Eloísa de Sa Moreira

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Produções bibliográficas

• 2016 MOREIRA, ELOISA S. ; SILVA, ISABELA M.W. ; LOURENÇO, NAILA ; MOREIRA, DANIELLE P. ; RIBEIRO, CINTIA M. ; MARTINS, ANA LUIZA B. ; GRIESI-OLIVEIRA, KARINA ; LAZAR, MONIZE ; COSTA, SILVIA S. ; NASLAVSKY, MICHEL S. ; ROCHA, KÁTIA M. ; AGUENA, MEIRE ; FETT-CONTE, AGNES C. ; ZATZ, MAYANA ; ROSENBERG, CARLA ; ZACHI, ELAINE C. ; BERTOLA, DÉBORA R. ; VADASZ, ESTEVÃO ; PASSOS-BUENO, MARIA RITA . Detection of small copy number variations (CNVs) in autism spectrum disorder (ASD) by custom array comparative genomic hybridization (aCGH). RES AUTISM SPECT DIS , v. 23, p. 145-151, 2016.

• 2015 UEDA, MIRIAM YH ; ALVARENGA, PAULO G ; REAL, JULIANA M ; MOREIRA, ELOISA DE SÁ ; WATANABE, ARIPUANÃ ; PASSOS-CASTILHO, ANA MARIA ; VESCOVI, MATHEUS ; NOVIS, YANA ; ROCHA, VANDERSON ; SEBER, ADRIANA ; OLIVEIRA, JOSE SR ; RODRIGUES, CELSO A ; GRANATO, CELSO FH . Optimisation of a quantitative polymerase chain reaction-based strategy for the detection and quantification of human herpesvirus 6 DNA in patients undergoing allogeneic haematopoietic stem cell transplantation. Memórias do Instituto Oswaldo Cruz (Online) , v. 110, p. 461-467, 2015.

• 2014 MOREIRA, DANIELLE P. ; GRIESI-OLIVEIRA, KARINA ; BOSSOLANI-MARTINS, ANA L. ; LOURENÇO, NAILA C. V. ; TAKAHASHI, VANESSA N. O. ; DA ROCHA, KÁTIA M. ; MOREIRA, ELOISA S. ; VADASZ, ESTEVÃO ; MEIRA, JOANNA GOES CASTRO ; BERTOLA, DEBORA ; HALLORAN, EOGHAN O? ; MAGALHÃES, TIAGO R. ; FETT-CONTE, AGNES C. ; PASSOS-BUENO, MARIA RITA . Investigation of 15q11-q13, 16p11.2 and 22q13 CNVs in Autism Spectrum Disorder Brazilian Individuals with and without Epilepsy. Plos One , v. 9, p. e107705, 2014.

• 2009 Mendes, CT ; MURY, FB ; MOREIRA, E. S. ; ALBERTO, F. L. ; Forlenza, OV ; DIAS-NETO, E. ; Gattaz, WF . Lithium reduces Gsk3b mRNA levels: implications for Alzheimer Disease. European Archives of Psychiatry and Clinical Neuroscience , v. 259, p. 16-22, 2009.

• 2009 ORABONA, G ; GRIESIOLIVEIRA, K ; VADASZ, E ; BULCAO, V ; TAKAHASHI, V ; MOREIRA, E ; FURIASILVA, M ; ROSMELO, A ; DOURADO, F ; MATIOLI, R . HTR1B and HTR2C in autism spectrum disorders in Brazilian families. Brain Research , v. 1250, p. 14-19, 2009.

• 2008 PINHEIRO, R ; DESAMOREIRA, E ; SILVA, M ; ALBERTO, F ; CHAUFFAILLE, M . FLT3 internal tandem duplication during myelodysplastic syndrome follow-up: a marker of transformation to acute myeloid leukemia. Cancer Genetics and Cytogenetics , v. 183, p. 89-93, 2008.

• 2008 Moyses, CB ; MOREIRA, E. S. ; Asprino, PF ; Guimaraes, GS ; ALBERTO, F. L. . Simultaneous detection of the C282Y, H63D and S65C mutations in the hemochromatosis gene using quenched-FRET real-time PCR. Brazilian Journal of Medical and Biological Research on line , v. 41, p. 833-838, 2008.

• 2008 Borri, D ; MOREIRA, E. S. ; ALBERTO, F. L. ; CHAUFFAILLE, M. L. . Acute promyelocytic leukemia with t(15;17): frequency of additional clonal chromosome abnormalities and FLT3 mutations. Leukemia & Lymphoma (Print) , v. 49, p. 2387-2389, 2008.

• 2007 Moreira, E. S. ; PINHEIRO, R. F. ; SILVA, M. R. ; GREGGIO, B. ; ALBERTO, F. L. ; CHAUFFAILLE, M. L. . FLT3 mutation and AML/ETO in a case of Myelodysplastic syndrome in transformation corroborates the two hit model of leukemogenesis. Leukemia Research , v. 31, p. 1015-1018, 2007.

• 2007 MATOS, C. A. ; PEREZ, R. M. ; LEMOS, L. B. ; MEDINA-PESTANA, J. O. ; LANZONI, V. P. ; ALBERTO, F. L. ; MOREIRA, E. S. ; SILVA, A. E. ; FERRAZ, M. L. . Factors associated with the intensity of liver fibrosis in renal transplant patients with hepatitis B virus infection. European Journal of Gastroenterology & Hepatology , v. 19, p. 653-657, 2007.

• 2005 Moreira, E. S. ; JEHEE, FS ; Johnson, D ; ALONSO, L.G. ; CAVALCANTI, D.P. ; ALBERTO, F. L. ; KOK, F. ; KIM, S. . Molecular screening for microdeletions at 9p22-p24 and 11q23-q24 in a large cohort of patients with trigonocephaly. Clinical Genetics , v. 67, p. 503-510, 2005.

