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Artigo de periodico
Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification (2013)
Hsu, Sandy Chan; Sears, Renee L.; Lemos, Roberta R.; Zatz, Mayana
Source: Neurogenetics. Unidade: IB
Subjects: MUTAÇÃO GENÉTICA, GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
HSU, Sandy Chan et al. Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification. Neurogenetics, v. 14, p. online, 2013Tradução . . Disponível em: https://doi.org/10.1007/s10048-012-0349-2. Acesso em: 04 nov. 2024.
APA
Hsu, S. C., Sears, R. L., Lemos, R. R., & Zatz, M. (2013). Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification. Neurogenetics, 14, online. doi:10.1007/s10048-012-0349-2
NLM
Hsu SC, Sears RL, Lemos RR, Zatz M. Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification [Internet]. Neurogenetics. 2013 ; 14 online.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1007/s10048-012-0349-2
Vancouver
Hsu SC, Sears RL, Lemos RR, Zatz M. Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification [Internet]. Neurogenetics. 2013 ; 14 online.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1007/s10048-012-0349-2
Artigo de periodico
New mutations in the ATM gene and clinical data of 25 AT patients (2011)
Demuth, Ilja; Dutrannoy, Véronique; Marques Júnior, Wilson; Neitzel, Heidemarie; Schindler, Detlev; Dimova, Ptja S.; Chrzanowaka, Krystyna H.; Bojinova, Veneta; Gregorek, Hanna; Graul-Neumann, Luitgard M.; ; Schulze, Ilka; Nicke, Marion; Bora, Elcin; Cankaya, Tufan; Oláh, Éva; Kiss, Csongor; Bessenyei, Beáta; Szakszon, Katalin; Gruber-Sedlmayr, Ursula; Kroisel, Peter Michael; Sodia, Sigrun; Goecke, Timm O.; Dörk, Thilo; Digweed, Martin; Sperling, Karl; Sá, Joaquim de; Lourenço, Charles Marques; Varon, Raymonda
Source: Neurogenetics. Unidade: FMRP
Subjects: DOENÇAS DO SISTEMA NERVOSO, DEGENERAÇÃO NEURAL, ATAXIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DEMUTH, Ilja et al. New mutations in the ATM gene and clinical data of 25 AT patients. Neurogenetics, v. 12, n. 4, p. 273-282, 2011Tradução . . Disponível em: https://doi.org/10.1007/s10048-011-0299-0. Acesso em: 04 nov. 2024.
APA
Demuth, I., Dutrannoy, V., Marques Júnior, W., Neitzel, H., Schindler, D., Dimova, P. S., et al. (2011). New mutations in the ATM gene and clinical data of 25 AT patients. Neurogenetics, 12( 4), 273-282. doi:10.1007/s10048-011-0299-0
NLM
Demuth I, Dutrannoy V, Marques Júnior W, Neitzel H, Schindler D, Dimova PS, Chrzanowaka KH, Bojinova V, Gregorek H, Graul-Neumann LM, , Schulze I, Nicke M, Bora E, Cankaya T, Oláh É, Kiss C, Bessenyei B, Szakszon K, Gruber-Sedlmayr U, Kroisel PM, Sodia S, Goecke TO, Dörk T, Digweed M, Sperling K, Sá J de, Lourenço CM, Varon R. New mutations in the ATM gene and clinical data of 25 AT patients [Internet]. Neurogenetics. 2011 ; 12( 4): 273-282.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1007/s10048-011-0299-0
Vancouver
Demuth I, Dutrannoy V, Marques Júnior W, Neitzel H, Schindler D, Dimova PS, Chrzanowaka KH, Bojinova V, Gregorek H, Graul-Neumann LM, , Schulze I, Nicke M, Bora E, Cankaya T, Oláh É, Kiss C, Bessenyei B, Szakszon K, Gruber-Sedlmayr U, Kroisel PM, Sodia S, Goecke TO, Dörk T, Digweed M, Sperling K, Sá J de, Lourenço CM, Varon R. New mutations in the ATM gene and clinical data of 25 AT patients [Internet]. Neurogenetics. 2011 ; 12( 4): 273-282.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1007/s10048-011-0299-0
Artigo de periodico
Compound Charcot-Marie-Tooth disease may determine unusual and milder phenotypes (2010)
Gouvêa, Silmara P.; Borghetti, Vinicius Horacio Stefani; Bueno, Keity Cristina; Genari, Adriana Borges; Lourenço, Charles Marques; Sobreira, Cláudia Ferreira da Rosa; Barreira, Amilton Antunes; Marques Júnior, Wilson
Source: Neurogenetics. Unidade: FMRP
Subjects: MUTAÇÃO GENÉTICA, DOENÇAS DO SISTEMA NERVOSO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GOUVÊA, Silmara P. et al. Compound Charcot-Marie-Tooth disease may determine unusual and milder phenotypes. Neurogenetics, v. 11, n. 1, p. 135-138, 2010Tradução . . Disponível em: https://doi.org/10.1007/s10048-009-0211-3. Acesso em: 04 nov. 2024.
