Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Alzira A. Siqueira-Carvalho"'
Autor:
Fábio Fernandes, Georgina del Cisne Jadán Luzuriaga, Guilherme Wesley Peixoto da Fonseca, Edileide Barros Correia, Alzira Alves Siqueira Carvalho, Ariane Vieira Scarlatelli Macedo, Otavio Rizzi Coelho-Filho, Phillip Scheinberg, Murillo Oliveira Antunes, Pedro Vellosa Schwartzmann, Sandrigo Mangini, Wilson Marques, Marcus Vinicius Simões
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-10 (2024)
Abstract Background Transthyretin amyloidosis (ATTR) is a multisystem disease caused by the deposition of fibrillar protein in organs and tissues. ATTR genotypes and phenotypes are highly heterogeneous. We present data on physical signs and symptoms,
Externí odkaz:
https://doaj.org/article/13652cdb50a54f85899e744d9db684ce
Autor:
Helga C. A. Azevedo, Lúcia I. Z. Mendonça, Paulo N. B. Salum, Mary S. Carvalho, Sueli K. Nagahashi-Marie, Alzira A. Siqueira-Carvalho, Maria A. Cerqueira, Umbertina C. Reed, José A. Levy
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 54, Iss 4, Pp 595-600 (1996)
Miotonia é o fenômeno da diminuição da velocidade de relaxamento muscular após contração, estímulo mecânico ou elétrico. As miotonias congênitas são afecções hereditárias e não apresentam distrofia muscular. Atualmente, a tendência
Externí odkaz:
https://doaj.org/article/5346dae2ce0f4bf09d59b9d46022fbc0
Autor:
Helga C. A. Azevedo, Mary S. Carvalho, Sueli K. Nagahashi -Marie, Martha N. S. Delgado, Alzira A. Siqueira-Carvalho, Paulo N. B. Salum, José A. Levy
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 54, Iss 1, Pp 114-119 (1996)
Os autores relatam o caso de paciente do sexo feminino de 18 anos de idade com fraqueza lentamente progressiva nos quatro membros desde a infância, sem antecedentes relevantes. O exame neurológico mostrou déficit motor discreto proximal e distal c
Externí odkaz:
https://doaj.org/article/ce27d0d294244efeba856aa741f6206f
Publikováno v:
Journal of Human Growth and Development. 31:465-469
Background: The involvement of the peripheral nervous system (PNS) in COVID-19 is rare and, to date, morphological aspects from muscle and nerve biopsies have not been reported. Here, we describe a case of Guillain-Barré Syndrome (GBS) related to CO
Autor:
Fabio Fernandes, Caio Cafezeiro, Renata Margarida do Val, Alexandra Patrícia Zilli Vieira, Wilson Marques, Edileide Barros Correia, Alzira Alves Siqueira Carvalho, Antonio Carlos Palandrini Chagas, Acary Souza Bulle Oliveira, Paulo Victor Sgobi de Souza, Wladimir Bocca Vieira de Resende Pinto, Ariane Vieira Scarlatelli Macedo, Murillo Oliveira Antunes, Pedro Vellosa Schwartzmann, Sandrigo Mangini, Marcus Vinicius Simões
Publikováno v:
ABC: Heart Failure & Cardiomyopathy. 1:86-89
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 69, Iss 6, Pp 992-992 (2011)
Externí odkaz:
https://doaj.org/article/c026423cd6a04dc28df20f37eb0c160d
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 62, Iss 2a, Pp 257-261 (2004)
Lipid-lowering drugs have been occasionally associated with neuromuscular symptoms and muscle biopsy changes. We reported the clinical course and the muscle biopsy in eight patients with hyperlipoproteinemia, treated with lipid -lowering drugs (stati
Autor:
Alzira Alves Siqueira Carvalho, Adriano Vieira, Hougelle Simplício, Satomi Fugygara, Solyon Maia Carvalho, Moacyr Pezati Rigueiro
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 63, Iss 1, Pp 160-162 (2005)
We report a case of a 26-year-old man who presented a lower motor neuron syndrome due to hyperparathyroidism. Electromyography showed neurogenic features with normal nerve conduction studies. Hypercalcemia led to the discovery of a primary hyperparat
Autor:
Maria Lígia de Araújo Cerqueira, P N B Salum, Umbertina Conti Reed, Helga C. A. Azevedo, J A Levy, Alzira A. Siqueira-Carvalho, Suely Kazue Nagahashi-Marie, M. S. Carvalho, Lucia Iracema Zanotto de Mendonça
Publikováno v:
Arquivos de Neuro-Psiquiatria. 54:595-600
Myotonia is the phenomenon of decrease of muscular relaxation rate, after either a contraction or a mechanical or electrical stimulus. Congenital myotonias are hereditary affections and do not present muscular dystrophy. The current trend is to group
Autor:
Sueli K. Nagahashi-Marie, Helga C. A. Azevedo, Alzira A. Siqueira-Carvalho, M. N. S. Delgado, J A Levy, P N B Salum, M. S. Carvalho
Publikováno v:
Arquivos de Neuro-Psiquiatria. 54:114-119
The authors report the case of a female patient, 18 years of age, with slowly progressing weakness in upper and lower limbs since childhood. There were no significant antecedents. The neurologic examination showed mild proximal and distal motor defic