खोज परिणाम - Maurizio Clementi

परिणाम को परिष्कृत करें
  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 द्वारा Christof Schaefer, Asher Ornoy, Maurizio Clementi, Reinhard Meister, Corinna Weber‐Schoendorfer

    प्रकाशित 2008
    पूर्ण पाठ प्राप्त करें
    Artigo
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    में बचाया:
  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 द्वारा Matteo Cassina, Marta Donà, Elena Di Gianantonio, Pietro Litta, Maurizio Clementi

    प्रकाशित 2014
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Revisão
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    में बचाया:
  3. 3
    Treatment of Hyperthyroidism in Pregnancy and Birth Defects

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

    प्रकाशित 2010
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
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    में बचाया:
  4. 4
    Optical Coherence Tomography in the Diagnosis of Optic Pathway Gliomas

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

    प्रकाशित 2013
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    Artigo
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    में बचाया:
  5. 5
    Comorbidity between headache and epilepsy in a pediatric headache center

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

    प्रकाशित 2010
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    Artigo
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    में बचाया:
  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 द्वारा Matteo Cassina, Luisa Frizziero, Enrico Opocher, Raffaele Parrozzani, Ugo Sorrentino, Elisabetta Viscardi, Giacomo Miglionico, Edoardo Midena, Maurizio Clementi, Eva Trevisson

    प्रकाशित 2019
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    Revisão
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    में बचाया:
  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 द्वारा Paola Riva, Lucia Corrado, Federica Natacci, Pierangela Castorina, Bai-Li Wu, Gretchen Schneider, Maurizio Clementi, Romano Tenconi, Bruce R. Korf, Lidia Larizza

    प्रकाशित 2000
    पूर्ण पाठ प्राप्त करें
    Artigo
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    में बचाया:
  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 द्वारा Marco Venturin, Paolo Guarnieri, Federica Natacci, M Stabile, Romano Tenconi, Maurizio Clementi, Carmen Hernández, Peter Thompson, Meena Upadhyaya, Lidia Larizza, Paola Riva

    प्रकाशित 2004
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Carta
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    में बचाया:
  9. 9
    Paroxetine and fluoxetine in pregnancy: a prospective, multicentre, controlled, observational study

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

    प्रकाशित 2008
    पूर्ण पाठ प्राप्त करें
    Artigo
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    में बचाया:
  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 द्वारा Angela Favaro, Maurizio Clementi, Renzo Manara, Romina Bosello, Monica Forzan, Alice Bruson, Elena Tenconi, Daniela Degortes, Francesca Titton, Francesco Di Salle, Paolo Santonastaso

    प्रकाशित 2013
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    Artigo
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    में बचाया:
  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 द्वारा Francesca Capon, Giuseppe Novelli, Sabrina Semprini, Maurizio Clementi, Maurizio Nudo, P Vultaggio, Chiara Maria Mazzanti, Tommaso Gobello, Annalisa Botta, Giuseppe Fabrizi, Bruno Dallapiccola

    प्रकाशित 1999
    पूर्ण पाठ प्राप्त करें
    Artigo
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    में बचाया:
  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 द्वारा Raffaele Parrozzani, Maurizio Clementi, Luisa Frizziero, Giacomo Miglionico, Pierdavide Perrini, Fabiano Cavarzeran, Olympia Kotsafti, Francesco Comacchio, Eva Trevisson, Enrica Convento, Stefano Fusetti, Edoardo Midena

    प्रकाशित 2015
    पूर्ण पाठ प्राप्त करें
    Artigo
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    में बचाया:
  13. 13
    Adverse effects of prenatal methimazole exposure

    Adverse effects of prenatal methimazole exposure द्वारा 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

    प्रकाशित 2001
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
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    में बचाया:
  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 द्वारा 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

    प्रकाशित 2007
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    Artigo
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    में बचाया:
  15. 15
    Advances in Alport syndrome diagnosis using next-generation sequencing

    Advances in Alport syndrome diagnosis using next-generation sequencing द्वारा 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

    प्रकाशित 2011
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    Artigo
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    में बचाया:
  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 द्वारा 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

    प्रकाशित 2019
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    Artigo
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    में बचाया:
  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 द्वारा 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

    प्रकाशित 1999
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    Artigo
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    में बचाया:
  18. 18
    Primary coenzyme Q10 deficiency presenting as fatal neonatal multiorgan failure

    Primary coenzyme Q10 deficiency presenting as fatal neonatal multiorgan failure द्वारा 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

    प्रकाशित 2015
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
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    में बचाया:
  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 द्वारा 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

    प्रकाशित 2017
    पूर्ण पाठ प्राप्त करें
    Revisão
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    में बचाया:
  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 द्वारा 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

    प्रकाशित 2014
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    Artigo
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    में बचाया:

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