Garibaldi M - Search Results

1

Eculizumab for myasthenic exacerbation during treatment with immune-checkpoint inhibitors.

Fionda L, Rossini E, Lauletta A, Leonardi L, Tufano L, Costanzo R, Marchetti P, Salvetti M, Garibaldi M, Morino S, Antonini G. Fionda L, et al. Among authors: garibaldi m. Neurol Sci. 2024 Mar;45(3):1243-1247. doi: 10.1007/s10072-023-07190-0. Epub 2023 Dec 18. Neurol Sci. 2024. PMID: 38108913

2

[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. BRAGE D, et al. Among authors: garibaldi m. Rev Neurol (Paris). 1963 Jun;108:979-83. Rev Neurol (Paris). 1963. PMID: 14092013 French. No abstract available.

3

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. Díaz-Manera J, et al. Among authors: garibaldi m. J Pathol. 2012 Dec;228(4):544-53. doi: 10.1002/path.4083. Epub 2012 Oct 5. J Pathol. 2012. PMID: 22847756

4

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. Renard D, et al. Among authors: garibaldi m. Am J Med Genet A. 2018 Aug;176(8):1760-1763. doi: 10.1002/ajmg.a.38843. Epub 2018 Jul 28. Am J Med Genet A. 2018. PMID: 30055030

5

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. Teveroni E, et al. Among authors: garibaldi m. J Clin Invest. 2017 Apr 3;127(4):1531-1545. doi: 10.1172/JCI89401. Epub 2017 Mar 6. J Clin Invest. 2017. PMID: 28263188 Free PMC article.

6

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

Brage D, Garibaldi MD, Intaglietta J, Buenaventura I, Famulari A. Brage D, et al. Among authors: garibaldi md. Int J Neurol. 1974;9(2):173-85. Int J Neurol. 1974. PMID: 4374443 No abstract available.

7

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. Garibaldi M, et al. Neuromuscul Disord. 2015 Nov;25(11):869-72. doi: 10.1016/j.nmd.2015.08.011. Epub 2015 Sep 7. Neuromuscul Disord. 2015. PMID: 26494409

8

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

Garibaldi M, Diaz-Manera J, Gallardo E, Antonini G. Garibaldi M, et al. Neurology. 2016 Jun 14;86(24):e250-1. doi: 10.1212/WNL.0000000000002772. Neurology. 2016. PMID: 27298456 No abstract available.

9

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. Garibaldi M, et al. J Neuromuscul Dis. 2016 Mar 3;3(1):111-114. doi: 10.3233/JND-150125. J Neuromuscul Dis. 2016. PMID: 27854204

10

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. Garibaldi M, et al. Clin Genet. 2017 May;91(5):780-786. doi: 10.1111/cge.12888. Epub 2016 Nov 23. Clin Genet. 2017. PMID: 27882542

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