A. Stachon

Molecular characterization of deletion breakpoints in adults with 22q11 deletion syndrome

R. Weksberg, A. Bassett, J. Squire, 2007, Human Genetics.

Gentamicin treatment in McArdle disease: Failure to correct myophosphorylase deficiency

N. Barbaro, S. DeArmond, G. Rabinovici, 2006, Neurology.

Dissemination of Evidence-Based Treatment for Pediatric Obsessive-Compulsive Disorder in the Southern Region of Brazil: Challenges and Future Directions

A. Stachon, Isabela Machado da Silva, 2014, Journal of Cognitive Psychotherapy.

Clinical and Molecular Characterization of Psychosis in 22q11 Deletion Syndrome

A. Stachon, 2010 .

New insights into the regulatory function of CYFIP1 in the context of WAVE- and FMRP-containing complexes

P. Szatmari, A. Giangrande, I. Caillé, 2017, Disease Models & Mechanisms.

Rett syndrome: clinical and molecular characterization of two Brazilian patients.

S. Raskin, A. Stachon, F. Assumpção, 2007, Arquivos de neuro-psiquiatria.

Anxiety Disorders and Perceptual Disturbances in Adolescents with 22q11.2 Deletion Syndrome Treated with SSRI: A Case Series.

Claire M. De Souza, A. Stachon, 2011, Journal of the Canadian Academy of Child and Adolescent Psychiatry = Journal de l'Academie canadienne de psychiatrie de l'enfant et de l'adolescent.

Assessment and Medication Management of Paediatric Obsessive-Compulsive Disorder

S. Stewart, D. Hezel, A. Stachon, 2012, Drugs.

Molecular diagnosis of 22q11.2 deletion and duplication by multiplex ligation dependent probe amplification

C. Cytrynbaum, R. Weksberg, P. Ray, 2007, American journal of medical genetics. Part A.