Search Result "22q11 deletion syndrome."


COMT Implication in Cognitive and Psychiatric Symptoms in Chromosome 22q11 Microdeletion Syndrome: A Selective Review

Journal: CNS & Neurological Disorders - Drug Targets
Volume: 11 Issue: 3 Year: 2012 Page: 273-281
Author(s): Marco Armando,Francesco Papaleo,Stefano Vicari

Syndromes with Orofacial Clefts

Ebook: Craniofacial Disorders - Orofacial Features and Peculiarities in Dental Treatment
Volume: 1 Year: 2017
Author(s): Beatriz Costa,Cleide Felício de Carvalho Carrara,Vivian de Agostino Biella Passos
Doi: 10.2174/9781681085166117010011

Mechanistic Approach to Understanding Psychosis Risk in Velocardiofacial Syndrome

Journal: Current Pediatric Reviews
Volume: 5 Issue: 2 Year: 2009 Page: 89-104
Author(s): Vandana Shashi, Margaret N. Berry, Matcheri S. Keshavan

Challenge and Therapeutic Studies Using Alpha-Methyl-para-Tyrosine (AMPT) in Neuropsychiatric Disorders: A Review

Journal: Central Nervous System Agents in Medicinal Chemistry
Volume: 8 Issue: 4 Year: 2008 Page: 249-256
Author(s): Oswald J.N. Bloemen, M. B. de Koning, E. Boot, J. Booij, T.A. M.J. van Amelsvoort

Catechol-O-Methyl Transferase as a Drug Target for Schizophrenia

Journal: CNS & Neurological Disorders - Drug Targets
Volume: 11 Issue: 3 Year: 2012 Page: 282-291
Author(s): Colm M.P. O’Tuathaigh,Lieve Desbonnet,Peter Lee,John L. Waddington

Research Article

Chromosomal Micro-aberration in a Saudi Family with Juvenile Myoclonic Epilepsy

Journal: CNS & Neurological Disorders - Drug Targets
Volume: 16 Issue: 9 Year: 2017 Page: 1010-1017
Author(s): Muhammad Imran Naseer,Mahmood Rasool,Adeel G. Chaudhary,Sameera Sogaty,Sajjad Karim,Hans-Juergen Schulten,Fehmida Bibi,Peter Natesan Pushparaj,Hussein A. Algahtani,Mohammad H. Al-Qahtani

Controlled Somatic and Germline Copy Number Variation in the Mouse Model

Journal: Current Genomics
Volume: 11 Issue: 6 Year: 2010 Page: 470-480
Author(s): Yann Herault, Arnaud Duchon, Damien Marechal, Matthieu Raveau, Patricia L. Pereira, Emilie Dalloneau, Veronique Brault

Tetralogy of Fallot and Hypoplastic Left Heart Syndrome – Complex Clinical Phenotypes Meet Complex Genetic Networks

Journal: Current Genomics
Volume: 16 Issue: 3 Year: 2015 Page: 141-158
Author(s): Harald Lahm,Patric Schon,Stefanie Doppler,Martina Dreßen,Julie Cleuziou,Marcus-Andre Deutsch,Peter Ewert,Rudiger Lange,Markus Krane

Extra Cardiac Defects in Fetuses with Congenital Heart Diseases

Ebook: Perinatal Cardiology-Part 2
Volume: 1 Year: 2020
Author(s): Alberto Borges Peixoto,Edward Araujo Júnior
Doi: 10.2174/9789811466557120010010

Assessment and Management of Velopharyngeal Insufficiency

Ebook: Otolaryngology for the Pediatrician
Volume: 1 Year: 2013
Author(s): Luke J. Schloegel,Diego A. Preciado
Doi: 10.2174/9781608054596113010013

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