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Effect of disease related biases on the subjective assessment of social functioning in Alzheimer's disease and schizophrenia patients.

Journal of psychiatric research

Jongs N, Penninx B, Arango C, Ayuso-Mateos JL, van der Wee N, Rossum IW, Saris IMJ, van Echteld A, Koops S, Bilderbeck AC, Raslescu A, Dawson GR, Sommer B, Marston H, Vorstman JA, Eijkemans MJ, Kas MJ.
PMID: 33221026
J Psychiatr Res. 2020 Nov 09; doi: 10.1016/j.jpsychires.2020.11.013. Epub 2020 Nov 09.

BACKGROUND: Questionnaires are the current hallmark for quantifying social functioning in human clinical research. In this study, we compared self- and proxy-rated (caregiver and researcher) assessments of social functioning in Schizophrenia (SZ) and Alzheimer's disease (AD) patients and evaluated...

Effect of disease related biases on the subjective assessment of social functioning in Alzheimer's disease and schizophrenia patients.

Journal of psychiatric research

Jongs N, Penninx B, Arango C, Ayuso-Mateos JL, van der Wee N, Rossum IW, Saris IMJ, van Echteld A, Koops S, Bilderbeck AC, Raslescu A, Dawson GR, Sommer B, Marston H, Vorstman JA, Eijkemans MJ, Kas MJ.
PMID: 33221026
J Psychiatr Res. 2022 Jan;145:302-308. doi: 10.1016/j.jpsychires.2020.11.013. Epub 2020 Nov 09.

BACKGROUND: Questionnaires are the current hallmark for quantifying social functioning in human clinical research. In this study, we compared self- and proxy-rated (caregiver and researcher) assessments of social functioning in Schizophrenia (SZ) and Alzheimer's disease (AD) patients and evaluated...

A novel pathogenic MLH1 missense mutation, c.112A > C, p.Asn38His, in six families with Lynch syndrome.

Hereditary cancer in clinical practice

van Riel E, Ausems MG, Hogervorst FB, Kluijt I, van Gijn ME, van Echtelt J, Scheidel-Jacobse K, Hennekam EF, Stulp RP, Vos YJ, Offerhaus GJ, Menko FH, Gille JJ.
PMID: 20704743
Hered Cancer Clin Pract. 2010 Aug 12;8(1):7. doi: 10.1186/1897-4287-8-7.

BACKGROUND: An unclassified variant (UV) in exon 1 of the MLH1 gene, c.112A > C, p.Asn38His, was found in six families who meet diagnostic criteria for Lynch syndrome. The pathogenicity of this variant was unknown. We aim to elucidate...

Structural abnormalities of the left ventricle in hypertrophic cardiomyopathy mutation carriers detectable before the development of hypertrophy.

Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation

Germans T, Wilde AA, van Echteld CJ, Kamp O, Pinto YM, van Rossum AC.
PMID: 18604279
Neth Heart J. 2007;15(4):161-3. doi: 10.1007/BF03085974.

No abstract available.

Showing 1 to 4 of 4 entries