Results 151 to 160 of about 7,742,036 (343)

Multiple Transition Abnormalities [PDF]

, 2020
openaire   +1 more source

Heterozygous Mutation of Drosophila Opa1 Causes the Development of Multiple Organ Abnormalities in an Age-Dependent and Organ-Specific Manner

, 2009
Parvin Shahrestani, Hung‐Tat Leung, Phung Khanh Le, William L. Pak, Stephanie Tse, Karen Ocorr, Taosheng Huang   +6 more
openalex   +2 more sources

Morphostructural MRI Abnormalities Related to Neuropsychiatric Disorders Associated to Multiple Sclerosis [PDF]

, 2013
Simona Bonavita, Gioacchino Tedeschi, Antonio Gallo   +2 more
openalex   +1 more source

Functional Connectivity Linked to Cognitive Recovery After Minor Stroke

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Patients with minor stroke exhibit slowed processing speed and generalized alterations in functional connectivity involving frontoparietal cortex (FPC). The pattern of connectivity evolves over time. In this study, we examine the relationship of functional connectivity patterns to cognitive performance, to determine ...
Vrishab Commuri, Isabella Dallasta, Ciaran Stone, Sophia Girgenti, Neda Gould, Rafael H. Llinas, Jonathan Z. Simon, Elisabeth Breese Marsh   +7 more
wiley   +1 more source

Population differences in the associations between chromosomal abnormalities and overall survival of multiple myeloma

Bei Wang, Benjamin A. Derman, Madina Sukhanova, Daniel Appelbaum, John Cursio, Wei Zhang, Andrzej Jakubowiak, Brian C.‐H. Chiu   +7 more
openalex   +1 more source

Abnormal Dosage Compensation of Reporter Genes Driven by the Drosophila Glass Multiple Reporter (GMR) Enhancer-Promoter

, 2011
Corey Laverty, Fang Li, Esther J. Belikoff, Maxwell J. Scott   +3 more
openalex   +2 more sources

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

Genomic alterations and abnormal expression of APE2 in multiple cancers [PDF]

, 2020
Katherine A. Jensen, Xinghua Shi, Shan Yan   +2 more
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

Clinician and radiologist chest radiography interpretation variability in a high-TB-burden setting. [PDF]

IJTLD Open
Navuluri N, Kipchirchir C, Lagat D, Birgen E, Kitur S, Thielman N, Que LG, Wools-Kaloustian K, Kussin PS, Tailor TD.   +9 more
europepmc   +1 more source