Cargando…

Brazilian consensus for diagnosis, management and treatment of hereditary transthyretin amyloidosis with peripheral neuropathy: second edition

Hereditary transthyretin amyloidosis with peripheral neuropathy (ATTRv-PN) is an autosomal dominant inherited sensorimotor and autonomic polyneuropathy with over 130 pathogenic variants identified in the TTR gene. Hereditary transthyretin amyloidosis with peripheral neuropathy is a disabling, progre...

Descripción completa

Detalles Bibliográficos
Autores principales:	Pinto, Marcus Vinicius, França, Marcondes Cavalcante, Gonçalves, Marcus Vinicius Magno, Machado-Costa, Marcela Câmara, Freitas, Marcos Raimundo Gomes de, Gondim, Francisco de Assis Aquino, Marrone, Carlo Domenico, Martinez, Alberto Rolim Muro, Moreira, Carolina Lavigne, Nascimento, Osvaldo J. M., Covaleski, Anna Paula Paranhos, Oliveira, Acary Souza Bulle de, Pupe, Camila Castelo Branco, Rodrigues, Marcia Maria Jardim, Rotta, Francisco Tellechea, Scola, Rosana Herminia, Marques, Wilson, Waddington-Cruz, Márcia
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Thieme Revinter Publicações Ltda. 2023
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10104762/ https://www.ncbi.nlm.nih.gov/pubmed/37059440 http://dx.doi.org/10.1055/s-0043-1764412

Ejemplares similares

Tafamidis for autonomic neuropathy in hereditary transthyretin (ATTR) amyloidosis: a review
por: Cruz, Márcia Waddington
Publicado: (2019)

A Review of Tafamidis for the Treatment of Transthyretin-Related Amyloidosis
por: Waddington Cruz, Márcia, et al.
Publicado: (2015)

Characteristics of Patients with Late- vs. Early-Onset Val30Met Transthyretin Amyloidosis from the Transthyretin Amyloidosis Outcomes Survey (THAOS)
por: Waddington-Cruz, Márcia, et al.
Publicado: (2021)

Feasibility of assessing progression of transthyretin amyloid polyneuropathy using nerve conduction studies: Findings from the Transthyretin Amyloidosis Outcomes Survey (THAOS)
por: Waddington‐Cruz, Márcia, et al.
Publicado: (2021)

Temporal Trends of Wild-Type Transthyretin Amyloid Cardiomyopathy in the Transthyretin Amyloidosis Outcomes Survey
por: Nativi-Nicolau, Jose, et al.
Publicado: (2021)

Estimating the global prevalence of transthyretin familial amyloid polyneuropathy
por: Schmidt, Hartmut H., et al.
Publicado: (2018)

Treatment of Dyslipidemia with Statins and Physical Exercises: Recent Findings of Skeletal Muscle Responses
por: Bonfim, Mariana Rotta, et al.
Publicado: (2015)

Update of the Brazilian consensus recommendations on Duchenne muscular dystrophy
por: Araujo, Alexandra Prufer de Queiroz Campos, et al.
Publicado: (2023)

Guideline of transthyretin-related hereditary amyloidosis for clinicians
por: Ando, Yukio, et al.
Publicado: (2013)

Early intervention with tafamidis provides long-term (5.5-year) delay of neurologic progression in transthyretin hereditary amyloid polyneuropathy
por: Waddington Cruz, Márcia, et al.
Publicado: (2016)

Early intervention with tafamidis provides long-term benefit in delaying neurological progression in patients with transthyretin familial amyloid polyneuropathy
por: Waddington-Cruz, Marcia, et al.
Publicado: (2015)

Optimal practices for the management of hereditary transthyretin amyloidosis: real-world experience from Japan, Brazil, and Portugal
por: Ando, Yukio, et al.
Publicado: (2023)

Evaluation of Mortality During Long-Term Treatment with Tafamidis for Transthyretin Amyloidosis with Polyneuropathy: Clinical Trial Results up to 8.5 Years
por: Merlini, Giampaolo, et al.
Publicado: (2020)

Epidemiological and clinical characteristics of symptomatic hereditary transthyretin amyloid polyneuropathy: a global case series
por: Waddington-Cruz, Márcia, et al.
Publicado: (2019)

Hereditary transthyretin-mediated amyloidosis with polyneuropathy: baseline anthropometric, demographic and disease characteristics of patients from a reference center
por: Sequeira, Vanessa Cristina Cunha, et al.
Publicado: (2021)

Liver‐directed drugs for transthyretin‐mediated amyloidosis
por: Brannagan, Thomas H., et al.
Publicado: (2022)

