المؤلفون: Calic, Zeljka, Peric, S, Vujnic, M, Bjelica, B, Bozovic, I, Basta, I, Rakocevic-Stojanovic, V, Bradshaw, A, Welgampola, M

المصدر: urn:ISSN:1351-5101 ; urn:ISSN:1468-1331

مصطلحات موضوعية: anzsrc-for: 1103 Clinical Sciences, anzsrc-for: 1109 Neurosciences

وصف الملف: application/octet-stream

Relation: http://hdl.handle.net/1959.4/unsworks_81001; https://unsworks.unsw.edu.au/bitstreams/f14fff60-7514-4fae-a288-1c0d4ecd3e7a/download; https://doi.org/10.26190/unsworks/28335

الاتاحة: http://hdl.handle.net/1959.4/unsworks_81001
https://unsworks.unsw.edu.au/bitstreams/f14fff60-7514-4fae-a288-1c0d4ecd3e7a/download
https://doi.org/10.26190/unsworks/28335

المؤلفون: Radovanović, Nemanja, Pesovic, J., Peric, S., Radenković, Lana, Brkušanin, Miloš, Brajušković, Goran, Rakocevic Stojanovic, V., Savić-Pavićević, Dušanka

Relation: 29th International Congress of the World Muscle Society. Neuromuscular Disorders. 2024, Prague, Czech Republic; https://biore.bio.bg.ac.rs/handle/123456789/7353

الاتاحة: https://biore.bio.bg.ac.rs/handle/123456789/7353

المؤلفون: Pešović, J., Bashtrykov, P., Perić, S., Radenković, Lana, Davidović, I., Radovanović, N., Brkušanin, Miloš, Rakočević-Stojanović, V., Savić-Pavićević, Dušanka

Relation: VII Congress of the Serbian Genetic Society, Zlatibor, Serbia; https://biore.bio.bg.ac.rs/handle/123456789/7349

الاتاحة: https://biore.bio.bg.ac.rs/handle/123456789/7349

المؤلفون: Radovanović, Nemanja, Pešović, J., Perić, S., Radenković, L., Brajušković, Goran, Rakočević Stojanović, V., Savić-Pavićević, Dušanka

Relation: the 56th European Society of Human Genetics (ESHG) Conference: Hybrid Posters. Eur J Hum Genet 32 (Suppl 1); https://biore.bio.bg.ac.rs/handle/123456789/7162

الاتاحة: https://biore.bio.bg.ac.rs/handle/123456789/7162

المؤلفون: Calic, Zeljka, Bjelica, Bogdan, Peric, Stojan, Vujnic, M, Rakocevic Stojanovic, V, Bradshaw, A, Welgampola, M

المصدر: 7th Congress of the European Academy of Neurology, Wiena, virtual, 2021-06-19 - 2021-08-22

وصف الملف: application/octet-stream

Relation: http://hdl.handle.net/1959.4/unsworks_77090; https://unsworks.unsw.edu.au/bitstreams/6ec1d2d3-4ae3-48a3-8156-633f910f541f/download; https://doi.org/10.26190/unsworks/28092

الاتاحة: http://hdl.handle.net/1959.4/unsworks_77090
https://unsworks.unsw.edu.au/bitstreams/6ec1d2d3-4ae3-48a3-8156-633f910f541f/download
https://doi.org/10.26190/unsworks/28092

المؤلفون: Topf A, Johnson K, Bates A, Phillips L, Chao KR, England EM, Laricchia KM, Mullen T, Valkanas E, Xu L, Bertoli M, Blain A, Casasus AB, Duff J, Mroczek M, Specht S, Lek M, Ensini M, MacArthur DG, Akay E, Alonso-Perez J, Baets J, Barisic N, Bastian A, Borell S, Chamova T, Claeys K, Colomer J, Coppens S, Deconinck N, de Ridder W, Diaz-Manera J, Dominguez-Gonzalez C, Duncan A, Durmus H, Fahmy NA, Farrugia ME, Fernandez-Torron R, Gonzalez-Quereda L, Haberlova J, von der Hagen M, Hahn A, Jakovcevic A, JericoPascual I, Kapetanovic S, Kenina V, Kirschner J, Klein A, Kolbel H, Kostera-Pruszczyk A, Kulshrestha R, Lahdetie J, Layegh M, Longman C, Lopezde Munain A, Loscher W, Lusakowska A, Maddison P, Magot A, Majumdar A, Marti P, MartinezArroyo A, Mazanec R, Mercier S, Mongini T, Muelas N, Nascimento A, Nafissi S, Omidi S, Ortez C, Paquay S, Pereon Y, Peric S, Ponzalino V, Rakocevic Stojanovic V, Remiche G, RodriguezSainz A, Rudnik S, SanchezAlbisua I, Santos M, Schara U, Shatillo A, Sertic J, Stephani U, Strang-Karlsson S, Sznajer Y, Tanev A, Tournev I, Van den Bergh P, Van Parijs V, Vilchez J, Vill K, Vissing J, Wallgren-Pettersson C, Wanschitz J, Willis T, Witting N, Zulaica M, Straub V

