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Annals of Human Genetics|April 23, 2005
Analysis of dystrophin gene deletions indicates that the hinge III region of the protein correlates with disease severityA Carsana, G Frisso, M R Tremolaterra, et al.Molecular and Cellular Probes|August 1, 1996
Allele frequency distributions at several variable number of tandem repeat (VNTR) and short tandem repeat (STR) loci in a restricted Caucasian population from south Italy and their evaluation for paternity and forensic useL Pastore, E Vuttariello, C Sarrantonio, et al.Clinical Chemistry|August 1, 1996
Differential diagnosis between hepatocellular carcinoma and cirrhosis through a discriminant function based on results for serum analytesG Castaldo, G Oriani, M M Lofrano, et al.Journal of Medical Genetics|June 1, 1996
Molecular epidemiology of cystic fibrosis mutations and haplotypes in southern Italy evaluated with an improved semiautomated robotic procedureG Castaldo, E Rippa, G Sebastio, et al.Neurobiology of Aging|November 30, 2005
Bilateral effects of unilateral intrastriatal GDNF on locomotor-excited and nonlocomotor-related striatal neurons in aged F344 ratsJohn A Stanford, Michael F Salvatore, Barry M Joyce, et al.Experimental Neurology|April 5, 2024
Aging accelerates locomotor decline in PINK1 knockout rats in association with decreased nigral, but not striatal, dopamine and tyrosine hydroxylase expressionIsabel Soto, Robert McManus, Walter Navarrete, et al.Minerva Urologica E Nefrologica = the Italian Journal of Urology and Nephrology|June 15, 2004
Gender and the progression of chronic renal diseases: does apoptosis make the difference?M T Gandolfo, D Verzola, F Salvatore, et al.Movement Disorders : Official Journal of the Movement Disorder Society|June 21, 2017
Ceftriaxone reduces L-dopa-induced dyskinesia severity in 6-hydroxydopamine parkinson's disease modelTanya Chotibut, Samantha Meadows, Ella A Kasanga, et al.Neuroscience|June 21, 2019
Glatiramer Acetate Reverses Motor Dysfunction and the Decrease in Tyrosine Hydroxylase Levels in a Mouse Model of Parkinson's DiseaseMadeline J Churchill, Mark A Cantu, Ella A Kasanga, et al.Clinical Chemistry|July 1, 1999
Detection of five rare cystic fibrosis mutations peculiar to Southern Italy: implications in screening for the disease and phenotype characterization for patients with homozygote mutationsG Castaldo, A Fuccio, C Cazeneuve, et al.Pageof 63