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Corrado Romano

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Michele Salemi; Maria Grazia Salluzzo; Cataldo Scavuzzo; Concetta Barone; Aldo E Calogero; Rita Anna Cantarella; Federico Ridolfo; Carmelo Romano; Corrado Romano; Paolo Bosco
KIF21A mRNA expression in patients with Down syndrome.
Daniela Di Benedetto; Giuseppa Di Vita; Lucia Castiglia; Mariangela Lo Giudice; Lucia Grillo; Sebastiano A Musumeci; Corrado Romano; Girolamo Aurelio Vitello; Marinella Zingale; Marco Fichera
6p22.3 deletion: report of a patient with autism, severe intellectual disability and electroencephalographic anomalies.
Corrado Romano; Carmelo Schepis
PTEN gene: a model for genetic diseases in dermatology.

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All Publications

2013: Michele Salemi; Maria Grazia Salluzzo; Cataldo Scavuzzo; Concetta Barone; Aldo E Calogero; Rita Anna Cantarella; Federico Ridolfo; Carmelo Romano; Corrado Romano; Paolo Bosco
KIF21A mRNA expression in patients with Down syndrome.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2013;34(4):569-71.
2013: Daniela Di Benedetto; Giuseppa Di Vita; Lucia Castiglia; Mariangela Lo Giudice; Lucia Grillo; Sebastiano A Musumeci; Corrado Romano; Girolamo Aurelio Vitello; Marinella Zingale; Marco Fichera
6p22.3 deletion: report of a patient with autism, severe intellectual disability and electroencephalographic anomalies.
Molecular cytogenetics 2013;6(1):4.
2012: Corrado Romano; Carmelo Schepis
PTEN gene: a model for genetic diseases in dermatology.
TheScientificWorldJournal 2012;2012():252457.
2012: Michele Salemi; Maria Grazia Salluzzo; Roberto Salluzzo; Cataldo Scavuzzo; Francesco Scillato; Maria Signorelli; Francesca Zolezzi; Concetta Barone; Dimos Kapetis; Corrado Romano; Carmelo Romano; Paolo Bosco
Gene expression profiling and qRT-PCR expression of RRP1B, PCNT, KIF21A and ADRB2 in leucocytes of Down's syndrome subjects.
Journal of genetics 2012;91(1):e18-23.
2012: Michele Salemi; Roberto Salluzzo; Cataldo Scavuzzo; Francesco Scillato; Aldo E Calogero; Filippo Caraci; Federico Ridolfo; Carmelo Romano; Corrado Romano; Concetta Barone; Paolo Bosco
Expression of LDOC1 mRNA in leucocytes of patients with Down's syndrome.
Journal of genetics 2012;91(1):95-8.
2012: Michele Salemi; Paolo Bosco; Roberto Castiglione; L Cimino; R A Condorelli; Sandro La Vignera; Corrado Romano; C Romano; Aldo E Calogero
Expression of STRBP mRNA in patients with cryptorchidism and Down's syndrome.
Journal of endocrinological investigation 2012;35(1):5-7.
2012: Daniela Concolino; M Fichera; Ornella Galesi; Maria Antonietta Iembo; R Marotta; MT Moricca; M Rapsomaniki; Corrado Romano; Pietro Strisciuglio
A de novo 8q22.2-24.3 duplication in a patient with mild phenotype.
European journal of medical genetics 2012;55(1):67-70.
2011: Michele Salemi; Concetta Barone; Mariaconcetta Giambirtone; Eleonora Gulotta; Maria Grazia Salluzzo; Corrado Romano; Carmelo Romano; Filippo Caraci; Cataldo Scavuzzo; Federico Ridolfo; Paolo Bosco
Differential expression of PARP1 mRNA in leucocytes of patients with Down's syndrome.
Journal of genetics 2011;90(3):469-72.
2011: Santhosh Girirajan; Carlos S Moreno; Wendy H Raskind; Corrado Romano; Neil Shafer; Margherita Silengo; Laura Vives; Tiffany H Vu; Stephen Warren; Carl Baker; Raphael Bernier; Zoran Brkanac; Bradley P Coe; Giovanni B Ferrero; Marco Fichera; Evan E Eichler
Relative burden of large CNVs on a range of neurodevelopmental phenotypes.
PLoS genetics 2011;7(11):e1002334.
2011: Michael E Talkowski; Devon Lamb Thrush; Margot I Van Allen; Bregje W M van Bon; Charles A Williams; Bai-Lin Wu; Lilei Zhang; Lesley C Ades; Yu An; Caroline Astbury; Dennis Bartholomew; Louise A Brueton; Colby Chiang; Bert B A de Vries; Carl Ernst; Marco Fichera; Julie M Gastier-Foster; James Gusella; Carrie Hanscom; Jeffrey W Innis; Sekar Kathiresan; Klaske D Lichtenbelt; Amelia M Lindgren; Cynthia C Morton; Sureni V Mullegama; Aditi Parikh; Robert E Pyatt; Elena A Repnikova; Corrado Romano; Jill A Rosenfeld; Douglas M Ruderfer; Stuart Schwartz; Lisa G Shaffer; Yiping Shen; Sarah H Elsea
Assessment of 2q23.1 microdeletion syndrome implicates MBD5 as a single causal locus of intellectual disability, epilepsy, and autism spectrum disorder.
American journal of human genetics 2011;89(4):551-63.
2011: Marcella Broli; Serafino Buono; Daniela Cevolani; Isabella Fiocchi; Elena Fontana; Roberto Gallassi; Roberto Giorda; Massimo Mastrangelo; Sebastiano Antonino Musumeci; Roberto Poda; Santina Reitano; Corrado Romano; Maria Savio; Marco Seri; Raffaele Agati; Bruno Bernardi; Bernardo Dalla Bernardina; Francesca Bisulli; Maria Clara Bonaglia; Girolamo Aurelio Vitello; Claudio Zucca; Orsetta Zuffardi; Paolo Tinuper
Definition of the neurological phenotype associated with dup (X)(p11.22-p11.23).
Epileptic disorders : international epilepsy journal with videotape 2011;13(3):240-51.
