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Mostrati risultati da 1 a 20 di 875
Titolo Data di pubblicazione Autori Tipo File Abstract
Complex IV change in the mitochondria respiratory chain of chronic external ophtalmoplegia : a review of our cases 1985 N. BresolinL. BetG. MeolaA. BordoniE. Nobile-OrazioG. Scarlato + Article (author) -
Oculopharyngeal myopathy with partial cytochrome c oxidase deficiency 1986 N. BresolinE. Nobile-OrazioL. BetF. FortunatoG. Scarlato + Article (author) -
Progressive cytochrome c oxidase deficiency in a case of Kearns-Sayre syndrome: morphological, immunological, and biochemical studies in muscle biopsies and autopsy tissues 1987 N. BresolinL. BetE. Nobile-OrazioG. Scarlato + Article (author) -
Cytochrome c oxidase during human fetal development 1989 N. BresolinE. ScarpiniL. BetF. FortunatoG. Scarlato + Article (author) -
A CASE OF MITOCHONDRIAL MYOPATHY, LACTIC-ACIDOSIS AND COMPLEX-I DEFICIENCY 1990 L. BETN. BRESOLING. MEOLAF. FORTUNATO + Article (author) -
[Expression of a defect in the respiratory chain in cultured human cells] 1991 G. MeolaV. SansoneN. BresolinG. Comi + Article (author) -
Multiple deletions of mitochondrial DNA in a patient with periodic attacks of paralysis 1993 G. ComiN. BresolinG. Scarlato + Article (author) -
Muscle glucose-6-phosphate dehydrogenase deficiency: restoration of enzymatic activity in hybrid myotubes 1993 G. MeolaV. SansoneN. Bresolin + Article (author) -
Chronic progressive external ophthalmoplegia: A correlative study of quantitative molecular data and histochemical and biochemical profile 1994 N. BresolinG. ComiG. Scarlato + Article (author) -
Neural regulation of acid maltase in an unusual adult onset deficiency 1994 G. MeolaV. SansoneN. Bresolin + Article (author) -
Ryanodine receptor gene point mutation and malignant hyperthermia susceptibility 1995 G. ComiN. BresolinG. Scarlato + Article (author) -
Early-onset cerebellar ataxia, myoclonus and hypogonadism in a case of mitochondrial complex III deficiency treated with vitamins K3 and C 1995 N. BresolinL. Bet + Article (author) -
Encefalomiopatie mitocondriali. Simposi in Medicina Clinica. Rivista Medica degli Ospedali di Milano IRCCS Ospedale Maggiore di Milano, Niguarda Cà Granda, San Carlo Borromeo e di Sesto S. Giovanni. The role of Molecular genetics in neurological diagnosis. Masson 89, (2): 177-186, 1995 1995 C. AusendaN. BresolinY. Torrente Article (author) -
Il trapianto di Mioblasti nelle Miopatie ereditarie 1996 N. BresolinC.D. AusendaY. Torrente + Book Part (author) -
The influence of coenzyme Q(10) on total serum calcium concentration in two patients with Kearns-Sayre Syndrome and hypoparathyroidism 1996 G. ComiN. Bresolin + Article (author) -
In Vivo Biolistic Technique in Control and Mdx Dystrophic Mice 1996 N. BresolinG.P. ComiY. Torrente + Article (author) -
5'azacytidine enhances exogenous gene expression in muscle 1997 Y. TorrenteS. CortiG. ComiN. Bresolin + Article (author) -
Intra-Aortic injection of myoblasts in Mdx mice: genetic and technetium-99m cell labeling and biodistribution 1997 N. BresolinY. TorrenteG.P. Comi + Article (author) -
La sindrome di Usher 1998 S. CortiN. Bresolin + Article (author) -
Extracorporeal circulation as a new experimental pathway for myoblast implantation in mdx mice 1999 Y. TorrenteR. Del BoS. CortiG.P. ComiG. ScarlatoN. Bresolin + Article (author) -
Mostrati risultati da 1 a 20 di 875
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