Broda P - Search Results

1

Impairment of caveolae formation and T-system disorganization in human muscular dystrophy with caveolin-3 deficiency.

Minetti C, Bado M, Broda P, Sotgia F, Bruno C, Galbiati F, Volonte D, Lucania G, Pavan A, Bonilla E, Lisanti MP, Cordone G. Minetti C, et al. Among authors: broda p. Am J Pathol. 2002 Jan;160(1):265-70. doi: 10.1016/S0002-9440(10)64370-2. Am J Pathol. 2002. PMID: 11786420 Free PMC article.

2

Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophy.

Minetti C, Sotgia F, Bruno C, Scartezzini P, Broda P, Bado M, Masetti E, Mazzocco M, Egeo A, Donati MA, Volonte D, Galbiati F, Cordone G, Bricarelli FD, Lisanti MP, Zara F. Minetti C, et al. Among authors: broda p. Nat Genet. 1998 Apr;18(4):365-8. doi: 10.1038/ng0498-365. Nat Genet. 1998. PMID: 9537420

3

Increased number of caveolae and caveolin-3 overexpression in Duchenne muscular dystrophy.

Repetto S, Bado M, Broda P, Lucania G, Masetti E, Sotgia F, Carbone I, Pavan A, Bonilla E, Cordone G, Lisanti MP, Minetti C. Repetto S, et al. Among authors: broda p. Biochem Biophys Res Commun. 1999 Aug 11;261(3):547-50. doi: 10.1006/bbrc.1999.1055. Biochem Biophys Res Commun. 1999. PMID: 10441463

4

Mutation in the CAV3 gene causes partial caveolin-3 deficiency and hyperCKemia.

Carbone I, Bruno C, Sotgia F, Bado M, Broda P, Masetti E, Panella A, Zara F, Bricarelli FD, Cordone G, Lisanti MP, Minetti C. Carbone I, et al. Among authors: broda p. Neurology. 2000 Mar 28;54(6):1373-6. doi: 10.1212/wnl.54.6.1373. Neurology. 2000. PMID: 10746614

5

POMT2 gene mutation in limb-girdle muscular dystrophy with inflammatory changes.

Biancheri R, Falace A, Tessa A, Pedemonte M, Scapolan S, Cassandrini D, Aiello C, Rossi A, Broda P, Zara F, Santorelli FM, Minetti C, Bruno C. Biancheri R, et al. Among authors: broda p. Biochem Biophys Res Commun. 2007 Nov 30;363(4):1033-7. doi: 10.1016/j.bbrc.2007.09.066. Epub 2007 Sep 25. Biochem Biophys Res Commun. 2007. PMID: 17923109

6

Aquaporin-4 expression is severely reduced in human sarcoglycanopathies and dysferlinopathies.

Assereto S, Mastrototaro M, Stringara S, Gazzerro E, Broda P, Nicchia GP, Svelto M, Bruno C, Nigro V, Lisanti MP, Frigeri A, Minetti C. Assereto S, et al. Among authors: broda p. Cell Cycle. 2008 Jul 15;7(14):2199-207. doi: 10.4161/cc.7.14.6272. Epub 2008 May 12. Cell Cycle. 2008. PMID: 18641458

7

[Muscle phosphorylase deficiency in childhood. A case report].

Bruno C, Iester A, Bado M, Morreale G, Broda P, Minetti C, Cordone A, Cordone G. Bruno C, et al. Among authors: broda p. Minerva Pediatr. 1994 Oct;46(10):459-62. Minerva Pediatr. 1994. PMID: 7808367 Italian.

8

POMGnT1 mutations in congenital muscular dystrophy: genotype-phenotype correlation and expanded clinical spectrum.

Biancheri R, Bertini E, Falace A, Pedemonte M, Rossi A, D'Amico A, Scapolan S, Bergamino L, Petrini S, Cassandrini D, Broda P, Manfredi M, Zara F, Santorelli FM, Minetti C, Bruno C. Biancheri R, et al. Among authors: broda p. Arch Neurol. 2006 Oct;63(10):1491-5. doi: 10.1001/archneur.63.10.1491. Arch Neurol. 2006. PMID: 17030669

9

Genetic and Early Clinical Manifestations of Females Heterozygous for Duchenne/Becker Muscular Dystrophy.

Papa R, Madia F, Bartolomeo D, Trucco F, Pedemonte M, Traverso M, Broda P, Bruno C, Zara F, Minetti C, Fiorillo C. Papa R, et al. Among authors: broda p. Pediatr Neurol. 2016 Feb;55:58-63. doi: 10.1016/j.pediatrneurol.2015.11.004. Epub 2015 Nov 26. Pediatr Neurol. 2016. PMID: 26718981

10

Novel TRIM32 mutation in sarcotubular myopathy.

Panicucci C, Traverso M, Baratto S, Romeo C, Iacomino M, Gemelli C, Tagliafico A, Broda P, Zara F, Bruno C, Minetti C, Fiorillo C. Panicucci C, et al. Among authors: broda p. Acta Myol. 2019 Mar 1;38(1):8-12. eCollection 2019 Mar. Acta Myol. 2019. PMID: 31309175 Free PMC article.

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