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Artigo de periodico
Secondary bruxism: a valid diagnosis or just a coincidental finding of additional masticatory muscle activity? a narrative review of literature (2024)
Conti, Paulo César Rodrigues ; Cunha, Carolina Ortigosa ; Conti, Ana Cláudia de Castro Ferreira ; Bonjardim, Leonardo Rigoldi ; Barbosa, Juliana Stuginski ; Costa, Yuri Martins
Source: Journal of Oral Rehabilitation. Unidade: FOB
Subjects: BRUXISMO, REFLUXO GASTROESOFÁGICO, APNEIA DO SONO TIPO OBSTRUTIVA, NEUROLOGIA
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ABNT
CONTI, Paulo César Rodrigues et al. Secondary bruxism: a valid diagnosis or just a coincidental finding of additional masticatory muscle activity? a narrative review of literature. Journal of Oral Rehabilitation, v. 51, n. Ja 2024, p. 74-86, 2024Tradução . . Disponível em: https://doi.org/10.1111/joor.13592. Acesso em: 17 out. 2024.
APA
Conti, P. C. R., Cunha, C. O., Conti, A. C. de C. F., Bonjardim, L. R., Barbosa, J. S., & Costa, Y. M. (2024). Secondary bruxism: a valid diagnosis or just a coincidental finding of additional masticatory muscle activity? a narrative review of literature. Journal of Oral Rehabilitation, 51( Ja 2024), 74-86. doi:10.1111/joor.13592
NLM
Conti PCR, Cunha CO, Conti AC de CF, Bonjardim LR, Barbosa JS, Costa YM. Secondary bruxism: a valid diagnosis or just a coincidental finding of additional masticatory muscle activity? a narrative review of literature [Internet]. Journal of Oral Rehabilitation. 2024 ; 51( Ja 2024): 74-86.[citado 2024 out. 17 ] Available from: https://doi.org/10.1111/joor.13592
Vancouver
Conti PCR, Cunha CO, Conti AC de CF, Bonjardim LR, Barbosa JS, Costa YM. Secondary bruxism: a valid diagnosis or just a coincidental finding of additional masticatory muscle activity? a narrative review of literature [Internet]. Journal of Oral Rehabilitation. 2024 ; 51( Ja 2024): 74-86.[citado 2024 out. 17 ] Available from: https://doi.org/10.1111/joor.13592
Trabalho de evento-resumo periodico
Merosin-positive congenital muscular dystrophy with cerebellar hypoplasia and mental retardation: report of three cases (2002)
Reed, Umbertina Conti; Gurgel-Giannetti, J.; Resende, M. B. D.; Ferreira, L. G.; Carvalho, M. S.; Marie, Suely Kazue Nagahashi
Source: Neuromuscular Disorders. Conference titles: International Congress of the World Muscle Society. Unidade: FM
Subjects: DISTROFIA MUSCULAR, NEUROLOGIA
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ABNT
REED, Umbertina Conti et al. Merosin-positive congenital muscular dystrophy with cerebellar hypoplasia and mental retardation: report of three cases. Neuromuscular Disorders. Oxford: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 17 out. 2024. , 2002
APA
Reed, U. C., Gurgel-Giannetti, J., Resende, M. B. D., Ferreira, L. G., Carvalho, M. S., & Marie, S. K. N. (2002). Merosin-positive congenital muscular dystrophy with cerebellar hypoplasia and mental retardation: report of three cases. Neuromuscular Disorders. Oxford: Faculdade de Medicina, Universidade de São Paulo.
