Results 241 to 250 of about 1,176,394 (331)

Cancer Precision Medicine in China

open access: yesGenomics, Proteomics & Bioinformatics, 2016
Hui Li
doaj   +1 more source

Precision medicine and music therapy for Parkinson's Disease. [PDF]

open access: yesClin Park Relat Disord
Li-Hua P, Jallow L, Tan Y, Bajinka O.
europepmc   +1 more source

Persistent Leukoencephalopathy Following H1N1 Infection Associated With a Novel MYRF Variant (p.Gly735Asp)

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Mutations in myelin regulatory factor (MYRF) are linked to demyelinating disorders. We report a 38‐year‐old male who developed acute symmetric leukoencephalopathy mimicking a stroke following an influenza A virus infection. While clinical symptoms markedly improved with corticosteroids, MRI revealed persistent white matter lesions, contrasting
Jinghan Hu   +5 more
wiley   +1 more source

Precision Medicine in Diabetic Retinopathy: The Role of Genetic and Epigenetic Biomarkers. [PDF]

open access: yesJ Clin Med
Kaštelan S   +4 more
europepmc   +1 more source

Fibrinogen Changes Before and After Intravenous Thrombolysis as Predictors of Cerebral Injury and Clinical Outcomes in Acute Ischemic Stroke: A Multicenter Prospective Cohort Study

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Plasma fibrinogen is essential in thrombosis and fibrinolysis, yet its dynamic changes pre‐ and post‐intravenous thrombolysis (IVT) for predicting brain injury severity and prognosis in acute ischemic stroke (AIS) patients remain unclear.
Wenhai Zhai   +28 more
wiley   +1 more source

Drug response in the era of precision medicine: A methodological review. [PDF]

open access: yesComput Struct Biotechnol J
Okyere D   +6 more
europepmc   +1 more source

Personalized Drug Delivery Systems: A New Era in Precision Medicine

open access: green
Sravanthi Gandu*, Madhukar Udutha, Uday Kiran Pathri
openalex   +1 more source

Dorsolateral Cervical Cord T2 Hyperintensity in KIF1C‐Related Disease (Spastic Paraplegia 58): Two Long‐Duration Cases

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Pathogenic variants in KIF1C cause Spastic Paraplegia 58 (SPG58), typically presenting with cerebellar ataxia and spastic paraparesis. We report two unrelated patients with spastic paraparesis, cerebellar ataxia, and tremor. Whole‐exome sequence analysis identified novel homozygous variants in the motor domain of KIF1C (NM_006612.6): c.921G>A (
Akihiko Mitsutake   +12 more
wiley   +1 more source

Rethinking Parkinson's disease genetics in the precision medicine era: why genomic diversity matters? [PDF]

open access: yesFront Genet
Pinheiro Gusmão CT   +7 more
europepmc   +1 more source

Home - About - Disclaimer - Privacy