Výsledky vyhledávání - Maurizio Clementi

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  1. 1
    Using observational cohort data for studying drug effects on pregnancy outcome—Methodological considerations

    Using observational cohort data for studying drug effects on pregnancy outcome—Methodological considerations Autor Christof Schaefer, Asher Ornoy, Maurizio Clementi, Reinhard Meister, Corinna Weber‐Schoendorfer

    Vydáno 2008
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  2. 2
    First-trimester exposure to metformin and risk of birth defects: a systematic review and meta-analysis

    First-trimester exposure to metformin and risk of birth defects: a systematic review and meta-analysis Autor Matteo Cassina, Marta Donà, Elena Di Gianantonio, Pietro Litta, Maurizio Clementi

    Vydáno 2014
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  3. 3
    Treatment of Hyperthyroidism in Pregnancy and Birth Defects

    Treatment of Hyperthyroidism in Pregnancy and Birth Defects Autor Maurizio Clementi, Elena Di Gianantonio, Matteo Cassina, Emanuele Leoncini, Lorenzo D. Botto, Pierpaolo Mastroiacovo

    Vydáno 2010
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  4. 4
    Optical Coherence Tomography in the Diagnosis of Optic Pathway Gliomas

    Optical Coherence Tomography in the Diagnosis of Optic Pathway Gliomas Autor Raffaele Parrozzani, Maurizio Clementi, Olympia Kotsafti, Giacomo Miglionico, Eva Trevisson, Gloria Orlando, Elisabetta Pilotto, Edoardo Midena

    Vydáno 2013
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  5. 5
    Comorbidity between headache and epilepsy in a pediatric headache center

    Comorbidity between headache and epilepsy in a pediatric headache center Autor Irene Toldo, Egle Perissinotto, Francesca Menegazzo, Clementina Boniver, Stefano Sartori, Leonardo Salviati, Maurizio Clementi, Pasquale Montagna, Pier Antonio Battistella

    Vydáno 2010
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  6. 6
    Optic Pathway Glioma in Type 1 Neurofibromatosis: Review of Its Pathogenesis, Diagnostic Assessment, and Treatment Recommendations

    Optic Pathway Glioma in Type 1 Neurofibromatosis: Review of Its Pathogenesis, Diagnostic Assessment, and Treatment Recommendations Autor Matteo Cassina, Luisa Frizziero, Enrico Opocher, Raffaele Parrozzani, Ugo Sorrentino, Elisabetta Viscardi, Giacomo Miglionico, Edoardo Midena, Maurizio Clementi, Eva Trevisson

    Vydáno 2019
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  7. 7
    NF1 Microdeletion Syndrome: Refined FISH Characterization of Sporadic and Familial Deletions with Locus-Specific Probes

    NF1 Microdeletion Syndrome: Refined FISH Characterization of Sporadic and Familial Deletions with Locus-Specific Probes Autor Paola Riva, Lucia Corrado, Federica Natacci, Pierangela Castorina, Bai-Li Wu, Gretchen Schneider, Maurizio Clementi, Romano Tenconi, Bruce R. Korf, Lidia Larizza

    Vydáno 2000
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  8. 8
    Mental retardation and cardiovascular malformations in NF1 microdeleted patients point to candidate genes in 17q11.2

    Mental retardation and cardiovascular malformations in NF1 microdeleted patients point to candidate genes in 17q11.2 Autor Marco Venturin, Paolo Guarnieri, Federica Natacci, M Stabile, Romano Tenconi, Maurizio Clementi, Carmen Hernández, Peter Thompson, Meena Upadhyaya, Lidia Larizza, Paola Riva

    Vydáno 2004
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  9. 9
    Paroxetine and fluoxetine in pregnancy: a prospective, multicentre, controlled, observational study

    Paroxetine and fluoxetine in pregnancy: a prospective, multicentre, controlled, observational study Autor Orna Diav‐Citrin, Svetlana Shechtman, Dafna Weinbaum, Rebecka Wajnberg, Meytal Avgil, Elena Di Gianantonio, Maurizio Clementi, Corinna Weber‐Schoendorfer, Christof Schaefer, Asher Ornoy

    Vydáno 2008
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  10. 10
    Catechol-O-methyltransferase genotype modifies executive functioning and prefrontal functional connectivity in women with anorexia nervosa

    Catechol-O-methyltransferase genotype modifies executive functioning and prefrontal functional connectivity in women with anorexia nervosa Autor Angela Favaro, Maurizio Clementi, Renzo Manara, Romina Bosello, Monica Forzan, Alice Bruson, Elena Tenconi, Daniela Degortes, Francesca Titton, Francesco Di Salle, Paolo Santonastaso

    Vydáno 2013
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  11. 11
    Searching for Psoriasis Susceptibility Genes in Italy: Genome Scan and Evidence for a New Locus on Chromosome 1

    Searching for Psoriasis Susceptibility Genes in Italy: Genome Scan and Evidence for a New Locus on Chromosome 1 Autor Francesca Capon, Giuseppe Novelli, Sabrina Semprini, Maurizio Clementi, Maurizio Nudo, P Vultaggio, Chiara Maria Mazzanti, Tommaso Gobello, Annalisa Botta, Giuseppe Fabrizi, Bruno Dallapiccola

    Vydáno 1999
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  12. 12
    In Vivo Detection of Choroidal Abnormalities Related to NF1: Feasibility and Comparison With Standard NIH Diagnostic Criteria in Pediatric Patients

