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Artigo de periodico
Congenital fiber type disproportion caused by TPM3 mutation: a report of two atypical cases (2020)
Moreno, Cristiane Araujo Martins; Harms, Matthew B; Bonnemann, Carsten; Zanoteli, Edmar ; Estephan, Eduardo de Paula; Fappi, Alan; Monges, Soledad; Lubieniecki, Fabiana; Abath Neto, Osorio Lopes; Reed, Umbertina Conti ; Donkervoort, Sandra
Source: Neuromuscular disorders. Unidade: FM
Subjects: BIOPOLÍMEROS, MIOPATIAS CONGÊNITAS ESTRUTURAIS, ESTUDO DE CASO
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ABNT
MORENO, Cristiane Araujo Martins; HARMS, Matthew B; BONNEMANN, Carsten; et al. Congenital fiber type disproportion caused by TPM3 mutation: a report of two atypical cases. Neuromuscular disorders, Oxford, v. 30, n. 1, p. 54-58, 2020. Disponível em: < https://observatorio.fm.usp.br/handle/OPI/35995 > DOI: 10.1016/j.nmd.2019.11.001.
APA
Moreno, C. A. M., Harms, M. B., Bonnemann, C., Zanoteli, E., Estephan, E. de P., Fappi, A., et al. (2020). Congenital fiber type disproportion caused by TPM3 mutation: a report of two atypical cases. Neuromuscular disorders, 30( 1), 54-58. doi:10.1016/j.nmd.2019.11.001
NLM
Moreno CAM, Harms MB, Bonnemann C, Zanoteli E, Estephan E de P, Fappi A, Monges S, Lubieniecki F, Abath Neto OL, Reed UC, Donkervoort S. Congenital fiber type disproportion caused by TPM3 mutation: a report of two atypical cases [Internet]. Neuromuscular disorders. 2020 ; 30( 1): 54-58.Available from: https://observatorio.fm.usp.br/handle/OPI/35995
Vancouver
Moreno CAM, Harms MB, Bonnemann C, Zanoteli E, Estephan E de P, Fappi A, Monges S, Lubieniecki F, Abath Neto OL, Reed UC, Donkervoort S. Congenital fiber type disproportion caused by TPM3 mutation: a report of two atypical cases [Internet]. Neuromuscular disorders. 2020 ; 30( 1): 54-58.Available from: https://observatorio.fm.usp.br/handle/OPI/35995
Artigo de periodico
Time Interval between First and Last Epileptic Seizures and Electroencephalogram Normalization in Benign Childhood Epilepsy with Centrotemporal Spikes: Influencing Factors (2020)
Miziara, Carmen Silvia Molleis Galego; Micheletto, Maria Laura Jorge; Serrano, Virginia Aparecida Gelmeti; Nakanishi, Denise Harumi; Serinolli, Mario Ivo; Manreza, Maria Luiza Giraldes de; Reed, Umbertina Conti
Source: Journal of pediatric epilepsy. Unidade: FM
Subjects: ELETROENCEFALOGRAFIA, EPILEPSIA, HISTÓRIA NATURAL DAS DOENÇAS, REGISTROS MÉDICOS
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ABNT
MIZIARA, Carmen Silvia Molleis Galego; MICHELETTO, Maria Laura Jorge; SERRANO, Virginia Aparecida Gelmeti; et al. Time Interval between First and Last Epileptic Seizures and Electroencephalogram Normalization in Benign Childhood Epilepsy with Centrotemporal Spikes: Influencing Factors. Journal of pediatric epilepsy, Stuttgart, v. 9, n. 02, p. 31-35, 2020. Disponível em: < https://observatorio.fm.usp.br/handle/OPI/36911 > DOI: 10.1055/s-0040-1709187.
APA
Miziara, C. S. M. G., Micheletto, M. L. J., Serrano, V. A. G., Nakanishi, D. H., Serinolli, M. I., Manreza, M. L. G. de, & Reed, U. C. (2020). Time Interval between First and Last Epileptic Seizures and Electroencephalogram Normalization in Benign Childhood Epilepsy with Centrotemporal Spikes: Influencing Factors. Journal of pediatric epilepsy, 9( 02), 31-35. doi:10.1055/s-0040-1709187
NLM
Miziara CSMG, Micheletto MLJ, Serrano VAG, Nakanishi DH, Serinolli MI, Manreza MLG de, Reed UC. Time Interval between First and Last Epileptic Seizures and Electroencephalogram Normalization in Benign Childhood Epilepsy with Centrotemporal Spikes: Influencing Factors [Internet]. Journal of pediatric epilepsy. 2020 ; 9( 02): 31-35.Available from: https://observatorio.fm.usp.br/handle/OPI/36911
Vancouver
Miziara CSMG, Micheletto MLJ, Serrano VAG, Nakanishi DH, Serinolli MI, Manreza MLG de, Reed UC. Time Interval between First and Last Epileptic Seizures and Electroencephalogram Normalization in Benign Childhood Epilepsy with Centrotemporal Spikes: Influencing Factors [Internet]. Journal of pediatric epilepsy. 2020 ; 9( 02): 31-35.Available from: https://observatorio.fm.usp.br/handle/OPI/36911
Artigo de periodico
Clinical features of collagen VI-related dystrophies: a large Brazilian cohort (2020)
Zanoteli, Edmar ; Soares, Priscilla Souza; Silva, Andre Macedo Serafim da; Camelo, Clara Gontijo; Fonseca, Alulin Tacio Quadros Santos Monteiro; Albuquerque, Marco Antinio Veloso; Moreno, Cristiane Araujo Martins ; Abath Neto, Osorio Lopes; Novo Filho, Gil Monteiro; Kulikowski, Leslie Domenici; Reed, Umbertina Conti
Source: Clinical neurology and neurosurgery. Unidade: FM
Subjects: DOENÇAS MUSCULARES, COLÁGENO, DISTROFIA MUSCULAR
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ABNT
ZANOTELI, Edmar; SOARES, Priscilla Souza; SILVA, Andre Macedo Serafim da; et al. Clinical features of collagen VI-related dystrophies: a large Brazilian cohort. Clinical neurology and neurosurgery, Amsterdam, v. 192, 2020. Disponível em: < https://observatorio.fm.usp.br/handle/OPI/35998 > DOI: 10.1016/j.clineuro.2020.105734.
