field_full_title_name

Anna Sułek, MD, PhD

Publikacje

• Małczyńska-Sims P., Chalimoniuk M., Sułek A. (2020): The Effect of Endurance Training on Brain-Derived Neurotrophic Factor and Inflammatory Markers in Healthy People and Parkinson's Disease. A Narrative Review. Front Physiol. 2020 Nov 19;11:578981. doi: 10.3389/fphys.2020.578981. PMID: 33329027; PMCID: PMC7711132.
• Bosak M., Sułek A., Łukasik M., Żak A., Słowik A., Lasek-Bal A. (2020): Genetic testing and the phenotype of Polish patients with Unverricht-Lundborg disease (EPM1) – A cohort study. Epilepsy Behav. 2020 Nov;112:107439. doi: 10.1016/j.yebeh.2020.107439. Epub 2020 Sep 10. PMID: 32920378.
• Frączek A., Potulska-Chromik A., Bednarska-Makaruk M., Sułek A., Obersztyn E., Braun-Walicka N., Ryniewicz B., Kostera-Pruszczyk A. (2020): Spinal muscular atrophy with an overlapping syndrome - "double trouble" or a potentially better outcome? Neurol Neurochir Pol. 2020;54(5):475-477. doi: 10.5603/PJNNS.a2020.0060. Epub 2020 Aug 5. PMID: 32757203.
• Nojszewska M., Lusakowska A., Gawel M., Sierdzinski J., Sulek A., Krysa W., Elert-Dobkowska E., Seroka A., Kaminska A.M., Kostera-Pruszczyk A. (2019): The needle EMG findings in myotonia congenita. J Electromyogr Kinesiol. 2019 Dec;49:102362. doi:10.1016/j.jelekin.2019.102362. Epub 2019 Oct 3. PMID: 31610484.
• Diallo A., Jacobi H., Cook A., Giunti P., Parkinson M.H., Labrum R., Durr A., Brice A., Charles P., Marelli C., Mariotti C., Nanetti L., Panzeri M., Castaldo A., Rakowicz M., Rola R., Sulek A., Schmitz-Hübsch T., Schöls L., Hengel H., Baliko L., Melegh B., Filla A., Antenora A., Infante J., Berciano J., van de Warrenburg B.P., Timmann D., Boesch S., Nachbauer W., Pandolfo M., Schulz J.B., Bauer P., Jun-Suk K., Klockgether T., Tezenas du Montcel S. (2019): Prediction of Survival With Long-Term Disease Progression in Most Common Spinocerebellar Ataxia. Mov Disord. 2019 Aug;34(8):1220-1227. doi: 10.1002/mds.27739. Epub 2019 Jun 18. PMID: 31211461.
• Lasek-Bal A., Lukasik M., Żak A., Sulek A., Bosak M. (2019): Unverricht-Lundborg disease: Clinical course and seizure management based on the experience of polish centers. Seizure. 2019 Jul;69:87-91. doi: 10.1016/j.seizure.2019.04.008. Epub 2019 Apr 10. PMID: 30999254.
• Elert-Dobkowska E., Stepniak I., Krysa W., Rakowicz M., Pilch J., Zaremba J., Sulek A. (2019): Next generation sequencing study reveals the broader variants spectrum of hereditary spastic paraplegia and related phenotypes. Neurogenetics, 2019, 20(1), 27-38, (DOI: 10.1007/s10048-019-00565-6) IF=3,090.
• Sulek A., Lusakowska A., Krysa W., Rajkiewicz M., Kaminska A., Nojszewska M., Kostera-Pruszczyk A., Zdzienicka E., Kubalska J., Rakowicz M., Szirkowiec W., Kwiecinski H., Zaremba J. (2018): Evidence for a relatively high proportion of DM2 mutations in a large group of Polish patients. Neurol Neurochir Pol. 2018 Nov - Dec;52(6):736-742. IF=0.641.
• Jacobi H., Tezenas du Montcel S., Bauer P., Giunti P., Cook A., Labrum R., ParkinsonM.H., Durr A., Brice A., Charles P., Marelli C., Mariotti C., Nanetti L., Sarro L., Rakowicz M., Sułek A., Sobańska A., Schmitz-Hübsch T., Schöls L., Hengel H., Baliko L., Melegh B., Filla A., Antenora A., Infante J., Berciano J., Van de Warrenburg B.P., Timmann D., Szymanski S., Boesch S., Nachbauer W., Kang J-S., Pandolfo M, Schulz J.B., Tanguy Melac A., Diallo A., Klockgether T. (2018): Long-term evolution of patient-reported outcome measures in spinocerebellar ataxias. J. Neurol. - 2018, vol. 265, nr 9, s. 2040-2051, (IF= 3.783)
