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Ebiomedicine|September 26, 2025
Broadening dementia risk models: building on the 2024 Lancet Commission report for a more inclusive global frameworkCyprian M Mostert, Chinedu Udeh-Momoh, Andrea Sylvia Winkler, et al.Public Health Nutrition|June 21, 2001
Anaemia in schoolchildren in eight countries in Africa and AsiaA Hall, E Bobrow, S Brooker, et al.Prehospital Emergency Care|August 26, 2014
Rationale, Methodology, and Implementation of a Dispatcher-assisted Cardiopulmonary Resuscitation Trial in the Asia-Pacific (Pan-Asian Resuscitation Outcomes Study Phase 2)Marcus Eng Hock Ong, Sang Do Shin, Hideharu Tanaka, et al.American Journal of Human Genetics|June 9, 2004
Mutations in the DLG3 gene cause nonsyndromic X-linked mental retardationPatrick Tarpey, Josep Parnau, Matthew Blow, et al.Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|September 27, 2021
Dementia in Africa: Current evidence, knowledge gaps, and future directionsRufus O Akinyemi, Joseph Yaria, Akin Ojagbemi, et al.Diabetes Care|April 22, 2018
Gaps in Guidelines for the Management of Diabetes in Low- and Middle-Income Versus High-Income Countries-A Systematic ReviewMayowa O Owolabi, Joseph O Yaria, Meena Daivadanam, et al.Plos One|April 9, 2019
The role of context in implementation research for non-communicable diseases: Answering the 'how-to' dilemmaMeena Daivadanam, Maia Ingram, Kristi Sidney Annerstedt, et al.American Journal of Human Genetics|April 17, 2007
Mutations in ZDHHC9, which encodes a palmitoyltransferase of NRAS and HRAS, cause X-linked mental retardation associated with a Marfanoid habitusF Lucy Raymond, Patrick S Tarpey, Sarah Edkins, et al.JAMA|May 20, 1992
Diagnosis of Duchenne and Becker muscular dystrophies by polymerase chain reaction. A multicenter studyJ S Chamberlain, J R Chamberlain, R G Fenwick, et al.American Journal of Human Genetics|August 2, 2007
Mutations in the BRWD3 gene cause X-linked mental retardation associated with macrocephalyMichael Field, Patrick S Tarpey, Raffaella Smith, et al.Pageof 52