Results 251 to 260 of about 125,324 (315)

The m.14484T>C MT‐ND6 Mutation Presenting with a Hereditary Spastic‐Paraparesis Phenotype

Movement Disorders Clinical Practice, EarlyView.
Gabriel Amorelli, Christelle Nilles, Gerald Pfeffer, Matthew Joel, Davide Martino   +4 more
wiley   +1 more source

Nebulized-Swallowed Albuterol for the Treatment of Food Impaction in Pediatric Patients with Eosinophilic Esophagitis: A Novel Nonendoscopic Approach. [PDF]

J Pediatr Clin Pract
Gunasekaran TS, Gorla K, Berman J, Bhardwaj V.   +3 more
europepmc   +1 more source

Improving Advance Care Planning for People with Parkinson's

Movement Disorders Clinical Practice, EarlyView.
Bradley Lonergan, Peter Miller, Elisabete Marques, Yen Tai, Anette Schrag   +4 more
wiley   +1 more source

What the "Voices" of Dysphagia Are Thinking about Its Future. [PDF]

Int Arch Otorhinolaryngol
Jotz GP, Jotz AV, Dornelles S, Velasco LC, Costa LF, Watanabe LMN, Vilela TGP, Alvarenga EHL, Macedo Filho ED, Manrique D, Elias VS, Mourão L, Furkim AM, Braga NMA, Silva RGD, Santos RS, Angelis EC.   +16 more
europepmc   +1 more source

The Importance of Neuropathology in a Complex Movement Disorder with Primary Familial Brain Calcification

Movement Disorders, EarlyView.
Ida Gugler, Per Svenningsson, Inger Nennesmo, Martin Paucar   +3 more
wiley   +1 more source

Pathogenic Variants in the PRKRA Gene Can Result in a Rapid‐Onset Dystonia‐Parkinsonism‐like Phenotype

Movement Disorders, EarlyView.
Maeve Bradley, Senan Maher, Christian Espinoza‐Vinces, Kathleen Gorman, Tim Lynch, Richard A. Walsh, Alberto J. Espay, Conor Fearon   +7 more
wiley   +1 more source