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Results: 1-17 |
Results: 17
Decreased platelet glutamate uptake and genetic risk factors in patients with Parkinson's disease
Authors: Ferrarese, C Tremolizzo, L Rigoldi, M Sala, G Begni, B Brighina, L Ricci, G Albizzati, MG Piolti, R Crosti, F Dalpra, L Frattola, L
Citation: C. Ferrarese et al., Decreased platelet glutamate uptake and genetic risk factors in patients with Parkinson's disease, NEUROL SCI, 22(1), 2001, pp. 65-66
Characterization of the genomic structure of the human neuronal nicotinic acetylcholine receptor CHRNA5/A3/B4 gene cluster and identification of novel intragenic polymorphisms
Authors: Duga, S Solda, G Asselta, R Bonati, MT Dalpra, L Malcovati, M Tenchini, ML
Citation: S. Duga et al., Characterization of the genomic structure of the human neuronal nicotinic acetylcholine receptor CHRNA5/A3/B4 gene cluster and identification of novel intragenic polymorphisms, J HUM GENET, 46(11), 2001, pp. 640-648
Relationship between clinical and genetic features in "inverted duplicatedchromosome 15" patients
Authors: Borgatti, R Piccinelli, P Passoni, D Dalpra, L Miozzo, M Micheli, R Gagliardi, C Balottin, U
Citation: R. Borgatti et al., Relationship between clinical and genetic features in "inverted duplicatedchromosome 15" patients, PED NEUROL, 24(2), 2001, pp. 111-116
Identification of a small supernumerary marker chromosome, r(2)(p10q11.2),and the problem of determining prognosis
Authors: Villa, N Riva, P Colombo, D Sala, E Mariani, S Zorloni, C Crosti, F Dalpra, L
Citation: N. Villa et al., Identification of a small supernumerary marker chromosome, r(2)(p10q11.2),and the problem of determining prognosis, PRENAT DIAG, 21(10), 2001, pp. 801-805
A patient defines the interstitial 1q deletion syndrome characterized by antithrombin III deficiency
Authors: Pallotta, R Dalpra, L Miozzo, M Ehresmann, T Fusilli, P
Citation: R. Pallotta et al., A patient defines the interstitial 1q deletion syndrome characterized by antithrombin III deficiency, AM J MED G, 104(4), 2001, pp. 282-286
Refined mapping of CHRNA3/A5/B4 gene cluster and its implications in ADNFLE
Authors: Bonati, MT Asselta, R Duga, S Ferini-Strambi, L Oldani, A Zucconi, M Malcovati, M Dalpra, L Tenchini, ML
Citation: Mt. Bonati et al., Refined mapping of CHRNA3/A5/B4 gene cluster and its implications in ADNFLE, NEUROREPORT, 11(10), 2000, pp. 2097-2101
A new biallelic polymorphism in intron 1 of the CHRNA4 gene may cause erroneous genotyping of a closely linked CA repeat marker
Authors: Bonati, MT Duga, S Asselta, R Ferini-Strambi, L Oldani, A Zucconi, M Malcovati, M Dalpra, L Tenchini, ML
Citation: Mt. Bonati et al., A new biallelic polymorphism in intron 1 of the CHRNA4 gene may cause erroneous genotyping of a closely linked CA repeat marker, MOL CELL PR, 14(6), 2000, pp. 373-380
Molecular definition of Xq common-deleted region in patients affected by premature ovarian failure
Authors: Marozzi, A Manfredini, E Tibiletti, MG Furlan, D Villa, N Vegetti, W Crosignani, PG Ginelli, E Meneveri, R Dalpra, L
Citation: A. Marozzi et al., Molecular definition of Xq common-deleted region in patients affected by premature ovarian failure, HUM GENET, 107(4), 2000, pp. 304-311
Premature ovarian failure
Authors: Vegetti, W Marozzi, A Manfredini, E Testa, G Alagna, F Nicolosi, A Caliari, I Taborelli, M Tibiletti, MG Dalpra, L Crosignani, PG
Citation: W. Vegetti et al., Premature ovarian failure, MOL C ENDOC, 161(1-2), 2000, pp. 53-57
Association between idiopathic premature ovarian failure and fragile X premutation
Authors: Marozzi, A Vegetti, W Manfredini, E Tibiletti, MG Testa, G Crosignani, PG Ginelli, E Meneveri, R Dalpra, L
Citation: A. Marozzi et al., Association between idiopathic premature ovarian failure and fragile X premutation, HUM REPR, 15(1), 2000, pp. 197-202
19p deletion in recurring leiomyosarcoma lesions from the same patient
Authors: Riva, P Dalpra, L Gualandri, V Volonte, M Miozzo, M Malgara, R Conti, AF Larizza, L
Citation: P. Riva et al., 19p deletion in recurring leiomyosarcoma lesions from the same patient, CANC GENET, 119(2), 2000, pp. 102-108
Monosomy and trisomy 1q44-qter in two sisters originating from a half cryptic 1q;15p translocation
Authors: Villa, N Sala, E Colombo, D Dell'Orto, M Grioni, D Dalpra, L
Citation: N. Villa et al., Monosomy and trisomy 1q44-qter in two sisters originating from a half cryptic 1q;15p translocation, J MED GENET, 37(8), 2000, pp. 612-615
A tumor suppressor locus in familial and sporadic chordoma maps to 1p36
Authors: Miozzo, M Dalpra, L Riva, P Volonte, M Macciardi, F Pericotti, S Tibiletti, MG Cerati, M Rohde, K Larizza, L Conti, AMF
Citation: M. Miozzo et al., A tumor suppressor locus in familial and sporadic chordoma maps to 1p36, INT J CANC, 87(1), 2000, pp. 68-72
FRAXA premutations are not a cause of familial premature ovarian failure
Authors: Marozzi, A Dalpra, L Ginelli, E Tibiletti, MG Crosignani, PG
Citation: A. Marozzi et al., FRAXA premutations are not a cause of familial premature ovarian failure, HUM REPR, 14(2), 1999, pp. 573-574
The idiopathic forms of premature menopause and early menopause show the same genetic pattern
Authors: Tibiletti, MG Testa, G Vegetti, W Alagna, F Taborelli, M Dalpra, L Bolis, PF Crosignani, PG
Citation: Mg. Tibiletti et al., The idiopathic forms of premature menopause and early menopause show the same genetic pattern, HUM REPR, 14(11), 1999, pp. 2731-2734
SER252PHE and 776INS3 mutations in the CHRNA4 gene are rare in the ItalianADNFLE population
Authors: Tenchini, ML Duga, S Bonati, MT Asselta, R Oldani, A Zucconi, M Malcovati, M Dalpra, L Ferini-Strambi, L
Citation: Ml. Tenchini et al., SER252PHE and 776INS3 mutations in the CHRNA4 gene are rare in the ItalianADNFLE population, SLEEP, 22(5), 1999, pp. 637-639
First cytogenetic study of a recurrent familial chordoma of the clivus
Authors: Dalpra, L Malgara, R Miozzo, M Riva, P Volonte, M Larizza, L Conti, AMF
Citation: L. Dalpra et al., First cytogenetic study of a recurrent familial chordoma of the clivus, INT J CANC, 81(1), 1999, pp. 24-30
Risultati: 1-17 |