المصدر: Genetics in Medicine, 2020

وصف الملف: application/pdf

Relation: https://eprints.ncl.ac.uk/267566; https://eprints.ncl.ac.uk/fulltext.aspx?url=267566/5017D509-DDA2-4331-9E22-C96779FB4397.pdf&pub_id=267566

الاتاحة: https://eprints.ncl.ac.uk/267566

المؤلفون: Calic, Z, Rakocevic-Stojanovic, V, Peric, S, Vujnic, M, Bjelica, B, Bozovic, I, Welgampola, M

المصدر: urn:ISSN:0022-510X ; Journal of the Neurological Sciences, 405, 36

مصطلحات موضوعية: anzsrc-for: 1103 Clinical Sciences, anzsrc-for: 1109 Neurosciences, anzsrc-for: 1701 Psychology

Relation: http://hdl.handle.net/1959.4/unsworks_63430; https://doi.org/10.1016/j.jns.2019.10.279

الاتاحة: http://hdl.handle.net/1959.4/unsworks_63430
https://doi.org/10.1016/j.jns.2019.10.279

المؤلفون: Radenković, Lana, Perić S., Pešović, Jovan, Radovanović, Nemanja, Brajušković, Goran, Rakočević Stojanović, V., Savić-Pavićević, Dušanka

Relation: IDMC-13: The 13 th Myotonic Dystrophy Consortium Meeting, June 22-25, Osaka, Japan.; Radenković L, Perić S, Pešović J, Radovanović N, Brajušković G, Rakočević Stojanović V, D Savić-Pavićević D. Cluster Analysis of Phenotypic Characteristics in patients with Myotonic dystrophy type 2. Electronic abstracts: Poster Presentation Abstract P-32. p. 108. IDMC-13: The 13 th Myotonic Dystrophy Consortium Meeting, June 22-25, Osaka, Japan.; https://biore.bio.bg.ac.rs/handle/123456789/5153

الاتاحة: https://biore.bio.bg.ac.rs/handle/123456789/5153

المؤلفون: Radovanović, Nemanja, Pešović, Jovan, Perić, S., Radenković, Lana, Vuković, J., Brkušanin, Miloš, Brajušković, Goran, Rakočević Stojanović, V., Savić-Pavićević, Dušanka

Relation: The 13 th Myotonic Dystrophy Consortium Meeting, June 22-25, Osaka, Japan.; Abstract S-2-2-5. p. 63. IDMC-13: The 13 th Myotonic Dystrophy Consortium Meeting, June 22-25, Osaka, Japan.; https://biore.bio.bg.ac.rs/handle/123456789/5152

الاتاحة: https://biore.bio.bg.ac.rs/handle/123456789/5152

المؤلفون: Pešović, Jovan, Perić, S., Radovanović, N., Radenković, Lana, Brkušanin, Miloš, Brajušković, Goran, Rakočević Stojanović, V., Savić-Pavićević, Dušanka

Relation: The 13 th Myotonic Dystrophy Consortium Meeting, June 22-25, Osaka, Japan.; Pešović J, Perić S, Radovanović N, Radenković L, Brkušanin M, Brajušković G, Rakočević Stojanović V, Savić-Pavićević D. CpG sites surrounding DMPK expansions are heterogeneously methylated in myotonic dystrophy type 1 patients with variant repeats. Electronic abstracts: Platform Presentation Abstract S-1-1-2. p. 40. IDMC-13: The 13 th Myotonic Dystrophy Consortium Meeting, June 22-25, Osaka, Japan.; https://biore.bio.bg.ac.rs/handle/123456789/5156

