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51

Defects in amphiphysin 2 (BIN1) and triads in several forms of centronuclear myopathies

Anne Toussaint, Belinda Simone Cowling, Karim Hnia, Michel Mohr, Anders Oldfors, Yannick Schwab, Uluc Yis, Thierry Maisonobe, Tanya Stojkovic, Carina Wallgren-Pettersson, Vincent Laugel, Andoni Echani

Journal:

Acta Neuropathologica

Year:

2011

Language:

english

File:

PDF, 2.18 MB

english, 2011

52

Multiple mitochondrial DNA deletions in hereditary inclusion body myopathy

Monica Jansson, Niklas Darin, Mårten Kyllerman, Tommy Martinsson, Jan Wahlström, A. Oldfors

Journal:

Acta Neuropathologica

Year:

2000

Language:

english

File:

PDF, 477 KB

english, 2000

53

Induced shift in myosin heavy chain expression in myosin myopathy by endurance training

Homa Tajsharghi, Katharina Stibrant Sunnerhagen, Niklas Darin, Mårten Kyllerman, Anders Oldfors

Journal:

Journal of Neurology

Year:

2004

Language:

english

File:

PDF, 2.04 MB

english, 2004

54

Immunohistochemical demonstration of different muscle fibre types in paraffin sections

A. OLDFORS, T. SEIDAL

Journal:

Year:

1989

Language:

english

File:

PDF, 399 KB

english, 1989

55

Local T-Cell Proliferation and Differentiation in Inflammatory Myopathies

C. LINDBERG, A. OLDFORS, A. TARKOWSKI

Journal:

Scandinavian Journal of Immunology

Year:

1995

Language:

english

File:

PDF, 2.34 MB

english, 1995

56

The effects of endurance training in persons with a hereditary myosin myopathy

K. S. Sunnerhagen, N. Darin, H. Tasjharghi, A. Oldfors

Journal:

Acta Neurologica Scandinavica

Year:

2004

Language:

english

File:

PDF, 110 KB

english, 2004

57

MELAS syndrome in a patient with a point mutation in MTTS1

C. Lindberg, A.-R. Moslemi, A. Oldfors

Journal:

Acta Neurologica Scandinavica

Year:

2008

Language:

english

File:

PDF, 257 KB

english, 2008

58

10.1038/5089

Wang, Jianming, Wilhelmsson, Hans, Graff, Caroline, Li, Hong, Oldfors, Anders, Rustin, Pierre, Brüning, Jens C., Kahn, C. Ronald, Clayton, David A., Barsh, Gregory S., Thorén, Peter, Larsson, Nils-Gör

Journal:

Nature Genetics

Year:

1999

Language:

english

File:

PDF, 590 KB

english, 1999

59

10.1038/81649

Larsson, Nils-Göran, Silva, José P., Köhler, Martin, Graff, Caroline, Oldfors, Anders, Magnuson, Mark A., Berggren, Per-Olof

Journal:

Nature Genetics

Year:

2000

Language:

english

File:

PDF, 11.50 MB

english, 2000

60

Mitochondrial transcription factor A is necessary for mtDNA maintance and embryogenesis in mice

Larsson, Nils-Göran, Wang, Jianming, Wilhelmsson, Hans, Oldfors, Anders, Rustin, Pierre, Lewandoski, Mark, Barsh, Gregory S., Clayton, David A.

Journal:

Nature Genetics

Year:

1998

File:

PDF, 825 KB

1998

61

Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy

Nicot, Anne-Sophie, Toussaint, Anne, Tosch, Valérie, Kretz, Christine, Wallgren-Pettersson, Carina, Iwarsson, Erik, Kingston, Helen, Garnier, Jean-Marie, Biancalana, Valérie, Oldfors, Anders

Journal:

Nature Genetics

Year:

2007

Language:

english

File:

PDF, 561 KB

english, 2007

62

Mutations and sequence variation in the human myosin heavy chain IIa gene (MYH2)

Tajsharghi, Homa, Darin, Niklas, Rekabdar, Elham, Kyllerman, Mårten, Wahlström, Jan, Martinsson, Tommy, Oldfors, Anders

Journal:

European Journal of Human Genetics

Year:

2005

Language:

english

File:

PDF, 88 KB

english, 2005

63

Low frequency of mtDNA point mutations in patients with PEO associated with POLG1 mutations

