Works matching IS 18661947 AND DT 2019 AND VI 11 AND IP 1

Results: 42

Initial eye gaze to faces and its functional consequence on face identification abilities in autism spectrum disorder.

Published in:

Journal of Neurodevelopmental Disorders, 2019, v. 11, n. 1, p. 1, doi. 10.1186/s11689-019-9303-z

By:

Schauder, Kimberly B.;
Park, Woon Ju;
Tsank, Yuliy;
Eckstein, Miguel P.;
Tadin, Duje;
Bennetto, Loisa

Publication type:

Article

Intellectual functioning and behavioural features associated with mosaicism in fragile X syndrome.

Published in:

Journal of Neurodevelopmental Disorders, 2019, v. 11, n. 1, p. 1, doi. 10.1186/s11689-019-9288-7

By:

Baker, Emma K.;
Arpone, Marta;
Vera, Solange Aliaga;
Bretherton, Lesley;
Ure, Alexandra;
Kraan, Claudine M.;
Bui, Minh;
Ling, Ling;
Francis, David;
Hunter, Matthew F.;
Elliott, Justine;
Rogers, Carolyn;
Field, Michael J.;
Cohen, Jonathan;
Maria, Lorena Santa;
Faundes, Victor;
Curotto, Bianca;
Morales, Paulina;
Trigo, Cesar;
Salas, Isabel

Publication type:

Article

Quantifying the resolution of spatial and temporal representation in children with 22q11.2 deletion syndrome.

Published in:

Journal of Neurodevelopmental Disorders, 2019, v. 11, n. 1, p. 1, doi. 10.1186/s11689-019-9301-1

By:

McCabe, Kathryn L.;
Popa, Abbie M.;
Durdle, Courtney;
Amato, Michele;
Cabaral, Margarita H.;
Cruz, Joshua;
Wong, Ling M.;
Harvey, Danielle;
Tartaglia, Nicole;
Simon, Tony J.

Publication type:

Article

Adaptation of the Clinical Dementia Rating Scale for adults with Down syndrome.

Published in:

Journal of Neurodevelopmental Disorders, 2019, v. 11, n. 1, p. 1, doi. 10.1186/s11689-019-9300-2

By:

Lessov-Schlaggar, Christina N.;
del Rosario, Olga L.;
Morris, John C.;
Ances, Beau M.;
Schlaggar, Bradley L.;
Constantino, John N.

Publication type:

Article

White matter and neurodevelopmental disorders: honoring Jean De Vellis through the work of the NICHD-funded intellectual and developmental disabilities research centers.

Published in:

2019

By:

Hazlett, Heather Cody;
Gallo, Vittorio

Publication type:

Editorial

In memory of Jean de Vellis (1935–2018).

Published in:

2019

By:

Bookheimer, Susan Y.;
Kornblum, Harley I.

Publication type:

Announcement

Reducing Th2 inflammation through neutralizing IL-4 antibody rescues myelination in IUGR rat brain.

Published in:

Journal of Neurodevelopmental Disorders, 2019, v. 11, n. 1, p. 1, doi. 10.1186/s11689-019-9297-6

By:

Zanno, Allison E.;
Romer, Micah A.;
Fox, Lauren;
Golden, Thea;
Jaeckle-Santos, Lane;
Simmons, Rebecca A.;
Grinspan, Judith B.

Publication type:

Article

The impact of expressive language development and the left inferior longitudinal fasciculus on listening and reading comprehension.

Published in:

Journal of Neurodevelopmental Disorders, 2019, v. 11, n. 1, p. 1, doi. 10.1186/s11689-019-9296-7

By:

Del Tufo, Stephanie N.;
Earle, F. Sayako;
Cutting, Laurie E.

Publication type:

Article

White matter as a monitoring biomarker for neurodevelopmental disorder intervention studies.

