Zobrazeno 1 - 10 of 201 pro vyhledávání: '"L. GARGANTINI"'
1
A new chromosome instability disorder
Autor: F. Lo Curto, D. Caufin, L. Gargantini, L. Minoli, Simonetta Lambiase, Paola Maraschio, Diletta Peretti, Orsetta Zuffardi
Publikováno v: Scopus-Elsevier
Chromosome analysis in a 31-year-old woman referred for primary amenorrhea, revealed a very high incidence of chromosome aberrations. She had microcephaly and immunodeficiency. Her healthy parents were consanguineous (1/32) and a younger sister, also
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aaa2da0ab5c3b1d7d70e869a2907e478
https://doi.org/10.1111/j.1399-0004.1986.tb01892.x
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2
The possible influences of B2A2 and B3A2 BCR/ABL protein structure on thrombopoiesis in chronic myeloid leukaemia
Autor: Roberto Perego, M Costantini, Enrica Morra, Cristina Bianchi, G Cornacchini, E Pungolino, L Gargantini, E Rovida
Publikováno v: European Journal of Cancer. 36:1395-1401
The Philadelphia chromosome, t(9;22)(q34;q11) gives rise more frequently, in chronic myeloid leukaemia (CML), to two BCR/ABL chimeric transcripts differing only by the absence of 75 nucleotides and defined as b2a2 and b3a2 types, encoding two 210-kDa
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27ae64e303bcf6d579c525c99094f220
https://doi.org/10.1016/s0959-8049(00)00128-3
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3
Treatment outcome and prognostic factors for primary mediastinal (thymic) B-cell lymphoma: a multicenter study of 106 patients
Autor: P. Möller, Carlo Bernasconi, Mario Lazzarino, Catherine Klersy, Marco Paulli, M. T. Rousset, E. Marra, J. Sträter, C. Manegold, Umberto Magrini, Umberto Gianelli, M. Gambacorta, L. Gargantini, T. Lavabre-Bertrand, Ester Orlandi
Publikováno v: Scopus-Elsevier
PURPOSE To define clinicopathologic features, response to treatment, and prognostic factors of primary mediastinal B-cell lymphoma (MBL), a CD20+ tumor recognized as a distinct entity among non-Hodgkin's lymphomas (NHL). PATIENTS AND METHODS One hund
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2db2b44e9293df868a62644b3a0a5a18
https://doi.org/10.1200/jco.1997.15.4.1646
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9
Neonatal hypotonia: don't forget the Prader-Willi syndrome
Autor: G, Trifirò, C, Livieri, L, Bosio, L, Gargantini, A, Corrias, G, Pozzan, A, Crinò
Publikováno v: Acta paediatrica (Oslo, Norway : 1992). 92(9)
During the neonatal period the diagnosis of the Prader-Willi syndrome (PWS) is difficult because the syndrome is expressed mainly by severe hypotonia at this age and the typical clinical features of later life are not yet present.To identify all the
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::35bf50439352da924c361372961b50b3
https://pubmed.ncbi.nlm.nih.gov/14599075
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10
Final height in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: the Italian experience
Autor: V L, Brunelli, G, Russo, S, Bertelloni, L, Gargantini, R, Balducci, L, Chiesa, C, Livieri, C, De Sanctis, S, Einaudi, R, Virdis, G, Saggese, G, Chiumello
Publikováno v: Journal of pediatric endocrinologymetabolism : JPEM. 16
To investigate the influence of target height (TH), gender, phenotype, glucocorticoid formulation and age at onset of treatment on final height (FH) in patients with 21-hydroxylase deficiency (21OHD).Clinical data of 93 patients--46 simple virilizing
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::c2e2f5d382b82222edc945d8b4c5b634
https://pubmed.ncbi.nlm.nih.gov/12729404
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