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Items: 41

1.

Human Factors Usability and Validation Studies of a Glucagon Autoinjector in a Simulated Severe Hypoglycemia Rescue Situation.

Valentine V, Newswanger B, Prestrelski S, Andre AD, Garibaldi M.

Diabetes Technol Ther. 2019 Jun 20. doi: 10.1089/dia.2019.0148. [Epub ahead of print]

PMID:
31219349
2.

Expanding the spectrum of genes responsible for hereditary motor neuropathies.

Previtali SC, Zhao E, Lazarevic D, Pipitone GB, Fabrizi GM, Manganelli F, Mazzeo A, Pareyson D, Schenone A, Taroni F, Vita G, Bellone E, Ferrarini M, Garibaldi M, Magri S, Padua L, Pennisi E, Pisciotta C, Riva N, Scaioli V, Scarlato M, Tozza S, Geroldi A, Jordanova A, Ferrari M, Molineris I, Reilly MM, Comi G, Carrera P, Devoto M, Bolino A.

J Neurol Neurosurg Psychiatry. 2019 Jun 5. pii: jnnp-2019-320717. doi: 10.1136/jnnp-2019-320717. [Epub ahead of print]

PMID:
31167812
3.

Reply to the letter entitled "Predictors of respiratory impairment in patients with myotonic dystrophy type 1".

Rossi S, Della Marca G, Ricci M, Perna A, Nicoletti TF, Brunetti V, Meleo E, Calvello M, Petrucci A, Antonini G, Bucci E, Licchelli L, Sancricca C, Massa R, Rastelli E, Botta A, Di Muzio A, Romano S, Garibaldi M, Silvestri G.

J Neurol Sci. 2019 May 24. pii: S0022-510X(19)30241-2. doi: 10.1016/j.jns.2019.05.025. [Epub ahead of print] No abstract available.

PMID:
31153591
4.

Prevalence and predictor factors of respiratory impairment in a large cohort of patients with Myotonic Dystrophy type 1 (DM1): A retrospective, cross sectional study.

Rossi S, Della Marca G, Ricci M, Perna A, Nicoletti TF, Brunetti V, Meleo E, Calvello M, Petrucci A, Antonini G, Bucci E, Licchelli L, Sancricca C, Massa R, Rastelli E, Botta A, Di Muzio A, Romano S, Garibaldi M, Silvestri G.

J Neurol Sci. 2019 Apr 15;399:118-124. doi: 10.1016/j.jns.2019.02.012. Epub 2019 Feb 7.

PMID:
30798109
5.

Thymomatous myasthenia gravis: novel association with HLA DQB1*05:01 and strengthened evidence of high clinical and serological severity.

Massa R, Greco G, Testi M, Rastelli E, Terracciano C, Frezza E, Garibaldi M, Marfia GA, Locatelli F, Mercuri NB, Pompeo E, Antonini G, Andreani M.

J Neurol. 2019 Apr;266(4):982-989. doi: 10.1007/s00415-019-09225-z. Epub 2019 Feb 11.

PMID:
30741378
6.

Nerve high-resolution ultrasonography in tangier disease.

Pasquale AD, Leonardi L, Fionda L, Vanoli F, Garibaldi M, Inghilleri M, Ceccanti M, Cambieri C, Onesti E, Antonini G.

Muscle Nerve. 2019 May;59(5):587-590. doi: 10.1002/mus.26427. Epub 2019 Feb 7.

PMID:
30680752
7.

'Dusty core disease' (DuCD): expanding morphological spectrum of RYR1 recessive myopathies.

Garibaldi M, Rendu J, Brocard J, Lacene E, Fauré J, Brochier G, Beuvin M, Labasse C, Madelaine A, Malfatti E, Bevilacqua JA, Lubieniecki F, Monges S, Taratuto AL, Laporte J, Marty I, Antonini G, Romero NB.

Acta Neuropathol Commun. 2019 Jan 5;7(1):3. doi: 10.1186/s40478-018-0655-5.

8.

