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Update of the Brazilian consensus recommendations on Duchenne muscular dystrophy.
Arq Neuropsiquiatr. 2023 Jan;81(1):81-94. doi: 10.1055/s-0043-1761466. Epub 2023 Mar 14.
Arq Neuropsiquiatr. 2023.
PMID: 36918011
Free PMC article.
Review.
Limb-girdle muscular dystrophy type 2A in Brazilian children.
Albuquerque MA, Abath Neto O, Silva FM, Zanoteli E, Reed UC.
Albuquerque MA, et al.
Arq Neuropsiquiatr. 2015 Dec;73(12):993-7. doi: 10.1590/0004-282X20150168.
Arq Neuropsiquiatr. 2015.
PMID: 26677118
Free article.
Item in Clipboard
Effect of the COVID-19 pandemic on patients with inherited neuromuscular disorders.
Moreno CAM, Camelo CG, Sampaio PHMA, Fonseca ATQSM, Estephan EP, Silva AMS, Pirola RN, Silva LHL, Lima KDF, Albuquerque MAV, Camelo Filho AE, Marques MVO, Yanagiura MT, Cavalcante WCP, Matsui Junior C, Isihi LMA, Mendonça RH, Pouza AFP, Carvalho MS, Reed UC, Zanoteli E.
Moreno CAM, et al. Among authors: albuquerque mav.
Arq Neuropsiquiatr. 2022 Jun;80(6):563-569. doi: 10.1590/0004-282X-ANP-2021-0166.
Arq Neuropsiquiatr. 2022.
PMID: 35946707
Free PMC article.
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Clinical features of collagen VI-related dystrophies: A large Brazilian cohort.
Zanoteli E, Soares PS, Silva AMSD, Camelo CG, Fonseca ATQSM, Albuquerque MAV, Moreno CAM, Lopes Abath Neto O, Novo Filho GM, Kulikowski LD, Reed UC.
Zanoteli E, et al. Among authors: albuquerque mav.
Clin Neurol Neurosurg. 2020 May;192:105734. doi: 10.1016/j.clineuro.2020.105734. Epub 2020 Feb 10.
Clin Neurol Neurosurg. 2020.
PMID: 32065942
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Clinical aspects of patients with sarcoglycanopathies under steroids therapy.
Albuquerque MA, Abath-Neto O, Maximino JR, Chadi G, Zanoteli E, Reed UC.
Albuquerque MA, et al.
Arq Neuropsiquiatr. 2014 Oct;72(10):768-72. doi: 10.1590/0004-282x20140126.
Arq Neuropsiquiatr. 2014.
PMID: 25337728
Free article.
Item in Clipboard
Phenotypic intermediate forms overlapping to Emery-Dreifuss and limb girdle muscular dystrophies caused by lamin A/C gene mutations.
Albuquerque MA, Pasqualin LM, Martins CA, Reed UC, Zanoteli E.
Albuquerque MA, et al.
Pediatr Neurol. 2014 May;50(5):e11-2. doi: 10.1016/j.pediatrneurol.2014.01.036. Epub 2014 Jan 24.
Pediatr Neurol. 2014.
PMID: 24656463
No abstract available.
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Congenital muscular dystrophy with dropped head linked to the LMNA gene in a Brazilian cohort.
Pasqualin LM, Reed UC, Costa TV, Quedas E, Albuquerque MA, Resende MB, Rutkowski A, Chadi G, Zanoteli E.
Pasqualin LM, et al.
Pediatr Neurol. 2014 Apr;50(4):400-6. doi: 10.1016/j.pediatrneurol.2013.11.010. Epub 2013 Nov 21.
Pediatr Neurol. 2014.
PMID: 24508248
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Proteus syndrome associated with hemimegalencephaly and Ohtahara syndrome: report of two cases.
Bastos H, da Silva PF, de Albuquerque MA, Mattos A, Riesgo RS, Ohlweiler L, Winckler MI, Bragatti JA, Duarte RD, Zandoná DI.
Bastos H, et al.
Seizure. 2008 Jun;17(4):378-82. doi: 10.1016/j.seizure.2007.11.001. Epub 2007 Dec 21.
Seizure. 2008.
PMID: 18082431
Free article.
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