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2022
Mark Towards a treatment for mitochondrial disease : current compounds in clinical development
Åsander Frostner, Eleonor ^LU ; Simon Serrano, Sonia ^LU ; Chamkha, Imen ^LU ; Elmer, Eskil ^LU ; Donnelly, Ellen and Hansson, Magnus ^LU (2022) In Bioenergetics Communications 2022(4). p.1-10
- Contribution to journal › Scientific review
Mark Statins Induce Locomotion and Muscular Phenotypes in Drosophila melanogaster That Are Reminiscent of Human Myopathy : Evidence for the Role of the Chloride Channel Inhibition in the Muscular Phenotypes
Al-Sabri, Mohamed H. ; Behare, Neha ; Alsehli, Ahmed M. ; Berkins, Samuel ; Arora, Aadeya ; Antoniou, Eirini ; Moysiadou, Eleni I. ; Anantha-Krishnan, Sowmya ; Cosmen, Patricia D. and Vikner, Johanna , et al. (2022) In Cells 11(22).
- Contribution to journal › Article
Mark Dominantly inherited myosin IIa myopathy caused by aberrant splicing of MYH2
Hedberg-Oldfors, Carola ; Elíasdóttir, Ólöf ; Geijer, Mats ^LU ; Lindberg, Christopher and Oldfors, Anders (2022) In BMC Neurology 22(1).
- Contribution to journal › Article
2020
Mark Loss of supervillin causes myopathy with myofibrillar disorganization and autophagic vacuoles
Hedberg-Oldfors, Carola ; Meyer, Robert ; Nolte, Kay ; Abdul Rahim, Yassir ^LU ; Lindberg, Christopher ; Karason, Kristjan ; Thuestad, Inger Johanne ; Visuttijai, Kittichate ; Geijer, Mats ^LU and Begemann, Matthias , et al. (2020) In Brain : a journal of neurology 143(8). p.2406-2420
- Contribution to journal › Article
2014
Mark Hereditary myopathy with early respiratory failure: occurrence in various populations
Palmio, Johanna ; Evila, Anni ; Chapon, Francoise ; Tasca, Giorgio ; Xiang, Fengqing ; Brådvik, Björn ^LU ; Eymard, Bruno ; Echaniz-Laguna, Andoni ; Laporte, Jocelyn and Karppa, Mikko , et al. (2014) In Journal of Neurology, Neurosurgery and Psychiatry 85(3). p.345-353
- Contribution to journal › Article
2012
Mark Myopathies associated with beta-tropomyosin mutations
Tajsharghi, H. ; Ohlsson, M. ; Palm, Lars ^LU and Oldfors, A. (2012) In Neuromuscular Disorders 22(11). p.923-933
- Contribution to journal › Scientific review
Mark Hereditary myopathy with early respiratory failure associated with a mutation in A-band titin
Ohlsson, Monica ; Hedberg, Carola ; Brådvik, Björn ^LU ; Lindberg, Christopher ; Tajsharghi, Homa ; Danielsson, Olof ; Melberg, Atle ; Udd, Bjarne ; Martinsson, Tommy and Oldfors, Anders (2012) In Brain 135(6). p.1682-1694
- Contribution to journal › Article
1996
Mark Myotonia in colchicine myoneuropathy
Rutkove, Seward B. ; De Girolami, Umberto ; Preston, David C. ; Freeman, Roy ; Nardin, Rachel A. ; Gouras, Gunnar K. ^LU ; Johns, Donald R. and Raynor, Elizabeth M. (1996) In Muscle and Nerve 19(7). p.870-875
- Contribution to journal › Article

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