Repositorio Dspace

Listar Enfermedades Neuromusculares por título

Listar Enfermedades Neuromusculares por título

Ordenar por:Orden:Resultados:

  • Long-Term Efficacy and Safety of Inotersen for Hereditary Transthyretin Amyloidosis: NEURO-TTR Open-Label Extension 2-Year Update (S27.008) 
    Brannagan, Thomas H.; Waddington Cruz, Marcia; Wang, Annabel K.; Polydefkis, Michael J.; Dyck, Peter J.; Khella, Sami; Plante-Bordeneuve, Violaine; Berk, John L.; Barroso, Fabio Adrián; Merlini, Giampaolo; Conceição, Isabel; Hughes, Steven G.; Kwoh, Jesse; Jung, Shiangtung W.; Guthrie, Spencer; Pollock, Michael; Benson, Merrill D.; Gertz, Morie; Coelho, Teresa (Lippincott Williams & Wilkins, 2019-03-09)
    Objective: To provide an update on the long-term efficacy and safety of inotersen, an antisense oligonucleotide inhibitor of transthyretin protein production, in patients with hereditary transthyretin amyloidosis (hATTR) ...
  • Long-Term Remission With Low-Dose Rituximab in Myasthenia Gravis: A Retrospective Study 
    Castiglione, Juan Ignacio; Rivero, Alberto Daniel; Barroso, Fabio Adrián; Brand, Patricio; Lautre, Andrea Rosana; Kohler, Alejandro Alfredo (Wolters Kluwer Health, 2022-08-31)
    Objetive: Rituximab (RTX) is a therapeutic option, for patients with myasthenia gravis (MG) not responding to conventional immunosuppressive treatment. In this cohort, we evaluated long-term efficacy of RTX in the treatment ...
  • Parasympathetic denervation of the heart: an early sign of symptomatic TTR-FAP 
    Barroso, Fabio Adrián; Badeigts, Agustina; Orellana, Lucas Gabriel; Lautre, Andrea Rosana; Lorefice, Fernando (Taylor & Francis, 2019-07-25)
    Autonomic nerves may become involved in Transthyretin Familial Amyloid Polyneuropathy (TTR-FAP), and autonomic dysfunction is considered a red flag for TTR-FAP Although autonomic symptoms are easy to recognize for clinicians, ...
  • Phenotypic characteristics of F64L, I68L, I107V, and S77Y ATTRv genotypes from the Transthyretin Amyloidosis Outcomes Survey (THAOS) 
    Gentile, Luca; Diemberger, Igor; Plante-Bordeneuve, Violaine; Mazzeo, Anna; Dori, Amir; Luigetti, Marco; Di Paolantonio, Andrea; Dispenzieri, Angela; Grogan, Martha; Waddington Cruz, Marcia; Adams, David; Inamo, Jocelyn; Kristen, Arnt V.; Cirami, Calogero Lino; Chapman, Doug; Gupta, Pritam; Glass, Oliver; Amass, Leslie; Barroso, Fabio Adrián (Public Library of Science, 2024-01-19)
    Transthyretin amyloidosis (ATTR amyloidosis) is a progressive, multi-systemic disease with wild-type (ATTRwt) and hereditary (ATTRv) forms. Over 130 variants associated with ATTRv amyloidosis have been identified, although ...
  • Phenotypic Differences of Glu89Gln Genotype in ATTR Amyloidosis From Endemic Loci: Update From THAOS 
    Gentile, Luca; Tournev, Ivailo; Amass, Leslie; Chapman, Doug; Mazzeo, Anna; THAOS investigators (Springer, 2021-06-19)
    Introduction Transthyretin amyloidosis (ATTR amyloidosis) is a progressive, clinically heterogeneous disease with spontaneous (wild-type) and hereditary (ATTRv) forms. The Glu89Gln variant is primarily associated with ...
  • Practice guideline for the treatment of familial amyloid polyneuropathy 
    Carretero, Marcelina; Sáez, María S.; Posadas Martínez, María L.; Aguirre, María A.; Sorroche, Patricia; Negro, Agustina; Calandra, Cristian R.; Salutto, Valeria; Lautre, Andrea Rosana; Conti, Eugenia; León Cejas, Luciana; Reisin, Ricardo C.; Nucifora, Elsa M.; Rugiero, Marcelo (Fundación Revista Medicina (Buenos Aires), 2022)
    This clinical practice guideline for the treatment of familial amyloid polyneuropathy is based on the best available evidence of clinical effectiveness. A list of questions was generated with a PICO format focused on the ...
  • Predicting Outcome in Guillain-Barré Syndrome: International Validation of the Modified Erasmus GBS Outcome Score 
    Doets, Alex Y.; Lingsma, Hester F.; Walgaard, Christa; Islam, Badrul; Papri, Nowshin; Davidson, Amy; Yamagishi, Yuko; Kusunoki, Susumu; Dimachkie, Mazen M.; Waheed, Waqar; Kolb, Noah; Islam, Zhahirul; Deen Mohammad, Quazi; Harbo, Thomas; Sindrup, Soren H.; Chavada, Govindsinh; Willison, Hugh J.; Casasnovas, Carlos; Barroso, Fabio Adrián; IGOS consortium (Lippincott Williams & Wilkins, 2021-12-22)
