• 5374 Citations
  • 38 h-Index
1976 …2019
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Fingerprint Dive into the research topics where Giovanni Meola is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 6 Similar Profiles
Myotonic Dystrophy Medicine & Life Sciences
Muscles Medicine & Life Sciences
Skeletal Muscle Medicine & Life Sciences
Myotonia Medicine & Life Sciences
Biopsy Medicine & Life Sciences
Muscular Diseases Medicine & Life Sciences
Skeletal Muscle Fibers Medicine & Life Sciences
Duchenne Muscular Dystrophy Medicine & Life Sciences

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Research Output 1976 2019

  • 5374 Citations
  • 38 h-Index
  • 233 Article
  • 6 Chapter
  • 2 Review article
  • 1 Comment/debate
1 Citation (Scopus)

Dysregulation of circular RNAs in myotonic dystrophy type 1

Voellenkle, C., Perfetti, A., Carrara, M., Fuschi, P., Renna, L. V., Longo, M., Sain, S. B., Cardani, R., Valaperta, R., Silvestri, G., Legnini, I., Bozzoni, I., Furling, D., Gaetano, C., Falcone, G., Meola, G. & Martelli, F., Apr 2 2019, In : International Journal of Molecular Sciences. 20, 8, 1938.

Research output: Contribution to journalArticle

Open Access
splicing
Myotonic Dystrophy
RNA
Muscle
RNA Splicing
3 Citations (Scopus)

Eight years after an international workshop on myotonic dystrophy patient registries: Case study of a global collaboration for a rare disease

Wood, L., Bassez, G., Bleyenheuft, C., Campbell, C., Cossette, L., Jimenez-Moreno, A. C., Dai, Y., Dawkins, H., Manera, J. A. D., Dogan, C., El Sherif, R., Fossati, B., Graham, C., Hilbert, J., Kastreva, K., Kimura, E., Korngut, L., Kostera-Pruszczyk, A., Lindberg, C., Lindvall, B. & 19 others, Luebbe, E., Lusakowska, A., Mazanec, R., Meola, G., Orlando, L., Takahashi, M. P., Peric, S., Puymirat, J., Rakocevic-Stojanovic, V., Rodrigues, M., Roxburgh, R., Schoser, B., Segovia, S., Shatillo, A., Thiele, S., Tournev, I., Van Engelen, B., Vohanka, S. & Lochmüller, H., Sep 5 2018, In : Orphanet Journal of Rare Diseases. 13, 1, 155.

Research output: Contribution to journalArticle

Myotonic Dystrophy
Rare Diseases
Registries
Education
Budgets
1 Citation (Scopus)

Flecainide-induced Brugada syndrome in a patient with skeletal muscle sodium channelopathy: A case report with critical therapeutical implications and review of the literature

Cavalli, M., Fossati, B., Vitale, R., Brigonzi, E., Ricigliano, V. A. G., Saraceno, L., Cardani, R., Pappone, C. & Meola, G., May 30 2018, In : Frontiers in Neurology. 9, MAY, 385.

Research output: Contribution to journalArticle

Channelopathies
Flecainide
Brugada Syndrome
Skeletal Muscle
Sodium
1 Citation (Scopus)

High-throughput analysis of the RNA-induced silencing complex in myotonic dystrophy type 1 patients identifies the dysregulation of miR-29c and its target ASB2

Cappella, M., Perfetti, A., Cardinali, B., Garcia-Manteiga, J. M., Carrara, M., Provenzano, C., Fuschi, P., Cardani, R., Renna, L. V., Meola, G., Falcone, G. & Martelli, F., Jul 1 2018, In : Cell Death and Disease. 9, 7, 729.

Research output: Contribution to journalArticle

RNA-Induced Silencing Complex
Myotonic Dystrophy
MicroRNAs
Messenger RNA
Biopsy

Incidence of amplification failure in DMPK allele due to allelic dropout event in a diagnostic laboratory

De Siena, C., Cardani, R., Brigonzi, E., Bosè, F., Fossati, B., Meola, G., Costa, E. & Valaperta, R., Sep 1 2018, In : Clinica Chimica Acta. 484, p. 111-116 6 p.

Research output: Contribution to journalArticle

Trinucleotide Repeats
Amplification
Assays
Alleles
Incidence