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Items: 29

1.

Web of the carotid artery: An under-recognized cause of ischemic stroke.

Pacei F, Quilici L, Mullin S, Innocenti A, Valvassori L, Nardone R, Bet L.

J Clin Neurosci. 2018 Apr;50:122-123. doi: 10.1016/j.jocn.2018.01.059. Epub 2018 Feb 7.

PMID:
29428268
2.

Hematopoietic Cell Transplantation-Specific Comorbidity Index Predicts Morbidity and Mortality in Autologous Stem Cell Transplantation.

Berro M, Arbelbide JA, Rivas MM, Basquiera AL, Ferini G, Vitriu A, Foncuberta C, Fernandez Escobar N, Requejo A, Milovic V, Yantorno S, Szelagoswki M, Martinez Rolon J, Bentolila G, Garcia JJ, Garcia P, Caeiro G, Castro M, Jaimovich G, Palmer S, Trucco JI, Bet LA, Shaw BE, Kusminsky GD.

Biol Blood Marrow Transplant. 2017 Oct;23(10):1646-1650. doi: 10.1016/j.bbmt.2017.06.014. Epub 2017 Jun 29.

3.

Electromechanical delay components during skeletal muscle contraction and relaxation in patients with myotonic dystrophy type 1.

Esposito F, Cè E, Rampichini S, Limonta E, Venturelli M, Monti E, Bet L, Fossati B, Meola G.

Neuromuscul Disord. 2016 Jan;26(1):60-72. doi: 10.1016/j.nmd.2015.09.013. Epub 2015 Sep 25.

4.

Spinal epidural abscess as a complication of cardiosurgery.

Pacei F, Bet L.

Neurol Sci. 2014 May;35(5):805-7. doi: 10.1007/s10072-014-1670-3. Epub 2014 Feb 12. No abstract available.

PMID:
24518990
5.

Vertebral artery dissection during Kung-Fu training.

Pacei F, Valvassori L, Bet L.

Neurol Sci. 2014 Feb;35(2):331-2. doi: 10.1007/s10072-013-1555-x. Epub 2013 Sep 26. No abstract available.

PMID:
24068483
6.

A case of Wernicke's encephalopathy due to oesophageal achalasia.

Pacei F, Mullin S, Colombo C, Viganò S, Bet L.

Neurol Sci. 2013 May;34(5):799-800. doi: 10.1007/s10072-012-1136-4. Epub 2012 Jun 24. No abstract available.

PMID:
22729531
7.

Bimodal administration of entacapone in Parkinson's disease patients improves motor control.

Bet L, Bareggi SR, Pacei F, Bondiolotti G, Meola G, Schapira AH.

Eur J Neurol. 2008 Mar;15(3):268-73. doi: 10.1111/j.1468-1331.2007.02043.x.

PMID:
18290846
8.

Ballooning-induced bradycardia during carotid stenting in primary stenosis and restenosis.

Nano G, Dalainas I, Bianchi P, Stegher S, Bet L, Malacrida G, Tealdi DG.

Neuroradiology. 2006 Aug;48(8):533-6. Epub 2006 May 3.

PMID:
16670918
9.

Poor metabolization of n-hexane in Parkinson's disease.

Canesi M, Perbellini L, Maestri L, Silvani A, Zecca L, Bet L, Pezzoli G.

J Neurol. 2003 May;250(5):556-60.

PMID:
12736734
10.

Late-onset mitochondrial neuromyopathy: an age-related phenomenon?

Toscano A, Santoro M, Vita G, Girlanda P, Sinicropi S, Fazio MC, Mazzeo A, Rodolico C, Aguennouz M, Bartolone S, Bet L, Comi GP, Messina C.

Arch Gerontol Geriatr. 1996;22 Suppl 1:577-83.

PMID:
18653097
11.

Early-onset cerebellar ataxia, myoclonus and hypogonadism in a case of mitochondrial complex III deficiency treated with vitamins K3 and C.

Toscano A, Fazio MC, Vita G, Cannavó S, Bresolin N, Bet L, Prelle A, Barbiroli B, Iotti S, Zaniol P, et al.

J Neurol. 1995 Mar;242(4):203-9.

PMID:
7798118
12.

Multiple sclerosis and mitochondrial myopathy: an unusual combination of diseases.

Bet L, Moggio M, Comi GP, Mariani C, Prelle A, Checcarelli N, Bordoni A, Bresolin N, Scarpini E, Scarlato G.

J Neurol. 1994 Jul;241(8):511-6.

PMID:
7964921
13.

Lipid storage myopathy in multiple acyl-CoA dehydrogenase deficiency: an adult case.

Mongini T, Doriguzzi C, Palmucci L, De Francesco A, Bet L, Manfredi L, Ponzetto C, Bresolin N.

Eur Neurol. 1992;32(3):170-6.

PMID:
1592075
14.