• Diallo A., Jacobi H., Cook A., Labrum R., Durr A., Brice A., Charles P., Marelli C., Mariotti C., Nanetti L., Panzeri M., Rakowicz M., Sobańska A., Sułek A., Schmitz-Hübsch T., Schöls L., Hengel H., Melegh B., Filla A., Infante J., Berciano J., Van de Warrenburg B.P., Timmann D., Boesch S., Pandolfo M., Schulz J.B., Bauer P., Giunti P., Kang J-S., Klockgether T., Tezenas du Montcel S. (2018): Survival in patients with spinocerebellar ataxia types 1, 2, 3, and 6 (EUROSCA): a longitudinal cohort study. Lancet Neurol. - 2018, vol.17, nr 4, s. 327-334, (IF= 27.144)
• Piekutowska-Abramczuk D., Kaliszewska M., Sułek A., Jurkowska N., Ołtarzewski M., Jabłońska E., Trubicka J., Głowacka A., Ciara E., Kowalski P., Langiewicz-Wojciechowska K., Tesarova M., Zeman J., Kierdaszuk B., Kuczyński D., Chmielewski D., Szymańska E., Bakuła A., Łusakowska A., Lipowska M., Brodacki B., Pera J., Dorobek M., Rydzanicz M., Płoski R., Chrzanowska K.H., Bartnik E., Placha G., Kamińska A., Kostera-Pruszczyk A., Krajewska-Walasek M., Tońska K., Pronicka E. (2018): The frequency of mitochondrial polymerase gamma related disorders in a large Polish population cohort. Mitochondrion. 2018 Nov 10. pii: S1567-7249(18)30184-3. doi: 10.1016/j.mito.2018.11.004. (IF=3.226)
• Krysa W., Sulek A., Rakowicz M., Szirkowiec W., Zaremba J.(2016): High relative frequency of SCA1 in Poland reflecting a potential founder effect. Neurol Sci. 2016 Aug;37(8):1319-25. IF=1.783.
• Günther S., Elert-Dobkowska E., Soehn A.S., Hinreiner S., Yoon G., Heller R., Hellenbroich Y., Hübner C.A., Ray P.N., Hehr U., Bauer P., Sulek A., Beetz C. (2016): High Frequency of Pathogenic Rearrangements in SPG11, and Extensive Contribution of Mutational Hotspots and Founder Alleles. Hum Mutat. Apr 13. doi: 10.1002/humu.23000. [Epub ahead of print]. (IF=5.089)
• Nojszewska M., Łusakowska A., Szmidt-Salkowska E., Gaweł M., Lipowska M., Sułek A., Krysa W., Rajkiewicz M., Seroka A., Kaczmarek K., Kamińska A.M. (2015): Peripheral nerve involvement in myotonic dystrophy type 2 - similar or different than in myotonic dystrophy type 1? Neurol Neurochir Pol. 2015;49(3):164-70. doi: 10.1016/j.pjnns.2015.04.008. Epub 2015 May 6. PubMed PMID: 26048604. (IF=0.747)
• Elert-Dobkowska E., Stepniak I., Krysa W., Rajkiewicz M., Rakowicz M., Sobanska A.,  Rudzinska M., Wasielewska A., Pilch J., Kubalska J., Lipczynska-Lojkowska W., Kulczycki J., Kurdziel K., Sikorska A., Beetz C., Zaremba J., Sulek A. (2015): Molecular spectrum of the SPAST, ATL1 and REEP1 gene mutations associated with the most common hereditary spastic paraplegias in a group of Polish patients. J Neurol Sci. 2015 Dec 15;359(1-2):35-9. IF=2,126.
• Jacobi H., du Montcel S.T., Bauer P., Giunti P., Cook A., Labrum R., Parkinson M.H., Durr A., Brice A., Charles P., Marelli C., Mariotti C., Nanetti L., Panzeri M., Rakowicz M., Sulek A, Sobanska A., Schmitz-Hübsch T., Schöls L., Hengel H., Baliko L., Melegh B., Filla A., Antenora A., Infante J., Berciano J., van de Warrenburg B.P., Timmann D., Szymanski S., Boesch S., Kang J.S., Pandolfo M., Schulz J.B., Molho S., Diallo A., Klockgether T. (2015): Long-term disease progression in spinocerebellar ataxia types 1, 2, 3, and 6: a longitudinal cohort study. Lancet Neurol. 2015 Nov;14(11):1101-8. pii: S1474-4422(15)00202-1. doi: 10.1016/S1474-4422(15)00202-1. (IF=23.468)
• Acewicz A., Wierzba-Bobrowicz T., Lewandowska E., Sienkiewicz-Jarosz H., Sulek A., Antczak J., Rakowicz M., Ryglewicz D. (2015): Morphological changes of skeletal muscle in spinal and bulbar muscular atrophy (SBMA), Kennedy's disease: a case report. Clin Neuropathol. 2015 Jul-Aug;34(4):199-206. doi: 10.5414/NP300829. PubMed PMID: 25828775. (IF=1,267)