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American Journal of Medical Genetics|January 1, 1987
Progressive form of multiple pterygium syndrome in association with nemalin-myopathy: report of a female followed for twelve yearsF Papadia, N Longo, L Serlenga, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 3, 2006
Classification of amyotrophic lateral sclerosis cases at presentation in epidemiological studiesS Zoccolella, E Beghi, L Serlenga, et al.
Rivista Di Neurologia|September 1, 1987
[Recessive hereditary ataxia with early onset. Clinical study of 27 cases]L Serlenga, M Trizio, G Pozio, et al.
European Neurology|January 1, 1982
Schwartz-Jampel syndrome with autosomal-dominant inheritanceE Ferrannini, T Perniola, G Krajewska, et al.
Revue Neurologique|September 1, 1975
[Oculopharyngeal myopathy. Histochemical observation of the muscles and concentration of immunoglobulins in the serum of an Italian family]G Campanella, A Filla, L Serlenga, et al.
Acta Neurologica|August 1, 1992
[Eye movement disorders in hereditary degenerative ataxia. Electro-oculographic study of 11 cases]L Serlenga, F Falco, V Castaldo, et al.
Rivista Di Patologia Nervosa E Mentale|March 1, 1983
[Lecithin therapy of hereditary ataxia]M Trizio, G Pozio, L Margari, et al.
Clinical Rheumatology|September 12, 2002
Mitochondrial disease mimicking polymyositis: a case reportA Corrado, F P Cantatore, L Serlenga, et al.
Neurology|January 16, 2008
Elevated plasma homocysteine levels in patients with amyotrophic lateral sclerosisS Zoccolella, I L Simone, P Lamberti, et al.
European Neurology|January 1, 1997
Freezing gait in Parkinson's diseaseP Lamberti, S Armenise, V Castaldo, et al.
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