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Huntington's Disease Does Not Appear to Increase the Risk of Diabetes Mellitus

Journal of neuroendocrinology, 2009-09, Vol.21 (9), p.770-776

2009

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Psychiatric and cognitive symptoms in Huntington's disease are modified by polymorphisms in catecholamine regulating enzyme genes

Clinical genetics, 2016-03, Vol.89 (3), p.320-327

2016

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P.1.i.037 Patients with seasonal affective disorder show seasonal fluctuations in their cerebral serotonin transporter binding

European neuropsychopharmacology, 2014-10, Vol.24, p.S319-S319

2014

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Impaired Glucose Tolerance in the R6/1 Transgenic Mouse Model of Huntington's Disease

Journal of neuroendocrinology, 2008-02, Vol.20 (2), p.165-172

2008

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P.4.030 Bright light dose correlates with change in striatal serotonin transporter binding in healthy Scandinavians

European neuropsychopharmacology, 2013-03, Vol.23, p.S92-S92

2013

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Hereditary spastic paraplegia with cerebellar ataxia: a complex phenotype associated with a new SPG4 gene mutation

European journal of neurology, 2004-12, Vol.11 (12), p.817-824

2004

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Genetic variants and brain binding potentials: Lost in translation?

NeuroImage (Orlando, Fla.), 2010-08, Vol.52 (S1), p.S27-S27

2010

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4p16.3 haplotype modifying age at onset of Huntington disease

Clinical genetics, 2009-03, Vol.75 (3), p.244-250

2009

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A novel presenilin 2 mutation (V393M) in early-onset dementia with profound language impairment

European journal of neurology, 2008-10, Vol.15 (10), p.1135-1139

2008

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Drosophila deoxyribonucleoside kinase mutants with enhanced ability to phosphorylate purine analogs

Gene therapy, 2007-09, Vol.14 (17), p.1278-1286

2007

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Mutations in exon 7 of the α-galactosidase a gene

Clinical therapeutics, 2007, Vol.29, p.S34-S34

2007

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Cag Repeat Expansion in Autosomal Dominant Pure Spastic Paraplegia Linked to Chromosome 2p21–p24

Human molecular genetics, 1997-10, Vol.6 (11), p.1811-1816

1997

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Functional and structural nerve fiber findings in heterozygote patients with Fabry disease

Pain (Amsterdam), 2009-09, Vol.145 (1-2), p.237-245

2009

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Autosomal dominant pure spastic paraplegia: a clinical, paraclinical, and genetic study

Journal of neurology, neurosurgery and psychiatry, 1998-01, Vol.64 (1), p.61-66

1998

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B19Lactate metabolism in the Huntington's disease mouse model R6/2

Journal of neurology, neurosurgery and psychiatry, 2012-09, Vol.83 (Suppl 1), p.A11-ai-A11

2012

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Mitotic and meiotic instability of the CAG trinucleotide repeat in spinocerebellar ataxia type 1

Human genetics, 1998-11, Vol.103 (5), p.564-569

1998

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B19 Lactate metabolism in the Huntington's disease mouse model R6/2

Journal of neurology, neurosurgery and psychiatry, 2012-09, Vol.83 (Suppl 1), p.A11-A11

2012

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Osteopenia: a common aspect of Fabry disease. Predictors of bone mineral density

Genetics in medicine, 2007-12, Vol.9 (12), p.812-818

2007

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H07 Primary skin fibroblast cultures in Huntington's disease research

Journal of neurology, neurosurgery and psychiatry, 2010-09, Vol.81 (Suppl 1), p.A35-A35

2010

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Five novel mutations in fourteen patients with Fabry disease

Human mutation, 2000-02, Vol.15 (2), p.207-208

2000

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Fabry disease: a new challenge in endocrinology and metabolism?

European journal of endocrinology, 2002-06, Vol.146 (6), p.741

2002

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Dentatorubral-pallidoluysian atrophy. Clinical features of a five-generation danish family

Movement disorders, 1996-09, Vol.11 (5), p.533-541

1996

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Fabry disease--a metabolic disorder with a challenge for endocrinologists?

Hormone research, 2002, Vol.58 (6), p.259-265

2002

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Elongated CAG repeats of the B37 gene in a Danish family with dentato-rubro-pallido-luysian atrophy

Human genetics, 1995-03, Vol.95 (3), p.313-318

1995

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Machado–Joseph disease in three Scandinavian families

Journal of the neurological sciences, 1998-04, Vol.156 (2), p.152-157

1998

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Huntington's Disease Does Not Appear to Increase the Risk of Diabetes Mellitus

Psychiatric and cognitive symptoms in Huntington's disease are modified by polymorphisms in catecholamine regulating enzyme genes

P.1.i.037 Patients with seasonal affective disorder show seasonal fluctuations in their cerebral serotonin transporter binding

Impaired Glucose Tolerance in the R6/1 Transgenic Mouse Model of Huntington's Disease

P.4.030 Bright light dose correlates with change in striatal serotonin transporter binding in healthy Scandinavians

Hereditary spastic paraplegia with cerebellar ataxia: a complex phenotype associated with a new SPG4 gene mutation

Genetic variants and brain binding potentials: Lost in translation?

4p16.3 haplotype modifying age at onset of Huntington disease

A novel presenilin 2 mutation (V393M) in early-onset dementia with profound language impairment

Drosophila deoxyribonucleoside kinase mutants with enhanced ability to phosphorylate purine analogs

Mutations in exon 7 of the α-galactosidase a gene

Cag Repeat Expansion in Autosomal Dominant Pure Spastic Paraplegia Linked to Chromosome 2p21–p24

Functional and structural nerve fiber findings in heterozygote patients with Fabry disease

Autosomal dominant pure spastic paraplegia: a clinical, paraclinical, and genetic study

B19Lactate metabolism in the Huntington's disease mouse model R6/2

Mitotic and meiotic instability of the CAG trinucleotide repeat in spinocerebellar ataxia type 1

B19 Lactate metabolism in the Huntington's disease mouse model R6/2

Osteopenia: a common aspect of Fabry disease. Predictors of bone mineral density

H07 Primary skin fibroblast cultures in Huntington's disease research

Five novel mutations in fourteen patients with Fabry disease

Fabry disease: a new challenge in endocrinology and metabolism?

Dentatorubral-pallidoluysian atrophy. Clinical features of a five-generation danish family

Fabry disease--a metabolic disorder with a challenge for endocrinologists?

Elongated CAG repeats of the B37 gene in a Danish family with dentato-rubro-pallido-luysian atrophy

Machado–Joseph disease in three Scandinavian families

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