❭ Research by medical division ❭ Clinical Neuroscience ❭ Department of Neurology ❭ Movement, neuromuscular disease and ALS ❭ Scientists ❭

Scientists

NameUnit(s)
Berge, Victoria-SeidlMolecular studies of Parkinson's disease [Toft]
Bjerknes, Silje KristinInger Marie Skogseid’s Project Group [Skogseid] ; Molecular studies of Parkinson's disease
Dietrichs, EspenClinical Studies of Movement Disorders
Elsais, AhmedClinical Studies of Movement Disorders
Frich, Jan ChristianClinical Studies of Movement Disorders
Gundersen, VidarClinical Studies of Movement Disorders
Iqbal, ZafarMolecular studies of Parkinson's disease [Toft]
Kerty, EmiliaClinical Studies of Movement Disorders
Kvernmo, Nadja Anette MyrvikInger Marie Skogseid’s Project Group [Skogseid]
Maniaol, Angelina HatløMyasthenia gravis and amyotrophic lateral sclerosis [Maniaol]
Popperud, Trine HaugClinical Studies of Movement Disorders
Siewers, VibekeInger Marie Skogseid’s Project Group [Skogseid]
Skogseid, Inger MarieInger Marie Skogseid’s Project Group [Skogseid]
Toft, MathiasMolecular studies of Parkinson's disease [Toft]
Wedding, Iselin MarieInger Marie Skogseid’s Project Group [Skogseid]

Home Department of Neurology Movement, neuromuscular disease and ALS

  • Molecular studies of Parkinson's disease
  • Clinical Studies of Movement Disorders
  • Inger Marie Skogseid's project group
  • Myasthenia and amyotrophic lateral sclerosis
  • Scientists
  • Publications

Recent publications

Vollstedt EJ, Schaake S, Lohmann K, Padmanabhan S, Brice A, Lesage S, Tesson C, Vidailhet M, Wurster I, Hentati F, Mirelman A, Giladi N, Marder K, Waters C, Fahn S, Kasten M, Brüggemann N, Borsche M, Foroud T, Tolosa E, Garrido A, Annesi G, Gagliardi M, Bozi M, Stefanis L et al. (2023)
Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort
Mov Disord (in press)
DOI 10.1002/mds.29288, PubMed 36692014

Yousaf H, Fatima A, Ali Z, Baig SM, Toft M, Iqbal Z (2022)
A Novel Nonsense Variant in GRM1 Causes Autosomal Recessive Spinocerebellar Ataxia 13 in a Consanguineous Pakistani Family
Genes (Basel), 13 (9)
DOI 10.3390/genes13091667, PubMed 36140834

Pihlstrøm L, Shireby G, Geut H, Henriksen SP, Rozemuller AJM, Tunold JA, Hannon E, Francis P, Thomas AJ, Love S, Mill J, van de Berg WDJ, Toft M (2022)
Epigenome-wide association study of human frontal cortex identifies differential methylation in Lewy body pathology
Nat Commun, 13 (1), 4932
DOI 10.1038/s41467-022-32619-z, PubMed 35995800

More publications

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