A case of mitochondrial myopathy, lactic acidosis and complex I deficiency.

Bet L, Bresolin N, Moggio M, Meola G, Prelle A, Schapira AH, Binzoni T, Chomyn A, Fortunato F, Cerretelli P, et al.

J Neurol. 1990 Nov;237(7):399-404.

PMID:
2125637
15.

Kearns-Sayre syndrome: different amounts of deleted mitochondrial DNA are present in several autoptic tissues.

Ponzetto C, Bresolin N, Bordoni A, Moggio M, Meola G, Bet L, Prelle A, Scarlato G.

J Neurol Sci. 1990 May;96(2-3):207-10.

PMID:
2376752
16.

[Mitochondrial encephalomyopathy].

Scarlato G, Bresolin N, Moggio M, Bet L, Meola G.

Recenti Prog Med. 1989 Dec;80(12):665-72. Italian.

PMID:
2560839
17.

Mitochondrial encephalomyopathies.

Scarlato G, Moggio M, Bet L, Gallanti A, Bresolin N.

Acta Neurol (Napoli). 1989 Oct;11(5):322-9. No abstract available.

PMID:
2603778
18.

Muscle glucose-6-phosphate dehydrogenase deficiency.

Bresolin N, Bet L, Moggio M, Meola G, Fortunato F, Comi G, Adobbati L, Geremia L, Pittalis S, Scarlato G.

J Neurol. 1989 May;236(4):193-8.

PMID:
2760630
19.

Cytochrome c oxidase during human fetal development.

Moggio M, Bresolin N, Scarpini E, Adobbati L, Prelle A, Gallanti A, Bet L, Fortunato F, Pellegrini G, Scarlato G.

Int J Dev Neurosci. 1989;7(1):5-14.

PMID:
2540623
20.

Endocrine involvement in mitochondrial encephalomyopathy with partial cytochrome c oxidase deficiency.

Doriguzzi C, Palmucci L, Mongini T, Bresolin N, Bet L, Comi G, Lala R.

J Neurol Neurosurg Psychiatry. 1989 Jan;52(1):122-5.

21.

Clinical and biochemical correlations in mitochondrial myopathies treated with coenzyme Q10.

Bresolin N, Bet L, Binda A, Moggio M, Comi G, Nador F, Ferrante C, Carenzi A, Scarlato G.

Neurology. 1988 Jun;38(6):892-9.

PMID:
3368070
22.

Body building and myoglobinuria: report of three cases.

Doriguzzi C, Palmucci L, Mongini T, Arnaudo E, Bet L, Bresolin N.

Br Med J (Clin Res Ed). 1988 Mar 19;296(6625):826-7. No abstract available.

23.

Immunological and biochemical studies and pilot therapeutic trial with ubidecarenone in Kearns-Sayre patients.

Bresolin N, Bet L, Ferrante C, Binda A, Carenzi A, Moggio M, Comi G, Scarlato G.

Adv Neurol. 1988;48:239-56. No abstract available.

PMID:
3334786
24.

Low doses of ketazolam in anxiety: a double-blind, placebo-controlled study.

Scarpini E, Baron PG, Bet L, Bottini G, Bresolin N, Meola G, Pezzoli G, Vallar G, Monza GC, Scarlato G.

Neuropsychobiology. 1988;20(2):74-7.

PMID:
2908133
25.

Biochemical and immunologic studies in a case of congenital myopathy with unusual morphologic features.

Biral D, Damiani E, Scarpini E, Bet L, Bresolin N, Moggio M, Pellegrini G, Barbieri S, Scarlato G.

Neurology. 1987 Oct;37(10):1658-62.

PMID:
3309721
26.

Muscle G6PD deficiency.

Bresolin N, Bet L, Moggio M, Meola G, Comi G, Gilardi A, Scarlato G.

Lancet. 1987 Jul 25;2(8552):212-3. No abstract available.

PMID:
2885660
27.

Progressive cytochrome c oxidase deficiency in a case of Kearns-Sayre syndrome: morphological, immunological, and biochemical studies in muscle biopsies and autopsy tissues.

Bresolin N, Moggio M, Bet L, Gallanti A, Prelle A, Nobile-Orazio E, Adobbati L, Ferrante C, Pellegrini G, Scarlato G.

Ann Neurol. 1987 Jun;21(6):564-72.

PMID:
3037990
28.

Childhood encephalomyopathy with cytochrome c oxidase deficiency, ataxia, muscle wasting, and mental impairment.

Angelini C, Bresolin N, Pegolo G, Bet L, Rinaldo P, Trevisan C, Vergani L.

Neurology. 1986 Aug;36(8):1048-52.

PMID:
3016603
29.

Carnitine and acyltransferase in experimental neurogenic atrophies: changes with treatment.

Bresolin N, Freddo L, Tegazzin V, Bet L, Armani M, Angelini C.

J Neurol. 1984;231(4):170-5.

PMID:
6512569

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