Italian recommendations for diagnosis and management of congenital myasthenic syndromes.

Maggi L, Bernasconi P, D'Amico A, Brugnoni R, Fiorillo C, Garibaldi M, Astrea G, Bruno C, Santorelli FM, Liguori R, Antonini G, Evoli A, Bertini E, Rodolico C, Mantegazza R.

Neurol Sci. 2019 Mar;40(3):457-468. doi: 10.1007/s10072-018-3682-x. Epub 2018 Dec 15.

PMID:
30554356
9.

Muscle MRI in a large cohort of patients with oculopharyngeal muscular dystrophy.

Alonso-Jimenez A, Kroon RHMJM, Alejaldre-Monforte A, Nuñez-Peralta C, Horlings CGC, van Engelen BGM, Olivé M, González L, Verges-Gil E, Paradas C, Márquez C, Garibaldi M, Gallano P, Rodriguez MJ, Gonzalez-Quereda L, Dominguez Gonzalez C, Vissing J, Fornander F, Eisum AV, García-Sobrino T, Pardo J, García-Figueiras R, Muelas N, Vilchez JJ, Kapetanovic S, Tasca G, Monforte M, Ricci E, Gomez MT, Bevilacqua JA, Diaz-Jara J, Zamorano II, Carlier RY, Laforet P, Pelayo-Negro A, Ramos-Fransi A, Martínez A, Marini-Bettolo C, Straub V, Gutiérrez G, Stojkovic T, Martín MA, Morís G, Fernández-Torrón R, Lopez De Munaín A, Cortes-Vicente E, Querol L, Rojas-García R, Illa I, Diaz-Manera J.

J Neurol Neurosurg Psychiatry. 2019 May;90(5):576-585. doi: 10.1136/jnnp-2018-319578. Epub 2018 Dec 8.

PMID:
30530568
10.

Widening the phenotypical spectrum of EGR2-related CMT: Unusual phenotype for R409W mutation.

Leonardi L, Garibaldi M, Fionda L, Vanoli F, Loreti S, Morino S, Antonini G.

Clin Neurophysiol. 2019 Jan;130(1):93-94. doi: 10.1016/j.clinph.2018.11.007. Epub 2018 Nov 22. No abstract available.

PMID:
30481651
11.

Lipid Myopathies.

Pennisi EM, Garibaldi M, Antonini G.

J Clin Med. 2018 Nov 23;7(12). pii: E472. doi: 10.3390/jcm7120472. Review.

12.

Core-rod myopathy due to a novel mutation in BTB/POZ domain of KBTBD13 manifesting as late onset LGMD.

Garibaldi M, Fattori F, Bortolotti CA, Brochier G, Labasse C, Verardo M, Servian-Morilla E, Gibellini L, Pinti M, Di Rocco G, Raffa S, Pennisi EM, Bertini ES, Paradas C, Romero NB, Antonini G.

Acta Neuropathol Commun. 2018 Sep 13;6(1):94. doi: 10.1186/s40478-018-0595-0. No abstract available.

13.

Inflammatory facioscapulohumeral muscular dystrophy type 2 in 18p deletion syndrome.

Renard D, Taieb G, Garibaldi M, Maues De Paula A, Bernard R, Lagha N, Cristofari G, Vovan C, Chaix C, Lévy N, Khau Van Kien P, Sacconi S.

Am J Med Genet A. 2018 Aug;176(8):1760-1763. doi: 10.1002/ajmg.a.38843. Epub 2018 Jul 28.

PMID:
30055030
14.

A 34-year longitudinal study on long-term cardiac outcomes in DM1 patients with normal ECG at baseline at an Italian clinical centre.

Bucci E, Testa M, Licchelli L, Frattari A, El Halabieh NA, Gabriele E, Pignatelli G, De Santis T, Fionda L, Vanoli F, Morino S, Garibaldi M, Di Pasquale A, Vanacore N, Botta A, Antonini G.

J Neurol. 2018 Apr;265(4):885-895. doi: 10.1007/s00415-018-8773-3. Epub 2018 Feb 10.

