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Author/Creator Łusakowska, Anna

1. Extending the clinical and mutational spectrum of TRIM32-related myopathies in a non-Hutterite population. Issue 4 (19th June 2018)

Authors:
Johnson, Katherine; De Ridder, Willem; Töpf, Ana; Bertoli, Marta; Phillips, Lauren; De Jonghe, Peter; Baets, Jonathan; Deconinck, Tine; Rakocevic Stojanovic, Vidosava; Perić, Stojan; Durmus, Hacer; Jamal-Omidi, Shirin; Nafissi, Shahriar; Mongini, Tiziana; Łusakowska, Anna; Busby, Mark; Miller, Ja...
Journal:
Journal of neurology, neurosurgery and psychiatry
Issue:
Volume 90:Issue 4(2019)
Page Start:
490
Record Type:
Journal Article
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2. Identification of exosomal muscle-specific miRNAs in serum of myotonic dystrophy patients relating to muscle disease progress. (16th June 2017)

Authors:
Koutsoulidou, Andrie; Photiades, Marinos; Kyriakides, Tassos C.; Georgiou, Kristia; Prokopi, Marianna; Kapnisis, Konstantinos; Łusakowska, Anna; Nearchou, Marianna; Christou, Yiolanda; Papadimas, George K.; Anayiotos, Andreas; Kyriakou, Kyriakos; Kararizou, Evangelia; Zamba Papanicolaou, Eleni; P...
Journal:
Human molecular genetics
Issue:
Volume 26:Number 17(2017:Sep. 01)
Page Start:
3285
Record Type:
Journal Article
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3. P47-T Could needle EMG still be helpful in diagnosis of myotonia congenita?. Issue 7 (July 2019)

Authors:
Nojszewska, Monika; Łusakowska, Anna; Gaweł, Małgorzata; Sierdziński, Janusz; Sułek, Anna; Krysa, Woiletta; Elert-Dobkowska, Ewelina; Seroka, Andrzej; Kamińska, Anna M.; Kostera-Pruszczyk, Anna
Journal:
Clinical neurophysiology
Issue:
Volume 130:Issue 7(2019:Jul.)
Page Start:
e52
Record Type:
Journal Article
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4. P48-T Short exercise and short exercise with cooling tests in recessive myotonia congenita (Becker disease). Issue 7 (July 2019)

Authors:
Nojszewska, Monika; Łusakowska, Anna; Gaweł, Malgorzata; Lipowska, Marta; Sierdziński, Janusz; Sułek, Anna; Krysa, Wioletta; Elert-Dobkowska, Ewelina; Seroka, Andrzej; Kamińska, Anna M.; Kostera-Pruszczyk, Anna
Journal:
Clinical neurophysiology
Issue:
Volume 130:Issue 7(2019:Jul.)
Page Start:
e53
Record Type:
Journal Article
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5. Recurrent K3E mutation in Cu/Zn superoxide dismutase gene associated with amyotrophic lateral sclerosis. Issue 7 (December 2013)

Authors:
Kuźma-Kozakiewicz, Magdalena; Berdyński, Mariusz; Morita, Mitsuya; Takahashi, Yuji; Kawata, Akihiro; Kaida, Ken-Ichi; Kaźmierczak, Beata; Łusakowska, Anna; Goto, Jun; Tsuji, Shoji; Żekanowski, Cezary; Kwieciński, Hubert
Journal:
Amyotrophic lateral sclerosis and frontotemporal degeneration
Issue:
Volume 14:Issue 7/8(2013)
Page Start:
608
Record Type:
Journal Article
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