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The International Journal of Artificial Organs|November 1, 1994
Removal of antiacetylcholine receptor antibodies by protein-A immunoadsorption in myasthenia gravisE Berta, P Confalonieri, O Simoncini, et al.Neuromuscular Disorders : NMD|March 4, 1999
Transforming growth factor-beta1 and fibrosis in congenital muscular dystrophiesP Bernasconi, C Di Blasi, M Mora, et al.Muscle & Nerve|July 1, 1983
Content of methylhistidines in normal and pathological human skeletal musclesE Mussini, F Cornelio, F Dworzak, et al.Pediatric Research|September 1, 1988
Hepatic and muscular presentations of carnitine palmitoyl transferase deficiency: two distinct entitiesF Demaugre, J P Bonnefont, G Mitchell, et al.American Journal of Human Genetics|January 1, 1995
A 1.5-Mb deletion in 17p11.2-p12 is frequently observed in Italian families with hereditary neuropathy with liability to pressure palsiesD Lorenzetti, D Pareyson, A Sghirlanzoni, et al.Nephron|January 1, 1989
L-carnitine addition to dialysis fluid. A therapeutic alternative for hemodialysis patientsG M Vacha, G Giorcelli, S d'Iddio, et al.Italian Journal of Neurological Sciences|May 1, 1981
Myasthenia gravis. Anti-acetylcholine receptor antibodiesD Cerrato, C Ariano, L La Mantia, et al.Neurology|November 1, 1984
Calcium and magnesium content in fetuses at risk and prenecrotic Duchenne muscular dystrophyT E Bertorini, F Cornelio, S K Bhattacharya, et al.Journal of Autoimmunity|August 1, 1990
Increased incidence of certain TCR and HLA genes associated with myasthenia gravis in ItaliansR Mantegazza, J R Oksenberg, F Baggi, et al.Biochemical Medicine and Metabolic Biology|August 1, 1994
Isolation of a new gene in the Friedreich ataxia candidate region on human chromosome 9 by cDNA direct selectionM Pandolfo, A Pizzuti, E Redolfi, et al.Pageof 16