Saana M Mönkäre

Clinical features and spectrum of NOTCH3 variants in Finnish patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)

Mönkäre, S., Kuuluvainen, L., Schleutker, J., Myllykangas, L. & Pöyhönen, M., nov. 2022, I: Acta Neurologica Scandinavica. 146, 5, s. 643-651 9 s.

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Genetic analysis reveals novel variants for vascular cognitive impairment

Mönkäre, S., Kuuluvainen, L., Schleutker, J., Bras, J., Roine, S., Pöyhönen, M., Guerreiro, R. & Myllykangas, L., juli 2022, I: Acta Neurologica Scandinavica. 146, 1, s. 42-50 9 s.

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Genetics of inherited small vessel diseases

Mönkäre, S., 2022, Helsinki: Helsingin yliopisto. 100 s.

Forskningsoutput: Avhandling › Doktorsavhandling › Samling av artiklar

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COL4A1 and COL4A2 Duplication Causes Cerebral Small Vessel Disease With Recurrent Early Onset Ischemic Strokes

Kuuluvainen, L., Mönkäre, S., Kokkonen, H., Zhao, F., Verkkoniemi-Ahola, A., Schleutker, J., Hakonen, A. H., Hartikainen, P., Pöyhönen, M. & Myllykangas, L., okt. 2021, I: Stroke. 52, 10, s. E624-E625 2 s.

Forskningsoutput: Tidskriftsbidrag › Brev › Vetenskaplig

PHACTR1 genetic variability is not critical in small vessel ischemic disease patients and PcomA recruitment in C57BL/6J mice

Messerschmidt, C., Foddis, M., Blumenau, S., Mueller, S., Bentele, K., Holtgrewe, M., Kun-Rodrigues, C., Alonso, I., Macario, M. D. C., Morgadinho, A. S., Velon, A. G., Santo, G., Santana, I., Mönkäre, S., Kuuluvainen, L., Schleutker, J., Pöyhönen, M., Myllykangas, L., Senatore, A. & Berchtold, D. & 14 andra, Winek, K., Meisel, A., Pavlovic, A., Kostic, V., Dobricic, V., Lohmann, E., Hanagasi, H., Guven, G., Bilgic, B., Bras, J., Guerreiro, R., Beule, D., Dirnagl, U. & Sassi, C., 16 mars 2021, I: Scientific Reports. 11, 1, 11 s., 6072.

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Saana M Mönkäre

Internationellt och inhemskt samarbete

Fördjupning

Clinical features and spectrum of NOTCH3 variants in Finnish patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)

Genetic analysis reveals novel variants for vascular cognitive impairment

Genetics of inherited small vessel diseases

COL4A1 and COL4A2 Duplication Causes Cerebral Small Vessel Disease With Recurrent Early Onset Ischemic Strokes

PHACTR1 genetic variability is not critical in small vessel ischemic disease patients and PcomA recruitment in C57BL/6J mice

Saana M Mönkäre

Internationellt och inhemskt samarbete

Publikationer

Clinical features and spectrum of NOTCH3 variants in Finnish patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)

Genetic analysis reveals novel variants for vascular cognitive impairment

Genetics of inherited small vessel diseases

COL4A1 and COL4A2 Duplication Causes Cerebral Small Vessel Disease With Recurrent Early Onset Ischemic Strokes

PHACTR1 genetic variability is not critical in small vessel ischemic disease patients and PcomA recruitment in C57BL/6J mice