Genuardi, E: search on Z-Library

The world's largest scientific articles store. 70,000,000+ articles for free.

Don't use scam websites

51

Polymorphisms of the prion protein gene in Italian patients with Creutzfeldt-Jakob disease

Mirella Salvatore, Maurizio Genuardi, Rosella Petraroli, Carlo Masullo, Marco D'Alessandro, Maurizio Pocchiari

Journal:

Year:

1994

Language:

english

File:

PDF, 593 KB

english, 1994

52

Double autosomal/gonosomal mosaic aneuploidy: study of nondisjunction in two cases with trisomy of chromosome 8

Daniele DeBrasi, Maurizio Genuardi, Antonio D'Agostino, Fabrizio Calvieri, Carla Tozzi, Stelio Varrone, Giovanni Neri

Journal:

Year:

1995

Language:

english

File:

PDF, 647 KB

english, 1995

53

Polymorphisms of the Prion Protein gene in italian patients with Creutzfeldt-Jakob disease

Mirella Salvatore, Maurizio Genuardi, Rosella Petraroli, Carlo Masullo, Marc D'Alessandro, Maurizio Pocchiari

Journal:

Year:

1995

Language:

english

File:

PDF, 31 KB

english, 1995

54

Localization of the HLA class 11-associated invariant chain gene to human chromosome band 5832

Maurizio Genuardi, Grady F. Saunders

Journal:

Year:

1988

Language:

english

File:

PDF, 344 KB

english, 1988

55

Partial tetrasomy 9 in an infant with clinical and radiological evidence of multiple joint dislocations

F. Calvieri, C. Tozzi, C. Benincori, M. V. Merulis, A. Bellussi, M. Genuardi, G. Neri

Journal:

European Journal of Pediatrics

Year:

1988

Language:

english

File:

PDF, 1.33 MB

english, 1988

56

National spending on mental health and substance abuse treatment by age of clients, 1997

Tami L. Mark, Henrick J. Harwood, David R. McKusick, Rosanna M. Coffey, Edward C. King, James S. Genuardi

Journal:

The Journal of Behavioral Health Services and Research

Year:

2003

Language:

english

File:

PDF, 845 KB

english, 2003

57

Characterization ofMLH1andMSH2alternative splicing and its relevance to molecular testing of colorectal cancer susceptibility

Maurizio Genuardi, Alessandra Viel, Daniela Bonora, Eugenia Capozzi, Alfonso Bellacosa, Francesca Leonardi, Roberta Valle, Andrea Ventura, Monica Pedroni, Mauro Boiocchi, G. Neri

Journal:

Year:

1998

Language:

english

File:

PDF, 114 KB

english, 1998

58

Inner ear abnormalities in four patients with dRTA and SNHL: clinical and genetic heterogeneity

Elena Andreucci, Benedetta Bianchi, Ilaria Carboni, Giancarlo Lavoratti, Marzia Mortilla, Claudio Fonda, Minna Bigozzi, Maurizio Genuardi, Sabrina Giglio, Ivana Pela

Journal:

Pediatric Nephrology

Year:

2009

Language:

english

File:

PDF, 211 KB

english, 2009

59

Schwannomatosis associated with multiple meningiomas due to a familialSMARCB1mutation

Costanza Bacci, Roberta Sestini, Aldesia Provenzano, Irene Paganini, Irene Mancini, Berardino Porfirio, Rossella Vivarelli, Maurizio Genuardi, Laura Papi

Journal:

Year:

2010

Language:

english

File:

PDF, 313 KB

english, 2010

60

Identification and Classification of Hereditary Nonpolyposis Colorectal Cancer (Lynch Syndrome): Adapting Old Concepts to Recent Advancements. Report from the Italian Association for the Study of Hereditary Colorectal Tumors Consensus Group

Maurizio Ponz de Leon, Lucio Bertario, Maurizio Genuardi, Giovanni Lanza, Cristina Oliani, Guglielmina Nadia Ranzani, Giovanni Battista Rossi, Liliana Varesco, Tiziana Venesio, Alessandra Viel

Journal:

Diseases of the Colon & Rectum

Year:

2007

Language:

english

File:

PDF, 268 KB

english, 2007

61

APALB2germline mutation associated with hereditary breast cancer in Italy

Laura Papi, Anna Laura Putignano, Caterina Congregati, Irene Piaceri, Ines Zanna, Francesco Sera, Doralba Morrone, Maurizio Genuardi, Domenico Palli

Journal:

Familial Cancer

Year:

2010

Language:

english

File:

PDF, 176 KB

english, 2010

62

Efficacy of a combination of human recombinant erythropoietin + 13-cis-retinoic acid and dihydroxylated vitamin D3 to improve moderate to severe anaemia in low/intermediate risk myelodysplastic syndromes

Dario Ferrero, Antonella Darbesio, Valentina Giai, Mariella Genuardi, Chiara Maria Dellacasa, Roberto Sorasio, Marilena Bertini, Mario Boccadoro

Journal:

British Journal of Haematology

Year:

2009

Language:

english

File:

PDF, 127 KB

english, 2009

63

Thyroid function and morphology in subjects with microdeletion of chromosome 22q11 (del(22)(q11))

Stefano Stagi, Elisabetta Lapi, Eleonora Gambineri, Roberto Salti, Maurizio Genuardi, Gloria Colarusso, Camilla Conti, Rita Jenuso, Francesco Chiarelli, Chiara Azzari, Maurizio De Martino

Journal:

Clinical Endocrinology

Year:

2010

Language:

english

File:

PDF, 161 KB

english, 2010

64

A novel microdeletion syndrome with loss of the MSH2 locus and hereditary non-polyposis colorectal cancer

E Lucci-Cordisco, M Zollino, S Baglioni, I Mancuso, R Lecce, F Gurrieri, A Crucitti, L Papi, G Neri, M Genuardi

Journal:

Clinical Genetics

Year:

2005

Language:

english

File:

PDF, 953 KB

english, 2005

65

A genetic model for determining MSH2 and MLH1 carrier probabilities based on family history and tumor microsatellite instability

F Marroni, C Pastrello, P Benatti, M Torrini, D Barana, EL Cordisco, A Viel, C Mareni, C Oliani, M Genuardi, JE Bailey-Wilson, M Ponz de Leon, S Presciuttini

Journal:

Clinical Genetics

Year:

2006

Language:

english

File:

PDF, 138 KB

english, 2006

66

Frequency of constitutional MSH6 mutations in a consecutive series of families with clinical suspicion of HNPCC

B Roncari, M Pedroni, S Maffei, C Di Gregorio, G Ponti, A Scarselli, L Losi, P Benatti, L Roncucci, C De Gaetani, L Camellini, E Lucci-Cordisco, R Tricarico, M Genuardi, M Ponz de Leon

Journal:

Clinical Genetics

Year:

2007

Language:

english

File:

PDF, 308 KB

english, 2007

67

Constitutional FLCN mutations in patients with suspected Birt–Hogg–Dubé syndrome ascertained for non-cutaneous manifestations

A Maffé, B Toschi, G Circo, D Giachino, S Giglio, A Rizzo, A Carloni, V Poletti, S Tomassetti, C Ginardi, S Ungari, M Genuardi

Journal:

Clinical Genetics

Year:

2011

Language:

english

File:

PDF, 600 KB

english, 2011

68

Fatal Malonyl CoA Decarboxylase Deficiency Due to Maternal Uniparental Isodisomy of the Telomeric End of Chromosome 16

S. Malvagia, L. Papi, A. Morrone, M. A. Donati, F. Ciani, E. Pasquini, G. La Marca, H. R. Scholte, M. Genuardi, E. Zammarchi

Journal:

Annals of Human Genetics

Year:

2007

Language:

english

File:

PDF, 186 KB

english, 2007

69

Microsatellite instability is not related to response to cisplatin-based chemotherapy in cervical cancer

A. Ercoli, G. Ferrandina, M. Genuardi, G.F. Zannoni, L. Cicchillitti, G. Raspaglio, S. Carrara, S. Mancuso, G. Scambia

Journal:

International Journal of Gynecological Cancer

Year:

2005

Language:

english

File:

PDF, 129 KB

english, 2005

70

A Single Mutation in the FGA Locus Responsible for False Homozygosities and Discrepancies Between Commercial Kits in an Unusual Paternity Test Case

Ugo Ricci, German Melean, Carlo Robino, Maurizio Genuardi

Journal:

Journal of Forensic Sciences

Year:

2007

Language:

english

File:

PDF, 272 KB

english, 2007

71

10.1038/15443

Bellacosa, Alfonso, Riccio, Antonio, Aaltonen, Lauri A., Godwin, Andrew K., Loukola, Anu, Percesepe, Antonio, Salovaara, Reijo, Masciullo, Valeria, Genuardi, Maurizio, Paravatou-Petsotas, Maria, Bassi

Journal:

Nature Genetics

Year:

1999

Language:

english

File:

PDF, 232 KB

english, 1999

72

Telomere length is an independent predictor of survival, treatment requirement and Richter's syndrome transformation in chronic lymphocytic leukemia

Rossi, D, Lobetti Bodoni, C, Genuardi, E, Monitillo, L, Drandi, D, Cerri, M, Deambrogi, C, Ricca, I, Rocci, A, Ferrero, S

Journal:

Year:

2009

Language:

english

File:

PDF, 406 KB

english, 2009

73

Lenalidomide, melphalan, prednisone and thalidomide (RMPT) for relapsed/refractory multiple myeloma

Larocca, A, Falco, P, Sanpaolo, G, Falcone, A P, Federico, V, Canepa, L, Crugnola, M, Genuardi, M, Magarotto, V, Palumbo, A

Journal:

Year:

2010

Language:

english

File:

PDF, 307 KB

english, 2010

74

Genetic testing among high-risk individuals in families with hereditary nonpolyposis colorectal cancer

Ponz de Leon, M, Benatti, P, Di Gregorio, C, Pedroni, M, Losi, L, Genuardi, M, Viel, A, Fornasarig, M, Lucci-Cordisco, E, Anti, M

Journal:

British Journal of Cancer

Year:

2004

Language:

english

File:

PDF, 103 KB

english, 2004

75

Mosaic trisomy 17 in amniocytes: phenotypic outcome, tissue distribution, and uniparental disomy studies

Genuardi, Maurizio, Tozzi, Carla, Pomponi, Maria Grazia, Stagni, Maria Letizia, Della Monica, Matteo, Scarano, Gioacchino, Calvieri, Fabrizio, Torrisi, Loredana, Neri, Giovanni

Journal:

European Journal of Human Genetics

Year:

1999

Language:

english

File:

PDF, 232 KB

english, 1999

76

Assessment of pathogenicity criteria for constitutional missense mutations of the hereditary nonpolyposis colorectal cancer genes MLH1 and MSH2

Genuardi, Maurizio, Carrara, Stefania, Anti, Marcello, Ponz de Leòn, Maurizio, Viel, Alessandra

Journal:

European Journal of Human Genetics

Year:

1999

Language:

english

File:

PDF, 157 KB

english, 1999

77

Stability of BAT26 in tumours of hereditary nonpolyposis colorectal cancer patients with MSH2 intragenic deletion

Pastrello, Chiara, Baglioni, Silvana, Tibiletti, Maria Grazia, Papi, Laura, Fornasarig, Mara, Morabito, Alberto, Agostini, Marco, Genuardi, Maurizio, Viel, Alessandra

Journal:

European Journal of Human Genetics

Year:

2005

Language:

english

File:

PDF, 173 KB

english, 2005

78

Reply to Jaskowski et al

Pastrello, Chiara, Tricarico, Rossella, Tibiletti, Maria Grazia, Papi, Laura, Fornasarig, Mara, Morabito, Alberto, Agostini, Marco, Genuardi, Maurizio, Viel, Alessandra

Journal:

European Journal of Human Genetics

Year:

2006

Language:

english

File:

PDF, 53 KB

english, 2006

79

Susceptibility to refractory ulcerative colitis is associated with polymorphism in the hMLH1 mismatch repair gene

Siro Bagnoli, Anna Laura Putignano, German Melean, Silvana Baglioni, Roberta Sestini, Monica Milla, Giuseppe d'Albasio, Maurizio Genuardi, Franco Pacini, Giacomo Trallori, Laura Papi

Journal:

Inflammatory Bowel Diseases

Year:

2004

Language:

english

File:

PDF, 67 KB

english, 2004

80

BRCA1-Related Malignancies in a Family Presenting with von Recklinghausen's Disease