2011: Maria Clara Bonaglia; Maria Teresa Bonati; Renato Borgatti; Armand Bottani; Anna Bremer; Alfredo Brusco; Antonella Cecconi; Roberto Ciccone; Bernardo Dalla Bernardina; Francesca Darra; Stefano D'Arrigo; Cristina De Agostini; Eleonora di Gregorio; Marco Fichera; Ornella Galesi; Sabrina Giglio; Stefania Gimelli; Roberto Giorda; Ursula Giussani; Rita Grasso; Donatella Greco; Lucia Grillo; Renzo Guerrini; Elisabetta Lapi; Elisa Mani; Susan Marelli; Nieves Martínez Guardia; Maria Luisa Martínez-Fernández; Maria Luisa Martinez-Frias; Emanuela Maserati; Massimo Molteni; Cristina Motta; Lucio Nitsch; Francesca Novara; Sara Osimani; Chiara Pantaleoni; Maria Grazia Patricelli; Pierluigi Politi; Emanuela Priolo; Santina Reitano; Daria Riva; Corrado Romano; Francesca Sciacca; Cristiano Termine; Annalisa Vetro; Leonardo Zoccante; Claudio Zucca; Britt-Marie Anderlid; Giulia Arrigo; Irene Bagnasco; Anna Baroncini; Frederique Bena; Silvana Beri; Stefania Bigoni; Orsetta Zuffardi
Molecular mechanisms generating and stabilizing terminal 22q13 deletions in 44 subjects with Phelan/McDermid syndrome.
PLoS genetics 2011;7(7):e1002173.
2011: Giuseppe Marangi; Federica Martinez; Marina Murdolo; Daniela Orteschi; Chiara Pantaleoni; Rosa Pettinato; Stefania Ricciardi; Corrado Romano; Gigliola Serra; Giovanni Sorge; Irene Toldo; Gessica Vasco; Enrico Alfei; Anna Baroncini; Domenica Battaglia; Chiara Biscione; Paolo Bonanni; Pietro Chiurazzi; Bruno Dallapiccola; Cecilia Daolio; Donatella Greco; Serena Lattante; Rosetta Lecce; Donatella Lettori; Cinzia Magnani; Marcella Zollino
The Pitt-Hopkins syndrome: report of 16 new patients and clinical diagnostic criteria.
American journal of medical genetics. Part A 2011;155A(7):1536-45.
2010: Carmelo Schepis; Maria Lentini; Pinella Failla; Lucia Castiglia; Marco Fichera; Corrado Romano
An unusual presentation of Becker Nevus.
European journal of dermatology : EJD 2010;20(4):522-3.
2010: Santhosh Girirajan; Jill A Rosenfeld; Gregory Cooper; Francesca Antonacci; Priscillia Siswara; Andy Itsara; Laura Vives; Tom Walsh; Shane E McCarthy; Carl Baker; Heather C Mefford; Jeffrey M Kidd; Sharon R Browning; Brian L Browning; Diane E Dickel; Deborah L Levy; Blake C Ballif; Kathryn Platky; Darren M Farber; Gordon C Gowans; Jessica J Wetherbee; Alexander Asamoah; David D Weaver; Paul R Mark; Jennifer Dickerson; Bhuwan P Garg; Sara A Ellingwood; Rosemarie Smith; Valerie C Banks; Wendy Smith; Marie T McDonald; Joe J Hoo; Beatrice N French; Cindy Hudson; John P Johnson; Jillian R Ozmore; John B Moeschler; Urvashi Surti; Luis F Escobar; Dima El-Khechen; Jerome L Gorski; Jennifer Kussmann; Bonnie Salbert; Yves Lacassie; Alisha Biser; Donna M McDonald-McGinn; Elaine H Zackai; Matthew A Deardorff; Tamim H Shaikh; Eric Haan; Kathryn L Friend; Marco Fichera; Corrado Romano; Jozef Gécz; Lynn E DeLisi; Jonathan Sebat; Mary-Claire King; Lisa Shaffer; Evan E Eichler
A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay.
Nature genetics 2010;42(3):203-9.
2010: L Grillo; S Reitano; G Belfiore; Angela Spalletta; Silvestra Amata; M Bottitta; C Barone; Michele Falco; M Fichera; Corrado Romano
Familial 1.1 Mb deletion in chromosome Xq22.1 associated with mental retardation and behavioural disorders in female patients.
European journal of medical genetics 2010;53(2):113-6.
2010: Bregje W M van Bon; David A Koolen; Louise Brueton; Dominic McMullan; Klaske D Lichtenbelt; Lesley C Adès; Gregory Peters; Kate Gibson; Susan Moloney; Francesca Novara; Tiziano Pramparo; Bernardo Dalla Bernardina; Leonardo Zoccante; Umberto Balottin; Fausta Piazza; Vanna Pecile; Paolo Gasparini; Veronica Guerci; Marleen Kets; Rolph Pfundt; Arjan P de Brouwer; Joris Veltman; Nicole de Leeuw; Meredith Wilson; Jayne Antony; Santina Reitano; Daniela Luciano; Marco Fichera; Corrado Romano; Han G Brunner; Orsetta Zuffardi; Bert B A de Vries
The 2q23.1 microdeletion syndrome: clinical and behavioural phenotype.
European journal of human genetics : EJHG 2010;18(2):163-70.
2010: Vincenza Barresi; Angela Ragusa; Marco Fichera; Nicolò Musso; Lucia Castiglia; Giancarlo Rappazzo; Salvatore Travali; Teresa Mattina; Corrado Romano; Guido Cocchi; Daniele F Condorelli
Decreased expression of GRAF1/OPHN-1-L in the X-linked alpha thalassemia mental retardation syndrome.
BMC medical genomics 2010;3():28.
2010: Luciana Musante; Stella-Amrei Kunde; Tina O Sulistio; Ute Fischer; Astrid Grimme; Suzanna G M Frints; Charles E Schwartz; Francisco Martínez; Corrado Romano; Hans-Hilger Ropers; Vera Kalscheuer
Common pathological mutations in PQBP1 induce nonsense-mediated mRNA decay and enhance exclusion of the mutant exon.
Human mutation 2010;31(1):90-8.