Wernicke Encephalopathy in COVID-19 Patients: Report of Three Cases
por: Branco de Oliveira, Marcus Vinicius, et al.
Publicado: (2021)

Genetic Determinants of Methicillin Resistance and Virulence among Staphylococcus aureus Isolates Recovered from Clinical and Surveillance Cultures in a Brazilian Teaching Hospital
por: Rodrigues, Marcus Vinicius Pimenta, et al.
Publicado: (2012)

Mild COVID-19 symptoms in a patient with multiple sclerosis in uninterrupted treatment with fingolimod
por: Medeiros da Silva, Marina, et al.
Publicado: (2022)

Definitions, phenomenology, diagnosis, and management of the disorders of laughter and crying in amyotrophic lateral sclerosis (ALS): Consensus from ALS and Motor Neuron Disease Scientific Department of the Brazilian Academy of Neurology
por: Gondim, Francisco de Assis Aquino, et al.
Publicado: (2023)

A Narrative Review of the Role of Transthyretin in Health and Disease
por: Liz, Marcia Almeida, et al.
Publicado: (2020)

Atypical reaction to anesthesia in Duchenne/Becker muscular dystrophy
por: Silva, Helga Cristina Almeida da, et al.
Publicado: (2017)

Clinical and genetic profile of patients enrolled in the Transthyretin Amyloidosis Outcomes Survey (THAOS): 14-year update
por: Dispenzieri, Angela, et al.
Publicado: (2022)

Neuropathy symptom and change: Inotersen treatment of hereditary transthyretin amyloidosis
por: Dyck, P. James B., et al.
Publicado: (2020)

Diffuse skin rash in tropical areas: Dengue fever or COVID-19?()()
por: Pastor Bandeira, Isabelle, et al.
Publicado: (2021)

Early Data on Long-term Impact of Inotersen on Quality-of-Life in Patients with Hereditary Transthyretin Amyloidosis Polyneuropathy: Open-Label Extension of NEURO-TTR
por: Yarlas, Aaron, et al.
Publicado: (2021)

Transthyretin interacts with actin regulators in a Drosophila model of familial amyloid polyneuropathy
por: I. Oliveira da Silva, Marina, et al.
Publicado: (2020)

Inotersen preserves or improves quality of life in hereditary transthyretin amyloidosis
por: Coelho, Teresa, et al.
Publicado: (2019)

Spontaneous pneumothorax: a fatal complication in HIV-infected patients
por: Picinin Safe, Izabella, et al.
Publicado: (2014)

Effect of postoperative tranexamic acid on recurrence rate and complications in chronic subdural hematomas patients: preliminary results of a randomized controlled clinical trial
por: de Paula, Marcus Vinícius Carneiro Torres, et al.
Publicado: (2023)

S-EMG signal compression based on domain transformation and spectral shape dynamic bit allocation
por: Trabuco, Marcel Henrique, et al.
Publicado: (2014)

Treatment of sleep central apnea with non-invasive mechanical ventilation with 2 levels of positive pressure (bilevel) in a patient with myotonic dystrophy type 1
por: Akamine, Ricardo Tera, et al.
Publicado: (2014)

Amyotrophic Lateral Sclerosis: New Perpectives and Update
por: Orsini, Marco, et al.
Publicado: (2015)

ω-Phonetoxins inhibit voltage-gated calcium Ca(V)2.2 ion channel splice isoforms of dorsal root ganglia
por: Castro-Junior, Célio, et al.
Publicado: (2023)

Frequency of hereditary transthyretin amyloidosis among elderly patients with transthyretin cardiomyopathy
por: Maestro‐Benedicto, Alba, et al.
Publicado: (2022)

Clinical, Histological, and Immunohistochemical Findings in Inclusion Body Myositis
por: de Camargo, Leonardo Valente, et al.
Publicado: (2018)

EGCG-Mediated Protection of Transthyretin Amyloidosis by Stabilizing Transthyretin Tetramers and Disrupting Transthyretin Aggregates
por: Zou, Huizhen, et al.
Publicado: (2023)

Marine Natural Products Against Tuberculosis
por: Nora De Souza, Marcus Vinícius
Publicado: (2006)

Plants and Fungal Products with Activity Against Tuberculosis
por: De Souza, Marcus Vinicius Nora
Publicado: (2005)

Complexity Measures of Heart-Rate Variability in Amyotrophic Lateral Sclerosis with Alternative Pulmonary Capacities
por: Pimentel, Renata M. M., et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_s5l3chfqplumlnid409h44oi4e