Results 181 to 190 of about 3,550,881 (351)

Tracking Motor Progression and Device‐Aided Therapy Eligibility in Parkinson's Disease

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To characterise the progression of motor symptoms and identify eligibility for device‐aided therapies in Parkinson's disease, using both the 5‐2‐1 criteria and a refined clinical definition, while examining differences across genetic subgroups.
David Ledingham, Sahana Sathyanarayana, Charlotte B. Stewart, Robyn Iredale, Victoria Foster, Debra Galley, Mark Baker, Nicola Pavese   +7 more
wiley   +1 more source

Effects of different polishing systems on the surface roughness, microhardness and gloss of 3D-printed resins. [PDF]

BMC Oral Health
Büyükpolat M, Aydin N, Karaoğlanoğlu S, Ersöz B, Öztürk F.   +4 more
europepmc   +1 more source

Corporate Policies with Permanent and Transitory Shocks

, 2016
Jean‐Paul Décamps, Sebastian Gryglewicz, Erwan Morellec, Stéphane Villeneuve   +3 more
openalex   +1 more source

Permanent and transitory earnings dynamics and lifetime income inequality in Sweden

, 2023
Johan Gustafsson, Johan Holmberg
openalex   +1 more source

The Diverse Neuromuscular Spectrum of VPS13A Disease

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective VPS13A disease (chorea‐acanthocytosis) is a rare neurodegenerative disorder caused by biallelic variants in VPS13A, typically presenting with hyperkinetic movement disorders, while neuromuscular signs are often mild. The aim of the project was to investigate the frequency and severity of neuromuscular impairment in VPS13A disease ...
Anne Buchberger, Evamaria Riedel, Marie Hackenberg, Alexander Mensch, Stefanie Beck‐Woedl, Joohyun Park, Tobias B. Haack, Bernhard Haslinger, Jan Kirschke, Holger Prokisch, Andreas Hermann, Christian Mawrin, Adrian Danek, Benedikt Schoser, Kevin Peikert, Marcus Deschauer, Isabell Cordts   +16 more
wiley   +1 more source

A Rare Case of Bilateral Mesiodens With Dens Invaginatus Obstructing Permanent Incisor Eruption. [PDF]

Clin Case Rep
Pourheidary H.
europepmc   +1 more source

Purkinje Cell Loss in Essential Tremor: Collective Data From 215 Brains Over a 21‐Year Period

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Essential tremor is a highly prevalent movement disorder. Pathological changes observed in essential tremor cerebella center around Purkinje cells and neighboring neuronal populations. Postmortem studies have variably, but not always, shown reduced Purkinje cell counts in essential tremor compared to controls.
Chloë A. Kerridge, Roberto S. Hernandez, Nora C. Hernandez, Phyllis L. Faust, Elan D. Louis   +4 more
wiley   +1 more source

Synchronous Dentigerous Cysts Managed by Decompression in Non-Syndromic Pediatric Patients: Two Cases with Three-Year Follow-Up. [PDF]

J Clin Med
Buljubasic A, Martinovic D, Mihovilovic A, Jerkovic K, Pojatina A, Rados A, Jerkovic D.   +6 more
europepmc   +1 more source

Copper vapor laser treatment of granuloma of the vermilion border of the lips arising as a complication after permanent make-up

, 2021
Igor Ponomarev, Yury N. Andrusenko, Sergey B. Topchiy, Lyudmila D. Shakina   +3 more
openalex   +2 more sources

Expanding Hereditary Spastic Paraplegias Limits: Biallelic SPAST Variants in Cerebral Palsy Mimics

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Hereditary spastic paraplegias (HSP) are rare neurodegenerative disorders marked by spasticity and lower limb weakness. The most common type, SPG4, is usually autosomal dominant and caused by SPAST gene variants, typically presenting as pure HSP.
Gregorio A. Nolasco, Mònica Roldán, Yalda Jamshidi, Ioannis Georvasilis, Rocío Jadraque Rodríguez, Reza Boostani, Ali Shoeibi, Lluís Armengol, Anna Codina, Ehsan Ghayoor Karimiani, Cristina Hernando‐Davalillo, Loreto Martorell, María Luisa Ramírez Almaraz, Jordi Muchart, Carlos Ortez, Andrés Nascimento, Roser Urreizti, Daniel Natera‐de Benito, Mercedes Serrano   +18 more
wiley   +1 more source