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Artigo de periodico
The relationship among HOXA10, estrogen receptor α, progesterone receptor, and progesterone receptor B proteins in rectosigmoid endometriosis: a tissue microarray study (2015)
Zanatta, Alysson; Pereira, Ricardo Mendes Alves; Rocha, André Monteiro da; Cogliati, Bruno; Baracat, Edmund Chada; Taylor, Hugh S; Motta, Eduardo Leme Alves da; Serafini, Paulo Cesar
Source: Reproductive Sciences. Unidades: FMVZ, FM
Subjects: ENDOMETRIOSE, GENES HOMEOBOX, RECEPTORES HORMONAIS
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ABNT
ZANATTA, Alysson et al. The relationship among HOXA10, estrogen receptor α, progesterone receptor, and progesterone receptor B proteins in rectosigmoid endometriosis: a tissue microarray study. Reproductive Sciences, v. 22, n. 1, p. 31-37, 2015Tradução . . Disponível em: https://doi.org/10.1177/1933719114549846. Acesso em: 08 jun. 2024.
APA
Zanatta, A., Pereira, R. M. A., Rocha, A. M. da, Cogliati, B., Baracat, E. C., Taylor, H. S., et al. (2015). The relationship among HOXA10, estrogen receptor α, progesterone receptor, and progesterone receptor B proteins in rectosigmoid endometriosis: a tissue microarray study. Reproductive Sciences, 22( 1), 31-37. doi:10.1177/1933719114549846
NLM
Zanatta A, Pereira RMA, Rocha AM da, Cogliati B, Baracat EC, Taylor HS, Motta ELA da, Serafini PC. The relationship among HOXA10, estrogen receptor α, progesterone receptor, and progesterone receptor B proteins in rectosigmoid endometriosis: a tissue microarray study [Internet]. Reproductive Sciences. 2015 ; 22( 1): 31-37.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1177/1933719114549846
Vancouver
Zanatta A, Pereira RMA, Rocha AM da, Cogliati B, Baracat EC, Taylor HS, Motta ELA da, Serafini PC. The relationship among HOXA10, estrogen receptor α, progesterone receptor, and progesterone receptor B proteins in rectosigmoid endometriosis: a tissue microarray study [Internet]. Reproductive Sciences. 2015 ; 22( 1): 31-37.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1177/1933719114549846
Artigo de periodico
Stem cells in endometrium and their role in the pathogenesis of endometriosis (2011)
Figueira, Paula Gabriela Marin; Abrão, Mauricio Simoes; Graciela Krikun,; Hugh Taylor
Source: Annals of the New York Academy of Sciences. Unidade: FM
Subjects: CÉLULAS-TRONCO, ENDOMETRIOSE (EEFEITOS ADVERSOS), ENDOMÉTRIO (FISIOPATOLOGIA)
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ABNT
FIGUEIRA, Paula Gabriela Marin et al. Stem cells in endometrium and their role in the pathogenesis of endometriosis. Annals of the New York Academy of Sciences, v. 1221, p. 10-17, 2011Tradução . . Disponível em: https://doi.org/10.1111/j.1749-6632.2011.05969.x. Acesso em: 08 jun. 2024.
APA
Figueira, P. G. M., Abrão, M. S., Graciela Krikun,, & Hugh Taylor,. (2011). Stem cells in endometrium and their role in the pathogenesis of endometriosis. Annals of the New York Academy of Sciences, 1221, 10-17. doi:10.1111/j.1749-6632.2011.05969.x
NLM
Figueira PGM, Abrão MS, Graciela Krikun, Hugh Taylor. Stem cells in endometrium and their role in the pathogenesis of endometriosis [Internet]. Annals of the New York Academy of Sciences. 2011 ; 1221 10-17.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1111/j.1749-6632.2011.05969.x
Vancouver
Figueira PGM, Abrão MS, Graciela Krikun, Hugh Taylor. Stem cells in endometrium and their role in the pathogenesis of endometriosis [Internet]. Annals of the New York Academy of Sciences. 2011 ; 1221 10-17.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1111/j.1749-6632.2011.05969.x
Artigo de periodico
A Comparison of the Consensus and Clinical Definitions of Pancreatitis With a Proposal to Redefine Post-Endoscopic Retrograde Cholangiopancreatography Pancreatitis (2010)
Arthjifon, Everson L. A.; Chu, Adrienne; Freeman, Martin; Sakai, Paulo; Usmani, Ashar; Kumar, Atul
Source: Pancreas. Unidade: FM
Subjects: PANCREATITE, DOENÇA AGUDA, TOMOGRAFIA COMPUTADORIZADA POR RAIOS X, COLANGIOGRAFIA
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ARTHJIFON, Everson L. A. et al. A Comparison of the Consensus and Clinical Definitions of Pancreatitis With a Proposal to Redefine Post-Endoscopic Retrograde Cholangiopancreatography Pancreatitis. Pancreas, v. 39, n. 4, p. 530-535, 2010Tradução . . Disponível em: https://doi.org/10.1097/MPA.0b013e3181c306c0. Acesso em: 08 jun. 2024.
