Zobrazeno 1 - 10
of 138
pro vyhledávání: '"Rebecca Parks"'
Autor:
Thomas C. Bulea, Amanda Guth, Nathan Sarkar, Andrew Gravunder, Bonnie Hodsdon, Kathleen Farrell, Leora E. Comis, Rebecca Parks, Hirity Shimellis, Vanessa Ndege, Pei-Shu Ho, Ami Mankodi
Publikováno v:
Neuromuscular Disorders. 32:321-331
Grip myotonia and weakness are attractive treatment response biomarkers in clinical trials of myotonic dystrophy type 1 (DM1). There is a need to develop simple, patient-friendly and reproducible methods of quantifying grip myotonia in multisite tria
Autor:
Melanie Quintana, William A. Gahl, Levent Bayman, Scott A. Van Wart, Colleen Jodarski, Claire T. Driscoll, Chia-Ying Liu, Nuria Carrillo, Carla Ciccone, Galen O. Joe, Scott M. Berry, Rebecca Parks, John D. Heiss, Bradley Class, May Christine V. Malicdan, Kennan Bradley, Petcharat Leoyklang, Joseph A. Shrader, John Perreault, Christopher S. Coffey, Christina Slota, Marjan Huizing
Publikováno v:
Genetics in Medicine
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BASE-Bielefeld Academic Search Engine
PURPOSE To evaluate the safety and efficacy of N-acetylmannosamine (ManNAc) in GNE myopathy, a genetic muscle disease caused by deficiency of the rate-limiting enzyme in N-acetylneuraminic acid (Neu5Ac) biosynthesis. METHODS We conducted an open-labe
Autor:
Jordan Wickstrom, Audrey Thurm, Dylan Hammond, Ariane Soldatos, An N Dang Do, Hanna Hildenbrand, Rebecca Parks, Forbes D. Porter, Kisha Jenkins, Katharine E. Alter, Thuy-Tien Nguyen, Cris Zampieri, Jesse Matsubara
Publikováno v:
Am J Med Genet A
In CLN3 disease, impairments in motor function are frequently reported to have later onset compared to visual and cognitive decline, but upper limb motor function has yet to be explored in this population. In a cohort of 22 individuals with CLN3, we
Autor:
Follman, Rebecca Parks1 rfollman@umd.edu
Publikováno v:
Proceedings of the Association for Information Science & Technology. 2015, Vol. 52 Issue 1, p1-8. 8p.
Publikováno v:
Marquee; 2007 Fourth Quarter, Vol. 39 Issue 4, p3-4, 2p, 2 Color Photographs
Autor:
Michael Weiner, Rebecca Parks, Joanne Daggy, Jessica Coffing, Cathy C. Schubert, James E. Slaven
Publikováno v:
Journal of the American Geriatrics Society. 67:818-824
OBJECTIVE Describe the implementation and effects of Mobile Acute Care for Elders (MACE) consultation at a Veterans Affairs Medical Center (VAMC). DESIGN Retrospective cohort analysis. INTERVENTION Veterans aged 65 or older who were admitted to the m
Publikováno v:
The Journal of Pediatrics. 199:206-211
Objectives To characterize the psychosocial profiles of adult women diagnosed with Turner syndrome before (early diagnosis) and at or after (late diagnosis) 13 years of age. Study design Women with Turner syndrome ages 22 and older at evaluation (n =
Autor:
Cathy C, Schubert, Rebecca, Parks, Jessica M, Coffing, Joanne, Daggy, James E, Slaven, Michael, Weiner
Publikováno v:
Journal of the American Geriatrics Society. 67(4)
Describe the implementation and effects of Mobile Acute Care for Elders (MACE) consultation at a Veterans Affairs Medical Center (VAMC).Retrospective cohort analysis.Veterans aged 65 or older who were admitted to the medicine service between October
Autor:
Follman, Rebecca Parks
Formal mentoring programs are a valuable tool for the professional development and socialization of new employees, and for the mentor. However, formal mentoring is often difficult to institutionalize. What are the indications that mentor and mentee s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::34912a7acfdfdbec89eb7ecfff7ea451
Autor:
M. Leach, M. McGuire, Fatou Tounkara, M. Waite, Jahannaz Dastgir, Leslie Nelson, Bonnie Hodsdon, James J. Collins, Ruhi Vasavada, Roxanna M. Bendixen, Elizabeth Harnett, Carsten G. Bönnemann, I. Arveson, Katherine G. Meilleur, Jeffrey S Elliott, Anne Rutkowski, Rebecca Parks, Sandra Donkervoort, Jocelyn Butrum, Michelle Hsia, Monal Punjabi, Melody M. Linton, Carmel Nichols, M. Jain, Katherine Keller
Congenital muscular dystrophy (CMD) comprises a rare group of genetic muscle diseases that present at birth or early during infancy. Two common subtypes of CMD are collagen VI-related muscular dystrophy (COL6-RD) and laminin alpha 2-related dystrophy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5b40bca3a9daed429877d059a135e09
https://europepmc.org/articles/PMC5318262/
https://europepmc.org/articles/PMC5318262/