Cordone G - Search Results

1

Disruption of muscle basal lamina in congenital muscular dystrophy with merosin deficiency.

Minetti C, Bado M, Morreale G, Pedemonte M, Cordone G. Minetti C, et al. Among authors: cordone g. Neurology. 1996 May;46(5):1354-8. doi: 10.1212/wnl.46.5.1354. Neurology. 1996. PMID: 8628482

2

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: cordone g. 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.

3

Abnormalities in the expression of beta-spectrin in Duchenne muscular dystrophy.

Minetti C, Tanji K, Rippa PG, Morreale G, Cordone G, Bonilla E. Minetti C, et al. Among authors: cordone g. Neurology. 1994 Jun;44(6):1149-53. doi: 10.1212/wnl.44.6.1149. Neurology. 1994. PMID: 8208414

4

Severe dystrophinopathy in a patient with congenital hypotonia.

Cordone G, Bado M, Morreale G, Pedemonte M, Minetti C. Cordone G, et al. Childs Nerv Syst. 1996 Aug;12(8):466-9. doi: 10.1007/BF00261626. Childs Nerv Syst. 1996. PMID: 8891365

5

Disorganization of dystrophin costameric lattice in Becker muscular dystrophy.

Minetti C, Cordone G, Beltrame F, Bado M, Bonilla E. Minetti C, et al. Among authors: cordone g. Muscle Nerve. 1998 Feb;21(2):211-6. doi: 10.1002/(sici)1097-4598(199802)21:2<211::aid-mus8>3.0.co;2-e. Muscle Nerve. 1998. PMID: 9466596

6

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: cordone g. Biochem Biophys Res Commun. 1999 Aug 11;261(3):547-50. doi: 10.1006/bbrc.1999.1055. Biochem Biophys Res Commun. 1999. PMID: 10441463

7

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: cordone g. Neurology. 2000 Mar 28;54(6):1373-6. doi: 10.1212/wnl.54.6.1373. Neurology. 2000. PMID: 10746614

8

Novel mutation in the CPT II gene in a child with periodic febrile myalgia and myoglobinuria.

Bruno C, Bado M, Minetti C, Cordone G, DiMauro S. Bruno C, et al. Among authors: cordone g. J Child Neurol. 2000 Jun;15(6):390-3. doi: 10.1177/088307380001500607. J Child Neurol. 2000. PMID: 10868782

9

[Congenital myopathies].

Cordone G, Bado M, Minetti C. Cordone G, et al. Minerva Pediatr. 1991 Mar;43(3):71-80. Minerva Pediatr. 1991. PMID: 1870529 Italian. No abstract available.

10

[Early myoclonic encephalopathy and spinal muscular atrophy type I].

Bado M, Bruno C, Morreale G, Parisi F, Minetti C, Cordone G. Bado M, et al. Among authors: cordone g. Minerva Pediatr. 1995 Jun;47(6):233-8. Minerva Pediatr. 1995. PMID: 7476749 Italian.

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