Zobrazeno 1 - 10
of 152
pro vyhledávání: '"R. Liutkevičienė"'
Publikováno v:
Neurologijos seminarai, Vol 26, Iss 3 (93) (2023)
Multiple sclerosis is a chronic autoimmune disease of the central nervous system. Multiple sclerosis causes demyelination, impaired nervous system function, and eventually neurodegeneration. Microglia are cells of the central nervous system that deve
Externí odkaz:
https://doaj.org/article/5283e92f7f9c4ccf8f064a3460fc8d13
Publikováno v:
Neurologijos seminarai, Vol 25, Iss 2(88) (2021)
Pituitary adenoma (PA) is a benign tumor of parenchymal cells in the adenohypophysis. Clinically significant PA occurs in 1 in 1064 of the population. Invasive PAs, pituitary carcinomas, are aggressive and can spread from sella turcica to other tissu
Externí odkaz:
https://doaj.org/article/65659f6635884eeb9dd5574fd8d75f9b
Autor:
A. Kubiliūtė, R. Liutkevičienė
Publikováno v:
Neurologijos seminarai, Vol 25, Iss 1(87) (2021)
Optic neuritis and multiple sclerosis are connected via processes of demyelination and neurodegeneration in the central nervous system. Immuno-modulated myelin sheathing and axonal loss causing irreversible neurological dysfunction can be found in bo
Externí odkaz:
https://doaj.org/article/3a174c36abea4af391fb64bcaf209f62
Publikováno v:
Neurologijos seminarai, Vol 25, Iss 1(87) (2021)
Neuromyelitis optica spectrum disorder (NMOSD) is a rare acute inflammatory disease of the central nervous system (CNS) predominantly affecting the optic nerve and the spinal cord. The main pathogenetic mechanism of NMOSD is the interaction of aquapo
Externí odkaz:
https://doaj.org/article/b3c3c8bf1cea4ba29c66a8871c07a194
Publikováno v:
Neurologijos seminarai, Vol 24, Iss 3(85) (2020)
Leber’s hereditary optic neuropathy (LHON) is one of the most common hereditary mitochondrial optic neuropathies characterized by bilateral, painless, subacute or acute loss of central vision. The disease usually develops between the ages of 15 and
Externí odkaz:
https://doaj.org/article/8dc99c58da6b49ebaaee44c9e4b7ba4c
Publikováno v:
Neurologijos seminarai, Vol 24, Iss 3(85) (2020)
Multiple sclerosis (MS) affects more than 2 million people worldwide. Lithuania has a high prevalence of multiple sclerosis. Optic neuritis (ON) occurs in 70% of patients with MS and it may be the initial presenting symptom in 25% of MS cases. Typica
Externí odkaz:
https://doaj.org/article/d0b9f5d2cf004bf485ef464cf5c6ed80
Autor:
V. Punytė, R. Liutkevičienė
Publikováno v:
Neurologijos seminarai, Vol 23, Iss 3(81) (2019)
Optic neuritis (ON) is characterized as an inflammation of the optic nerve. Based on etiology, ON is classified to typical and atypical forms. Typical ON is often related to multiple sclerosis while atypical ON can be caused by various infections, au
Externí odkaz:
https://doaj.org/article/d7bce27b95ef44a2b5bfd70eae7cb0e6
Autor:
J. Katelytė, R. Liutkevičienė
Publikováno v:
Neurologijos seminarai, Vol 23, Iss 2(80) (2019)
Optic neuritis (ON) is a quite common condition and most neurologists are familiar with it. However, some studies show that at least 10% of cases are overdiagnosed. The most common mistake of diagnosing ON is wrong terminology and other illnesses whi
Externí odkaz:
https://doaj.org/article/2e7a79db4d45481ab4a4486745b1352f
Publikováno v:
Neurologijos seminarai, Vol 22, Iss 4(78) (2018)
Leber hereditary optic neuropathy (LHON) is one of the most common inherited mitochondrial optic neuropathies, caused by mitochondrial DNA mutations. Three most common mutations, namely m.11778G>A, m.14484T>G, and m.3460G>A, account for the majority
Externí odkaz:
https://doaj.org/article/c424153c89ec425992184f3477a361ca
Autor:
I. Povilaitytė, R. Liutkevičienė
Publikováno v:
Neurologijos seminarai, Vol 22, Iss 4(78) (2018)
Leber hereditary optic neuropathy (LHON) is the most common hereditary optical neuropathy caused by primary mutations in mitochondrial DNA. LHON manifests as opticnerve atrophy and loss of central vision. In about 70% of LHON cases three major mutati
Externí odkaz:
https://doaj.org/article/e98c9149e2b9414c83c706f46b0bbaec