Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Ana Carolina dos Santos Jorge"'
Autor:
Paulo Victor Sgobbi Souza, Gliciane Afonso, Wladimir Bocca Vieira de Rezende Pinto, Paulo de Lima Serrano, Bruno de Mattos Lombardi Badia, Igor Braga Farias, Ana Carolina dos Santos Jorge, Roberta Ismael Lacerda Machado, Icaro França Navarro Pinto, Glenda Barbosa Barros, Helvia Bertoldo de Oliveira, Samia Rogatis Calil, Cibele Franz, Acary Souza Bulle Oliveira
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-11 (2023)
Abstract Background Porphyrias are a rare group of disease due to inherited defects of heme synthesis with important systemic manifestations and great burden of disease for patients and families due to the exceptional course of disease with disabling
Externí odkaz:
https://doaj.org/article/e991abfc8f334db599cba5bf626ab962
Autor:
Paulo Victor Sgobbi de Souza, Wladimir Bocca Vieira de Rezende Pinto, Igor Braga Farias, Bruno de Mattos Lombardi Badia, Icaro França Navarro Pinto, Gustavo Carvalho Costa, Carolina Maria Marin, Ana Carolina dos Santos Jorge, Emília Correia Souto, Paulo de Lima Serrano, Roberta Ismael Lacerda Machado, Marco Antônio Troccoli Chieia, Enrico Bertini, Acary Souza Bulle Oliveira
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-11 (2021)
Abstract Background Amyotrophic Lateral Sclerosis (ALS) is a rare, progressive, and fatal neurodegenerative disease due to upper and lower motor neuron involvement with symptoms classically occurring in adulthood with an increasing recognition of juv
Externí odkaz:
https://doaj.org/article/c91e9548ecc64b80805575c606c17e22
Autor:
Paulo Victor Sgobbi de Souza, Igor Braga Farias, Paulo de Lima Serrano, Bruno de Mattos Lombardi Badia, Ana Carolina dos Santos Jorge, Glenda Barbosa Barros, Hélvia Bertoldo de Oliveira, Samia Rogatis Calil, Isabela Danziato Fernandes, Roberta Correa Ribeiro, Vinícius Lopes Braga, Roberta Ismael Lacerda Machado, Marco Antônio Troccoli Chieia, Wladimir Bocca Vieira de Rezende Pinto, Acary Souza Bulle Oliveira
Publikováno v:
Sclerosis. 1:22-26
A 38-year-old Brazilian man presented with slowly progressive quadriparesis since age 11 years. He progressed over 15 years with symptoms restricted to the lower limbs, and since then, with a progressive compromise of the upper limbs. His deceased br
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4fccd7123841bf15f64a0254af49a31d
https://doi.org/10.3390/sclerosis1010004
https://doi.org/10.3390/sclerosis1010004
Autor:
Carolina Maria Marin, Acary Souza Bulle Oliveira, Gustavo Carvalho Costa, Wladimir Bocca Vieira de Rezende Pinto, Roberta Ismael Lacerda Machado, Paulo de Lima Serrano, Emília Correia Souto, Bruno de Mattos Lombardi Badia, Enrico Bertini, Paulo Victor Sgobbi de Souza, Igor Braga Farias, Ana Carolina Dos Santos Jorge, Marco Antônio Troccoli Chieia, Icaro França Navarro Pinto
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-11 (2021)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
Background Amyotrophic Lateral Sclerosis (ALS) is a rare, progressive, and fatal neurodegenerative disease due to upper and lower motor neuron involvement with symptoms classically occurring in adulthood with an increasing recognition of juvenile pre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::840485c064d960b5f07fa56ae98d0b70
https://doaj.org/article/c91e9548ecc64b80805575c606c17e22
https://doaj.org/article/c91e9548ecc64b80805575c606c17e22