Results 151 to 160 of about 279,596 (299)

Low math anxiety prevents math achievement decline for urban but not rural Chinese schoolchildren. [PDF]

Front Psychol
Ying Z, Chungang H, Haiying Y, Pavlova A, Malykh A, Malykh S.   +5 more
europepmc   +1 more source

Nonverbal Communication

Higher Brain Function Research, 2013
Jasmin Tiro, Simon J. Craddock Lee, Steven E. Lipshultz, Tracie L. Miller, James D. Wilkinson, Miriam A. Mestre, Barbara Resnick, Donna Miller, Cristina A. Fernandez, David J. Lee, Martica H. Hall, Deborah Lee Young-Hyman, Deborah Lee Young-Hyman, Jennifer Pellowski, Barbara Resnick, Natalie E. Bustillo, Jennifer Pellowski, Vaughn Bryant, Anne Frankel, Riyad Khanfer, Benjamin I. Felleman, G. Alan Marlatt, Hansel Tookes, Deborah M. Stringer, Johan Denollet, Louise C. Hawkley, J. Rick Turner, Wiebke Arlt, Ana Vitlic, Emil C. Toescu, Ornit Chiba-Falek, Elliott A. Beaton, Yori Gidron, Yori Gidron, Yori Gidron, Robert J. Gatchel, Matthew T. Knauf, Marijke Couck, Mustafa Al’Absi, Richard Hoffman, Yori Gidron, Yori Gidron, Leigh A. Sharma, Susan Dorsey, Motohiro Nakajima, Mustafa Al’Absi, Jed E. Rose, Alyssa Haney, Michele L. Okun, Sarah Aldred, Magne Arve Flaten, J. Rick Turner, Salvatore Insana, Elizabeth Galik, Sabrina Segal, Chad Barrett, William Whang, Steven Gambert, Lisa Harnack, Steven Gambert   +59 more
openaire   +3 more sources

Swallowing and Communication in Cockayne Syndrome: Clinical Characteristics and Management

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Cockayne syndrome (CS) is an ultrarare genetic disorder associated with genes encoding proteins involved in DNA repair. The clinical course of CS involves neurodevelopmental and neurodegenerative features, including swallowing and communication impairments.
Abigail M. Spoden, Katlyn E. McGrattan, Peter B. Kang   +2 more
wiley   +1 more source

Misconceptions About Nonverbal Cues to Deception: A Covert Threat to the Justice System?

Frontiers in Psychology, 2020
Vincent Denault, Vincent Denault, Vincent Denault   +2 more
doaj   +1 more source

Psychodynamic treatments taking an embodied perspective and their effect on depressive symptomatology: a systematic review and meta-analysis of randomized controlled trials. [PDF]

Front Psychol
Heider M, Sulz S, Franzen G.
europepmc   +1 more source

35 Individuals With HUWE1‐Related Neurodevelopmental Disorder and Suggested Clinical Evaluations

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT HUWE1 (HECT, UBA, and WWE Domain Containing E3 Ubiquitin Protein Ligase1, OMIM 300697), located at Xp11.22, encodes a ubiquitin ligase that is highly conserved across species. Genetic variants in HUWE1 described in multiple independent studies cause X‐linked intellectual disability, including in the patients identified by Juberg, Marsidi, and ...
Mindy H. Li, Deziree L. Coleman, Kelsey Hogan, Danielle Luz, Lindsay Bhandari, Newell Belnap, Tiffany Busa, Charles Coutton, Klaus Dieterich, Svetlana Gorokhova, Clara Hildebrandt, Rachel Logan, Milena Mariani, Manuela Morleo, Vincenzo Nigro, John Pappas, Rachel Rabin, Kelly Schoch, Angelo Selicorni, Vandana Shashi, Rebecca Spillmann, Jennifer Sullivan, Charlotte Tardy, Samantha A. Schrier Vergano, Brock Grill, Kristin Baranano   +25 more
wiley   +1 more source

Teaching French Language and Culture with French Feature Films on Videocassettes [PDF]

, 1988
Scanlan, Timothy
core   +2 more sources

Long‐Term Follow Up of Two Patients With Variants in the Cluster 1031‐1159 of TRRAP Gene: Expanding the Phenotype of Developmental Delay With or Without Dysmorphic Facies and Autism

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The transformation/transcription domain‐associated protein (TRRAP) gene encodes a large multidomain protein, a member of the phosphatidylinositol 3‐kinase‐related kinase (PIKK) family. TRRAP is a component of the histone acetyltransferase (HAT) complex, and it plays an important role in gene transcription, DNA repair, and cell‐cycle regulation.
Roseli Maria Zechi‐Ceide, Vinicius Contrucci Dantas Segarra, Siulan Vendramini‐Pittoli, Henrique Regonaschi Serigatto, Luiza Virmond, Heloisa Marcelina da Cunha Palhares, Fernanda Jehee, Ana Cristina Victorino Krepischi, Carla Rosenberg, Carlos Henrique Paiva Grangeiro, Nancy Mizue Kokitsu‐Nakata   +10 more
wiley   +1 more source

Early Warning Signs of Autism: A Systematic Review of Nonverbal Behavioral Markers and Early Developmental Red Flags in Children Under 36 Months. [PDF]

Cureus
Ahmad HRM, Hasan Alqudah Q, Elkhalifa HEE, Merghani AS, Abusbaih RR, Ghaleb AN, Mohamed Elhassan OOO, Ahmed A, Jibreel M.   +8 more
europepmc   +1 more source

Clinical, Behavioral and Neuroradiological Phenotype in an Italian Cohort of Patients With Xia Gibbs Syndrome: A Multicenter Cross‐Sectional Study and Systematic Literature Review

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Heterozygous variants in the AHDC1 gene are associated with Xia Gibbs Syndrome (XGS), a genetic disorder with a highly variable phenotype. Cognitive impairment, motor delay, language delay, neonatal hypotonia, and sleep apnea are considered “cardinal” signs of the disease.
Giulia Cinelli, Stefania Della Vecchia, Patrizia Bergonzini, Elisa Caramaschi, Elisabetta Spezia, Claudia Parenti, Simona Filomena Madeo, Laura Lucaccioni, Cavalleri Francesca, Marisa Pugliese, Federico Raviglione, Clara Colonna, Olga Calabrese, Ilaria Stanghellini, Maria Carmen Marongiu, Enrico Biagioni, Anna Rita Ferrari, Roberta Battini, Lorenzo Iughetti   +18 more
wiley   +1 more source