2009: Lorena Travaglini; Francesco Brancati; Tania Attie-Bitach; Sophie Audollent; Enrico Bertini; Josseline Kaplan; Isabelle Perrault; Miriam Iannicelli; Brunella Mancuso; Luciana Rigoli; Jean-Michel Rozet; Dominika Swistun; Jerlyn Tolentino; Bruno Dallapiccola; Joseph G Gleeson; Enza Maria Valente; A Zankl; R Leventer; P Grattan-Smith; A Janecke; M D'Hooghe; Y Sznajer; R Van Coster; L Demerleir; K Dias; C Moco; A Moreira; C Ae Kim; Gustavo Maegawa; D Petkovic; G M H Abdel-Salam; A Abdel-Aleem; M S Zaki; I Marti; S Quijano-Roy; S Sigaudy; P de Lonlay; S Romano; R Touraine; M Koenig; C Lagier-Tourenne; J Messer; P Collignon; N Wolf; H Philippi; Sophia Kitsiou-Tzeli; S Halldorsson; J Johannsdottir; P Ludvigsson; S R Phadke; V Udani; B Stuart; A Magee; D Lev; M Michelson; B Ben-Zeev; R Fischetto; F Benedicenti; F Stanzial; R Borgatti; P Accorsi; S Battaglia; E Fazzi; L Giordano; L Pinelli; L Boccone; S Bigoni; A Ferlini; M A Donati; G Caridi; M T Divizia; F Faravelli; G Ghiggeri; A Pessagno; M Briguglio; S Briuglia; C D Salpietro; G Tortorella; A Adami; P Castorina; F Lalatta; G Marra; D Riva; Barbara Scelsa; L Spaccini; Graziella Uziel; E Del Giudice; A M Laverda; K Ludwig; A Permunian; A Suppiej; S Signorini; C Uggetti; R Battini; M Di Giacomo; M R Cilio; M L Di Sabato; V Leuzzi; P Parisi; M Pollazzon; M Silengo; R De Vescovi; D Greco; Corrado Romano; M Cazzagon; A Simonati; A A Al-Tawari; L Bastaki; A Mégarbané; V Sabolic Avramovska; M M de Jong; P Stromme; R Koul; A Rajab; M Azam; C Barbot; L Martorell Sampol; B Rodriguez; I Pascual-Castroviejo; S Teber; B Anlar; S Comu; E Karaca; H Kayserili; A Yüksel; M Akcakus; L Al Gazali; L Sztriha; D Nicholl; C G Woods; C Bennett; J Hurst; E Sheridan; A Barnicoat; Raoul Hennekam; M Lees; E Blair; S Bernes; H Sanchez; A E Clark; E DeMarco; C Donahue; Elliott H Sherr; J Hahn; T D Sanger; T E Gallager; W B Dobyns; C Daugherty; K S Krishnamoorthy; D Sarco; Christopher Walsh; T McKanna; J Milisa; W K Chung; D C De Vivo; Hillary Raynes; R Schubert; A Seward; D G Brooks; A Goldstein; J Caldwell; E Finsecke; B L Maria; K Holden; R P Cruse; K J Swoboda; D Viskochil
Expanding CEP290 mutational spectrum in ciliopathies.
American journal of medical genetics. Part A 2009;149A(10):2173-80.
2009: Roberto Giorda; M Clara Bonaglia; Silvana Beri; Marco Fichera; Francesca Novara; Pamela Magini; Jill Urquhart; Freddie H Sharkey; Claudio Zucca; Rita Grasso; Susan Marelli; Lucia Castiglia; Daniela Di Benedetto; Sebastiano A Musumeci; Girolamo A Vitello; Pinella Failla; Santina Reitano; Emanuela Avola; Francesca Bisulli; Paolo Tinuper; Massimo Mastrangelo; Isabella Fiocchi; Luigina Spaccini; Claudia Torniero; Elena Fontana; Sally Ann Lynch; Jill Clayton-Smith; Graeme Black; Philippe Jonveaux; Bruno Leheup; Marco Seri; Corrado Romano; Bernardo dalla Bernardina; Orsetta Zuffardi
Complex segmental duplications mediate a recurrent dup(X)(p11.22-p11.23) associated with mental retardation, speech delay, and EEG anomalies in males and females.
American journal of human genetics 2009;85(3):394-400.
2009: F Brancati; L Bernardini; D P Cavalcanti; Corrado Romano; A Novelli; B Dallapiccola
Genome rearrangements in patients with blepharophimosis, mental retardation and hypothyroidism, so-called Young-Simpson syndrome.
Clinical genetics 2009;76(2):210-3.
2009: B W M van Bon; H C Mefford; B Menten; D A Koolen; A J Sharp; W M Nillesen; Jeffrey W Innis; T J L de Ravel; C L Mercer; M Fichera; H Stewart; L E Connell; K Ounap; K Lachlan; B Castle; N Van der Aa; Conny van Ravenswaaij-Arts; M A Nobrega; C Serra-Juhé; I Simonic; N de Leeuw; R Pfundt; E M Bongers; C Baker; P Finnemore; S Huang; V K Maloney; J A Crolla; M van Kalmthout; M Elia; G Vandeweyer; J P Fryns; S Janssens; N Foulds; S Reitano; K Smith; S Parkel; Bart Loeys; C G Woods; A Oostra; F Speleman; A C Pereira; A Kurg; Lionel Willatt; S J L Knight; J R Vermeesch; Corrado Romano; J C Barber; G Mortier; L A Pérez-Jurado; F Kooy; H G Brunner; Evan E Eichler; T Kleefstra; B B A de Vries
Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome.
Journal of medical genetics 2009;46(8):511-23.
2009: Michele Salemi; Corrado Romano; Concetta Barone; Francesco Calí; Filippo Caraci; Corrado Romano; Cataldo Scavuzzo; Francesco Scillato; Maria Grazia Salluzzo; Maria Piccione; Manuela Martines; Giovanni Corsello; Ferdinando Nicoletti; Paolo Bosco
SPANX-B and SPANX-C (Xq27 region) gene dosage analysis in Down's syndrome subjects with undescended testes.
Journal of genetics 2009;88(1):93-7.
2009: A K Nicholas; E A Swanson; James Cox; Gulshan Karbani; S Malik; Kelly Springell; Daniel J Hampshire; M Ahmed; Jacquelyn Bond; D Di Benedetto; M Fichera; Corrado Romano; W B Dobyns; C Geoffrey Woods
The molecular landscape of ASPM mutations in primary microcephaly.
Journal of medical genetics 2009;46(4):249-53.
2009: Nathalie Van der Aa; Liesbeth Rooms; Geert Vandeweyer; Jenneke van den Ende; Edwin Reyniers; Marco Fichera; Corrado Romano; Barbara Delle Chiaie; Geert R Mortier; Björn Menten; Anne Destrée; Isabelle Maystadt; Katrin Männik; Ants Kurg; Tiia Reimand; Dom McMullan; Christine Oley; Louise Brueton; Ernie M H F Bongers; Bregje W M van Bon; Rolph Pfund; Sebastien Jacquemont; Alessandra Ferrarini; Danielle Martinet; Connie Schrander-Stumpel; Alexander P A Stegmann; Suzanna G M Frints; Bert B A de Vries; Berten Ceulemans; R Frank Kooy
Fourteen new cases contribute to the characterization of the 7q11.23 microduplication syndrome.
