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Factors behind Antibiotic Therapy: A Survey of Primary Care Pediatricians in Lombardy
Author / Creator:Perrone, Pier Mario ; Picca, Marina ; Carrozzo, Romeo ; Agostoni, Carlo Virginio ; Marchisio, Paola ; Milani, Gregorio Paolo ; Castaldi, Silvana
Publisher:Switzerland: MDPI AG
Journal title:International journal of environmental research and public health, 2024-08, Vol.21 (8), p.1091
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Recurrent upper respiratory tract infections in early childhood: a newly defined clinical condition
Author / Creator:Corsello, Antonio ; Milani, Gregorio Paolo ; Picca, Marina ; Buzzetti, Roberto ; Carrozzo, Romeo ; Gambino, Mirko ; Chiaffoni, Giovanni ; Marchisio, Paola ; Mameli, Chiara
Publisher:England: BioMed Central
Journal title:Italian journal of pediatrics, 2024-02, Vol.50 (1), p.30-30, Article 30
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Leading reasons for antibiotic prescriptions in pediatric respiratory infections: influence of fever in a primary care setting
Author / Creator:Picca, Marina ; Carrozzo, Romeo ; Milani, Gregorio Paolo ; Corsello, Antonio ; Macchi, Marina ; Buzzetti, Roberto ; Marchisio, Paola ; Mameli, Chiara
Publisher:Pisa: BioMed Central
Journal title:Italian journal of pediatrics, 2023-09, Vol.49 (1), p.1-131, Article 131
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Reciprocal translocations: a trap for cytogenetists?
Author / Creator:Ciccone, Roberto ; Giorda, Roberto ; Gregato, Giuliana ; Guerrini, Renzo ; Giglio, Sabrina ; Carrozzo, Romeo ; Bonaglia, Maria Clara ; Priolo, Emanuela ; Laganà, Carmelo ; Tenconi, Romano ; Rocchi, Mariano ; Pramparo, Tiziano ; Zuffardi, Orsetta ; Rossi, Elena
Publisher:Heidelberg: Springer
Journal title:Human genetics, 2005-10, Vol.117 (6), p.571-582
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Human piebaldism: six novel mutations of the proto-oncogene KIT
Author / Creator:Syrris, Petros ; Heathcote, Kirsten ; Carrozzo, Romeo ; Devriendt, Koen ; Elçioglu, Nursel ; Garrett, Christine ; McEntagart, Meriel ; Carter, Nicholas D.
Publisher:New York: Wiley Subscription Services, Inc., A Wiley Company
Journal title:Human mutation, 2002-09, Vol.20 (3), p.234-234
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Identification of novel RP2 mutations in a subset of X-linked retinitis pigmentosa families and prediction of new domains
Author / Creator:Miano, Maria Giuseppina ; Testa, Francesco ; Filippini, Francesco ; Trujillo, Mariajosè ; Conte, Ivan ; Lanzara, Carmela ; Millán, Josè Maria ; De Bernardo, Carmelilia ; Grammatico, Barbara ; Mangino, Massimo ; Torrente, Isabella ; Carrozzo, Romeo ; Simonelli, Francesca ; Rinaldi, Ernesto ; Ventruto, Valerio ; D'Urso, Michele ; Ayuso, Carmen ; Ciccodicola, Alfredo
Publisher:New York: John Wiley & Sons, Inc
Journal title:Human mutation, 2001-08, Vol.18 (2), p.109-119
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Opposite deletions/duplications of the X chromosome: two novel reciprocal rearrangements
Author / Creator:Giglio, Sabrina ; Pirola, Barbara ; Arrigo, Giulia ; Dagrada, Paolo ; Bardoni, Barbara ; Bernardi, Franca ; Russo, Giovanni ; Argentiero, Luisa ; Forabosco, Antonino ; Carrozzo, Romeo ; Zuffardi, Orsetta
Publisher:England: Nature Publishing Group
Journal title:European journal of human genetics : EJHG, 2000-01, Vol.8 (1), p.63-70
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Isolation of a Miller–Dicker lissencephaly gene containing G protein β-subunit-like repeats
Author / Creator:Reiner, Orly ; Carrozzo, Romeo ; Shen, Ying ; Wehnert, Manfred ; Faustinella, Fabrizia ; Dobyns, William B. ; Caskey, C. Thomas ; Ledbetter, David H.
Publisher:London: Nature Publishing Group UK
Journal title:Nature (London), 1993-08, Vol.364 (6439), p.717-721
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Cryptic telomeric rearrangements in subjects with mental retardation associated with dysmorphism and congenital malformations
Author / Creator:Rossi, Elena ; Piccini, Flavia ; Zollino, Marcella ; Neri, Giovanni ; Caselli, Desirée ; Tenconi, Romano ; Castellan, Claudio ; Carrozzo, Romeo ; Danesino, Cesare ; Zuffardi, Orsetta ; Ragusa, Angela ; Castiglia, Lucia ; Galesi, Ornella ; Greco, Donatella ; Romano, Corrado ; Pierluigi, Mauro ; Perfumo, Chiara ; Di Rocco, Maia ; Faravelli, Francesca ; Bricarelli, Franca Dagna ; Bonaglia, MariaClara ; Bedeschi, MariaFrancesca ; Borgatti, Renato
Publisher:London: BMJ
Journal title:Journal of medical genetics, 2001-06, Vol.38 (6), p.417-420
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Molecular and functional analysis of SUMF1 mutations in multiple sulfatase deficiency
Author / Creator:Cosma, Maria Pia ; Pepe, Stefano ; Parenti, Giancarlo ; Settembre, Carmine ; Annunziata, Ida ; Wade-Martins, Richard ; Domenico, Carmela Di ; Natale, Paola Di ; Mankad, Anuj ; Cox, Barbara ; Uziel, Graziella ; Mancini, Grazia M.S. ; Zammarchi, Enrico ; Donati, Maria Alice ; Kleijer, Wim J. ; Filocamo, Mirella ; Carrozzo, Romeo ; Carella, Massimo ; Ballabio, Andrea
Publisher:Hoboken: Wiley Subscription Services, Inc., A Wiley Company
Journal title:Human mutation, 2004-06, Vol.23 (6), p.576-581
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A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules
Author / Creator:Franco, Brunella ; Guioli, Silvana ; Pragliola, Antonella ; Incerti, Barbara ; Bardoni, Barbara ; Tonlorenzi, Rossana ; Carrozzo, Romeo ; Maestrini, Elena ; Pieretti, Maura ; Taillon-Miller, Patricia ; Brown, Carolyn J. ; Willard, Huntington F. ; Lawrence, Charles ; Persico, M. Graziella ; Camerino, Giovanna ; Ballabio, Andrea
Publisher:London: Nature Publishing
Journal title:Nature (London), 1991-10, Vol.353 (6344), p.529-536
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Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness
Author / Creator:Masmoudi, Saber ; Antonarakis, Stylianos E. ; Schwede, Torsten ; Ghorbel, Abdel Monem ; Gratri, M'hamed ; Pappasavas, Marie-Pierre ; Drira, Mohamed ; Elgaied-Boulila, Amel ; Wattenhofer, Marie ; Rossier, Colette ; Scott, Hamish S. ; Ayadi, Hammadi ; Guipponi, Michel
Publisher:New York: John Wiley & Sons, Inc
Journal title:Human mutation, 2001-08, Vol.18 (2), p.101-108
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Human piebaldism: six novel mutations of the proto-oncogene KIT: MUTATIONS IN BRIEF
Author / Creator:Syrris, Petros ; Heathcote, Kirsten ; Carrozzo, Romeo ; Devriendt, Koen ; Elçioglu, Nursel ; Garrett, Christine ; McEntagart, Meriel ; Carter, Nicholas D.
Journal title:Human mutation, 2002-09, Vol.20 (3), p.234-234
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ArticlesPeer ReviewedFull Text
Molecular and functional analysis ofSUMF1 mutations in multiple sulfatase deficiency
Author / Creator:Cosma, Maria Pia ; Pepe, Stefano ; Parenti, Giancarlo ; Settembre, Carmine ; Annunziata, Ida ; Wade-Martins, Richard ; Domenico, Carmela Di ; Natale, Paola Di ; Mankad, Anuj ; Cox, Barbara ; Uziel, Graziella ; Mancini, Grazia M.S. ; Zammarchi, Enrico ; Donati, Maria Alice ; Kleijer, Wim J. ; Filocamo, Mirella ; Carrozzo, Romeo ; Carella, Massimo ; Ballabio, Andrea
Journal title:Human mutation, 2004-06, Vol.23 (6), p.576-581
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Identification of novel RP2 mutations in a subset of X-linked retinitis pigmentosa families and prediction of new domains: RP2 Mutations and Functional Domains
Author / Creator:Miano, Maria Giuseppina ; Testa, Francesco ; Filippini, Francesco ; Trujillo, Mariajosè ; Conte, Ivan ; Lanzara, Carmela ; Millán, Josè Maria ; De Bernardo, Carmelilia ; Grammatico, Barbara ; Mangino, Massimo ; Torrente, Isabella ; Carrozzo, Romeo ; Simonelli, Francesca ; Rinaldi, Ernesto ; Ventruto, Valerio ; D’Urso, Michele ; Ayuso, Carmen ; Ciccodicola, Alfredo
Journal title:Human mutation, 2001-08, Vol.18 (2), p.109-119
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Identification of two paralogous regions mapping to the short and long arms of human chromosome 2 comprising LIS1 pseudogenes
Author / Creator:Fogli, A. ; Giglio, S. ; Arrigo, G. ; Lo Nigro, C. ; Zollo, M. ; Viggiano, L. ; Rocchi, M. ; Archidiacono, N. ; Zuffardi, O. ; Carrozzo, R.
Publisher:Basel, Switzerland: S. Karger AG
Journal title:Cytogenetic and genome research, 1999-01, Vol.86 (3-4), p.225-232
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Factors behind Antibiotic Therapy: A Survey of Primary Care Pediatricians in Lombardy

