Quantum and classical statistical mechanics of a class of non-Hermitian HamiltoniansJONES, H. F; MOREIRA, E. S.Journal of physics. A, Mathematical and theoretical (Print). 2010, Vol 43, Num 5, issn 1751-8113, 055307.1-055307.11Article

An adaptive intrusion detection system using Neural NetworksBONIFACIO, J. M; MOREIRA, E. S; CANSIAN, A. M et al.IFIP TC11 conferenceIFIP TC11 conferenceSEC '98 : international conference on information securitySEC '98 : international conference on information security. 1998, pp 418-428, isbn 3-85403-116-5Conference Paper

Partial α-sarcoglycan deficiency with retention of the dystrophin-glycoprotein complex in a LGMD2D familyVAINZOF, M; MOREIRA, E. S; CANOVAS, M et al.Muscle & nerve. 2000, Vol 23, Num 6, pp 984-988, issn 0148-639XArticle

A first missense mutation in the δ sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2f (LGMD2F) in Brazilian sarcoglycanopathiesMOREIRA, E. S; VAINZOF, M; MARIE, S. K et al.Journal of medical genetics. 1998, Vol 35, Num 11, pp 951-953, issn 0022-2593Article

HTR1B and HTR2C in autism spectrum disorders in Brazilian familiesORABONA, G. M; GRIESI-OLIVEIRA, K; OTTO, P et al.Brain research. 2009, Vol 1250, pp 14-19, issn 0006-8993, 6 p.Article

Seven autosomal recessive limb-girdle muscular dystrophies in the Brazilian population : From LGMD2A to LGMD2GPASSOS-BUENO, M. R; VAINZOF, M; MOREIRA, E. S et al.American journal of medical genetics. 1999, Vol 82, Num 5, pp 392-398, issn 0148-7299Article

Confirmation of the 2p locus for the mild autosomal recessive limb-girdle muscular dystrophy gene (LGMD2B) in three families allows refinement of the candidate regionPASSOS-BUENO, M. R; RAMAISA BASHIR; STRACHAN, T et al.Genomics (San Diego, Calif.). 1995, Vol 27, Num 1, pp 192-195, issn 0888-7543Article

Deficiency of α-actinin-3 (ACTN3) occurs in different forms of muscular dystrophyVAINZOF, M; COSTA, C. S; MARIE, S. K et al.Neuropediatrics. 1997, Vol 28, Num 4, pp 223-228, issn 0174-304XArticle

The seventh form of autosomal recessive limb-girdle muscular dystrophy is mapped to 17q11-12MOREIRA, E. S; VAINZOF, M; MARIE, S. K et al.American journal of human genetics. 1997, Vol 61, Num 1, pp 151-159, issn 0002-9297Article

Main clinical features of the three mapped autosomal recessive limb-girdle muscular dystrophies and estimated proportion of each form in 13 Brazilian familiesPASSOS-BUENO, M. R; MOREIRA, E. S; STRACHAN, T et al.Journal of medical genetics. 1996, Vol 33, Num 2, pp 97-102, issn 0022-2593Article

A common missense mutation in the adhalin gene in three unrelated Brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophyRITA PASSOS BUENO, M; MOREIRA, E. S; VAINZOF, M et al.Human molecular genetics (Print). 1995, Vol 4, Num 7, pp 1163-1167, issn 0964-6906Article

Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethoninMOREIRA, E. S; WILTSHIRE, T. J; JENNE, D. E et al.Nature genetics. 2000, Vol 24, Num 2, pp 163-166, issn 1061-4036Article

A gene which causes severe ocular alterations and occipital encephalocele (Knobloch syndrome) is mapped to 21q22.3SERTIE, A. L; QUIMBY, M; MOREIRA, E. S et al.Human molecular genetics (Print). 1996, Vol 5, Num 6, pp 843-848, issn 0964-6906, 5 p.Article

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 LGMDPASSOS-BUENO, M. R; MOREIRA, E. S; VAINZOF, M et al.Human molecular genetics (Print). 1996, Vol 5, Num 6, pp 815-820, issn 0964-6906Article

The sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophiesVAINZOF, M; PASSOS-BUENO, M. R; KUNKEL, L. M et al.Human molecular genetics (Print). 1996, Vol 5, Num 12, pp 1963-1969, issn 0964-6906Article

In vitro activity of meglumine antimoniate, a pentavalent antimonial drug, on Leishmania promastigotesMOREIRA, E. S. A; PETRILLO-PEIXOTO, M. L.Brazilian journal of medical and biological research. 1991, Vol 24, Num 5, pp 459-469, issn 0100-879X, 11 p.Article

Actinobacillus actinomycetemcomitans genetic heterogeneity: amplification of JP2-like Itx promoter pattern correlated with specific arbitrarily primed polymerase chain reaction (AP-PCR) genotypes from human but not marmoset Brazilian isolatesSADDI-ORTEGA, L; CARVALHO, M. A. R; CISALPINO, P. S et al.Canadian journal of microbiology. 2002, Vol 48, Num 7, pp 602-610, issn 0008-4166, 9 p.Article

Glucantime susceptibility of Leishmania promastigotes under variable growth conditionsMOREIRA, E. S. A; DE ARAUJO SOARES, R. M; PETRILLO-PEIXOTO, M. DE L et al.Parasitology research (1987). 1995, Vol 81, Num 4, pp 291-295, issn 0932-0113Article

Antibacterial activity of Brazilian propolis and fractions against oral anaerobic bacteriaSANTOS, F. A; BASTOS, E. M. A; UZEDA, M et al.Journal of ethnopharmacology. 2002, Vol 80, Num 1, pp 1-7, issn 0378-8741Article

Brazilian propolis: Physicochemical properties, plant origin and antibacterial activity on periodontopathogensSANTOS, F. A; BASTOS, E. M. A. F; MAIA, A. B. R. A et al.PTR. Phytotherapy research. 2003, Vol 17, Num 3, pp 285-289, issn 0951-418X, 5 p.Article

Cell surface carbohydrates and in vivo infectivity of glucantime-sensitive and resistant Leishmania (Viannia) guyanensis cell linesGAZOLA, K. C. P; FERREIRA, A. V. B; ANACLETO, C et al.Parasitology research (1987). 2001, Vol 87, Num 11, pp 935-940, issn 0932-0113Article

Leishmania (V.) guyanensis : isolation and characterization of glucantime-resistant cell linesFERREIRA-PINTO, K. C; MIRANDA-VILELA, A. L; ANACLETO, C et al.Canadian journal of microbiology. 1996, Vol 42, Num 9, pp 944-949, issn 0008-4166Article

Genetic diversity of Saccharomyces cerevisiae strains during the 24 h fermentative cycle for the production of the artisanal Brazilian cachaçaGUERRA, J. B; ARAUJO, R. A. C; PATARO, C et al.Letters in applied microbiology. 2001, Vol 33, Num 2, pp 106-111, issn 0266-8254Article