APA
Zanoteli, E., Soares, P. S., Silva, A. M. S. da, Camelo, C. G., Fonseca, A. T. Q. S. M., Albuquerque, M. A. V., et al. (2020). Clinical features of collagen VI-related dystrophies: a large Brazilian cohort. Clinical neurology and neurosurgery, 192. doi:10.1016/j.clineuro.2020.105734
NLM
Zanoteli E, Soares PS, Silva AMS da, Camelo CG, Fonseca ATQSM, Albuquerque MAV, Moreno CAM, Abath Neto OL, Novo Filho GM, Kulikowski LD, Reed UC. Clinical features of collagen VI-related dystrophies: a large Brazilian cohort [Internet]. Clinical neurology and neurosurgery. 2020 ; 192Available from: https://observatorio.fm.usp.br/handle/OPI/35998
Vancouver
Zanoteli E, Soares PS, Silva AMS da, Camelo CG, Fonseca ATQSM, Albuquerque MAV, Moreno CAM, Abath Neto OL, Novo Filho GM, Kulikowski LD, Reed UC. Clinical features of collagen VI-related dystrophies: a large Brazilian cohort [Internet]. Clinical neurology and neurosurgery. 2020 ; 192Available from: https://observatorio.fm.usp.br/handle/OPI/35998
Artigo de periodico
Combining neuropsychological tests to improve the assessment of arithmetic difficulties in children with ADHD (2020)
Rezende, Angelo R. T; Pacheco, Sandra P; Branco, Sulamy C. C; Fernandes, Rosangela D. C; Boldrini, Carla R; Doria Filho, Ulysses; Bazan, Paulo R; Amaro Junior, Edson ; Reed, Umbertina Conti ; Casella, Erasmo Barbante
Source: Arquivos de Neuro-Psiquiatria. Unidade: FM
Subjects: TRANSTORNO DO DEFICIT DE ATENÇÃO COM HIPERATIVIDADE, ESTIMULANTES DO SISTEMA NERVOSO CENTRAL, TESTES NEUROPSICOLÓGICOS
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ABNT
REZENDE, Angelo R. T; PACHECO, Sandra P; BRANCO, Sulamy C. C; et al. Combining neuropsychological tests to improve the assessment of arithmetic difficulties in children with ADHD. Arquivos de Neuro-Psiquiatria, Sao Paulo Sp, v. 78, n. 4, p. 193-198, 2020. Disponível em: < https://observatorio.fm.usp.br/handle/OPI/35915 > DOI: 10.1590/0004-282X20190178.
APA
Rezende, A. R. T., Pacheco, S. P., Branco, S. C. C., Fernandes, R. D. C., Boldrini, C. R., Doria Filho, U., et al. (2020). Combining neuropsychological tests to improve the assessment of arithmetic difficulties in children with ADHD. Arquivos de Neuro-Psiquiatria, 78( 4), 193-198. doi:10.1590/0004-282X20190178
NLM
Rezende ART, Pacheco SP, Branco SCC, Fernandes RDC, Boldrini CR, Doria Filho U, Bazan PR, Amaro Junior E, Reed UC, Casella EB. Combining neuropsychological tests to improve the assessment of arithmetic difficulties in children with ADHD [Internet]. Arquivos de Neuro-Psiquiatria. 2020 ; 78( 4): 193-198.Available from: https://observatorio.fm.usp.br/handle/OPI/35915
Vancouver
Rezende ART, Pacheco SP, Branco SCC, Fernandes RDC, Boldrini CR, Doria Filho U, Bazan PR, Amaro Junior E, Reed UC, Casella EB. Combining neuropsychological tests to improve the assessment of arithmetic difficulties in children with ADHD [Internet]. Arquivos de Neuro-Psiquiatria. 2020 ; 78( 4): 193-198.Available from: https://observatorio.fm.usp.br/handle/OPI/35915
Artigo de periodico
Clinicogenetic lessons from 370 patients with autosomal recessive limb-girdle muscular dystrophy (2019)
Winckler, Pablo B; Silva, Andre M. S. da; Coimbra-Neto, Antonio R; Carvalho, Elmano; Cavalcanti, Eduardo B. U; Sobreira, Claudia F. R; Marrone, Carlo D; Machado-costa, Marcela C; Reed, Umbertina Conti ; Zanoteli, Edmar
Source: Clinical genetics. Unidade: FM
Subjects: DISTROFIA MUSCULAR, DIAGNÓSTICO DIFERENCIAL, GENÓTIPOS, FENÓTIPOS, PROGNÓSTICO
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ABNT
WINCKLER, Pablo B; SILVA, Andre M. S. da; COIMBRA-NETO, Antonio R; et al. Clinicogenetic lessons from 370 patients with autosomal recessive limb-girdle muscular dystrophy. Clinical genetics, Hoboken, v. 96, n. 4, p. 341-353, 2019. Disponível em: < http://observatorio.fm.usp.br/handle/OPI/34049 > DOI: 10.1111/cge.13597.