Published in:

Journal of Neurodevelopmental Disorders, 2019, v. 11, n. 1, p. 1, doi. 10.1186/s11689-019-9295-8

By:

Swanson, Meghan R.;
Hazlett, Heather C.

Publication type:

Article

Spatiotemporal development of spinal neuronal and glial populations in the Ts65Dn mouse model of Down syndrome.

Published in:

Journal of Neurodevelopmental Disorders, 2019, v. 11, n. 1, p. 1, doi. 10.1186/s11689-019-9294-9

By:

Aziz, Nadine M.;
Klein, Jenny A.;
Brady, Morgan R.;
Olmos-Serrano, Jose Luis;
Gallo, Vittorio;
Haydar, Tarik F.

Publication type:

Article

Early white matter development is abnormal in tuberous sclerosis complex patients who develop autism spectrum disorder.

Published in:

Journal of Neurodevelopmental Disorders, 2019, v. 11, n. 1, p. 1, doi. 10.1186/s11689-019-9293-x

By:

Prohl, Anna K.;
Scherrer, Benoit;
Tomas-Fernandez, Xavier;
Davis, Peter E.;
Filip-Dhima, Rajna;
Prabhu, Sanjay P.;
Peters, Jurriaan M.;
Bebin, E. Martina;
Krueger, Darcy A.;
Northrup, Hope;
Wu, Joyce Y.;
Sahin, Mustafa;
Warfield, Simon K.;
on behalf of the TACERN Study Group;
Goyal, Monisha;
Pearson, Deborah A.;
Williams, Marian E.;
Hanson, Ellen;
Bing, Nicole;
Kent, Bridget

Publication type:

Article

Mitochondrial aminoacyl-tRNA synthetase disorders: an emerging group of developmental disorders of myelination.

Published in:

Journal of Neurodevelopmental Disorders, 2019, v. 11, n. 1, p. 1, doi. 10.1186/s11689-019-9292-y

By:

Fine, Amena Smith;
Nemeth, Christina L.;
Kaufman, Miriam L.;
Fatemi, Ali

Publication type:

Article

A diffusion-weighted imaging tract-based spatial statistics study of autism spectrum disorder in preschool-aged children.

Published in:

Journal of Neurodevelopmental Disorders, 2019, v. 11, n. 1, p. 1, doi. 10.1186/s11689-019-9291-z

By:

Andrews, Derek Sayre;
Lee, Joshua K.;
Solomon, Marjorie;
Rogers, Sally J.;
Amaral, David G.;
Nordahl, Christine Wu

Publication type:

Article

Refining the concept of GFAP toxicity in Alexander disease.

Published in:

Journal of Neurodevelopmental Disorders, 2019, v. 11, n. 1, p. 1, doi. 10.1186/s11689-019-9290-0

By:

Messing, Albee

Publication type:

Article

The role of glia in epilepsy, intellectual disability, and other neurodevelopmental disorders in tuberous sclerosis complex.

Published in:

Journal of Neurodevelopmental Disorders, 2019, v. 11, n. 1, p. 1, doi. 10.1186/s11689-019-9289-6

By:

Wong, Michael

Publication type:

Article

Are there shared neural correlates between dyslexia and ADHD? A meta-analysis of voxel-based morphometry studies.

Published in:

Journal of Neurodevelopmental Disorders, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s11689-019-9287-8

By:

McGrath, Lauren M.;
Stoodley, Catherine J.

Publication type:

Article

Quantitative gait assessment in children with 16p11.2 syndrome.

Published in:

Journal of Neurodevelopmental Disorders, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s11689-019-9286-9

By:

Goldman, Sylvie;
McCullough, Aston K.;
Young, Sally Dunaway;
Mueller, Carly;
Stahl, Adrianna;
Zoeller, Audrey;
Abbruzzese, Laurel Daniels;
Rao, Ashwini K.;
Montes, Jacqueline

Publication type:

Article

Vocabulary comprehension in adults with fragile X syndrome (FXS).

