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Mostrati risultati da 61 a 77 di 77
Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
A Hunter Patient with a Severe Phenotype Reveals Two Large Deletions and Two Duplications Extending 1.2 Mb Distally to IDS Locus 2014 ZANETTI, ALESSANDRATOMANIN, ROSELLARAMPAZZO, ANGELICARIGON, CHIARAGASPAROTTO, NICOLETTACASSINA, MATTEOCLEMENTI, MAURIZIOSCARPA, MAURIZIO JIMD REPORTS - -
Pregnancy outcome in women exposed to antiepileptic drugs: Teratogenic role of maternal epilepsy and its pharmacologic treatment. 2013 CASSINA, MATTEOCLEMENTI, MAURIZIO + REPRODUCTIVE TOXICOLOGY - -
Analysis of p53 polymorphisms in individuals with multiple melanocytic nevi 2013 BRUSON, ALICEZATTRA, EDOARDOCASSINA, MATTEOBALDO, VINCENZOCLEMENTI, MAURIZIOALAIBAC, MAURO SALVATORE ALESSANDRO + EUROPEAN JOURNAL OF DERMATOLOGY - -
Recurrent HERV-H-Mediated 3q13.2-q13.31 Deletions Cause a Syndrome of Hypotonia and Motor, Language, and Cognitive Delays 2013 CASSINA, MATTEO + HUMAN MUTATION - -
Congenital pulmonary airway malformation (CPAM) [congenital cystic adenomatoid malformation] associated with tracheoesophageal fistula and agensesis of the corpus callosum. 2012 PIZZI, MARCOFASSAN, MATTEOLUDWIG, KATHRINCASSINA, MATTEOSALMASO, ROBERTO + FETAL AND PEDIATRIC PATHOLOGY - -
Genetic susceptibility to teratogens: State of the art. 2012 CASSINA, MATTEOSALVIATI, LEONARDOCLEMENTI, MAURIZIO + REPRODUCTIVE TOXICOLOGY - -
Pharmacologic treatment of hyperthyroidism during pregnancy. 2012 CASSINA, MATTEOCLEMENTI, MAURIZIO + BIRTH DEFECTS RESEARCH. PART A, CLINICAL AND MOLECULAR TERATOLOGY - -
Copper and bezafibrate cooperate to rescue cytochrome c oxidase deficiency in cells of patients with sco2 mutations. 2012 CASARIN, ALBERTODOIMO, MARABASSO, GIUSEPPECASSINA, MATTEORIZZUTO, ROSARIOCLEMENTI, MAURIZIOTREVISSON, EVASALVIATI, LEONARDO + ORPHANET JOURNAL OF RARE DISEASES - -
Haploinsufficiency of COQ4 causes coenzymeQ10 deficiency 2012 SALVIATI, LEONARDOTREVISSON, EVACASARIN, ALBERTODOIMO, MARACASSINA, MATTEODesbats MASARTORI, GEPPO + JOURNAL OF MEDICAL GENETICS - -
Eating-induced epileptic spasms in a boy with MECP2 duplication syndrome: insights into pathogenesis of genetic epilepsies. 2012 CASSINA, MATTEOTOLDO, IRENENOSADINI, MARGHERITACLEMENTI, MAURIZIOSartori S. + EPILEPTIC DISORDERS - -
Pregnancy outcome in women exposed to leflunomide before or during pregnancy. 2012 CASSINA, MATTEO + ARTHRITIS AND RHEUMATISM - -
Infantile epilepsy associated with mosaic 2q24 duplication including SCN2A and SCN3A. 2011 CASSINA, MATTEOCLEMENTI, MAURIZIO + SEIZURE - -
Treatment of Hyperthyroidism in Pregnancy and Birth Defects 2010 CLEMENTI, MAURIZIOCASSINA, MATTEO + THE JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM - -
Migraine therapy during pregnancy and lactation 2010 CASSINA, MATTEOTOLDO, IRENEBATTISTELLA, PIER ANTONIOCLEMENTI, MAURIZIO + EXPERT OPINION ON DRUG SAFETY - -
First trimester diclofenac exposure and pregnancy outcome 2010 CASSINA, MATTEOCLEMENTI, MAURIZIO + REPRODUCTIVE TOXICOLOGY - -
Medications in pregnancy and lactation. 2009 CLEMENTI, MAURIZIOCASSINA, MATTEO + OBSTETRICS AND GYNECOLOGY - -
Therapy of inflammatory bowel diseases in pregnancy and lactation. 2009 CASSINA, MATTEOFABRIS, LUCAOKOLICSANYI, LAJOSCLEMENTI, MAURIZIO + EXPERT OPINION ON DRUG SAFETY - -
Mostrati risultati da 61 a 77 di 77
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