DI MAURO, ROSSANA SIMONA

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Dominantly inherited mitochondrial myopathy with multiple deletions of mitochondrial DNA: Clinical, morphologic, and biochemical studies

1991 Servidei, S.; Zeviani, M.; Manfredi, G.; Ricci, E.; Silvestri, G.; Bertini, E.; Gellera, C.; Di Mauro, S.; Di Donate, S.; Tonali, P.

Hepatocerebral form of mitochondrial DNA depletion syndrome: Novel MPV17 mutations

2008 Spinazzola, A.; Santer, R.; Akman, O. H.; Tsiakas, K.; Schaefer, H.; Ding, X.; Karadimas, C. L.; Shanske, S.; Ganesh, J.; Di Mauro, S.; Zeviani, M.

MELAS syndrome: characteristic migrainous and epileptic features and maternal transmission

1988 Montagna, P; Gallassi, R; Medori, R; Govoni, E; Zeviani, M; Di Mauro, S; Lugaresi, E; Andermann, F

Titolo	Data di pubblicazione	Autori	Rivista	Serie	Titolo libro
Dominantly inherited mitochondrial myopathy with multiple deletions of mitochondrial DNA: Clinical, morphologic, and biochemical studies	1991	Servidei S.Zeviani M.Manfredi G.Ricci E.Silvestri G.Bertini E.Gellera C.Di Mauro S.Di Donate S.Tonali P. + -	NEUROLOGY	-	-
Hepatocerebral form of mitochondrial DNA depletion syndrome: Novel MPV17 mutations	2008	Spinazzola A.Santer R.Akman O. H.Tsiakas K.Schaefer H.Ding X.Karadimas C. L.Shanske S.Ganesh J.Di Mauro S.Zeviani M. + -	ARCHIVES OF NEUROLOGY	-	-
MELAS syndrome: characteristic migrainous and epileptic features and maternal transmission	1988	Montagna, PGallassi, RMedori, RGovoni, EZeviani, MDi Mauro, SLugaresi, EAndermann, F + -	NEUROLOGY	-	-