State of New York Public Employment Relations Board Decisions from May 27, 2011 [PDF]
BD_Mtng_5_27_2011.pdf: 547 downloads, before Oct.
New York State Public Employment Relations Board
core +1 more source
Gender and Racial Disparities in Diagnostic Radiology Residency Programs: A Decade of Trends and Implications for Diversity and Inclusion [PDF]
Imran Bitar +4 more
openalex +1 more source
X + Y Scheduling Models in Internal Medicine Residency Programs: A National Survey of Program Directors' Perspectives [PDF]
Craig Noronha +6 more
openalex +1 more source
Physician Empathy in Public and Private Internal Medicine Residency Training Programs in Pasig City [PDF]
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
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]
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
Punitive Residency Revocation: The Most Recent Tool of Forcible Transfer [PDF]
Community Action Center at Al-Quds University
openalex +1 more source
Relationship Between Neurologic Symptoms and Signs and FMR1 Genotype in Premutation Carriers
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
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

