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List of works by Olof Sydow

A rare truncating mutation in ADH1C (G78Stop) shows significant association with Parkinson disease in a large international sample

scientific article published in January 2005

Abnormal erythrocyte survival in patients with myotonic dystrophy.

scientific article

Adenosine for pain relief in a patient with intractable secondary erythromelalgia.

scientific article published on January 1997

Alcohol dehydrogenase alleles in Parkinson's disease

scientific article published on 01 September 2000

Altered enzymatic activity and allele frequency of OMI/HTRA2 in Alzheimer's disease

scientific article published on 16 December 2010

Association between the estrogen receptor beta gene and age of onset of Parkinson's disease

scientific article published in September 2004

Association of a polymorphism in the ABCB1 gene with Parkinson's disease

scientific article

Association of a protective paraoxonase 1 (PON1) polymorphism in Parkinson's disease

scientific article published on 13 June 2012

Association study of two genetic variants in mitochondrial transcription factor A (TFAM) in Alzheimer's and Parkinson's disease

scientific article published on 10 May 2007

Carbohydrate composition of erythrocyte membranes and glycosidase activities in serum in patients with myotonic dystrophy, limb-girdle dystrophy and congenital myotonia

scientific article published on 01 March 1984

Cerebellar alpha-synuclein levels are decreased in Parkinson's disease and do not correlate with SNCA polymorphisms associated with disease in a Swedish material

scientific article published on 7 July 2008

Cyclooxygenase-2 polymorphisms in Parkinson's disease

scientific article published in April 2007

Cytochrome P450 2E1 gene polymorphisms/haplotypes and Parkinson's disease in a Swedish population

scientific article published on 21 April 2009

DJ-1 Mutations are Rare in a Swedish Parkinson Cohort

scientific article

Dopamine autoreceptor function is lost in advanced Parkinson's disease

scientific article

Further evidence for an association of the paraoxonase 1 (PON1) Met-54 allele with Parkinson's disease

scientific article

Genetic Screening of the Mitochondrial Rho GTPases MIRO1 and MIRO2 in Parkinson's Disease

scientific article published on 3 April 2012

Genetic studies of the protein kinase AKT1 in Parkinson's disease

scientific article published on 29 June 2011

Interaction of polymorphisms in the genes encoding interleukin-6 and estrogen receptor beta on the susceptibility to Parkinson's disease

scientific article published in February 2005

Interim analysis of long-term intraduodenal levodopa infusion in advanced Parkinson disease

scientific article published on 12 June 2012

Investigation of genes coding for inflammatory components in Parkinson's disease

scientific article published in May 2005

Investigation of genes related to familial forms of Parkinson's disease--with focus on the Parkin gene

scientific article published on 05 March 2008

LRRK2 expression linked to dopamine-innervated areas

scientific article published in April 2006

Lack of association between the BDNF Val66Met polymorphism and Parkinson's disease in a Swedish population

scientific article

Leucine-rich repeat kinase 2 (LRRK2) mutations in a Swedish Parkinson cohort and a healthy nonagenarian

scientific article published on 01 October 2006

Levodopa-carbidopa intestinal gel (LCIG) treatment in routine care of patients with advanced Parkinson's disease: An open-label prospective observational study of effectiveness, tolerability and healthcare costs.

scientific article published on 4 June 2016

Long-term beneficial effects of adrenal medullary autografts supported by nerve growth factor in Parkinson's disease.

scientific article published on November 1995

Long-term efficacy of thalamic deep brain stimulation for tremor: double-blind assessments

scientific article published in February 2003

Multicentre European study of thalamic stimulation for parkinsonian tremor: a 6 year follow-up

scientific article published on 26 September 2007

NURR1 Mutations in cases of schizophrenia and manic-depressive disorder

article

NURR1 promoter polymorphisms: Parkinson's disease, schizophrenia, and personality traits.

scientific article published in July 2003

Neuromuscular and psychomotor abnormalities in patients with schizophrenia and their first-degree relatives

scientific article published on 01 July 2000

No Association Between rs7077361 in ITGA8 and Parkinson's Disease in Sweden

scientific article published on 30 June 2016

PITX3 polymorphism is associated with early onset Parkinson's disease

scientific article published on 16 April 2008

Possible involvement of a mitochondrial translation initiation factor 3 variant causing decreased mRNA levels in Parkinson's disease

scientific article published on 14 June 2010

Quantitative estimation of abnormal microheterogeneity of serum transferrin in alcoholics

scientific article published on 01 January 1980

S18Y in ubiquitin carboxy-terminal hydrolase L1 (UCH-L1) associated with decreased risk of Parkinson's disease in Sweden

scientific article published on 06 February 2007

Sialic acid concentration in erythrocyte membrane subfractions in patients with myotonic dystrophy and healthy controls ⬇️

scientific article published on February 29, 1988

Sialic acid content in serum IgG from patients with myotonic dystrophy compared with healthy controls

scientific article published on 01 November 1989

Sialyltransferase activity in erythrocyte membranes and serum in patients with myotonic dystrophy

scientific article published on 01 October 1988

Strong association between glucocerebrosidase mutations and Parkinson's disease in Sweden

scientific article published on 03 May 2016

The HLA-DRA variation rs3129882 is not associated with Parkinson's disease in Sweden

scientific article

The physical state of the erythrocyte membrane in myotonic dystrophy.

scientific article published on October 1989

The sialic acid and galactose concentrations in erythrocyte membranes in patients with myotonic dystrophy, limb-girdle and facioscapulohumeral dystrophy

scientific article published on 01 June 1983

Variations of the CAG trinucleotide repeat in DNA polymerase γ (POLG1) is associated with Parkinson's disease in Sweden

scientific article

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