Lista de obras - Olof Sydow - Dominio Público Uruguay

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

artículo científico publicado en 2005

Abnormal erythrocyte survival in patients with myotonic dystrophy.

artículo científico publicado en 1985

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

artículo científico publicado en 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

artículo científico publicado en 2010

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

artículo científico publicado en 2004

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

artículo científico publicado en 2009

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

artículo científico publicado en 2012

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

artículo científico publicado en 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

artículo científico publicado en 2008

Cyclooxygenase-2 polymorphisms in Parkinson's disease

artículo científico publicado en 2007

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

artículo científico publicado en 2009

DJ-1 Mutations are Rare in a Swedish Parkinson Cohort

artículo científico publicado en 2011

Dopamine autoreceptor function is lost in advanced Parkinson's disease

artículo científico publicado en 1999

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

artículo científico publicado en 2002

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

artículo científico publicado en 2012

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

artículo científico publicado en 2011

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

artículo científico publicado en 2005

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

artículo científico publicado en 2012

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

artículo científico publicado en 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

artículo científico publicado en 2006

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

artículo científico publicado en 2003

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

artículo científico publicado en 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.

artículo científico publicado en 2016

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

artículo científico publicado en 1995

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

artículo científico publicado en 2003

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

artículo científico publicado en 2007

NURR1 Mutations in cases of schizophrenia and manic-depressive disorder

article

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

artículo científico publicado en 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

artículo científico publicado en 2016

PITX3 polymorphism is associated with early onset Parkinson's disease

artículo científico publicado en 2008

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

artículo científico publicado en 2010

Quantitative estimation of abnormal microheterogeneity of serum transferrin in alcoholics

artículo científico publicado en 1980

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

artículo científico publicado en 2007

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

artículo científico publicado el 29 de febrero de 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

artículo científico publicado en 1988

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

artículo científico publicado en 2016

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

artículo científico publicado en 2013

The physical state of the erythrocyte membrane in myotonic dystrophy.

artículo científico publicado en 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

artículo científico publicado en 2010

Lista de obras de Olof Sydow

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

Abnormal erythrocyte survival in patients with myotonic dystrophy.

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

Alcohol dehydrogenase alleles in Parkinson's disease

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

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

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

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

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

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

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

Cyclooxygenase-2 polymorphisms in Parkinson's disease

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

DJ-1 Mutations are Rare in a Swedish Parkinson Cohort

Dopamine autoreceptor function is lost in advanced Parkinson's disease

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

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

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

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

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

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

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

LRRK2 expression linked to dopamine-innervated areas

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

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

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.

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

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

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

NURR1 Mutations in cases of schizophrenia and manic-depressive disorder

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

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

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

PITX3 polymorphism is associated with early onset Parkinson's disease

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

Quantitative estimation of abnormal microheterogeneity of serum transferrin in alcoholics

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

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

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

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

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

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

The physical state of the erythrocyte membrane in myotonic dystrophy.

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

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