Research output per year
Research output per year
Search results
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2024
Diagnosing Monogenic Stroke at Younger Age
Ilinca, A., Kafantari, E., Wallenius, J., Kristoffersson, U., Englund, E., Puschmann, A. & Lindgren, A. G., 2024 Dec 1, In: Stroke. 55, 12, p. 2846-2855 10 p.Research output: Contribution to journal › Article › peer-review
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Clinical and genetic analyses of a Swedish patient series diagnosed with ataxia
Gorcenco, S., Kafantari, E., Wallenius, J., Karremo, C., Alinder, E., Dobloug, S., Landqvist Waldö, M., Englund, E., Ehrencrona, H., Wictorin, K., Karrman, K. & Puschmann, A., 2024, In: Journal of Neurology. 271, 1, p. 526-542Research output: Contribution to journal › Article › peer-review
Open Access -
Exonic trinucleotide repeat expansions in ZFHX3 cause spinocerebellar ataxia type 4: A poly-glycine disease
Wallenius, J., Kafantari, E., Jhaveri, E., Gorcenco, S., Ameur, A., Karremo, C., Dobloug, S., Karrman, K., de Koning, T., Ilinca, A., Landqvist Waldö, M., Arvidsson, A., Persson, S., Englund, E., Ehrencrona, H. & Puschmann, A., 2024, In: American Journal of Human Genetics. 111, 1, p. 82-95Research output: Contribution to journal › Article › peer-review
Open Access -
2021
MAP3K6 Mutations in a Neurovascular Disease Causing Stroke, Cognitive Impairment, and Tremor
Ilinca, A., Englund, E., Samuelsson, S., Truvé, K., Kafantari, E., Martinez-Majander, N., Putaala, J., Håkansson, C., Lindgren, A. G. & Puschmann, A., 2021 Feb, In: Neurology: Genetics. 7, 1, e548.Research output: Contribution to journal › Article › peer-review
Open Access -
2020
New generation genetic testing entering the clinic
Gorcenco, S., Ilinca, A., Almasoudi, W., Kafantari, E., Lindgren, A. G. & Puschmann, A., 2020 Apr 1, In: Parkinsonism and Related Disorders. 73, p. 72-84 13 p.Research output: Contribution to journal › Article › peer-review
Open Access