Results 241 to 250 of about 792,865 (388)

A novel method to assess motor planning deficits in patients with parkinson's disease and mild cognitive impairment. [PDF]

Sci Rep
Maffitt NJ, Banerjee S, Sarkar S, Majumdar S, Choudhury S, Kumar H, Soteropoulos DS, Kraskov A.   +7 more
europepmc   +1 more source

Neuropsychological methods in mild cognitive impairment

, 2004
Valérie Hahn‐Barma, Céline Chamayou, Christina Rogan, Marie Sarazin, Bruno Dubois   +4 more
openalex   +1 more source

Speech and Language Disorders Associated With 7q31 Deletions Implicating FOXP2

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Some 7q31 deletions encompass FOXP2, a gene long associated with speech and language disorders. Intragenic pathogenic FOXP2 variants cause FOXP2‐related speech and language disorder, which has been well characterized in the literature. Conversely, the phenotype associated with 7q31 deletions is neglected.
Lottie D. Morison, Ruth Braden, David J. Amor, Angela T. Morgan   +3 more
wiley   +1 more source

Research progress of multimodal biomarkers in the early diagnosis of mild cognitive impairment in Parkinson's disease. [PDF]

Front Neurol
Guo H, Shen X, Lyu M, Zhou G, Chen C, Xing B, Xie Y.   +6 more
europepmc   +1 more source

Regulatory aspects of mild cognitive impairment: toward a harmonized perspective

, 2004
Peter J. Whitehouse
openalex   +1 more source

Mild Cognitive Impairment

Journal of the Korean Neurological Association, 2016
Ae Young Lee, Eungseok Oh
openaire   +2 more sources

CLCN4‐Related Neurodevelopmental Condition: Characterization of Speech and Language Abilities

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Speech and language difficulties are a core feature of the CLCN4‐related neurodevelopmental condition, but these have not been well described. Here we systematically phenotype speech and language in 13 participants (10 female, aged 1 year 10 months–41 years 10 months) with pathogenic CLCN4 variants (12 missense de novo, 1 premature stop codon ...
Alexandra Garrett, Vera M. Kalscheuer, Rebeca Ridings Figueroa, Elizabeth E. Palmer, Angela T. Morgan   +4 more
wiley   +1 more source

Hippocampal iron patterns in aging and mild cognitive impairment. [PDF]

Front Aging Neurosci
Kagerer SM, Vionnet L, van Bergen JMG, Meyer R, Gietl AF, Pruessmann KP, Hock C, Unschuld PG.   +7 more
europepmc   +1 more source

PET Network Abnormalities and Cognitive Decline in Patients with Mild Cognitive Impairment [PDF]

, 2005
Davangere P. Devanand, Christian Habeck, Matthias H. Tabert, Nikolaos Scarmeas, Gregory H. Pelton, James R. Moeller, Brett D. Mensh, Tyler Tarabula, Ronald L. Van Heertum, Yaakov Stern   +9 more
openalex   +1 more source

Trisomy 5p: Long Recognized, Rarely Published‐ Three New Cases and Review of the Literature

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Complete trisomy 5p is a rare chromosomal disorder caused by a duplication of the short arm of chromosome 5. Current data suggest that complete trisomy 5p presents as a distinct clinical syndrome including but not limited to seizures, developmental delays, facial dysmorphisms, failure to thrive, and recurrent respiratory infections.
Gabriela J. Kim, Kristen N. Lee, Amanda B. Pritchard   +2 more
wiley   +1 more source