Zobrazeno 1 - 10
of 104
pro vyhledávání: '"Vidosava Rakocevic-Stojanovic"'
Autor:
Milija Mijajlovic, Ivo Bozovic, Aleksandra Pavlovic, Vidosava Rakocevic-Stojanovic, Sanja Gluscevic, Amalija Stojanovic, Ivana Basta, Giovanni Meola, Stojan Peric
Publikováno v:
Heliyon, Vol 10, Iss 5, Pp e26856- (2024)
Introduction: Myotonic dystrophy type 1 (DM1) and 2 (DM2) are genetically determined progressive muscular disorders with multisystemic affection, including brain involvement. Transcranial sonography (TCS) is a reliable diagnostic tool for the investi
Externí odkaz:
https://doaj.org/article/119b45579f9b4ba49855f8a94f9a9c72
Autor:
Stojan Peric, Jelena Zlatar, Luka Nikolic, Vukan Ivanovic, Jovan Pesovic, Ivana Petrovic Djordjevic, Svetlana Sreckovic, Dusanka Savic-Pavicevic, Giovanni Meola, Vidosava Rakocevic-Stojanovic
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
IntroductionMyotonic dystrophy type 2 (DM2) is a rare autosomal dominant multisystemic disease with highly variable clinical presentation. Several case reports and one cohort study suggested a significant association between DM2 and autoimmune diseas
Externí odkaz:
https://doaj.org/article/64b68df33c9d40bc8b3fb5062abb08d0
Autor:
Libby Wood, Guillaume Bassez, Corinne Bleyenheuft, Craig Campbell, Louise Cossette, Aura Cecilia Jimenez-Moreno, Yi Dai, Hugh Dawkins, Jorge Alberto Diaz Manera, Celine Dogan, Rasha el Sherif, Barbara Fossati, Caroline Graham, James Hilbert, Kristinia Kastreva, En Kimura, Lawrence Korngut, Anna Kostera-Pruszczyk, Christopher Lindberg, Bjorn Lindvall, Elizabeth Luebbe, Anna Lusakowska, Radim Mazanec, Giovani Meola, Liannna Orlando, Masanori P. Takahashi, Stojan Peric, Jack Puymirat, Vidosava Rakocevic-Stojanovic, Miriam Rodrigues, Richard Roxburgh, Benedikt Schoser, Sonia Segovia, Andriy Shatillo, Simone Thiele, Ivailo Tournev, Baziel van Engelen, Stanislav Vohanka, Hanns Lochmüller
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-11 (2018)
Abstract Background Myotonic Dystrophy is the most common form of muscular dystrophy in adults, affecting an estimated 10 per 100,000 people. It is a multisystemic disorder affecting multiple generations with increasing severity. There are currently
Externí odkaz:
https://doaj.org/article/cc2d675314b54dc3be1bfaec5e0a7e85
Autor:
Libby Wood, Guillaume Bassez, Corinne Bleyenheuft, Craig Campbell, Louise Cossette, Aura Cecilia Jimenez-Moreno, Yi Dai, Hugh Dawkins, Jordi Díaz-Manera, Celine Dogan, Rasha el Sherif, Barbara Fossati, Caroline Graham, James Hilbert, Kristinia Kastreva, En Kimura, Lawrence Korngut, Anna Kostera-Pruszczyk, Christopher Lindberg, Bjorn Lindvall, Elizabeth Luebbe, Anna Lusakowska, Radim Mazanec, Giovani Meola, Liannna Orlando, Masanori P. Takahashi, Stojan Peric, Jack Puymirat, Vidosava Rakocevic-Stojanovic, Miriam Rodrigues, Richard Roxburgh, Benedikt Schoser, Sonia Segovia, Andriy Shatillo, Simone Thiele, Ivailo Tournev, Baziel van Engelen, Stanislav Vohanka, Hanns Lochmüller
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-1 (2019)
The original version of this article [1] unfortunately included an error to an author’s name. Author Jordi Díaz-Manera was erroneously presented as Jorge Alberto Diaz Manera. The correct author name has been included in the author list of this Cor
Externí odkaz:
https://doaj.org/article/3d421795de054b8797ffba84621edb38
Autor:
Stojan Peric, Ilija Gunjic, Neda Delic, Olivera Stojiljkovic Tamas, Biljana Salak-Djokic, Jovan Pesovic, Ivana Petrovic Djordjevic, Vukan Ivanovic, Dusanka Savic-Pavicevic, Giovanni Meola, Vidosava Rakocevic-Stojanovic
Publikováno v:
Neuromuscular Disorders. 32:743-748
Myotonic dystrophy type 2 (DM2) is an autosomal dominant multisystemic disorder. Previous studies conducted on small cohorts of DM2 patients indicated presence of a cognitive dysfunction. We aimed to assess cognitive functions in a larger cohort of S
Autor:
Jelena Ilic Zivojinovic, Katarina Djurdjevic, Ivo Bozovic, Giovanni Meola, Marina Peric, Ana Azanjac Arsic, Ivana Basta, Vidosava Rakocevic-Stojanovic, Stojan Peric
Publikováno v:
Neurological Sciences.
Introduction Myotonic dystrophy type 1 (DM1) is the most prevalent muscular dystrophy in adults. People with DM1 might represent a high-risk population for respiratory infections, including COVID-19. Our aim was to evaluate the characteristics of COV
Autor:
Dejan Aleksic, Sanja Milenkovic, Milena Jankovic, Zorica Stevic, Vidosava Rakocevic-Stojanovic, Stojan Peric
Publikováno v:
Vojnosanitetski pregled. 80:87-89
Introduction. Histopathological findings of various inclusions were reported in the central nervous system of amyotrophic lateral sclerosis (ALS) patients but not in the peripheral nerves. Case report. We present a 66-year-old man with lower limb wea
Autor:
Jasmina Maksic, Nela Maksimovic, Lukas Rasulic, Olgica Milankov, Ana Marjanovic, Dragana Cvetkovic, Vidosava Rakocevic-Stojanovic, Ivana Novakovic
Publikováno v:
Vojnosanitetski pregled (2023) 80(3):201-207
Background/Aim. Duchenne muscular dystrophy (MD) and Becker MD are caused by mutations in the gene for dystrophin (DMD). They are X chromosome-linked recessive diseases where males are affected, and females are healthy carriers of the mutation in mos
Publikováno v:
Neuromuscular Disorders. 31:681-694
Myotonic dystrophy type 2 (DM2) is an autosomal dominant multisystemic disorder caused by CCTG repeats expansion in the first intron of the CNBP gene. In this review we focus on the brain involvement in DM2, including its pathogenic mechanisms, micro
Autor:
Vukan, Ivanovic, Stojan, Peric, Jovan, Pesovic, Radoje, Tubic, Ivo, Bozovic, Ivana, Petrovic Djordjevic, Dusanka, Savic-Pavicevic, Giovanni, Meola, Vidosava, Rakocevic-Stojanovic
Publikováno v:
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology.
Myotonic dystrophy type 2 (DM2) is a rare, multisystemic, autosomal dominant disease with highly variable clinical presentation. DM2 is considered to be highly underdiagnosed.The aim of this study was to determine which symptoms, signs, and diagnosti