    In Vivo Detection of Choroidal Abnormalities Related to NF1: Feasibility and Comparison With Standard NIH Diagnostic Criteria in Pediatric Patients Autor Raffaele Parrozzani, Maurizio Clementi, Luisa Frizziero, Giacomo Miglionico, Pierdavide Perrini, Fabiano Cavarzeran, Olympia Kotsafti, Francesco Comacchio, Eva Trevisson, Enrica Convento, Stefano Fusetti, Edoardo Midena

    Vydáno 2015
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  13. 13
    Adverse effects of prenatal methimazole exposure

    Adverse effects of prenatal methimazole exposure Autor Elena Di Gianantonio, Christof Schaefer, P Mastroiacovo, Maxime Cournot, Francesco Benedicenti, Minke Reuvers, Brunella Occupati, Elisabeth Robert, B Bellemin, Antonio Addis, Judy Arnon, Maurizio Clementi

    Vydáno 2001
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  14. 14
    Visual outcome of a cohort of children with neurofibromatosis type 1 and optic pathway glioma followed by a pediatric neuro-oncology program

    Visual outcome of a cohort of children with neurofibromatosis type 1 and optic pathway glioma followed by a pediatric neuro-oncology program Autor Paola Dalla Via, Enrico Opocher, Maria Luisa Pinello, Milena Calderone, Elisabetta Viscardi, Maurizio Clementi, Pier Antonio Battistella, Anna Maria Laverda, Liviana Da Dalt, Giorgio Perilongo

    Vydáno 2007
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  15. 15
    Advances in Alport syndrome diagnosis using next-generation sequencing

    Advances in Alport syndrome diagnosis using next-generation sequencing Autor Rosangela Artuso, Chiara Fallerini, Laura Dosa, Francesca Scionti, Maurizio Clementi, Guido Garosi, Laura Massella, Maria Carmela Epistolato, Roberta Mancini, Francesca Mari, Ilaria Longo, Francesca Ariani, Alessandra Renieri, Mirella Bruttini

    Vydáno 2011
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  16. 16
    Breast cancer in neurofibromatosis 1: survival and risk of contralateral breast cancer in a five country cohort study

    Breast cancer in neurofibromatosis 1: survival and risk of contralateral breast cancer in a five country cohort study Autor D. Gareth Evans, Roope A. Kallionpää, Maurizio Clementi, Eva Trevisson, Victor-Felix Mautner, Sacha J. Howell, Lauren Lewis, O. Zehou, Sirkku Peltonen, Antonella Brunello, Elaine F. Harkness, P. Wolkenstein, Juha Peltonen

    Vydáno 2019
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  17. 17
    Genetic analysis in Italian families with inflammatory bowel disease supports linkage to the IBD1 locus – A GISC study

    Genetic analysis in Italian families with inflammatory bowel disease supports linkage to the IBD1 locus – A GISC study Autor Vito Annese, Anna Latiano, P. Bovio, Paola Forabosco, Ada Piepoli, Giovanni Lombardi, Arnaldo Andreoli, Marco Astegiano, Paolo Gionchetti, Gabriele Riegler, G Sturniolo, Maurizio Clementi, Eric Rappaport, Paolo Fortina, Marcella Devoto, Paolo Gasparini, Angelo Andriulli

    Vydáno 1999
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  18. 18
    Primary coenzyme Q10 deficiency presenting as fatal neonatal multiorgan failure

    Primary coenzyme Q10 deficiency presenting as fatal neonatal multiorgan failure Autor María Andrea Desbats, Annalisa Vetro, Ivan Limongelli, G. Lunardi, Alberto Casarin, Mara Doimo, Marco Spinazzi, C. Angelini, Giovanna Cenacchi, Alberto Burlina, María Hernández, Lino Chiandetti, Maurizio Clementi, Eva Trevisson, Plácido Navas, Orsetta Zuffardi, Leonardo Salviati

    Vydáno 2015
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  19. 19
    Catechol‐<i>O</i>‐Methyltransferase (COMT) Val158Met Polymorphism and Eating Disorders: Data From a New Biobank and Meta‐Analysis of Previously Published Studies

    Catechol‐<i>O</i>‐Methyltransferase (COMT) Val158Met Polymorphism and Eating Disorders: Data From a New Biobank and Meta‐Analysis of Previously Published Studies Autor Enrico Collantoni, Marco Solmi, Davide Gallicchio, Paolo Santonastaso, Paolo Meneguzzo, André F. Carvalho, Brendon Stubbs, Maurizio Clementi, Claudia Pinato, Monica Forzan, Matteo Cassina, Francesca Fontana, I. Piva, Roberta Siani, Pierandrea Salvo, Elena Tenconi, Nicola Veronese, Christoph U. Correll, Angela Favaro

    Vydáno 2017
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  20. 20
    p.Arg1809Cys substitution in neurofibromin is associated with a distinctive NF1 phenotype without neurofibromas

    p.Arg1809Cys substitution in neurofibromin is associated with a distinctive NF1 phenotype without neurofibromas Autor Valentina Pinna, Valentina Lanari, Paola Daniele, Federica Consoli, Emanuele Agolini, Katia Margiotti, Irene Bottillo, Isabella Torrente, Alessandro Bruselles, Caterina Fusilli, Anna Ficcadenti, Sara Bargiacchi, Eva Trevisson, Monica Forzan, Sandra Giustini, Chiara Leoni, Giuseppe Zampino, M. Cristina Digilio, Bruno Dallapiccola, Maurizio Clementi, Marco Tartaglia, Alessandro De Luca

    Vydáno 2014
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