Published in:

Journal of Neurodevelopmental Disorders, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s11689-019-9285-x

By:

Hoffmann, Anne;
Krause, Sue Ellen;
Wuu, Joanne;
Leurgans, Sue;
Guter, Stephen J.;
Block, Sandra S.;
Salt, Jeff;
Cook, Edwin;
Maino, Dominick M.;
Berry-Kravis, Elizabeth

Publication type:

Article

Behavioural and psychological characteristics in Pitt-Hopkins syndrome: a comparison with Angelman and Cornelia de Lange syndromes.

Published in:

Journal of Neurodevelopmental Disorders, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s11689-019-9282-0

By:

Watkins, Alice;
Bissell, Stacey;
Moss, Jo;
Oliver, Chris;
Clayton-Smith, Jill;
Haye, Lorraine;
Heald, Mary;
Welham, Alice

Publication type:

Article

Developmental divergence: motor trajectories in children with fragile X syndrome with and without co-occurring autism.

Published in:

Journal of Neurodevelopmental Disorders, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s11689-019-9281-1

By:

Will, Elizabeth A.;
Bishop, Somer L.;
Roberts, Jane E.

Publication type:

Article

Early negative affect in males and females with fragile X syndrome: implications for anxiety and autism.

Published in:

Journal of Neurodevelopmental Disorders, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s11689-019-9284-y

By:

Wall, Carla A.;
Hogan, Abigail L.;
Will, Elizabeth A.;
McQuillin, Samuel;
Kelleher, Bridgette L.;
Roberts, Jane E.

Publication type:

Article

Within-task variability on standardized language tests predicts autism spectrum disorder: a pilot study of the Response Dispersion Index.

Published in:

Journal of Neurodevelopmental Disorders, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s11689-019-9283-z

By:

Hare-Harris, Abby E.;
Mitchel, Marissa W.;
Myers, Scott M.;
Mitchel, Aaron D.;
King, Brian R.;
Ruocco, Brittany G.;
Martin, Christa Lese;
Flax, Judy F.;
Brzustowicz, Linda M.

Publication type:

Article

Assessing general cognitive and adaptive abilities in adults with Down syndrome: a systematic review.

Published in:

Journal of Neurodevelopmental Disorders, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s11689-019-9279-8

By:

Hamburg, Sarah;
Lowe, Bryony;
Startin, Carla Marie;
Padilla, Concepcion;
Coppus, Antonia;
Silverman, Wayne;
Fortea, Juan;
Zaman, Shahid;
Head, Elizabeth;
Handen, Benjamin L.;
Lott, Ira;
Song, Weihong;
Strydom, André

Publication type:

Article

Magnetoencephalographic (MEG) brain activity during a mental flexibility task suggests some shared neurobiology in children with neurodevelopmental disorders.

Published in:

Journal of Neurodevelopmental Disorders, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s11689-019-9280-2

By:

Mogadam, Alexandra;
Keller, Anne E.;
Arnold, Paul D.;
Schachar, Russell;
Lerch, Jason P.;
Anagnostou, Evdokia;
Pang, Elizabeth W.

Publication type:

Article

Phenotypic characterization of individuals with SYNGAP1 pathogenic variants reveals a potential correlation between posterior dominant rhythm and developmental progression.

Published in:

Journal of Neurodevelopmental Disorders, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s11689-019-9276-y

By:

Jimenez-Gomez, Andres;
Niu, Sizhe;
Andujar-Perez, Fabiola;
McQuade, Elizabeth A.;
Balasa, Alfred;
Huss, David;
Coorg, Rohini;
Quach, Michael;
Vinson, Sherry;
Risen, Sarah;
Holder, J. Lloyd

Publication type:

Article

STXBP1-associated neurodevelopmental disorder: a comparative study of behavioural characteristics.