European journal of medical genetics 2009;52(2-3):94-100.
2009: Ingo Helbig; Heather C Mefford; Andrew J Sharp; Michel Guipponi; Marco Fichera; Andre Franke; Hiltrud Muhle; Carolien de Kovel; Carl Baker; Sarah von Spiczak; Katherine L Kron; Ines Steinich; Ailing A Kleefuss-Lie; Costin Leu; Verena Gaus; Bettina Schmitz; Karl M Klein; Philipp S Reif; Felix Rosenow; Yvonne Weber; Holger Lerche; Fritz Zimprich; Lydia Urak; Karoline Fuchs; Martha Feucht; Pierre Genton; Pierre Thomas; Frank Visscher; Gerrit-Jan de Haan; Rikke Steensbjerre Møller; Helle Hjalgrim; Daniela Luciano; Michael Wittig; Michael Nothnagel; Christian E Elger; Peter Nürnberg; Corrado Romano; Alain Malafosse; Bobby P C Koeleman; Dick Lindhout; Ulrich Stephani; Stefan Schreiber; Evan E Eichler; Thomas Sander
15q13.3 microdeletions increase risk of idiopathic generalized epilepsy.
Nature genetics 2009;41(2):160-2.
2008: Heather C Mefford; andrew sharp; Carl Baker; Andy Itsara; Zhaoshi Jiang; Karen Buysse; Shuwen Huang; Viv K Maloney; John A Crolla; Diana Baralle; Amanda Collins; Catherine Mercer; Koen Norga; Thomy de Ravel; koenraad devriendt; Ernie M H F Bongers; Nicole de Leeuw; William Reardon; stefania gimelli; Frederique Bena; Raoul Hennekam; Alison Male; Lorraine Gaunt; Jill Clayton-Smith; Ingrid Simonic; Soo Mi Park; Sarju G Mehta; Serena Nik-Zainal; C Geoffrey Woods; Helen V Firth; Georgina Parkin; Marco Fichera; Santina Reitano; Mariangela Lo Giudice; Kelly E Li; Iris Casuga; Adam Broomer; Bernard Conrad; Markus Schwerzmann; Lorenz Räber; Sabina Gallati; Pasquale Striano; Antonietta Coppola; John L Tolmie; Edward S Tobias; Chris Lilley; Lluis Armengol; Yves Spysschaert; Patrick Verloo; Anja De Coene; Linde Goossens; Geert Mortier; Frank Speleman; Ellen van Binsbergen; Marcel R Nelen; Ron Hochstenbach; Martin Poot; Louise Gallagher; Michael Gill; Jon McClellan; Mary-Claire King; Regina Regan; Cindy Skinner; Roger E Stevenson; Stylianos Antonarakis; Caifu Chen; Xavier Estivill; Björn Menten; Giorgio Gimelli; Susan Gribble; Stuart Schwartz; James S Sutcliffe; Tom Walsh; Samantha J L Knight; Jonathan Sebat; Corrado Romano; Charles E Schwartz; Joris Veltman; Bert B A de Vries; Joris R Vermeesch; John C K Barber; Lionel Willatt; May Tassabehji; Evan E Eichler
Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes.
The New England journal of medicine 2008;359(16):1685-99.
2008: Pinella Failla; Corrado Romano; Santina Reitano; Daniela Di Benedetto; Lucia Grillo; Marco Fichera; Lucia Castiglia
12q12 deletion: a new patient contributing to genotype-phenotype correlation.
American journal of medical genetics. Part A 2008;146A(10):1354-7.
2008: Carmelo Schepis; Donatella Greco; Maddalena Siragusa; Corrado Romano
Cerebriform plantar hyperplasia: the major cutaneous feature of Proteus syndrome.
International journal of dermatology 2008;47(4):374-6.
2008: andrew sharp; Heather C Mefford; Kelly Li; Carl Baker; Cindy Skinner; Roger E Stevenson; Richard J Schroer; Francesca Novara; Manuela De Gregori; Roberto Ciccone; Adam Broomer; Iris Casuga; Yu Wang; Chunlin Xiao; Catalin Barbacioru; Giorgio Gimelli; Bernardo Dalla Bernardina; Claudia Torniero; Roberto Giorda; Regina Regan; Victoria Murday; Sahar Mansour; Marco Fichera; Lucia Castiglia; Pinella Failla; ventura Mario; Zhaoshi Jiang; Gregory Cooper; Samantha J L Knight; Corrado Romano; Orsetta Zuffardi; Caifu Chen; Charles E Schwartz; Evan E Eichler
A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures.
Nature genetics 2008;40(3):322-8.
2008: D Greco; Corrado Romano; S Reitano; C Barone; D D Benedetto; Lucia Castiglia; Marco Fichera; Ornella Galesi; M Zingale; Serafino Buono; Vera Uliana; Richard Caselli; Roberto Canitano; Giuseppe Hayek; Alessandra Renieri
Three new patients with dup(17)(p11.2p11.2) without autism.
Clinical genetics 2008;73(3):294-6.
2008: David A Koolen; Erik A Sistermans; Willy Nilessen; Samantha J L Knight; Regina Regan; Yan T Liu; R Frank Kooy; Liesbeth Rooms; Corrado Romano; Marco Fichera; Albert Schinzel; Alessandra Baumer; Britt-Marie Anderlid; Jacqueline Schoumans; Ad Geurts van Kessel; Magnus Nordenskjold; Bert B A de Vries
Identification of non-recurrent submicroscopic genome imbalances: the advantage of genome-wide microarrays over targeted approaches.
European journal of human genetics : EJHG 2008;16(3):395-400.
2008: Agatino Battaglia; H Eugene Hoyme; Bruno Dallapiccola; Elaine Zackai; Louanne Hudgins; Donna McDonald-McGinn; Nadia Bahi-Buisson; Corrado Romano; Charles A Williams; Lisa L Brailey; Lisa L Braley; Sameer M Zuberi; John C Carey
Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation.
Pediatrics 2008;121(2):404-10.