APA
Gouvêa, S. P., Borghetti, V. H. S., Bueno, K. C., Genari, A. B., Lourenço, C. M., Sobreira, C. F. da R., et al. (2010). Compound Charcot-Marie-Tooth disease may determine unusual and milder phenotypes. Neurogenetics, 11( 1), 135-138. doi:10.1007/s10048-009-0211-3
NLM
Gouvêa SP, Borghetti VHS, Bueno KC, Genari AB, Lourenço CM, Sobreira CF da R, Barreira AA, Marques Júnior W. Compound Charcot-Marie-Tooth disease may determine unusual and milder phenotypes [Internet]. Neurogenetics. 2010 ; 11( 1): 135-138.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1007/s10048-009-0211-3
Vancouver
Gouvêa SP, Borghetti VHS, Bueno KC, Genari AB, Lourenço CM, Sobreira CF da R, Barreira AA, Marques Júnior W. Compound Charcot-Marie-Tooth disease may determine unusual and milder phenotypes [Internet]. Neurogenetics. 2010 ; 11( 1): 135-138.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1007/s10048-009-0211-3
Artigo de periodico
Reevaluation of a large family defines a new locus for x-linked recessive pure spastic paraplegia (SPG34) on chromosome Xq25 (2008)
Macedo-Souza, Lúcia Inês; Kok, Fernando; Santos, Silvana; Licinio, Luciana; Lezirovitz, Karina; Nascimento, Rafaella Maria Pessutti; Bueno, Clarissa; Martyn, Marcília; Leão, Emília Katiane Embiruçu de Araujo; Zatz, Mayana
Source: Neurogenetics. Unidade: IB
Assunto: GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MACEDO-SOUZA, Lúcia Inês et al. Reevaluation of a large family defines a new locus for x-linked recessive pure spastic paraplegia (SPG34) on chromosome Xq25. Neurogenetics, v. 9, n. 3, p. 225-226, 2008Tradução . . Disponível em: https://doi.org/10.1007/s10048-008-0130-8. Acesso em: 04 nov. 2024.
APA
Macedo-Souza, L. I., Kok, F., Santos, S., Licinio, L., Lezirovitz, K., Nascimento, R. M. P., et al. (2008). Reevaluation of a large family defines a new locus for x-linked recessive pure spastic paraplegia (SPG34) on chromosome Xq25. Neurogenetics, 9( 3), 225-226. doi:10.1007/s10048-008-0130-8
NLM
Macedo-Souza LI, Kok F, Santos S, Licinio L, Lezirovitz K, Nascimento RMP, Bueno C, Martyn M, Leão EKE de A, Zatz M. Reevaluation of a large family defines a new locus for x-linked recessive pure spastic paraplegia (SPG34) on chromosome Xq25 [Internet]. Neurogenetics. 2008 ; 9( 3): 225-226.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1007/s10048-008-0130-8
Vancouver
Macedo-Souza LI, Kok F, Santos S, Licinio L, Lezirovitz K, Nascimento RMP, Bueno C, Martyn M, Leão EKE de A, Zatz M. Reevaluation of a large family defines a new locus for x-linked recessive pure spastic paraplegia (SPG34) on chromosome Xq25 [Internet]. Neurogenetics. 2008 ; 9( 3): 225-226.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1007/s10048-008-0130-8
Artigo de periodico
Inter-laboratory comparison of DNA preservation in archival paraffin-embedded human brain tissue from participating centres on four continents (2001)
Kösel, S.; Grasbon-Frodl, E. M.; Arima, K.; Chimelli, L.; Hahn, M.; Hashizume, Y.; Hulette, C.; Ikeda, K.; Jacobsen, P. F.; Jones, M.; Kobayashi, M.; Love, S.; Mizutani, T.; Rosemberg, Sergio; Sasaki, A.; Smith, T. W.; Takahashi, H.; Vortmeyer, A. O.
Source: Neurogenetics. Unidade: FM
Subjects: DNA, CROMATOGRAFIA LÍQUIDA DE ALTA EFICIÊNCIA, DNA MITOCONDRIAL, REAÇÃO EM CADEIA POR POLIMERASE, ULTRAFILTRAÇÃO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KÖSEL, S. et al. Inter-laboratory comparison of DNA preservation in archival paraffin-embedded human brain tissue from participating centres on four continents. Neurogenetics, v. 3, p. 163-170, 2001Tradução . . Disponível em: https://doi.org/10.1007/s100480100114. Acesso em: 04 nov. 2024.
APA
Kösel, S., Grasbon-Frodl, E. M., Arima, K., Chimelli, L., Hahn, M., Hashizume, Y., et al. (2001). Inter-laboratory comparison of DNA preservation in archival paraffin-embedded human brain tissue from participating centres on four continents. Neurogenetics, 3, 163-170. doi:10.1007/s100480100114
NLM
Kösel S, Grasbon-Frodl EM, Arima K, Chimelli L, Hahn M, Hashizume Y, Hulette C, Ikeda K, Jacobsen PF, Jones M, Kobayashi M, Love S, Mizutani T, Rosemberg S, Sasaki A, Smith TW, Takahashi H, Vortmeyer AO. Inter-laboratory comparison of DNA preservation in archival paraffin-embedded human brain tissue from participating centres on four continents [Internet]. Neurogenetics. 2001 ; 3 163-170.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1007/s100480100114
Vancouver
Kösel S, Grasbon-Frodl EM, Arima K, Chimelli L, Hahn M, Hashizume Y, Hulette C, Ikeda K, Jacobsen PF, Jones M, Kobayashi M, Love S, Mizutani T, Rosemberg S, Sasaki A, Smith TW, Takahashi H, Vortmeyer AO. Inter-laboratory comparison of DNA preservation in archival paraffin-embedded human brain tissue from participating centres on four continents [Internet]. Neurogenetics. 2001 ; 3 163-170.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1007/s100480100114

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