• 2004 SOGAYAR, M. C. ; CAMARGO, A. A. ; BETTONI, F. ; CARRARO, D. M. ; PIRES, L. C. ; PARMIGIANI, R. B. ; MOREIRA, E. S. ; ROSÁRIO, D. ; LATORRE, M. O. ; SIMPSON, A. J. G. ; CRUZ, L. O. ; DEGAKI, T. L. ; FILHO, F. C. ; LUDWIG-FAPESP TRANSCRIPT FINISHING INITIATIVE . A transcript finishing initiative for closing gaps in the human transcriptome.. Genome Research , v. 14, p. 1413-1423, 2004.

• 2004 Maranduba, Carlos Magno da Costa ; S? Moreira, Elo?sa ; M?ller Orabona, Guilherme ; C?ssia Pavanello, Rita ; Vianna-Morgante, Angela M. ; Rita Passos-Bueno, Maria . Does the P172H mutation at theTM4SF2 gene cause X-linked mental retardation?. American Journal of Medical Genetics , v. 124A, p. 413-415, 2004.

• 2003 Moreira, E. S. ; VAINZOF, M. ; SUZUKI, O. T. ; PAVANELLO, R. C. M. ; ZATZ, M. ; PASSOS-BUENO, M. R. . Genotype-phenotype correlations in 35 Brazilian families with sarcoglycanopathies including the description of three novel mutations. Journal of Medical Genetics , v. 40, p. 12e-12, 2003.

• 2002 VAINZOF, M. ; MOREIRA, E. S. ; SUZUKI, O. T. ; FAULKNER, G. ; VALLE, G. ; BEGGS, A. H. ; CARPEN, O. ; GURGEL-GIANNETI, J. ; TSANACLIS, A. M. ; SILVA, H. C. ; PASSOS-BUENO, M. R. ; ZATZ, M. . Telethonin protein expression in neuromuscular disorders. Biochimica et Biophysica Acta. Molecular Basis of Disease , v. 1588, p. 33-40, 2002.

• 2001 VAINZOF, M. ; ANDERSON, L. V. B. ; MCNALLY. E. M. ; DAVIS, D. B. ; FAULKNER, G. ; VALLE, G. ; MOREIRA, E. S. ; PAVANELLO, R. C. M. ; PASSOS-BUENO, M. R. ; ZATZ, M. . Dysferlin Protein Analysis in Limb-Girdle Muscular Dystrophies. Journal of Molecular Neuroscience , v. 17, p. 71-80, 2001.

• 2001 IUGHETTI, P. ; SUZUKI, O. T. ; GODOI, P. H. ; ALVES, V. A. ; SERTIÉ, A. L. ; ZORICK, T. ; SOARES, F. ; CAMARGO, A. A. ; MOREIRA, E. S. ; LORETO, C. ; MOREIRA-FILHO, C. A. ; SIMPSON, A. J. G. ; OLIVA, G. ; PASSOS-BUENO, M. R. . A polymorphism in endostatin, an angiogenesis inhibitor, predisposes for the development of prostatic adenocarcinoma.. Cancer Research (Chicago, Ill.) , v. 61, p. 7375-7378, 2001.

• 2001 CAMARGO, A. A. ; SAMAIA, H. P. ; DIAS-NETO, E. ; SIMÃO, D. F. ; SOARES, F. ; MOREIRA, E. S. ; NUNES, D. N. ; CORREA, R. G. ; ZALCBERG, H. ; CARVALHO, A. F. ; REIS, L. F. ; BRENTANI, R. R. ; SIMPSON, A. J. G. ; et al. . From the Cover: The contribution of 700,000 ORF sequence tags to the definition of the human transcriptome. Proceedings of the National Academy of Sciences of the United States of America , v. 98, p. 12103-12108, 2001.

• 2000 Moreira, E. S. ; WILTSHIRE, T. ; FAULKNER, G. ; Vainzof, M. ; SUZUKI, O. T. ; VALLE, G. ; REEVES, R. H. ; Zatz, M. ; Passos-Bueno, M. R. ; JENNE, D. . Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethonin. Nature Genetics (Print) , v. 24, p. 163-166, 2000.

• 2000 VAINZOF, M. ; MOREIRA, E. S. ; CANOVAS, M. ; ANDERSON, L. V. B. ; PAVANELLO, R. C. M. ; PASSOS-BUENO, M. R. ; ZATZ, M. . Partial α-sarcoglycan deficiency with retention of the dystrophin-glycoprotein complex in a LGMD2D family. Muscle & Nerve (Print) , v. 23, p. 984-988, 2000.

• 1999 VAINZOF, M. ; MOREIRA, E. S. ; FERRAZ, G. ; PASSOS-BUENO, M. R. ; MARIE, S. K. ; ZATZ, M. . 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, 1999.

• 1999 PASSOS-BUENO, M. R. ; VAINZOF, M. ; MOREIRA, E. S. ; ZATZ, M. . Seven autosomal recessive limb-girdle muscular dystrophies in the Brazilian population: from LGMD2A to LGMD2G. American Journal of Medical Genetics (Print) (Cessou em 2002. Foi desdobrado em três: ISSN 1552-4825, 1552-4841 e 1552-4868) , v. 82, p. 392-398, 1999.

• 1998 Moreira, E. S. ; Vainzof, M. ; MARIE, S. K. ; NIGRO, V. ; Zatz, M. ; Passos-Bueno, M. R. . A first missense mutation in the delta sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathies.. Journal of Medical Genetics , v. 35, p. 951-953, 1998.

• 1998 BUSHBY, KATE ; BASHIR, RUMAISA ; BRITTON, STEPHEN ; STRACHAN, TOM ; KEERS, SHARON ; VAFIADAKI, ELIZABETH ; LAKO, MAJLINDA ; RICHARD, ISABELLE ; MARCHAND, SYLVIE ; BOURG, NATHALIE ; ARGOV, ZOHAR ; SADEH, MENACHEM ; MAHJNEH, IBRAHIM ; MARCONI, GIAMPIERO ; PASSOS-BUENO, MARIA RITA ; MOREIRA, ELOISA DE S ; ZATZ, MAYANA ; BECKMANN, JACQUES S. . A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B. Nature Genetics (Print) , v. 20, p. 37-42, 1998.

