Motoneuron afterhyperpolarisation duration in amyotrophic lateral sclerosis von Piotrkiewicz, Maria, Hausmanowa‐Petrusewicz, Irena

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Analysis of double discharges in amyotrophic lateral sclerosis von Piotrkiewicz, Maria, Kudina, Lydia, Mierzejewska, Jolanta, Hausmanowa-Petrusewicz, Irena

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Novel Col12A1 variant expands the clinical picture of congenital myopathies with extracellular matrix defects von Punetha, Jaya, Kesari, Akanchha, Hoffman, Eric P., Gos, Monika, Kamińska, Anna, Kostera‐Pruszczyk, Anna, Hausmanowa‐Petrusewicz, Irena, Hu, Ying, Zou, Yaqun, Bönnemann, Carsten G., JȨdrzejowska, Maria

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The inner nuclear membrane protein Emerin regulates β-catenin activity by restricting its accumulation in the nucleus von Markiewicz, Ewa, Tilgner, Katarzyna, Barker, Nick, van de Wetering, Mark, Clevers, Hans, Dorobek, Margareth, Hausmanowa-Petrusewicz, Irena, Ramaekers, Frans CS, Broers, Jos LV, Blankesteijn, W Matthijs, Salpingidou, Georgia, Wilson, Robert G, Ellis, Juliet A, Hutchison, Christopher J

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Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2 von Monaco, Anthony P, Bolino, Alessandra, Muglia, Maria, Conforti, Francesca Luisa, LeGuern, Eric, Salih, Mustafa A.M, Georgiou, Domna-Maria, Christodoulou, Kyproula, Hausmanowa-Petrusewicz, Irena, Mandich, Paola, Schenone, Angelo, Gambardella, Antonio, Bono, Franco, Quattrone, Aldo, Devoto, Marcella

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Simulation studies on the motor unit potentials with satellite components in amyotrophic lateral sclerosis and spinal muscle atrophy von Zalewska, Ewa, Rowinska-Marcinska, Katarzyna, Gawel, Małgorzata, Hausmanowa-Petrusewicz, Irena

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Dysfunctional lamins as mediators of oxidative stress in Emery-Dreifuss muscular dystrophy von Niebroj-Dobosz, Irena, Sokołowska, Beata, Madej-Pilarczyk, Agnieszka, Marchel, Michał, Hausmanowa-Petrusewicz, Irena

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SIMPLE mutations in Charcot‐Marie‐Tooth disease and the potential role of its protein product in protein degradation von Saifi, Gulam Mustafa, Szigeti, Kinga, Wiszniewski, Wojciech, Shy, Michael E., Krajewski, Karen, Hausmanowa‐Petrusewicz, Irena, Kochanski, Andrzej, Reeser, Suzanne, Mancias, Pedro, Butler, Ian, Lupski, James R.

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Spinal muscular atrophy: a delayed development hypothesis von HAUSMANOWA -PETRUSEWICZ, Irena, VRBOVA, Gerta

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Incidence of Spinal Muscular Atrophy in Poland – More Frequent than Predicted? von Jedrzejowska, Maria, Milewski, Michal, Zimowski, Janusz, Zagozdzon, Pawel, Kostera-Pruszczyk, Anna, Borkowska, Janina, Sielska, Danuta, Jurek, Marta, Hausmanowa-Petrusewicz, Irena

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Progeroid syndrome with scleroderma-like skin changes associated with homozygous R435C LMNA mutation von Madej-Pilarczyk, Agnieszka, Rosińska-Borkowska, Danuta, Rękawek, Joanna, Marchel, Michał, Szaluś, Ewa, Jabłońska, Stefania, Hausmanowa-Petrusewicz, Irena

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A collaborative study on the natural history of childhood and juvenile onset proximal spinal muscular atrophy (type II and III SMA): 569 patients von Zerres, Klaus, Rudnik-Schöneborn, Sabine, Forrest, Eric, Lusakowska, Anna, Borkowska, Janina, Hausmanowa-Petrusewicz, Irena

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A dystrophin missense mutation showing persistence of dystrophin and dystrophin-associated proteins yet a severe phenotype von Goldberg, Laura R., Hausmanowa-Petrusewicz, Irena, Fidzianska, Anna, Duggan, David J., Steinberg, Lisa S., Hoffman, Eric P.

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Cardiac involvement in laminopathies – short invited review von Nigro, Gerardo, Carboni, Nicola, Marchel, Michal, Palladino, Alberto, Madej-Pilarczyk, Agnieszka, Opolski, Grzegorz, Hausmanowa-Petrusewicz, Irena, Politano, Luisa

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108th ENMC International Workshop, 3rd Workshop of the MYO-CLUSTER project: EUROMEN, 7th International Emery-Dreifuss Muscular Dystrophy (EDMD) Workshop, 13–15 September 2002, Naar... von Bonne, Gisèle, Yaou, Rabah Ben, Béroud, Christophe, Boriani, Giuseppe, Brown, Sue, de Visser, Marianne, Duboc, Denis, Ellis, Juliet, Hausmanowa-Petrusewicz, Irena, Lattanzi, Giovanna, Merlini, Luciano, Morris, Glenn, Muntoni, Francesco, Opolski, Grzegorz, Pinto, Yigal M, Sangiuolo, Federica, Toniolo, Daniela, Trembath, Richard, van Berlo, Jop H, van der Kooi, Anneke J, Wehnert, Manfred

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Late-onset Charcot-Marie-Tooth type 2 disease with hearing impairment associated with a novel Pro105Thr mutation in the MPZ gene von Kabzińska, Dagmara, Korwin-Piotrowska, Teresa, Drechsler, Hanna, Drac, Hanna, Hausmanowa-Petrusewicz, Irena, Kochański, Andrzej

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Assessment of Human Motoneuron Afterhyperpolarization Duration in Health and Disease von Maria, Piotrkiewicz, Lydia, Kudina, Jia-Jin, Jason Chen, Irena, Hausmanowa-Petrusewicz

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Correlating motor unit morphology with bioelectrical activity – A simulation study von Zalewska, Ewa, Hausmanowa-Petrusewicz, Irena

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Shape irregularity of motor unit potentials in some neuromuscular disorders von Zalewska, Ewa, Rowińska-Marcińska, Katarzyna, MD, PhD, Irena Hausmanowa-Petrusewicz

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Meiotic stability and genotype - phenotype correlation of the trinucleotide repeat in X-linked spinal and bulbar muscular atrophy von La Spada, Albert R, Roling, Daniel B, Harding, Anita E, Warner, Carolyn L, Spiegel, Roland, Hausmanowa-Petrusewicz, Irena, Yee, Woon-Chee, Fischbeck, Kenneth H

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