Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Ivana, Petrovic Djordjevic"'
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:
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:
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