• 1998 MCNALLY. E. M. ; MOREIRA, E. S. ; DUGGAN, D. J. ; BÖNNEMANN, C. G. ; LISANTI, M. P. ; LIDOV, H. G. W. ; VAINZOF, M. ; PASSOS-BUENO, M. R. ; HOFFMAN, E. P. ; ZATZ, M. ; KUNKEL, L. M. . Caveolin-3 in muscular dystrophy.. Human Molecular Genetics (Print) , v. 7, p. 871-877, 1998.

• 1997 Moreira, E. S. ; Vainzof, M. ; MARIE, S. K. ; SERTIE, A. L. ; Zatz, M. ; Passos-Bueno, M. R. . The Seventh Form of Autosomal Recessive Limb-Girdle Muscular Dystrophy Is Mapped to 17q11-12. American Journal of Human Genetics , v. 61, p. 151-159, 1997.

• 1997 VAINZOF, M. ; COSTA, C. S. ; MARIE, S. K. ; MOREIRA, E. S. ; REED, U. ; PASSOS-BUENO, M. R. ; BEGGS, A. H. ; ZATZ, M. . Deficiency of α-Actinin-3 (ACTN3) Occurs in Different Forms of Muscular Dystrophy. Neuropediatrics , v. 28, p. 223-228, 1997.

• 1996 Moreira, E. S. ; NIGRO, V. ; PILUSO, G. ; Vainzof, M. ; BELSITO, A. ; POLITANO, L. ; PUCA, A. A. ; Passos-Bueno, M. R. ; Zatz, M. . Autosomal recessive limbgirdle muscular dystrophy, LGMD2F, is caused by a mutation in the δ-sarcoglycan gene. Nature Genetics (Print) , v. 14, p. 195-198, 1996.

• 1996 Passos-Bueno, M. R. ; Moreira, E. S. ; Vainzof, M. ; MARIE, S. K. ; Zatz, M. . Linkage analysis in autosomal recessive limb-girdle muscular dystrophy (AR LGMD) maps a sixth form to 5q33-34 (LGMD2F) and indicates that there is at least one more subtype of AR LGMD.. Human Molecular Genetics (Print) , v. 5, p. 815-820, 1996.

• 1996 SERTIÉ, A. L. ; QUIMBY, M. ; MOREIRA, E. S. ; ZATZ, M. ; ANTONARAKIS, S. E. ; PASSOS-BUENO, M. R. . A gene which causes severe ocular alterations and occipital encephalocele (Knobloch syndrome) is mapped to 21q22.2.. Human Molecular Genetics (Print) , v. 5, p. 843-847, 1996.

• 1996 BÖNNEMANN, C. G. ; PASSOS-BUENO, M. R. ; MCNALLY. E. M. ; VAINZOF, M. ; MOREIRA, E. S. ; MARIE, S. K. ; PAVANELLO, R. C. M. ; NOGUCHI, S. ; OZAWA, E. ; ZATZ, M. ; KUNKEL, L. M. . Genomic screening for β-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2E (LGMD2E).. Human Molecular Genetics (Print) , v. 5, p. 1953-1961, 1996.

• 1996 VAINZOF, M. ; PASSOS-BUENO, M. R. ; CANOVAS, M. ; MOREIRA, E. S. ; PAVANELLO, R. C. M. ; MARIE, S. K. ; ANDERSON, L. V. B. ; BÖNNEMANN, C. G. ; MCNALLY. E. M. ; NIGRO, V. ; KUNKEL, L. M. ; ZATZ, M. . The sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophies.. Human Molecular Genetics , v. 5, p. 1963-1969, 1996.

• 1996 MCNALLY. E. M. ; PASSOS-BUENO, M. R. ; BÖNNEMANN, C. G. ; VAINZOF, M. ; MOREIRA, E. S. ; LIDOV, H. G. W. ; OTHMANE, K. B. ; DENTON, P. H. ; VANCE, J. M. ; ZATZ, M. ; KUNKEL, L. M. . Mild and severe muscular dystrophy caused by a single γ-sarcoglycan mutation.. American Journal of Human Genetics , v. 59, p. 1040-1047, 1996.

• 1996 PASSOS-BUENO, M. R. ; MOREIRA, E. S. ; MARIE, S. K. ; BASHIR, R. ; VASQUES, L. R. ; LOVE, D. R. ; VAINZOF, M. ; IUGHETTI, P. ; OLIVEIRA, J. R. ; BAKKER, E. ; STRACHAN, T. ; BUSHBY, K. ; ZATZ, M. . Main clinical features for the three mapped autosomal recessive limb-girdle muscular dystrophies and estimated proportion of each form in 13 Brazilian families.. Journal of Medical Genetics , v. 33, p. 97-102, 1996.

• 1995 PASSOS-BUENO, M. R. ; MOREIRA, E. S. ; VAINZOF, M. ; CHAMBERLAIN, J. ; MARIE, S. K. ; PEREIRA, L. ; AKIYAMA, J. ; ROBERDS, S. ; CAMPBELL, K. ; ZATZ, M. . A common missense mutation in the adhalin gene in three unrelated Brazilian families with a realtively mild form of autosomal recessive limb-girdle muscular dystrophy.. Human Molecular Genetics , v. 4, p. 1163-1167, 1995.

• 1995 PASSOS-BUENO, M. R. ; BASHIR, R. ; MOREIRA, E. S. ; VASQUES, L. R. ; MARIE, S. K. ; VAINZOF, M. ; IUGHETTI, P. ; BAKKER, E. ; KEERS, S. ; STEPHENSON, A. ; STRACHAN, T. ; BUSHBY, K. ; ZATZ, M. . Confirmation of the 2p Locus for the Mild Autosomal Recessive Limb-Girdle Muscular Dystrophy Gene (LGMD2B) in Three Families Allows Refinement of the Candidate Region. Genomics (San Diego, Calif.) , v. 27, p. 192-195, 1995.

