ReP USP - Resultado da busca

Artigo de periodico
STAC3 variants cause a congenital myopathy with distinctive dysmorphic features and malignant hyperthermia susceptibility (2018)
Zaharieva, Irina T; Sarkozy, Anna; Munot, Pinki; Manzur, Adnan; O'grady, Gina; Rendu, John; Malfatti, Eduardo; Amthor, Helge; Servais, Laurent; Urtizberea, J. Andoni; Zanoteli, Edmar
Source: Human mutation. Unidade: FM
Subjects: MIOPATIAS CONGÊNITAS ESTRUTURAIS, HIPERTERMIA MALIGNA, PROTEÍNAS MUSCULARES, CONTRAÇÃO MUSCULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZAHARIEVA, Irina T et al. STAC3 variants cause a congenital myopathy with distinctive dysmorphic features and malignant hyperthermia susceptibility. Human mutation, v. 39, n. 12, p. 1980-1994, 2018Tradução . . Disponível em: https://doi.org/10.1002/humu.23635. Acesso em: 23 out. 2025.
APA
Zaharieva, I. T., Sarkozy, A., Munot, P., Manzur, A., O'grady, G., Rendu, J., et al. (2018). STAC3 variants cause a congenital myopathy with distinctive dysmorphic features and malignant hyperthermia susceptibility. Human mutation, 39( 12), 1980-1994. doi:10.1002/humu.23635
NLM
Zaharieva IT, Sarkozy A, Munot P, Manzur A, O'grady G, Rendu J, Malfatti E, Amthor H, Servais L, Urtizberea JA, Zanoteli E. STAC3 variants cause a congenital myopathy with distinctive dysmorphic features and malignant hyperthermia susceptibility [Internet]. Human mutation. 2018 ; 39( 12): 1980-1994.[citado 2025 out. 23 ] Available from: https://doi.org/10.1002/humu.23635
Vancouver
Zaharieva IT, Sarkozy A, Munot P, Manzur A, O'grady G, Rendu J, Malfatti E, Amthor H, Servais L, Urtizberea JA, Zanoteli E. STAC3 variants cause a congenital myopathy with distinctive dysmorphic features and malignant hyperthermia susceptibility [Internet]. Human mutation. 2018 ; 39( 12): 1980-1994.[citado 2025 out. 23 ] Available from: https://doi.org/10.1002/humu.23635
Artigo de periodico
ClinVar database of global familial hypercholesterolemia-associated DNA variants (2018)
Iacocca, Michael A; Santos, Raul D
Source: Human mutation. Unidade: FM
Subjects: HIPERCOLESTEROLEMIA, DOENÇAS GENÉTICAS, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
IACOCCA, Michael A e SANTOS, Raul D. ClinVar database of global familial hypercholesterolemia-associated DNA variants. Human mutation, v. 39, n. 11, p. 1631-1640, 2018Tradução . . Disponível em: https://doi.org/10.1002/humu.23634. Acesso em: 23 out. 2025.
APA
Iacocca, M. A., & Santos, R. D. (2018). ClinVar database of global familial hypercholesterolemia-associated DNA variants. Human mutation, 39( 11), 1631-1640. doi:10.1002/humu.23634
NLM
Iacocca MA, Santos RD. ClinVar database of global familial hypercholesterolemia-associated DNA variants [Internet]. Human mutation. 2018 ; 39( 11): 1631-1640.[citado 2025 out. 23 ] Available from: https://doi.org/10.1002/humu.23634
Vancouver
Iacocca MA, Santos RD. ClinVar database of global familial hypercholesterolemia-associated DNA variants [Internet]. Human mutation. 2018 ; 39( 11): 1631-1640.[citado 2025 out. 23 ] Available from: https://doi.org/10.1002/humu.23634
Artigo de periodico
Risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germline RET mutations located in exon 10 (2011)
