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Christopher Lindberg

Showing results (21-30 of 56) with videos related to

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Journal of Neurology|July 27, 2023
Inclusion body myositis with early onset: a population-based studyUlrika Lindgren, Carola Hedberg-Oldfors, Rille Pullerits, et al.
Neuromuscular Disorders : NMD|November 22, 2011
Myopathy in a woman and her daughter associated with a novel splice site MTM1 mutationCarola Hedberg, Christopher Lindberg, Gyöngyvér Máthé, et al.
Journal of Neuropathology and Experimental Neurology|March 9, 2005
Mitochondrial myopathy and rhabdomyolysis associated with a novel nonsense mutation in the gene encoding cytochrome c oxidase subunit IGittan Kollberg, Ali-Reza Moslemi, Christopher Lindberg, et al.
Journal of Nephrology|August 5, 2021
Estimation of kidney function in patients with primary neuromuscular diseases: is serum cystatin C a better marker of kidney function than creatinine?Annika Aldenbratt, Christopher Lindberg, Elias Johannesson, et al.
Neurology. Genetics|July 9, 2020
COX deficiency and leukoencephalopathy due to a novel homozygous <i>APOPT1/COA8</i> mutationCarola Hedberg-Oldfors, Niklas Darin, Christer Thomsen, et al.
Behavioral and Brain Functions : BBF|May 21, 2010
Depression in Myotonic Dystrophy type 1: clinical and neuronal correlatesStefan Winblad, Christer Jensen, Jan-Eric Månsson, et al.
BMC Neurology|November 15, 2022
Dominantly inherited myosin IIa myopathy caused by aberrant splicing of MYH2Carola Hedberg-Oldfors, Ólöf Elíasdóttir, Mats Geijer, et al.
The New England Journal of Medicine|April 2, 2010
Glycogenin-1 deficiency and inactivated priming of glycogen synthesisAli-Reza Moslemi, Christopher Lindberg, Johanna Nilsson, et al.
Neuromuscular Disorders : NMD|March 26, 2026
Living with Duchenne muscular dystrophy as an adult: motor function, ventilatory assistance and health-related quality of lifeLisa Wahlgren, Sara Nordström, Anna-Karin Kroksmark, et al.
Annals of Neurology|October 2, 2003
Myosin storage myopathy associated with a heterozygous missense mutation in MYH7Homa Tajsharghi, Lars-Eric Thornell, Christopher Lindberg, et al.
Pageof 6

Showing results (21-30 of 56) with videos related to

Sort By:
Pageof 6
Journal of Neurology|July 27, 2023
Inclusion body myositis with early onset: a population-based studyUlrika Lindgren, Carola Hedberg-Oldfors, Rille Pullerits, et al.
Neuromuscular Disorders : NMD|November 22, 2011
Myopathy in a woman and her daughter associated with a novel splice site MTM1 mutationCarola Hedberg, Christopher Lindberg, Gyöngyvér Máthé, et al.
Journal of Neuropathology and Experimental Neurology|March 9, 2005
Mitochondrial myopathy and rhabdomyolysis associated with a novel nonsense mutation in the gene encoding cytochrome c oxidase subunit IGittan Kollberg, Ali-Reza Moslemi, Christopher Lindberg, et al.
Journal of Nephrology|August 5, 2021
Estimation of kidney function in patients with primary neuromuscular diseases: is serum cystatin C a better marker of kidney function than creatinine?Annika Aldenbratt, Christopher Lindberg, Elias Johannesson, et al.
Neurology. Genetics|July 9, 2020
COX deficiency and leukoencephalopathy due to a novel homozygous <i>APOPT1/COA8</i> mutationCarola Hedberg-Oldfors, Niklas Darin, Christer Thomsen, et al.
Behavioral and Brain Functions : BBF|May 21, 2010
Depression in Myotonic Dystrophy type 1: clinical and neuronal correlatesStefan Winblad, Christer Jensen, Jan-Eric Månsson, et al.
BMC Neurology|November 15, 2022
Dominantly inherited myosin IIa myopathy caused by aberrant splicing of MYH2Carola Hedberg-Oldfors, Ólöf Elíasdóttir, Mats Geijer, et al.
The New England Journal of Medicine|April 2, 2010
Glycogenin-1 deficiency and inactivated priming of glycogen synthesisAli-Reza Moslemi, Christopher Lindberg, Johanna Nilsson, et al.
Neuromuscular Disorders : NMD|March 26, 2026
Living with Duchenne muscular dystrophy as an adult: motor function, ventilatory assistance and health-related quality of lifeLisa Wahlgren, Sara Nordström, Anna-Karin Kroksmark, et al.
Annals of Neurology|October 2, 2003
Myosin storage myopathy associated with a heterozygous missense mutation in MYH7Homa Tajsharghi, Lars-Eric Thornell, Christopher Lindberg, et al.
Pageof 6