APA
Arthjifon, E. L. A., Chu, A., Freeman, M., Sakai, P., Usmani, A., & Kumar, A. (2010). A Comparison of the Consensus and Clinical Definitions of Pancreatitis With a Proposal to Redefine Post-Endoscopic Retrograde Cholangiopancreatography Pancreatitis. Pancreas, 39( 4), 530-535. doi:10.1097/MPA.0b013e3181c306c0
NLM
Arthjifon ELA, Chu A, Freeman M, Sakai P, Usmani A, Kumar A. A Comparison of the Consensus and Clinical Definitions of Pancreatitis With a Proposal to Redefine Post-Endoscopic Retrograde Cholangiopancreatography Pancreatitis [Internet]. Pancreas. 2010 ; 39( 4): 530-535.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1097/MPA.0b013e3181c306c0
Vancouver
Arthjifon ELA, Chu A, Freeman M, Sakai P, Usmani A, Kumar A. A Comparison of the Consensus and Clinical Definitions of Pancreatitis With a Proposal to Redefine Post-Endoscopic Retrograde Cholangiopancreatography Pancreatitis [Internet]. Pancreas. 2010 ; 39( 4): 530-535.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1097/MPA.0b013e3181c306c0
Artigo de periodico
Obsessive–compulsive disorder: a review of the diagnostic criteria and possible subtypes and dimensional specifiers for DSM-V (2010)
Leckman, James F.; Denys, Damiaan; Simpson, H. Blair; Mataix-Cols, David; Hollander, Eric; Sanjaya Saxena; Miguel, Euripedes C.; Rauch, Scott L.; Wayne K. Goodman, Wayne K.; Phillips, Katharine A.; Stein, Dan J.
Source: Depression and Anxiety. Unidade: FM
Subjects: TRANSTORNO OBSSESSIVO COMPULSIVO (DIAGNÓSTICO), TRANSTORNO OBSESSIVO-COMPULSIVO (CLASSIFICAÇÃO)
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LECKMAN, James F. et al. Obsessive–compulsive disorder: a review of the diagnostic criteria and possible subtypes and dimensional specifiers for DSM-V. Depression and Anxiety, v. 27, n. 6, p. 507-527, 2010Tradução . . Disponível em: https://doi.org/10.1002/da.20669. Acesso em: 08 jun. 2024.
APA
Leckman, J. F., Denys, D., Simpson, H. B., Mataix-Cols, D., Hollander, E., Sanjaya Saxena,, et al. (2010). Obsessive–compulsive disorder: a review of the diagnostic criteria and possible subtypes and dimensional specifiers for DSM-V. Depression and Anxiety, 27( 6), 507-527. doi:10.1002/da.20669
NLM
Leckman JF, Denys D, Simpson HB, Mataix-Cols D, Hollander E, Sanjaya Saxena, Miguel EC, Rauch SL, Wayne K. Goodman WK, Phillips KA, Stein DJ. Obsessive–compulsive disorder: a review of the diagnostic criteria and possible subtypes and dimensional specifiers for DSM-V [Internet]. Depression and Anxiety. 2010 ; 27( 6): 507-527.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1002/da.20669
Vancouver
Leckman JF, Denys D, Simpson HB, Mataix-Cols D, Hollander E, Sanjaya Saxena, Miguel EC, Rauch SL, Wayne K. Goodman WK, Phillips KA, Stein DJ. Obsessive–compulsive disorder: a review of the diagnostic criteria and possible subtypes and dimensional specifiers for DSM-V [Internet]. Depression and Anxiety. 2010 ; 27( 6): 507-527.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1002/da.20669
Artigo de periodico
Validation of the University of Sao Paulo Sensory Phenomena Scale: Initial Psychometric Properties (2009)
Rosário, Maria Conceição do; Prado, Helena da Silva; Borcato, Sonia; Diniz, Juliana Belo; Shavitt, Roseli Gedanke; Hounie, Ana Gabriela; Mathis, Maria Eugenia; Mostrorosa, Rosana Savio; Velloso, Patricia; Perin, Eduardo Alliende; Fossaluza, Victor ; Pereira, Carlos Alberto de Bragança ; Geller, Daniel; Leckman, James; Miguel, Euripedes
Source: CNS Spectrums: International Journal of Neuropsychiatric Medicine. Unidades: IME, FM
Assunto: PSICOMETRIA
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ROSÁRIO, Maria Conceição do et al. Validation of the University of Sao Paulo Sensory Phenomena Scale: Initial Psychometric Properties. CNS Spectrums: International Journal of Neuropsychiatric Medicine, v. 14, n. 6, p. 315-232, 2009Tradução . . Disponível em: https://doi.org/10.1017/s1092852900020319. Acesso em: 08 jun. 2024.
