Zobrazeno 1 - 10
of 98
pro vyhledávání: '"Burnei G"'
Publikováno v:
Annals of Clinical and Medical Case Reports.
Publikováno v:
Journal of Medicine and Life
This paper presented a special case and shortly described the congenital malformations of a child operated at the age of 2 years and 7 months. Medical literature does not mention the cases of double or triple congenital scoliosis. 54 patients were tr
Publikováno v:
Journal of Medicine and Life
Rationale::In its most severe form, developmental dysplasia of the hip (DDH) is one of the most common congenital malformations. Uncorrected developmental dysplasia of the hip is associated with long-term morbidity such as gait abnormalities, chronic
Autor:
Burnei, G.1,2,3 mscburnei@yahoo.com, Gavriliu, S.1,2,3, Vlad, C.1, Georgescu, I.1, Ghita, R. A.1,3, Dughilă, C.1,3, Japie, E. M.1, Onilă, A.1
Publikováno v:
Journal of Medicine & Life. Jul-Sep2015, Vol. 8 Issue 3, p388-397. 10p.
Publikováno v:
Journal of Medicine and Life
This paper presented a special case and shortly described the congenital malformations of a child operated at the age of 2 years and 7 months. Medical literature does not mention the cases of double or triple congenital scoliosis. 54 patients were tr
Autor:
Iagăru, N.1 nicolae.iagaru@gmail.com, Burnei, G.2, Arndt, R.3, Plaiasu, Vasilica4, Enculescu, Augustina2, Vlad, C.2
Publikováno v:
Romanian Journal of Rheumatology / Revista Romana de Reumatologie. 2014, Vol. 23 Issue 4, p216-220. 5p.
Autor:
Popescu, M. D.1,2 popescumariadelia@yahoo.com, Burnei, G.1,2, Draghici, L.1,3, Draghici, I.1,2
Publikováno v:
Journal of Medicine & Life. Oct-Dec2014, Vol. 7 Issue 4, p563-566. 4p.
Autor:
Burnei, G.1,2,3 mscburnei@yahoo.com, Gavriliu, Ş.1,2,3, Nepaliuc, I.4, Vlad, C.2,3, Drăgoescu, M.2, Georgescu, I.2,3, Ghita, R. A.2, Muntean, L.5, Pârvan, A. A.6, Dughilă, C.7, Ţiripa, I.2, Hamei, Ş.8, Klinaku, l.9
Publikováno v:
Journal of Medicine & Life. Oct-Dec2014, Vol. 7 Issue 4, p595-600. 6p.
Publikováno v:
European Spine Journal. 23:262-266
Even if diastematomyelia is a rare condition, it always has to be identified in case of diagnosing and treating a case of congenital scoliosis. The consequence of missing the diagnosis of such a malformation may be devastating to the involved patient
Autor:
Burnei, G.1, Ghiţă, R. A.1, Pârvan, A. A.2, Japie, E.1, Gavriliu, Ș1 banteo@gmail.com, Georgescu, I.1, Nayef, T. El.1, Ţiripa, I.1, Hamei, Ş3
Publikováno v:
Journal of Medicine & Life. Oct-Dec2013, Vol. 6 Issue 4, p365-368. 4p.