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Cephalalgia : an International Journal of Headache|October 1, 2008
Correlation between abnormal brain excitability and emotional symptomatology in paediatric migraineM Valeriani, F Galli, S Tarantino, et al.Giornale Italiano Di Cardiologia|May 1, 1997
Restrictive cardiomyopathy due to desmin accumulation in a family with evidence of autosomal dominant inheritanceE Zachara, E Bertini, E Lioy, et al.Human Heredity|December 22, 1998
A novel mutation (R271X) in the myotubularin gene causes a severe miotubular myopathyA De Luca, I Torrente, M Mangino, et al.Acta Paediatrica (Oslo, Norway : 1992). Supplement|June 5, 2004
A mitochondrial ATPase 6 mutation is associated with Leigh syndrome in a family and affects proton flow and adenosine triphosphate output when modeled in Escherichia coliR Carrozzo, T Rizza, S Lucioli, et al.Human Molecular Genetics|March 1, 1997
Linkage mapping of benign familial infantile convulsions (BFIC) to chromosome 19qM Guipponi, F Rivier, F Vigevano, et al.Seizure|November 29, 2019
De novo Absence Status Epilepticus in a pediatric cohort: Electroclinical pattern in a multicenter Italian patients cohortC Pepi, E Cesaroni, P Striano, et al.Neurology|December 25, 2002
A severe variant of childhood ataxia with central hypomyelination/vanishing white matter leukoencephalopathy related to EIF21B5 mutationA Fogli, C Dionisi-Vici, F Deodato, et al.Muscle & Nerve|February 1, 1997
Maternally inherited cardiomyopathy: a new phenotype associated with the A to G AT nt.3243 of mitochondrial DNA (MELAS mutation)G Silvestri, E Bertini, S Servidei, et al.Law and Human Behavior|June 7, 2012
Field reliability of the SAVRY with juvenile probation officers: Implications for trainingGina M Vincent, Laura S Guy, Samantha L Fusco, et al.Current Medicinal Chemistry|February 7, 2012
Glutamate and multiple sclerosisM Frigo, M G Cogo, M L Fusco, et al.Pageof 29