• MOREIRA, E. S. ; Vainzof, M. ; Zatz, M. ; Passos-Bueno, M. R. . Limb Girdle Muscular Dystrophy Type 2G. In: Florian Lang. (Org.). Encyclopedia of Molecular Mechanisms of Disease. 1ed.Berlin: Springer, 2009, v. 1, p. 1183-1184.

• PASSOS-BUENO, M. R. ; MOREIRA, E. S. . Ferramentas Básicas da Genética Molecular Humana.. In: Luís Mir; Carlos Alberto Moreira-Filho. (Org.). Genômica. São Paulo: Editora Atheneu, 2003, v. , p. 43-67.

• BIAGINI, S. ; COSTA, P. A. ; DALE, C. S. ; REAL, J. M. ; MOREIRA, E. S. ; CARVALHO, C. R. R. ; SCHETTINO, G. P. P. ; WENDEL, S. ; AZEVEDO, L. C. P. . EFFECTS OF STORED RED BLOOD CELL TRANSFUSION IN CARDIOPULMONARY FUNCTION AND INFLAMMATION: AN EXPERIMENTAL MECHANISTIC STUDY. In: 32nd International Congress of the International Society of Blood Transfusion, 2012, Cancun. Vox Sanguinis, 2012. v. 103. p. 21-21.

• SILVA, I. M. W. ; MOREIRA, ELOISA S. ; LOURENÇO, NAILA C. V. ; BOSSOLANI-MARTINS, A. L. ; LAZAR, M. ; ROCHA, K. M. ; AGUENA, M. ; MARCO-ANTONIO, D. S. ; FETT-CONTE, A. C. ; ROSENBERG, C. ; VADASZ, E. ; Passos-Bueno, M. R. . Contribution of Small Copy Number Variations (CNVs) to Autism Spectrum Disorder (ASD). In: 2015 International Meeting for Autism Research, 2015, Salt Lake CIty. IMFAR 2015 Program Book & Abstracts, 2015.

• UEDA, M. Y. H. ; REAL, J. M. ; OLIVEIRA, P. G. A. G. ; MOREIRA, E. S. ; REIS, L. F. ; GRANATO, C. F. H. ; RODRIGUES, C. A. . Detection and Quantification of Eight Herpesviruses in Patients undergoing Allogeneic Stem Cell Transplantation in Brazil. In: 11th International Congress on Inflammation/ XXXVIII Brazilian Congress of Immunology, 2013, Natal. Abstractsof the 11th International Congress on Inflammation/ XXXVIII Brazilian Congress of Immunology, 2013.

• RIBEIRO, C. M. ; MOREIRA, E. S. ; MARTINS, A. L. B. ; MORALES, A. G. ; FERREIRA, S. G. ; TAKAHASHI, V. N. O. ; MOREIRA, D. P. ; GRIESI-OLIVEIRA, K. ; CONTE, A. C. F. ; ROSENBERG, C. ; VADASZ, E. ; PASSOS-BUENO, MARIA RITA . Use of a custom-designed array-CGH to identify small CNVs in nonsyndromic Autism Spectrum Disorders. In: 63rd Annual Meeting of the American Society of Human Genetics, 2013, Boston. Abstracts of the 63rd Annual Meeting of the American Society of Human Genetics, 2013.

• UEDA, M. Y. H. ; REAL, J. M. ; OLIVEIRA, P. G. A. G. ; MOREIRA, E. S. ; REIS, L. F. ; GRANATO, C. F. H. ; RODRIGUES, C. A. . A New Strategy Based On qPCR to Optimize Detection and Quantification of Eight Herpesviruses in Patients Undergoing Allogeneic Hematopoietic Stem Cell Transplantation. In: 54th American Society of Hematology Annual Meeting, 2012, Atlanta. Blood, 2012. v. 120. p. 3044.

• PEREIRA, K. M. C. ; FARIA, A. G. A. ; Moreira, E. S. ; SANTOS, V. C. ; GRECCO, M. ; SILVA, N. P. ; ANDRADE, L. E. C. . Associação entre o Número de Cópias de C4A e C4B e Lúpus Eritematoso Sistêmico. In: XXXI Reunião Anual da SPAIC/ XIV Congresso Luso-Brasileiro de Alergologia e Imunologia Clínica, 2010, Madeira. XXXI Reunião Anual da SPAIC/ XIV Congresso Luso-Brasileiro de Alergologia e Imunologia Clínica, 2010.

• PEREIRA, K. M. C. ; FARIA, A. G. A. ; Moreira, E. S. ; SANTOS, V. C. ; GRECCO, M. ; SILVA, N. P. ; ANDRADE, L. E. C. . Low C4A Gene Copy Number in Systemic Lupus Erythematosus.. In: American College of Rheumatology/Association of Rheumatology Health Professionals Annual Scientific Meeting, 2010, Atlanta. Arthritis Rheum, 2010. v. 62. p. 498.

• CHAUFFAILLE, M. L. ; Borri, D ; MOREIRA, E. S. ; ALBERTO, F. L. . Acute promyelocytic acute leuekemia with t(15;17): frequency of additional clonal chromosome abnormalities and FLT3. In: 31o Congresso da Sociedade Brasileir de Hematologia e Hemoterapia, 2008, São Paulo. Rev. Bras. Hematol. Hemoter., 2008. v. 30. p. 102.

• ORABONA, G. M. ; MOREIRA, E. S. ; AVELAR, L. O. ; GRIESI-OLIVEIRA, K. ; VADASZ, E. ; BIASON, L. M. ; MATIOLLI, S. ; OTTO, P. ; PASSOS-BUENO, M. R. . Haplotype analyses of the serotonin receptor 2C gene (HTR2C) show evidence of association with male affected with autism spectrum disorders. In: 59th Annual Meeting of the American Society of Human Genetics, 2005, Salt Lake City. Am. J. Hum. Genet., 2005.

