Zobrazeno 1 - 10
of 471
pro vyhledávání: '"A D, Forrest"'
Autor:
Bruce D. Forrest, Namita A. Goyal, Thomas R. Fleming, Paige M. Bracci, Neil R. Brett, Zaeem Khan, Michelle Robinson, Ari Azhir, Michael McGrath
Publikováno v:
Biomedicines, Vol 12, Iss 10, p 2367 (2024)
Background/Objectives: The aim of this study was to estimate the effect of a 6 months’ treatment course of the innate immune modulator NP001 (a pH-adjusted intravenous formulation of purified sodium chlorite), on disease progression, as measured by
Externí odkaz:
https://doaj.org/article/d472239dee954f209612297801e36085
Publikováno v:
Biomedicines, Vol 12, Iss 10, p 2362 (2024)
Background/objective: Amyotrophic lateral sclerosis (ALS) is a diagnosis that incorporates a heterogeneous set of neurodegenerative processes into a single progressive and uniformly fatal disease making the development of a uniformly applicable thera
Externí odkaz:
https://doaj.org/article/d42e9120670f43a3aa48168a2fa01089
Autor:
MILLS, D. FORREST1,2 fmills@sbts.edu
Publikováno v:
Journal of the Evangelical Theological Society. Sep2023, Vol. 66 Issue 3, p523-538. 16p.
Publikováno v:
Cells, Vol 12, Iss 7, p 1031 (2023)
Amyotrophic lateral sclerosis (ALS) is a clinical diagnosis used to define a neurodegenerative process that involves progressive loss of voluntary muscle function and leads to death within 2–5 years after diagnosis, in most cases because of respira
Externí odkaz:
https://doaj.org/article/84e2ee8b77b943fbbd627f70088db07b
Autor:
Christopher B. Forrest, Kathryn D. Forrest, Jennifer L. Clegg, Anna de la Motte, Sandra Amaral, Andrew B. Grossman, Susan L. Furth
Publikováno v:
Journal of Patient-Reported Outcomes, Vol 4, Iss 1, Pp 1-7 (2020)
Abstract Background PROMIS Pediatric patient-reported outcome measures were developed with children from the general population, and their content validity has not been established in children with chronic disease. This study was done to evaluate the
Externí odkaz:
https://doaj.org/article/6be60f6714c349f28b8edd551a49f79b
Autor:
Alexandra D. Forrest, Danielle M. Vuncannon, Jane E. Ellis, Zvi Grunwald, Frederick S. Kaplan
Publikováno v:
Case Reports in Obstetrics and Gynecology, Vol 2022 (2022)
Objective. To evaluate maternal and fetal outcomes in pregnant patients with fibrodysplasia ossificans progressiva (FOP; OMIM#135100), an ultrarare genetic disorder characterized by progressive heterotopic ossification of soft tissues and cumulative
Externí odkaz:
https://doaj.org/article/15bb9c60754e43b68701f459073102e3
Autor:
D. Kim, E. Atenafu, D. Forrest, I. Bence-Bruckler, L. Savoie, M.-M. Keating, L. Busque, R. Delage, A. Xenocostas, E. Liew, P. Laneuville, K. Paulson, T. Stockley, J. Lipton, B. Leber
Publikováno v:
HemaSphere, Vol 6, Pp 59-60 (2022)
Externí odkaz:
https://doaj.org/article/ab7685c77d8742969d612cced8d251cc
Autor:
R. Henderson, Y. Eissa, R. Stubbins, Y. Abou Mourad, S. Chung, D. Forrest, K. Hay, F. Kuchenbauer, S. Nantel, T. Nevill, M. Power, J. Rodrigo, C. Roy, D. Sanford, K. Song, H. Sutherland, C. Toze, J. White, S. Narayanan
Publikováno v:
HemaSphere, Vol 6, Pp 441-442 (2022)
Externí odkaz:
https://doaj.org/article/68b8b1edb13d4c37829d9760a10998dc
Publikováno v:
Biomedicines, Vol 10, Iss 11, p 2907 (2022)
Amyotrophic lateral sclerosis (ALS) is a heterogeneous, progressive, and universally fatal neurodegenerative disease. A subset of ALS patients has measurable plasma levels of lipopolysaccharide (LPS) and C-reactive protein (CRP) consistent with low-g
Externí odkaz:
https://doaj.org/article/30722db4787c4e8c8b9fb21165019488
Autor:
William Douglas Woody, Joshua M. Stewart, Krista D. Forrest, Lourdes Janet Camacho, Skye A. Woestehoff, Karlee R. Provenza, Alexis T. Walker, Steven J. Powner
Publikováno v:
Cogent Psychology, Vol 5, Iss 1 (2018)
Triers of fact evaluated trial materials involving disputed confessions, false-evidence ploys (FEPs) during interrogation, and expert testimony. In two experiments, we assessed pre-deliberation and post-deliberation trial decisions as well as individ
Externí odkaz:
https://doaj.org/article/309d82f314fc49cb8557318b308e78e1