APA
Rosário, M. C. do, Prado, H. da S., Borcato, S., Diniz, J. B., Shavitt, R. G., Hounie, A. G., et al. (2009). Validation of the University of Sao Paulo Sensory Phenomena Scale: Initial Psychometric Properties. CNS Spectrums: International Journal of Neuropsychiatric Medicine, 14( 6), 315-232. doi:10.1017/s1092852900020319
NLM
Rosário MC do, Prado H da S, Borcato S, Diniz JB, Shavitt RG, Hounie AG, Mathis ME, Mostrorosa RS, Velloso P, Perin EA, Fossaluza V, Pereira CA de B, Geller D, Leckman J, Miguel E. Validation of the University of Sao Paulo Sensory Phenomena Scale: Initial Psychometric Properties [Internet]. CNS Spectrums: International Journal of Neuropsychiatric Medicine. 2009 ; 14( 6): 315-232.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1017/s1092852900020319
Vancouver
Rosário MC do, Prado H da S, Borcato S, Diniz JB, Shavitt RG, Hounie AG, Mathis ME, Mostrorosa RS, Velloso P, Perin EA, Fossaluza V, Pereira CA de B, Geller D, Leckman J, Miguel E. Validation of the University of Sao Paulo Sensory Phenomena Scale: Initial Psychometric Properties [Internet]. CNS Spectrums: International Journal of Neuropsychiatric Medicine. 2009 ; 14( 6): 315-232.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1017/s1092852900020319
Artigo de periodico
Biliary and Pancreatic Dysgenesis in Mice Harboring a Mutation in Pkhd1 (2008)
Gallagher,Anna-Rachel; Esquivel, Ernie L.; Briere, Tiffany S.; Tian, Xin; Mitobe, Michihiro; Menezes, Luis F.; Markowitz, Glen S.; Jain, Dhanpat; Onuchic, Luiz F.; Somlo, Stefan
Source: American Journal of Pathology. Unidade: FM
Subjects: CISTOS, RIM (PATOLOGIA, DOENÇAS HEREDITÁRIAS (GENÉTICA), MUTAÇÃO GENÉTICA, MODELOS ANIMAIS, CAMUNDONGOS, FIBROSE CÍSTICA
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ABNT
GALLAGHER, Anna-Rachel et al. Biliary and Pancreatic Dysgenesis in Mice Harboring a Mutation in Pkhd1. American Journal of Pathology, v. 172, n. 2, p. 417-429, 2008Tradução . . Disponível em: https://doi.org/10.2353/ajpath.2008.070381. Acesso em: 08 jun. 2024.
APA
Gallagher, A. -R., Esquivel, E. L., Briere, T. S., Tian, X., Mitobe, M., Menezes, L. F., et al. (2008). Biliary and Pancreatic Dysgenesis in Mice Harboring a Mutation in Pkhd1. American Journal of Pathology, 172( 2), 417-429. doi:10.2353/ajpath.2008.070381
NLM
Gallagher A-R, Esquivel EL, Briere TS, Tian X, Mitobe M, Menezes LF, Markowitz GS, Jain D, Onuchic LF, Somlo S. Biliary and Pancreatic Dysgenesis in Mice Harboring a Mutation in Pkhd1 [Internet]. American Journal of Pathology. 2008 ; 172( 2): 417-429.[citado 2024 jun. 08 ] Available from: https://doi.org/10.2353/ajpath.2008.070381
Vancouver
Gallagher A-R, Esquivel EL, Briere TS, Tian X, Mitobe M, Menezes LF, Markowitz GS, Jain D, Onuchic LF, Somlo S. Biliary and Pancreatic Dysgenesis in Mice Harboring a Mutation in Pkhd1 [Internet]. American Journal of Pathology. 2008 ; 172( 2): 417-429.[citado 2024 jun. 08 ] Available from: https://doi.org/10.2353/ajpath.2008.070381
Artigo de periodico
Comprehensive genomic analysis of PKHD1 mutations in ARPKD cohorts (2005)
Sharp, A. M.; Messiaen, L. M.; Page, G.; Gubler, M-C; Antignac, C.; Onuchic, Luiz Fernando; Somlo, S.; Germino, G. G.; Guay-Woodford, L. M.