• FERRAZ, M. L. ; MATOS, C. A. ; PEREZ, R. M. ; PACHECO, M. S. ; LEMOS, L. B. ; ALBERTO, F. L. ; MOREIRA, E. S. ; MEDINA-PESTANA, J. O. ; SILVA, A. E. . Carga viral do vírus da hepatite B em transplantados renais: comparação entre pacientes HBeAg positivo e negativo. In: XVIII Congresso Brasileiro de Hepatologia, 2005, Camp do Jordão. GED, 2005. v. 24. p. 61.

• FERRAZ, M. L. ; MOUTINHO, R. S. ; MATOS, C. A. ; PEREZ, R. M. ; ALBERTO, F. L. ; MOREIRA, E. S. ; MEDINA-PESTANA, J. O. ; LANZONI, V. P. ; SILVA, A. E. . Estudo comparativo da infecção pelo HBV entre portadores de insuficiência renal crônica (IRC) e transplantados renais com HBeAg positivo. In: XVIII Congresso Brasileiro de Hepatologia, 2005, Campos do Jordão. GED, 2005. v. 24. p. 6.

• FERRAZ, M. L. ; MATOS, C. A. ; PEREZ, R. M. ; PACHECO, M. S. ; LEMOS, L. B. ; ALBERTO, F. L. ; MOREIRA, E. S. ; MEDINA-PESTANA, J. O. ; SILVA, A. E. . Fatores associados à fibrose hepática avançada em transplantados renais com infecção pelo vírus da hepatite B. In: XVIII Congresso Brasileiro de Hepatologia, 2005, Campos do Jordão. GED, 2005. v. 24. p. 6.

• FERRAZ, M. L. ; MATOS, C. A. ; PEREZ, R. M. ; PACHECO, M. S. ; LEMOS, L. B. ; ALBERTO, F. L. ; MOREIRA, E. S. ; MEDINA-PESTANA, J. O. ; SILVA, A. E. . Impacto da co-infecção pelo HCV nos níveis de HBV-DNA em transplantados renais com HBsAg positivo. In: XVIII Congresso Brasileiro de Hepatologia, 2005, Campos do Jordão. GED, 2005. v. 24. p. 15.

• FIGUEIREDO, M. S. ; MIYASHIRO, K. ; MOREIRA, E. S. ; ALBERTO, F. L. . Toxoplasma gondii detection using a multiplex, semi automated, real-time PCR assay. In: 2005 Annual Meeting of the American Association of Clinical Chemistry, 2005, Orlando. Clinical Chemistry, 2005. v. 51. p. A170-A171.

• FIGUEIREDO, M. S. ; PERES, T. S. ; MOREIRA, E. S. ; MIYASHIRO, K. ; KOIDE, S. S. ; ALBERTO, F. L. . Bioinformatics tools for automation of DNA sequence analyses in the clinical laboratory setting. In: 2005 Annual Meeting of the American Association of Clinical Chemistry, 2005, Orlando. Clinical Chemistry, 2005. v. 51. p. A222-A222.

• AVELAR, L. O. ; MOREIRA, E. S. ; ORABONA, G. M. ; VADASZ, E ; VIANNA-MORGANTE, A. M. ; PASSOS-BUENO, M. R. . Estudo de associação entre o gene ATF2 e os transtornos do espectro autista. In: 50o. Congresso Brasileiro de Genética, 2004, Florianópolis. Anais do 50o. Congresso Brasileiro de Genética, 2004. p. 813.

• ORABONA, G. M. ; MOREIRA, E. S. ; AVELAR, L. O. ; VADASZ, E ; VIANNA-MORGANTE, A. M. ; PASSOS-BUENO, M. R. . Estudo de associação entre genes de receptores de serotonina e o autismo. In: 50o. Congresso Brasileiro de Genética, 2004, Florianópolis. Anais do 50o. Congresso Brasileiro de Genética, 2004. p. 819.

• MOREIRA, E. S. ; ORABONA, G. M. ; AVELAR, L. O. ; VADASZ, E. ; BIASON, L. M. ; TAKAHASHI, V. N. O. ; ABE, K. ; Vianna-Morgante, Angela M. ; PASSOS-BUENO, M. R. . Molecular and cytogenetic analyses in Brazilian patients affected by autism spectrum disorders. In: 53rd Annual Meeting of the American Society of Human Genetics, 2003, Los Angeles. Am. J. Hum. Genet., 2003.

• VAINZOF, M. ; CANOVAS, M. ; GOUVEIA, T. L. ; MOREIRA, E. S. ; PASSOS-BUENO, M. R. ; ZATZ, M. . Sarcoglicanopatias: estudo da organização das proteínas do complexo sarcoglicano nas famílias brasileiras. In: XIII Jornada Brasileira de Doenças Neuromusculares, 2002, Ribeirão Preto. Anais da XIII Jornada Brasileira de Doenças Neuromusculares, 2002. v. 2002.

• PAULA, F. ; VAINZOF, M. ; MOREIRA, E. S. ; PASSOS-BUENO, M. R. ; PAVANELLO, R. C. M. ; MATIOLI, S. ; NIGRO, V. ; ZATZ, M. . Clinical Variability in Calpainopathy: What Makes the Difference?. In: Xth International Congress on Neuromuscular Diseases, 2002, Vancouver. Journal of the Neurological Sciences, 2002. v. 199. p. P285.

• MOREIRA, E. S. ; ORABONA, G. M. ; TAKAHASHI, V ; VADASZ, E ; BIASON, L. M. ; ROSENBERG, R. ; VIANNA-MORGANTE, A. M. ; PASSOS-BUENO, M. R. . Análise do gene FMR1 e cromossômica em pacientes brasileiros com autismo. In: 48 Congresso Nacional de Genética, 2002, Aguas de Lindoia. Anais do 48 Congresso Nacional de Genética, 2002. p. GH081.

