Results 271 to 280 of about 16,814,361 (358)

Discovery and Targeted Proteomic Studies Reveal Striatal Markers Validated for Huntington's Disease

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Clinical trials for Huntington's disease (HD) enrolling persons before clinical motor diagnosis (CMD) lack validated biomarkers. This study aimed to conduct an unbiased discovery analysis and a targeted examination of proteomic biomarkers scrutinized by clinical validation. Methods Cerebrospinal fluid was obtained from PREDICT‐HD and
Daniel Chelsky, Cara Joyce, H. Jeremy Bockholt, Paul A. Rudnick, William H. Adams, Fiona McAllister, Justin W. Smock, Michael A. Newton, Jane S. Paulsen   +8 more
wiley   +1 more source

Occurrence of human infection with Salmonella Typhi in sub-Saharan Africa. [PDF]

Sci Data
Kim JH, Parajulee P, Nguyen TT, Wasunkar S, Mogasale V, Park SE, Panzner U, Mogeni OD, Im J, Marks F.   +9 more
europepmc   +1 more source

The effects of class wide peer tutoring on fifth grade students' weekly spelling test performance.

, 2013
Lindsay Kryszak
openalex   +1 more source

Effectiveness and Safety of Nusinersen and Risdiplam in Spinal Muscular Atrophy: A Systematic Review

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Spinal Muscular Atrophy (SMA) is a rare genetic disorder marked by progressive muscle weakness and mobility loss. It has a profound physical, emotional and social impact on patients and caregivers, requiring comprehensive medical and supportive care.
Amin Mehrabian, Peter Auguste, Amy Grove, Anna Brown, Janette Parr, Mubarak Patel, Furqan Butt, Jeremiah Donoghue, Mehdi Yousefi, Jo Parsons   +9 more
wiley   +1 more source

Usefulness of Cerebrospinal Fluid Alzheimer's disease biomarkers in older patients: Evidence from a national multicenter prospective study. [PDF]

J Prev Alzheimers Dis
Decaix T, Mouton-Liger F, Dumurgier J, Cognat E, Vrillon A, Hugon J, Hourregue C, Bouaziz-Amar E, Wallon D, Muraine MQ, Troussière AC, Magnin E, Duron E, Philippi N, Blanc F, Gabelle A, Croisile B, Jager A, Pasquier F, Schraen S, Sayette V, Beaufils É, Miguet-Alfonsi C, Paquet C, Lilamand M.   +24 more
europepmc   +1 more source

Clinical and economic impact of genome-wide non-invasive prenatal testing (NIPT) as a first-tier screening method compared to targeted NIPT and first-trimester combined testing: A modeling study

Lisanne van Prooyen Schuurman, Harry J. de Koning, E. Meier, Robert-Jan H. Galjaard, Nicolien T. van Ravesteyn   +4 more
openalex   +1 more source

Genome-wide association testing of Biolog GenIII phenotypes vs. accessory genome presence/absence

, 2019
Florent Lassalle
openalex   +1 more source

An Out‐of‐Place Etiology: Recognizing FMR1 Premutation in the Memory Clinic

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT The FMR1 gene premutation (55–200 CGG repeats) is usually associated with a wide range of symptoms and phenotypes within the Fragile X‐tremor/ataxia syndrome (FXTAS), but may also manifest as predominant or isolated cognitive decline. We describe three male patients referred for progressive cognitive impairment and behavioral changes. Standard
Guido Greco, Caterina Motta, Enrica Marchionni, Maria Rosaria D'Apice, Carlangelo Carrese, Giuseppe Novelli, Alessandro Martorana, Chiara Giuseppina Bonomi   +7 more
wiley   +1 more source

Unraveling Homocysteine's Role in Dementia: No Specific Association with Alzheimer's Disease, but a Connection to White Matter Hyperintensities. [PDF]

Aging Dis
Decaix T, Lilamand M, Götze K, Mouton-Liger F, Cognat E, Hugon J, Bouaziz-Amar E, Sindzingre L, Dumurgier J, Paquet C.   +9 more
europepmc   +1 more source

Plate technique adaptation of the widal test.

Indian journal of pathology & microbiology, 1981
S K, Hamsavadani, R, Vasanthakumari, M, Mallika   +2 more
openaire   +1 more source