Source: Journal of Medical Genetics. Unidade: FM
Subjects: GENOMAS (ANÁLISE), NEFROPATIAS (GENÉTICA), MUTAÇÃO GENÉTICA, POLIMORFISMO
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ABNT
SHARP, A. M. et al. Comprehensive genomic analysis of PKHD1 mutations in ARPKD cohorts. Journal of Medical Genetics, v. 42, p. 336-349, 2005Tradução . . Disponível em: https://doi.org/10.1136/jmg.2004.024489. Acesso em: 08 jun. 2024.
APA
Sharp, A. M., Messiaen, L. M., Page, G., Gubler, M. -C., Antignac, C., Onuchic, L. F., et al. (2005). Comprehensive genomic analysis of PKHD1 mutations in ARPKD cohorts. Journal of Medical Genetics, 42, 336-349. doi:10.1136/jmg.2004.024489
NLM
Sharp AM, Messiaen LM, Page G, Gubler M-C, Antignac C, Onuchic LF, Somlo S, Germino GG, Guay-Woodford LM. Comprehensive genomic analysis of PKHD1 mutations in ARPKD cohorts [Internet]. Journal of Medical Genetics. 2005 ; 42 336-349.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1136/jmg.2004.024489
Vancouver
Sharp AM, Messiaen LM, Page G, Gubler M-C, Antignac C, Onuchic LF, Somlo S, Germino GG, Guay-Woodford LM. Comprehensive genomic analysis of PKHD1 mutations in ARPKD cohorts [Internet]. Journal of Medical Genetics. 2005 ; 42 336-349.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1136/jmg.2004.024489
Artigo de periodico
A family study of early-onset obsessive-compulsive disorder (2005)
Rosario-Campos, Maria Conceição do; Leckman, James F.; Curi, Mariana; Quatrano, Susan; Katsovitch, Lylia; Miguel, Euripedes C.; Pauls, David L.
Source: American Journal of Medical Genetics Part A. Unidade: FM
Subjects: TRANSTORNO OBSESSIVO-COMPULSIVO (GENÉTICA), INFÂNCIA, COMORBIDADE, TIQUES (GENÉTICA)
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ABNT
ROSARIO-CAMPOS, Maria Conceição do et al. A family study of early-onset obsessive-compulsive disorder. American Journal of Medical Genetics Part A, v. 136B, n. 1, p. 92-97, 2005Tradução . . Disponível em: https://doi.org/10.1002/ajmg.b.30149. Acesso em: 08 jun. 2024.
APA
Rosario-Campos, M. C. do, Leckman, J. F., Curi, M., Quatrano, S., Katsovitch, L., Miguel, E. C., & Pauls, D. L. (2005). A family study of early-onset obsessive-compulsive disorder. American Journal of Medical Genetics Part A, 136B( 1), 92-97. doi:10.1002/ajmg.b.30149
NLM
Rosario-Campos MC do, Leckman JF, Curi M, Quatrano S, Katsovitch L, Miguel EC, Pauls DL. A family study of early-onset obsessive-compulsive disorder [Internet]. American Journal of Medical Genetics Part A. 2005 ; 136B( 1): 92-97.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1002/ajmg.b.30149
Vancouver
Rosario-Campos MC do, Leckman JF, Curi M, Quatrano S, Katsovitch L, Miguel EC, Pauls DL. A family study of early-onset obsessive-compulsive disorder [Internet]. American Journal of Medical Genetics Part A. 2005 ; 136B( 1): 92-97.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1002/ajmg.b.30149
Artigo de periodico
A HIF1a Regulatory Loop Links Hypoxia and Mitochondrial Signals in Pheochromocytomas (2005)
Dahia, Patricia L. M.; Ross, Ken N.; Wright, Matthew E.; Hayashida, César Y.; Santagata, Sandro; Barontini, Marta; Kung, Andrew L.; Sanso, Gabriela; Powers, James F.; Tischler, Arthur S.; Hodin, Richard; Heitritter, Shannon; Moore, Francis; Dluhy, Robert; Sosa, Julie Ann; Ocal, I. Tolgay; Benn, Diana E.; Marsh, Deborah J.; Robinson, Bruce G.; Schneider, Katherine; Garber, Judy; Arum, Seth M.; Korbonits, Márta; Grossman, Ashley; Pigny, Pascal; Toledo, S. P. A.; Nosé, Vania; Li, Cheng; Stiles, Charles D.