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Recurrent upper respiratory tract infections in early childhood: a newly defined clinical condition

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Leading reasons for antibiotic prescriptions in pediatric respiratory infections: influence of fever in a primary care setting

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Reciprocal translocations: a trap for cytogenetists?

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Human piebaldism: six novel mutations of the proto-oncogene KIT

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Identification of novel RP2 mutations in a subset of X-linked retinitis pigmentosa families and prediction of new domains

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Opposite deletions/duplications of the X chromosome: two novel reciprocal rearrangements

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Isolation of a Miller–Dicker lissencephaly gene containing G protein β-subunit-like repeats

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Cryptic telomeric rearrangements in subjects with mental retardation associated with dysmorphism and congenital malformations

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Molecular and functional analysis of SUMF1 mutations in multiple sulfatase deficiency

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A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules

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Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness

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Human piebaldism: six novel mutations of the proto-oncogene KIT: MUTATIONS IN BRIEF

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Molecular and functional analysis ofSUMF1 mutations in multiple sulfatase deficiency

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Identification of novel RP2 mutations in a subset of X-linked retinitis pigmentosa families and prediction of new domains: RP2 Mutations and Functional Domains

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Identification of two paralogous regions mapping to the short and long arms of human chromosome 2 comprising LIS1 pseudogenes

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