Haugarvoll, K
33  results:
?
1

Hereditary diffuse leukoencephalopathy with spheroids with ..:

Sundal, C. ; Baker, M. ; Karrenbauer, V....
European Journal of Neurology.  22 (2014)  2 - p. 328-333 , 2014
 
?
2

Parkinson disease: Associated disorders in the Norwegian po..:

Skeie, G.O. ; Muller, B. ; Haugarvoll, K...
Parkinsonism & Related Disorders.  19 (2013)  1 - p. 53-55 , 2013
 
?
3

Severe nigrostriatal degeneration without clinical parkinso..:

Tzoulis, C. ; Tran, G.T. ; Schwarzlmüller, T....
Journal of the Neurological Sciences.  333 (2013)  - p. e101 , 2013
 
?
 
?
6

P1.057 Novel compound heterozygous tyrosine hydroxylase mut..:

Haugarvoll, K. ; Bindoff, L.
Parkinsonism & Related Disorders.  15 (2009)  - p. S43 , 2009
 
?
 
?
9

Meta-analysis of whole-exome sequencing data from two indep..:

Gaare, Johannes Jernqvist ; Sanchez Nido, Gonzalo ; Dölle, Christian...
Gaare, J.J., Nido, G., Dölle, C., Sztromwasser,, P., Alves, G., Tysnes, O-B., Haugarvoll, K., Tzoulis, C. (2020) Meta-analysis of whole-exome sequencing data from two independent cohorts finds no evidence for rare variant enrichment in Parkinson disease associated loci. PLOS ONE, 15(10), e0239824 , 1-9..  , 2020
 
?
 
?
 
1-15