2007: M De Gregori; R Ciccone; P Magini; T Pramparo; stefania gimelli; J Messa; F Novara; Annalisa Vetro; E Rossi; P Maraschio; M C Bonaglia; C Anichini; G B Ferrero; M Silengo; E Fazzi; A Zatterale; R Fischetto; C Previderé; S Belli; A Turci; G Calabrese; F Bernardi; E Meneghelli; M Riegel; M Rocchi; S Guerneri; F Lalatta; L Zelante; Corrado Romano; M Fichera; T Mattina; G Arrigo; M Zollino; S Giglio; Fortunato Lonardo; A Bonfante; A Ferlini; F Cifuentes; H Van Esch; liesbeth backx; A Schinzel; J R Vermeesch; O Zuffardi
Cryptic deletions are a common finding in "balanced" reciprocal and complex chromosome rearrangements: a study of 59 patients.
Journal of medical genetics 2007;44(12):750-62.
2007: Corrado Romano; Samantha J L Knight; Christa Lese Martin; Bert B A de Vries
3rd International Meeting on Cryptic Chromosomal Rearrangements in Mental Retardation and Autism.
European journal of human genetics : EJHG 2007;15(10):1098-101.
2007: Vanna Micheli; Silvia Sestini; Veronica Parri; Marco Fichera; Corrado Romano; Francesca Ariani; Ilaria Longo; Francesca Mari; Mirella Bruttini; Alessandra Renieri; Ilaria Meloni
RSK2 enzymatic assay as a second level diagnostic tool in Coffin-Lowry syndrome.
Clinica chimica acta; international journal of clinical chemistry 2007;384(1-2):35-40.
2007: Caterina Proto; Daniela Romualdi; Rosa Maria Cento; Corrado Romano; Giuseppe Campagna; Antonio Lanzone
Free and total leptin serum levels and soluble leptin receptors levels in two models of genetic obesity: the Prader-Willi and the Down syndromes.
Metabolism: clinical and experimental 2007;56(8):1076-80.
2007: Pinella Failla; Corrado Romano; A Alberti; A Vasta; Serafino Buono; Lucia Castiglia; D Luciano; Daniela Di Benedetto; Marco Fichera; Ornella Galesi
Schizophrenia in a patient with subtelomeric duplication of chromosome 22q.
Clinical genetics 2007;71(6):599-601.
2007: Jean-Louis Guéant; Nicodème W Chabi; Rosa-Maria Guéant-Rodriguez; Osvaldo M Mutchinick; Renée Debard; Corinne Payet; Xiaohong Lu; Christian Villaume; Jean-Pierre Bronowicki; Edward V Quadros; Ambaliou Sanni; Emile K Amouzou; Bing Xia; Min Chen; Guido Anello; Paolo Bosco; Corrado Romano; Heidy R Arrieta; Beatríz E Sánchez; Antonino Romano; Bernard Herbeth; Wafaa Anwar; Farès Namour
Environmental influence on the worldwide prevalence of a 776C->G variant in the transcobalamin gene (TCN2).
Journal of medical genetics 2007;44(6):363-7.
2007: A Alberti; Corrado Romano; Michele Falco; Francesco Calì; Pietro Schinocca; Ornella Galesi; Angela Spalletta; Daniela Di Benedetto; Marco Fichera
1.5 Mb de novo 22q11.21 microduplication in a patient with cognitive deficits and dysmorphic facial features.
Clinical genetics 2007;71(2):177-82.
2007: Michele Salemi; Corrado Romano; Letizia Ragusa; Giuseppa Di Vita; Roberto Salluzzo; Ileana Oteri; Maria Luisa Trovato; Corrado Romano; Filippo Caraci; Ferdinando Nicoletti; Paolo Bosco
A new 6-bp SOX-3 polyalanine tract deletion does not segregate with mental retardation.
Genetic testing 2007;11(2):124-7.
2006: Sebastiano A Musumeci; Maurizio Elia; Marco Fichera; Carmelo Amato; Raffaele Ferri; Corrado Romano; A Federico
Nail aplasia, microcephaly, severe mental retardation and MRI abnormalities: report of two unrelated cases.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2006;27(6):425-31.
2006: David A Koolen; Lisenka E L M Vissers; Rolph Pfundt; Nicole de Leeuw; Samantha J L Knight; Regina Regan; R Frank Kooy; Edwin Reyniers; Corrado Romano; Marco Fichera; Albert Schinzel; Alessandra Baumer; Britt-Marie Anderlid; Jacqueline Schoumans; Nine V A M Knoers; Ad Geurts van Kessel; Erik A Sistermans; Joris Veltman; Han G Brunner; Bert B A de Vries
A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism.
Nature genetics 2006;38(9):999-1001.
2006: Corrado Romano
2nd international meeting on cryptic chromosomal rearrangements in mental retardation and autism.
European journal of human genetics : EJHG 2006;14(9):1058.
2006: Maurizio Elia; Pasquale Striano; Marco Fichera; Roberto Gaggero; Lucia Castiglia; Ornella Galesi; Michela Malacarne; Mauro Pierluigi; Carmelo Amato; Sebastiano A Musumeci; Corrado Romano; Silvia Majore; Paola Grammatico; Federico Zara; Salvatore Striano; Francesca Faravelli
6q terminal deletion syndrome associated with a distinctive EEG and clinical pattern: a report of five cases.
Epilepsia 2006;47(5):830-8.
2006: Rosa-Maria Guéant-Rodriguez; Jean-Louis Guéant; Renée Debard; Sylvie Thirion; Lu Xiao Hong; Jean-Pierre Bronowicki; Farès Namour; Nicodème W Chabi; Ambaliou Sanni; Guido Anello; Paolo Bosco; Corrado Romano; Emile K Amouzou; Heidy R Arrieta; Beatríz E Sánchez; Antonino Romano; Bernard Herbeth; Jean-Claude Guilland; Osvaldo M Mutchinick
Prevalence of methylenetetrahydrofolate reductase 677T and 1298C alleles and folate status: a comparative study in Mexican, West African, and European populations.
The American journal of clinical nutrition 2006;83(3):701-7.
2006: Antonino Romano; Rosa Pettinato; Maria Andriolo; Marinella Viola; Rosa-Maria Guéant-Rodriguez; Rocco Valluzzi; Corrado Romano; Maurizio Elia; Maria Teresa Ventura; Jean-Louis Guéant
Hypersensitivity to aromatic anticonvulsants: in vivo and in vitro cross-reactivity studies.
Current pharmaceutical design 2006;12(26):3373-81.
2005: Michele Falco; Corrado Romano; Antonino Alberti; Donatella Greco; Carmela Scuderi; Emanuela Avola; Pinella Failla; Serena Belli; John Tolmie; Silvestra Amata; Marco Fichera
Identification of novel mutations in patients with Coffin-Lowry syndrome by a denaturing HPLC-based assay.
Clinical chemistry 2005;51(12):2356-8.