• PAULA, F. ; VAINZOF, M. ; MOREIRA, E. S. ; PASSOS-BUENO, M. R. ; BUSHBY, K. ; BASHIR, R. ; ZATZ, M. . Novel Dysferlin Mutations in Brazilian LGMD2B Patients. In: 51st Annual Meeting of the American Society of Human Genetics, 2001, San Diego. Am. J. Hum. Genet., 2001. v. 69. p. 639.

• VAINZOF, M. ; FAULKNER, G. ; VALLE, G. ; BEGGS, A. H. ; CARPEN, O. ; SALMIKANGAS, P. ; WALLGREN-PETTERSSON, C. ; MOREIRA, E. S. ; PASSOS-BUENO, M. R. ; ZATZ, M. . Sarcomeric proteins and Neuromuscular disorders. In: 51st Annual Meeting of the American Society of Human Genetics, 2001, San Diego. Am. J. Hum. Genet., 2001. v. 69. p. 638.

• VAINZOF, M. ; FAULKNER, G. ; VALLE, G. ; BEGGS, A. H. ; CARPEN, O. ; SALMIKANGAS, P. ; WALLGREN-PETTERSSON, C. ; LABEIT, S. ; GURGEL-GIANNETI, J. ; MOREIRA, E. S. ; PASSOS-BUENO, M. R. ; ZATZ, M. . The role of sarcomeric proteins in neuromuscular disorders. In: 6th International Congress of the World Muscle Society, 2001, Utah. Neuromusc. Disord., 2001. v. 11. p. 629.

• PAULA, F. ; VAINZOF, M. ; MOREIRA, E. S. ; PASSOS-BUENO, M. R. ; ZATZ, M. . Screening of dysferlin mutations in LGMD Brazilian patients. In: 6th International Congress of the World Muscle Society, 2001, Utah. Neuromusc. Disord., 2001. v. 11. p. 627.

• VAINZOF, M. ; MOREIRA, E. S. ; PAULA, F. ; PAVANELLO, R. C. M. ; Passos-Bueno, M. R. ; Zatz, M. . Protein Analysis In Autosomal Recessive Limb-girdle Muscular Dystrophies (AR-lgmd). In: 10th International congress of Human Genetics, 2001, Viena. European Journal of Human Genetics, 2001. v. 9. p. P1503.

• PAULA, F. ; VIEGAS, R. ; KAI, A. ; MOREIRA, E. S. ; PASSOS-BUENO, M. R. ; VAINZOF, M. ; NIGRO, V. ; ZATZ, M. . Recurrent Basque and Brazilian Mutation in LGMD2A (Calpainopathy) Brazilian Families. In: 10th International congress of Human Genetics, 2001, Viena. European Journal of Human Genetics, 2001. v. 9. p. P1504.

• VAINZOF, M. ; MOREIRA, E. S. ; PASSOS-BUENO, M. R. ; ZANOTELI, E. ; Gurgel-Giannetti, J. G. ; RIBEIRO, A. ; SILVA, H. C. A. ; TSANACLIS, A. M. C. ; ZATZ, M. . Effect of Telethonin Deficiency in LGMD-2G and Its Expression in Other Forms of Muscular Dystrophies and Congenital Myopathies. In: 23RD ANNUAL CARRELL-KRUSEN SYMPOSIUM, 2001, Dallas. Journal of Child Neurology, 2001. v. 16. p. S5-2.

• VAINZOF, M. ; MOREIRA, E. S. ; PASSOS-BUENO, M. R. ; FAULKNER, G. ; VALLE, G. ; ZANOTELI, E. ; GURGEL-GIANNETI, J. ; RIBEIRO, A. ; SILVA, H. C. A. ; TSANACLIS, A. M. ; ZATZ, M. . The effect of telethonin deficiency in LGMD-2G and its expression in other forms of muscular dystrophies and congenital myopathies. In: 50th Annual Meeting of the American Society of Human Genetics, 2000, Philadelphia. Am. J. Hum. Genet., 2000. v. 67. p. 379-379.

• VAINZOF, M. ; PAVANELLO, R. C. M. ; ANDERSON, L. V. B. ; MOREIRA, E. S. ; PASSOS-BUENO, M. R. ; ZATZ, M. . Dysferlin analysis in autosomal recessive limb-girdle muscular dystrophies (AR-LGMD). In: 5th International Congress of the World Muscle Society, 2000, South Africa. Neuromusc. Disord., 2000. v. 10. p. 364.

• VAINZOF, M. ; MOREIRA, E. S. ; FAULKNER, G. ; VALLE, G. ; GURGEL-GIANNETI, J. ; ZATZ, M. . Telethonin expression in the autosomal recessive limb-girdle muscular dystrophies. In: 5th International Congress of the World Muscle Society, 2000, South Africa. Neuromusc. Disord., 2000. v. 10. p. 364.

• PAULA, F. ; VAINZOF, M. ; KAI, A. ; MOREIRA, E. S. ; PASSOS-BUENO, M. R. ; ZATZ, M. . Screening of calpain mutations in Brazilian LGMD2A patients suggests preferential involvement of three exons. In: 5th International Congress of the World Muscle Society, 2000, South Africa. Neuromusc. Disord., 2000. v. 10. p. 354.

• VAINZOF, M. ; ANDERSON, L. V. B. ; MOREIRA, E. S. ; PAVANELLO, R. C. M. ; PASSOS-BUENO, M. R. ; ZATZ, M. . Calpain 3: Characterization of the primary defect in LGMD2A and analysis of its secondary effect in other LGMDs. In: 52nd annual Meeting of the American Academy of Neurology, 2000, San Diego. Neurol., 2000. v. 54.

• PAULA, F. ; MOREIRA, E. S. ; BERNARDINO, A. ; KAI, A. ; PASSOS-BUENO, M. R. ; VAINZOF, M. ; ZATZ, M. . Recurrent LGMD2A (Calpainopathy) Mutations in Brazilian Patients. In: 50th Annual Meeting of the American Society of Human Genetics, 2000, Philadelphia. Am. J. Hum. Genet., 2000. v. 67. p. 251-251.

