Results 201 to 210 of about 339,240 (318)

Cognitive Dysfunction Precedes Neuropathology and Motor Abnormalities in the YAC128 Mouse Model of Huntington's Disease [PDF]

, 2005
Jeremy M. Van Raamsdonk, Jacqueline Pearson, Elizabeth Slow, Sazzad M. Hossain, Blair R. Leavitt, Michael R. Hayden   +5 more
openalex   +1 more source

A Pilot Study to Evaluate Neurodevelopmental Outcomes in a Pediatric Cohort With Genodermatoses

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Our study aimed to evaluate cognitive function in individuals with genetic skin disorders involving neuroectoderm (n = 8) compared to individuals with only ectoderm or mesoderm (n = 16) involvement. We hypothesized that neuroectodermal involvement would result in poorer neurocognitive performance.
Sneha A. Rangu, Kierstin Keller, Dong Li, Hope Thomas, Nora O'Connor, Abbas F. Jawad, Allison Thomas, Nina H. Thomas, Hakon Hakonarson, Leslie Castelo‐Soccio, Sarah E. Sheppard   +10 more
wiley   +1 more source

Basic research on postoperative cognitive dysfunction in the past decade: a bibliometric analysis. [PDF]

Front Aging Neurosci
Wu H, Song J, Hu Z, Li H, Zhou Q, Dai C, Gao Y, Ma W.   +7 more
europepmc   +1 more source

Predictors of Cognitive Dysfunction After Subarachnoid Hemorrhage

, 2002
Kurt T. Kreiter, Daphne Copeland, Gary L. Bernardini, Joseph E Bates, Shelley Peery, Jan Claassen, Yanru Du, Yaakov Stern, E. Sander Connolly, Stephan A. Mayer   +9 more
openalex   +1 more source

GABA Targets for the Treatment of Cognitive Dysfunction in Schizophrenia [PDF]

, 2005
David W. Volk, David A. Lewis
openalex   +1 more source

Clinical Insights Into Nabais Sá‐De Vries Syndrome due to a Novel SPOP Mutation: Neuromotor, Cognitive, Adaptive, Behavioral, and Neurovisual Features

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Nabais Sá‐De Vries syndrome (NSDVS) is an extremely rare autosomal dominant disorder caused by SPOP mutations. To date, only 10 cases have been described presenting with intellectual disability, neurological signs and symptoms, and a variable association of dysmorphic features.
Jessica Galli, Erika Loi, Federica Zanardini, Giovanna Baldoni, Francesca Novara, Serena Panigada, Roberto Ciccone, Maria Rosa Cutrì, Alice Bertoletti, Lorenzo Pinelli, Elisa Fazzi   +10 more
wiley   +1 more source

Developing a consensus statement for psychosocial support in active surveillance for prostate cancer

BJUI Compass, Volume 4, Issue 1, Page 104-113, January 2023., 2023
Abstract Purpose Our objective was to prioritise the psychosocial support needs of men on active surveillance for prostate cancer and to develop a consensus statement to provide guidance on best practice psychosocial support for men choosing active surveillance and their families.
Kerri Beckmann, Declan Cahill, Christian Brown, Mieke Van Hemelrijck, Netty Kinsella   +4 more
wiley   +1 more source

Origins of cognitive dysfunction in schizophrenia: clues from age at onset [PDF]

, 2005
Eileen M. Joyce
openalex   +1 more source

Natural History of NAA15‐Related Neurodevelopmental Disorder Through Adolescence

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The NatA N‐terminal acetyltransferase complex is composed of the NAA10 catalytic subunit and the auxiliary subunits NAA15 and HYPK. While those with variants in the enzymatic subunit develop Ogden Syndrome, individuals with variants in the NAA15 coding region develop NAA15‐related neurodevelopmental syndrome, which presents with a wide array ...
Rikhil Makwana, Carolina Christ, Rahi Patel, Elaine Marchi, Randie Harpell, Gholson J. Lyon   +5 more
wiley   +1 more source

Cognitive Dysfunction in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome-Aetiology and Potential Treatments. [PDF]

Int J Mol Sci
Bansal AS, Seton KA, Brooks JCW, Carding SR.   +3 more
europepmc   +1 more source