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Items: 1 to 50 of 51

1.

Autophagy markers LC3 and p62 accumulate in immune-mediated necrotizing myopathy.

Girolamo F, Lia A, Annese T, Giannini M, Amati A, D'Abbicco D, Tampoia M, Virgintino D, Ribatti D, Serlenga L, Iannone F, Trojano M.

Muscle Nerve. 2019 Sep;60(3):315-327. doi: 10.1002/mus.26608. Epub 2019 Jun 21.

PMID:
31172530
2.

Overexpression of autophagic proteins in the skeletal muscle of sporadic inclusion body myositis.

Girolamo F, Lia A, Amati A, Strippoli M, Coppola C, Virgintino D, Roncali L, Toscano A, Serlenga L, Trojano M.

Neuropathol Appl Neurobiol. 2013 Dec;39(7):736-49. doi: 10.1111/nan.12040.

PMID:
23452291
3.

Mitochondrial genome aberrations in skeletal muscle of patients with motor neuron disease.

Artuso L, Zoccolella S, Favia P, Amati A, Capozzo R, Logroscino G, Serlenga L, Simone I, Gasparre G, Petruzzella V.

Amyotroph Lateral Scler Frontotemporal Degener. 2013 May;14(4):261-6. doi: 10.3109/21678421.2012.735239. Epub 2012 Oct 24.

PMID:
23134511
4.

Clinical features and new molecular findings in muscle phosphofructokinase deficiency (GSD type VII).

Musumeci O, Bruno C, Mongini T, Rodolico C, Aguennouz M, Barca E, Amati A, Cassandrini D, Serlenga L, Vita G, Toscano A.

Neuromuscul Disord. 2012 Apr;22(4):325-30. doi: 10.1016/j.nmd.2011.10.022. Epub 2011 Nov 30.

PMID:
22133655
5.

Autoimmune autonomic ganglionopathy: a possible postganglionic neuropathy.

Manganelli F, Dubbioso R, Nolano M, Iodice R, Pisciotta C, Provitera V, Ruggiero L, Serlenga L, Barbieri F, Santoro L.

Arch Neurol. 2011 Apr;68(4):504-7. doi: 10.1001/archneurol.2011.60.

PMID:
21482929
6.

A new locus on 3p23-p25 for an autosomal-dominant limb-girdle muscular dystrophy, LGMD1H.

Bisceglia L, Zoccolella S, Torraco A, Piemontese MR, Dell'Aglio R, Amati A, De Bonis P, Artuso L, Copetti M, Santorelli FM, Serlenga L, Zelante L, Bertini E, Petruzzella V.

Eur J Hum Genet. 2010 Jun;18(6):636-41. doi: 10.1038/ejhg.2009.235. Epub 2010 Jan 13.

7.

Molecular analysis in a family presenting with a mild form of late-onset autosomal dominant chronic progressive external ophthalmoplegia.

Negro R, Zoccolella S, Dell'aglio R, Amati A, Artuso L, Bisceglia L, Lavolpe V, Papa S, Serlenga L, Petruzzella V.

Neuromuscul Disord. 2009 Jun;19(6):423-6. doi: 10.1016/j.nmd.2009.04.008. Epub 2009 May 9.

PMID:
19428252
8.

Motoneuron disease after electric injury: a case report.

Zoccolella S, Masi G, Mezzapesa D, Carnicella F, Iliceto G, Lamberti P, Serlenga L.

Neurol Sci. 2008 Feb;29(1):47-9. doi: 10.1007/s10072-008-0860-2. Epub 2008 Apr 1.

PMID:
18379742
9.

Elevated plasma homocysteine levels in patients with amyotrophic lateral sclerosis.

Zoccolella S, Simone IL, Lamberti P, Samarelli V, Tortelli R, Serlenga L, Logroscino G.

Neurology. 2008 Jan 15;70(3):222-5. doi: 10.1212/01.wnl.0000297193.53986.6f.

PMID:
18195267
10.

Predictors of long survival in amyotrophic lateral sclerosis: a population-based study.

Zoccolella S, Beghi E, Palagano G, Fraddosio A, Guerra V, Samarelli V, Lepore V, Simone IL, Lamberti P, Serlenga L, Logroscino G.

J Neurol Sci. 2008 May 15;268(1-2):28-32. Epub 2007 Nov 19.

