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Results:
1-17
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Results: 17
Authors:
Oldfors, A
Fyhr, IM
Citation: A. Oldfors et Im. Fyhr, Inclusion body myositis: genetic factors, aberrant protein expression, andautoimmunity, CURR OP RH, 13(6), 2001, pp. 469-475
Authors:
Rantanen, A
Jansson, M
Oldfors, A
Larsson, NG
Citation: A. Rantanen et al., Downregulation of Tfam and mtDNA copy number during mammalian spermatogenesis, MAMM GENOME, 12(10), 2001, pp. 787-792
Authors:
Darin, N
Oldfors, A
Moslemi, AR
Holme, E
Tulinius, M
Citation: N. Darin et al., The incidence of mitochondrial encephalomyopathies in childhood: Clinical features and morphological, biochemical, and DNA abnormalities, ANN NEUROL, 49(3), 2001, pp. 377-383
Authors:
Larsson, NG
Oldfors, A
Citation: Ng. Larsson et A. Oldfors, Mitochondrial myopathies, ACT PHYSL S, 171(3), 2001, pp. 385-393
Authors:
Silva, JP
Kohler, M
Graff, C
Oldfors, A
Magnuson, MA
Berggren, PO
Larsson, NG
Citation: Jp. Silva et al., Impaired insulin secretion and beta-cell loss in tissue-specific knockout mice with mitochondrial diabetes, NAT GENET, 26(3), 2000, pp. 336-340
Authors:
Martinsson, T
Oldfors, A
Darin, N
Berg, K
Tajsharghi, H
Kyllerman, M
Wahlstrom, J
Citation: T. Martinsson et al., Autosomal dominant myopathy: Missense mutation (Glu-706 -> Lys) in the myosin heavy chain IIa gene, P NAS US, 97(26), 2000, pp. 14614-14619
Authors:
Moslemi, AR
Selimovic, N
Bergh, CH
Oldfors, A
Citation: Ar. Moslemi et al., Fatal dilated cardiomyopathy associated with a mitochondrial DNA deletion, CARDIOLOGY, 94(1), 2000, pp. 68-71
Authors:
Kjellman, UW
Hallgren, P
Bergh, CH
Lycke, J
Oldfors, A
Wiklund, L
Citation: Uw. Kjellman et al., Weaning from mechanical support in a patient with acute heart failure and multiple sclerosis, ANN THORAC, 69(2), 2000, pp. 628-630
Authors:
Jansson, M
Darin, N
Kyllerman, M
Martinsson, T
Wahlstrom, J
Oldfors, A
Citation: M. Jansson et al., Multiple mitochondrial DNA deletions in hereditary inclusion body myopathy, ACT NEUROP, 100(1), 2000, pp. 23-28
Authors:
Oldfors, A
Lindberg, C
Citation: A. Oldfors et C. Lindberg, Inclusion body myositis, CURR OP NEU, 12(5), 1999, pp. 527-533
Authors:
Wang, JM
Wilhelmsson, H
Graff, C
Li, H
Oldfors, A
Rustin, P
Bruning, JC
Kahn, CR
Clayton, DA
Barsh, GS
Thoren, P
Larsson, NG
Citation: Jm. Wang et al., Dilated cardiomyopathy and atrioventricular conduction blocks induced by heart-specific inactivation of mitochondrial DNA gene expression, NAT GENET, 21(1), 1999, pp. 133-137
Authors:
Houshmand, M
Lindberg, C
Moslemi, AR
Oldfors, A
Holme, E
Citation: M. Houshmand et al., A novel heteroplasmic point mutation in the mitochondrial tRNA(Lys) gene in a sporadic case of mitochondrial encepharomyopathy: De novo mutation and no transmission to the offspring, HUM MUTAT, 13(3), 1999, pp. 203-209
Authors:
Melberg, A
Oldfors, A
Blomstrom-Lundqvist, C
Stalberg, E
Carlsson, B
Larsson, E
Lidell, C
Eeg-Olofsson, KE
Wikstrom, G
Henriksson, KG
Dahl, N
Citation: A. Melberg et al., Autosomal dominant myofibrillar myopathy with arrhythmogenic right ventricular cardiomyopathy linked to chromosome 10q, ANN NEUROL, 46(5), 1999, pp. 684-692
Authors:
Annerstedt, M
Herlitz, H
Molne, J
Oldfors, A
Westberg, G
Citation: M. Annerstedt et al., Rhabdomyolysis and acute renal failure associated with influenza virus type A, SC J UROL N, 33(4), 1999, pp. 260-264
Authors:
Moslemi, AR
Melberg, A
Holme, E
Oldfors, A
Citation: Ar. Moslemi et al., Autosomal dominant progressive external ophthalmoplegia - Distribution of multiple mitochondrial DNA deletions, NEUROLOGY, 53(1), 1999, pp. 79-84
Authors:
Martinsson, T
Darin, N
Kyllerman, M
Oldfors, A
Hallberg, B
Wahlstrom, J
Citation: T. Martinsson et al., Dominant hereditary inclusion-body myopathy gene (IBM3) maps to chromosomeregion 17p13.1, AM J HU GEN, 64(5), 1999, pp. 1420-1426
Authors:
Fyhr, IM
Moslemi, AR
Lindberg, C
Oldfors, A
Citation: Im. Fyhr et al., T cell receptor beta-chain repertoire in inclusion body myositis, J NEUROIMM, 91(1-2), 1998, pp. 129-134
Risultati:
1-17
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