Hakutulokset - Elisa Grillo
- Näytetään 1 - 4 yhteensä 4 tuloksesta
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1
Efficacy of Antioxidant Supplementation to Non-Surgical Periodontal Therapy on Metabolic Control in Type 2 Diabetes Patients: A Network Meta-Analysis Tekijä Araújo, Elisa Grillo, de Oliveira, Domitilla Marchiori Sant’Anna Leal, Martins, Carolina Castro, Stefani, Cristine Miron
Julkaistu 2022Teksti -
2
Revealing the Complexity of a Monogenic Disease: Rett Syndrome Exome Sequencing Tekijä Elisa Grillo, Caterina Lo Rizzo, Laura Bianciardi, Veronica Bizzarri, Margherita Baldassarri, Ottavia Spiga, Simone Furini, Claudio De Felice, Cinzia Signorini, Silvia Leoncini, Alessandra Pecorelli, Lucia Ciccoli, Maria Antonietta Mencarelli, Joussef Hayek, Ilaria Meloni, Francesca Ariani, Francesca Mari, Alessandra Renieri
Julkaistu 2013Artigo -
3
NF1 microdeletions in neurofibromatosis type 1: from genotype to phenotype Tekijä Éric Pasmant, Audrey Sabbagh, Gill Spurlock, Ingrid Laurendeau, Elisa Grillo, Marie-José Hamel, Ludovic Martin, S. Barbarot, Bruno Leheup, Diana Rodriguez, Didier Lacombe, Hélène Dollfus, Laurent Pasquier, Bertrand Isidor, S. Ferkal, Jean Soulier, Marc Sanson, Anne Dieux‐Coëslier, Ivan Bièche, Béatrice Parfait, Michel Vidaud, P. Wolkenstein, Meena Upadhyaya, Dominique Vidaud
Julkaistu 2010Artigo -
4
Analysis of the Phenotypes in the Rett Networked Database Tekijä Elisa Frullanti, Filomena Tiziana Papa, Elisa Grillo, Angus Clarke, Bruria Ben‐Zeev, Mercédes Pineda, Nadia Bahi‐Buisson, Thierry Bienvenu, Judith Armstrong, Ana Roche Martínez, Francesca Mari, Andreea Nissenkorn, Caterina Lo Rizzo, Edvige Veneselli, Silvia Russo, Aglaia Vignoli, Giorgio Pini, Milena Djurić, Anne‐Marie Bisgaard, Kirstine Ravn, Vlatka Mejaški Bošnjak, Joussef Hayek, Rajni Khajuria, Barbara Montomoli, Francesca Cogliati, Maria Pintaudi, Kinga Hadzsiev, Dana Craiu, V. Yu. Voinova, Aleksandra Djukic, Laurent Villard, Alessandra Renieri
Julkaistu 2019Artigo
Työkalut:
Liittyvät aiheet
Biology
Gene
Genetics
Phenotype
MECP2
Medicine
Rett syndrome
Bioinformatics
Breakpoint
Chromosome
Comparative genomic hybridization
Copy-number variation
Disease
Exome
Exome sequencing
Genome
Genotype
Intellectual disability
Internal medicine
Microdeletion syndrome
Mutation
Neurodevelopmental disorder
Neurofibromatosis
Neurofibromatosis type I
Neuroscience
Pediatrics