Pregled bibliografske jedinice broj: 73485
Congenital muscular dystrophy (CMD) with merosin deficiency (MD) and leukoencephalopathy (L) - phenotyphe studies in two patients
Congenital muscular dystrophy (CMD) with merosin deficiency (MD) and leukoencephalopathy (L) - phenotyphe studies in two patients // European Journal of Paediatric Neurology / Dubowitz, Victor; Caesar, Paul (ur.).
London : Philadelphia (PA) : Sydney : Tokyo : Toronto: W.B. Saunders Company Ltd, 2001. (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 73485 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Congenital muscular dystrophy (CMD) with merosin deficiency (MD) and leukoencephalopathy (L) - phenotyphe studies in two patients
Autori
Cvitanović-Šojat, Ljerka ; Mejaški-Bošnjak, Vlatka ; Bonneman, C ; Mucić-Šucić, Branka ; Gojmerac, Tomislav ; Hajžić, Tomislav Franjo ; Hanefeld, Folker ; Šojat, T
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
European Journal of Paediatric Neurology
/ Dubowitz, Victor; Caesar, Paul - London : Philadelphia (PA) : Sydney : Tokyo : Toronto : W.B. Saunders Company Ltd, 2001
Skup
4th International Congress of the European Paediatric Neurology Society
Mjesto i datum
Baden-Baden, Njemačka, 12.09.2001. - 16.09.2001
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
Congenital muscular dystrophy; Merosin deficiency; Leukoencephalopathy
Sažetak
Our work has shown that in patients with unclassified CMD, MR of the brain may reveal a pattern of white matter abnormalities to suggest laminin-alpha2 (LA2) deficiency in muscle (also reffered to as merosin.
Izvorni jezik
Engleski