PMID:
18021808
11.

Analysis of survival and prognostic factors in amyotrophic lateral sclerosis: a population based study.

Zoccolella S, Beghi E, Palagano G, Fraddosio A, Guerra V, Samarelli V, Lepore V, Simone IL, Lamberti P, Serlenga L, Logroscino G; SLAP Registry.

J Neurol Neurosurg Psychiatry. 2008 Jan;79(1):33-7. Epub 2007 Jun 5.

PMID:
17550991
12.

ALS multidisciplinary clinic and survival. Results from a population-based study in Southern Italy.

Zoccolella S, Beghi E, Palagano G, Fraddosio A, Guerra V, Lepore V, Simone IL, Lamberti P, Serlenga L, Logroscino G.

J Neurol. 2007 Aug;254(8):1107-12. Epub 2007 Apr 13.

PMID:
17431705
13.

Riluzole and amyotrophic lateral sclerosis survival: a population-based study in southern Italy.

Zoccolella S, Beghi E, Palagano G, Fraddosio A, Guerra V, Samarelli V, Lepore V, Simone IL, Lamberti P, Serlenga L, Logroscino G; SLAP registry.

Eur J Neurol. 2007 Mar;14(3):262-8.

PMID:
17355545
14.

A case of vacuolar myopathy during the course of chronic hepatitis C.

Zoccolella S, Serlenga L, Amati A, Lavolpe V, Minerva N, Agremorz M, Toscano A, Lamberti P.

Funct Neurol. 2006 Jul-Sep;21(3):167-9.

PMID:
17049137
15.

Predictors of delay in the diagnosis and clinical trial entry of amyotrophic lateral sclerosis patients: a population-based study.

Zoccolella S, Beghi E, Palagano G, Fraddosio A, Samarelli V, Lamberti P, Lepore V, Serlenga L, Logroscino G; SLAP registry.

J Neurol Sci. 2006 Dec 1;250(1-2):45-9. Epub 2006 Aug 22.

PMID:
16920152
16.

Signs and symptoms at diagnosis of amyotrophic lateral sclerosis: a population-based study in southern Italy.

Zoccolella S, Beghi E, Palagano G, Fraddosio A, Samarelli V, Lamberti P, Lepore V, Serlenga L, Logroscino G; SLAP registry.

Eur J Neurol. 2006 Jul;13(7):789-92.

PMID:
16834713
17.

Unusual clinical presentation of a patient carrying a novel single 1.8 kb deletion of mitochondrial DNA.

Zoccolella S, Torraco A, Amati A, Lamberti P, Serlenga L, Papa S, Petruzzella V.

Funct Neurol. 2006 Jan-Mar;21(1):39-41.

PMID:
16735000
18.

Classification of amyotrophic lateral sclerosis cases at presentation in epidemiological studies.

Zoccolella S, Beghi E, Serlenga L, Logroscino G.

Neurol Sci. 2005 Dec;26(5):330-3.

PMID:
16388367
19.

Incidence of amyotrophic lateral sclerosis in southern Italy: a population based study.

Logroscino G, Beghi E, Zoccolella S, Palagano R, Fraddosio A, Simone IL, Lamberti P, Lepore V, Serlenga L; SLAP Registry.

J Neurol Neurosurg Psychiatry. 2005 Aug;76(8):1094-8.

20.

Cerebellar ataxia as atypical manifestation of the 3243A>G MELAS mutation.

Petruzzella V, Zoccolella S, Amati A, Torraco A, Lamberti P, Carnicella F, Serlenga L, Papa S.

Clin Genet. 2004 Jan;65(1):64-5. No abstract available.

PMID:
15032978
21.

ALS-plus: 5 cases of concomitant amyotrophic lateral sclerosis and parkinsonism.

Zoccolella S, Palagano G, Fraddosio A, Russo I, Ferrannini E, Serlenga L, Maggio F, Lamberti S, Iliceto G.

Neurol Sci. 2002 Sep;23 Suppl 2:S123-4.

PMID:
12548374
22.

Mitochondrial disease mimicking polymyositis: a case report.

Corrado A, Cantatore FP, Serlenga L, Amati A, Petruzzella V, Lapadula G.

Clin Rheumatol. 2002 Sep;21(5):411-4.