APA
Winckler, P. B., Silva, A. M. S. da, Coimbra-Neto, A. R., Carvalho, E., Cavalcanti, E. B. U., Sobreira, C. F. R., et al. (2019). Clinicogenetic lessons from 370 patients with autosomal recessive limb-girdle muscular dystrophy. Clinical genetics, 96( 4), 341-353. doi:10.1111/cge.13597
NLM
Winckler PB, Silva AMS da, Coimbra-Neto AR, Carvalho E, Cavalcanti EBU, Sobreira CFR, Marrone CD, Machado-costa MC, Reed UC, Zanoteli E. Clinicogenetic lessons from 370 patients with autosomal recessive limb-girdle muscular dystrophy [Internet]. Clinical genetics. 2019 ; 96( 4): 341-353.Available from: http://observatorio.fm.usp.br/handle/OPI/34049
Vancouver
Winckler PB, Silva AMS da, Coimbra-Neto AR, Carvalho E, Cavalcanti EBU, Sobreira CFR, Marrone CD, Machado-costa MC, Reed UC, Zanoteli E. Clinicogenetic lessons from 370 patients with autosomal recessive limb-girdle muscular dystrophy [Internet]. Clinical genetics. 2019 ; 96( 4): 341-353.Available from: http://observatorio.fm.usp.br/handle/OPI/34049
Artigo de periodico-carta/editorial
Global Central Nervous System Atrophy in Spinal Muscular Atrophy Type 0 [Carta] (2019)
Mendonca, Rodrigo H; Rocha, Antonio J; Lozano-Arango, Andres; Diaz, Astry B; Castiglioni, Claudia; Silva, Andre M. S; Reed, Umbertina Conti ; Kulikowski, Leslie; Paramonov, Ida; Zanoteli, Edmar
Source: Annals of neurology. Unidade: FM
Subjects: ATROFIA MUSCULAR, DOENÇAS DA MEDULA ESPINHAL, DOENÇAS DO SISTEMA NERVOSO CENTRAL, CONVULSÕES, PROTEÍNAS DE TRANSPORTE, APOPTOSE, PROTEÍNAS DO TECIDO NERVOSO, GENES REGULADORES, FENÓTIPOS
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ABNT
MENDONCA, Rodrigo H; ROCHA, Antonio J; LOZANO-ARANGO, Andres; et al. Global Central Nervous System Atrophy in Spinal Muscular Atrophy Type 0 [Carta]. Annals of neurology[S.l: s.n.], 2019.Disponível em: DOI: 10.1002/ana.25597.
APA
Mendonca, R. H., Rocha, A. J., Lozano-Arango, A., Diaz, A. B., Castiglioni, C., Silva, A. M. S., et al. (2019). Global Central Nervous System Atrophy in Spinal Muscular Atrophy Type 0 [Carta]. Annals of neurology. Hoboken. doi:10.1002/ana.25597
NLM
Mendonca RH, Rocha AJ, Lozano-Arango A, Diaz AB, Castiglioni C, Silva AMS, Reed UC, Kulikowski L, Paramonov I, Zanoteli E. Global Central Nervous System Atrophy in Spinal Muscular Atrophy Type 0 [Carta] [Internet]. Annals of neurology. 2019 ; 86( 5): 803-803.Available from: http://observatorio.fm.usp.br/handle/OPI/34038
Vancouver
Mendonca RH, Rocha AJ, Lozano-Arango A, Diaz AB, Castiglioni C, Silva AMS, Reed UC, Kulikowski L, Paramonov I, Zanoteli E. Global Central Nervous System Atrophy in Spinal Muscular Atrophy Type 0 [Carta] [Internet]. Annals of neurology. 2019 ; 86( 5): 803-803.Available from: http://observatorio.fm.usp.br/handle/OPI/34038
Artigo de periodico
Severe brain involvement in 5q spinal muscular atrophy type 0 (2019)
Mendonca, Rodrigo H; Rocha, Antonio J; Lozano-arango, Andres; Diaz, Astry B; Castiglioni, Claudia; Silva, Andre M. S; Reed, Umbertina Conti ; Kulikowski, Leslie; Paramonov, Ida; Zanoteli, Edmar
Source: Annals of neurology. Unidade: FM
Subjects: ATROFIA MUSCULAR, ANORMALIDADES DO SISTEMA NERVOSO, SEQUENCIAMENTO GENÉTICO, RESSONÂNCIA MAGNÉTICA, RECÉM-NASCIDO, LACTENTES
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ABNT
MENDONCA, Rodrigo H; ROCHA, Antonio J; LOZANO-ARANGO, Andres; et al. Severe brain involvement in 5q spinal muscular atrophy type 0. Annals of neurology, Hoboken, v. 86, n. 3, p. 458-462, 2019. Disponível em: < http://observatorio.fm.usp.br/handle/OPI/34443 > DOI: 10.1002/ana.25549.