NLM
Reed UC, Gurgel-Giannetti J, Resende MBD, Ferreira LG, Carvalho MS, Marie SKN. Merosin-positive congenital muscular dystrophy with cerebellar hypoplasia and mental retardation: report of three cases. Neuromuscular Disorders. 2002 ; 12( 7-8): 765.[citado 2024 out. 17 ]
Vancouver
Reed UC, Gurgel-Giannetti J, Resende MBD, Ferreira LG, Carvalho MS, Marie SKN. Merosin-positive congenital muscular dystrophy with cerebellar hypoplasia and mental retardation: report of three cases. Neuromuscular Disorders. 2002 ; 12( 7-8): 765.[citado 2024 out. 17 ]
Trabalho de evento-resumo periodico
Rod distribution and muscles fibers type modification in the progression of nemaline myopathy (2002)
Gurgel-Giannetti, J.; Zanoteli, E.; Werneck, L. C.; Reed, Umbertina Conti; Beggs, A. H.; Marie, Suely Kazue Nagahashi; Fireman, M. A. T.; Oliveira, A. S. B.; Zatz, Mayana ; Vainzof, Mariz
Source: Neuromuscular Disorders. Conference titles: International Congress of the World Muscle Society. Unidades: FM, IB
Assunto: NEUROLOGIA
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ABNT
GURGEL-GIANNETTI, J. et al. Rod distribution and muscles fibers type modification in the progression of nemaline myopathy. Neuromuscular Disorders. Oxford: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 17 out. 2024. , 2002
APA
Gurgel-Giannetti, J., Zanoteli, E., Werneck, L. C., Reed, U. C., Beggs, A. H., Marie, S. K. N., et al. (2002). Rod distribution and muscles fibers type modification in the progression of nemaline myopathy. Neuromuscular Disorders. Oxford: Faculdade de Medicina, Universidade de São Paulo.
NLM
Gurgel-Giannetti J, Zanoteli E, Werneck LC, Reed UC, Beggs AH, Marie SKN, Fireman MAT, Oliveira ASB, Zatz M, Vainzof M. Rod distribution and muscles fibers type modification in the progression of nemaline myopathy. Neuromuscular Disorders. 2002 ; 12( 7-8): 767 res. G.P.6.11.[citado 2024 out. 17 ]
Vancouver
Gurgel-Giannetti J, Zanoteli E, Werneck LC, Reed UC, Beggs AH, Marie SKN, Fireman MAT, Oliveira ASB, Zatz M, Vainzof M. Rod distribution and muscles fibers type modification in the progression of nemaline myopathy. Neuromuscular Disorders. 2002 ; 12( 7-8): 767 res. G.P.6.11.[citado 2024 out. 17 ]
Trabalho de evento-resumo periodico
Amyotrophic lateral sclerosis (ALS) in Brazil: prospective evaluation of 90 patients (2001)
Silva, H. C. A.; Callegaro, D.; Hirata, M. T. A.; Broto, M. W. I.; Marchiori, P. E.; Scaff, Milberto
Source: Amyotrophic Lateral Sclerosis and other Motor Neuron Disorders. Conference titles: International Symposium on ALS/MND. Unidade: FM
Assunto: NEUROLOGIA
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ABNT
SILVA, H. C. A. et al. Amyotrophic lateral sclerosis (ALS) in Brazil: prospective evaluation of 90 patients. Amyotrophic Lateral Sclerosis and other Motor Neuron Disorders. London: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 17 out. 2024. , 2001
APA
Silva, H. C. A., Callegaro, D., Hirata, M. T. A., Broto, M. W. I., Marchiori, P. E., & Scaff, M. (2001). Amyotrophic lateral sclerosis (ALS) in Brazil: prospective evaluation of 90 patients. Amyotrophic Lateral Sclerosis and other Motor Neuron Disorders. London: Faculdade de Medicina, Universidade de São Paulo.
NLM
Silva HCA, Callegaro D, Hirata MTA, Broto MWI, Marchiori PE, Scaff M. Amyotrophic lateral sclerosis (ALS) in Brazil: prospective evaluation of 90 patients. Amyotrophic Lateral Sclerosis and other Motor Neuron Disorders. 2001 ; 2 54 res. P3.[citado 2024 out. 17 ]
Vancouver
Silva HCA, Callegaro D, Hirata MTA, Broto MWI, Marchiori PE, Scaff M. Amyotrophic lateral sclerosis (ALS) in Brazil: prospective evaluation of 90 patients. Amyotrophic Lateral Sclerosis and other Motor Neuron Disorders. 2001 ; 2 54 res. P3.[citado 2024 out. 17 ]
Trabalho de evento-resumo periodico
Identification and analysis of the motor systems at work on oral language production in amyotrophic lateral sclerosis (2001)
Paiva, L. S.; Silva, H. C. A.; Mansur, Letícia Lessa; Callegaro, D.; Scaff, Milberto; Marchiori, P. E.
