Results 21 to 30 of about 44,172 (225)

Expanded Phenotype of PAX2-Related Papillorenal Syndrome: A Case Featuring FSGS, Atypical Retinopathy, Cerebellar Hypoplasia, and ADHD. [PDF]

Clin Case Rep
ABSTRACT Papillorenal syndrome (PAPRS), or renal coloboma syndrome, is a rare autosomal dominant disorder caused by PAX2 mutations. It classically manifests with renal hypodysplasia and optic nerve anomalies. However, recent literature suggests an expanding phenotypic spectrum.
Sultana N, Mamun AA, Begum A.
europepmc   +2 more sources

A comprehensive longitudinal analysis of changes during Attention Deficit Hyperactive Disorder pharmacological treatments: Relationships between clinical measures, QbCheck and Conners CPT-II. [PDF]

JCPP Adv
Abstract Background This study aims to evaluate the clinical value of using QbCheck in routine Attention Deficit Hyperactive Disorder (ADHD) clinics by investigating longitudinal inter‐domain relationships between objective neurocognitive outcomes of QbCheck and subjective clinical outcomes: ADHD core symptoms, impairment and quality of life (QoL ...
Lee S, Testa R, Johnson B, Coghill D.
europepmc   +2 more sources

Lewis Atterbury Conner [PDF]

Circulation, 1998
Lewis Atterbury Conner, one of the founding group of the American Heart Association in 1924 and its first president in 1924 to 1925, is honored by the Lewis Conner Memorial Lecture at the annual American Heart Association Scientific Sessions. Conner was born in New Albany, Ind, and received the degree of bachelor of philosophy from the Sheffield ...
C F, Wooley, D, Schneider, A A, Lerner
openaire   +2 more sources

Moderators, mediators and nonspecific predictors of outcome after cognitive rehabilitation of executive functions in a randomised controlled trial [PDF]

, 2017
Moderators, mediators and nonspecific predictors of treatment after cognitive rehabilitation of executive functions in a randomised controlled trial Objective: To explore moderators, mediators and nonspecific predictors of executive functioning after ...
Evans, Jonathan, Løvstad, Marianne, Schanke, Anne-Kristine, Solbakk, Anne-Kristin, Stubberud, Jan, Tornås, Sveinung   +5 more
core   +1 more source

Brain biomarkers and pre-injury cognition are associated with long-term cognitive outcome in children with traumatic brain injury

BMC Pediatrics, 2017
Background Children with traumatic brain injury (TBI) are frequently at risk of long-term impairments of attention and executive functioning but these problems are difficult to predict.
Amy A. Wilkinson, Maureen Dennis, Nevena Simic, Margot J. Taylor, Benjamin R. Morgan, Helena Frndova, Karen Choong, Craig Campbell, Douglas Fraser, Vicki Anderson, Anne-Marie Guerguerian, Russell Schachar, Jamie Hutchison, For the Canadian Critical Care Trials Group (CCCTG), The Canadian Critical Care Translational Biology Group (CCCTBG)   +14 more
doaj   +1 more source

Gender differences in adolescents' academic motivation and classroom behaviour [PDF]

, 2013
© 2013 Taylor & Francis. The present study investigated gender differences in adolescents’ academic motivation and classroom behaviour and gender differences in the extent to which motivation was associated with, and predicted, classroom behaviour ...
Bugler, Myfanwy, McGeown, Sarah P., St Clair-Thompson, Helen   +2 more
core   +1 more source

Testosterone therapy in men with prostate cancer: literature review, clinical experience, and recommendations

Asian Journal of Andrology, 2015
For several decades any diagnosis of prostate cancer (PCa) has been considered an absolute contraindication to the use of testosterone (T) therapy in men.
Abraham Morgentaler, William P Conners
doaj   +1 more source

Methylphenidate Response Prediction in ADHD

Pediatric Neurology Briefs, 1994
Predictors of response to methylphenidate (MPH) among 47 children with ADHD and mental retardation (MR) were studied at the University of Pittsburgh School of Medicine, and the Western Psychiatric Institute and Clinic, Pittsburgh, PA.
J Gordon Millichap
doaj   +1 more source

Novel mutations expand the clinical spectrum of DYNC1H1-associated spinal muscular atrophy [PDF]

, 2015
OBJECTIVE To expand the clinical phenotype of autosomal dominant congenital spinal muscular atrophy with lower extremity predominance (SMA-LED) due to mutations in the dynein, cytoplasmic 1, heavy chain 1 (DYNC1H1) gene.
Al-Lozi, Muhammad T, Baas, Frank, Baloh, Robert H, Benatar, Michael, Calissano, Mattia, Chong, W K Kling, Cirak, Sebahattin, Connolly, Anne M, de Goede, Christian G E L, De Visser, Marianne, Fallon, Penny, Foley, A Reghan, Hadjikoumi, Irene, Hafezparast, Majid, Harms, Matthew B, Klein, Andrea, Mansour, Sahar, Manzur, Adnan Y, Martínez Arroyo, Amaia, Mcwilliam, Catherine, Mercuri, Eugenio, Muntoni, Francesco, Nixon, John, Overweg-Plandsoen, W C G Truus, Phadke, Rahul, Pitt, Matthew, Reilly, Mary M, Robb, Stephanie, Rodriguez Sanz, Aida, Rossor, Alexander M, Scoto, Mariacristina, Sewry, Caroline, Taylor, J Paul, Yang, Michele   +33 more
core   +1 more source

Culturally Appropriate Assessment of Functional Impairment in Diverse Children: Validation of the ADHD-FX Scale With an At-Risk Community Sample [PDF]

, 2017
Objective: In an effort to reduce disparities in ADHD diagnoses and treatment across cultures, the current study sought to establish initial psychometric and cultural properties of the ADHD-FX: a culturally sensitive assessment measure of functional ...
Gerdes, Alyson C., Haack, Lauren Marie
core   +1 more source