PMID:
12223994
23.

A case of concomitant amyotrophic lateral sclerosis and HIV infection.

Zoccolella S, Carbonara S, Minerva D, Palagano G, Bruno F, Ferrannini E, Iliceto G, Serlenga L, Lamberti P.

Eur J Neurol. 2002 Mar;9(2):180-2. No abstract available.

PMID:
11882063
24.

A randomized controlled trial of recombinant interferon beta-1a in ALS. Italian Amyotrophic Lateral Sclerosis Study Group.

Beghi E, ChiĆ² A, Inghilleri M, Mazzini L, Micheli A, Mora G, Poloni M, Riva R, Serlenga L, Testa D, Tonali P.

Neurology. 2000 Jan 25;54(2):469-74.

PMID:
10668716
25.

Spinocerebellar ataxia type 2 in southern Italy: a clinical and molecular study of 30 families.

Filla A, De Michele G, Santoro L, Calabrese O, Castaldo I, Giuffrida S, Restivo D, Serlenga L, Condorelli DF, Bonuccelli U, Scala R, Coppola G, Caruso G, Cocozza S.

J Neurol. 1999 Jun;246(6):467-71.

PMID:
10431773
26.

Mitochondrial DNA deletions in oculopharyngeal muscular dystrophy.

Lezza AM, Cormio A, Gerardi P, Silvestri G, Servidei S, Serlenga L, Cantatore P, Gadaleta MN.

FEBS Lett. 1997 Nov 24;418(1-2):167-70.

27.

Freezing gait in Parkinson's disease.

Lamberti P, Armenise S, Castaldo V, de Mari M, Iliceto G, Tronci P, Serlenga L.

Eur Neurol. 1997;38(4):297-301.

PMID:
9434089
28.

Autosomal dominant cerebellar ataxia type I. Clinical and molecular study in 36 Italian families including a comparison between SCA1 and SCA2 phenotypes.

Filla A, De Michele G, Campanella G, Perretti A, Santoro L, Serlenga L, Ragno M, Calabrese O, Castaldo I, De Joanna G, Cocozza S.

J Neurol Sci. 1996 Oct;142(1-2):140-7.

PMID:
8902734
29.

Short-latency median nerve somatosensory evoked potentials in three cases of parkinsonism and dopa responsive dystonia.

Margari L, de Mari M, Lamberti P, Iliceto G, Serlenga L, Perniola T, Rossini PM, Ferrari E.

Funct Neurol. 1995 Mar-Apr;10(2):99-105.

PMID:
7557558
30.

Effect of L-dopa on oculogyric crises in a case of dopa-responsive dystonia.

Lamberti P, de Mari M, Iliceto G, Caldarola M, Serlenga L.

Mov Disord. 1993 Apr;8(2):236-7. No abstract available.

PMID:
8474501
31.

[Eye movement disorders in hereditary degenerative ataxia. Electro-oculographic study of 11 cases].

Serlenga L, Falco F, Castaldo V, Caldarazzo M, Federici A.

Acta Neurol (Napoli). 1992 Aug-Dec;14(4-6):440-50. Italian.

PMID:
1293987
32.

[Plasmapheresis in neuromuscular diseases. Personal cases].

Affuso R, Dimonte D, Pagliarulo R, Serlenga L, Simone IL, Specchio LM, Lamberti P.

Acta Neurol (Napoli). 1989 Apr-Jun;11(2-3):200-10. Italian.

PMID:
2782116
33.

[Recessive hereditary ataxia with early onset. Clinical study of 27 cases].

Serlenga L, Trizio M, Pozio G, Oteri G, Caldarazzo M.

Riv Neurol. 1987 Sep-Oct;57(5):285-9. Italian.

PMID:
3445070
34.

Hereditary sensory and autonomic neuropathy presenting as ataxia.

Serlenga L, Trizio M, Pozio G, Di Pietro F.

Acta Neurol (Napoli). 1987 Feb;9(1):12-8. No abstract available.

PMID:
3577864
35.
36.

[Sporadic distal myopathy with early onset. Description of a case].

Pozio G, Trizio M, Trojano M, Lochi L, Serlenga L.

Acta Neurol (Napoli). 1986 Jun;8(3):304-9. Italian. No abstract available.

PMID:
3739780
37.