APA
Mendonca, R. H., Rocha, A. J., Lozano-arango, A., Diaz, A. B., Castiglioni, C., Silva, A. M. S., et al. (2019). Severe brain involvement in 5q spinal muscular atrophy type 0. Annals of neurology, 86( 3), 458-462. doi:10.1002/ana.25549
NLM
Mendonca RH, Rocha AJ, Lozano-arango A, Diaz AB, Castiglioni C, Silva AMS, Reed UC, Kulikowski L, Paramonov I, Zanoteli E. Severe brain involvement in 5q spinal muscular atrophy type 0 [Internet]. Annals of neurology. 2019 ; 86( 3): 458-462.Available from: http://observatorio.fm.usp.br/handle/OPI/34443
Vancouver
Mendonca RH, Rocha AJ, Lozano-arango A, Diaz AB, Castiglioni C, Silva AMS, Reed UC, Kulikowski L, Paramonov I, Zanoteli E. Severe brain involvement in 5q spinal muscular atrophy type 0 [Internet]. Annals of neurology. 2019 ; 86( 3): 458-462.Available from: http://observatorio.fm.usp.br/handle/OPI/34443
Artigo de periodico
Cognitive performance of children with spinal muscular atrophy: a systematic review (2019)
Polido, Graziela Jorge; Miranda, Mariana Mangini Vaz de; Carvas Junior, Nelson; Mendonça, Rodrigo de Holanda; Caromano, Fátima Aparecida ; Reed, Umbertina Conti ; Zanoteli, Edmar ; Voos, Mariana Callil
Source: Dementia & neuropsychologia. Unidade: FM
Subjects: ATROFIA MUSCULAR, MEDULA ESPINHAL, COGNIÇÃO, TRANSTORNOS COGNITIVOS, CRIANÇAS, REVISÃO SISTEMÁTICA
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ABNT
POLIDO, Graziela Jorge; MIRANDA, Mariana Mangini Vaz de; CARVAS JUNIOR, Nelson; et al. Cognitive performance of children with spinal muscular atrophy: a systematic review. Dementia & neuropsychologia, São Paulo, v. 13, n. 4, p. 436-443, 2019. Disponível em: < http://observatorio.fm.usp.br/handle/OPI/35304 > DOI: 10.1590/1980-57642018dn13-040011.
APA
Polido, G. J., Miranda, M. M. V. de, Carvas Junior, N., Mendonça, R. de H., Caromano, F. A., Reed, U. C., et al. (2019). Cognitive performance of children with spinal muscular atrophy: a systematic review. Dementia & neuropsychologia, 13( 4), 436-443. doi:10.1590/1980-57642018dn13-040011
NLM
Polido GJ, Miranda MMV de, Carvas Junior N, Mendonça R de H, Caromano FA, Reed UC, Zanoteli E, Voos MC. Cognitive performance of children with spinal muscular atrophy: a systematic review [Internet]. Dementia & neuropsychologia. 2019 ; 13( 4): 436-443.Available from: http://observatorio.fm.usp.br/handle/OPI/35304
Vancouver
Polido GJ, Miranda MMV de, Carvas Junior N, Mendonça R de H, Caromano FA, Reed UC, Zanoteli E, Voos MC. Cognitive performance of children with spinal muscular atrophy: a systematic review [Internet]. Dementia & neuropsychologia. 2019 ; 13( 4): 436-443.Available from: http://observatorio.fm.usp.br/handle/OPI/35304
Artigo de periodico
Clinical and molecular findings in a cohort of ANO5-related myopathy (2019)
Silva, Andre M. S; Coimbra-neto, Antonio R; Souza, Paulo Victor S; Winckler, Pablo B; Goncalves, Marcus V. M; Cavalcanti, Eduardo B. U; Carvalho, Alzira A. D. S; Sobreire, Claudia F. D. R; Reed, Umbertina Conti ; Zanoteli, Edmar
Source: Annals of clinical and translational neurology. Unidade: FM
Subjects: DISTROFIA MUSCULAR, PROTEÍNAS DA MEMBRANA, PROTEÍNAS DE TRANSPORTE, MUTAÇÃO GENÉTICA, DIAGNÓSTICO HISTOLÓGICO, RESSONÂNCIA MAGNÉTICA, ANÁLISE DE SEQUÊNCIA DE DNA
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ABNT
SILVA, Andre M. S; COIMBRA-NETO, Antonio R; SOUZA, Paulo Victor S; et al. Clinical and molecular findings in a cohort of ANO5-related myopathy. Annals of clinical and translational neurology, Hoboken, v. 6, n. 7, p. 1225-1238, 2019. Disponível em: < http://observatorio.fm.usp.br/handle/OPI/33500 > DOI: 10.1002/acn3.50801.
APA
Silva, A. M. S., Coimbra-neto, A. R., Souza, P. V. S., Winckler, P. B., Goncalves, M. V. M., Cavalcanti, E. B. U., et al. (2019). Clinical and molecular findings in a cohort of ANO5-related myopathy. Annals of clinical and translational neurology, 6( 7), 1225-1238. doi:10.1002/acn3.50801
NLM
Silva AMS, Coimbra-neto AR, Souza PVS, Winckler PB, Goncalves MVM, Cavalcanti EBU, Carvalho AADS, Sobreire CFDR, Reed UC, Zanoteli E. Clinical and molecular findings in a cohort of ANO5-related myopathy [Internet]. Annals of clinical and translational neurology. 2019 ; 6( 7): 1225-1238.Available from: http://observatorio.fm.usp.br/handle/OPI/33500
Vancouver
Silva AMS, Coimbra-neto AR, Souza PVS, Winckler PB, Goncalves MVM, Cavalcanti EBU, Carvalho AADS, Sobreire CFDR, Reed UC, Zanoteli E. Clinical and molecular findings in a cohort of ANO5-related myopathy [Internet]. Annals of clinical and translational neurology. 2019 ; 6( 7): 1225-1238.Available from: http://observatorio.fm.usp.br/handle/OPI/33500
Artigo de periodico
The clinical spectrum of the congenital myasthenic syndrome resulting from COL13A1 mutations (2019)
Cruz, Pedro M. Rodriguez; Cossins, Judith; Estephan, Eduardo de Paula; Munell, Francina; Selby, Kathryn; Hirano, Michio; Maroofin, Reza; Mehrjardi, Mohammad Yahya Vahidi; Zanoteli, Edmar ; Reed, Umbertina Conti
Source: Brain. Unidade: FM
Subjects: DOENÇAS DA JUNÇÃO NEUROMUSCULAR, PROTEÍNAS DE MATRIZ EXTRACELULARES, SINAPSE, MUTAÇÃO GENÉTICA, RECEPTORES ADRENÉRGICOS, AMINAS
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ABNT
CRUZ, Pedro M. Rodriguez; COSSINS, Judith; ESTEPHAN, Eduardo de Paula; et al. The clinical spectrum of the congenital myasthenic syndrome resulting from COL13A1 mutations. Brain, Oxford, v. 142, p. 1547-1560, 2019. Disponível em: < http://observatorio.fm.usp.br/handle/OPI/33503 > DOI: 10.1093/brain/awz107.