Source: PLOS Genetics. Unidade: FM
Subjects: MITOCÔNDRIAS (ANÁLISE), FEOCROMOCITOMA (ENZIMOLOGIA), MUTAÇÃO GENÉTICA
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ABNT
DAHIA, Patricia L. M. et al. A HIF1a Regulatory Loop Links Hypoxia and Mitochondrial Signals in Pheochromocytomas. PLOS Genetics, v. 1, n. 1, p. 72-80, 2005Tradução . . Disponível em: https://doi.org/10.1371/journal.pgen.0010008. Acesso em: 08 jun. 2024.
APA
Dahia, P. L. M., Ross, K. N., Wright, M. E., Hayashida, C. Y., Santagata, S., Barontini, M., et al. (2005). A HIF1a Regulatory Loop Links Hypoxia and Mitochondrial Signals in Pheochromocytomas. PLOS Genetics, 1( 1), 72-80. doi:10.1371/journal.pgen.0010008
NLM
Dahia PLM, Ross KN, Wright ME, Hayashida CY, Santagata S, Barontini M, Kung AL, Sanso G, Powers JF, Tischler AS, Hodin R, Heitritter S, Moore F, Dluhy R, Sosa JA, Ocal IT, Benn DE, Marsh DJ, Robinson BG, Schneider K, Garber J, Arum SM, Korbonits M, Grossman A, Pigny P, Toledo SPA, Nosé V, Li C, Stiles CD. A HIF1a Regulatory Loop Links Hypoxia and Mitochondrial Signals in Pheochromocytomas [Internet]. PLOS Genetics. 2005 ; 1( 1): 72-80.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1371/journal.pgen.0010008
Vancouver
Dahia PLM, Ross KN, Wright ME, Hayashida CY, Santagata S, Barontini M, Kung AL, Sanso G, Powers JF, Tischler AS, Hodin R, Heitritter S, Moore F, Dluhy R, Sosa JA, Ocal IT, Benn DE, Marsh DJ, Robinson BG, Schneider K, Garber J, Arum SM, Korbonits M, Grossman A, Pigny P, Toledo SPA, Nosé V, Li C, Stiles CD. A HIF1a Regulatory Loop Links Hypoxia and Mitochondrial Signals in Pheochromocytomas [Internet]. PLOS Genetics. 2005 ; 1( 1): 72-80.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1371/journal.pgen.0010008
Trabalho de evento-resumo periodico
Initial characterization of polyductin, the PKHD1 gene product (2003)
Menezes, L. F.; Cai, Y.; Nagasawa, Y.; Almeida, F.; Somlo, S.; Guay Woodford, L. M.; Germino, G. G.; Onuchic, Luiz Fernando
Source: Journal of the American Society of Nephrology. Conference titles: Accredited Sponsor: The American Society of Nephrology. Unidade: FM
Subjects: NEFROLOGIA, GENES
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ABNT
MENEZES, L. F. et al. Initial characterization of polyductin, the PKHD1 gene product. Journal of the American Society of Nephrology. Philadelphia: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 08 jun. 2024. , 2003
APA
Menezes, L. F., Cai, Y., Nagasawa, Y., Almeida, F., Somlo, S., Guay Woodford, L. M., et al. (2003). Initial characterization of polyductin, the PKHD1 gene product. Journal of the American Society of Nephrology. Philadelphia: Faculdade de Medicina, Universidade de São Paulo.
