Որոնման արդյունքները - Francesca Cogliati
- Ցուցադրվում են 1 - 5 արդյունքները 5
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1
Novel mutations in the CDKL5 gene, predicted effects and associated phenotypes Silvia Russo, Margherita Marchi, Francesca Cogliati, Maria Teresa Bonati, Maria Pintaudi, E. Veneselli, Veronica Saletti, M. R. Balestrini, Bruria Ben‐Zeev, Lidia Larizza
Հրապարակվել է 2009Artigo -
2
Epilepsy in Rett syndrome: Clinical and genetic features Maria Pintaudi, Maria Grazia Calevo, Aglaia Vignoli, Elena Biggi Parodi, Francesca Aiello, M. G. Baglietto, Joussef Hayek, Sabrina Buoni, Alessandra Renieri, Silvia Russo, Francesca Cogliati, Lucio Giordano, Maria Paola Canevini, Edvige Veneselli
Հրապարակվել է 2010Artigo -
3
Mutations in the Small GTPase Gene RAB39B Are Responsible for X-linked Mental Retardation Associated with Autism, Epilepsy, and Macrocephaly Maila Giannandrea, Veronica Bianchi, Maria Lidia Mignogna, A. Sirri, Salvatore Carrabino, Errico D’Elia, Matteo Vecellio, Silvia Russo, Francesca Cogliati, Lidia Larizza, Hans‐Hilger Ropers, Andreas Tzschach, Vera M. Kalscheuer, Barbara Oehl‐Jaschkowitz, Cindy Skinner, Charles E. Schwartz, Jozef Gécz, Hilde Van Esch, Martine Raynaud, Jamel Chelly, Arjan P.M. de Brouwer, Daniela Toniolo, Patrizia D’Adamo
Հրապարակվել է 2010Artigo -
4
The phenotype of <i>SCN8A</i> developmental and epileptic encephalopathy Elena Gardella, Carla Marini, Marina Trivisano, Mark P. Fitzgerald, Michael Alber, Katherine B. Howell, Francesca Darra, Sabrina Siliquini, Bigna K. Bölsterli, Silva Masnada, Anna Pichiecchio, Katrine M. Johannesen, Birgit Jepsen, Elena Fontana, Gaia Anibaldi, Silvia Russo, Francesca Cogliati, Martino Montomoli, Nicola Specchio, Guido Rubboli, Pierangelo Veggiotti, Sándor Beniczky, Markus Wolff, Ingo Helbig, Federico Vigevano, Ingrid E. Scheffer, Renzo Guerrini, Rikke S. Møller
Հրապարակվել է 2018Artigo -
5
Analysis of the Phenotypes in the Rett Networked Database 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
Հրապարակվել է 2019Artigo
Որոնման գործիքներ:
Առնչվող խորագիր
Biology
Gene
Genetics
Phenotype
MECP2
Medicine
Rett syndrome
Epilepsy
Mutation
Pediatrics
Allele
Angelman syndrome
Bioinformatics
Cell biology
Encephalopathy
Endoplasmic reticulum
Environmental health
Epilepsy syndromes
Exon
GTPase
Golgi apparatus
Haploinsufficiency
Human genetics
Internal medicine
Missense mutation
Neuroscience
Population
Psychiatry
Psychology
RNA