الاتاحة: https://biore.bio.bg.ac.rs/handle/123456789/5156

المؤلفون: Wood L, Bassez G, Bleyenheuft C, Campbell C, Cossette L, Jimenez-Moreno AC, Dai Y, Dawkins H, Diaz-Manera J, Dogan C, El Sherif R, Fossati B, Graham C, Hilbert J, Kastreva K, Kimura E, Korngut L, Kostera-Pruszczyk A, Lindberg C, Lindvall B, Luebbe E, Lusakowska A, Mazanec R, Meola G, Orlando L, Takahashi MP, Peric S, Puymirat J, Rakocevic-Stojanovic V, Rodrigues M, Roxburgh R, Schoser B, Segovia S, Shatillo A, Thiele S, Tournev I, Van Engelen B, Vohanka S, Lochmuller H

المصدر: Orphanet Journal of Rare Diseases, 5 September 2018

وصف الملف: application/pdf

Relation: https://eprints.ncl.ac.uk/251454; https://eprints.ncl.ac.uk/fulltext.aspx?url=251454/B1B52020-BE93-47D8-AF04-6ADC75A8A148.pdf&pub_id=251454

الاتاحة: https://eprints.ncl.ac.uk/251454

المؤلفون: Vujnic, M, Peric, S, Calic, Z, Benovic, N, Nisic, T, Pesovic, J, Savic-Pavicevic, D, Rakocevic-Stojanovic, V

المصدر: urn:ISSN:1128-2460 ; urn:ISSN:2532-1900 ; Acta Myologica, 37, 4, 252-256

مصطلحات موضوعية: Obesity, Genetics, Cardiovascular, Nutrition, Clinical Research, Diabetes, 6.1 Pharmaceuticals, 6 Evaluation of treatments and therapeutic interventions, Metabolic and endocrine, 3 Good Health and Well Being, Adult, Cardiovascular Diseases, Female, Humans, Hyperlipidemias, Hypertension, Hypertriglyceridemia, Insulin Resistance, Male, Metabolic Syndrome, Middle Aged, Myotonic Dystrophy, Needs Assessment, Quality of Life, Risk Factors, Serbia, myotonic dystrophy type 2, anzsrc-for: 1102 Cardiorespiratory Medicine and Haematology, anzsrc-for: 1103 Clinical Sciences

وصف الملف: application/pdf

Relation: http://hdl.handle.net/1959.4/unsworks_58296; https://unsworks.unsw.edu.au/bitstreams/5e277641-1361-42d8-b889-9656f85755fb/download

الاتاحة: http://hdl.handle.net/1959.4/unsworks_58296
https://unsworks.unsw.edu.au/bitstreams/5e277641-1361-42d8-b889-9656f85755fb/download

المؤلفون: Topf A., Johnson K., Bates A., Phillips L., Chao K. R., England E. M., Laricchia K. M., Mullen T., Valkanas E., Xu L., Bertoli M., Blain A., Casasus A. B., Duff J., Mroczek M., Specht S., Lek M., Ensini M., MacArthur D. G., Akay E., Alonso-Perez J., Baets J., Barisic N., Bastian A., Borell S., Chamova T., Claeys K., Colomer J., Coppens S., Deconinck N., de Ridder W., Diaz-Manera J., Dominguez-Gonzalez C., Duncan A., Durmus H., Fahmy N. A., Farrugia M. E., Fernandez-Torron R., Gonzalez-Quereda L., Haberlova J., von der Hagen M., Hahn A., Jakovcevic A., JericoPascual I., Kapetanovic S., Kenina V., Kirschner J., Klein A., Kolbel H., Kostera-Pruszczyk A., Kulshrestha R., Lahdetie J., Layegh M., Longman C., Lopezde Munain A., Loscher W., Lusakowska A., Maddison P., Magot A., Majumdar A., Marti P., MartinezArroyo A., Mazanec R., Mercier S., Mongini T., Muelas N., Nascimento A., Nafissi S., Omidi S., Ortez C., Paquay S., Pereon Y., Peric S., Ponzalino V., Rakocevic Stojanovic V., Remiche G., RodriguezSainz A., Rudnik S., SanchezAlbisua I., Santos M., Schara U., Shatillo A., Sertic J., Stephani U., Strang-Karlsson S., Sznajer Y., Tanev A., Tournev I., Van den Bergh P., Van Parijs V., Vilchez J., Vill K., Vissing J., Wallgren-Pettersson C., Wanschitz J., Willis T., Witting N., Zulaica M., Straub V.