Source: Amyotrophic Lateral Sclerosis and other Motor Neuron Disorders. Conference titles: International Symposium on ALS/MND. Unidade: FM
Assunto: NEUROLOGIA
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ABNT
PAIVA, L. S. et al. Identification and analysis of the motor systems at work on oral language production in amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis and other Motor Neuron Disorders. London: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 17 out. 2024. , 2001
APA
Paiva, L. S., Silva, H. C. A., Mansur, L. L., Callegaro, D., Scaff, M., & Marchiori, P. E. (2001). Identification and analysis of the motor systems at work on oral language production in amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis and other Motor Neuron Disorders. London: Faculdade de Medicina, Universidade de São Paulo.
NLM
Paiva LS, Silva HCA, Mansur LL, Callegaro D, Scaff M, Marchiori PE. Identification and analysis of the motor systems at work on oral language production in amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis and other Motor Neuron Disorders. 2001 ; 2 88 res. P54.[citado 2024 out. 17 ]
Vancouver
Paiva LS, Silva HCA, Mansur LL, Callegaro D, Scaff M, Marchiori PE. Identification and analysis of the motor systems at work on oral language production in amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis and other Motor Neuron Disorders. 2001 ; 2 88 res. P54.[citado 2024 out. 17 ]
Trabalho de evento-resumo periodico
Importance of the physical therapeutic program in muscular force and the functional state in patients with amyotrophic lateral sclerosis during 6 months (2001)
Pedroso, J. P. C.; Ramirez, C.; Silva, H. C. A.; Callegaro, D.; Marchiori, P. E.; Scaff, Milberto; Piemonte, Maria Elisa Pimentel
Source: Amyotrophic Lateral Sclerosis and other Motor Neuron Disorders. Conference titles: International Symposium on ALS/MND. Unidade: FM
Assunto: NEUROLOGIA
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ABNT
PEDROSO, J. P. C. et al. Importance of the physical therapeutic program in muscular force and the functional state in patients with amyotrophic lateral sclerosis during 6 months. Amyotrophic Lateral Sclerosis and other Motor Neuron Disorders. London: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 17 out. 2024. , 2001
APA
Pedroso, J. P. C., Ramirez, C., Silva, H. C. A., Callegaro, D., Marchiori, P. E., Scaff, M., & Piemonte, M. E. P. (2001). Importance of the physical therapeutic program in muscular force and the functional state in patients with amyotrophic lateral sclerosis during 6 months. Amyotrophic Lateral Sclerosis and other Motor Neuron Disorders. London: Faculdade de Medicina, Universidade de São Paulo.
NLM
Pedroso JPC, Ramirez C, Silva HCA, Callegaro D, Marchiori PE, Scaff M, Piemonte MEP. Importance of the physical therapeutic program in muscular force and the functional state in patients with amyotrophic lateral sclerosis during 6 months. Amyotrophic Lateral Sclerosis and other Motor Neuron Disorders. 2001 ; 2 94 res. P63.[citado 2024 out. 17 ]
Vancouver
Pedroso JPC, Ramirez C, Silva HCA, Callegaro D, Marchiori PE, Scaff M, Piemonte MEP. Importance of the physical therapeutic program in muscular force and the functional state in patients with amyotrophic lateral sclerosis during 6 months. Amyotrophic Lateral Sclerosis and other Motor Neuron Disorders. 2001 ; 2 94 res. P63.[citado 2024 out. 17 ]
Artigo de periodico
Role of central adenosine in the respiratory and thermoregulatory responses to hypoxia (2000)
Barros, Renata C H; Branco, Luiz Guilherme de Siqueira
Source: Anatomic Nervous System. Unidade: FORP
Assunto: NEUROLOGIA
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ABNT
BARROS, Renata C H e BRANCO, Luiz Guilherme de Siqueira. Role of central adenosine in the respiratory and thermoregulatory responses to hypoxia. Anatomic Nervous System, v. 11, n. 1, p. 193-197, 2000Tradução . . Disponível em: https://doi.org/10.1097/00001756-200001170-00038. Acesso em: 17 out. 2024.
