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Human Genetics|January 18, 2022
Biochemical analysis of novel NAA10 variants suggests distinct pathogenic mechanisms involving impaired protein N-terminal acetylationNina McTiernan, Lisbeth Tranebjærg, Anna S Bjørheim, et al.
Hispanic Health Care International : the Official Journal of the National Association of Hispanic Nurses|April 26, 2021
A Culturally Relevant Care Model to Reduce Health Disparities Among Medicaid RecipientsAndrew Johnson, Anita Murcko, Anabell Castro Thompson, et al.
Psychology Research and Behavior Management|June 10, 2024
Social Activities and Depressive Symptoms Among Elderly Based on Rural and Urban Differences in China: a National Cross-Sectional StudyWeiyun Jin, Mark Stephan Felix, Seung Chun Paek, et al.
Health & Social Care in the Community|April 7, 2021
Scoping review: Health needs of the family caregivers of elderly stroke survivorsMark Stephan Felix, Thi Ngoc Phuc Le, Min Wei, et al.
American Journal of Medical Genetics. Part A|November 15, 2014
Truncating mutations in the last exon of NOTCH3 cause lateral meningocele syndromeKaren W Gripp, Katherine M Robbins, Nara L Sobreira, et al.
Health & Social Care in the Community|October 13, 2021
Scoping review: Influence of cisgender male and female genders on health literacy of the elderly peopleMark Stephan Felix, Patreeya Kitcharoen, Thi Ngoc Phuc Le, et al.
Magnetic Resonance in Medicine|October 4, 2024
Fast 3D 31P mapping with a weighted stack of spiral trajectory at 7 TMark Stephan Widmaier, Antonia Kaiser, Salomé Baup, et al.
Human Mutation|April 3, 2014
Mutation update and genotype-phenotype correlations of novel and previously described mutations in TPM2 and TPM3 causing congenital myopathiesMinttu Marttila, Vilma-Lotta Lehtokari, Steven Marston, et al.
Human Genetics|October 20, 2014
De novo mutations in beta-catenin (CTNNB1) appear to be a frequent cause of intellectual disability: expanding the mutational and clinical spectrumAlma Kuechler, Marjolein H Willemsen, Beate Albrecht, et al.
Nature Communications|August 22, 2024
Loss of symmetric cell division of apical neural progenitors drives DENND5A-related developmental and epileptic encephalopathyEmily Banks, Vincent Francis, Sheng-Jia Lin, et al.
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