NLM
Menezes LF, Cai Y, Nagasawa Y, Almeida F, Somlo S, Guay Woodford LM, Germino GG, Onuchic LF. Initial characterization of polyductin, the PKHD1 gene product. Journal of the American Society of Nephrology. 2003 ; 14[citado 2024 jun. 08 ]
Vancouver
Menezes LF, Cai Y, Nagasawa Y, Almeida F, Somlo S, Guay Woodford LM, Germino GG, Onuchic LF. Initial characterization of polyductin, the PKHD1 gene product. Journal of the American Society of Nephrology. 2003 ; 14[citado 2024 jun. 08 ]
Artigo de periodico
Milder presentation of recessive polycystic kidney disease requires presence of amino acid substitution mutation (2003)
Furu, Laszlo; Senderek, Jan; Gharavi, Ali; Hou, Xiaoying; Esquivel, Ernie L.; Nagasawa, Yasuyuki; Avner, Ellis; Germino, Gregory; Guay-Woodford, Lisa; Somlo, Stefan; Büttner, Reinhard; Zerres, Klaus; Onuchic, Luiz Fernando
Source: Journal of the American Society of Nephrology. Conference titles: Accredited Sponsor: The American Society of Nephrology. Unidade: FM
Subjects: NEFROLOGIA, GENES, AMINOÁCIDOS
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ABNT
FURU, Laszlo et al. Milder presentation of recessive polycystic kidney disease requires presence of amino acid substitution mutation. Journal of the American Society of Nephrology, v. 14, 2003Tradução . . Acesso em: 08 jun. 2024.
APA
Furu, L., Senderek, J., Gharavi, A., Hou, X., Esquivel, E. L., Nagasawa, Y., et al. (2003). Milder presentation of recessive polycystic kidney disease requires presence of amino acid substitution mutation. Journal of the American Society of Nephrology, 14.
NLM
Furu L, Senderek J, Gharavi A, Hou X, Esquivel EL, Nagasawa Y, Avner E, Germino G, Guay-Woodford L, Somlo S, Büttner R, Zerres K, Onuchic LF. Milder presentation of recessive polycystic kidney disease requires presence of amino acid substitution mutation. Journal of the American Society of Nephrology. 2003 ; 14[citado 2024 jun. 08 ]
Vancouver
Furu L, Senderek J, Gharavi A, Hou X, Esquivel EL, Nagasawa Y, Avner E, Germino G, Guay-Woodford L, Somlo S, Büttner R, Zerres K, Onuchic LF. Milder presentation of recessive polycystic kidney disease requires presence of amino acid substitution mutation. Journal of the American Society of Nephrology. 2003 ; 14[citado 2024 jun. 08 ]
Artigo de periodico
Spectrum of mutations in the gene for autosomal recessive polycystic kidney disease (ARPKD/PKHD1) (2003)
Bergmann, Carsten; Senderek, Jan; Sedlacek, Beate; Pegiazoglou, Ioannis; Puglia, Patricia; Eggermann, Thomas; Rudnick-Schöneborn, Sabine; Furu, Laszlo; Baca, Monica de; Germino, Gregory; Guay-Woodford, Lisa; Somlo, Stefan; Moser, Markus; Büttner, Reinhard; Zerres, Klaus; Onuchic, Luiz Fernando
Source: Journal of the American Society of Nephrology. Conference titles: Accredited Sponsor: The American Society of Nephrology. Unidade: FM
Subjects: NEFROLOGIA, GENES
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ABNT
BERGMANN, Carsten et al. Spectrum of mutations in the gene for autosomal recessive polycystic kidney disease (ARPKD/PKHD1). Journal of the American Society of Nephrology, v. 14, 2003Tradução . . Acesso em: 08 jun. 2024.
APA
Bergmann, C., Senderek, J., Sedlacek, B., Pegiazoglou, I., Puglia, P., Eggermann, T., et al. (2003). Spectrum of mutations in the gene for autosomal recessive polycystic kidney disease (ARPKD/PKHD1). Journal of the American Society of Nephrology, 14.
NLM
Bergmann C, Senderek J, Sedlacek B, Pegiazoglou I, Puglia P, Eggermann T, Rudnick-Schöneborn S, Furu L, Baca M de, Germino G, Guay-Woodford L, Somlo S, Moser M, Büttner R, Zerres K, Onuchic LF. Spectrum of mutations in the gene for autosomal recessive polycystic kidney disease (ARPKD/PKHD1). Journal of the American Society of Nephrology. 2003 ; 14[citado 2024 jun. 08 ]
Vancouver
Bergmann C, Senderek J, Sedlacek B, Pegiazoglou I, Puglia P, Eggermann T, Rudnick-Schöneborn S, Furu L, Baca M de, Germino G, Guay-Woodford L, Somlo S, Moser M, Büttner R, Zerres K, Onuchic LF. Spectrum of mutations in the gene for autosomal recessive polycystic kidney disease (ARPKD/PKHD1). Journal of the American Society of Nephrology. 2003 ; 14[citado 2024 jun. 08 ]
Trabalho de evento-resumo periodico
Current status of the PKHDI region transcription map (2000)
Onuchic, Luiz Fernando; Furu, L.; Nagasawa, Y.; Lakings, Alicia; Mangasser Stephan, K.; Avner, Ellis D.; Zerres, Klaus; Guay Woodford, Lisa M.; Somlo, Stefan; Germino, Gregory G.