APA
Barros, R. C. H., & Branco, L. G. de S. (2000). Role of central adenosine in the respiratory and thermoregulatory responses to hypoxia. Anatomic Nervous System, 11( 1), 193-197. doi:10.1097/00001756-200001170-00038
NLM
Barros RCH, Branco LG de S. Role of central adenosine in the respiratory and thermoregulatory responses to hypoxia [Internet]. Anatomic Nervous System. 2000 ; 11( 1): 193-197.[citado 2024 out. 17 ] Available from: https://doi.org/10.1097/00001756-200001170-00038
Vancouver
Barros RCH, Branco LG de S. Role of central adenosine in the respiratory and thermoregulatory responses to hypoxia [Internet]. Anatomic Nervous System. 2000 ; 11( 1): 193-197.[citado 2024 out. 17 ] Available from: https://doi.org/10.1097/00001756-200001170-00038
Artigo de periodico-carta/editorial
Central nervous system involvement in a novel connexin 32 mutation affecting identical twins. [Carta] (1999)
Sweeney, M. G.; Wood, Nicholas W.; Wroe, S. J.; Marques, W.
Source: Journal of Neurology, Neurosurgery and Psychiatry. Unidade: FMRP
Assunto: NEUROLOGIA
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ABNT
SWEENEY, M. G. et al. Central nervous system involvement in a novel connexin 32 mutation affecting identical twins. [Carta]. Journal of Neurology, Neurosurgery and Psychiatry. London: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 17 out. 2024. , 1999
APA
Sweeney, M. G., Wood, N. W., Wroe, S. J., & Marques, W. (1999). Central nervous system involvement in a novel connexin 32 mutation affecting identical twins. [Carta]. Journal of Neurology, Neurosurgery and Psychiatry. London: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Sweeney MG, Wood NW, Wroe SJ, Marques W. Central nervous system involvement in a novel connexin 32 mutation affecting identical twins. [Carta]. Journal of Neurology, Neurosurgery and Psychiatry. 1999 ; 66( 6): 803-804.[citado 2024 out. 17 ]
Vancouver
Sweeney MG, Wood NW, Wroe SJ, Marques W. Central nervous system involvement in a novel connexin 32 mutation affecting identical twins. [Carta]. Journal of Neurology, Neurosurgery and Psychiatry. 1999 ; 66( 6): 803-804.[citado 2024 out. 17 ]
Artigo de periodico
Further evidence for the organisation of the four sarcoglycans proteins within the dystrophin-glycoprotein complex (1999)
Vainzof, Mariz ; Moreira, E. S.; Ferraz, G.; Passos-Bueno, Maria Rita ; Marie, Suely Kazue Nagahashi; Zatz, Mayana
Source: European Journal of Human Genetics. Unidades: IB, FM
Assunto: NEUROLOGIA
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ABNT
VAINZOF, Mariz et al. Further evidence for the organisation of the four sarcoglycans proteins within the dystrophin-glycoprotein complex. European Journal of Human Genetics, v. 7, p. 251-254, 1999Tradução . . Disponível em: https://doi.org/10.1038/sj.ejhg.5200263. Acesso em: 17 out. 2024.
