Memmi M - Search Results

1

FKBP12.6 deficiency and defective calcium release channel (ryanodine receptor) function linked to exercise-induced sudden cardiac death.

Wehrens XH, Lehnart SE, Huang F, Vest JA, Reiken SR, Mohler PJ, Sun J, Guatimosim S, Song LS, Rosemblit N, D'Armiento JM, Napolitano C, Memmi M, Priori SG, Lederer WJ, Marks AR. Wehrens XH, et al. Among authors: memmi m. Cell. 2003 Jun 27;113(7):829-40. doi: 10.1016/s0092-8674(03)00434-3. Cell. 2003. PMID: 12837242 Free article.

2

Brugada syndrome and sudden cardiac death in children.

Priori SG, Napolitano C, Giordano U, Collisani G, Memmi M. Priori SG, et al. Among authors: memmi m. Lancet. 2000 Mar 4;355(9206):808-9. doi: 10.1016/S0140-6736(99)05277-0. Lancet. 2000. PMID: 10711933

3

Gene specific therapy for arrhythmogenic disorders.

Priori SG, Ronchetti E, Memmi M. Priori SG, et al. Among authors: memmi m. Ital Heart J. 2000 Sep;1 Suppl 3:S52-4. Ital Heart J. 2000. PMID: 11003025 No abstract available.

4

Novel characteristics of a misprocessed mutant HERG channel linked to hereditary long QT syndrome.

Ficker E, Thomas D, Viswanathan PC, Dennis AT, Priori SG, Napolitano C, Memmi M, Wible BA, Kaufman ES, Iyengar S, Schwartz PJ, Rudy Y, Brown AM. Ficker E, et al. Among authors: memmi m. Am J Physiol Heart Circ Physiol. 2000 Oct;279(4):H1748-56. doi: 10.1152/ajpheart.2000.279.4.H1748. Am J Physiol Heart Circ Physiol. 2000. PMID: 11009462 Free article.

5

Mechanisms of I(Ks) suppression in LQT1 mutants.

Bianchi L, Priori SG, Napolitano C, Surewicz KA, Dennis AT, Memmi M, Schwartz PJ, Brown AM. Bianchi L, et al. Among authors: memmi m. Am J Physiol Heart Circ Physiol. 2000 Dec;279(6):H3003-11. doi: 10.1152/ajpheart.2000.279.6.H3003. Am J Physiol Heart Circ Physiol. 2000. PMID: 11087258 Free article.

6

Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia.

Priori SG, Napolitano C, Tiso N, Memmi M, Vignati G, Bloise R, Sorrentino V, Danieli GA. Priori SG, et al. Among authors: memmi m. Circulation. 2001 Jan 16;103(2):196-200. doi: 10.1161/01.cir.103.2.196. Circulation. 2001. PMID: 11208676

7

Novel arrhythmogenic mechanism revealed by a long-QT syndrome mutation in the cardiac Na(+) channel.

Abriel H, Cabo C, Wehrens XH, Rivolta I, Motoike HK, Memmi M, Napolitano C, Priori SG, Kass RS. Abriel H, et al. Among authors: memmi m. Circ Res. 2001 Apr 13;88(7):740-5. doi: 10.1161/hh0701.089668. Circ Res. 2001. PMID: 11304498

8

Inherited Brugada and long QT-3 syndrome mutations of a single residue of the cardiac sodium channel confer distinct channel and clinical phenotypes.

Rivolta I, Abriel H, Tateyama M, Liu H, Memmi M, Vardas P, Napolitano C, Priori SG, Kass RS. Rivolta I, et al. Among authors: memmi m. J Biol Chem. 2001 Aug 17;276(33):30623-30. doi: 10.1074/jbc.M104471200. Epub 2001 Jun 15. J Biol Chem. 2001. PMID: 11410597 Free article.

9

Involvement of the cardiac ryanodine receptor/calcium release channel in catecholaminergic polymorphic ventricular tachycardia.

Marks AR, Priori S, Memmi M, Kontula K, Laitinen PJ. Marks AR, et al. Among authors: memmi m. J Cell Physiol. 2002 Jan;190(1):1-6. doi: 10.1002/jcp.10031. J Cell Physiol. 2002. PMID: 11807805 Review.

10

Clinical and molecular characterization of patients with catecholaminergic polymorphic ventricular tachycardia.

Priori SG, Napolitano C, Memmi M, Colombi B, Drago F, Gasparini M, DeSimone L, Coltorti F, Bloise R, Keegan R, Cruz Filho FE, Vignati G, Benatar A, DeLogu A. Priori SG, et al. Among authors: memmi m. Circulation. 2002 Jul 2;106(1):69-74. doi: 10.1161/01.cir.0000020013.73106.d8. Circulation. 2002. PMID: 12093772

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