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Analysis and comparison of the 4b core protein gene of avipoxviruses from wild birds: Evidence for interspecies spatial phylogenetic variation

Archives of virology, 2004-10, Vol.149 (10), p.2035-2046

2004

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G.P.277

Neuromuscular disorders : NMD, 2014-10, Vol.24 (9), p.900-900

2014

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P.8.1 Muscle biopsy findings in Limb Girdle muscle Dystrophy 2I (LGMD2I)

Neuromuscular disorders : NMD, 2013-10, Vol.23 (9), p.779-780

2013

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P2.17 Fukutin-related protein resides in the Golgi cisternae of human skeletal muscle fibres and forms disulfide-linked homodimers via an N-terminal interaction interface

Neuromuscular disorders : NMD, 2011-10, Vol.21 (9), p.665-666

2011

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P2.19 Norwegian patients with Limb Girdle Muscular Dystrophy 2I structural changes and immunhistochemistry related to clinical findings and genotype–fenotype

Neuromuscular disorders : NMD, 2011-10, Vol.21 (9), p.666-666

2011

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Myotonia congenita and myotonic dystrophy in the same family: coexistence of a CLCN1 mutation and expansion in the CNBP (ZNF9) gene

Clinical genetics, 2011-12, Vol.80 (6), p.574-580

2011

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Socio-demographic Characteristics of Suicides in the Nenets Autonomous Okrug, Northwestern Russia

European psychiatry, 2015-03, Vol.30, p.949-949

2015

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MOTOR NEURON DISORDERS AND NEUROPATHIES: EP.246 Kennedy disease in two sisters with biallelic CAG expansions of the androgen receptor gene

Neuromuscular disorders : NMD, 2021-10, Vol.31, p.S123-S124

2021

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MOTOR NEURON DISORDERS AND NEUROPATHIES

Neuromuscular disorders : NMD, 2021-10, Vol.31, p.S123-S124

2021

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EM.P.2.09 Spectrum of mutations and phenotypic variability in FKRP-related disease in Norway

Neuromuscular disorders : NMD, 2009-09, Vol.19 (8), p.554-554

2009

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Enzyme replacement therapy for alpha-mannosidosis: 12 months follow-up of a single centre, randomised, multiple dose study

Journal of inherited metabolic disease, 2013-11, Vol.36 (6), p.1015-1024

2013

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EP.98Next-generation sequencing-based molecular diagnosis of neuromuscular patients: results of three years experience

Neuromuscular disorders : NMD, 2019-10, Vol.29, p.S181-S181

2019

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Lactococcin A, a new bacteriocin from Lactococcus lactis subsp. cremoris: isolation and characterization of the protein and its gene

Journal of Bacteriology, 1991-06, Vol.173 (12), p.3879-3887

1991

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Identification of a New Locus for Autosomal Dominant Non-Syndromic Hearing Impairment (DFNA7) in a Large Norwegian Family

Human molecular genetics, 1996-08, Vol.5 (8), p.1187-1191

1996

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α-Mannosidosis:Functional Cloning of the Lysosomal α-Mannosidase cDNA and Identification of a Mutation in Two Affected Siblings

Human molecular genetics, 1997-05, Vol.6 (5), p.717-726

1997

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MUSCLE HOMEOSTASIS: P.125Protein homeostasis in LGMD2I

Neuromuscular disorders : NMD, 2019-10, Vol.29, p.S85-S85

2019

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MUSCLE HOMEOSTASIS

Neuromuscular disorders : NMD, 2019-10, Vol.29, p.S85

2019

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G.P.277: LGMD2I: Is there a relationship between clinical phenotype, morphological alterations and level of alpha-dystroglycan glycosylation in patients with the same FKRP genotype?