APA
Cruz, P. M. R., Cossins, J., Estephan, E. de P., Munell, F., Selby, K., Hirano, M., et al. (2019). The clinical spectrum of the congenital myasthenic syndrome resulting from COL13A1 mutations. Brain, 142, 1547-1560. doi:10.1093/brain/awz107
NLM
Cruz PMR, Cossins J, Estephan E de P, Munell F, Selby K, Hirano M, Maroofin R, Mehrjardi MYV, Zanoteli E, Reed UC. The clinical spectrum of the congenital myasthenic syndrome resulting from COL13A1 mutations [Internet]. Brain. 2019 ; 142 1547-1560.Available from: http://observatorio.fm.usp.br/handle/OPI/33503
Vancouver
Cruz PMR, Cossins J, Estephan E de P, Munell F, Selby K, Hirano M, Maroofin R, Mehrjardi MYV, Zanoteli E, Reed UC. The clinical spectrum of the congenital myasthenic syndrome resulting from COL13A1 mutations [Internet]. Brain. 2019 ; 142 1547-1560.Available from: http://observatorio.fm.usp.br/handle/OPI/33503
Artigo de periodico
Therapeutic advances in 5q-linked spinal muscular atrophy (2018)
Reed, Umbertina Conti; Zanoteli, Edmar
Source: Arquivos de Neuro-Psiquiatria. Unidade: FM
Subjects: RATOS, MUTAÇÃO GENÉTICA, ESTRATÉGIAS TERAPÊUTICAS, DOENÇAS DO SISTEMA NERVOSO PERIFÉRICO, ATROFIA MUSCULAR
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ABNT
REED, Umbertina Conti; ZANOTELI, Edmar. Therapeutic advances in 5q-linked spinal muscular atrophy. Arquivos de Neuro-Psiquiatria, Sao Paulo Sp, v. 76, n. 4, p. 265-272, 2018. Disponível em: < http://dx.doi.org/10.1590/0004-282X20180011 > DOI: 10.1590/0004-282X20180011.
APA
Reed, U. C., & Zanoteli, E. (2018). Therapeutic advances in 5q-linked spinal muscular atrophy. Arquivos de Neuro-Psiquiatria, 76( 4), 265-272. doi:10.1590/0004-282X20180011
NLM
Reed UC, Zanoteli E. Therapeutic advances in 5q-linked spinal muscular atrophy [Internet]. Arquivos de Neuro-Psiquiatria. 2018 ; 76( 4): 265-272.Available from: http://dx.doi.org/10.1590/0004-282X20180011
Vancouver
Reed UC, Zanoteli E. Therapeutic advances in 5q-linked spinal muscular atrophy [Internet]. Arquivos de Neuro-Psiquiatria. 2018 ; 76( 4): 265-272.Available from: http://dx.doi.org/10.1590/0004-282X20180011
Artigo de periodico
Clinical and imaging hallmarks of the MYH7-related myopathy with severe axial involvement (2018)
Dabaj, Ivana; Reed, Umbertina Conti; Zanoteli, Edmar
Source: Muscle & nerve. Unidade: FM
Subjects: IMAGEM POR RESSONÂNCIA MAGNÉTICA, MUTAÇÃO GENÉTICA, MÚSCULOS, BIÓPSIA
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ABNT
DABAJ, Ivana; REED, Umbertina Conti; ZANOTELI, Edmar. Clinical and imaging hallmarks of the MYH7-related myopathy with severe axial involvement. Muscle & nerve, Hoboken, v. 58, n. 2, p. 224-234, 2018. Disponível em: < http://dx.doi.org/10.1002/mus.26137 > DOI: 10.1002/mus.26137.
APA
Dabaj, I., Reed, U. C., & Zanoteli, E. (2018). Clinical and imaging hallmarks of the MYH7-related myopathy with severe axial involvement. Muscle & nerve, 58( 2), 224-234. doi:10.1002/mus.26137
NLM
Dabaj I, Reed UC, Zanoteli E. Clinical and imaging hallmarks of the MYH7-related myopathy with severe axial involvement [Internet]. Muscle & nerve. 2018 ; 58( 2): 224-234.Available from: http://dx.doi.org/10.1002/mus.26137
Vancouver
Dabaj I, Reed UC, Zanoteli E. Clinical and imaging hallmarks of the MYH7-related myopathy with severe axial involvement [Internet]. Muscle & nerve. 2018 ; 58( 2): 224-234.Available from: http://dx.doi.org/10.1002/mus.26137
Artigo de periodico
Theraputic advances in 5q-linked spinal muscular atrophy (2018)
Reed, Umbertina Conti; Zanoteli, Edmar
Source: Arquivos de Neuro-Psiquiatria. Unidade: FM
Subjects: ATROFIA MUSCULAR, DOENÇAS NEURODEGENERATIVAS, DOENÇAS GENÉTICAS, TERAPIAS COMPLEMENTARES
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ABNT
REED, Umbertina Conti; ZANOTELI, Edmar. Theraputic advances in 5q-linked spinal muscular atrophy. Arquivos de Neuro-Psiquiatria, São Paulo, v. 76, n. 04, p. 265-272, 2018. Disponível em: < http://dx.doi.org/10.1590/0004-282x20180011 > DOI: 10.1590/0004-282x20180011.
