, I
Vitelli, F
Bruttini, M
Cusano, R
Loffredo, P
Longo, I
Renieri, A
Citation: C. De Bona et al., Preserved speech variant is allelic of classic Rett syndrome, EUR J HUM G, 8(5), 2000, pp. 325-330
Authors:
Vitelli, F
Meloni, I
Fineschi, S
Favara, F
Storlazzi, CT
Rocchi, M
Renieri, A
Citation: F. Vitelli et al., Identification and characterization of mouse orthologs of the AMMECR1 and FACL4 genes deleted in AMME syndrome: orthology of Xq22.3 and MmuXF1-F3, CYTOG C GEN, 88(3-4), 2000, pp. 259-263
Authors:
Bruttini, M
Vitelli, F
Meloni, I
Rizzari, C
Della Volpe, M
Mazzucco, G
De Marchi, M
Renieri, A
Citation: M. Bruttini et al., Mosaicism in Alport syndrome and genetic counselling, J MED GENET, 37(9), 2000, pp. 717-719
Authors:
Blasi, MA
Rinaldi, R
Renieri, A
Petrucci, R
De Bernardo, C
Bruttini, M
Grammatico, P
Citation: Ma. Blasi et al., Dot-and-fleck retinopathy in Alport syndrome caused by a novel mutation inthe COL4A5 gene, AM J OPHTH, 130(1), 2000, pp. 130-131
Authors:
Meloni, I
Bruttini, M
Longo, I
Mari, F
Rizzolio, F
D'Adamo, P
Denvriendt, K
Fryns, JP
Toniolo, D
Renieri, A
Citation: I. Meloni et al., A mutation in the Rett syndrome gene, MECP2, causes X-linked mental retardation and progressive spasticity in males, AM J HU GEN, 67(4), 2000, pp. 982-985
Authors:
Dattoli, G
Mezi, L
Migliorati, M
Renieri, A
Citation: G. Dattoli et al., Storage ring free electron laser dynamics, with the inclusion of bunch lengthening and energy spread increasing effects, EUR PHY J D, 6(3), 1999, pp. 375-381
Authors:
Gallerano, GP
Doria, A
Giovenale, E
Renieri, A
Citation: Gp. Gallerano et al., Compact free electron lasers: From Cerenkov to waveguide free electron lasers, INFR PHYS T, 40(3), 1999, pp. 161-174
Authors:
Dattoli, G
Ottaviani, PL
Renieri, A
Citation: G. Dattoli et al., High-gain FEL output power vs. the saturation intensity, NUOV CIM B, 114(5), 1999, pp. 605-608
Authors:
Piccini, M
Vitelli, F
Seri, M
Galietta, LJV
Moran, O
Bulfone, A
Banfi, S
Pober, B
Renieri, A
Citation: M. Piccini et al., KCNE1-like gene is deleted in AMME contiguous gene syndrome: Identification and characterization of the human and mouse homologs, GENOMICS, 60(3), 1999, pp. 251-257
Authors:
Vitelli, F
Piccini, M
Caroli, F
Franco, B
Malandrini, A
Pober, B
Jonsson, O
Sorrentino, V
Renieri, A
Citation: F. Vitelli et al., Identification and characterization of a highly conserved protein absent in the Alport syndrome (A), mental retardation (M), midface hypoplasia (M), and elliptocytosis (E) contiguous gene deletion syndrome (AMME), GENOMICS, 55(3), 1999, pp. 335-340
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
Authors:
Fimiani, M
Seri, M
Rubegni, P
Cusano, R
De Aloe, G
Forabosco, P
Devoto, M
Andreassi, L
Renieri, A
Citation: M. Fimiani et al., Autosomal dominant aplasia cutis congenita: report of a large Italian family and no hint for candidate chromosomal regions, ARCH DERM R, 291(12), 1999, pp. 637-642
Authors:
Piccini, M
Casari, G
Zhou, JH
Bruttini, M
Li Volti, S
Ballabio, A
Renieri, A
Citation: M. Piccini et al., Evidence for genetic heterogeneity in benign familial hematuria, AM J NEPHR, 19(4), 1999, pp. 464-467
Authors:
Dattoli, G
Mezi, L
Migliorati, M
Palumbo, L
Renieri, A
Citation: G. Dattoli et al., Storage ring free electron lasers and saw-tooth instability, NUCL INST A, 433(3), 1999, pp. 683-689
Authors:
Vitelli, F
Villanova, M
Malandrini, A
Bruttini, M
Piccini, M
Merlini, L
Guazzi, G
Renieri, A
Citation: F. Vitelli et al., Inheritance of a 38-kb fragment in apparently sporadic facioscapulohumeralmuscular dystrophy, MUSCLE NERV, 22(10), 1999, pp. 1437-1441
LINE-1 elements at the sites of molecular rearrangements in Alport syndrome - Diffuse leiomyomatosis
Authors:
Segal, Y
Peissel, B
Renieri, A
de Marchi, M
Ballabio, A
Pei, Y
Zhou, J
Citation: Y. Segal et al., LINE-1 elements at the sites of molecular rearrangements in Alport syndrome - Diffuse leiomyomatosis, AM J HU GEN, 64(1), 1999, pp. 62-69
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