Håkan Widner
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- 2010
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Mark
Hereditary Parkinson's Disease of Unknown Genetic Cause in Two Families from Southern Sweden
2010) 24th Annual Symposium on Etiology, Pathogenesis and Treatment of Parkinsons Disease and Other Movement Disorders In Movement Disorders 25(6).(
- Contribution to journal › Published meeting abstract
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Mark
Characterization of Lewy Body Pathology in 12-and 16-Year Old Intrastriatal Mesencephalic Grafts Surviving in a Patient with Parkinson's Disease
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- Contribution to journal › Published meeting abstract
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Mark
Presentation, Diagnosis, and Management of Multiple System Atrophy in Europe: Final Analysis of the European Multiple System Atrophy Registry
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- Contribution to journal › Article
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Mark
Study of Intracerebroventricular Administration of SNN0031 (rhPDGF-BB) to Patients with Parkinson's Disease (PD), Using an Implanted Pump System
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- Contribution to journal › Published meeting abstract
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Mark
Efficacy and Safety of the Dopaminergic Stabilizer Pridopidine (ACR16) in Patients With Huntington's Disease.
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- Contribution to journal › Article
- 2009
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Mark
Alpha-synuclein multiplications with parkinsonism, dementia or progressive myoclonus?
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- Contribution to journal › Article
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Mark
Recommendations on the diagnosis and management of Niemann-Pick disease type C
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- Contribution to journal › Debate/Note/Editorial
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Mark
Herman Lundborg did not describe Unverricht-Lundborg disease: hyperekplexia in a Swedish family with hereditary Parkinson's disease due to alpha-synuclein multiplications
2009) 13th Congress of the European-Federation-of-Neurological-Societies In European Journal of Neurology 16. p.153-153(
- Contribution to journal › Published meeting abstract
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Mark
Long-term neurological outcome after cardiac arrest and therapeutic hypothermia.
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- Contribution to journal › Article
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Mark
A Swedish family with de novo alpha-synuclein A53T mutation: Evidence for early cortical dysfunction.
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- Contribution to journal › Article