PMID:
29429070
15.

Erratum to: Muscle MRI in neutral lipid storage disease (NLSD).

Garibaldi M, Tasca G, Diaz-Manera J, Ottaviani P, Laschena F, Pantoli D, Gerevini S, Fiorillo C, Maggi L, Tasca E, D'Amico A, Musumeci O, Toscano A, Bruno C, Massa R, Angelini C, Bertini E, Antonini G, Pennisi EM.

J Neurol. 2017 Jul;264(7):1343-1344. doi: 10.1007/s00415-017-8528-6. No abstract available.

PMID:
28608302
16.

Muscle MRI in neutral lipid storage disease (NLSD).

Garibaldi M, Tasca G, Diaz-Manera J, Ottaviani P, Laschena F, Pantoli D, Gerevini S, Fiorillo C, Maggi L, Tasca E, D'Amico A, Musumeci O, Toscano A, Bruno C, Massa R, Angelini C, Bertini E, Antonini G, Pennisi EM.

J Neurol. 2017 Jul;264(7):1334-1342. doi: 10.1007/s00415-017-8498-8. Epub 2017 May 13. Erratum in: J Neurol. 2017 Jun 12;:.

17.

Neutral Lipid Storage Diseases: clinical/genetic features and natural history in a large cohort of Italian patients.

Pennisi EM, Arca M, Bertini E, Bruno C, Cassandrini D, D'amico A, Garibaldi M, Gragnani F, Maggi L, Massa R, Missaglia S, Morandi L, Musumeci O, Pegoraro E, Rastelli E, Santorelli FM, Tasca E, Tavian D, Toscano A, Angelini C; Italian NLSD Group.

Orphanet J Rare Dis. 2017 May 12;12(1):90. doi: 10.1186/s13023-017-0646-9.

18.

Estrogens enhance myoblast differentiation in facioscapulohumeral muscular dystrophy by antagonizing DUX4 activity.

Teveroni E, Pellegrino M, Sacconi S, Calandra P, Cascino I, Farioli-Vecchioli S, Puma A, Garibaldi M, Morosetti R, Tasca G, Ricci E, Trevisan CP, Galluzzi G, Pontecorvi A, Crescenzi M, Deidda G, Moretti F.

J Clin Invest. 2017 Apr 3;127(4):1531-1545. doi: 10.1172/JCI89401. Epub 2017 Mar 6.

19.

Prognostic factors in prostate cancer patients treated by radical external beam radiotherapy.

Garibaldi E, Gabriele D, Maggio A, Delmastro E, Garibaldi M, Russo F, Bresciani S, Stasi M, Gabriele P.

Panminerva Med. 2017 Sep;59(3):210-220. doi: 10.23736/S0031-0808.17.03232-3. Epub 2017 Mar 3.

PMID:
28256120
20.

Recessive MYPN mutations cause cap myopathy with occasional nemaline rods.

Lornage X, Malfatti E, Chéraud C, Schneider R, Biancalana V, Cuisset JM, Garibaldi M, Eymard B, Fardeau M, Boland A, Deleuze JF, Thompson J, Carlier RY, Böhm J, Romero NB, Laporte J.

Ann Neurol. 2017 Mar;81(3):467-473. doi: 10.1002/ana.24900. Epub 2017 Mar 20.

PMID:
28220527
21.

Long term follow-up of cerebrovascular abnormalities in late onset Pompe disease (LOPD).

Garibaldi M, Sacconi S, Antonini G, Desnuelle C.

J Neurol. 2017 Mar;264(3):589-590. doi: 10.1007/s00415-017-8396-0. Epub 2017 Jan 24. No abstract available.

PMID:
28120044
22.

A novel gain-of-function mutation in ORAI1 causes late-onset tubular aggregate myopathy and congenital miosis.

Garibaldi M, Fattori F, Riva B, Labasse C, Brochier G, Ottaviani P, Sacconi S, Vizzaccaro E, Laschena F, Romero NB, Genazzani A, Bertini E, Antonini G.

