Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Natalia Oliva"'
Autor:
Silvio Mayke Leite, Eriem Micaela Gonçalo Sena Santos, Mariana Regolin Almeida, Natalia Oliva, Gabriella Goulart Stevanato, João Pedro Nunes Gasque, Leonir Bueno Ribeiro, Leandro Dalcin Castilha
Publikováno v:
Acta Scientiarum: Animal Sciences, Vol 46, Iss 1 (2024)
This review aimed to address all relevant parts of the digestive physiology of rabbits, before and after weaning, with a view to enabling greater understanding of these phases and reducing the mortality of kits. The biggest bottlenecks in Brazilian r
Externí odkaz:
https://doaj.org/article/f5fbe658176a457f82fb03caa802a154
Publikováno v:
Human Genome Variation, Vol 11, Iss 1, Pp 1-6 (2024)
Abstract Chromosomal heteromorphisms (CHs) are morphological variations predominantly found in constitutive heterochromatic regions of the genome, primarily composed of tandemly repetitive sequences of satellite DNA. Although not completely devoid of
Externí odkaz:
https://doaj.org/article/1b6cd479731042bc8e3f809ef43c7f81
Publikováno v:
Pediatric dermatology. 33(1)
BACKGROUND The current treatment of keloids includes surgery, intralesional steroids, and radiotherapy, among others. Radiotherapy is not recommended in children due to its effects on growing tissues. Our aim was to study intralesional triamcinilone
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49596a1cc7aeec3d29d2e5edead16992
https://pubmed.ncbi.nlm.nih.gov/26758090
https://pubmed.ncbi.nlm.nih.gov/26758090
Autor:
Telma Luís, Cristina Candeias, Sara Domingues, Natália Oliva-Teles, Céu Mota, Cláudia Falcão Reis
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 61, Iss 1, Pp 150-152 (2022)
Objective: To present prenatal diagnosis and cytogenetic characterization of a unique pattern of partial tetrasomy 18 mosaicism. Case report: A 34-year-old woman underwent amniocentesis at 25 weeks of gestation due to anomalies detected in obstetric
Externí odkaz:
https://doaj.org/article/9939018d3faf47e09019fa730a20d29f
Autor:
Jorge Diogo Da Silva, Natália Oliva-Teles, Nataliya Tkachenko, Joana Fino, Mariana Marques, Ana Maria Fortuna, Dezso David
Publikováno v:
Biomedicines, Vol 11, Iss 1, p 12 (2022)
The genetic complexity of neurodevelopmental disorders (NDD), combined with a heterogeneous clinical presentation, makes accurate assessment of their molecular bases and pathogenic mechanisms challenging. Our purpose is to reveal the pathogenic varia
Externí odkaz:
https://doaj.org/article/8bbe1e18206e44ee8ed510f6cbda8464
Autor:
Borovecki, Ana, Einarsdóttir, Jónína, O'Mathúna, Dónal, Pospieszna, Paulina, Stern, Orly Maya, Teles, Natália Oliva
Publikováno v:
In The Lancet 11-17 April 2015 385(9976):1391-1391
Akademický článek
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Autor:
Ana Rita Soares, Gabriela Soares, Manuela Mota-Freitas, Natália Oliva-Teles, Ana Maria Fortuna
Publikováno v:
Acta Médica Portuguesa, Vol 32, Iss 7-8 (2019)
Introduction: Intellectual disability affects 2% – 3% of the general population, with a chromosomal abnormality being found in 4% – 28% of these patients and a cryptic subtelomeric abnormality in 3% – 16%. In most cases, these subtelomeric rear
Externí odkaz:
https://doaj.org/article/724086fa16534922a3d9add6cb9ca66a
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
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Autor:
Maria de Fátima Oliveira dos Santos, Alessandro de Oliveira Silva, Débora de Paiva Lucena, Thalita Esther Oliveira dos Santos, Ana Laís Oliveira dos Santos, Natália Oliva Teles
Publikováno v:
Revista de Ciências da Saúde Nova Esperança, Vol 10, Iss 2, Pp 91-101 (2012)
O presente artigo enfoca o sigilo profissional que faz parte dos valores éticos e das determinações legais que devem ser seguidas pelos profissionais de saúde, constituindo-se dever inerente ao desempenho da profissão médica, o que caracteriza
Externí odkaz:
https://doaj.org/article/f2e31e3ac9ac449e8e9f13fbbd827ae8