Published in:

Journal of Neurodevelopmental Disorders, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s11689-019-9278-9

By:

O'Brien, Sinéad;
Ng-Cordell, Elise;
Astle, Duncan E.;
Scerif, Gaia;
Baker, Kate

Publication type:

Article

A phase 1/2, open-label assessment of the safety, tolerability, and efficacy of transdermal cannabidiol (ZYN002) for the treatment of pediatric fragile X syndrome.

Published in:

Journal of Neurodevelopmental Disorders, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s11689-019-9277-x

By:

Heussler, Helen;
Cohen, Jonathan;
Silove, Natalie;
Tich, Nancy;
Bonn-Miller, Marcel O.;
Du, Wei;
O'Neill, Carol;
Sebree, Terri

Publication type:

Article

Electroencephalographic spectral power as a marker of cortical function and disease severity in girls with Rett syndrome.

Published in:

Journal of Neurodevelopmental Disorders, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s11689-019-9275-z

By:

Roche, Katherine J.;
LeBlanc, Jocelyn J.;
Levin, April R.;
O'Leary, Heather M.;
Baczewski, Lauren M.;
Nelson, Charles A.

Publication type:

Article

Infant regulatory function acts as a protective factor for later traits of autism spectrum disorder and attention deficit/hyperactivity disorder but not callous unemotional traits.

Published in:

Journal of Neurodevelopmental Disorders, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s11689-019-9274-0

By:

Bedford, Rachael;
Gliga, Teodora;
Hendry, Alexandra;
Jones, Emily J. H.;
Pasco, Greg;
Charman, Tony;
Johnson, Mark H.;
Pickles, Andrew

Publication type:

Article

A Brazilian cohort of individuals with Phelan-McDermid syndrome: genotype-phenotype correlation and identification of an atypical case.

Published in:

Journal of Neurodevelopmental Disorders, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s11689-019-9273-1

By:

Samogy-Costa, Claudia Ismania;
Varella-Branco, Elisa;
Monfardini, Frederico;
Ferraz, Helen;
Fock, Rodrigo Ambrósio;
Barbosa, Ricardo Henrique Almeida;
Pessoa, André Luiz Santos;
Perez, Ana Beatriz Alvarez;
Lourenço, Naila;
Vibranovski, Maria;
Krepischi, Ana;
Rosenberg, Carla;
Passos-Bueno, Maria Rita

Publication type:

Article

Children with facial paralysis due to Moebius syndrome exhibit reduced autonomic modulation during emotion processing.

Published in:

Journal of Neurodevelopmental Disorders, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s11689-019-9272-2

By:

De Stefani, Elisa;
Ardizzi, Martina;
Nicolini, Ylenia;
Belluardo, Mauro;
Barbot, Anna;
Bertolini, Chiara;
Garofalo, Gioacchino;
Bianchi, Bernardo;
Coudé, Gino;
Murray, Lynne;
Ferrari, Pier Francesco

Publication type:

Article

Novel pathogenic variants and multiple molecular diagnoses in neurodevelopmental disorders.

Published in:

Journal of Neurodevelopmental Disorders, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s11689-019-9270-4

By:

Trinh, Joanne;
Kandaswamy, Krishna Kumar;
Werber, Martin;
Weiss, Maximilian E. R.;
Oprea, Gabriela;
Kishore, Shivendra;
Lohmann, Katja;
Rolfs, Arndt

Publication type:

Article

Impaired neurodevelopmental pathways in autism spectrum disorder: a review of signaling mechanisms and crosstalk.

Published in:

Journal of Neurodevelopmental Disorders, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s11689-019-9268-y

By:

Kumar, Santosh;
Reynolds, Kurt;
Ji, Yu;
Gu, Ran;
Rai, Sunil;
Zhou, Chengji J.

Publication type:

Article

Lesser suppression of response to bright visual stimuli and visual abnormality in children with autism spectrum disorder: a magnetoencephalographic study.