Marcello Ceccaroni, Maurizio Genuardi, Francesco Legge, Emanuela Lucci-Cordisco, Stefania Carrara, Franca D'Amico, Stefano Greggi, Giovanni Scambia

Journal:

Gynecologic Oncology

Year:

2002

Language:

english

File:

PDF, 58 KB

english, 2002

81

Chronic myelogenous leukemia in the course of chronic lymphocytic leukemia: Evidence for an independent clonal origin

Marcella Zollino, Maurizio Genuardi, Paola Tanci, Giorgio Mango, Carlo Rumi, Rosalba Mancini, Giovanni Neri

Journal:

Leukemia Research

Year:

1991

Language:

english

File:

PDF, 1.81 MB

english, 1991

82

Constitutional trisomy 8 and myelodysplasia: Report of a case and review of the literature

M. Zollino, M. Genuardi, J. Bajer, A. Tornesello, S. Mastrangelo, G. Zampino, R. Mastrangelo, G. Neri

Journal:

Leukemia Research

Year:

1995

Language:

english

File:

PDF, 318 KB

english, 1995

83

First report of t(8;21)(q22;q22) in a case of de novo acute monoblastic leukemia

M. Christina Cox-Froncillo, Maurizio Genuardi, Jolanta Bajer, Esther Livdi, Gaspare Adorno, Adriano Venditti, Mario Masi, Paolo Giudiceandrea, Giovanni Neri, Giuseppe Papa

Journal:

Cancer Genetics and Cytogenetics

Year:

1995

Language:

english

File:

PDF, 219 KB

english, 1995

84

Machine-aided indexing at NASA

June P. Silvester, Michael T. Genuardi, Paul H. Klingbiel

Journal:

Information Processing & Management

Year:

1994

Language:

english

File:

PDF, 1.22 MB

english, 1994

85

Germline mutations in MEN1 and BRCA1 genes in a woman with familial multiple endocrine neoplasia type 1 and inherited breast–ovarian cancer syndromes: a case report

Laura Papi, Domenico Palli, Laura Masi, Anna Laura Putignano, Caterina Congregati, Ines Zanna, Francesca Marini, Francesca Giusti, Ettore Luzi, Francesco Tonelli, Maurizio Genuardi, Maria Luisa Brandi

Journal:

Cancer Genetics and Cytogenetics

Year:

2009

Language:

english

File:

PDF, 123 KB

english, 2009

86

Partial duplication of chromosome 1q preceding the development of an L3 lymphoblastic leukemia with t(8;14), secondary to treatment for Hodgkin's disease

M. Zollino, M. Genuardi, R. De Santis, G. Leone, R. Marra, R. Mancini, G. Mango, G. Neri

Journal:

European Journal of Haematology

Year:

1988

Language:

english

File:

PDF, 1010 KB

english, 1988

87

High resolution melting analysis for a rapid identification of heterozygous and homozygous sequence changes in theMUTYHgene

Rossella Tricarico, Francesca Crucianelli, Antonio Alvau, Claudio Orlando, Roberta Sestini, Francesco Tonelli, Rosa Valanzano, Maurizio Genuardi

Journal:

Year:

2011

Language:

english

File:

PDF, 945 KB

english, 2011

88

Brachy/ectrodactyly and absence or hypoplasia of the fibula: an autosomal dominant condition with low penetrance and variable expressivity

M. Genuardi, M. Zollino, A. Bellussi, W. Fuhrmann, G. Neri

Journal:

Clinical Genetics

Year:

1990

Language:

english

File:

PDF, 601 KB

english, 1990

89

Dosage analysis at the CSF1 and CSF1R loci in a new case of partial trisomy 5q

M. Genuardi, R. Flamia, G. Palka, G. Parruti, G. Nsri

Journal:

Clinical Genetics

Year:

1992

Language:

english

File:

PDF, 383 KB

english, 1992

90

Dicentric chromosome Y associated with Leydig cell agenesis and sex reversal

Maurizio Genuardi, Barbara Bardoni, Giovanna Floridia, Pietro Chiurazzi, Gioacchino Scarano, Marcella Zollino, Nicola Garcea, Maria Enrica Martini-Neri, Giovanni Neri

Journal:

Clinical Genetics

Year:

1995

Language:

english

File:

PDF, 811 KB

english, 1995

91

Sexual contact tracing outcome in adolescent chlamydial and gonococcal cervicitis cases

