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Mostrati risultati da 1 a 20 di 27
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Open prospective study on oxcarbazepine in epilepsy in children: a preliminary report. 2006 Franzoni E;Garone C;Sarajlija J;Gualandi S;Malaspina E;Cecconi I;Moscano FC;Marchiani V
Unusual diagnosis in a child suffering from juvenile Alexander disease: clinical and imaging report. 2006 Franzoni E;Van der Knaap MS;Errani A;Colonnelli MC;Bracceschi R;Malaspina E;Moscano FC;Garone C;Sarajlija J;Zimmerman RA;Salomons GS;Bernardi B
Preliminary report on effects of oxcarbazepine-treatment on serum lipid levels in children. 2006 Franzoni E;Marchiani V;Cecconi I;Moscano FC;Gualandi S;Garone C;Sarajlija J;Malaspina E
Topiramate: effects on serum lipids and lipoproteins levels in children. 2007 Franzoni E;Verrotti A;Sarajlija J;Garone C;Matricardi S;Salerno GG;Monti M;Chiarelli F
No kinetic interaction between levetiracetam and cyclosporine: a case report. 2007 Franzoni E;Sarajlija J;Garone C;Malaspina E;Marchiani V
Levetiracetam or oxcarbazepine as monotherapy in newly diagnosed benign epilepsy of childhood with centrotemporal spikes (BECTS): an open-label, parallel group trial. 2007 Coppola G;Franzoni E;Verrotti A;Garone C;Sarajlija J;Operto FF;Pascotto A
Prospective study on long-term treatment with oxcarbazepine in pediatric epilepsy. 2009 Franzoni E;Gentile V;Pellicciari A;Garone C;Iero L;Gualandi S;Cordelli DM;Cecconi I;Moscano FC;Marchiani V;Errani A
SAFA: A new measure to evaluate psychiatric symptoms detected in a sample of children and adolescents affected by eating disorders. Correlations with risk factors. 2009 Franzoni E;Monti M;Pellicciari A;Muratore C;Verrotti A;Garone C;Cecconi I;Iero L;Gualandi S;Savarino F;Gualandi P
Progressive cerebral white matter involvement in a patient with Congenital Cataracts Facial Dysmorphisms Neuropathy (CCFDN). 2010 Cordelli DM;Garone C;Marchiani V;Lodi R;Tonon C;Ferrari S;Seri M;Franzoni E
Metabolic myopathies. 2010 DiMauro S;Garone C;Naini A
Intracerebral large artery disease in Aicardi-Goutières syndrome implicates SAMHD1 in vascular homeostasis. 2010 Ramesh V;Bernardi B;Stafa A;Garone C;Franzoni E;Abinun M;Mitchell P;Mitra D;Friswell M;Nelson J;Shalev SA;Rice GI;Gornall H;Szynkiewicz M;Aymard F;Ganesan V;Prendiville J;Livingston JH;Crow YJ
A new case of idiopathic hemiplegia hemiconvulsion syndrome. 2010 Franzoni E;Garone C;Marchiani V;Brunetto D;Tonon C;Lodi R;Bernardi B
Historical perspective on mitochondrial medicine. 2010 DiMauro S;Garone C
FA2H-related disorders: a novel c.270+3A>T splice-site mutation leads to a complex neurodegenerative phenotype. 2011 Garone C;Pippucci T;Cordelli DM;Zuntini R;Castegnaro G;Marconi C;Graziano C;Marchiani V;Verrotti A;Seri M;Franzoni E
Clinical and genetic spectrum of mitochondrial neurogastrointestinal encephalomyopathy. 2011 Garone C;Tadesse S;Hirano M
Metabolic disorders of fetal life: glycogenoses and mitochondrial defects of the mitochondrial respiratory chain. 2011 Dimauro S;Garone C
Next-generation sequencing reveals DGUOK mutations in adult patients with mitochondrial DNA multiple deletions. 2012 Ronchi D;Garone C;Bordoni A;Gutierrez Rios P;Calvo SE;Ripolone M;Ranieri M;Rizzuti M;Villa L;Magri F;Corti S;Bresolin N;Mootha VK;Moggio M;DiMauro S;Comi GP;Sciacco M
Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus. 2012 Anderson BH;Kasher PR;Mayer J;Szynkiewicz M;Jenkinson EM;Bhaskar SS;Urquhart JE;Daly SB;Dickerson JE;O'Sullivan J;Leibundgut EO;Muter J;Abdel-Salem GM;Babul-Hirji R;Baxter P;Berger A;Bonafé L;Brunstom-Hernandez JE;Buckard JA;Chitayat D;Chong WK;Cordelli DM;Ferreira P;Fluss J;Forrest EH;Franzoni E;Garone C;Hammans SR;Houge G;Hughes I;Jacquemont S;Jeannet PY;Jefferson RJ;Kumar R;Kutschke G;Lundberg S;Lourenço CM;Mehta R;Naidu S;Nischal KK;Nunes L;Ounap K;Philippart M;Prabhakar P;Risen SR;Schiffmann R;Soh C;Stephenson JB;Stewart H;Stone J;Tolmie JL;van der Knaap MS;Vieira JP;Vilain CN;Wakeling EL;Wermenbol V;Whitney A;Lovell SC;Meyer S;Livingston JH;Baerlocher GM;Black GC;Rice GI;Crow YJ
Molecular diagnosis of infantile mitochondrial disease with targeted next-generation sequencing. 2012 Calvo SE;Compton AG;Hershman SG;Lim SC;Lieber DS;Tucker EJ;Laskowski A;Garone C;Liu S;Jaffe DB;Christodoulou J;Fletcher JM;Bruno DL;Goldblatt J;Dimauro S;Thorburn DR;Mootha VK
CoQ(10) deficiencies and MNGIE: two treatable mitochondrial disorders. 2012 Hirano M;Garone C;Quinzii CM
Mostrati risultati da 1 a 20 di 27
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