Results 161 to 170 of about 463,400 (366)

State of New York Public Employment Relations Board Decisions from May 27, 2011 [PDF]

open access: yes, 2011
BD_Mtng_5_27_2011.pdf: 547 downloads, before Oct.
New York State Public Employment Relations Board
core   +1 more source

X + Y Scheduling Models in Internal Medicine Residency Programs: A National Survey of Program Directors' Perspectives [PDF]

open access: bronze, 2017
Craig Noronha   +6 more
openalex   +1 more source

Physician Empathy in Public and Private Internal Medicine Residency Training Programs in Pasig City [PDF]

open access: hybrid, 2020
Melody Hope L Lee Yu   +5 more
openalex   +1 more source

The Role of Calcitonin Gene‐Related Peptide in High‐Altitude Headache: A Prospective Field Study

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective High‐altitude headache (HAH) is a common neurological condition associated with rapid ascent to high altitude. The pathophysiological mechanisms underlying HAH remain incompletely understood. Calcitonin gene‐related peptide (CGRP), a neuropeptide implicated in migraine pathophysiology, may play a key role in the pathophysiology of ...
Roman Schniepp   +4 more
wiley   +1 more source

"The good days are amazing", an evaluation of the Writer's in Prison Network [PDF]

open access: yes, 2012
The Writers in Prison Network (WIPN) was established and appointed by the Arts Council in April 1998 to administer the Writers in Residence in Prison Scheme.
Albertson, Katherine, O'Keeffe, Caroline
core  

Relationship Between Neurologic Symptoms and Signs and FMR1 Genotype in Premutation Carriers

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background and Objectives Fragile X‐associated Tremor/Ataxia Syndrome (FXTAS) is the most severe late‐onset condition caused by a premutation in the FMR1 gene, characterized by expanded CGG triplet repeats of 55–200. Clinical presentations of FXTAS, including gait ataxia, kinetic tremor, cognitive decline, and rare Parkinsonism, are linked to ...
Flora Tassone   +8 more
wiley   +1 more source

RNA Sequencing Resolves Cryptic Pathogenic Variants in Mitochondrial Disease

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Mitochondrial diseases are the most common inherited metabolic disorders, characterized by pronounced clinical and genetic heterogeneity that complicates molecular diagnosis. Although DNA‐based sequencing approaches have become standard in genetic testing, up to half of patients remain without a definitive diagnosis.
Zhimei Liu   +21 more
wiley   +1 more source

Home - About - Disclaimer - Privacy