المساهمون: Topf A., Johnson K., Bates A., Phillips L., Chao K.R., England E.M., Laricchia K.M., Mullen T., Valkanas E., Xu L., Bertoli M., Blain A., Casasus A.B., Duff J., Mroczek M., Specht S., Lek M., Ensini M., MacArthur D.G., Akay E., Alonso-Perez J., Baets J., Barisic N., Bastian A., Borell S., Chamova T., Claeys K., Colomer J., Coppens S., Deconinck N., de Ridder W., Diaz-Manera J., Dominguez-Gonzalez C., Duncan A., Durmus H., Fahmy N.A., Farrugia M.E., Fernandez-Torron R., Gonzalez-Quereda L., Haberlova J., von der Hagen M., Hahn A., Jakovcevic A., JericoPascual I., Kapetanovic S., Kenina V., Kirschner J., Klein A., Kolbel H., Kostera-Pruszczyk A., Kulshrestha R., Lahdetie J., Layegh M., Longman C., Lopezde Munain A., Loscher W., Lusakowska A., Maddison P., Magot A., Majumdar A., Marti P., MartinezArroyo A., Mazanec R., Mercier S., Mongini T., Muelas N., Nascimento A., Nafissi S., Omidi S., Ortez C., Paquay S., Pereon Y., Peric S., Ponzalino V., Rakocevic Stojanovic V., Remiche G., RodriguezSainz A., Rudnik S., SanchezAlbisua I., Santos M., Schara U., Shatillo A., Sertic J., Stephani U., Strang-Karlsson S., Sznajer Y., Tanev A., Tournev I., Van den Bergh P., Van Parijs V., Vilchez J., Vill K., Vissing J., Wallgren-Pettersson C., Wanschitz J., Willis T., Witting N., Zulaica M., Straub V.

مصطلحات موضوعية: genetic diagnosi, limb-girdle weakne, neuromuscular disease, next-generation sequencing, targeted exome analysis

Relation: info:eu-repo/semantics/altIdentifier/pmid/32528171; info:eu-repo/semantics/altIdentifier/wos/WOS:000539889800001; volume:22; issue:9; firstpage:1478; lastpage:1488; numberofpages:11; journal:GENETICS IN MEDICINE; http://hdl.handle.net/2318/1786318; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85086267166

الاتاحة: http://hdl.handle.net/2318/1786318
https://doi.org/10.1038/s41436-020-0840-3

المؤلفون: Howard J. F., Bril V., Vu T., Karam C., Peric S., Margania T., Murai H., Bilinska M., Shakarishvili R., Smilowski M., Guglietta A., Ulrichts P., Vangeneugden T., Utsugisawa K., Verschuuren J., Mantegazza R., De Bleeker J., De Koning K., De Mey K., De Pue A., Mercelis R., Wyckmans M., Vinck C., Wagemaekers L., Baets J., Ng E., Shabanpour J., Daniyal L., Mannan S., Katzberg H., Genge A., Siddiqi Z., Junkerova J., Horakova J., Reguliova K., Tyblova M., Jurajdova I., Novakova I., Jakubikova M., Pitha J., Vohanka S., Havelkova K., Horak T., Bednarik J., Horakova M., Meisel A., Remstedt D., Heibutzki C., Kohler S., Hoffman S., Stascheit F., Vissing J., Zafirakos L., Khatri K. K., Autzen A., Godtfeldt Stemmerik M. P., Andersen H., Attarian S., Tsiskaridze A., Rozsa C., Jakab G. M., Toth S., Szabo G., Bors D., Szabo E., Campanella A., Vanoli F., Frangiamore R., Antozzi C., Bonanno S., Maggi L., Giossi R., Sacca F., Marsili A., Imbriglio T., Antonini G., Alfieri G., Morino S., Garibaldi M., Fionda L., Leonardi L., Konno S., Uzawa A., Sakuma K., Watanabe C., Ozawa Y., Yasuda M., Onishi Y., Samukawa M., Tsuda T., Suzuki Y., Ishida S., Watanabe G., Takahashi M., Nakamura H., Sugano E., Kubota T., Imai T., Mari Suzuki., Mori A., Yamamoto D., Ikeda K., Hisahara S., Masuda M., Takaki M., Minemoto K., Ido N., Naito M., Okubo Y., Sugimoto T., Takematsu Y., Kamei A., Shimizu M., Naito H., Nomura E., Van Heur M., Peters A., Tannemaat M., Ruiter A., Keene K., Halas M., Szczudlik A., Pinkosz M., Frasinska M., Zwolinska G., Kostera-Pruszczyk A., Golenia A., Szczudlik P., Szczechowski L., Marek E., Poverennova I., Urtaeva L., Kuznetsova N., Romanova T., Nadezhda M., Lapochka E., Korobko D., Vergunova I., Melnikova A., Bulatova E., Antipenko E., Bozovic I., Lavrnic D., Rakocevic Stojanovic V., Beydoun S., Akhter S., Malekniazi A., Darki L., Pimentel N., Cannon V., Chopra M., Traub R., Mozaffar T., Turner I., Habib A., Goyal N., Kak M., Velasquez E., Lam L., Suresh N., Farias J., Jones S., Wagoner M., Eggleston D., Bertorini T., Benzel C., Henegar R., Pillai R., Bharavaju-Sanka R., Paiz C., Jackson C., Ruzhansky K., Dimitrova D., Visser A., Chahin N., Levine T., Lisak R., Jia K., Mada F., Bernitsas E., Pasnoor M., Roath K., Colgan S., Currence M., Heim A., Barohn R., Dimachkie M., Statland J., Jawdat O., Jabari D., Farmakidis C., Gilchrist J., Li Y., Caristo I., Hastings D., Anthony Morren J., Weiss M., Muppidi S., Nguyen T., Welsh L., So Y., Pulley M., Bailey C., Smith L., Berger A., Sahagian G., Camberos Y., Frishberg B.

