Literature DB >> 28283807

Identification of the Genetic Cause for Childhood Disintegrative Disorder by Whole-Exome Sequencing.

Zhu Wen1, Tian-Lin Cheng2, Da-Zhi Yin2, Shi-Bang Sun1, Zheng Wang2, Shun-Ying Yu1, Yi Zhang3,4, Zilong Qiu5, Ya-Song Du6.   

Abstract

Mesh：

Year:  2017        PMID： 28283807      PMCID： PMC5567535          DOI： 10.1007/s12264-017-0119-0

Source DB:  PubMed          Journal:  Neurosci Bull        ISSN： 1995-8218            Impact factor:   5.203


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  12 in total

Review 1.  Childhood disintegrative disorder: should it be considered a distinct diagnosis?

Authors:  C N Hendry
Journal:  Clin Psychol Rev       Date:  2000-01

2.  Brief report: childhood disintegrative disorder: a brief examination of eight case studies.

Authors:  Kendra J Homan; Michael W Mellon; Daniel Houlihan; Maja Z Katusic
Journal:  J Autism Dev Disord       Date:  2011-04

3.  The UCLA-University of Utah epidemiologic survey of autism: the etiologic role of rare diseases.

Authors:  E R Ritvo; A Mason-Brothers; B J Freeman; C Pingree; W R Jenson; W M McMahon; P B Petersen; L B Jorde; A Mo; A Ritvo
Journal:  Am J Psychiatry       Date:  1990-12       Impact factor: 18.112

4.  Acquired autistic behaviors in children with mucopolysaccharidosis type IIIA.

Authors:  Robin K Rumsey; Kyle Rudser; Kathleen Delaney; Michael Potegal; Chester B Whitley; Elsa Shapiro
Journal:  J Pediatr       Date:  2014-02-25       Impact factor: 4.406

5.  Inherited metabolic disorders in Turkish patients with autism spectrum disorders.

Authors:  Ertugrul Kiykim; Cigdem Aktuglu Zeybek; Tanyel Zubarioglu; Serif Cansever; Cengiz Yalcinkaya; Erdogan Soyucen; Ahmet Aydin
Journal:  Autism Res       Date:  2015-06-07       Impact factor: 5.216

Review 6.  Sanfilippo syndrome: a mini-review.

Authors:  M J Valstar; G J G Ruijter; O P van Diggelen; B J Poorthuis; F A Wijburg
Journal:  J Inherit Metab Dis       Date:  2008-04-04       Impact factor: 4.982

7.  Case report: an unexpected link between partial deletion of the SHANK3 gene and Heller's dementia infantilis, a rare subtype of autism spectrum disorder.

Authors:  Anne Philippe; Yann Craus; Marlène Rio; Nadia Bahi-Buisson; Nathalie Boddaert; Valérie Malan; Jean-Paul Bonnefont; Laurence Robel
Journal:  BMC Psychiatry       Date:  2015-10-21       Impact factor: 3.630

Review 8.  Mucopolysaccharidosis type III (Sanfilippo syndrome) and misdiagnosis of idiopathic developmental delay, attention deficit/hyperactivity disorder or autism spectrum disorder.

Authors:  Frits A Wijburg; Grzegorz Węgrzyn; Barbara K Burton; Anna Tylki-Szymańska
Journal:  Acta Paediatr       Date:  2013-02-06       Impact factor: 2.299

9.  Autism Diagnostic Interview-Revised (ADI-R) Algorithms for Toddlers and Young Preschoolers: Application in a Non-US Sample of 1,104 Children.

Authors:  Annelies de Bildt; Sjoerd Sytema; Eric Zander; Sven Bölte; Harald Sturm; Nurit Yirmiya; Maya Yaari; Tony Charman; Erica Salomone; Ann LeCouteur; Jonathan Green; Ricardo Canal Bedia; Patricia García Primo; Emma van Daalen; Maretha V de Jonge; Emilía Guðmundsdóttir; Sigurrós Jóhannsdóttir; Marija Raleva; Meri Boskovska; Bernadette Rogé; Sophie Baduel; Irma Moilanen; Anneli Yliherva; Jan Buitelaar; Iris J Oosterling
Journal:  J Autism Dev Disord       Date:  2015-07

Review 10.  Sanfilippo syndrome: causes, consequences, and treatments.

Authors:  Anthony O Fedele
Journal:  Appl Clin Genet       Date:  2015-11-25
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  2 in total

1.  Recent Research Progress in Autism Spectrum Disorder.

Authors:  Xiang Yu; Zilong Qiu; Dai Zhang
Journal:  Neurosci Bull       Date:  2017-03-11       Impact factor: 5.203

Review 2.  NGS Technologies as a Turning Point in Rare Disease Research , Diagnosis and Treatment.

Authors:  Ana Fernandez-Marmiesse; Sofia Gouveia; Maria L Couce
Journal:  Curr Med Chem       Date:  2018-01-30       Impact factor: 4.530
  2 in total

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