Search Results - "Galera, Marcial F."

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    Evaluation of the maturational auditory process in children with the infection by Zika congenital syndrome by Lucas, Priscila de A, Santos, Walkiria B, de Oliveira, Thalita M, Galera, Marcial F

    Published in Revista CEFAC (01-03-2024)
    “…ABSTRACT Purpose: to analyze the absolute latencies of waves I. III and V and the interpeak intervals I-III. III-V and I-V of the ABR recorded from different…”
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    Journal Article
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    Erythrocytic changes in patients with Systemic Lupus Erythematosus by Matos, Marilia B. P., Dias, Eliane P., Arruda, Augusto C., Aguiar Junior, Nestor A., Galera, Marcial F., Leite, Cristhiane A.

    Published in Medicina (Sao Paulo. 197?) (02-02-2016)
    “…Objective: We assessed the prevalence of erythrocytic changes in patients with SLE, at Cuiabá University General Hospital (UNIC-HGU). Methods: blood samples…”
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    Ethical issues related to the access to orphan drugs in Brazil: the case of mucopolysaccharidosis type I by Boy, Raquel, Schwartz, Ida V D, Krug, Bárbara C, Santana-da-Silva, Luiz C, Steiner, Carlos E, Acosta, Angelina X, Ribeiro, Erlane M, Galera, Marcial F, Leivas, Paulo G C, Braz, Marlene

    Published in Journal of medical ethics (01-04-2011)
    “…Background/AimsMucopolysaccharidosis type I (MPS I) is a rare lysosomal storage disorder treated with bone marrow transplantation or enzyme replacement therapy…”
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    Molecular identification of chromosome Y sequences in Brazilian patients with Turner syndrome by Araújo, Claudinéia, Galera, Marcial F., Galera, Bianca B., Silvestre, Flávia G., Medeiros, Sebastião F.

    Published in Gynecological endocrinology (01-01-2008)
    “…The investigation of Y-specific sequences in patients with Turner Syndrome (TS) with karyotype 45,X or mosaic, has a fundamental role in the clinical…”
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    Deletion of 17p13 and LIS1 Gene Mutation in Isolated Lissencephaly Sequence by Elias, Renata C., Galera, Marcial F., Schnabel, Beatriz, Briones, Marcelo R.S., Borri, Maria L., Lipay, Monica, Carvalheira, Gianna, Brunoni, Decio, Melaragno, Maria I.

    Published in Pediatric neurology (01-07-2006)
    “…Classical lissencephaly is a neuroblast migration disorder that occurs either as isolated lissencephaly sequence or in association with malformation syndromes,…”
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    Evaluation of a protocol for postmortem examination of stillbirths and neonatal deaths with congenital anomalies by Cernach, Mirlene C S P, Patrício, Francy R S, Galera, Marcial F, Moron, Antonio F, Brunoni, Decio

    Published in Pediatric and developmental pathology (01-07-2004)
    “…A study was conducted on 75 perinatal deaths with congenital anomalies through clinical, radiographic, cytogenetic, and autopsy evaluation, and the diagnoses…”
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    Avaliação do processo maturacional auditivo em crianças portadoras da síndrome da infecção congênita pelo Zika vírus by Lucas, Priscila de A, Santos, Walkiria B, Oliveira, Thalita M de, Galera, Marcial F

    Published in Revista CEFAC (2024)
    “…RESUMO Objetivo: analisar as latências absolutas das ondas I. III e V e os intervalos interpicos I-III. III-V e I-V do Potencial Evocado Auditivo de Tronco…”
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    Association of Polymorphisms in the DNA Repair Genes XRCC1 and XRCC3 with Systemic Lupus Erythematosus by Da Silva, Cristhiane A. Leite, Galera, Marcial F., Festi, Regiane R., Espinosa, Mariano M., Fernandes, Vander, Blaskievicz, Paula H., Dias, Eliane P.

    Published in The open rheumatology journal (28-02-2019)
    “…Background: Evidence suggests that DNA damage is implicated in the development of Systemic Lupus Erythematosus (SLE). Objective: Investigate the possible…”
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    Ceratocone e retardo mental entre irmãos by Boianovsky, Celso, Freitas, Denise de, Moura, Rita Cristina M. R., Galera, Marcial F.

    Published in Arquivos brasileiros de oftalmologia (01-06-1995)
    “…RESUMO Apresentamos dois irmãos com a associação de retardo mental e ceratocone bilateral, filhos de pais consangüíneos, onde a avaliação genealógica sugere um…”
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