APA
Reed, U. C., & Zanoteli, E. (2018). Theraputic advances in 5q-linked spinal muscular atrophy. Arquivos de Neuro-Psiquiatria, 76( 04), 265-272. doi:10.1590/0004-282x20180011
NLM
Reed UC, Zanoteli E. Theraputic advances in 5q-linked spinal muscular atrophy [Internet]. Arquivos de Neuro-Psiquiatria. 2018 ; 76( 04): 265-272.Available from: http://dx.doi.org/10.1590/0004-282x20180011
Vancouver
Reed UC, Zanoteli E. Theraputic advances in 5q-linked spinal muscular atrophy [Internet]. Arquivos de Neuro-Psiquiatria. 2018 ; 76( 04): 265-272.Available from: http://dx.doi.org/10.1590/0004-282x20180011
Artigo de periodico
A novel ATP1A2 mutation in a patient with hypokalaemic periodic paralysis and CNS symptoms (2018)
Castaneda, Marisol Sampedro; Zanoteli, Edmar; Scalco, Renata S.; Scaramuzzi, Vinicius; Caldas, Vitor Marques; Reed, Umbertina Conti; Silva, Andre Macedo Serafim da; O'callaghan, Benjamin; Phadke, Rahul; Bugiardini, Enrico
Source: Brain. Unidade: FM
Subjects: DOENÇAS MUSCULARES, POTÁSSIO, PARESIA, PROTEÍNAS DE TRANSPORTE, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CASTANEDA, Marisol Sampedro; ZANOTELI, Edmar; SCALCO, Renata S.; et al. A novel ATP1A2 mutation in a patient with hypokalaemic periodic paralysis and CNS symptoms. Brain, Oxford, v. 141, p. 3308-3318, 2018. Disponível em: < http://observatorio.fm.usp.br/handle/OPI/30867 > DOI: 10.1093/brain/awy283.
APA
Castaneda, M. S., Zanoteli, E., Scalco, R. S., Scaramuzzi, V., Caldas, V. M., Reed, U. C., et al. (2018). A novel ATP1A2 mutation in a patient with hypokalaemic periodic paralysis and CNS symptoms. Brain, 141, 3308-3318. doi:10.1093/brain/awy283
NLM
Castaneda MS, Zanoteli E, Scalco RS, Scaramuzzi V, Caldas VM, Reed UC, Silva AMS da, O'callaghan B, Phadke R, Bugiardini E. A novel ATP1A2 mutation in a patient with hypokalaemic periodic paralysis and CNS symptoms [Internet]. Brain. 2018 ; 141 3308-3318.Available from: http://observatorio.fm.usp.br/handle/OPI/30867
Vancouver
Castaneda MS, Zanoteli E, Scalco RS, Scaramuzzi V, Caldas VM, Reed UC, Silva AMS da, O'callaghan B, Phadke R, Bugiardini E. A novel ATP1A2 mutation in a patient with hypokalaemic periodic paralysis and CNS symptoms [Internet]. Brain. 2018 ; 141 3308-3318.Available from: http://observatorio.fm.usp.br/handle/OPI/30867
Artigo de periodico
Clinical variability of early-onset congenital myasthenic syndrome due to biallelic RAPSN mutations in Brazil (2018)
Estephan, Eduardo de Paula; Zambon, Antonio Alberto; Marchiori, Paulo Euripedes; Silva, Andre Macedo Serafim da; Caldas, Vitor Marques; Moreno, Cristiane Araujo Martins; Reed, Umbertina Conti; Horvath, Rita; Topf, Ana; Lochmueller, Hanns
Source: Neuromuscular disorders. Unidade: FM
Subjects: DOENÇAS DA JUNÇÃO NEUROMUSCULAR, RECEPTORES DE ACETILCOLINA, ESTUDOS DE COORTES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ESTEPHAN, Eduardo de Paula; ZAMBON, Antonio Alberto; MARCHIORI, Paulo Euripedes; et al. Clinical variability of early-onset congenital myasthenic syndrome due to biallelic RAPSN mutations in Brazil. Neuromuscular disorders, Oxford, v. 28, n. 11, p. 961-964, 2018. Disponível em: < http://observatorio.fm.usp.br/handle/OPI/29973 > DOI: 10.1016/j.nmd.2018.08.007.
