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Search on : ROSELINO, ANA MARIA [Author]
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 Roselino, Ana Maria et al. An outbreak of scalp white piedra in a Brazilian children day care. Rev. Inst. Med. trop. S. Paulo, Oct 2008, vol.50, no.5, p.307-309. ISSN 0036-4665


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 Roselino, Ana Maria et al. L. (L.) chagasi in aids and visceral leishmaniasis (kala-azar) co-infection. Rev. Inst. Med. trop. S. Paulo, Aug 2008, vol.50, no.4, p.251-254. ISSN 0036-4665


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 Gomes, Ciro Martins et al. Accuracy of mucocutaneous leishmaniasis diagnosis using polymerase chain reaction: systematic literature review and meta-analysis. Mem. Inst. Oswaldo Cruz, Apr 2015, vol.110, no.2, p.157-165. ISSN 0074-0276
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 Medeiros, Angela Rapela, Silva Jr, Wilson A and Roselino, Ana Maria DNA sequencing confirms the involvement of Leishmania (L.) amazonensis in american tegumentary leishmaniasis in the state of São Paulo, Brazil. Clinics, 2008, vol.63, no.4, p.451-456. ISSN 1807-5932
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 Soares, Killarney Ataide et al. Field validation of a Leishmania (Leishmania) mexicana exo-antigens ELISA for diagnosing tegumentary leishmaniasis in regions of Leishmania (Viannia) predominance. Braz J Infect Dis, June 2015, vol.19, no.3, p.302-307. ISSN 1413-8670
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 Gomes, Ciro Martins et al. Complementary exams in the diagnosis of american tegumentary leishmaniasis. An. bras. dermatol., Sept 2014, vol.89, no.5, p.701-709. ISSN 0365-0596
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 Ambiel, Marcela Vendruscolo and Roselino, Ana Maria Prevalence of Metabolic Syndrome and its components in a Brazilian sample of pemphigus patients. An. bras. dermatol., Sept 2014, vol.89, no.5, p.752-756. ISSN 0365-0596
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 Cumming, Moema Mignac et al. Doença de Mucha-Habermann (variante febril úlcero-necrótica) com acometimento mucoso exuberante: relato de caso. An. Bras. Dermatol., Dez 2009, vol.84, no.6, p.655-658. ISSN 0365-0596


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 Brito, Moema Mignac Cumming et al. Citologia de Tzanck: redescobrindo uma antiga ferramenta diagnóstica. An. Bras. Dermatol., Ago 2009, vol.84, no.4, p.431-433. ISSN 0365-0596


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 Brochado, Maria José Franco et al. Polimorfismo Val247Leu do gene β2-glicoproteína 1 pode justificar a gênese de anticorpos antiβ2GP1 e síndrome do anticorpo antifosfolípide na hanseníase multibacilar. An. Bras. Dermatol., Ago 2009, vol.84, no.4, p.355-359. ISSN 0365-0596


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