Results 61 to 70 of about 151,971 (294)

Genomic Contributors to Congenital Diaphragmatic Hernia: Results of Exome Sequencing in 560 Probands and Cross Reference of Findings in an Independent Cohort

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT There is a strong genetic contribution to the etiology of congenital diaphragmatic hernia (CDH). This study evaluated genetic testing results and diagnostic yield for fetuses and children with CDH. This was a retrospective cohort study of exome sequencing (ES) performed at GeneDx for fetuses and children ≤ 18 years of age with CDH compared ...
Justin Blair, Kevin Carratu, Natalie E. Rintoul, Holly L. Hedrick, William H. Peranteau, Catherine M. Avitabile, Kirsty McWalter, Paul Kruszka, Ian D. Krantz, K. Taylor Wild   +9 more
wiley   +1 more source

Effectiveness of hypnotherapy in the treatment of attention-deficit/hyperactivity disorder

Revista Electrónica Dr. Zoilo E. Marinello Vidaurreta, 2021
Background: attention-deficit/hyperactivity disorder is inconsistent with the development of the individual and frequent during childhood.Objective: to assess the effectiveness of a hypnotherapeutic model in patients with attention-deficit/hyperactivity ...
Adolfo Rafael Lambert-Delgado, Alberto Erconvaldo Cobián-Mena, Gabriel Pérez-Almoza, Julio Armando Sánchez-Delgado, Nailé Edita Sánchez-Lara   +4 more
doaj  

Selected intervention approaches available for children diagnosed with attention deficit and hyperactivity disorder [PDF]

, 2001
Plan BThis study had a two-fold purpose. First, to review, analyze, criticize, and draw sets of implications from literature regarding material on multimodal intervention approaches for students who had attention deficit-hyperactivity disorder.
Brunke, Gina L.
core  

Gray’s revised Reinforcement Sensitivity Theory in relation to Attention-Deficit/Hyperactivity and Tourette-like behaviors in the general population [PDF]

, 2015
Attention-Deficit/Hyperactivity Disorder (ADHD) and Tourette Syndrome (TS) present as distinct conditions clinically; however, they show comorbidity and inhibitory control deficits have been proposed to underlie both.
Kantini, Ebrahim, Kantini, E, Checkley, HLR, Cassaday, HJ, Heym, Nadja, Heym, N, Checkley, Hannah L.R., Cassaday, Helen J.   +7 more
core   +1 more source

Phenotype Expansion of Malan Syndrome: New Cases and a Review of the Literature

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Malan syndrome is an ultra‐rare overgrowth syndrome caused by pathogenic variants or deletions in nuclear factor one X (NFIX) located at 19p13.2. Here, we report a comprehensive literature review and phenotyping of known patients with Malan syndrome and present a novel cohort of eight patients.
Alex F. Nisbet, Sylvie A. Adams, Zoe S. Katz, Christal G. Delagrammatikas, Kosuke Izumi, Winifred Sigal, Kim Ventarola, Elaine H. Zackai, Julia E. Reid, Grant T. Liu, Jennifer M. Kalish   +10 more
wiley   +1 more source

High‐Resolution Genomic Characterization of WAGR Spectrum Disorder: Insights From a Novel Cohort and Literature Synthesis, and Validation of Patient‐Reported Data

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT WAGR spectrum disorder (WAGRSD) is an ultra‐rare congenital disorder caused by heterozygous deletion of chromosome 11p13. While classically associated with Wilms tumor, Aniridia, Genitourinary anomalies, and a Range of developmental delays, accurate delineation of the deletion is critical for prognosis because the phenotypic spectrum extends ...
Andrew M. George, Bamelak T. Duki, Zoe S. Katz, Aravind Viswanathan, Suzanne P. MacFarland, Evan R. Hathaway, Caitlin Monahan, John Morris, Kelly L. Trout, Shari M. Krantz, Arupa Ganguly, Jennifer M. Kalish   +11 more
wiley   +1 more source

Practitioner review: pathways to care for ADHD - a systematic review of barriers and facilitators [PDF]

, 2015
Background. Attention-Deficit/Hyperactivity Disorder (ADHD) is a common neurodevelopmental disorder starting in childhood that may persist into adulthood.
Walid Sorour (7243601), Daley, David, Schneider, Justine, Schneider, J, Moldavsky, Maria, Maria Moldavsky (7243589), Kapil Sayal (119323), Daley, D, Puja Kochhar (7243595), Kochhar, P, Moldavsky, M, Mills, Jon, Sayal, K, David Daley (625223), Mills, J, Coates, Janine, Justine Schneider (4182823), Wright, Nicola, Sorour, W, Ipsita Chakrabarti (7243592), Chakrabarti, Ipsita, Sayal, Kapil, Sorour, Walid, Chakrabarti, I, Nicola Wright (834999), Kochhar, Puja, Janine Coates (3089055), Jon Mills (7243598), Coates, J, Wright, N   +29 more
core   +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

The measurement of the symptoms of ADHD in the NICHQ Vanderbilt Assessment Scale for Parent (VADPRS) and for Teacher (VADTRS)

Psychiatria i Psychologia Kliniczna, 2014
The presence of several inattentive or hyperactive, impulsive symptoms in two or more situations (at home, school, in other activities) is required for the diagnosis of attention deficit hyperactivity disorder. There is clear evidence that the symptoms
Halina Kądziela-Olech
doaj   +1 more source

Are language production problems apparent in adults who no longer meet diagnostic criteria for attention-deficit/hyperactivity disorder?

, 2012
In this study, we examined sentence production in a sample of adults (N = 21) who had had attention-deficit/hyperactivity disorder (ADHD) as children, but as adults no longer met DSM-IV diagnostic criteria (APA, 2000).
Veld, Sean N., Sean N. Veld, Veld, Sean, Engelhardt, Paul, Fernanda Ferreira, Engelhardt, Paul E., Nigg, Joel T., Ferreira, Fernanda, Paul E. Engelhardt, Joel T. Nigg   +9 more
core   +1 more source