Source: Journal of the American Society of Nephrology. Conference titles: Annual Meeting of the American Society of Nephrology. Unidade: FM
Assunto: NEFROLOGIA
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ABNT
ONUCHIC, Luiz Fernando et al. Current status of the PKHDI region transcription map. Journal of the American Society of Nephrology. Toronto: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 08 jun. 2024. , 2000
APA
Onuchic, L. F., Furu, L., Nagasawa, Y., Lakings, A., Mangasser Stephan, K., Avner, E. D., et al. (2000). Current status of the PKHDI region transcription map. Journal of the American Society of Nephrology. Toronto: Faculdade de Medicina, Universidade de São Paulo.
NLM
Onuchic LF, Furu L, Nagasawa Y, Lakings A, Mangasser Stephan K, Avner ED, Zerres K, Guay Woodford LM, Somlo S, Germino GG. Current status of the PKHDI region transcription map. Journal of the American Society of Nephrology. 2000 ; 11 396A.[citado 2024 jun. 08 ]
Vancouver
Onuchic LF, Furu L, Nagasawa Y, Lakings A, Mangasser Stephan K, Avner ED, Zerres K, Guay Woodford LM, Somlo S, Germino GG. Current status of the PKHDI region transcription map. Journal of the American Society of Nephrology. 2000 ; 11 396A.[citado 2024 jun. 08 ]
Artigo de periodico
Genomic structure of the gene for the human P1 protein (MCM3) and its exclusion as a candidate for atosomal recessive polycystic kidney disease (2000)
Hofmann, Yvonne; Becker, Jutta; Wright, Felicia; Avner, Ellis D.; Mrug, Michal; Guay Woodford, Lisa M.; Somlo, Stefan; Zerres, Klaus; Germino, Gregory G.; Onuchic, Luiz Fernando
Source: European Journal of Human Genetics. Unidade: FM
Assunto: GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
HOFMANN, Yvonne et al. Genomic structure of the gene for the human P1 protein (MCM3) and its exclusion as a candidate for atosomal recessive polycystic kidney disease. European Journal of Human Genetics, n. 8, p. 163-6, 2000Tradução . . Disponível em: https://doi.org/10.1038/sj.ejhg.5200426. Acesso em: 08 jun. 2024.
APA
Hofmann, Y., Becker, J., Wright, F., Avner, E. D., Mrug, M., Guay Woodford, L. M., et al. (2000). Genomic structure of the gene for the human P1 protein (MCM3) and its exclusion as a candidate for atosomal recessive polycystic kidney disease. European Journal of Human Genetics, ( 8), 163-6. doi:10.1038/sj.ejhg.5200426
NLM
Hofmann Y, Becker J, Wright F, Avner ED, Mrug M, Guay Woodford LM, Somlo S, Zerres K, Germino GG, Onuchic LF. Genomic structure of the gene for the human P1 protein (MCM3) and its exclusion as a candidate for atosomal recessive polycystic kidney disease [Internet]. European Journal of Human Genetics. 2000 ;( 8): 163-6.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1038/sj.ejhg.5200426
Vancouver
Hofmann Y, Becker J, Wright F, Avner ED, Mrug M, Guay Woodford LM, Somlo S, Zerres K, Germino GG, Onuchic LF. Genomic structure of the gene for the human P1 protein (MCM3) and its exclusion as a candidate for atosomal recessive polycystic kidney disease [Internet]. European Journal of Human Genetics. 2000 ;( 8): 163-6.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1038/sj.ejhg.5200426
Artigo de periodico-carta/editorial
Immune reactivity of HTLV-IIa- infected Kayapo Indians with HTLV-IIb extended tax epitope (1997)
Lal, Renu B.; Pardi, Diane; Switzer, William; Segurado, Aluísio Augusto Cotrim; Black, Francis
Source: Journal of Acquired Immune Deficiency Syndromes and Human Retrovirology. Unidade: FM
Assunto: IMUNOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LAL, Renu B. et al. Immune reactivity of HTLV-IIa- infected Kayapo Indians with HTLV-IIb extended tax epitope. Journal of Acquired Immune Deficiency Syndromes and Human Retrovirology. New York: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 08 jun. 2024. , 1997
APA
Lal, R. B., Pardi, D., Switzer, W., Segurado, A. A. C., & Black, F. (1997). Immune reactivity of HTLV-IIa- infected Kayapo Indians with HTLV-IIb extended tax epitope. Journal of Acquired Immune Deficiency Syndromes and Human Retrovirology. New York: Faculdade de Medicina, Universidade de São Paulo.