Frank-Raue, Karin; Rybicki, Lisa A.; Erlic, Zoran; Schweizer, Heiko; Winter, Aurelia; Milos, Ioana; Toledo, Sergio Pereira de Almeida; Toledo, Rodrigo A.; Tavares, Marcos R.; Alevizaki, Maria; Mian, Caterina; Siggelkow, Heide; Hüfner, Michael; Wohllk, Nelson; Opocher, Giuseppe; Dvořáková, Šárka; Bendlova, Bela; Czetwertynska, Małgorzata; Skasko, Elżbieta; Barontini, Marta; Sanso, Gabriela; Vorländer, Christian; Maia, Ana Luiza; Patocs, Attila; Links, Thera P.; de Groot, Jan Willem; Kerstens, Michiel N.; Valk, Gerlof D.; Miehle, Konstanze; Musholt, Thomas J.; Biarnes, Josefina; Damjanovic, Svetozar; Muresan, Mihaela; Wüster, Christian; Fassnacht, Martin; Peczkowska, Mariola; Fauth, Christine; Golcher, Henriette; Walter, Martin A.; Pichl, Josef; Raue, Friedhelm; Eng, Charis; Neumann, Hartmut P. H.
Source: Human mutation. Unidade: FM
Subjects: NEOPLASIA ENDÓCRINA MÚLTIPLA (GENÉTICA), FATORES DE CRESCIMENTO, NEOPLASIAS DA TIREOIDE, GENÓTIPOS, CARCINOMA MEDULAR, FENÓTIPOS, METÁSTASE NEOPLÁSICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FRANK-RAUE, Karin et al. Risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germline RET mutations located in exon 10. Human mutation, v. 32, n. 1, p. 51-58, 2011Tradução . . Disponível em: http://onlinelibrary.wiley.com/doi/10.1002/humu.21385/pdf. Acesso em: 23 out. 2025.
APA
Frank-Raue, K., Rybicki, L. A., Erlic, Z., Schweizer, H., Winter, A., Milos, I., et al. (2011). Risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germline RET mutations located in exon 10. Human mutation, 32( 1), 51-58. doi:10.1002/humu.21385
NLM
Frank-Raue K, Rybicki LA, Erlic Z, Schweizer H, Winter A, Milos I, Toledo SP de A, Toledo RA, Tavares MR, Alevizaki M, Mian C, Siggelkow H, Hüfner M, Wohllk N, Opocher G, Dvořáková Š, Bendlova B, Czetwertynska M, Skasko E, Barontini M, Sanso G, Vorländer C, Maia AL, Patocs A, Links TP, de Groot JW, Kerstens MN, Valk GD, Miehle K, Musholt TJ, Biarnes J, Damjanovic S, Muresan M, Wüster C, Fassnacht M, Peczkowska M, Fauth C, Golcher H, Walter MA, Pichl J, Raue F, Eng C, Neumann HPH. Risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germline RET mutations located in exon 10 [Internet]. Human mutation. 2011 ; 32( 1): 51-58.[citado 2025 out. 23 ] Available from: http://onlinelibrary.wiley.com/doi/10.1002/humu.21385/pdf
Vancouver
Frank-Raue K, Rybicki LA, Erlic Z, Schweizer H, Winter A, Milos I, Toledo SP de A, Toledo RA, Tavares MR, Alevizaki M, Mian C, Siggelkow H, Hüfner M, Wohllk N, Opocher G, Dvořáková Š, Bendlova B, Czetwertynska M, Skasko E, Barontini M, Sanso G, Vorländer C, Maia AL, Patocs A, Links TP, de Groot JW, Kerstens MN, Valk GD, Miehle K, Musholt TJ, Biarnes J, Damjanovic S, Muresan M, Wüster C, Fassnacht M, Peczkowska M, Fauth C, Golcher H, Walter MA, Pichl J, Raue F, Eng C, Neumann HPH. Risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germline RET mutations located in exon 10 [Internet]. Human mutation. 2011 ; 32( 1): 51-58.[citado 2025 out. 23 ] Available from: http://onlinelibrary.wiley.com/doi/10.1002/humu.21385/pdf
Artigo de periodico
Detailed haplotype analysis at the TP53 Locus in p.R337H mutation carriers (2010)
Garritano, Sonia; Palmero, Edenir Inez; Olivier, Magali; Martel-Planche, Ghyslaine; Calvez-Kelm, Florence Lee; Brugiéres, Laurence; Vargas, Fernando Regla; Brentani, Ricardo Renzo; Ashton-Prolla, Patricia; Landi, Stefano; Tavtigian, Sean V; Hainaut, Pierre; Achatz, Maria Isabel W
