Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Virginija Danylaité Karrenbauer"'
Autor:
Daiva Valadkevičienė, Dalius Jatužis, Irena Žukauskaitė, Virginija Danylaitė Karrenbauer, Indre Bileviciute-Ljungar
Publikováno v:
Journal of Rehabilitation Medicine, Vol 56 (2024)
Objective: To evaluate the Comprehensive International Classification of Functioning, Disability and Health (ICF) Core Set for multiple sclerosis with regard to the Brief ICF Core Set for multiple sclerosis. Design: Descriptive cross-sectional singl
Externí odkaz:
https://doaj.org/article/3a54136740ee48fd91e73994dec7db0b
Autor:
Andrius Kavaliunas, Ali Manouchehrinia, Virginija Danylaite Karrenbauer, Hanna Gyllensten, Anna Glaser, Kristina Alexanderson, Jan Hillert
Publikováno v:
PLoS ONE, Vol 12, Iss 1, p e0169460 (2017)
Multiple sclerosis (MS) is a disease with profound heterogeneity in clinical course.To analyze sources and levels of income among MS patients in relation to disease phenotype with a special focus on identifying differences/similarities between primar
Externí odkaz:
https://doaj.org/article/a8b17cb8227e4b9c9e1306587ce67c15
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-7 (2021)
Abstract Multiple sclerosis (MS) patients with immunoglobulin gamma (IgG) oligoclonal bands (OCB) in the cerebrospinal fluid (CSF) have different genetic backgrounds and brain MRI features compared to those without. In this study, we aimed to determi
Externí odkaz:
https://doaj.org/article/01d6be95c1a141ee8ecd58413c1b49a1
Autor:
Jinming Han, Heela Sarlus, Zbigniew K. Wszolek, Virginija Danylaité Karrenbauer, Robert A. Harris
Publikováno v:
Acta Neuropathologica Communications, Vol 8, Iss 1, Pp 1-12 (2020)
Abstract CSF1R-related leukoencephalopathy is an adult-onset leukoencephalopathy with axonal spheroids and pigmented glia caused by colony stimulating factor 1 receptor (CSF1R) gene mutations. The disease has a global distribution and currently has n
Externí odkaz:
https://doaj.org/article/197bf60a7caf4469bbe3bfa70d8d93ef
Autor:
Igal Rosenstein, Oluf Andersen, Daniel Victor, Elisabet Englund, Tobias Granberg, Carola Hedberg‐Oldfors, Katarina Jood, Yusran Ady Fitrah, Takeshi Ikeuchi, Virginija Danylaité Karrenbauer
Publikováno v:
Acta Neurologica Scandinavica. 145:599-609
Colony stimulating factor 1 receptor (CSF1R)-related leukoencephalopathy is a rare, genetic disease caused by heterozygous mutations in the CSF1R gene with rapidly progressive neurodegeneration, behavioral, cognitive, motor disturbances.To describe f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2702e0aecca616cacf717e5f8641ce6c
https://doi.org/10.1111/ane.13589
https://doi.org/10.1111/ane.13589
Autor:
Goda‐Camille Mickeviciute, Monika Valiuskyte, Michael Plattén, Zbigniew K. Wszolek, Oluf Andersen, Virginija Danylaité Karrenbauer, Benjamin V. Ineichen, Tobias Granberg
Publikováno v:
Journal of Internal Medicine. 291:269-282
Colony-stimulating factor 1 receptor (CSF1R)-related leukoencephalopathy is a rare but fatal microgliopathy. The diagnosis is often delayed due to multifaceted symptoms that can mimic several other neurological disorders. Imaging provides diagnostic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82de0dcfe76c157dab7285aa77877608
https://doi.org/10.1111/joim.13420
https://doi.org/10.1111/joim.13420
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-6 (2021)
Scientific Reports
Scientific Reports
To investigate whether cerebrospinal fluid (CSF) markers differ between pediatric-onset multiple sclerosis (PoMS, onset
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5fcc1d285ecc00fb0d448ebb4981a72
https://doaj.org/article/19ee7f7483874f38ac49d944e5ce2b46
https://doaj.org/article/19ee7f7483874f38ac49d944e5ce2b46
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-7 (2021)
Scientific Reports
Scientific Reports
Multiple sclerosis (MS) patients with and without the oligoclonal band (OCB) distribution of immunoglobulin gamma (IgG) in the cerebrospinal fluid (CSF) has a different genetic background and brain MRI features. In this study we have aimed to determi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4ca19f2a38fcaa25725d54fac92dd50
https://doaj.org/article/01d6be95c1a141ee8ecd58413c1b49a1
https://doaj.org/article/01d6be95c1a141ee8ecd58413c1b49a1
Publikováno v:
Acta Neurologica Scandinavica. 143:587-601
Multiple sclerosis (MS) is a challenging and disabling condition, predominantly affecting individuals in their early life, and has an impact functionally, financially, and on quality of life. However, there is a lack of systematic approach towards as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f14a1d52e4297be2da8a74193ddd11e
https://doi.org/10.1111/ane.13411
https://doi.org/10.1111/ane.13411
Autor:
null Igal Rosenstein, null Oluf Andersen, null Daniel Victor, null Elisabet Englund, null Tobias Granberg, null Carola Hedberg‐Oldfors, null Katarina Jood, null Yusran Ady Fitrah, null Takeshi Ikeuchi, null Virginija Danylaité Karrenbauer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::daed6d3e7f7f0c38044d0b775c16c18e
https://doi.org/10.1111/ane.13589/v2/response1
https://doi.org/10.1111/ane.13589/v2/response1
