Maria Gardberg
Publications
- Clinically variable nemaline myopathy in a three-generation family caused by mutation of the skeletal muscle alpha-actin gene (2018)
- Neuromuscular Disorders
(A1 Refereed original research article in a scientific journal) - Desmoid tumors of the head and neck: Two decades in a single tertiary care unit and review of the literature (2018)
- Ear Nose and Throat Journal
(A2 Refereed review article in a scientific journal ) - Formin Proteins FHOD1 and INF2 in Triple-Negative Breast Cancer: Association With Basal Markers and Functional Activities (2018)
- Breast Cancer: Basic and Clinical Research
(A1 Refereed original research article in a scientific journal) - Kun katse jähmettyy - muista mitokondriotaudin mahdollisuus (2018)
- Duodecim
(D1 Article in a professional journal) - Left cerebral hemisphere hydrophilic polymer embolism associated with endovascular WEB treatment of a ruptured aneurysm of the anterior cerebral artery (2018)
- Legal Medicine
(A1 Refereed original research article in a scientific journal) - Negative C-11-PIB PET Predicts Lack of Alzheimer's Disease Pathology in Postmortem Examination (2018)
- Journal of Alzheimer's Disease
(A1 Refereed original research article in a scientific journal) - Somatostatin receptor expression in lymphomas: a source of false diagnosis of neuroendocrine tumor at 68Ga-DOTANOC PET/CT imaging (2018)
- Acta Oncologica
(A1 Refereed original research article in a scientific journal) - Some DNM2 mutations cause extremely severe congenital myopathy and phenocopy myotubular myopathy (2018)
- Acta Neuropathologica Communications
(B1 Non-refereed article in a scientific journal) - Dopamine transporter imaging does not predict the number of nigral neurons in Parkinson disease (2017)
- Neurology
(A1 Refereed original research article in a scientific journal) - FHOD1 formin is upregulated in melanomas and modifies proliferation and tumor growth (2017)
- Experimental Cell Research
(A1 Refereed original research article in a scientific journal) - SNCA mutation p.Ala53Glu is derived from a common founder in the Finnish population (2017)
- Neurobiology of Aging
(A1 Refereed original research article in a scientific journal) - Somatostatin receptor 2A in gliomas: Association with oligodendrogliomas and favourable outcome (2017)
- Oncotarget
(A1 Refereed original research article in a scientific journal) - The m.7510T > C mutation: Hearing impairment and a complex neurologic phenotype (2017)
- Brain and Behavior
(A1 Refereed original research article in a scientific journal) - WHO:n aivokasvainluokitus (2017)
- Moodi
(D1 Article in a professional journal) - Comparison of Somatostatin Receptor 2-Targeting PET Tracers in the Detection of Mouse Atherosclerotic Plaques (2016)
- Molecular Imaging and Biology
(A1 Refereed original research article in a scientific journal) - FMNL2/FMNL3 formins are linked with oncogenic pathways and predict melanoma outcome (2016)
- Journal of Pathology: Clinical Research
(A1 Refereed original research article in a scientific journal) - Scedosporium apiospermum as a rare cause of central skull base osteomyelitis. (2016)
- Medical Mycology Case Reports
(A1 Refereed original research article in a scientific journal) - Creutzfeldt-Jakobin taudin ilmiasu ja ilmaantuvuus Suomessa vuosina 1997-2013 (2015)
- Duodecim
(A1 Refereed original research article in a scientific journal) - Formin proteins in normal tissues and cancer (2015) Gardberg Maria
(G5 Article dissertation ) - Microglial activation correlates with disease progression in multiple sclerosis (2015) E. Rissanen, J. Tuisku, M. Gardberg, A.M. Dickens, M. Sucksdorff, J. Rokka, T. Paavilainen, R. Parkkola, J.O. Rinne, L. Airas
(Other publication)