Clin Genet. 2017 May;91(5):780-786. doi: 10.1111/cge.12888. Epub 2016 Nov 23.

PMID:
27882542
23.

Novel Dominant Mutation in BIN1 Gene Causing Mild Centronuclear Myopathy Revealed by Myalgias and CK Elevation.

Garibaldi M, Böhm J, Fattori F, Koch C, Surace C, Ottaviani P, Laschena F, Laporte J, Bertini E, Antonini G, Romero NB.

J Neuromuscul Dis. 2016 Mar 3;3(1):111-114.

PMID:
27854204
24.

Teaching Video NeuroImages: The Beevor sign in late-onset Pompe disease.

Garibaldi M, Diaz-Manera J, Gallardo E, Antonini G.

Neurology. 2016 Jun 14;86(24):e250-1. doi: 10.1212/WNL.0000000000002772. No abstract available.

PMID:
27298456
25.

External beam radiotherapy with dose escalation in 1080 prostate cancer patients: definitive outcome and dose impact.

Garibaldi E, Gabriele D, Maggio A, Delmastro E, Garibaldi M, Bresciani S, Ortega C, Stasi M, Gabriele P.

Panminerva Med. 2016 Jun;58(2):121-9. Epub 2016 Jan 19.

PMID:
26785374
26.

Dropped-head in recessive oculopharyngeal muscular dystrophy.

Garibaldi M, Pennisi EM, Bruttini M, Bizzarri V, Bucci E, Morino S, Talerico C, Stoppacciaro A, Renieri A, Antonini G.

Neuromuscul Disord. 2015 Nov;25(11):869-72. doi: 10.1016/j.nmd.2015.08.011. Epub 2015 Sep 7.

PMID:
26494409
27.

Percentage of positive prostate biopsies independently predicts biochemical outcome following radiation therapy for prostate cancer.

Gabriele D, Garibaldi M, Girelli G, Taraglio S, Duregon E, Gabriele P, Guiot C, Bollito E; CONSORTIUM THE EUREKA.

Panminerva Med. 2016 Jun;58(2):109-14. Epub 2015 Jul 24.

PMID:
26211465
28.

The Human Pathogen Streptococcus pyogenes Releases Lipoproteins as Lipoprotein-rich Membrane Vesicles.

Biagini M, Garibaldi M, Aprea S, Pezzicoli A, Doro F, Becherelli M, Taddei AR, Tani C, Tavarini S, Mora M, Teti G, D'Oro U, Nuti S, Soriani M, Margarit I, Rappuoli R, Grandi G, Norais N.

Mol Cell Proteomics. 2015 Aug;14(8):2138-49. doi: 10.1074/mcp.M114.045880. Epub 2015 May 27.

29.

Exploiting intracardiac and surface recording modalities for atrial signal extraction in atrial fibrillation.

Garibaldi M, Zarzoso V.

Conf Proc IEEE Eng Med Biol Soc. 2013;2013:6015-8. doi: 10.1109/EMBC.2013.6610923.

PMID:
24111110
30.

Predicting catheter ablation outcome in persistent atrial fibrillation using atrial dominant frequency and related spectral features.

Garibaldi M, Zarzoso V, Latcu DG, Saoudi N.

Conf Proc IEEE Eng Med Biol Soc. 2012;2012:613-6. doi: 10.1109/EMBC.2012.6346006.

PMID:
23365967
31.

The increase of pericyte population in human neuromuscular disorders supports their role in muscle regeneration in vivo.

Díaz-Manera J, Gallardo E, de Luna N, Navas M, Soria L, Garibaldi M, Rojas-García R, Tonlorenzi R, Cossu G, Illa I.

J Pathol. 2012 Dec;228(4):544-53. doi: 10.1002/path.4083. Epub 2012 Oct 5.

PMID:
22847756
32.

Multi high-throughput approach for highly selective identification of vaccine candidates: the Group A Streptococcus case.