2005: Carmelo Schepis; C Barone; G C Lazzaro Danzuso; Corrado Romano
Alopecia areata in Down syndrome: a clinical evaluation.
Journal of the European Academy of Dermatology and Venereology : JEADV 2005;19(6):769-70.
2005: Lucia Castiglia; Marco Fichera; Corrado Romano; Ornella Galesi; L Grillo; Maurizio Sturnio; Pinella Failla
Narrowing the candidate region for congenital diaphragmatic hernia in chromosome 15q26: contradictory results.
American journal of human genetics 2005;77(5):892-4; author reply 894-5.
2005: Michele Falco; Daniela Luciano; Maurizio Sturnio; Angela Spalletta; Domenico Scionti; Mariangela Lo Giudice; Corrado Romano; Marco Fichera
Denaturing HPLC-based assay for detection of ATRX gene mutations.
Clinical chemistry 2005;51(7):1314-5.
2005: Jean-Louis Guéant; Guido Anello; Paolo Bosco; Rosa-Maria Guéant-Rodríguez; Antonino Romano; Concetta Barone; Philippe Gérard; Corrado Romano
Homocysteine and related genetic polymorphisms in Down's syndrome IQ.
Journal of neurology, neurosurgery, and psychiatry 2005;76(5):706-9.
2005: Carmelo Schepis; D Greco; Maddalena Siragusa; Corrado Romano
Piezogenic pedal papules during Prader-Willi syndrome.
Journal of the European Academy of Dermatology and Venereology : JEADV 2005;19(1):136-7.
2003: Jean-Louis Guéant; Rosa-Maria Guéant-Rodriguez; Guido Anello; Paolo Bosco; laurent brunaud; Corrado Romano; Raffaele Ferri; Antonino Romano; Mirande Candito; Bernard Namour
Genetic determinants of folate and vitamin B12 metabolism: a common pathway in neural tube defect and Down syndrome?
Clinical chemistry and laboratory medicine : CCLM / FESCC 2003;41(11):1473-7.
2003: Paolo Bosco; Rosa-Maria Guéant-Rodriguez; Guido Anello; Concetta Barone; Farès Namour; Filippo Caraci; Antonino Romano; Corrado Romano; Jean-Louis Guéant
Methionine synthase (MTR) 2756 (A --> G) polymorphism, double heterozygosity methionine synthase 2756 AG/methionine synthase reductase (MTRR) 66 AG, and elevated homocysteinemia are three risk factors for having a child with Down syndrome.
American journal of medical genetics. Part A 2003;121A(3):219-24.
2003: Carmelo Schepis; D Greco; Pinella Failla; Maddalena Siragusa; Corrado Romano; M Scaffidi; A Sindoni
Medial telangiectatic sacral nevi and MCA/MR syndromes.
Pediatric dermatology 2003;20(4):370-1.
2003: Martine Raynaud; Sabine Dessay; Nathalie Ronce; John Opitz; Marcus E Pembrey; Corrado Romano; Claude Moraine; Sylvain Briault
Skewed X chromosome inactivation in carriers is not a constant finding in FG syndrome.
European journal of human genetics : EJHG 2003;11(4):352-6.
2002: Marco Fichera; Eugenia Borgione; Emanuela Avola; Silvestra Amata; Maurizio Sturnio; Corrado Romano; Angela Ragusa
A new MRXS locus maps to the X chromosome pericentromeric region: a new syndrome or narrow definition of Sutherland-Haan genetic locus?
Journal of medical genetics 2002;39(4):276-80.
2002: Corrado Romano; Rosa Pettinato; Letizia Ragusa; Concetta Barone; Antonino Alberti; Pinella Failla
Is there a relationship between zinc and the peculiar comorbidities of Down syndrome?
Down's syndrome, research and practice : the journal of the Sarah Duffen Centre / University of Portsmouth 2002;8(1):25-8.
2002: Carmelo Schepis; Concetta Barone; Maddalena Siragusa; Rosa Pettinato; Corrado Romano
An updated survey on skin conditions in Down syndrome.
Dermatology (Basel, Switzerland) 2002;205(3):234-8.
2001: Marco Fichera; M Silengo; Angela Spalletta; Mariangela Lo Giudice; Corrado Romano; Angela Ragusa
Prenatal diagnosis of ATR-X syndrome in a fetus with a new G>T splicing mutation in the XNP/ATR-X gene.
Prenatal diagnosis 2001;21(9):747-51.
2001: Margherita Bonamico; Paolo Mariani; Helene M Danesi; M Crisogianni; P Failla; G Gemme; A R Quartino; A Giannotti; Massimo Castro; Fiorella Balli; M Lecora; generoso andria; Graziella Guariso; Orazio Gabrielli; Carlo Catassi; Rosanna Lazzari; N A Balocco; Stefano De Virgiliis; Franco Culasso; Corrado Romano
Prevalence and clinical picture of celiac disease in italian down syndrome patients: a multicenter study.
Journal of pediatric gastroenterology and nutrition 2001;33(2):139-43.
2001: Guido Anello; Jean-Louis Guéant; Corrado Romano; Concetta Barone; Rosa Pettinato; T Pillot; R Rodriguez; A Romano; Paolo Bosco
Allele varepsilon4 of apolipoprotein E gene is less frequent in Down syndrome patient of the Sicilian population and has no influence on the grade of mental retardation.
Neuroscience letters 2001;306(1-2):129-31.
2001: Rosa Maria Cento; Mario Ciampelli; Caterina Proto; M Le Donne; Corrado Romano; Antonio Lanzone
Neuroendocrine features of pubertal development in females with mental retardation.
Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology 2001;15(3):178-83.
2001: E Rossi; F Piccini; Marcella Zollino; Giovanni Neri; Desiree Caselli; Romano Tenconi; C Castellan; R Carrozzo; Cesare Danesino; Orsetta Zuffardi; Angela Ragusa; Lucia Castiglia; Ornella Galesi; D Greco; Corrado Romano; Mauro Pierluigi; C Perfumo; Maja Di Rocco; Francesca Faravelli; Franca Dagna Bricarelli; Maria Clara Bonaglia; Maria Francesca Bedeschi; Renato Borgatti
Cryptic telomeric rearrangements in subjects with mental retardation associated with dysmorphism and congenital malformations.
Journal of medical genetics 2001;38(6):417-20.
2001: D Greco; Corrado Romano; M Elia
Facial and skeletal malformations, mental retardation, aganglionosis, and neurogenic muscle weakness: a variant of Niikawa-Kuroki syndrome or a new syndrome?