• VAINZOF, M. ; MOREIRA, E. S. ; CANOVAS, M. ; SUZUKI, O. T. ; PAVANELLO, R. C. M. ; PASSOS-BUENO, M. R. ; ZATZ, M. . Partial a-sarcoglycan (a-SG) deficiency associated with the retention of the SG complex in a LGMD2D family. In: 49th Annual Meeting of the American Society of Human Genetics, 1999, San Francisco. Am. J. Hum. Genet., 1999. v. 65. p. 494-494.

• MOREIRA, E. S. ; WILTSHIRE, T. ; VAINZOF, M. ; REEVES, R. H. ; ZATZ, M. ; PASSOS-BUENO, M. R. . Physical mapping of the candidate region for the gene causing Limb-Girdle Muscular Dystrophy type 2G (LGMD2G). In: 49th Annual Meeting of the American Society of Human Genetics, 1999, San Francisco. Am. J. Hum. Genet., 1999. v. 65. p. 415-415.

• VAINZOF, M. ; MOREIRA, E. S. ; CANOVAS, M. ; SUZUKI, O. T. ; PAVANELLO, R. C. M. ; COSTA, C. S. ; PASSOS-BUENO, M. R. . Deficiência parcial de a-sarcolgicana (a-SG) associada à manutenção do complexo sarcoglicano em uma família com a forma 2D da Distrofia Muscular tipo Cinturas (DMC). In: 45o Congresso Nacional de Genética, 1999, Gramado. Genet. Mol. Biol., 1999. v. 22. p. 247.

• MOREIRA, E. S. ; WILTSHIRE, T. ; VAINZOF, M. ; REEVES, R. H. ; ZATZ, M. ; PASSOS-BUENO, M. R. . Mapeamento físico da região candidata para o gene associado à forma 2G da Distrofia Muscular tipo Cinturas (DMC). In: 45o Congresso Nacional de Genética, 1999, Gramado. Genet. Mol. Biol., 1999. v. 22. p. 250.

• MOREIRA, E. S. ; SUZUKI, O. T. ; VAINZOF, M. ; MARIE, S. K. ; ZATZ, M. ; PASSOS-BUENO, M. R. . Estudo de correlação genótipo-fenótipo nas sarcoglicanopatias tipo 2D e 2E. In: 45o Congresso Nacional de Genética, 1999, Gramado. Genet. Mol. Biol., 1999. v. 22. p. 253.

• VAINZOF, M. ; ANDERSON, L. V. B. ; MOREIRA, E. S. ; PASSOS-BUENO, M. R. ; PAVANELLO, R. C. M. ; ZATZ, M. . LGMD2A: muscle calpain analysis in Brazilian LGMD patients. In: 4th International Congress of the World Muscle society, 1999, Antalya. Neuromusc. Disord., 1999. v. 9. p. 506.

• VAINZOF, M. ; MOREIRA, E. S. ; PASSOS-BUENO, M. R. ; ZATZ, M. . Sarcoglycanopathies and limb-girdle syndromes: diagnostic insights. In: IX International Congress on Neuromuscular Diseases, 1998, Adelaide. Muscle & Nerve, 1998. v. 7. p. S3.

• MOREIRA, E. S. ; VAINZOF, M. ; MARIE, S. K. ; NIGRO, V. ; ZATZ, M. ; PASSOS-BUENO, M. R. . Distrofia Muscular de Cinturas (DMC) tipo 2F: Caracterização de mutações em famílias brasileiras. In: 44o Congresso Nacional de Genética, 1998, Águas de Lindóia. Genet. Mol. Biol., 1998. v. 21. p. 295.

• ALBUQUERQUE, F. D. ; MOREIRA, E. S. ; MCNALLY. E. M. ; PASSOS-BUENO, M. R. ; ZATZ, M. . Triagem de mutações no gene da caveolina e estudos de ligação em famílias de dois afetados por DMC. In: 43o Congresso Nacional de Genética, 1997, Goiânia. Rev. Bras. Genet., 1997. v. 20. p. 220.

• MOREIRA, E. S. ; VAINZOF, M. ; MARIE, S. K. ; SERTIE, A. L. ; ZATZ, M. ; PASSOS-BUENO, M. R. . Proporção e variabilidade clínica entre as formas autossômicas recessivas da Distrofia Muscular tipo Cinturas (DMC) em famílias brasileiras. In: 43o Congresso Nacional de Genética, 1997, Goiânia. Rev. Bras. Genet., 1997. v. 20. p. 220.

• MOREIRA, E. S. ; VAINZOF, M. ; MARIE, S. K. ; ZATZ, M. ; PASSOS-BUENO, M. R. . A sétima forma autossômica recessiva da Distrofia Muscular tipo Cinturas (LGMD2G) está mapeada em 17q11-12. In: 43o Congresso Nacional de Genética, 1997, Goiânia. Rev. Bras. Genet., 1997. v. 20. p. 220.

• MOREIRA, E. S. ; PASSOS-BUENO, M. R. ; VAINZOF, M. ; MARIE, S. K. ; ZATZ, M. . Linkage analysis in autosomal recessive limb-girdle muscular dystrophy (AR LGMD) maps a sixth form to 5q33-34 and indicates that there is at least one more subtype of AR LGMD. In: 9th International Congress of Human Genetics, 1996, Rio de Janeiro. Braz. J. Genet., 1996. v. 19. p. 245.

• PASSOS-BUENO, M. R. ; VAINZOF, M. ; MARIE, S. K. ; MOREIRA, E. S. ; OLIVEIRA, J. R. ; ZATZ, M. . Molecular and clinical findings in the six forms of autosomal recessive limb-girdle muscular dystrophies. In: 9th International Congress of Human Genetics, 1996, Rio de Janeiro. Braz. J. Genet., 1996. v. 19. p. 86.