Bensi G, Mora M, Tuscano G, Biagini M, Chiarot E, Bombaci M, Capo S, Falugi F, Manetti AG, Donato P, Swennen E, Gallotta M, Garibaldi M, Pinto V, Chiappini N, Musser JM, Janulczyk R, Mariani M, Scarselli M, Telford JL, Grifantini R, Norais N, Margarit I, Grandi G.

Mol Cell Proteomics. 2012 Jun;11(6):M111.015693. doi: 10.1074/mcp.M111.015693. Epub 2012 Jan 27.

33.

A surface protein of Streptococcus suis serotype 2 identified by proteomics protects mice against infection.

Mandanici F, Gómez-Gascón L, Garibaldi M, Olaya-Abril A, Luque I, Tarradas C, Mancuso G, Papasergi S, Bárcena JA, Teti G, Beninati C, Rodríguez-Ortega MJ.

J Proteomics. 2010 Nov 10;73(12):2365-9. doi: 10.1016/j.jprot.2010.07.009. Epub 2010 Jul 23.

PMID:
20656083
34.

Immunoprotective activities of a Streptococcus suis pilus subunit in murine models of infection.

Garibaldi M, Rodríguez-Ortega MJ, Mandanici F, Cardaci A, Midiri A, Papasergi S, Gambadoro O, Cavallari V, Teti G, Beninati C.

Vaccine. 2010 Apr 30;28(20):3609-16. doi: 10.1016/j.vaccine.2010.01.009. Epub 2010 Jan 14.

PMID:
20079873
35.

Plasminogen- and fibronectin-binding protein B is involved in the adherence of Streptococcus pneumoniae to human epithelial cells.

Papasergi S, Garibaldi M, Tuscano G, Signorino G, Ricci S, Peppoloni S, Pernice I, Lo Passo C, Teti G, Felici F, Beninati C.

J Biol Chem. 2010 Mar 5;285(10):7517-24. doi: 10.1074/jbc.M109.062075. Epub 2010 Jan 4.

36.

Immunogenic mimics of Brucella lipopolysaccharide epitopes.

Beninati C, Garibaldi M, Lo Passo C, Mancuso G, Papasergi S, Garufi G, Pernice I, Teti G, Felici F.

Peptides. 2009 Oct;30(10):1936-9. doi: 10.1016/j.peptides.2009.07.009. Epub 2009 Jul 22.

PMID:
19631246
37.

Erectile dysfunction in myotonic dystrophy type 1 (DM1).

Antonini G, Clemenzi A, Bucci E, Morino S, Garibaldi M, Sepe-Monti M, Giubilei F, Novelli G.

J Neurol. 2009 Apr;256(4):657-9. doi: 10.1007/s00415-009-0912-4. Epub 2009 Apr 27. No abstract available.

PMID:
19444536
38.

Taking your board to the next level: a conversation with eight philanthropy board leaders.

Hurt G, Mills GM, Burress R, Ulvila L, Law J, Smith D, Garibaldi M, Ziegler J.

AHP J. 2007 Fall:8-9, 11, 13 passim. No abstract available.

PMID:
17929374
39.

[Percutaneous thromboembolization of the internal maxillary arteries for control of posterior epistaxis].

Berkstein A, Bernardo Boleaga K, Klinckwort T, Garibaldi M.

An Otorrinolaringol Ibero Am. 1981;8(1):31-8. Spanish. No abstract available.

PMID:
7258575
40.

Alcohol and nervous system with special reference to the enolic neuropathies.

Brage D, Garibaldi MD, Intaglietta J, Buenaventura I, Famulari A.

Int J Neurol. 1974;9(2):173-85. No abstract available.

PMID:
4374443
41.

[PARTIAL AND CONGENITAL STENOSIS OF THE AQUEDUCT OF SYLVIUS BY GLIOSIS. (CLINICAL, SURGICAL AND ANATOMO-PATHOLOGICAL OBSERVATION)].

BRAGE D, COPELLO I, MOREA R, CICHERO E, GARIBALDI M.

Rev Neurol (Paris). 1963 Jun;108:979-83. French. No abstract available.

PMID:
14092013

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