نتایج جستجو برای: neurodevelopmental disorder

تعداد نتایج: 603172  

Journal: :Epidemiology and Psychiatric Sciences 1999

Journal: :Arquivos De Neuro-psiquiatria 2023

Case presentation: PHAPS, male, 9 years old, being followed up at the neuropediatric outpatient clinic for a history of seizures since 1 year and 6 months, focal epilepsy with in type left side, eyelid myoclonus drooling, subsequent generalization. At seven he started behavioral changes stereotypies. Delayed neuropsychomotor development: sustained cervical 3 lallation year, articulation first w...

Journal: :Materia socio-medica 2016
Mladenka Vukojevic Ines Trninic Arta Dodaj Masa Malenica Tatjana Barisic Sandra Stojic

GOAL To analyze the appearance of neurodevelopmental disorders in children delivered post-term and to find out whether prolonged pregnancy may be a cause of such disorders in a selected group participants. PATIENTS AND METHODS This study included a cohort of 34 children born post-term suffering from neurodevelopmental disorders who were treated at the Service for psycho-physiological and spea...

2010
Jessica E. Van Schijndel Gerard J.M Martens

The complex neurodevelopmental disorder schizophrenia is thought to be induced by an interaction between predisposing genes and environmental stressors. In order to get a better insight into the aetiology of this complex disorder, animal models have been developed. In this review, we summarize mRNA expression profiling studies on neurodevelopmental, pharmacological and genetic animal models for...

Journal: :Journal of the American Academy of Child and Adolescent Psychiatry 2014
Lauren M McGrath Dongmei Yu Christian Marshall Lea K Davis Bhooma Thiruvahindrapuram Bingbin Li Carolina Cappi Gloria Gerber Aaron Wolf Frederick A Schroeder Lisa Osiecki Colm O'Dushlaine Andrew Kirby Cornelia Illmann Stephen Haddad Patience Gallagher Jesen A Fagerness Cathy L Barr Laura Bellodi Fortu Benarroch O Joseph Bienvenu Donald W Black Michael H Bloch Ruth D Bruun Cathy L Budman Beatriz Camarena Danielle C Cath Maria C Cavallini Sylvain Chouinard Vladimir Coric Bernadette Cullen Richard Delorme Damiaan Denys Eske M Derks Yves Dion Maria C Rosário Valsama Eapen Patrick Evans Peter Falkai Thomas V Fernandez Helena Garrido Daniel Geller Hans J Grabe Marco A Grados Benjamin D Greenberg Varda Gross-Tsur Edna Grünblatt Gary A Heiman Sian M J Hemmings Luis D Herrera Ana G Hounie Joseph Jankovic James L Kennedy Robert A King Roger Kurlan Nuria Lanzagorta Marion Leboyer James F Leckman Leonhard Lennertz Christine Lochner Thomas L Lowe Gholson J Lyon Fabio Macciardi Wolfgang Maier James T McCracken William McMahon Dennis L Murphy Allan L Naarden Benjamin M Neale Erika Nurmi Andrew J Pakstis Michele T Pato Carlos N Pato John Piacentini Christopher Pittenger Yehuda Pollak Victor I Reus Margaret A Richter Mark Riddle Mary M Robertson David Rosenberg Guy A Rouleau Stephan Ruhrmann Aline S Sampaio Jack Samuels Paul Sandor Brooke Sheppard Harvey S Singer Jan H Smit Dan J Stein Jay A Tischfield Homero Vallada Jeremy Veenstra-VanderWeele Susanne Walitza Ying Wang Jens R Wendland Yin Yao Shugart Euripedes C Miguel Humberto Nicolini Ben A Oostra Rainald Moessner Michael Wagner Andres Ruiz-Linares Peter Heutink Gerald Nestadt Nelson Freimer Tracey Petryshen Danielle Posthuma Michael A Jenike Nancy J Cox Gregory L Hanna Helena Brentani Stephen W Scherer Paul D Arnold S Evelyn Stewart Carol A Mathews James A Knowles Edwin H Cook David L Pauls Kai Wang Jeremiah M Scharf

OBJECTIVE Obsessive-compulsive disorder (OCD) and Tourette syndrome (TS) are heritable neurodevelopmental disorders with a partially shared genetic etiology. This study represents the first genome-wide investigation of large (>500 kb), rare (<1%) copy number variants (CNVs) in OCD and the largest genome-wide CNV analysis in TS to date. METHOD The primary analyses used a cross-disorder design ...

Journal: :Scientific reports 2016
Muideen O Bakare Mashudat A Bello-Mojeed Kerim M Munir Oluwayemi C Ogun Julian Eaton

Late diagnosis and interventions characterize childhood neurodevelopmental disorders in Sub-Saharan Africa. This has negatively impacted on the prognosis of the children with neurodevelopmental disorders. This study examined the prevalence and pattern of neurodevelopmental delays among children under the age of 3 years attending immunization clinics in Lagos State, Nigeria and also affords oppo...

Journal: :BJPsych Advances 2022

SUMMARY This editorial introduces the first of two special issues BJPsych Advances on neurodevelopmental disorders, including intellectual disability, autism spectrum disorder, attention-deficit hyperactivity disorder and epilepsy. issue is intended to offer a clinical tool kit for mental health professionals giving guidance assessment management these disorders associated conditions, such as b...

2015
JC McPartland

Glossary Applied behavior analysis A category of intervention approach for ASD based on principles of reinforcing desired behaviors to effect behavior change, usually improvement in social-communication skills. Examples include Discrete Trial Intervention, Pivotal Response Training, and the Early Start Denver Model. Asperger’s disorder A neurodevelopmental disorder characterized by impairments ...

Journal: :Neurology 2016
Hannah Stamberger Marina Nikanorova Marjolein H Willemsen Patrizia Accorsi Marco Angriman Hartmut Baier Ira Benkel-Herrenbrueck Valérie Benoit Mauro Budetta Almuth Caliebe Gaetano Cantalupo Giuseppe Capovilla Gianluca Casara Carolina Courage Marie Deprez Anne Destrée Robertino Dilena Corrie E Erasmus Madeleine Fannemel Roar Fjær Lucio Giordano Katherine L Helbig Henrike O Heyne Joerg Klepper Gerhard J Kluger Damien Lederer Monica Lodi Oliver Maier Andreas Merkenschlager Nina Michelberger Carlo Minetti Hiltrud Muhle Judith Phalin Keri Ramsey Antonino Romeo Jens Schallner Ina Schanze Marwan Shinawi Kristel Sleegers Katalin Sterbova Steffen Syrbe Monica Traverso Andreas Tzschach Peter Uldall Rudy Van Coster Helene Verhelst Maurizio Viri Susan Winter Markus Wolff Martin Zenker Leonardo Zoccante Peter De Jonghe Ingo Helbig Pasquale Striano Johannes R Lemke Rikke S Møller Sarah Weckhuysen

OBJECTIVE To give a comprehensive overview of the phenotypic and genetic spectrum of STXBP1 encephalopathy (STXBP1-E) by systematically reviewing newly diagnosed and previously reported patients. METHODS We recruited newly diagnosed patients with STXBP1 mutations through an international network of clinicians and geneticists. Furthermore, we performed a systematic literature search to review ...

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