Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Andrea Stachon"'
Autor:
Sabiha Abekhoukh, H. Bahar Sahin, Mauro Grossi, Samantha Zongaro, Thomas Maurin, Irene Madrigal, Daniele Kazue-Sugioka, Annick Raas-Rothschild, Mohamed Doulazmi, Pilar Carrera, Andrea Stachon, Steven Scherer, Maria Rita Drula Do Nascimento, Alain Trembleau, Ignacio Arroyo, Peter Szatmari, Isabel M. Smith, Montserrat Milà, Adam C. Smith, Angela Giangrande, Isabelle Caillé, Barbara Bardoni
Publikováno v:
Disease Models & Mechanisms, Vol 10, Iss 4, Pp 463-474 (2017)
Cytoplasmic FMRP interacting protein 1 (CYFIP1) is a candidate gene for intellectual disability (ID), autism, schizophrenia and epilepsy. It is a member of a family of proteins that is highly conserved during evolution, sharing high homology with its
Externí odkaz:
https://doaj.org/article/b879a391863543d5b04344b33425077a
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 65, Iss 1, Pp 36-40 (2007)
BACKGROUND: Rett syndrome (RS) is recognized as a pan-ethnic condition. Since the identification of mutations in the MECP2 gene, more patients have been diagnosed, and a broad spectrum of phenotypes has been reported. There is a lack of phenotype-gen
Externí odkaz:
https://doaj.org/article/4df70da031de4a4baabb1a542c4772cb
Publikováno v:
Journal of cognitive psychotherapy. 28(3)
Pediatric obsessive-compulsive disorder (OCD) is a prevalent condition that responds well to specialized treatment including cognitive behavioral therapy (CBT) or serotonin reuptake inhibitors or their combination. In Brazil, the dissemination of evi
Publikováno v:
Arquivos de Neuro-Psiquiatria v.65 n.1 2007
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
Arquivos de Neuro-Psiquiatria, Volume: 65, Issue: 1, Pages: 36-40, Published: MAR 2007
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
Arquivos de Neuro-Psiquiatria, Volume: 65, Issue: 1, Pages: 36-40, Published: MAR 2007
BACKGROUND: Rett syndrome (RS) is recognized as a pan-ethnic condition. Since the identification of mutations in the MECP2 gene, more patients have been diagnosed, and a broad spectrum of phenotypes has been reported. There is a lack of phenotype-gen
Autor:
Ahmed Teebi, Adam C. Smith, Peter N. Ray, Leona Fishman, Rosanna Weksberg, Roberto Mendoza-Londono, Berivan Baskin, Cheryl Cytrynbaum, Andrea Shugar, Regan Klatt, Andrea Stachon
Publikováno v:
American Journal of Medical Genetics Part A. :2924-2930
22q11 Deletion syndrome (22q11DS) is the most common microdeletion syndrome in humans, occurring with an incidence of 1 in 4,000. In most cases the submicroscopic deletion spans 3 Mb, but there are a number of other overlapping and non-overlapping de
Autor:
Stephen Meyn, Anne S. Bassett, Jeremy A. Squire, Rosanna Weksberg, Laura Moldovan, Eva W.C. Chow, Andrea Stachon, Jane Bayani
Publikováno v:
Human Genetics. 120:837-845
22q11 Deletion syndrome (22q11DS) is a common microdeletion syndrome with variable expression, including congenital and later onset conditions such as schizophrenia. Most studies indicate that expression does not appear to be related to length of the
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::939b34202153b69a3b708b91634208d0
http://www.scopus.com/inward/record.url?eid=2-s2.0-34547647249&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-34547647249&partnerID=MN8TOARS
Autor:
Andrea Stachon
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::97b33d3fe5055a30718ffbd04b5506e3
http://www.scopus.com/inward/record.url?eid=2-s2.0-33847725525&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-33847725525&partnerID=MN8TOARS
Publikováno v:
Journal of Cognitive Psychotherapy; 2014, Vol. 28 Issue 3, p198-210, 13p
Autor:
Lewin, Adam B., Storch, Eric A.
Publikováno v:
Journal of Cognitive Psychotherapy; 2014, Vol. 28 Issue 3, p151-155, 5p