Works matching IS 18661947 AND DT 2016 AND VI 8 AND IP 1

Results: 12

An investigation of NFXL1, a gene implicated in a study of specific language impairment.

Published in:

Journal of Neurodevelopmental Disorders, 2016, v. 8, n. 1, p. 1, doi. 10.1186/s11689-016-9146-9

By:

Nudel, Ron

Publication type:

Article

Development, behavior, and biomarker characterization of Smith-Lemli-Opitz syndrome: an update.

Published in:

Journal of Neurodevelopmental Disorders, 2016, v. 8, n. 1, p. 1, doi. 10.1186/s11689-016-9145-x

By:

Thurm, Audrey;
Tierney, Elaine;
Farmer, Cristan;
Albert, Phebe;
Joseph, Lisa;
Swedo, Susan;
Bianconi, Simona;
Bukelis, Irena;
Wheeler, Courtney;
Sarphare, Geeta;
Lanham, Diane;
Wassif, Christopher;
Porter, Forbes

Publication type:

Article

Specific pattern of maturation and differentiation in the formation of cortical tubers in tuberous sclerosis omplex (TSC): evidence from layer-specific marker expression.

Published in:

Journal of Neurodevelopmental Disorders, 2016, v. 8, n. 1, p. 1, doi. 10.1186/s11689-016-9142-0

By:

Mühlebner, Angelika;
Iyer, Anand;
van Scheppingen, Jackelien;
Anink, Jasper;
Jansen, Floor;
Veersema, Tim;
Braun, Kees;
Spliet, Wim;
van Hecke, Wim;
Söylemezoğlu, Figen;
Feucht, Martha;
Krsek, Pavel;
Zamecnik, Josef;
Bien, Christian;
Polster, Tilman;
Coras, Roland;
Blümcke, Ingmar;
Aronica, Eleonora

Publication type:

Article

Developmental trajectories of executive functions in 22q11.2 deletion syndrome.

Published in:

Journal of Neurodevelopmental Disorders, 2016, v. 8, n. 1, p. 1, doi. 10.1186/s11689-016-9141-1

By:

Maeder, Johanna;
Schneider, Maude;
Bostelmann, Mathilde;
Debbané, Martin;
Glaser, Bronwyn;
Menghetti, Sarah;
Schaer, Marie;
Eliez, Stephan

Publication type:

Article

Reduced engagement with social stimuli in 6-month-old infants with later autism spectrum disorder: a longitudinal prospective study of infants at high familial risk.

Published in:

Journal of Neurodevelopmental Disorders, 2016, v. 8, n. 1, p. 1, doi. 10.1186/s11689-016-9139-8

By:

Jones, E.;
Venema, K.;
Earl, R.;
Lowy, R.;
Barnes, K.;
Estes, A.;
Dawson, G.;
Webb, S.

Publication type:

Article

Neural selectivity for communicative auditory signals in Phelan-McDermid syndrome.

Published in:

Journal of Neurodevelopmental Disorders, 2016, v. 8, n. 1, p. 1, doi. 10.1186/s11689-016-9138-9

By:

Wang, A.;
Lim, Teresa;
Jamison, Jesslyn;
Bush, Lauren;
Soorya, Latha;
Tavassoli, Teresa;
Siper, Paige;
Buxbaum, Joseph;
Kolevzon, Alexander

Publication type:

Article

Limited impact of Cntn4 mutation on autism-related traits in developing and adult C57BL/6J mice.

Published in:

Journal of Neurodevelopmental Disorders, 2016, v. 8, n. 1, p. 1, doi. 10.1186/s11689-016-9140-2

By:

Molenhuis, Remco;
Bruining, Hilgo;
Remmelink, Esther;
de Visser, Leonie;
Loos, Maarten;
Burbach, J.;
Kas, Martien

Publication type:

Article

Neural selectivity for communicative auditory signals in Phelan-McDermid syndrome.

Published in:

Journal of Neurodevelopmental Disorders, 2016, v. 8, n. 1, p. 1, doi. 10.1186/s11689-016-9138-9

By:

Wang, A.;
Lim, Teresa;
Jamison, Jesslyn;
Bush, Lauren;
Soorya, Latha;
Tavassoli, Teresa;
Siper, Paige;
Buxbaum, Joseph;
Kolevzon, Alexander

Publication type:

Article

Journal of Neurodevelopmental Disorders reviewer acknowledgement 2015.

Published in:

Journal of Neurodevelopmental Disorders, 2016, v. 8, n. 1, p. 1, doi. 10.1186/s11689-016-9137-x

By:

Piven, Joseph

Publication type:

Article

Genomic sequencing of a dyslexia susceptibility haplotype encompassing ROBO1.

Published in:

Journal of Neurodevelopmental Disorders, 2016, v. 8, n. 1, p. 1, doi. 10.1186/s11689-016-9136-y

By:

Massinen, Satu;
Wang, Jingwen;
Laivuori, Krista;
Bieder, Andrea;
Tapia Paez, Isabel;
Jiao, Hong;
Kere, Juha

Publication type:

Article

Atypical functional connectivity in resting-state networks of individuals with 22q11.2 deletion syndrome: associations with neurocognitive and psychiatric functioning.

Published in:

Journal of Neurodevelopmental Disorders, 2016, v. 8, n. 1, p. 1, doi. 10.1186/s11689-016-9135-z

By:

Mattiaccio, Leah;
Coman, Ioana;
Schreiner, Matthew;
Antshel, Kevin;
Fremont, Wanda;
Bearden, Carrie;
Kates, Wendy

Publication type:

Article

Mavoglurant in adolescents with fragile X syndrome: analysis of Clinical Global Impression-Improvement source data from a double-blind therapeutic study followed by an open-label, long-term extension study.

Published in:

Journal of Neurodevelopmental Disorders, 2016, v. 8, n. 1, p. 1, doi. 10.1186/s11689-015-9134-5

By:

Bailey, Donald;
Berry-Kravis, Elizabeth;
Wheeler, Anne;
Raspa, Melissa;
Merrien, Florence;
Ricart, Javier;
Koumaras, Barbara;
Rosenkranz, Gerd;
Tomlinson, Mark;
von Raison, Florian;
Apostol, George

Publication type:

Article