    Background and objectives: The clinical course and outcome of the Guillain-Barré syndrome (GBS) are diverse and vary among regions. The modified Erasmus GBS Outcome Score (mEGOS), developed with data from Dutch patients, ...
  • Pseudo One-And-A-Half Syndrome in a Myasthenia Gravis Patient 
    Marrodán, Mariano; Castiglione, Juan Ignacio; Wainberg, Florencia N.; Rivero, Alberto Daniel (Neurological Society of India, 2022-09)
  • Risk factors for respiratory failure among hospitalized patients with Guillain-Barré syndrome 
    Maskin, Luis Patricio; Wilken, Miguel; Rodríguez Lucci, Federico; Wisnivesky, J. P.; Barroso, Fabio Adrián; Wainsztein, Néstor Adrián (Elsevier, 2021-05-30)
    Background: Guillain-Barré syndrome (GBS) is an acute inflammatory polyneuropathy that can lead to respiratory failure. In this study, we evaluate early clinical risk factors for respiratory failure at the time of hospital ...
  • Síndrome miasteniforme de Lambert-Eaton 
    Hernández, Micaela Anahí; Kohler, Alejandro Alfredo; Marrodán, Mariano; Lautre, Andrea Rosana; Brand, Patricio; Nogués, Martín; Barroso, Fabio Adrián (Revista De Neurología, 2021-08-01)
    Introducción. El síndrome miasteniforme de Lambert-Eaton (LEMS) es una patología paraneoplásica (T-LEMS) o idiopática autoinmunitaria (NT-LEMS) ocasionada por autoanticuerpos contra los canales de calcio dependientes del ...
  • Terapias inmunomoduladoras e inmunosupresoras en polineuropatía desmielinizante inflamatoria crónica refractaria. Revisión de la literatura 
    Zambrano, Darío; Alessandro, Lucas; Barroso, Fabio Adrián (Elsevier, 2021-05-19)
    Introducción La polineuropatía desmielinizante inflamatoria crónica (CIDP) se define como una neuropatía inmunomediada con recaídas y remisiones o un curso progresivo en el tiempo superior a 2 meses. En la mayoría de los ...
  • Transverse Myelitis in Systemic Lupus Erythematosus: Clinical Features and Prognostic Factors in a Large Cohort of Latin American Patients. 
    Chiganer, Edson Hernán; Lessa, Carmen Flora; Di Pace, José Luis; Perassolo, Mónica Beatriz; Carnero Contentti, Edgar; Alessandro, Lucas; Correale, Jorge; Farfan, María Fernanda; Galiana, Graciana Lourdes; Benavides, Marvin Sánchez; Pacello, Franco; Stagno, Mauro; Cardozo, Analía; Cantero, María Belén Nacimiento; Elizaur López, Juan Gabriel; Delgadillo, Pedro Daniel; Melgarejo, Patricia; Acosta Colman, Isabel; Vázquez Báez, Marcos Aurelio; Correa Díaz, Edgar Patricio; Jácome Sánchez, Elisa Carolina; Linares, Magaly Alva; Zamora Tehozol, Erick Adrian; Fragoso-Loyo, Hilda Esther; Quintanilla-González, Lauro; Batún-Garrido, José Antonio de Jesús; Sato, Emilia Inoue; do Reis-Neto, Edgard Torres; Carreño Nigro, María Angela; Hryb, Javier Pablo (Lippincott Williams & Wilkins, 2020-02-05)
    Background: Acute transverse myelitis (ATM) is an infrequent but severe complication of systemic lupus erythematosus (SLE). The purpose of study was to describe clinical features and prognostic factors of patients with ...
  • Treatment-related fluctuations in Guillain-Barré syndrome​: clinical features and predictors of recurrence 
    Alessandro, Lucas; Castiglione, Juan Ignacio; Brand, Patricio; Bruno, Verónica; Barroso, Fabio Adrián (Associacao Arquivos De Neuro-Psiquitria Dr Oswaldo Lange, 2022-05)
    Background: A treatment-related fluctuation (TRF) in a patient with Guillain-Barré syndrome (GBS) is defined as clinical deterioration within two months of symptom onset following previous stabilization or improvements ...
  • Utilidad de la identificación de anticuerpos en neuropatías periféricas, neuronopatías y ganglionopatías: revisión 
    Reisin, Ricardo C.; Salutto, Valeria L.; Aguirre, Florencia; Álvarez, Valeria; Barroso, Fabio Adrián; Bendersky, Mariana; Berardo, Andrés; Bettini, Mariela; Borrelli, Mariano M.; Chaves, Marcelo; Cisneros, Elisa M.; Conti, Eugenia; Crespo, José Manuel; di Egidio, Mariana; Figueredo, María Alejandra; Gargiulo, Gisella; Jáuregui, Agustín; Landriscina, Paula; Cejas, Luciana León; Tillard, Belén; Grupo de Trabajo de Enfermedades Neuromusculares de la Sociedad Neurológica Argentina (Sociedad Argentina de Neurología, 2020-04-04)
    Introducción En los últimos años la identificación de anticuerpos y gammapatías monoclonales ha permitido comprender la fisiopatología y favorecer el diagnóstico y tratamiento de una multiplicidad de neuropatías ...

Buscar en DSpace


Listar

Mi cuenta