المساهمون: Howard, J. F., Bril, V., Vu, T., Karam, C., Peric, S., Margania, T., Murai, H., Bilinska, M., Shakarishvili, R., Smilowski, M., Guglietta, A., Ulrichts, P., Vangeneugden, T., Utsugisawa, K., Verschuuren, J., Mantegazza, R., De Bleeker, J., De Koning, K., De Mey, K., De Pue, A., Mercelis, R., Wyckmans, M., Vinck, C., Wagemaekers, L., Baets, J., Ng, E., Shabanpour, J., Daniyal, L., Mannan, S., Katzberg, H., Genge, A., Siddiqi, Z., Junkerova, J., Horakova, J., Reguliova, K., Tyblova, M., Jurajdova, I., Novakova, I., Jakubikova, M., Pitha, J., Vohanka, S., Havelkova, K., Horak, T., Bednarik, J., Horakova, M., Meisel, A., Remstedt, D., Heibutzki, C., Kohler, S., Hoffman, S., Stascheit, F., Vissing, J., Zafirakos, L., Khatri, K. K., Autzen, A., Godtfeldt Stemmerik, M. P., Andersen, H., Attarian, S., Tsiskaridze, A., Rozsa, C., Jakab, G. M., Toth, S., Szabo, G., Bors, D., Szabo, E., Campanella, A., Vanoli, F., Frangiamore, R., Antozzi, C., Bonanno, S., Maggi, L., Giossi, R., Sacca, F., Marsili, A., Imbriglio, T., Antonini, G., Alfieri, G., Morino, S., Garibaldi, M., Fionda, L., Leonardi, L., Konno, S., Uzawa, A., Sakuma, K., Watanabe, C., Ozawa, Y., Yasuda, M., Onishi, Y., Samukawa, M., Tsuda, T., Suzuki, Y., Ishida, S., Watanabe, G., Takahashi, M., Nakamura, H., Sugano, E., Kubota, T., Imai, T., Mari, Suzuki., Mori, A.

مصطلحات موضوعية: efgartigimod, myasthenia gravi, fc fragment

Relation: info:eu-repo/semantics/altIdentifier/pmid/34146511; info:eu-repo/semantics/altIdentifier/wos/WOS:000687268300012; volume:20; issue:7; firstpage:526; lastpage:536; numberofpages:11; journal:LANCET NEUROLOGY; http://hdl.handle.net/11573/1558042; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85107960986

الاتاحة: http://hdl.handle.net/11573/1558042
https://doi.org/10.1016/S1474-4422(21)00159-9

المؤلفون: Calic, Z, Bjelica, B, Peric, S, Vujnic, M, Bozovic, I, Rakocevic-Stojanovic, V, Bradshaw, A, Welgampola, M

مصطلحات الفهرس: 1103 Clinical Sciences, 1109 Neurosciences, text, Conference Paper

URL: http://handle.unsw.edu.au/1959.4/unsworks_78224
https://orcid.org/0000-0003-0635-016X
https://orcid.org/0000-0003-0635-016X
European Journal of Neurology
28
7th Congress of the European Academy of Neurology

المؤلفون: Johnson K., De Ridder W., Topf A., Bertoli M., Phillips L., De Jonghe P., Baets J., Deconinck T., Rakocevic Stojanovic V., Peric S., Durmus H., Jamal-Omidi S., Nafissi S., Mongini T., Lusakowska A., Busby M., Miller J., Norwood F., Hudson J., Barresi R., Lek M., Macarthur D. G., Straub V.