APA
Estephan, E. de P., Zambon, A. A., Marchiori, P. E., Silva, A. M. S. da, Caldas, V. M., Moreno, C. A. M., et al. (2018). Clinical variability of early-onset congenital myasthenic syndrome due to biallelic RAPSN mutations in Brazil. Neuromuscular disorders, 28( 11), 961-964. doi:10.1016/j.nmd.2018.08.007
NLM
Estephan E de P, Zambon AA, Marchiori PE, Silva AMS da, Caldas VM, Moreno CAM, Reed UC, Horvath R, Topf A, Lochmueller H. Clinical variability of early-onset congenital myasthenic syndrome due to biallelic RAPSN mutations in Brazil [Internet]. Neuromuscular disorders. 2018 ; 28( 11): 961-964.Available from: http://observatorio.fm.usp.br/handle/OPI/29973
Vancouver
Estephan E de P, Zambon AA, Marchiori PE, Silva AMS da, Caldas VM, Moreno CAM, Reed UC, Horvath R, Topf A, Lochmueller H. Clinical variability of early-onset congenital myasthenic syndrome due to biallelic RAPSN mutations in Brazil [Internet]. Neuromuscular disorders. 2018 ; 28( 11): 961-964.Available from: http://observatorio.fm.usp.br/handle/OPI/29973
Artigo de periodico
A common CHRNE mutation in Brazilian patients with congenital myasthenic syndrome (2018)
Estephan, Eduardo de Paula; Marchiori, Paulo Euripedes; Reed, Umbertina Conti; Zanoteli, Edmar
Source: Journal of neurology. Unidade: FM
Subjects: MIASTENIA GRAVIS, MUTAÇÃO GENÉTICA, SINAIS E SINTOMAS, BRASIL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ESTEPHAN, Eduardo de Paula; MARCHIORI, Paulo Euripedes; REED, Umbertina Conti; ZANOTELI, Edmar. A common CHRNE mutation in Brazilian patients with congenital myasthenic syndrome. Journal of neurology, Heidelberg, v. 265, n. 3, p. 708-713, 2018. Disponível em: < http://dx.doi.org/10.1007/s00415-018-8736-8 > DOI: 10.1007/s00415-018-8736-8.
APA
Estephan, E. de P., Marchiori, P. E., Reed, U. C., & Zanoteli, E. (2018). A common CHRNE mutation in Brazilian patients with congenital myasthenic syndrome. Journal of neurology, 265( 3), 708-713. doi:10.1007/s00415-018-8736-8
NLM
Estephan E de P, Marchiori PE, Reed UC, Zanoteli E. A common CHRNE mutation in Brazilian patients with congenital myasthenic syndrome [Internet]. Journal of neurology. 2018 ; 265( 3): 708-713.Available from: http://dx.doi.org/10.1007/s00415-018-8736-8
Vancouver
Estephan E de P, Marchiori PE, Reed UC, Zanoteli E. A common CHRNE mutation in Brazilian patients with congenital myasthenic syndrome [Internet]. Journal of neurology. 2018 ; 265( 3): 708-713.Available from: http://dx.doi.org/10.1007/s00415-018-8736-8
Artigo de periodico
Muscle biopsy with dystrophic pattern and rimmed vacuoles: GNE myopathy in a Brazilian patient (2017)
Estephan, Eduardo de Paula; Moreno, Cristiane Araújo Martins; Silva, André Macedo Serafim da; Mendonça, Rodrigo de Holanda; Abath Neto, Osório; Nishimura, Patrícia Yoshi; Galindo, Layla Testa; Zanoteli, Edmar; Reed, Umbertina Conti
Source: Arquivos de Neuro-Psiquiatria. Unidade: FM
Subjects: BIÓPSIA, DOENÇAS GENÉTICAS, MÚSCULOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ESTEPHAN, Eduardo de Paula; MORENO, Cristiane Araújo Martins; SILVA, André Macedo Serafim da; et al. Muscle biopsy with dystrophic pattern and rimmed vacuoles: GNE myopathy in a Brazilian patient. Arquivos de Neuro-Psiquiatria, São Paulo, v. 75, n. 1, p. 72-73, 2017. Disponível em: < http://www.scielo.br/pdf/anp/v75n1/0004-282X-anp-75-01-0072.pdf > DOI: 10.1590/0004-282X20160171.
APA
Estephan, E. de P., Moreno, C. A. M., Silva, A. M. S. da, Mendonça, R. de H., Abath Neto, O., Nishimura, P. Y., et al. (2017). Muscle biopsy with dystrophic pattern and rimmed vacuoles: GNE myopathy in a Brazilian patient. Arquivos de Neuro-Psiquiatria, 75( 1), 72-73. doi:10.1590/0004-282X20160171
NLM
Estephan E de P, Moreno CAM, Silva AMS da, Mendonça R de H, Abath Neto O, Nishimura PY, Galindo LT, Zanoteli E, Reed UC. Muscle biopsy with dystrophic pattern and rimmed vacuoles: GNE myopathy in a Brazilian patient [Internet]. Arquivos de Neuro-Psiquiatria. 2017 ; 75( 1): 72-73.Available from: http://www.scielo.br/pdf/anp/v75n1/0004-282X-anp-75-01-0072.pdf
Vancouver
Estephan E de P, Moreno CAM, Silva AMS da, Mendonça R de H, Abath Neto O, Nishimura PY, Galindo LT, Zanoteli E, Reed UC. Muscle biopsy with dystrophic pattern and rimmed vacuoles: GNE myopathy in a Brazilian patient [Internet]. Arquivos de Neuro-Psiquiatria. 2017 ; 75( 1): 72-73.Available from: http://www.scielo.br/pdf/anp/v75n1/0004-282X-anp-75-01-0072.pdf
Artigo de periodico
Translation and validation of the Life Satisfaction Index for Adolescents scale with neuromuscular disorders: LSI-A Brazil (2017)
Simon, Valdecir Antonio; Zanoteli, Edmar; Simon, Margarete Andreozzi Vaz Pereira; Resende, Maria Bernadete Dutra de; Reed, Umbertina Conti
Source: Arquivos de Neuro-Psiquiatria. Unidade: FM
Subjects: ESTUDO DE VALIDAÇÃO, ADOLESCENTES, VALIDAÇÃO DE MODELOS, DOENÇAS NEUROMUSCULARES, BRASIL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SIMON, Valdecir Antonio; ZANOTELI, Edmar; SIMON, Margarete Andreozzi Vaz Pereira; RESENDE, Maria Bernadete Dutra de; REED, Umbertina Conti. Translation and validation of the Life Satisfaction Index for Adolescents scale with neuromuscular disorders: LSI-A Brazil. Arquivos de Neuro-Psiquiatria, São Paulo, v. 75, n. 8, p. 553-562, 2017. Disponível em: < http://www.scielo.br/pdf/anp/v75n8/0004-282X-anp-75-08-0553.pdf > DOI: 10.1590/0004-282X20170103 C.
