Zobrazeno 1 - 10
of 109
pro vyhledávání: '"Vitalie Vacaras"'
Autor:
Andreea-Cristina Paraschiv, Vitalie Vacaras, Cristina Nistor, Cristiana Vacaras, Stefan Strilciuc, Dafin F Muresanu
Publikováno v:
Microbial Cell, Vol 11, Pp 106-115 (2024)
Gut microbiota has complex immune functions, related to different pathologies, including multiple sclerosis (MS).This study evaluated the influence of treatments on gut microbiota in people with MS (PwMS). The research comprised 60 participants, incl
Externí odkaz:
https://doaj.org/article/53cae5724a4a4ffe8d6f407e0c813bcb
Autor:
Oliviu-Florentiu Sarb, Adriana-Daniela Sarb, Maria Iacobescu, Irina-Maria Vlad, Mircea-Vasile Milaciu, Lorena Ciurmarnean, Vitalie Vacaras, Alina-Ioana Tantau
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 11, p 5676 (2024)
Inflammatory bowel diseases (IBDs) are characterized by chronic gastrointestinal inflammation due to abnormal immune responses to gut microflora. The gut–brain axis is disrupted in IBDs, leading to neurobiological imbalances and affective symptoms.
Externí odkaz:
https://doaj.org/article/9b06c8b14f144bdfb398958d2a7ca80e
Publikováno v:
JMIR Research Protocols, Vol 12, p e50546 (2023)
BackgroundMild cognitive impairment (MCI) and Alzheimer’s disease (AD) might be more frequent in patients with inflammatory bowel disease (IBD), but the relationship between these 2 entities is yet to be entirely established. Certain blood biomarke
Externí odkaz:
https://doaj.org/article/b28d10a0174d4a94ad326fed219d5be0
Autor:
Vitalie Vacaras, Andreea-Cristina Paraschiv, Silvina Iluț, Cristiana Vacaras, Cristina Nistor, Gheorghe-Eduard Marin, Andra Maria Schiopu, Dorian-Traian Nistor, Ștefan Cristian Vesa, Dafin Fior Mureșanu
Publikováno v:
Brain Sciences, Vol 14, Iss 3, p 243 (2024)
Multiple sclerosis (MS) is a demyelinating central nervous system disease that leads to neurological disability. Brain-derived neurotrophic factors (BDNFs) are neurotrophins involved in neurodegenerative disorders. This study analysed the relationshi
Externí odkaz:
https://doaj.org/article/5647bead718842b08c06d3ab2213ac71
Publikováno v:
Romanian Journal of Neurology, Vol 20, Iss 1, Pp 107-114 (2021)
Introduction. Cryptogenic stroke represents 25% of all cases. Paradoxical embolism is a common case in people under 45 years old who have patent foramen ovale. Case presentation. 44-years old patient with left motor deficit, dysarthria and dizziness
Externí odkaz:
https://doaj.org/article/50d910aa8dfd49a281ea79fedcdc744b
Autor:
Tudor Arsenescu, Radu Chifor, Tiberiu Marita, Andrei Santoma, Andrei Lebovici, Daniel Duma, Vitalie Vacaras, Alexandru Florin Badea
Publikováno v:
Sensors, Vol 23, Iss 5, p 2806 (2023)
The aim of this study was to evaluate the feasibility of a noninvasive and low-operator-dependent imaging method for carotid-artery-stenosis diagnosis. A previously developed prototype for 3D ultrasound scans based on a standard ultrasound machine an
Externí odkaz:
https://doaj.org/article/4dd7ef9816354eea99e8488a4a0914f2
Publikováno v:
Case Reports in Neurology, Vol 12, Iss 3, Pp 339-347 (2020)
Stiff person syndrome (SPS) is a rare neurologic disorder, characterized by muscle rigidity and spasms. Anti-glutamic acid decarboxylase (anti-GAD) antibodies are associated with the classic form of SPS, while antibodies against amphiphysin are assoc
Externí odkaz:
https://doaj.org/article/b7b7273cb8dc48efae3334c1cc83bfcf
Autor:
Silvina Ilut, Bianca O. Pirlog, Radu Pirlog, Andreea Nutu, Vitalie Vacaras, Sebastian M. Armean
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 18, p 10221 (2022)
Acute ischemic stroke (AIS) represents an important cause of disability and death. Since only a minor percentage of patients with AIS are eligible for acute therapy, the management of risk factors is mandatory. An important risk factor of AIS is hype
Externí odkaz:
https://doaj.org/article/9c2afdfcc01a4eb4806ba854609a1ebe
Publikováno v:
Romanian Journal of Neurology, Vol 17, Iss 4, Pp 200-203 (2018)
Fabry disease is a rare genetic disease involving a deficiency of an enzyme. A decrease in the enzyme activity leads to a selective suffering of specific anatomic and functional structures resulting in heteromorphic clinical signs that increase the d
Externí odkaz:
https://doaj.org/article/fa1763a888124ae495407378bfa1e136
Publikováno v:
Romanian Journal of Neurology, Vol 17, Iss 2, Pp 113-118 (2018)
Wilson disease (hepatolenticular degeneration) is due to a genetic abnormality inherited in an autosomal recessive manner that leads to impairment of cellular copper transport. The clinical manifestations of Wilson disease are predominantly hepatic,
Externí odkaz:
https://doaj.org/article/7f37c8ef48244aecaa576ffab063c138