المساهمون: Johnson K., De Ridder W., Topf A., Bertoli M., Phillips L., De Jonghe P., Baets J., Deconinck T., Rakocevic Stojanovic V., Peric S., Durmus H., Jamal-Omidi S., Nafissi S., Mongini T., Lusakowska A., Busby M., Miller J., Norwood F., Hudson J., Barresi R., Lek M., Macarthur D.G., Straub V.

مصطلحات موضوعية: Muscle disease, Muscular dystrophy, Myopathy, Neuromuscular, Adult, Ethnic Group, Female, Human, Magnetic Resonance Imaging, Male, Middle Aged, Muscle, Skeletal, Muscular Disease, Muscular Dystrophies, Limb-Girdle, Mutation, Transcription Factor, Tripartite Motif Protein, Ubiquitin-Protein Ligases

Relation: info:eu-repo/semantics/altIdentifier/pmid/29921608; info:eu-repo/semantics/altIdentifier/wos/WOS:000471115600024; volume:90; issue:4; firstpage:490; lastpage:493; numberofpages:4; journal:JOURNAL OF NEUROLOGY, NEUROSURGERY AND PSYCHIATRY; http://hdl.handle.net/2318/1786348; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85063253675

الاتاحة: http://hdl.handle.net/2318/1786348
https://doi.org/10.1136/jnnp-2018-318288

المؤلفون: Fatehi, F., Okhovat, A. A., Nilipour, Y., Mroczek, M., Straub, V., Töpf, A., Palibrk, A., Peric, S., Rakocevic Stojanovic, V., Najmabadi, H., Nafissi, S.

المساهمون: Ultragenyx Pharmaceutical, Genzyme, National Heart, Lung, and Blood Institute, Muscular Dystrophy UK, National Human Genome Research Institute, National Eye Institute, Limb Girdle Muscular Dystrophy 2i Research Fund

المصدر: European Journal of Neurology ; volume 27, issue 11, page 2257-2266 ; ISSN 1351-5101 1468-1331

الاتاحة: http://dx.doi.org/10.1111/ene.14402
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fene.14402
https://onlinelibrary.wiley.com/doi/pdf/10.1111/ene.14402
https://onlinelibrary.wiley.com/doi/full-xml/10.1111/ene.14402

المؤلفون: Bozovic, I., Peric, S., Basta, I., Rakocevic-Stojanovic, V., Lavrnic, D., Stevic, Z., Radovanovic, S.

المصدر: Journal of Clinical Neuroscience ; volume 80, page 6-10 ; ISSN 0967-5868

الاتاحة: http://dx.doi.org/10.1016/j.jocn.2020.08.009
https://api.elsevier.com/content/article/PII:S0967586820314508?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S0967586820314508?httpAccept=text/plain

المؤلفون: Paunic, T., Peric, S., Parojcic, A., Dusanka, S. -P, Vujnic, M., Pesovic, J., Basta, I., Lavrnic, D., Rakocevic-Stojanovic, V.

المصدر: Acta Myologica
Scopus-Elsevier

مصطلحات موضوعية: musculoskeletal diseases, Adult, Male, paranoid, compulsive, Millon Clinical Multiaxial Inventory, Original Articles, Anxiety, Middle Aged, quality of life, personality, Compulsive Behavior, Educational Status, Humans, Myotonic Dystrophy, Female, Age of Onset, myotonic dystrophy type 2, Somatoform Disorders, Paranoid Behavior

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::6c2bc3d99cb51efc4b0a79a81cb46bc5
http://europepmc.org/articles/PMC5479103

المؤلفون: Peric S, Stevanovic J, Johnson K, Kosac A, Peric M, Brankovic M, Marjanovic A, Jankovic M, Banko B, Milenkovic S, Durdic M, Bozovic I, Glumac JN, Lavrnic D, Maksimovic R, Milic-Rasic V, Rakocevic-Stojanovic V

المصدر: Acta Myologica, 1 September 2019

Relation: https://eprints.ncl.ac.uk/262285

الاتاحة: https://eprints.ncl.ac.uk/262285