Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Ezequiel Piccione"'
Autor:
Navnika Gupta, Afsaneh Shirani, Lakshman Arcot Jayagopal, Ezequiel Piccione, Elizabeth Hartman, Rana Khalil Zabad
Publikováno v:
Brain Sciences, Vol 12, Iss 9, p 1124 (2022)
Autoantibodies against nodal and paranodal proteins, specifically anti-neurofascin antibodies (ANFAs), have been recently described in central and peripheral nervous system demyelinating disorders. We retrospectively reviewed the charts of six indivi
Externí odkaz:
https://doaj.org/article/54e8875ca1f0485682c36860bc62dbe9
Autor:
Erin Dennis, Elizabeth Hartman, Nicolas Cortes-Penfield, Ezequiel Piccione, Pariwat Thaisetthawatkul
Publikováno v:
Journal of Clinical Neuromuscular Disease. 24:147-156
Autor:
Rana Zabad, Krystian Solis, Courtney Venegas, Erin Dennis, Ezequiel Piccione, Brian Westerhuis, Lakshman Arcot Jayagopal
Publikováno v:
Sunday, April 23.
Publikováno v:
Neurology. 97(10)
A 40-year-old woman presented to the neuromuscular clinic for evaluation of chronic right shoulder weakness of 1-year duration. During that time, she noticed progressive difficulties lifting her right arm overhead and reaching for objects on the back
Autor:
Ahmed Bayoumi, Ahmad Armouti, Mohammad Aladawi, Mohamed Elfil, Deaa Abu Jazar, Ezequiel Piccione, Baha Abu-Esheh
Publikováno v:
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques. 49(1)
Background:In January 2020, the first case of Guillain Barre syndrome (GBS) due to COVID-19 was documented in China. GBS is known to be postinfectious following several types of infections. Although causality can only be proven through large epidemio
Publikováno v:
Neurohospitalist
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b6b0411240fd2a02f80f8c8b5320462
https://europepmc.org/articles/PMC8689532/
https://europepmc.org/articles/PMC8689532/
Autor:
Ezequiel Piccione, Navya Joseph
Publikováno v:
Journal of Clinical Neuromuscular Disease. 21:54-56
Publikováno v:
Journal of Clinical Neuromuscular Disease. 20:207-209
We report a 73-year-old man with Val142Ile transthyretin (TTR) amyloidosis and an atypical clinical presentation of upper-extremity-predominant neuropathy without significant autonomic or cardiac involvement. TTR familial amyloid polyneuropathy commo
Autor:
P. James B. Dyck, J. Americo Fernandes, Ezequiel Piccione, Laetitia Truong, Pariwat Thaisetthawatkul
Publikováno v:
Journal of clinical neuromuscular disease. 20(1)
Objectives Mild inflammatory diabetic neuropathies (IDNs) overlap with diabetic sensorimotor neuropathy (DPN) in clinical presentation and electrophysiological and laboratory tests. This study is to determine whether IDN can be differentiated from DP
Publikováno v:
Medicine
Rationale: Sensory neuronopathy can be a devastating peripheral nervous system disorder. Profound loss in joint position is associated with sensory ataxia, and reflects degeneration of large-sized dorsal root ganglia. Prompt recognition of sensory ne