Results 161 to 170 of about 607,748 (277)

[Oral rehabilitation in Sotos syndrome: case report and scoping review of the literature]. [PDF]

open access: yesRev Cient Odontol (Lima)
Trabucco V, Stuardo-Parada A, Leiva C.
europepmc   +1 more source

Agradecimientos a los revisores

open access: yes, 2018
[ES]El comit? cient?fico de FarmaJournal quiere agradecer la colaboraci?n durante el proceso de revisi?n de los art?culos de investigaci?n publicados en este n?mero a varios profesores de la Facultad de Farmacia de la Universidad de Salamanca.
openaire   +5 more sources

SPG4 and Dementia: Expanding the Clinical Spectrum

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Hereditary spastic paraplegia (HSP) is a group of disorders characterized by progressive spasticity and lower limb weakness, with mutations in SPG4/SPAST being the most common cause. Detailed studies and clinical and molecular comparisons across different populations are missing.
Emanuele Panza   +19 more
wiley   +1 more source

Radiocarpal Fracture Dislocation: Minimally Invasive Treatment Assisted by Arthoscopic - Case Report. [PDF]

open access: yesRev Bras Ortop (Sao Paulo)
Aita MA   +5 more
europepmc   +1 more source

The 2017 international classification of the Ehlers–Danlos syndromes

open access: yesAmerican Journal of Medical Genetics. Part C, Seminars in Medical Genetics, 2017
F. Malfait   +44 more
semanticscholar   +1 more source

Revisores

open access: yesRevista Brasileira de Horticultura Ornamental, 2013
openaire   +3 more sources

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

[Early diagnosis of congenital craniofacial differences: a systematic review of current evidence]. [PDF]

open access: yesRev Cient Odontol (Lima)
Cáceres Matta SV   +2 more
europepmc   +1 more source

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

Home - About - Disclaimer - Privacy