Broccolini A - Search Results

1

Movement disorders following mechanical thrombectomy resulting in ischemic lesions of the basal ganglia: An emerging clinical entity.

Rigon L, Genovese D, Piano C, Brunetti V, Guglielmi V, Cimmino AT, Scala I, Citro S, Bentivoglio AR, Rollo E, Di Iorio R, Broccolini A, Morosetti R, Monforte M, Frisullo G, Caliandro P, Pedicelli A, Caricato A, Masone G, Calabresi P, Marca GD. Rigon L, et al. Among authors: broccolini a. Eur J Neurol. 2024 May;31(5):e16219. doi: 10.1111/ene.16219. Epub 2024 Feb 1. Eur J Neurol. 2024. PMID: 38299441

2

Novel GNE mutations in Italian families with autosomal recessive hereditary inclusion-body myopathy.

Broccolini A, Ricci E, Cassandrini D, Gliubizzi C, Bruno C, Tonoli E, Silvestri G, Pescatori M, Rodolico C, Sinicropi S, Servidei S, Zara F, Minetti C, Tonali PA, Mirabella M. Broccolini A, et al. Hum Mutat. 2004 Jun;23(6):632. doi: 10.1002/humu.9252. Hum Mutat. 2004. PMID: 15146476

3

Localization of survival motor neuron protein in human apoptotic-like and regenerating muscle fibers, and neuromuscular junctions.

Broccolini A, Engel WK, Askanas V. Broccolini A, et al. Neuroreport. 1999 Jun 3;10(8):1637-41. doi: 10.1097/00001756-199906030-00003. Neuroreport. 1999. PMID: 10501549

4

Constitutive activation of MAPK cascade in acute quadriplegic myopathy.

Di Giovanni S, Molon A, Broccolini A, Melcon G, Mirabella M, Hoffman EP, Servidei S. Di Giovanni S, et al. Among authors: broccolini a. Ann Neurol. 2004 Feb;55(2):195-206. doi: 10.1002/ana.10811. Ann Neurol. 2004. PMID: 14755723

5

Pharmacological rescue of the dystrophin-glycoprotein complex in Duchenne and Becker skeletal muscle explants by proteasome inhibitor treatment.

Assereto S, Stringara S, Sotgia F, Bonuccelli G, Broccolini A, Pedemonte M, Traverso M, Biancheri R, Zara F, Bruno C, Lisanti MP, Minetti C. Assereto S, et al. Among authors: broccolini a. Am J Physiol Cell Physiol. 2006 Feb;290(2):C577-82. doi: 10.1152/ajpcell.00434.2005. Epub 2005 Sep 28. Am J Physiol Cell Physiol. 2006. PMID: 16192300 Free article.

6

Gene expression profiling in the early phases of DMD: a constant molecular signature characterizes DMD muscle from early postnatal life throughout disease progression.

Pescatori M, Broccolini A, Minetti C, Bertini E, Bruno C, D'amico A, Bernardini C, Mirabella M, Silvestri G, Giglio V, Modoni A, Pedemonte M, Tasca G, Galluzzi G, Mercuri E, Tonali PA, Ricci E. Pescatori M, et al. Among authors: broccolini a. FASEB J. 2007 Apr;21(4):1210-26. doi: 10.1096/fj.06-7285com. Epub 2007 Jan 30. FASEB J. 2007. PMID: 17264171

7

Redox factor-1 in muscle biopsies of patients with inclusion-body myositis.

Broccolini A, Engel WK, Alvarez RB, Askanas V. Broccolini A, et al. Neurosci Lett. 2000 Jun 16;287(1):1-4. doi: 10.1016/s0304-3940(00)01156-3. Neurosci Lett. 2000. PMID: 10841976

8

The drastic reduction of SMN protein in SMA I spinal cord motor neurons is not due to inefficient transcription.

Mirabella M, Servidei S, Broccolini A, Gandolfi N, Ricci E, Neri G, Tonali P, Brahe C. Mirabella M, et al. Among authors: broccolini a. Neurogenetics. 1999 Apr;2(2):97-100. doi: 10.1007/s100480050059. Neurogenetics. 1999. PMID: 10369885

9

Novel immunolocalization of alpha-synuclein in human muscle of inclusion-body myositis, regenerating and necrotic muscle fibers, and at neuromuscular junctions.

Askanas V, Engel WK, Alvarez RB, McFerrin J, Broccolini A. Askanas V, et al. Among authors: broccolini a. J Neuropathol Exp Neurol. 2000 Jul;59(7):592-8. doi: 10.1093/jnen/59.7.592. J Neuropathol Exp Neurol. 2000. PMID: 10901230

10

Analysis of MTMR1 expression and correlation with muscle pathological features in juvenile/adult onset myotonic dystrophy type 1 (DM1) and in myotonic dystrophy type 2 (DM2).

Santoro M, Modoni A, Masciullo M, Gidaro T, Broccolini A, Ricci E, Tonali PA, Silvestri G. Santoro M, et al. Among authors: broccolini a. Exp Mol Pathol. 2010 Oct;89(2):158-68. doi: 10.1016/j.yexmp.2010.05.007. Epub 2010 Jun 1. Exp Mol Pathol. 2010. PMID: 20685272

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