Results 91 to 100 of about 2,725,849 (257)

Bi‐ and Mono‐Allelic RFC1 Expansion in a North American Cohort With Idiopathic Axonal Neuropathy

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective RFC1 biallelic repeat expansion is increasingly recognized as a cause of chronic idiopathic axonal polyneuropathy (CIAP), but it remains challenging to know who to test. This study aims to determine the prevalence of biallelic and monoallelic RFC1 expansions and their corresponding neuropathy phenotypes in CIAP patients and identify ...
Amro M. Stino   +25 more
wiley   +1 more source

Total phenol content in seed coat of three cultivars of Phaseolus vulgaris L.

open access: yesBiotecnología Vegetal, 2016
The colors of the common bean (Phaseolus vulgaris L.) are related to some of their properties. The objective of this work was to determine the total phenol content in the seed coat of three different bean cultivars. Seeds of the cultivars 'Delicias 364' (
Yenisey Gutierrez Sánchez   +7 more
doaj  

Black Gorringes Evening Coat

open access: yes, 2010
Black belted evening coat; large shoulder pads, gathered and draped from shoulders. Black cord edging down centre front of coat. lined; internal jigger button at waist. Label: Gorringes London SW1. Maker: Gorringes. Date: 1940 - 1949 - from the The Betty
The Betty Smithers Design Collection at Staffordshire University   +1 more
core  

Seven novel KIT mutations in horses with white coat colour phenotypes

open access: yes, 2009
White coat colour in horses is inherited as a monogenic autosomal dominant trait showing a variable expression of coat depigmentation. Mutations in the KIT gene have previously been shown to cause white coat colour phenotypes in pigs, mice and humans. We
Rieder, S.   +17 more
core   +1 more source

Long‐Term Neurologic Exam Findings in People Diagnosed and Treated During Acute HIV Infection

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Evaluate clinical and laboratory correlates of abnormal neurologic exam findings after acute HIV infection (AHI). Methods Participants from the RV254/SEARCH 010 cohort in Bangkok underwent standardized neurologic examinations at Weeks 0 (AHI), 12, 96, and 288 following antiretroviral therapy (ART).
Kathryn B. Holroyd   +118 more
wiley   +1 more source

Natural Frequencies of Levodopa‐Induced Dyskinesia in Parkinson's Disease

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objectives Abnormal involuntary movements, known as dyskinesias, are common complications of levodopa treatment in patients with Parkinson's disease and can significantly impair quality of life. The underlying pathophysiology remains unclear, and current therapeutic options are limited.
Ioannis U. Isaias   +3 more
wiley   +1 more source

The Dirty White Coat

open access: yes, 2018
Learning Objectives: Review the potential germs spread by our white coat To think about how we could limit the spread of germs/contamination To review the selected article critically Determine the relevance of our practice and us as physicians To ...
Reaves, MD, Bruce
core   +1 more source

Childs Coat

open access: yes, 2010
Child's Coat - from the The Betty Smithers Design Collection at Staffordshire University.
The Betty Smithers Design Collection at Staffordshire University   +1 more
core  

White coat impact on children

open access: yes, 2023
The objective of this work is to thoroughly examine and define the differences related to the "white coat effect" and "white coat hypertension," taking into account both adult and pediatric forms.
Klimashevska, Veronika   +1 more
core  

Validation of a Cellular Imaging‐Based Method as a Potential Biomarker for SPG4 Hereditary Spastic Paraplegia

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Hereditary Spastic Paraplegia (HSP) comprises a group of rare genetic diseases characterized by length‐dependent axonal degeneration of the corticospinal tracts and dorsal columns, whose main clinical feature is spastic gait. Pathogenic variants in the SPG4 gene cause Spastic Paraplegia Type 4 (SPG4‐HSP), the most common form of HSP.
Gaia Fattorini   +12 more
wiley   +1 more source

Home - About - Disclaimer - Privacy