Zobrazeno 1 - 10
of 477
pro vyhledávání: '"Alina Costina"'
Autor:
Dana Elena Mîndru, Elena Țarcă, Elena Emanuela Braha, Alexandrina-Ștefania Curpăn, Solange Tamara Roșu, Dana-Teodora Anton-Păduraru, Heidrun Adumitrăchioaiei, Valentin Bernic, Ioana-Alexandra Pădureț, Alina Costina Luca
Publikováno v:
Diagnostics, Vol 14, Iss 5, p 491 (2024)
Gangliosidosis (ORPHA: 79255) is an autosomal recessive lysosomal storage disease (LSD) with a variable phenotype and an incidence of 1:200000 live births. The underlying genotype is comprised GLB1 mutations that lead to β-galactosidase deficiency a
Externí odkaz:
https://doaj.org/article/480718db861a49fe9175c58b96e4f112
Autor:
Alina Costina Luca, Simona Georgiana David, Alexandru Gabriel David, Viorel Țarcă, Ioana-Alexandra Pădureț, Dana Elena Mîndru, Solange Tamara Roșu, Eduard Vasile Roșu, Heidrun Adumitrăchioaiei, Jana Bernic, Elena Cojocaru, Elena Țarcă
Publikováno v:
Life, Vol 13, Iss 10, p 2056 (2023)
Cardiovascular disease is the leading cause of mortality and morbidity throughout the world, accounting for 16.7 million deaths each year. The underlying pathological process for the majority of cardiovascular diseases is atherosclerosis, a slowly pr
Externí odkaz:
https://doaj.org/article/35aecf1f0faa4628a9afbbe8cc990ba6
Autor:
Ioannis Mavroudis, Ioana-Miruna Balmus, Alin Ciobica, Mircea Nicusor Nicoara, Alina Costina Luca, Dragos Octavian Palade
Publikováno v:
Life, Vol 13, Iss 9, p 1924 (2023)
(1) Background: In this study, we aimed to explore the regulatory mechanism of miR-124-3p microglial exosomes, as they were previously reported to modulate neuroinflammation and promote neuronal repair following traumatic brain injury (TBI). (2) Meth
Externí odkaz:
https://doaj.org/article/15899985eba44c099a6e88e12cce6525
Autor:
Petru Fabian Lungu, Corina-Miruna Lungu, Alin Ciobîcă, Ioana Miruna Balmus, Alexandra Boloș, Romeo Dobrin, Alina Costina Luca
Publikováno v:
Brain Sciences, Vol 13, Iss 7, p 1004 (2023)
Metacognition essentially represents “thinking about thinking”, or the individual’s capacity to control and monitor their own cognitive processes. Metacognition impairment in schizophrenia represents a core feature of the disease, and, in the l
Externí odkaz:
https://doaj.org/article/3f841f3244b2498a85327e6500d98cab
Autor:
Dana Elena Mîndru, Gabriela Păduraru, Carmen Daniela Rusu, Elena Țarcă, Alice Nicoleta Azoicăi, Solange Tamara Roșu, Alexandrina-Ștefania Curpăn, Irina Mihaela Ciomaga Jitaru, Ioana Alexandra Pădureț, Alina Costina Luca
Publikováno v:
Medicina, Vol 59, Iss 6, p 1113 (2023)
Foreign body aspiration (FBA) is a frequent diagnosis in children. In the absence of other lung conditions, such as asthma or chronic pulmonary infections, this manifests as a sudden onset of cough, dyspnea, and wheezing. The differential diagnosis i
Externí odkaz:
https://doaj.org/article/73afcccb9ba9451e808679e38abf373a
Autor:
Ioannis Mavroudis, Foivos Petridis, Ioana-Miruna Balmus, Alin Ciobica, Dragos Lucian Gorgan, Alina Costina Luca
Publikováno v:
Diagnostics, Vol 13, Iss 8, p 1367 (2023)
(1) Background: While mild traumatic brain injuries (TBIs) are a major public health issue, post-concussion syndrome (PCS) remains a controversial entity. In both cases, the clinical diagnosis is mainly based on the symptoms and brain imaging evaluat
Externí odkaz:
https://doaj.org/article/be0ccffd2ab743648c6af519dc63c36a
Autor:
Elena Țarcă, Dina Al Namat, Alina Costina Luca, Vasile Valeriu Lupu, Razan Al Namat, Ancuța Lupu, Laura Bălănescu, Jana Bernic, Lăcrămioara Ionela Butnariu, Mihaela Moscalu, Marius Valeriu Hînganu
Publikováno v:
Diagnostics, Vol 13, Iss 8, p 1413 (2023)
Omphalocele is the most common ventral abdominal wall defect. Omphalocele is associated with other significant anomalies in up to 80% of cases, among which the cardiac ones are the most frequent. The aim of our paper is to highlight, through a review
Externí odkaz:
https://doaj.org/article/f47ce04deca54ce18905ebf4f19ef707
Autor:
Smaranda Diaconescu, Cristina Rusu, Laura Bozomitu, Alina Costina Luca, Ecaterina Vlad, Oana-Larisa Ciobanu-Matei, Ramona Babici, Silvia Strat, Lorenza Donea
Publikováno v:
Romanian Journal of Pediatrics, Vol 69, Iss 2, Pp 162-165 (2020)
The article discusses a clinical case of late-onset Pompe disease in a 15-year and 6-month-old adolescent hospitalised in a Paediatric Gastroenterology department to investigate persistent liver cytolysis, without response to hepatoprotective therapy
Externí odkaz:
https://doaj.org/article/744f63c2082c47fd8396358c5b7a181c
Autor:
Smaranda Diaconescu, Cristina Rusu, Laura Bozomitu, Alina Costina Luca, Ecaterina Vlad, Oana-Larisa Ciobanu-Matei, Ramona Babici, Silvia Strat, Lorenza Donea
Publikováno v:
Romanian Journal of Pediatrics, Vol 69, Iss 2, Pp 166-169 (2020)
Articolul pune în discuţie un caz clinic de boală Pompe forma tardivă la un adolescent în vârstă de 15 ani și 6 luni, internat într-un serviciu de gastroenterologie pediatrică pentru investigarea unei citolize hepatice persistente, fără r
Externí odkaz:
https://doaj.org/article/72f752af53b64c4ba0f2f4ee65d5fa00
Autor:
Stefana Maria Moisa, Elena-Lia Spoiala, Laura Mihaela Trandafir, Lacramioara Ionela Butnariu, Ingrith-Crenguta Miron, Antonela Ciobanu, Adriana Mocanu, Anca Ivanov, Carmen Iulia Ciongradi, Ioan Sarbu, Anamaria Ciubara, Carmen Daniela Rusu, Alina Costina Luca, Alexandru Burlacu
Publikováno v:
Medicina, Vol 59, Iss 2, p 362 (2023)
Diamond–Blackfan anemia is a rare (6–7 million live births), inherited condition manifesting as severe anemia due to the impaired bone marrow production of red blood cells. We present the unusual case of a six month old infant with a de novo muta
Externí odkaz:
https://doaj.org/article/a46cf09496f74c4c89a4e59eab18eb32