Rana M - Search Results

1

Cardiomyopathy may be the only clinical manifestation in female carriers of Duchenne muscular dystrophy.

Mirabella M, Servidei S, Manfredi G, Ricci E, Frustaci A, Bertini E, Rana M, Tonali P. Mirabella M, et al. Among authors: rana m. Neurology. 1993 Nov;43(11):2342-5. doi: 10.1212/wnl.43.11.2342. Neurology. 1993. PMID: 8232953

2

Manifesting heterozygotes in McArdle's disease: clinical, morphological and biochemical studies in a family.

Manfredi G, Silvestri G, Servidei S, Ricci E, Mirabella M, Bertini E, Papacci M, Rana M, Tonali P. Manfredi G, et al. Among authors: rana m. J Neurol Sci. 1993 Mar;115(1):91-4. doi: 10.1016/0022-510x(93)90071-6. J Neurol Sci. 1993. PMID: 8468596

3

A novel mitochondrial DNA point mutation in the tRNA(Ile) gene is associated with progressive external ophtalmoplegia.

Silvestri G, Servidei S, Rana M, Ricci E, Spinazzola A, Paris E, Tonali P. Silvestri G, et al. Among authors: rana m. Biochem Biophys Res Commun. 1996 Mar 27;220(3):623-7. doi: 10.1006/bbrc.1996.0453. Biochem Biophys Res Commun. 1996. PMID: 8607814

4

Maternally inherited cardiomyopathy: a new phenotype associated with the A to G AT nt.3243 of mitochondrial DNA (MELAS mutation).

Silvestri G, Bertini E, Servidei S, Rana M, Zachara E, Ricci E, Tonali P. Silvestri G, et al. Among authors: rana m. Muscle Nerve. 1997 Feb;20(2):221-5. doi: 10.1002/(sici)1097-4598(199702)20:2<221::aid-mus13>3.0.co;2-5. Muscle Nerve. 1997. PMID: 9040662

5

A late-onset mitochondrial myopathy is associated with a novel mitochondrial DNA (mtDNA) point mutation in the tRNA(Trp) gene.

Silvestri G, Rana M, DiMuzio A, Uncini A, Tonali P, Servidei S. Silvestri G, et al. Among authors: rana m. Neuromuscul Disord. 1998 Jun;8(5):291-5. doi: 10.1016/s0960-8966(98)00037-6. Neuromuscul Disord. 1998. PMID: 9673981

6

Single-fiber PCR in MELAS(3243) patients: correlations between intratissue distribution and phenotypic expression of the mtDNA(A3243G) genotype.

Silvestri G, Rana M, Odoardi F, Modoni A, Paris E, Papacci M, Tonali P, Servidei S. Silvestri G, et al. Among authors: rana m. Am J Med Genet. 2000 Sep 18;94(3):201-6. doi: 10.1002/1096-8628(20000918)94:3<201::aid-ajmg5>3.0.co;2-2. Am J Med Genet. 2000. PMID: 10995506

7

Pathogenic role of mtDNA duplications in mitochondrial diseases associated with mtDNA deletions.

Odoardi F, Rana M, Broccolini A, Mirabella M, Modoni A, D'Amico A, Papacci M, Tonali P, Servidei S, Silvestri G. Odoardi F, et al. Among authors: rana m. Am J Med Genet A. 2003 Apr 30;118A(3):247-54. doi: 10.1002/ajmg.a.20006. Am J Med Genet A. 2003. PMID: 12673655

8

An out-of-frame cytochrome b gene deletion from a patient with parkinsonism is associated with impaired complex III assembly and an increase in free radical production.

Rana M, de Coo I, Diaz F, Smeets H, Moraes CT. Rana M, et al. Ann Neurol. 2000 Nov;48(5):774-81. Ann Neurol. 2000. PMID: 11079541

9

Human mitochondrial DNA with large deletions repopulates organelles faster than full-length genomes under relaxed copy number control.

Diaz F, Bayona-Bafaluy MP, Rana M, Mora M, Hao H, Moraes CT. Diaz F, et al. Among authors: rana m. Nucleic Acids Res. 2002 Nov 1;30(21):4626-33. doi: 10.1093/nar/gkf602. Nucleic Acids Res. 2002. PMID: 12409452 Free PMC article.

10

Explantation of infected fenestrated endovascular aortic repair device.

Hanif H, Massie P, Danczyk R, Clark R, Rana MA. Hanif H, et al. Among authors: rana ma. J Vasc Surg Cases Innov Tech. 2024 Nov 19;11(1):101686. doi: 10.1016/j.jvscit.2024.101686. eCollection 2025 Feb. J Vasc Surg Cases Innov Tech. 2024. PMID: 39839271 Free PMC article. No abstract available.

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