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Artigo de periodico
Expanding MAPT p.V363I Mutation Phenotype: An Overlapping of PSP-CBS and Posterior Cortical Atrophy (2023)
Parmera, Jacy Bezerra ; Coutinho, Artur Martins Novaes ; Guimarães, Thiago Gonçalves; Yamamoto, Joyce Yuri Silvestre ; Takada, Leonel Tadao ; Nitrini, Ricardo ; Barbosa, Egberto Reis ; Brucki, Sonia Maria Dozzi
Source: Movement disorders clinical practice. Unidade: FM
Subjects: FENÓTIPOS, BIOMARCADORES, DOENÇAS NEURODEGENERATIVAS, DOENÇAS CEREBRAIS
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ABNT
PARMERA, Jacy Bezerra et al. Expanding MAPT p.V363I Mutation Phenotype: An Overlapping of PSP-CBS and Posterior Cortical Atrophy. Movement disorders clinical practice, v. 10, n. 4, p. 716-718, 2023Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/53947. Acesso em: 24 set. 2024.
APA
Parmera, J. B., Coutinho, A. M. N., Guimarães, T. G., Yamamoto, J. Y. S., Takada, L. T., Nitrini, R., et al. (2023). Expanding MAPT p.V363I Mutation Phenotype: An Overlapping of PSP-CBS and Posterior Cortical Atrophy. Movement disorders clinical practice, 10( 4), 716-718. doi:10.1002/mdc3.13671
NLM
Parmera JB, Coutinho AMN, Guimarães TG, Yamamoto JYS, Takada LT, Nitrini R, Barbosa ER, Brucki SMD. Expanding MAPT p.V363I Mutation Phenotype: An Overlapping of PSP-CBS and Posterior Cortical Atrophy [Internet]. Movement disorders clinical practice. 2023 ; 10( 4): 716-718.[citado 2024 set. 24 ] Available from: https://observatorio.fm.usp.br/handle/OPI/53947
Vancouver
Parmera JB, Coutinho AMN, Guimarães TG, Yamamoto JYS, Takada LT, Nitrini R, Barbosa ER, Brucki SMD. Expanding MAPT p.V363I Mutation Phenotype: An Overlapping of PSP-CBS and Posterior Cortical Atrophy [Internet]. Movement disorders clinical practice. 2023 ; 10( 4): 716-718.[citado 2024 set. 24 ] Available from: https://observatorio.fm.usp.br/handle/OPI/53947
Artigo de periodico
Biallelic Loss-of-Function NDUFA12 Variants Cause a Wide Phenotypic Spectrum from Leigh/Leigh-Like Syndrome to Isolated Optic Atrophy (2022)
Magrinelli, Francesca; Cali, Elisa; Braga, Vinicius Lopes; Yis, Uluc; Tomoum, Hoda; Shamseldin, Hanan; Raiman, Julian; Kernstock, Christoph; Rezende Filho, Flavio Moura; Kok, Fernando
Source: Movement disorders clinical practice. Unidade: FM
Subjects: ATROFIA MUSCULAR, DISTROFIA MUSCULAR, FENÓTIPOS, OLHO
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ABNT
MAGRINELLI, Francesca et al. Biallelic Loss-of-Function NDUFA12 Variants Cause a Wide Phenotypic Spectrum from Leigh/Leigh-Like Syndrome to Isolated Optic Atrophy. Movement disorders clinical practice, v. 9, n. 2, p. 218-228, 2022Tradução . . Disponível em: https://doi.org/10.1002/mdc3.13398. Acesso em: 24 set. 2024.