[HMSN type II with autosomal recessive transmission. Description of 2 cases with early onset].

Trizio M, Pozio G, Coviello V, Serlenga L.

Acta Neurol (Napoli). 1986 Jun;8(3):234-9. Italian. No abstract available.

PMID:
3017060
38.

Central core disease and congenital scoliosis. Study of one case.

Pozio G, De Giorgi G, Trizio W, Mariani G, Trizio M, Serlenga L.

Acta Neurol (Napoli). 1985 Oct;7(5):425-31. No abstract available.

PMID:
4061153
39.

Centronuclear myopathy. Report of a sporadic case.

Serlenga L, Pozio G, Trizio M, Pavia T.

Acta Neurol (Napoli). 1985 Oct;7(5):416-24. No abstract available.

PMID:
4061152
40.

[Lecithin therapy of hereditary ataxia].

Trizio M, Pozio G, Margari L, Massagli A, Serlenga L.

Riv Patol Nerv Ment. 1983 Mar-Apr;104(2):49-59. Italian.

PMID:
6679921
41.

Friedreich's ataxia: electrophysiological and histological findings.

Caruso G, Santoro L, Perretti A, Serlenga L, Crisci C, Ragno M, Barbieri F, Filla A.

Acta Neurol Scand. 1983 Jan;67(1):26-40.

PMID:
6837264
42.

Schwartz-Jampel syndrome with autosomal-dominant inheritance.

Ferrannini E, Perniola T, Krajewska G, Serlenga L, Trizio M.

Eur Neurol. 1982;21(3):137-46.

PMID:
7117301
43.

[Vestibulo-oculomotor reflexes in relation to the level of consciousness. V. Changes induced by non-hypnotic psychopharmacological agents in induced nystagmus in man].

Puca F, Genco S, Serlenga L, Brignone A, Specchio LM.

Riv Neurol. 1976 Sep-Oct;46(5):367-77. Italian. No abstract available.

PMID:
1025679
44.

[Effects of apomorphine on the vestibulo-ocular reflex in normal subjects and in patients with parkinsonism].

Serlenga L, Genco S, Puca FM, Specchio LM, Brignone A.

Boll Soc Ital Biol Sper. 1975 Oct 30;51(20):1382-6. Italian. No abstract available.

PMID:
1085153
45.

[Effects of dopamine on the vestibulo-ocular reflex in parkinsonism].

Genco S, Puca FM, Serlenga L, Brignone A, Specchio LM.

Boll Soc Ital Biol Sper. 1975 Oct 30;51(20):1375-81. Italian. No abstract available.

PMID:
1085152
46.

[Modifications induced by antidepressant drugs on the vestibulo-ocular reflex in man].

Specchio LM, Brignone A, Puca FM, Genco S, Serlenga L.

Boll Soc Ital Biol Sper. 1975 Oct 30;51(20):1369-74. Italian. No abstract available.

PMID:
1085151
47.

[Oculopharyngeal myopathy. Histochemical observation of the muscles and concentration of immunoglobulins in the serum of an Italian family].

Campanella G, Filla A, Serlenga L, Federico A, Buscaino GA.

Rev Neurol (Paris). 1975 Sep;131(9):615-28. French.

PMID:
1224116
48.

[Analysis of the patterns of potentials during normal nocturnal sleep and in the course of central depression induced with gamma-hydroxybutyrate].

Ventrella O, Brignone A, Genco S, Puca FM, Serlenga L.

Boll Soc Ital Biol Sper. 1974 Jun 15;50(11):752-8. Italian. No abstract available.

PMID:
4447691
49.

[Neuromelanin and schizophrenia. Preliminary histochemical study].

Buscaino GA, Gullotta F, De Giacomo P, Serlenga L, Perniola T.

Acta Neurol (Napoli). 1972 Mar-Apr;27(2):208-12. Italian. No abstract available.

PMID:
5042261
50.

[Unusual nueromusclular pathology. 2: Clinical, muscular histoenzymatic and electromyographic aspects of a case of generalized spastic rigidity causing falls (stiff-man syndrome?)].

Buscaino GA, Campanella G, Serlenga L, Labianca O.

Acta Neurol (Napoli). 1970 Sep-Oct;25(5):509-23. Italian. No abstract available.

PMID:
5491151

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