Source: Human mutation. Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, POLIMORFISMO, NEOPLASIAS (GENÉTICA), RISCO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GARRITANO, Sonia et al. Detailed haplotype analysis at the TP53 Locus in p.R337H mutation carriers. Human mutation, v. 31, n. 2, p. 143-150, 2010Tradução . . Disponível em: https://doi.org/10.1002/humu.21151. Acesso em: 23 out. 2025.
APA
Garritano, S., Palmero, E. I., Olivier, M., Martel-Planche, G., Calvez-Kelm, F. L., Brugiéres, L., et al. (2010). Detailed haplotype analysis at the TP53 Locus in p.R337H mutation carriers. Human mutation, 31( 2), 143-150. doi:10.1002/humu.21151
NLM
Garritano S, Palmero EI, Olivier M, Martel-Planche G, Calvez-Kelm FL, Brugiéres L, Vargas FR, Brentani RR, Ashton-Prolla P, Landi S, Tavtigian SV, Hainaut P, Achatz MIW. Detailed haplotype analysis at the TP53 Locus in p.R337H mutation carriers [Internet]. Human mutation. 2010 ; 31( 2): 143-150.[citado 2025 out. 23 ] Available from: https://doi.org/10.1002/humu.21151
Vancouver
Garritano S, Palmero EI, Olivier M, Martel-Planche G, Calvez-Kelm FL, Brugiéres L, Vargas FR, Brentani RR, Ashton-Prolla P, Landi S, Tavtigian SV, Hainaut P, Achatz MIW. Detailed haplotype analysis at the TP53 Locus in p.R337H mutation carriers [Internet]. Human mutation. 2010 ; 31( 2): 143-150.[citado 2025 out. 23 ] Available from: https://doi.org/10.1002/humu.21151
Artigo de periodico
Wilson disease: novel mutations in the ATP7B gene and clinical correlation in Brazilian patients (2004)
Deguti, Marta M.; Genschel, Janine; Cançado, Eduardo L. R.; Barbosa, Egberto R.; Bochow, Bettina; Mucennic, Marcos; Porta, Gilda; Lochs, Herbert; Carrilho, Flair J.; Schmidt, Hartmut H.-J.
Source: Human mutation. Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, FENÓTIPOS, GENÓTIPOS, DOENÇAS GENÉTICAS (DIAGNÓSTICO), DOENÇAS DEGENERATIVAS (GENÉTICA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DEGUTI, Marta M. et al. Wilson disease: novel mutations in the ATP7B gene and clinical correlation in Brazilian patients. Human mutation, v. 23, n. 4, p. online, 2004Tradução . . Disponível em: https://doi.org/10.1002/humu.9227. Acesso em: 23 out. 2025.
APA
Deguti, M. M., Genschel, J., Cançado, E. L. R., Barbosa, E. R., Bochow, B., Mucennic, M., et al. (2004). Wilson disease: novel mutations in the ATP7B gene and clinical correlation in Brazilian patients. Human mutation, 23( 4), online. doi:10.1002/humu.9227
NLM
Deguti MM, Genschel J, Cançado ELR, Barbosa ER, Bochow B, Mucennic M, Porta G, Lochs H, Carrilho FJ, Schmidt HH-J. Wilson disease: novel mutations in the ATP7B gene and clinical correlation in Brazilian patients [Internet]. Human mutation. 2004 ; 23( 4): online.[citado 2025 out. 23 ] Available from: https://doi.org/10.1002/humu.9227
Vancouver
Deguti MM, Genschel J, Cançado ELR, Barbosa ER, Bochow B, Mucennic M, Porta G, Lochs H, Carrilho FJ, Schmidt HH-J. Wilson disease: novel mutations in the ATP7B gene and clinical correlation in Brazilian patients [Internet]. Human mutation. 2004 ; 23( 4): online.[citado 2025 out. 23 ] Available from: https://doi.org/10.1002/humu.9227