NLM
Lal RB, Pardi D, Switzer W, Segurado AAC, Black F. Immune reactivity of HTLV-IIa- infected Kayapo Indians with HTLV-IIb extended tax epitope. Journal of Acquired Immune Deficiency Syndromes and Human Retrovirology. 1997 ; 14( 5): 476-477.[citado 2024 jun. 08 ]
Vancouver
Lal RB, Pardi D, Switzer W, Segurado AAC, Black F. Immune reactivity of HTLV-IIa- infected Kayapo Indians with HTLV-IIb extended tax epitope. Journal of Acquired Immune Deficiency Syndromes and Human Retrovirology. 1997 ; 14( 5): 476-477.[citado 2024 jun. 08 ]
Artigo de periodico
EBV Infectious in Brazil: III - Infectious mononucleosis (1981)
Carvalho, Renato Piza de Souza; Evans, Alfred S.; Pannuti, Claudio Sergio; Frost, Patricia; Grossman, L.; Jamra, Michel A.
Source: Revista do Instituto de Medicina Tropical de São Paulo. Unidades: ICB, FM
Assunto: MICROBIOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CARVALHO, Renato Piza de Souza et al. EBV Infectious in Brazil: III - Infectious mononucleosis. Revista do Instituto de Medicina Tropical de São Paulo, v. 23, n. 4, p. 167-172, 1981Tradução . . Acesso em: 08 jun. 2024.
APA
Carvalho, R. P. de S., Evans, A. S., Pannuti, C. S., Frost, P., Grossman, L., & Jamra, M. A. (1981). EBV Infectious in Brazil: III - Infectious mononucleosis. Revista do Instituto de Medicina Tropical de São Paulo, 23( 4), 167-172.
NLM
Carvalho RP de S, Evans AS, Pannuti CS, Frost P, Grossman L, Jamra MA. EBV Infectious in Brazil: III - Infectious mononucleosis. Revista do Instituto de Medicina Tropical de São Paulo. 1981 ; 23( 4): 167-172.[citado 2024 jun. 08 ]
Vancouver
Carvalho RP de S, Evans AS, Pannuti CS, Frost P, Grossman L, Jamra MA. EBV Infectious in Brazil: III - Infectious mononucleosis. Revista do Instituto de Medicina Tropical de São Paulo. 1981 ; 23( 4): 167-172.[citado 2024 jun. 08 ]
Artigo de periodico
A case-control study of Hodgkin's disease in Brazil: II. Seroepidemiologic studies in cases and family members (1980)
Evans, Alfred S.; Kirchhoff, Louis V.; Pannuti, Cláudio Sérgio; Carvalho, Renato Piza de Souza; McClelland, Karen E.
Source: American Journal of Epidemiology. Unidades: ICB, FM
Assunto: MICROBIOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
EVANS, Alfred S. et al. A case-control study of Hodgkin's disease in Brazil: II. Seroepidemiologic studies in cases and family members. American Journal of Epidemiology, v. 112, n. 5, p. 609-618, 1980Tradução . . Acesso em: 08 jun. 2024.
APA
Evans, A. S., Kirchhoff, L. V., Pannuti, C. S., Carvalho, R. P. de S., & McClelland, K. E. (1980). A case-control study of Hodgkin's disease in Brazil: II. Seroepidemiologic studies in cases and family members. American Journal of Epidemiology, 112( 5), 609-618.
NLM
Evans AS, Kirchhoff LV, Pannuti CS, Carvalho RP de S, McClelland KE. A case-control study of Hodgkin's disease in Brazil: II. Seroepidemiologic studies in cases and family members. American Journal of Epidemiology. 1980 ; 112( 5): 609-618.[citado 2024 jun. 08 ]
Vancouver
Evans AS, Kirchhoff LV, Pannuti CS, Carvalho RP de S, McClelland KE. A case-control study of Hodgkin's disease in Brazil: II. Seroepidemiologic studies in cases and family members. American Journal of Epidemiology. 1980 ; 112( 5): 609-618.[citado 2024 jun. 08 ]

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