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of 9
pro vyhledávání: '"Laura Durão Ferreira"'
Autor:
Valdemir Vicente da Silva Júnior, Laura Durão Ferreira, Lílian Rodrigues Alves, Adriane Borges Cabral, Paula Regina Luna de Araújo Jácome, Paulo Sérgio Ramos de Araújo, Ana Catarina de Souza Lopes, Maria Amélia Vieira Maciel
Publikováno v:
Revista da Sociedade Brasileira de Medicina Tropical, Vol 50, Iss 6, Pp 764-768
Abstract INTRODUCTION: Pseudomonas aeruginosa, an important pathogen globally, presents several resistance mechanisms. This study aimed to investigate the presence of bla GES in clinical isolates of Pseudomonas aeruginosa obtained from various clinic
Externí odkaz:
https://doaj.org/article/3b95cd49529f4620b26e4d8012fda001
Autor:
Rhonda E. Schnur, Rayssa L. Borges-Medeiros, Jenny Thies, João Ricardo Mendes de Oliveira, Laura Durão Ferreira, Christina Lam
Publikováno v:
American Journal of Medical Genetics Part A. 179:2228-2232
Primrose syndrome (PRIMS), a rare genetic disorder with several clinical findings including intellectual disability, macrocephaly, typical facial features, and muscle wasting, is caused by heterozygous variants in the ZBTB20 gene. We report the cases
Publikováno v:
Journal of Molecular Neuroscience. 67:441-444
Primary familial brain calcification (PFBC) is a rare neurodegenerative disorder characterized by symmetrical and bilateral brain calcification. It is typically inherited as an autosomal dominant disorder, and de novo variants have also been describe
Publikováno v:
Journal of molecular neuroscience : MN. 71(12)
Raine syndrome is a rare, often lethal autosomal recessive condition marked by congenital malformations that range in severity. Considering that several case reports of this syndrome describe cases of stillbirth or perinatal death, information about
Publikováno v:
Journal of Molecular Neuroscience. 70:1255-1256
Primary familial brain calcification (PFBC) is a well-known genetic condition that has recently had a surge of autosomal recessive cases. We recently reported a case of autosomal recessive PFBC on a 54-year-old Brazilian patient with a novel homozygo
Publikováno v:
The Journal of Neuropsychiatry and Clinical Neurosciences. 30:291-293
Publikováno v:
Journal of the neurological sciences. 379
Highlights • Primary familial brain calcification (PFBC) has diverse presentations • Impairment beyond the brain has been described in PFBC patients • Findings emphasized here include elevated CSF-Pi and white matter hyperintensities • Such a
Publikováno v:
Brain. 142:e51-e51
Autor:
Laura Durão Ferreira, Valdemir Vicente da Silva Júnior, Adriane Borges Cabral, Paulo Sérgio Ramos de Araújo, Ana Catarina de Souza Lopes, Paula Regina Luna de Araújo Jácome, Maria Amélia Vieira Maciel, Lílian Rodrigues Alves
Publikováno v:
Revista da Sociedade Brasileira de Medicina Tropical, Vol 50, Iss 6, Pp 764-768
Revista da Sociedade Brasileira de Medicina Tropical, Volume: 50, Issue: 6, Pages: 764-768, Published: DEC 2017
Revista da Sociedade Brasileira de Medicina Tropical v.50 n.6 2017
Revista da Sociedade Brasileira de Medicina Tropical
Sociedade Brasileira de Medicina Tropical (SBMT)
instacron:SBMT
Revista da Sociedade Brasileira de Medicina Tropical, Volume: 50, Issue: 6, Pages: 764-768, Published: DEC 2017
Revista da Sociedade Brasileira de Medicina Tropical v.50 n.6 2017
Revista da Sociedade Brasileira de Medicina Tropical
Sociedade Brasileira de Medicina Tropical (SBMT)
instacron:SBMT
INTRODUCTION: Pseudomonas aeruginosa, an important pathogen globally, presents several resistance mechanisms. This study aimed to investigate the presence of bla GES in clinical isolates of Pseudomonas aeruginosa obtained from various clinical specim