Artigo de periodico
PKHD1 mutations in autosomal recessive polycystic kidney disease (ARPKD) (2004)
Bergmann, Carsten; Senderek, Jan; Kupper, Fabian; Schneider, Frank; Dornia, Christian; Windelen, Ellen; Eggermann, Thomas; Rudnik-Schoneborn, Sabine; Kirfel, Jutta; Furu, Laszlo; Onuchic, Luiz F.; Rossetti, Sandro; Harris, Peter C.; Somlo, Stefan; Guay-Woodford, Lisa; Germino, Gregory G.; Moser, Markus; Buttner, Reinhard; Zerresm, Klaus
Source: Human mutation. Unidade: FM
Subjects: CISTOS, RIM (FISIOPATOLOGIA), GENÓTIPOS, MUTAÇÃO GENÉTICA, ANTICORPOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BERGMANN, Carsten et al. PKHD1 mutations in autosomal recessive polycystic kidney disease (ARPKD). Human mutation, v. 23, n. 5, p. 453-463, 2004Tradução . . Disponível em: http://onlinelibrary.wiley.com/doi/10.1002/humu.20029/pdf. Acesso em: 23 out. 2025.
APA
Bergmann, C., Senderek, J., Kupper, F., Schneider, F., Dornia, C., Windelen, E., et al. (2004). PKHD1 mutations in autosomal recessive polycystic kidney disease (ARPKD). Human mutation, 23( 5), 453-463. Recuperado de http://onlinelibrary.wiley.com/doi/10.1002/humu.20029/pdf
NLM
Bergmann C, Senderek J, Kupper F, Schneider F, Dornia C, Windelen E, Eggermann T, Rudnik-Schoneborn S, Kirfel J, Furu L, Onuchic LF, Rossetti S, Harris PC, Somlo S, Guay-Woodford L, Germino GG, Moser M, Buttner R, Zerresm K. PKHD1 mutations in autosomal recessive polycystic kidney disease (ARPKD) [Internet]. Human mutation. 2004 ; 23( 5): 453-463.[citado 2025 out. 23 ] Available from: http://onlinelibrary.wiley.com/doi/10.1002/humu.20029/pdf
Vancouver
Bergmann C, Senderek J, Kupper F, Schneider F, Dornia C, Windelen E, Eggermann T, Rudnik-Schoneborn S, Kirfel J, Furu L, Onuchic LF, Rossetti S, Harris PC, Somlo S, Guay-Woodford L, Germino GG, Moser M, Buttner R, Zerresm K. PKHD1 mutations in autosomal recessive polycystic kidney disease (ARPKD) [Internet]. Human mutation. 2004 ; 23( 5): 453-463.[citado 2025 out. 23 ] Available from: http://onlinelibrary.wiley.com/doi/10.1002/humu.20029/pdf
Artigo de periodico
Novel point mutations in the dystrophin gene (1997)
Zatz, Mayana ; Passos-Bueno, Maria Rita
Source: Human mutation. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZATZ, Mayana e PASSOS-BUENO, Maria Rita. Novel point mutations in the dystrophin gene. Human mutation, n. 10, p. 217-222, 1997Tradução . . Disponível em: https://doi.org/10.1002/(sici)1098-1004(1997)10:3%3C217::aid-humu7%3E3.3.co;2-o. Acesso em: 23 out. 2025.
APA
Zatz, M., & Passos-Bueno, M. R. (1997). Novel point mutations in the dystrophin gene. Human mutation, ( 10), 217-222. doi:10.1002/(sici)1098-1004(1997)10:3%3C217::aid-humu7%3E3.3.co;2-o
NLM
Zatz M, Passos-Bueno MR. Novel point mutations in the dystrophin gene [Internet]. Human mutation. 1997 ;( 10): 217-222.[citado 2025 out. 23 ] Available from: https://doi.org/10.1002/(sici)1098-1004(1997)10:3%3C217::aid-humu7%3E3.3.co;2-o
Vancouver
Zatz M, Passos-Bueno MR. Novel point mutations in the dystrophin gene [Internet]. Human mutation. 1997 ;( 10): 217-222.[citado 2025 out. 23 ] Available from: https://doi.org/10.1002/(sici)1098-1004(1997)10:3%3C217::aid-humu7%3E3.3.co;2-o

USP Schools

ReP

Filtros

Departament

Authors

USP affiliated authors

Subjects

Funding Agencies