APA
Simon, V. A., Zanoteli, E., Simon, M. A. V. P., Resende, M. B. D. de, & Reed, U. C. (2017). Translation and validation of the Life Satisfaction Index for Adolescents scale with neuromuscular disorders: LSI-A Brazil. Arquivos de Neuro-Psiquiatria, 75( 8), 553-562. doi:10.1590/0004-282X20170103 C
NLM
Simon VA, Zanoteli E, Simon MAVP, Resende MBD de, Reed UC. Translation and validation of the Life Satisfaction Index for Adolescents scale with neuromuscular disorders: LSI-A Brazil [Internet]. Arquivos de Neuro-Psiquiatria. 2017 ; 75( 8): 553-562.Available from: http://www.scielo.br/pdf/anp/v75n8/0004-282X-anp-75-08-0553.pdf
Vancouver
Simon VA, Zanoteli E, Simon MAVP, Resende MBD de, Reed UC. Translation and validation of the Life Satisfaction Index for Adolescents scale with neuromuscular disorders: LSI-A Brazil [Internet]. Arquivos de Neuro-Psiquiatria. 2017 ; 75( 8): 553-562.Available from: http://www.scielo.br/pdf/anp/v75n8/0004-282X-anp-75-08-0553.pdf
Parte de monografia/livro
Doenças neuromusculares (2017)
Fonseca, Alulin Tácio Quadros Santos Monteiro; Zanoteli, Edmar; Reed, Umbertina Conti
Source: Tratado de neurologia infantil. Unidade: FM
Subjects: NEURÔNIOS, ATROFIA MUSCULAR, DOENÇAS NEUROMUSCULARES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FONSECA, Alulin Tácio Quadros Santos Monteiro; ZANOTELI, Edmar; REED, Umbertina Conti. Doenças neuromusculares. In: Tratado de neurologia infantil[S.l: s.n.], 2017.
APA
Fonseca, A. T. Q. S. M., Zanoteli, E., & Reed, U. C. (2017). Doenças neuromusculares. In Tratado de neurologia infantil. São Paulo: Atheneu.
NLM
Fonseca ATQSM, Zanoteli E, Reed UC. Doenças neuromusculares. In: Tratado de neurologia infantil. São Paulo: Atheneu; 2017.
Vancouver
Fonseca ATQSM, Zanoteli E, Reed UC. Doenças neuromusculares. In: Tratado de neurologia infantil. São Paulo: Atheneu; 2017.
Artigo de periodico
Validation of the Expression and Emotion Scale for Children with attention deficit hyperactivity disorder into Brazilian Portuguese (2017)
Simon, Margarete Andreozzi Vaz Pereira; Reed, Umbertina Conti; Vaughan, Brigette; Simon, Valdecir Antonio; Casella, Erasmo Barbante
Source: Arquivos de Neuro-Psiquiatria. Unidade: FM
Subjects: HIPERATIVIDADE, CRIANÇAS, ADOLESCENTES, VALIDAÇÃO DE MODELOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SIMON, Margarete Andreozzi Vaz Pereira; REED, Umbertina Conti; VAUGHAN, Brigette; SIMON, Valdecir Antonio; CASELLA, Erasmo Barbante. Validation of the Expression and Emotion Scale for Children with attention deficit hyperactivity disorder into Brazilian Portuguese. Arquivos de Neuro-Psiquiatria, São Paulo, v. 75, n. 8, p. 563-569, 2017. Disponível em: < http://www.scielo.br/pdf/anp/v75n8/0004-282X-anp-75-08-0563.pdf > DOI: 10.1590/0004-282x20170105.
APA
Simon, M. A. V. P., Reed, U. C., Vaughan, B., Simon, V. A., & Casella, E. B. (2017). Validation of the Expression and Emotion Scale for Children with attention deficit hyperactivity disorder into Brazilian Portuguese. Arquivos de Neuro-Psiquiatria, 75( 8), 563-569. doi:10.1590/0004-282x20170105
NLM
Simon MAVP, Reed UC, Vaughan B, Simon VA, Casella EB. Validation of the Expression and Emotion Scale for Children with attention deficit hyperactivity disorder into Brazilian Portuguese [Internet]. Arquivos de Neuro-Psiquiatria. 2017 ; 75( 8): 563-569.Available from: http://www.scielo.br/pdf/anp/v75n8/0004-282X-anp-75-08-0563.pdf
Vancouver
Simon MAVP, Reed UC, Vaughan B, Simon VA, Casella EB. Validation of the Expression and Emotion Scale for Children with attention deficit hyperactivity disorder into Brazilian Portuguese [Internet]. Arquivos de Neuro-Psiquiatria. 2017 ; 75( 8): 563-569.Available from: http://www.scielo.br/pdf/anp/v75n8/0004-282X-anp-75-08-0563.pdf

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