Results 201 to 210 of about 1,747,298 (334)
The Targeted Management (TEAM) Intervention for Reducing Stroke Risk in African American Men: Rationale and Study Design of a Prospective Randomized Controlled Trial
, 2021 Carolyn H. Still, Chris Burant, Shirley M. Moore, Doug Einstadter, Cheryl Killion, Charles S. Modlin, Sophia Sundararajan, John D Thornton, Jackson T. Wright, Martha Sajatovic +9 moreopenalex +2 more sourcesMolecular Profiling of Genes Associated With Methylphenidate Pathway Therapy and Discovery of New Variants in Amazonian Amerindian Populations
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.ABSTRACT
In Attention Deficit Hyperactivity Disorder (ADHD), methylphenidate is one of the most widely used drugs, in which patient response significantly impacts prognosis. This study aimed to characterize the molecular profile of 10 genes associated with methylphenidate therapy.Aline Pasquini Santos, Tatiane Carinta de Souza, Kaio Evandro Cardoso Aguiar, Ana Caroline Alves da Costa, Natasha Monte, Juliana Carla Gomes Rodrigues, Giovanna Gilioli da Costa Nunes, Rita de Cássia Calderaro Coelho, Ândrea Ribeiro‐dos‐Santos, André Maurício Ribeiro dos Santos, Sandro José de Souza, Sidney Emanuel Batista dos Santos, Rommel Mario Rodriguez Burbano, Marianne Rodrigues Fernandes, Ney Pereira Carneiro dos Santos +14 morewiley +1 more sourceContributions of selenoproteins to breast cancer etiology and racial disparity. [PDF]
Cancer Causes ControlBera S, Liu L, Ma W, Xu Z, Sverdlov M, Deaton R, Macias V, Valyi-Nagy K, Kajdacsy-Balla A, Hoskins K, Wiley EL, Kastrati I, Diamond AM. +12 moreeuropepmc +1 more sourcePain coping skills training for African Americans with osteoarthritis study: baseline participant characteristics and comparison to prior studies
, 2019 Kelli D. Allen, Liubov Arbeeva, Crystal W. Cené, Cynthia J. Coffman, Kimberlea F Grimm, Erin Haley, Francis J. Keefe, Caroline T Nagle, Eugene Ž. Oddone, Tamara J. Somers, Yashika Watkins, Lisa C. Campbell +11 moreopenalex +1 more sourceDescriptive Epidemiology From the Myhre Syndrome Foundation Registry: The Value of Self‐Reported Data
American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.ABSTRACT
Myhre syndrome is an ultrarare genetic disease characterized by short stature, distinct craniofacial features, cardiovascular and respiratory fibrosis and stenosis, neurodevelopmental delays, autism, intellectual disability, and hearing loss. The natural history of Myhre syndrome is still not fully understood due to a small patient population ...Mary K. Young, Armelle Pindon, Maggie R. Brand, Kate Wears, Katherine H. Young, Alyssa Mendel, Michael J. Lyons +6 morewiley +1 more sourceAnalysis of Acute Myocardial Infarction Mortality Trends in the African American Population in the United States (1999 - 2020). [PDF]
Cardiol ResGondal MUR, Rovenstine L, Alam F, Baig M, Appiah NK, Acharya A, Khalid F, Khan H, Sarker P, Kiyani Z, Khan T, Jaleel S. +11 moreeuropepmc +1 more sourcePsychiatric Comorbidities and Treatment Modalities in Children With Osteogenesis Imperfecta: A Systematic Review of Mental Health
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT
To evaluate the prevalence of psychiatric signs and symptoms and describe psychotherapeutic and psychopharmacological interventions among children with osteogenesis imperfecta (OI). PRISMA guidelines were followed, and the study was registered in PROSPERO (CRD42024588284). Studies (n = 1419) were identified across five databases.Julia M. Morales, Camille F. Villar, Beatriz Varman, Gianna M. Colombo, Danqi Li, Sarah J. Sadek, Marie‐Eve Robinson, Chaya N. Murali, Kara Ayers, Jocelyn Gomez, Brendan Lee, V. Reid Sutton, Eric A. Storch, Andrew D. Wiese +13 morewiley +1 more source