Journal of child neurology 2001;16(4):296-8.
2001: Carmelo Schepis; Pinella Failla; Maddalena Siragusa; Corrado Romano
An additional case of macular phylloid mosaicism.
Dermatology (Basel, Switzerland) 2001;202(1):73.
2001: Carmelo Schepis; D Greco; Maddalena Siragusa; Dario Batolo; Corrado Romano
Rubinstein-Taybi syndrome with epidermal nevus: a case report.
Pediatric dermatology 2001;18(1):34-7.
2001: Eugenia Borgione; Mariangela Lo Giudice; Ornella Galesi; Lucia Castiglia; Pinella Failla; Corrado Romano; Angela Ragusa; Marco Fichera
How microsatellite analysis can be exploited for subtelomeric chromosomal rearrangement analysis in mental retardation.
Journal of medical genetics 2001;38(1):E1.
2000: Angela E Lin; PH Birch; Bruce Korf; Romano Tenconi; Michihito Niimura; M Poyhonen; K Armfield Uhas; M Sigorini; Raffaele Virdis; Corrado Romano; E Bonioli; P Wolkenstein; E K Pivnick; M Lawrence; JM Friedman
Cardiovascular malformations and other cardiovascular abnormalities in neurofibromatosis 1.
American journal of medical genetics 2000;95(2):108-17.
2000: C Barone; Rosa Pettinato; Emanuela Avola; A Alberti; D Greco; Pinella Failla; Corrado Romano
Comparison of three probiotics in the treatment of acute diarrhea in mentally retarded children.
Minerva pediatrica 2000;52(3):161-5.
2000: Maddalena Siragusa; Corrado Romano; N Batticane; Dario Batolo; Carmelo Schepis
A new family with Papillon-Lefèvre syndrome: effectiveness of etretinate treatment.
Cutis; cutaneous medicine for the practitioner 2000;65(3):151-5.
2000: Carmelo Schepis; D Greco; Paolo Bosco; Angela Ragusa; Corrado Romano
Medial telangiectatic sacral nevi (Types A and C) associated with Williams syndrome.
Dermatology (Basel, Switzerland) 2000;201(3):285-6.
1999: S M Pueschel; Corrado Romano; Pinella Failla; C Barone; Rosa Pettinato; A Castellano Chiodo; D L Plumari
A prevalence study of celiac disease in persons with Down syndrome residing in the United States of America.
Acta paediatrica (Oslo, Norway : 1992) 1999;88(9):953-6.
1999: A Alberti; P Pirrone; M Elia; R H Waring; Corrado Romano
Sulphation deficit in "low-functioning" autistic children: a pilot study.
Biological psychiatry 1999;46(3):420-4.
1999: Deborah J Marsh; JB Kum; Kathryn L Lunetta; M J Bennett; RJ Gorlin; S F Ahmed; J Bodurtha; C Crowe; M A Curtis; Majed Dasouki; T Dunn; H Feit; M T Geraghty; J M Graham; Shirley V Hodgson; A Hunter; Bruce Korf; D Manchester; S Miesfeldt; Victoria Murday; Katherine L Nathanson; M Parisi; B Pober; Corrado Romano; Charis Eng
PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome.
Human molecular genetics 1999;8(8):1461-72.
1999: Carmelo Schepis; D Greco; Corrado Romano
Cardiofaciocutaneous (CFC) syndrome.
The Australasian journal of dermatology 1999;40(2):111-3.
1999: Laurent Villard; M C Bonino; fatima abidi; Angela Ragusa; Jérôme Belougne; Anne-Marie Lossi; L Seaver; J P Bonnefont; Corrado Romano; Marco Fichera; D Lacombe; André Hanauer; Nicole Philip; C Schwartz; Michel Fontés
Evaluation of a mutation screening strategy for sporadic cases of ATR-X syndrome.
Journal of medical genetics 1999;36(3):183-6.
1999: Josefina Ramunni; Letizia Ragusa; Emanuela Arvat; Laura Gianotti; B Maccagno; Roberta Giordano; Rosa Pettinato; C Barone; Corrado Romano; Ezio Ghigo
Young adults with Down's syndrome show increased corticotrope responsiveness to hCRH or hexarelin, a peptidyl GH secretagogue.
Journal of endocrinological investigation 1999;22(10 Suppl):57-8.
1999: Carmelo Schepis; A Alberti; Maddalena Siragusa; Corrado Romano
Progressive cribriform and zosteriform hyperpigmentation: the late-onset feature of linear and whorled nevoid hypermelanosis associated with congenital neurological, skeletal and cutaneous anomalies.
Dermatology (Basel, Switzerland) 1999;199(1):72-3.
1999: Corrado Romano; P Pirrone; Maddalena Siragusa; Carmelo Schepis; Vittorio Cavallari
An additional case of linear and whorled nevoid hypermelanosis associated with birth defects and mental retardation.
Pediatric dermatology 1999;16(1):71-3.
1998: Letizia Ragusa; MR Valetto; Caterina Proto; A Alberti; Corrado Romano; A Rossodivita; Ginevra Corneli; Claudia Baffoni; Fabio Lanfranco; Gianluca Aimaretti; F Colabucci; Ezio Ghigo
IGF-I levels in prepubertal and pubertal children with Down syndrome.
Minerva endocrinologica 1998;23(2):31-6.
1998: Carmelo Schepis; D Greco; Maddalena Siragusa; Dario Batolo; Corrado Romano
An intriguing case of LEOPARD syndrome.
Pediatric dermatology 1998;15(2):125-8.
1998: Carmelo Schepis; Pinella Failla; Maddalena Siragusa; R Palazzo; Corrado Romano
Failure of fluoxetine to modify the skin-picking behaviour of Prader-Willi syndrome.
The Australasian journal of dermatology 1998;39(1):57-8.
1998: Marco Fichera; Corrado Romano; Lucia Castiglia; Pinella Failla; C Ruberto; Silvestra Amata; D Greco; Carlos Cardoso; Michel Fontés; Angela Ragusa
New mutations in XNP/ATR-X gene: a further contribution to genotype/phenotype relationship in ATR/X syndrome. Mutations in brief no. 176. Online.
Human mutation 1998;12(3):214.
1997: Sylvain Briault; R Hill; A Shrimpton; D Zhu; M Till; Nathalie Ronce; P Margaritte-Jeannin; M Baraitser; Helen Middleton-Price; Sue Malcolm; E Thompson; J Hoo; G Wilson; Corrado Romano; Agnès Guichet; Marcus E Pembrey; Michel Fontes; A Poustka; Claude Moraine
A gene for FG syndrome maps in the Xq12-q21.31 region.
