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Anna Birve

Kontaktinformation
Befattning:	Forskningsingenjör, förste
Verksam vid:	Farmakologi och klinisk neurovetenskap
Avdelning:	Klinisk neurovetenskap
Adress:	Umeå universitet SE-901 85 Umeå Sverige
Besöksadress:
Tel:	+46 90 785 29 47
E-postadress:	anna.birve@neuro.umu.se E-post
Webbsida:	http://www.neuropharm.umu.se Webbsida

Publikationer

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Författare	Titel	År	Fulltext
Akimoto, Chizuru Forsgren, Lars Linder, Jan; et al.	No GGGGCC-hexanucleotide repeat expansion in C9ORF72 in parkinsonism patients in Sweden Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 14(1): 26-29	2013	-
Ingre, Caroline Landers, JE Rizik, N; et al.	A novel phosphorylation site mutation in profilin 1 revealed in a large screen of US, Nordic and German amyotrophic lateral sclerosis/frontotemporal dementia cohorts Neurobiology of Aging, 34(6): 1708.e1-1708.e6	2013	-
Graffmo, Karin S. Forsberg, Karin Bergh, Johan; et al.	Expression of wild-type human superoxide dismutase-1 in mice causes amyotrophic lateral sclerosis Human Molecular Genetics, 22(1): 51-60	2013	-
Weishaupt, Jochen H Waibel, Stefan Birve, Anna; et al.	A novel optineurin truncating mutation and three glaucoma-associated missense variants in patients with familial amyotrophic lateral sclerosis in Germany Neurobiology of Aging, 34(5): 1516.e9-1516.e15	2013	-
Ingre, Caroline Press, R. Birve, Anna; et al.	Mutations in VAPB are relatively frequent in the Swedish population, but not associated with ALS European Journal of Neurology, 19(SI, Suppl 1): 82-82	2012	-
Weber, M Neuwirth, C Thierbach, J; et al.	ALS patients with SOD1 mutations in Switzerland show very diverse phenotypes and extremely long survival Journal of Neurology, Neurosurgery and Psychiatry, 83(3): 351-353	2012	-
Bogaert, Elke Goris, An Van Damme, Philip; et al.	Polymorphisms in the GluR2 gene are not associated with amyotrophic lateral sclerosis Neurobiology of Aging, 33(2): 418-420	2012	-
van Es, Michael A Schelhaas, Helenius J van Vught, Paul W J; et al.	Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis Annals of Neurology, 70(6): 964-973	2011	-
Brotherton, Terrell Polak, Meraida Kelly, Crystal; et al.	A novel ALS SOD1 C6S mutation with implications for aggregation related toxicity and genetic counseling Amyotrophic Lateral Sclerosis and other Motor Neuron Disorders, 12(3): 215-219	2011	-
Blauw, Hylke M Al-Chalabi, Ammar Andersen, Peter M; et al.	A large genome scan for rare CNVs in amyotrophic lateral sclerosis Human Molecular Genetics, 19(20): 4091-4099	2010	-

Sidansvarig: Kerstin Gruffman
2010-11-02