Published in:

Journal of Neurodevelopmental Disorders, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s11689-019-9266-0

By:

Aoki, Sho;
Kagitani-Shimono, Kuriko;
Matsuzaki, Junko;
Hanaie, Ryuzo;
Nakanishi, Mariko;
Tominaga, Koji;
Nagai, Yukie;
Mohri, Ikuko;
Taniike, Masako

Publication type:

Article

Using kinematic analyses to explore sensorimotor control impairments in children with 22q11.2 deletion syndrome.

Published in:

Journal of Neurodevelopmental Disorders, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s11689-019-9271-3

By:

Cunningham, Adam C.;
Hill, Liam;
Mon-Williams, Mark;
Peall, Kathryn J.;
Linden, David E. J.;
Hall, Jeremy;
Owen, Michael J.;
van den Bree, Marianne B. M.

Publication type:

Article

Lifespan trajectory of affect in Cornelia de Lange syndrome: towards a neurobiological hypothesis.

Published in:

Journal of Neurodevelopmental Disorders, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s11689-019-9269-x

By:

Groves, Laura;
Moss, Joanna;
Crawford, Hayley;
Nelson, Lisa;
Stinton, Chris;
Singla, Gursharan;
Oliver, Chris

Publication type:

Article

In the line-up: deleted genes associated with DiGeorge/22q11.2 deletion syndrome: are they all suspects?

Published in:

Journal of Neurodevelopmental Disorders, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s11689-019-9267-z

By:

Motahari, Zahra;
Moody, Sally Ann;
Maynard, Thomas Michael;
LaMantia, Anthony-Samuel

Publication type:

Article

Cognitive training for children and adolescents with fragile X syndrome: a randomized controlled trial of Cogmed.

Published in:

Journal of Neurodevelopmental Disorders, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s11689-019-9264-2

By:

Hessl, David;
Schweitzer, Julie B.;
Nguyen, Danh V.;
McLennan, Yingratana A.;
Johnston, Cindy;
Shickman, Ryan;
Chen, Yanjun

Publication type:

Article

Adaptation to different communicative contexts: an eye tracking study of autistic adults.

Published in:

Journal of Neurodevelopmental Disorders, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s11689-019-9265-1

By:

Parish-Morris, Julia;
Pallathra, Ashley A.;
Ferguson, Emily;
Maddox, Brenna B.;
Pomykacz, Alison;
Perez, Leat S.;
Bateman, Leila;
Pandey, Juhi;
Schultz, Robert T.;
Brodkin, Edward S.

Publication type:

Article

Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders.

Published in:

Journal of Neurodevelopmental Disorders, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s11689-019-9263-3

By:

Costain, Gregory;
Walker, Susan;
Argiropoulos, Bob;
Baribeau, Danielle A.;
Bassett, Anne S.;
Boot, Erik;
Devriendt, Koen;
Kellam, Barbara;
Marshall, Christian R.;
Prasad, Aparna;
Serrano, Moises A.;
Stavropoulos, D. James;
Twede, Hope;
Vermeesch, Joris R.;
Vorstman, Jacob A. S.;
Scherer, Stephen W.

Publication type:

Article

Differentiating social preference and social anxiety phenotypes in fragile X syndrome using an eye gaze analysis: a pilot study.

Published in:

Journal of Neurodevelopmental Disorders, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s11689-019-9262-4

By:

Hong, Michael P.;
Eckert, Eleanor M.;
Pedapati, Ernest V.;
Shaffer, Rebecca C.;
Dominick, Kelli C.;
Wink, Logan K.;
Sweeney, John A.;
Erickson, Craig A.

Publication type:

Article

Static and dynamic postural control deficits in aging fragile X mental retardation 1 (FMR1) gene premutation carriers.

Published in:

Journal of Neurodevelopmental Disorders, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s11689-018-9261-x

By:

Wang, Zheng;
Khemani, Pravin;
Schmitt, Lauren M.;
Lui, Su;
Mosconi, Matthew W.

Publication type:

Article