American journal of medical genetics 1997;73(1):87-90.
1997: Carmelo Schepis; C Barone; Maddalena Siragusa; Corrado Romano
Prevalence of atopic dermatitis in patients with Down syndrome: a clinical survey.
Journal of the American Academy of Dermatology 1997;36(6 Pt 1):1019-21.
1997: Maddalena Siragusa; Corrado Romano; Vittorio Cavallari; Carmelo Schepis
Localized elastosis perforans serpiginosa in a boy with Down syndrome.
Pediatric dermatology 1997;14(3):244-6.
1997: Pinella Failla; Corrado Romano; Carmelo Schepis
Hypomelanosis of Ito: a syndrome requiring a multisystem approach.
The Australasian journal of dermatology 1997;38(2):65-70.
1996: Maurizio Elia; Sebastiano A Musumeci; Raffaele Ferri; D Greco; Corrado Romano; S Del Gracco; M C Stefanini
Saethre-Chotzen syndrome: a clinical, EEG and neuroradiological study.
Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery 1996;12(11):699-704.
1996: Pinella Failla; C Ruberto; M C Pagano; M Lombardo; G Bottaro; Bruno Perichon; Rajagopal Krishnamoorthy; Corrado Romano; Angela Ragusa
Celiac disease in Down's syndrome with HLA serological and molecular studies.
Journal of pediatric gastroenterology and nutrition 1996;23(3):303-6.
1996: Carmelo Schepis; Corrado Romano
Cutaneous findings in the mentally retarded.
International journal of dermatology 1996;35(5):317-22.
1996: Rosa Maria Cento; Letizia Ragusa; Caterina Proto; A Alberti; Corrado Romano; Gustavo Boemi; F Colabucci; Antonio Lanzone
Basal body temperature curves and endocrine pattern of menstrual cycles in Down syndrome.
Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology 1996;10(2):133-7.
1996: Carmelo Schepis; D Greco; Maddalena Siragusa; Corrado Romano
What syndrome is this? Lesch-Nyhan syndrome.
Pediatric dermatology 1996;13(2):169-70.
1996: Carmelo Schepis; Maddalena Siragusa; R Palazzo; Dario Batolo; Corrado Romano
Milia-like idiopathic calcinosis cutis: an unusual dermatosis associated with Down syndrome.
The British journal of dermatology 1996;134(1):143-6.
1995: M Elia; R Di Lello; Corrado Romano; Carmelo Schepis
A case of FG syndrome with gingival hyperplasia and keloids.
Pediatric dermatology 1995;12(4):387-9.
1995: Sebastiano A Musumeci; Maurizio Elia; Raffaele Ferri; Corrado Romano; C Scuderi; S Del Gracco
A further family with epilepsy, dementia and yellow teeth: the Kohlschütter syndrome.
Brain & development 1995;17(2):133-8; discussion 142-3.
1994: Carmelo Schepis; Pinella Failla; Maddalena Siragusa; Corrado Romano
Skin-picking: the best cutaneous feature in the recognization of Prader-Willi syndrome.
International journal of dermatology 1994;33(12):866-7.
1994: Carmelo Schepis; Maddalena Siragusa; R Palazzo; Dario Batolo; Corrado Romano
Perforating milia-like idiopathic calcinosis cutis and periorbital syringomas in a girl with Down syndrome.
Pediatric dermatology 1994;11(3):258-60.
1994: Corrado Romano; M Baraitser; E Thompson
A clinical follow-up of British patients with FG syndrome.
Clinical dysmorphology 1994;3(2):104-14.
1992: Letizia Ragusa; Corrado Romano; P Failla; Caterina Proto; F Colabucci
Growth hormone subnormality in Down syndrome.
American journal of medical genetics 1992;43(5):894-5.
1991: Corrado Romano; R M Ragusa; F Scillato; D Greco; G Amato; C Barletta
Phenotypic and phoniatric findings in mosaic cri du chat syndrome.
American journal of medical genetics 1991;39(4):391-5.
1991: Valentino Romano; G Mascali; V Chiavetta; R M Ragusa; C Barletta; Corrado Romano; F Mollica; T Mattina; A Gross; W Ted Brown
RFLP analysis in 5 Sicilian families with the fragile X syndrome.
American journal of medical genetics 1991;38(2-3):347-8.
1990: N Batticane; Maria Concetta Morale; Corrado Romano; N Cutuli; Bianca Marchetti
Brain dysfunction and the immune system: lymphocyte's beta-adrenergic receptor in Down syndrome.
Pharmacological research : the official journal of the Italian Pharmacological Society 1990;22 Suppl 1():49-50.
1990: Salvatore Leonardi; Salvatore Musumeci; A Sciacca; D Greco; Corrado Romano
Reliability of intradermal vaccination against hepatitis B for accelerated prophylaxis.
The Pediatric infectious disease journal 1990;9(7):520.
1990: Corrado Romano; A Tiné; G Fazio; Renata Rizzo; R M Colognola; Giovanni Sorge; P Bergonzi; Lorenzo Pavone
Seizures in patients with trisomy 21.
American journal of medical genetics. Supplement 1990;7():298-300.
1988: M Filippello; G Scimone; P Morello; G Cuccia; G Ventimiglia; Corrado Romano
[Study of stereopsis using the Lang and Titmus stereo-tests to assess the presence of changes in binocular vision of children with mental retardation].
Minerva pediatrica 1988;40(8):473-6.
1988: Giovanni Neri; S Sanfilippo; L Pavone; F Mollica; I Barberi; L Giuffrè; Corrado Romano; T Mattina; M Cammarata; M G Ragusa
The fragile X in Sicily: an epidemiological survey.
American journal of medical genetics 1988;30(1-2):665-72.
1988: G Milone; L Conti; Renata Rizzo; Santo Sanfilippo; V Sammito; Corrado Romano
A dermatoglyphic study of a group of Sicilian children with fragile-X syndrome.
American journal of medical genetics 1988;30(1-2):177-83.
1988: G Neri; V Sammito; Corrado Romano; Santo Sanfilippo; J M Opitz
Facial midline defect in the fetal alcohol syndrome: embryogenetic considerations in two clinical cases.
American journal of medical genetics 1988;29(3):477-82.
1988: Salvatore Musumeci; A D'Agata; Corrado Romano; R Patané; D Cutrona
Ichthyosis and neutral lipid storage disease.
American journal of medical genetics 1988;29(2):377-82.