APA
Magrinelli, F., Cali, E., Braga, V. L., Yis, U., Tomoum, H., Shamseldin, H., et al. (2022). Biallelic Loss-of-Function NDUFA12 Variants Cause a Wide Phenotypic Spectrum from Leigh/Leigh-Like Syndrome to Isolated Optic Atrophy. Movement disorders clinical practice, 9( 2), 218-228. doi:10.1002/mdc3.13398
NLM
Magrinelli F, Cali E, Braga VL, Yis U, Tomoum H, Shamseldin H, Raiman J, Kernstock C, Rezende Filho FM, Kok F. Biallelic Loss-of-Function NDUFA12 Variants Cause a Wide Phenotypic Spectrum from Leigh/Leigh-Like Syndrome to Isolated Optic Atrophy [Internet]. Movement disorders clinical practice. 2022 ; 9( 2): 218-228.[citado 2024 set. 24 ] Available from: https://doi.org/10.1002/mdc3.13398
Vancouver
Magrinelli F, Cali E, Braga VL, Yis U, Tomoum H, Shamseldin H, Raiman J, Kernstock C, Rezende Filho FM, Kok F. Biallelic Loss-of-Function NDUFA12 Variants Cause a Wide Phenotypic Spectrum from Leigh/Leigh-Like Syndrome to Isolated Optic Atrophy [Internet]. Movement disorders clinical practice. 2022 ; 9( 2): 218-228.[citado 2024 set. 24 ] Available from: https://doi.org/10.1002/mdc3.13398
Artigo de periodico-carta/editorial
Deep brain stimulation in patients with isolated generalized dystonia caused by PRKRA mutation (2019)
Casagrande, Sara Carvalho Barbosa ; Listik, Clarice ; Coelho, Daniel Boari; Limongi, Joao Carlos Papaterra; Teixeira, Luis Augusto; Teixeira, Manoel Jacobsen; Barbosa, Egberto Reis; Cury, Rubens Gisbert
Source: Movement disorders clinical practice. Unidades: EEFE, FM
Subjects: ESTIMULAÇÃO CEREBRAL, MUTAÇÃO GENÉTICA, DOENÇAS GENÉTICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CASAGRANDE, Sara Carvalho Barbosa et al. Deep brain stimulation in patients with isolated generalized dystonia caused by PRKRA mutation. Movement disorders clinical practice. Hoboken: Escola de Educação Física e Esporte, Universidade de São Paulo. Disponível em: https://doi.org/10.1002/mdc3.12811. Acesso em: 24 set. 2024. , 2019
APA
Casagrande, S. C. B., Listik, C., Coelho, D. B., Limongi, J. C. P., Teixeira, L. A., Teixeira, M. J., et al. (2019). Deep brain stimulation in patients with isolated generalized dystonia caused by PRKRA mutation. Movement disorders clinical practice. Hoboken: Escola de Educação Física e Esporte, Universidade de São Paulo. doi:10.1002/mdc3.12811
NLM
Casagrande SCB, Listik C, Coelho DB, Limongi JCP, Teixeira LA, Teixeira MJ, Barbosa ER, Cury RG. Deep brain stimulation in patients with isolated generalized dystonia caused by PRKRA mutation [Internet]. Movement disorders clinical practice. 2019 ;3 .[citado 2024 set. 24 ] Available from: https://doi.org/10.1002/mdc3.12811
Vancouver
Casagrande SCB, Listik C, Coelho DB, Limongi JCP, Teixeira LA, Teixeira MJ, Barbosa ER, Cury RG. Deep brain stimulation in patients with isolated generalized dystonia caused by PRKRA mutation [Internet]. Movement disorders clinical practice. 2019 ;3 .[citado 2024 set. 24 ] Available from: https://doi.org/10.1002/mdc3.12811
Artigo de periodico-carta/editorial
Progressive Myoclonic Epilepsy Type 8 Due to CERS1 Deficiency [editorial]: A Novel Mutation with Prominent Ataxia (2018)
Godeiro Junior, Clecio de Oliveira; Kok, Fernando; Vale, Thiago Cardoso; Afonso, Cintia Oliveira de Melo; Pedroso, Jose Luiz; Barsotiini, Orlando G.
Source: Movement disorders clinical practice. Unidade: FM
Subjects: EPILEPSIA, ATAXIA, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GODEIRO JUNIOR, Clecio de Oliveira et al. Progressive Myoclonic Epilepsy Type 8 Due to CERS1 Deficiency [editorial]: A Novel Mutation with Prominent Ataxia. Movement disorders clinical practice. Hoboken: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://doi.org/10.1002/mdc3.12610. Acesso em: 24 set. 2024. , 2018
APA
Godeiro Junior, C. de O., Kok, F., Vale, T. C., Afonso, C. O. de M., Pedroso, J. L., & Barsotiini, O. G. (2018). Progressive Myoclonic Epilepsy Type 8 Due to CERS1 Deficiency [editorial]: A Novel Mutation with Prominent Ataxia. Movement disorders clinical practice. Hoboken: Faculdade de Medicina, Universidade de São Paulo. doi:10.1002/mdc3.12610
NLM
Godeiro Junior C de O, Kok F, Vale TC, Afonso CO de M, Pedroso JL, Barsotiini OG. Progressive Myoclonic Epilepsy Type 8 Due to CERS1 Deficiency [editorial]: A Novel Mutation with Prominent Ataxia [Internet]. Movement disorders clinical practice. 2018 ; 5( 3): 330-332.[citado 2024 set. 24 ] Available from: https://doi.org/10.1002/mdc3.12610
Vancouver
Godeiro Junior C de O, Kok F, Vale TC, Afonso CO de M, Pedroso JL, Barsotiini OG. Progressive Myoclonic Epilepsy Type 8 Due to CERS1 Deficiency [editorial]: A Novel Mutation with Prominent Ataxia [Internet]. Movement disorders clinical practice. 2018 ; 5( 3): 330-332.[citado 2024 set. 24 ] Available from: https://doi.org/10.1002/mdc3.12610

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