Neuromuscular disorders : NMD, 2014-10, Vol.24 (9-10), p.900-900

2014

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Purification and Characterization of Recombinant Human Lysosomal α-Mannosidase

Molecular genetics and metabolism, 2001-05, Vol.73 (1), p.18-29

2001

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Modulation of Disease Severity of Dystrophic Epidermolysis Bullosa By a Splice Site Mutation in Combination with a Missense Mutation in the COL7A1 Gene

Human molecular genetics, 1997-07, Vol.6 (7), p.1125-1135

1997

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Spectrum of Mutations in α-Mannosidosis

American journal of human genetics, 1999, Vol.64 (1), p.77-88

1999

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LONG-TERM EFFECT OF BRIEF INTERVENTION IN AT-RISK ALCOHOL DRINKERS: A 9-YEAR FOLLOW-UP STUDY

Alcohol and alcoholism (Oxford), 2004-11, Vol.39 (6), p.548-551

Nilssen, Odd

2004

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P.36 - Limb girdle muscular dystrophy type 2I: Lack of correlation between clinical severity, histopathological alterations and levels of glycosylated α-dystroglycan in patients homozygous for the common FKRP mutation

Neuromuscular disorders : NMD, 2017-10, Vol.27, p.S109-S109

2017

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Limb girdle muscular dystrophy type 2I: Lack of correlation between clinical severity, histopathological alterations and levels of glycosylated α-dystroglycan in patients homozygous for the common FKRP mutation

Neuromuscular disorders : NMD, 2017-10, Vol.27, p.S109

2017

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Premature cardiovascular mortality and alcohol consumption before death in Arkhangelsk, Russia: an analysis of a consecutive series of forensic autopsies

International journal of epidemiology, 2011-12, Vol.40 (6), p.1519-1529

2011

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Analysis and comparison of the 4b core protein gene of avipoxviruses from wild birds: Evidence for interspecies spatial phylogenetic variation

G.P.277

P.8.1 Muscle biopsy findings in Limb Girdle muscle Dystrophy 2I (LGMD2I)

P2.17 Fukutin-related protein resides in the Golgi cisternae of human skeletal muscle fibres and forms disulfide-linked homodimers via an N-terminal interaction interface

P2.19 Norwegian patients with Limb Girdle Muscular Dystrophy 2I structural changes and immunhistochemistry related to clinical findings and genotype–fenotype

Myotonia congenita and myotonic dystrophy in the same family: coexistence of a CLCN1 mutation and expansion in the CNBP (ZNF9) gene

Socio-demographic Characteristics of Suicides in the Nenets Autonomous Okrug, Northwestern Russia

MOTOR NEURON DISORDERS AND NEUROPATHIES: EP.246 Kennedy disease in two sisters with biallelic CAG expansions of the androgen receptor gene

MOTOR NEURON DISORDERS AND NEUROPATHIES

EM.P.2.09 Spectrum of mutations and phenotypic variability in FKRP-related disease in Norway

Enzyme replacement therapy for alpha-mannosidosis: 12 months follow-up of a single centre, randomised, multiple dose study

EP.98Next-generation sequencing-based molecular diagnosis of neuromuscular patients: results of three years experience

Lactococcin A, a new bacteriocin from Lactococcus lactis subsp. cremoris: isolation and characterization of the protein and its gene

Identification of a New Locus for Autosomal Dominant Non-Syndromic Hearing Impairment (DFNA7) in a Large Norwegian Family

α-Mannosidosis:Functional Cloning of the Lysosomal α-Mannosidase cDNA and Identification of a Mutation in Two Affected Siblings

MUSCLE HOMEOSTASIS: P.125Protein homeostasis in LGMD2I

MUSCLE HOMEOSTASIS

G.P.277: LGMD2I: Is there a relationship between clinical phenotype, morphological alterations and level of alpha-dystroglycan glycosylation in patients with the same FKRP genotype?

Purification and Characterization of Recombinant Human Lysosomal α-Mannosidase

Modulation of Disease Severity of Dystrophic Epidermolysis Bullosa By a Splice Site Mutation in Combination with a Missense Mutation in the COL7A1 Gene

Spectrum of Mutations in α-Mannosidosis

LONG-TERM EFFECT OF BRIEF INTERVENTION IN AT-RISK ALCOHOL DRINKERS: A 9-YEAR FOLLOW-UP STUDY

P.36 - Limb girdle muscular dystrophy type 2I: Lack of correlation between clinical severity, histopathological alterations and levels of glycosylated α-dystroglycan in patients homozygous for the common FKRP mutation

Limb girdle muscular dystrophy type 2I: Lack of correlation between clinical severity, histopathological alterations and levels of glycosylated α-dystroglycan in patients homozygous for the common FKRP mutation

Premature cardiovascular mortality and alcohol consumption before death in Arkhangelsk, Russia: an analysis of a consecutive series of forensic autopsies

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