[HTML][HTML] Gene network reconstruction reveals cell cycle and antiviral genes as major drivers of cervical cancer
Although human papillomavirus was identified as an aetiological factor in cervical cancer,
the key human gene drivers of this disease remain unknown. Here we apply an unbiased …
the key human gene drivers of this disease remain unknown. Here we apply an unbiased …
Prevalence and duration of breast milk feeding in very preterm infants: A 3‐year follow‐up study and a systematic literature review
C Rodrigues, R Teixeira, MJ Fonseca… - Paediatric and …, 2018 - Wiley Online Library
Abstract Background The World Health Organization recommends exclusive breast milk
feeding until 6 months and continuing up to 2 years of age; little is known about whether very …
feeding until 6 months and continuing up to 2 years of age; little is known about whether very …
Cord blood levels of IL-6, IL-8 and IL-10 may be early predictors of bronchopulmonary dysplasia in preterm newborns small for gestational age
G Rocha, E Proença, A Guedes, C Carvalho… - Disease …, 2012 - content.iospress.com
Introduction: Various cytokines have been associated to the occurrence of
bronchopulmonary dysplasia (BPD) in preterm neonates. AIM: To establish an association …
bronchopulmonary dysplasia (BPD) in preterm neonates. AIM: To establish an association …
[HTML][HTML] The influence of Aloe vera with mesenchymal stem cells from dental pulp on bone regeneration: characterization and treatment of non-critical defects of the …
IMV Soares, GVO Fernandes, LC Cavalcante… - Journal of Applied Oral …, 2019 - SciELO Brasil
Objective This study aimed to evaluate the inflammatory effect and bone formation in sterile
surgical failures after implantation of a collagen sponge with mesenchymal stem cells from …
surgical failures after implantation of a collagen sponge with mesenchymal stem cells from …
New approach reveals CD28 and IFNG gene interaction in the susceptibility to cervical cancer
VB Guzman, A Yambartsev… - Human molecular …, 2008 - academic.oup.com
Cervical cancer is a complex disease with multiple environmental and genetic determinants.
In this study, we sought an association between polymorphisms in immune response genes …
In this study, we sought an association between polymorphisms in immune response genes …
[HTML][HTML] Prenatal diagnosis and management of a fetal goiter hypothyroidism due to dyshormonogenesis
CM Figueiredo, I Falcão, J Vilaverde… - Case Reports in …, 2018 - hindawi.com
Fetal goiter is a rare disorder not expected to be found during a healthy woman's pregnancy.
It can be a prenatal manifestation of congenital hypothyroidism due to thyroid …
It can be a prenatal manifestation of congenital hypothyroidism due to thyroid …
[HTML][HTML] Aloe vera as vehicle to mineral trioxide aggregate: study in bone repair
JLM Fé, CA Coelho, GM Damascena… - … de Odontologia da …, 2014 - SciELO Brasil
AIM: Mineral trioxide aggregate (MTA) was associated to Aloe vera to verify the coadjutant
action of that medicinal plant in the bone neoformation process in tibia of rats. MATERIAL …
action of that medicinal plant in the bone neoformation process in tibia of rats. MATERIAL …
Congenital disorders of glycosylation with neonatal presentation
C Resende, C Carvalho, A Alegria, D Oliveira… - Case …, 2014 - casereports.bmj.com
Congenital disorders of glycosylation (CDG) are a group of hereditary diseases
characterised by deficiency of enzymes involved in proteins glycosylation. We describe the …
characterised by deficiency of enzymes involved in proteins glycosylation. We describe the …
Neonatal pericardial effusion: case report and review of the literature
CF Liz, S Domingues, L Pinho, L Lopes… - Journal of Pediatric and …, 2020 - jpnim.com
Pericardial effusion (PCE) is a rare condition in neonates. The most common cause is
iatrogenic due to central venous catheters (CVCs) and symptoms vary from asymptomatic to …
iatrogenic due to central venous catheters (CVCs) and symptoms vary from asymptomatic to …
A Novel Noonan Syndrome RAF1 Mutation: Lethal Course in a Preterm Infant
A Ratola, HM Silva, A Guedes, C Mota, AC Braga… - Pediatric Reports, 2015 - mdpi.com
Noonan syndrome is a relatively common and heterogeneous genetic disorder, associated
with congenital heart defect in about 50% of the cases. If the defect is not severe, life …
with congenital heart defect in about 50% of the cases. If the defect is not severe, life …