Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Andreea Jercan"'
Autor:
Gabriela Neculae, Robert Adam, Andreea Jercan, Sorina Bădeliță, Catherina Tjahjadi, Mirela Draghici, Claudiu Stan, Jeroen J. Bax, Bogdan A. Popescu, Nina Ajmone Marsan, Daniel Coriu, Ruxandra Jurcuț
Publikováno v:
ESC Heart Failure, Vol 11, Iss 5, Pp 2825-2834 (2024)
Abstract Aims Systemic amyloidosis represents a heterogeneous group of diseases resulting from amyloid fibre deposition. The purpose of this study is to establish a differential diagnosis algorithm targeted towards the two most frequent subtypes of C
Externí odkaz:
https://doaj.org/article/70340846daa34f3497295c6b85d66e68
Autor:
Carmen Saguna, Nicoleta Mariana Berbec, Marian Platon, Alexandra Marcoci, Andreea Jercan, Andrei Colita, Mihai Emanuel Gherghe, Dana-Georgiana Nedelea, Romica Cergan, Cristian Scheau, Serban Dragosloveanu
Publikováno v:
Life, Vol 14, Iss 9, p 1124 (2024)
We present the case of a 66 year-old male patient who developed severe postoperative thrombocytopenia after revision total hip arthroplasty. The patient underwent surgery in a dedicated orthopedics hospital and was initially managed in the intensive
Externí odkaz:
https://doaj.org/article/da4e0df9d777424a949c6dec8ab20c3b
Autor:
Robert Daniel Adam, Daniel Coriu, Andreea Jercan, Sorina Bădeliţă, Bogdan A. Popescu, Thibaud Damy, Ruxandra Jurcuţ
Publikováno v:
ESC Heart Failure, Vol 8, Iss 4, Pp 2380-2396 (2021)
Abstract Cardiac amyloidosis is a restrictive cardiomyopathy determined by the accumulation of amyloid, which is represented by misfolded protein fragments in the cardiac extracellular space. The main classification of systemic amyloidosis is determi
Externí odkaz:
https://doaj.org/article/c781c9da04a2447cb4974a9852f8cd07
Autor:
Andreea Jercan, Amalia Ene, Ruxandra Jurcut, Mirela Draghici, Sorina Badelita, Mihaela Dragomir, Camelia Dobrea, Monica Popescu, Dumitru Jardan, Emanuel Stoica, Speranta Iacob, Ionela Codita, Claudiu Stan, Daniel Coriu
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-8 (2020)
Abstract Background In Romania, 23 patients have been diagnosed with hereditary transthyretin amyloidosis (ATTRh), 18 of whom have the Glu54Gln mutation. This retrospective cohort included all patients with Glu54Gln-mutated ATTRh who were diagnosed i
Externí odkaz:
https://doaj.org/article/c2b271c673c24582aaa937c8667f0036
Autor:
Dumitru Jardan, Andreea Jercan, Emanuel Stoica, Sorina Badelita, Amalia Ene, Ionela Codita, Mihaela Dragomir, Speranta Iacob, Monica Popescu, Claudiu Stan, Camelia Dobrea, Daniel Coriu, Ruxandra Jurcut, Mirela Draghici
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-8 (2020)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
Background In Romania, 23 patients have been diagnosed with hereditary transthyretin amyloidosis (ATTRh), 18 of whom have the Glu54Gln mutation. This retrospective cohort included all patients with Glu54Gln-mutated ATTRh who were diagnosed in Romania
Autor:
Mirela Draghici, Andreea Jercan, Sorina Nicoleta Badelita, Ruxandra Maria Irimia, Alexandra Eugenia Bastian, Camelia Dobrea, Monica Popescu, Daniel Coriu
Publikováno v:
Medicine. 100:e28267
Autor:
Speranta Iacob, Andreea Jercan, Sorina Badelita, Camelia Dobrea, Ruxandra Jurcut, Monica Popescu, Mihaela Ghioca, Razvan Iacob, Liana Gheorghe, Daniel Coriu
Publikováno v:
Journal of Hepatology. 73:S782
Autor:
Mirela Draghici, Andreea Jercan, Sorina Badelita, Daniel Coriu, Speranta Iacob, Emanuel Stoica
Publikováno v:
Amyloid. 26:31-32
Transthyretin hereditary amyloidosis is a rare disease and thus far considered to be limited to certain geographical areas. Recently, with the intensification of genetic screening possibilities, ne...
Publikováno v:
Documenta Haematologica. 34:39-44
Hereditary spherocytosis is an inherited hemolytic anemia due to red cell membrane defects, characterised by chronic hemolysis with different severity degrees, splenomegaly and microspherocytosis on the peripheral blood film. Among the possible compl
Autor:
Liliana Gheorghe, Daniel Coriu, Andreea Jercan, Sorina Badelita, Cristian Gheorghe, Speranta Iacob, Mihaela Lita, Razvan Iacob
Publikováno v:
Gastroenterology. 154:S-729