M. Kim Oh, John R. Boker, Frank J. Genuardi, Gretchen A. Cloud, Julia Reynolds, J. Bart Hodgens

Journal:

Journal of Adolescent Health

Year:

1996

Language:

english

File:

PDF, 494 KB

english, 1996

92

Beliefs of third-year medical students regarding adolescent medicine

Frank J. Genuardi, Marsha S. Sturdevant

Journal:

Journal of Adolescent Health

Year:

1996

Language:

english

File:

PDF, 143 KB

english, 1996

93

A proteomics approach to identify changes in protein profiles in serum of Familial Adenomatous Polyposis patients

Barbara Quaresima, Telma Crugliano, Marco Gaspari, Maria Concetta Faniello, Paola Cosimo, Rosa Valanzano, Maurizio Genuardi, Mario Cannataro, Pierangelo Veltri, Francesco Baudi, Patrizia Doldo, Giovan

Journal:

Year:

2008

Language:

english

File:

PDF, 631 KB

english, 2008

94

Endometrial cancer and somatic G>T KRAS transversion in patients with constitutional MUTYH biallelic mutations

Rossella Tricarico, Paola Bet, Benedetta Ciambotti, Carmela Di Gregorio, Beatrice Gatteschi, Viviana Gismondi, Benedetta Toschi, Francesco Tonelli, Liliana Varesco, Maurizio Genuardi

Journal:

Year:

2009

Language:

english

File:

PDF, 160 KB

english, 2009

95

Introduction of the DNase in forensic analysis

G. Melean, U. Ricci, M. Genuardi

Journal:

International Congress Series

Year:

2006

Language:

english

File:

PDF, 85 KB

english, 2006

96

Lone and secondary nonvalvular atrial fibrillation: Role of a genetic susceptibility

Cinzia Fatini, Elena Sticchi, Francesca Gensini, Anna Maria Gori, Rossella Marcucci, Meri Lenti, Antonio Michelucci, Maurizio Genuardi, Rosanna Abbate, Gian Franco Gensini

Journal:

International Journal of Cardiology

Year:

2007

Language:

english

File:

PDF, 138 KB

english, 2007

97

Erratum to “Effects of dexamethasone on the growth and epidermal growth factor receptor expression of the OVCA 433 ovarian cancer cells” [Mol. Cell. Endocrinol. 83 (1992) 183–193]

G. Ferrandina, G. Scambia, P. Benedetti Panici, G. Bonanno, R. De Vincenzo, C. Rumi, S. Bussa, M. Genuardi, V. Romano Spica, S. Mancuso

Journal:

Molecular and Cellular Endocrinology

Year:

2006

Language:

english

File:

PDF, 45 KB

english, 2006

98

Morquio A syndrome due to Maternal Uniparental Isodisomy of the telomeric end of chromosome 16

S. Catarzi, L. Giunti, F. Papadia, O. Gabrielli, R. Guerrini, M.A. Donati, M. Genuardi, A. Morrone

Journal:

Molecular Genetics and Metabolism

Year:

2012

Language:

english

File:

PDF, 435 KB

english, 2012

99

Adolescent medicine faculty development needs

Frank J Genuardi, Elisa A Zenni

Journal:

Journal of Adolescent Health

Year:

2001

Language:

english

File:

PDF, 189 KB

english, 2001

100

Genetic STRs variation in a large population from Tuscany (Italy)

Ilaria Carboni, Anna Lucia Nutini, Berardino Porfirio, Maurizio Genuardi, Ugo Ricci

Journal:

Forensic Science International: Genetics

Year:

2007

Language:

english

File:

PDF, 92 KB

english, 2007

To build up a library is to create a life. It’s never just a random collection of books.

— Carlos María Domínguez

Official channel

Z-Library Desktop Launcher

Z-Library Since 2009 support@z-lib.do

EnglishРусскийEspañolItalianoελληνικάاللغة العربيةBahasa IndonesiaBahasa Malaysiaहिन्दीDeutschFrançaisPortuguêsУкраїнськаPolski中文繁體中文日本語Tiếng ViệtAzərbaycan DiliՀայոց լեզուภาษาไทยTürk Diliქართველიবাংলাپښتوతెలుగుاردو한국어SrpskiБългарски