APA
Vainzof, M., Moreira, E. S., Ferraz, G., Passos-Bueno, M. R., Marie, S. K. N., & Zatz, M. (1999). Further evidence for the organisation of the four sarcoglycans proteins within the dystrophin-glycoprotein complex. European Journal of Human Genetics, 7, 251-254. doi:10.1038/sj.ejhg.5200263
NLM
Vainzof M, Moreira ES, Ferraz G, Passos-Bueno MR, Marie SKN, Zatz M. Further evidence for the organisation of the four sarcoglycans proteins within the dystrophin-glycoprotein complex [Internet]. European Journal of Human Genetics. 1999 ; 7 251-254.[citado 2024 out. 17 ] Available from: https://doi.org/10.1038/sj.ejhg.5200263
Vancouver
Vainzof M, Moreira ES, Ferraz G, Passos-Bueno MR, Marie SKN, Zatz M. Further evidence for the organisation of the four sarcoglycans proteins within the dystrophin-glycoprotein complex [Internet]. European Journal of Human Genetics. 1999 ; 7 251-254.[citado 2024 out. 17 ] Available from: https://doi.org/10.1038/sj.ejhg.5200263
Trabalho de evento-resumo periodico
Neuropathology of the eye-the-tiger sign in hallervorden-spats syndrome (1995)
Rosemberg, Sérgio; Barbosa, E R; Menezes Netto, J R; Santos, C R
Source: Developmental Medicine and Child Neurology. Conference titles: European Paediatric Neurology Society Meeting. Unidade: FM
Assunto: NEUROLOGIA
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ABNT
ROSEMBERG, Sérgio et al. Neuropathology of the eye-the-tiger sign in hallervorden-spats syndrome. Developmental Medicine and Child Neurology. London: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 17 out. 2024. , 1995
APA
Rosemberg, S., Barbosa, E. R., Menezes Netto, J. R., & Santos, C. R. (1995). Neuropathology of the eye-the-tiger sign in hallervorden-spats syndrome. Developmental Medicine and Child Neurology. London: Faculdade de Medicina, Universidade de São Paulo.
NLM
Rosemberg S, Barbosa ER, Menezes Netto JR, Santos CR. Neuropathology of the eye-the-tiger sign in hallervorden-spats syndrome. Developmental Medicine and Child Neurology. 1995 ;37( 3 suppl.72): 108.[citado 2024 out. 17 ]
Vancouver
Rosemberg S, Barbosa ER, Menezes Netto JR, Santos CR. Neuropathology of the eye-the-tiger sign in hallervorden-spats syndrome. Developmental Medicine and Child Neurology. 1995 ;37( 3 suppl.72): 108.[citado 2024 out. 17 ]
Artigo de periodico
Common missense mutation in the adhalin gene in three unrelated brazilian families with a relatively mild form of autosomal recessive limb girdle muscular dystrophy (1995)
Passos-Bueno, Maria Rita ; Moreira, E S; Vainzof, Mariz ; Chamberlain, J; Marie, Suely Kazue Nagahashi; Pereira, L; Akujama, J Y; Roberds, S; Campbell, K P; Zatz, Mayana
Source: Human Molecular Genetics. Unidade: FM
Assunto: NEUROLOGIA
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ABNT
PASSOS-BUENO, Maria Rita et al. Common missense mutation in the adhalin gene in three unrelated brazilian families with a relatively mild form of autosomal recessive limb girdle muscular dystrophy. Human Molecular Genetics, v. 4 , n. 7 , p. 1163-7, 1995Tradução . . Disponível em: https://doi.org/10.1093/hmg/4.7.1163. Acesso em: 17 out. 2024.
APA
Passos-Bueno, M. R., Moreira, E. S., Vainzof, M., Chamberlain, J., Marie, S. K. N., Pereira, L., et al. (1995). Common missense mutation in the adhalin gene in three unrelated brazilian families with a relatively mild form of autosomal recessive limb girdle muscular dystrophy. Human Molecular Genetics, 4 ( 7 ), 1163-7. doi:10.1093/hmg/4.7.1163
NLM
Passos-Bueno MR, Moreira ES, Vainzof M, Chamberlain J, Marie SKN, Pereira L, Akujama JY, Roberds S, Campbell KP, Zatz M. Common missense mutation in the adhalin gene in three unrelated brazilian families with a relatively mild form of autosomal recessive limb girdle muscular dystrophy [Internet]. Human Molecular Genetics. 1995 ;4 ( 7 ): 1163-7.[citado 2024 out. 17 ] Available from: https://doi.org/10.1093/hmg/4.7.1163
Vancouver
Passos-Bueno MR, Moreira ES, Vainzof M, Chamberlain J, Marie SKN, Pereira L, Akujama JY, Roberds S, Campbell KP, Zatz M. Common missense mutation in the adhalin gene in three unrelated brazilian families with a relatively mild form of autosomal recessive limb girdle muscular dystrophy [Internet]. Human Molecular Genetics. 1995 ;4 ( 7 ): 1163-7.[citado 2024 out. 17 ] Available from: https://doi.org/10.1093/hmg/4.7.1163

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