• SERTIE, A. L. ; QUIMBY, M. ; MOREIRA, E. S. ; MURRAY, J. ; ZATZ, M. ; PASSOS-BUENO, M. R. . COL6A1 and COL6A2 as candidate genes for Knobloch Syndrome. In: 9th International Congress of Human Genetics, 1996, Rio de Janeiro. Braz. J. Genet., 1996. v. 19. p. 246.

• VAINZOF, M. ; PASSOS-BUENO, M. R. ; MOREIRA, E. S. ; BÖNNEMANN, C. G. ; MCNALLY. E. M. ; ANDERSON, L. V. B. ; NIGRO, V. ; KUNKEL, L. M. ; ZATZ, M. . The sarcoglycan complex in the six Autosomal Recessive Limb-Girdle Muscular Dystrophy (AR-LGMD). In: 46th Anual Meeting Of The American Society Of Human Genetics, 1996, San Francisco. Am. J. Hum. Genet., 1996. v. 59. p. A290.

• MOREIRA, E. S. ; SERTIE, A. L. ; MARIE, S. K. ; VAINZOF, M. ; ZATZ, M. ; PASSOS-BUENO, M. R. . Estudo de ligação em famílias com Distrofia Muscular tipo Cinturas (DMC). In: 41o Congresso Nacional de Genética, 1995, Caxambu. Rev. Bras. Genet., 1995. v. 18. p. 555.

• PASSOS-BUENO, M. R. ; MOREIRA, E. S. ; VAINZOF, M. ; PEREIRA, L. ; MARIE, S. K. ; AKIYAMA, J. ; ZATZ, M. . Uma mesma mutação no gene da adalina pode causar formas graves e leves de Distrofia Muscular tipo Cinturas (DMC). In: 41o Congresso Nacional de Genética, 1995, Caxambu. Rev. Bras. Genet., 1995. v. 18. p. 556.

• SERTIE, A. L. ; MARIE, S. K. ; MOREIRA, E. S. ; ZATZ, M. ; PASSOS-BUENO, M. R. . Síndrome de Knobloch: é causada por um gene de desenvolvimento?. In: 41o Congresso Nacional de Genética, 1995, Caxambu. Rev. Bras. Genet., 1995. v. 18. p. 553.

• PASSOS-BUENO, M. R. ; MOREIRA, E. S. ; VASQUES, L. R. ; MARIE, S. K. ; IUGHETTI, P. ; VAINZOF, M. ; BASHIR, R. ; BUSHBY, K. ; BAKKER, E. ; ZATZ, M. . Confirmation of a third locus at 2p for autosomal recessive limb-girdle muscular dystrophy indicates that at least 4 genes are responsible for this condition. In: 44th Annual Meeting of the American Societ of Human Genetics, 1994, Montreal. Am. J. Hum. Genet., 1994. v. 55. p. A199.

• OLIVEIRA, P. G. A. G. ; UEDA, M. Y. H. ; REAL, J. M. ; MOREIRA, ELOISA S. ; OLIVEIRA, J. S. R. ; GONCALVES, M. V. ; GINANI, V. C. ; OLIVEIRA, O. M. ; SEBER, A. ; NOVIS, Y. ; ROCHA, V. ; GRANATO, C. F. H. ; RODRIGUES, C. A. . Simultaneous quantification of the eight human herpesviruses in allogeneic hematopoietic stem cell transplantation. Transplantation , 2015.

• PEREIRA, K. ; PERAZZIO, S. ; FARIA, A. ; Moreira, E. S. ; SANTOS, V. ; GRECCO, M. ; SILVA, N. ; ANDRADE, L. E. . Impact of C4, C4A and C4B gene copy number variation in the susceptibility, phenotype and progression of systemic lupus erythematosus 2015 (Artigo científico).

• MOREIRA, ELOISA S. ; SILVA, I. M. W. ; LOURENCO, N. ; MOREIRA, DANIELLE P. ; RIBEIRO, C. M. ; MARTINS, A. L. B. ; LAZAR, M. ; COSTA, S. S. ; ROCHA, K. M. ; AGUENA, M. ; FETT-CONTE, A. ; ROSENBERG, C. ; BERTOLA, D. R. ; VADASZ, E. ; Passos-Bueno, M. R. . Detection of small copy number variations (CNVs) in Autism Spectrum Disorder (ASD) by custom array comparative genomic hybridization (aCGH) 2015 (Artigo científico).

Outras produções

Projetos de pesquisa

• 2008 - Atual

  Identificação de alterações moleculares em neoplasias hematológicas, Situação: Em andamento; Natureza: Pesquisa. , Integrantes: Eloisa de Sá Moreira - Integrante / CHAUFFAILLE, M. L. - Coordenador.

• 2004 - 2007

  Caracterização de alterações moleculares em doenças mielodisplásicas, Situação: Concluído; Natureza: Pesquisa. , Integrantes: Eloisa de Sá Moreira - Integrante / Fernando Lopes Alberto - Integrante / CHAUFFAILLE, M. L. - Coordenador., Financiador(es): Fundação de Amparo à Pesquisa do Estado de São Paulo - Auxílio financeiro., Número de produções C, T & A: 3

• 2001 - Atual

  Identificação de genes e mecanismos moleculares associados aos transtornos autistas, Projeto certificado pelo(a) coordenador(a) Maria Rita dos Santos e Passos Bueno em 02/10/2013., Situação: Em andamento; Natureza: Pesquisa. , Integrantes: Eloisa de Sá Moreira - Integrante / PASSOS-BUENO, M. R. - Coordenador.

• 2000 - 2001

  Transcript Finishing Initiative, Situação: Concluído; Natureza: Pesquisa. , Integrantes: Eloisa de Sá Moreira - Integrante / Anamaria Aranha Camargo - Coordenador / Andrew John George Simpson - Integrante / SOGAYAR, M. C. - Integrante / SOUZA, S. J. - Integrante., Financiador(es): Fundação de Amparo à Pesquisa do Estado de São Paulo - Bolsa., Número de produções C, T & A: 1

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