Kollberg, Gittan, Jansson, Monica, Pérez-Bercoff, Åsa, Melberg, Atle, Lindberg, Christopher, Holme, Elisabeth, Moslemi, Ali-Reza, Oldfors, Anders

Journal:

European Journal of Human Genetics

Year:

2005

Language:

english

File:

PDF, 212 KB

english, 2005

64

Effects of a R133W β-tropomyosin mutation on regulation of muscle contraction in single human muscle fibres

Julien Ochala, Mingxin Li, Homa Tajsharghi, Eva Kimber, Mar Tulinius, Anders Oldfors, Lars Larsson

Journal:

The Journal of Physiology

Year:

2007

Language:

english

File:

PDF, 467 KB

english, 2007

65

Defective regulation of contractile function in muscle fibres carrying an E41K β-tropomyosin mutation

Julien Ochala, Meishan Li, Monica Ohlsson, Anders Oldfors, Lars Larsson

Journal:

The Journal of Physiology

Year:

2008

Language:

english

File:

PDF, 1.21 MB

english, 2008

66

Congenital myasthenic syndrome with tubular aggregates caused byGFPT1mutations

Guergueltcheva, Velina, Müller, Juliane S., Dusl, Marina, Senderek, Jan, Oldfors, Anders, Lindbergh, Christopher, Maxwell, Susan, Colomer, Jaume, Mallebrera, Cecilia Jimenez, Nascimento, Andres

Journal:

Journal of Neurology

Year:

2012

Language:

english

File:

PDF, 844 KB

english, 2012

67

Inflammation and response to steroid treatment in limb-girdle muscular dystrophy 2I

N. Darin, A.-K. Kroksmark, A.-C. Åhlander, A.-R. Moslemi, A. Oldfors, M. Tulinius

Journal:

European Journal of Paediatric Neurology

Year:

2007

Language:

english

File:

PDF, 598 KB

english, 2007

68

Phenotypic and genotypic variability in Alpers syndrome

Kalliopi Sofou, Ali-Reza Moslemi, Gittan Kollberg, Ingibjörg Bjarnadóttir, Anders Oldfors, Inger Nennesmo, Elisabeth Holme, Már Tulinius, Niklas Darin

Journal:

European Journal of Paediatric Neurology

Year:

2012

Language:

english

File:

PDF, 764 KB

english, 2012

69

T cell receptor β-chain repertoire in inclusion body myositis

Ing-Marie Fyhr, Ali-Reza Moslemi, Christopher Lindberg, Anders Oldfors

Journal:

Journal of Neuroimmunology

Year:

1998

Language:

english

File:

PDF, 515 KB

english, 1998

70

MNP025 Myozyme treatment in a boy with a mild form of infantile-onset Pompe disease

M. Tulinius, A.-K. Kroksmark, I. Östman-Smith, A. Oldfors, J.-E. Månsson

Journal:

European Journal of Paediatric Neurology

Year:

2007

Language:

english

File:

PDF, 45 KB

english, 2007

71

MNP026 Clinical variation in distal arthrogryposis type 1, 2A and 2B with MYH3-mutations

E. Kimber, H. Tajsharghi, A.-K. Kroksmark, A. Oldfors, M. Tulinius

Journal:

European Journal of Paediatric Neurology

Year:

2007

Language:

english

File:

PDF, 45 KB

english, 2007

72

Changes in specific gravity as a sign of disturbed brain maturation in protein-deprived rats

Anders Oldfors, Patrick Sourander, Lars-Erik Linder, Barbro B. Johansson

Journal:

Acta Neurologica Scandinavica

Year:

1986

Language:

english

File:

PDF, 127 KB

english, 1986

73

Clinical and muscle biopsy findings in malignant hyperthermia susceptibility

E. Ranklev, KG Henriksson, R. Fletcher, K. Germundsson, A. Oldfors, H. Kalimo

Journal:

Acta Neurologica Scandinavica

Year:

1986

Language:

english

File:

PDF, 672 KB

english, 1986

74

Inclusion body myositis: clinical, morphological, physiological and laboratory findings in 18 cases

C. Lindberg, Ll. Persson, J. Björkander, A. Oldfors

Journal:

Acta Neurologica Scandinavica

Year:

1994

Language:

english

File:

PDF, 1.61 MB

english, 1994

75

Episodes of exercise-induced dark urine and myalgia in LGMD 2I

C. Lindberg, C. Sixt, A. Oldfors

Journal:

Acta Neurologica Scandinavica

Year:

2012

Language:

english

File:

PDF, 136 KB

english, 2012

76

Distal arthrogryposis: clinical and genetic findings

Eva Kimber, Homa Tajsharghi, Anna-Karin Kroksmark, Anders Oldfors, Már Tulinius

Journal:

Acta Paediatrica

Year:

2012

Language:

english

File:

PDF, 293 KB

english, 2012

77

THE EFFECT OF β-ADRENERGIC BLOCKADE ON THE MYOPATHIC CHANGES IN EXPERIMENTAL HYPERTHYROIDISM IN RATS

ULF AngerÅS, ANDERS Oldfors, PER-OLOF Hasselgren

Journal:

Year:

1986

Language:

english

File:

PDF, 1016 KB

english, 1986

78

A freeze-fracture study of the perineurium in normal and protein-deprived rats

N. G. Beamish, C. Stolinski, P. K. Thomas, R. H. M. King, A. Oldfors

Journal:

Year:

1991

Language:

english

File:

PDF, 5.36 MB

english, 1991

79

The influence of maternal protein deprivation on the developmental pattern of serum immunoreactive insulin-like growth factor 1 (IGF-1) levels

VICKI R. SARA, KERSTIN HALL, SHELLY MENOLASCINO, BARBRO SJÖGREN, LENNART WETTERBERG, KRISTINA MÜNTZING, ANDERS OLDFORS, PATRICK SOURANDER

Journal:

Acta Physiologica

Year:

1986

Language:

english

File:

PDF, 367 KB

english, 1986

80

Effects of growth hormone on skeletal muscle. II. Studies on regeneration and denervation in adult rats

M. ULLMAN, H. ALAMEDDINE, A. SKOTTNER, A. OLDFORS

Journal:

Acta Physiologica

Year:

1989

Language:

english

File:

PDF, 883 KB

english, 1989

81

Effects of growth hormone on skeletal muscle. I. Studies on normal adult rats

M. ULLMAN, A. OLDFORS

Journal:

Acta Physiologica

Year:

1989

Language:

english

File:

PDF, 441 KB

english, 1989

82

Effects of growth hormone on muscle regeneration and IGF-I concentration in old rats

M. ULLMAN, A. ULLMAN, H. SOMMERLAND, A. SKOTTNER, A. OLDFORS

Journal:

Acta Physiologica

Year:

1990

Language:

english

File:

PDF, 388 KB

english, 1990

83

PERMEABILITY OF THE PERINEURIUM OF SMALL NERVE FASCICLES: AN ULTRASTRUCTURAL STUDY USING FERRITIN IN RATS

Journal:

Neuropathology and Applied Neurobiology

Year:

1981

Language:

english

File:

PDF, 888 KB

english, 1981

84

THE PERMEABILITY OF THE BASAL LAMINA AT THE NEUROMUSCULAR JUNCTION. AN ULTRASTRUCTURAL STUDY OF RAT SKELETAL MUSCLE USING PARTICULATE TRACERS

A. OLDFORS, M. FARDEAU

Journal:

Neuropathology and Applied Neurobiology

Year:

1983

Language:

english

File:

PDF, 1.17 MB

english, 1983

85

X-linked myotubular myopathy: clinical and pathological findings in a family

A. Oldfors, M. Kyllerman, J. Wahlström, C. Darnfors, K. G. Henriksson

Journal:

Clinical Genetics

Year:

1989

Language:

english

File:

PDF, 853 KB

english, 1989

86

X-linked myotubular myopathy: a linkage study

Catarina Darnfors, H. E. Börje Larsson, Anders Oldfors, Mårten Kyllerman, Karl-Henrik Gustavson, Gunnar Bjursell, Jan Wahlström

Journal:

Clinical Genetics

Year:

1990

Language:

english

File:

PDF, 321 KB

english, 1990

87

Duchenne muscular dystrophy and spinal muscular atrophy type I segregating in the same family

Anders Oldfors, Tommy Martinsson, Ingemar Tessin, Jan Wahlström, Shu Wang

Journal:

Clinical Genetics

Year:

1994

Language:

english

File:

PDF, 821 KB

english, 1994

88

Low Levels of Mitochondrial Transcription Factor A in Mitochondrial DNA Depletion

N.G. Larsson, A. Oldfors, E. Holme, D.A. Clayton

Journal:

Biochemical and Biophysical Research Communications

Year:

1994

File:

PDF, 645 KB

1994

89

Effects of nandrolone propionate on experimental tumor growth and cancer cachexia

Eva Lydén, Elisabet Cvetkovska, Thomas Westin, Anders Oldfors, Bassam Soussi, Bertil Gustafsson, Staffan Edström

Journal:

Year:

1995

Language:

english

File:

PDF, 2.07 MB

english, 1995

90

Early-onset myopathy with tubular aggregates

Már H. Tulinius, Anita Lundberg, Anders Oldfors

Journal:

Pediatric Neurology

Year:

1996

Language:

english

File:

PDF, 1.06 MB

english, 1996

91

Inheritance and expression of mitochondrial DNA point mutations

Elisabeth Holme, Már H. Tulinius, Nils-Göran Larrson, Anders Oldfors

Journal:

Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease

Year:

1995

Language:

english

File:

PDF, 346 KB

english, 1995

92

Molecular pathogenesis of a new glycogenosis caused by a glycogenin-1 mutation

Johanna Nilsson, Adnan Halim, Ali-Reza Moslemi, Anders Pedersen, Jonas Nilsson, Göran Larson, Anders Oldfors

Journal:

Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease

Year:

2012

Language:

english

File:

PDF, 1.01 MB

english, 2012

93

A patient with two mitochondrial DNA mutations causing PEO and LHON

Atle Melberg, Ali-Reza Moslemi, Oscar Palm, Raili Raininko, Erik Stålberg, Anders Oldfors

Journal:

European Journal of Medical Genetics

Year:

2009

Language:

english

File:

PDF, 85 KB

english, 2009

94

Different tissue distribution of a mitochondrial DNA duplication and the corresponding deletion in a patient with a mild mitochondrial encephalomyopathy: deletion in muscle, duplication in blood

Massoud Houshmand, Ann Gardner, Tore Hällström, Kristina Müntzing, Anders Oldfors, Elisabeth Holme

Journal:

Neuromuscular Disorders

Year:

2004

Language:

english

File:

PDF, 446 KB

english, 2004

95

Follow-up of nemaline myopathy in two patients with novel mutations in the skeletal muscle alpha-actin gene (ACTA1)

M. Ohlsson, H. Tajsharghi, N. Darin, M. Kyllerman, A. Oldfors

Journal:

Neuromuscular Disorders

Year:

2004

Language:

english

File:

PDF, 380 KB

english, 2004

96

Novel mutations in the thymidine kinase 2 gene (TK2) associated with fatal mitochondrial myopathy and mitochondrial DNA depletion

Már Tulinius, Ali-Reza Moslemi, Niklas Darin, Elisabeth Holme, Anders Oldfors

Journal:

Neuromuscular Disorders

Year:

2005

Language:

english

File:

PDF, 346 KB

english, 2005

97

Early onset myopathy with a novel mutation in the Selenoprotein N gene (SEPN1)

Homa Tajsharghi, Niklas Darin, Mar Tulinius, Anders Oldfors

Journal:

Neuromuscular Disorders

Year:

2005

Language:

english

File:

PDF, 183 KB

english, 2005

98

Mitochondrial myopathy with exercise intolerance and retinal dystrophy in a sporadic patient with a G583A mutation in the mt tRNAphe gene

N. Darin, G. Kollberg, A-R. Moslemi, M. Tulinius, E. Holme, M. Andersson Grönlund, S. Andersson, A. Oldfors

Journal:

Neuromuscular Disorders

Year:

2006

Language:

english

File:

PDF, 192 KB

english, 2006

99

G.P.3 07 Mitochondrial myopathy with exercise intolerance and retinal dystrophy in a sporadic patient with a G583A mutation in the mt tRNAphe gene

A.R. Moslemi, N. Darin, G. Kolberg, M. Tulinius, E. Holme, M. Andersson Grönlund, S. Andersson, A. Oldfors

Journal:

Neuromuscular Disorders

Year:

2006

Language:

english

File:

PDF, 46 KB

english, 2006

100

P.P.3 02 Raised troponin T in inclusion body myositis is common and serum levels are persistent over time

C. Lindberg, L. Klintberg, A. Oldfors

Journal:

Neuromuscular Disorders

Year:

2006

Language:

english

File:

PDF, 45 KB

english, 2006

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