Teresa Sevilla
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Explore the profile of Teresa Sevilla including associated specialties, affiliations and a list of published articles.
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137
Citations
1406
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Recent Articles
1.
Cortese A, Dohrn M, Curro R, Negri S, Lassuthova P, Pisciotta C, et al.
Brain
. 2025 Feb;
PMID: 39938083
Biallelic loss-of-function mutations in the sorbitol dehydrogenase (SORD) gene cause the most common recessive type of Charcot-Marie-Tooth disease (CMT), CMT-SORD. However, the full genotype-phenotype spectrum and progression of the disease...
2.
Antozzi C, Vu T, Ramchandren S, Nowak R, Farmakidis C, Bril V, et al.
Lancet Neurol
. 2025 Jan;
24(2):105-116.
PMID: 39862879
Background: Given burdensome side-effects and long latency for efficacy with conventional agents, there is a continued need for generalised myasthenia gravis treatments that are safe and provide consistently sustained, long-term...
3.
Canos-Verdecho A, Bermejo A, Castel B, Izquierdo R, Robledo R, Gallach E, et al.
J Clin Med
. 2025 Jan;
14(2).
PMID: 39860657
The aim of this study was to evaluate the effects of spinal cord stimulation (SCS) on pain, neuropathic symptoms, and other health-related metrics in patients with chronic painful peripheral neuropathy...
4.
de Frutos F, Herrador L, Peiro-Aventin B, Eiros R, Limeres Freire J, Zorio E, et al.
Rev Esp Cardiol (Engl Ed)
. 2025 Jan;
PMID: 39827963
Introduction And Objectives: In recent years, several cases of hereditary transthyretin amyloidosis (ATTRv) due to the p.Val142Ile variant have been described in patients without African ancestry. The aim of this...
5.
Muelas N, Carretero-Vilarroig L, Marti P, Azorin I, Frasquet M, Poyatos-Garcia J, et al.
J Neurol
. 2025 Jan;
272(1):97.
PMID: 39775307
Background: Distal myopathies (MPDs) are heterogeneous diseases of complex diagnosis whose prevalence and distribution in specific populations are unknown. Methods: Demographic, clinical, genetic, neurophysiological, histopathological and muscle imaging characteristics of...
6.
Losada Lopez I, Gonzalez-Moreno J, Buades Reines J, Sevilla T, Martinez Valle F, Galan Davila L, et al.
J Clin Med
. 2025 Jan;
13(24.
PMID: 39768509
Hereditary transthyretin amyloidosis (ATTRv) is an autosomal-dominant systemic disease, where amyloid fibrils accumulate especially in the peripheral and autonomic nervous systems and in the heart. The aim of the present...
7.
Marti P, Pitarch-Castellano I, Muelas N, Azorin I, Fores L, Vilchez R, et al.
Neurology
. 2024 Dec;
104(1):e210116.
PMID: 39666917
Background And Objectives: Persistent elevation of serum creatine kinase levels (hyperCKemia) as an isolated manifestation presents a diagnostic challenge. Genetic myopathies are frequently involved; however, studies using next-generation sequencing (NGS)...
8.
Bustamante-Munguira J, Arevalo Abascal A, Amoros Rivera C, Feliz Perez D, Blasco-Turrion S, Sevilla T, et al.
JACC Cardiovasc Interv
. 2024 Dec;
17(23):2835-2838.
PMID: 39663067
No abstract available.
9.
Cabello-Murgui J, Jimenez-Jimenez J, Vilchez J, Azorin I, Marti-Martinez P, Millet E, et al.
Eur J Neurol
. 2024 Sep;
31(12):e16485.
PMID: 39287469
Background And Purpose: ITPR3 encodes type 3 inositol-tri-phosphate receptor (IPR3), a protein expressed in Schwann cells, predominantly in the paranodal region, and involved in the regulation of Ca release from...
10.
Galan Davila L, Martinez Valle F, Buades Reines J, Gonzalez-Moreno J, Losada Lopez I, Sevilla T, et al.
Orphanet J Rare Dis
. 2024 Sep;
19(1):323.
PMID: 39242501
Background: Variant transthyretin amyloidosis (ATTRv) is a rare multisystemic disorder caused by mutations in the transthyretin (TTR) gene. The aim of the present work was to describe the clinical profile...