Gennarelli M - Search Results

1

Prediction of myotonic dystrophy clinical severity based on the number of intragenic [CTG]n trinucleotide repeats.

Gennarelli M, Novelli G, Andreasi Bassi F, Martorell L, Cornet M, Menegazzo E, Mostacciuolo ML, Martinez JM, Angelini C, Pizzuti A, Baiget M, Dallapiccola B. Gennarelli M, et al. Am J Med Genet. 1996 Nov 11;65(4):342-7. doi: 10.1002/(SICI)1096-8628(19961111)65:4<342::AID-AJMG18>3.0.CO;2-U. Am J Med Genet. 1996. PMID: 8923947

2

Expansion of the myotonic dystrophy gene in Italian and Spanish patients.

Melchionda S, Cobo A, Gennarelli M, Martorell L, Fattorini C, Baiget M, Lopez de Munain A, Johnson K, Shelbourne P, Novelli G, et al. Melchionda S, et al. Among authors: gennarelli m. J Med Genet. 1992 Nov;29(11):789-90. doi: 10.1136/jmg.29.11.789. J Med Genet. 1992. PMID: 1453428 Free PMC article.

3

3' creatine kinase (M-type) polymorphisms linked to myotonic dystrophy in Italian and Spanish populations.

Gennarelli M, Novelli G, Cobo A, Baiget M, Dallapiccola B. Gennarelli M, et al. Hum Genet. 1991 Oct;87(6):654-6. doi: 10.1007/BF00201719. Hum Genet. 1991. PMID: 1682233

4

Postzygotic instability of the myotonic dystrophy p[AGC] in repeat supported by larger expansions in muscle and reduced amplifications in sperm.

Massari A, Gennarelli M, Menegazzo E, Pizzuti A, Silani V, Mastrogiacomo I, Pagani E, Angelini C, Scarlato G, Novelli G, et al. Massari A, et al. Among authors: gennarelli m. J Neurol. 1995 Jun;242(6):379-83. doi: 10.1007/BF00868393. J Neurol. 1995. PMID: 7561966

5

Discordant clinical outcome in myotonic dystrophy relatives showing (CTG)n > 700 repeats.

Novelli G, Gennarelli M, Menegazzo E, Angelini C, Dallapiccola B. Novelli G, et al. Among authors: gennarelli m. Neuromuscul Disord. 1995 Mar;5(2):157-9. doi: 10.1016/0960-8966(94)00044-a. Neuromuscul Disord. 1995. PMID: 7767095

6

Meiotic drive at the myotonic dystrophy locus.

Gennarelli M, Dallapiccola B, Baiget M, Martorell L, Novelli G. Gennarelli M, et al. J Med Genet. 1994 Dec;31(12):980. doi: 10.1136/jmg.31.12.980. J Med Genet. 1994. PMID: 7891386 Free PMC article. No abstract available.

7

The dynamic genomics of myotonic dystrophy and its clinical relevance: an overview.

Novelli G, Gennarelli M, Fattorini C, Abbruzzese C, Dallapiccola B. Novelli G, et al. Among authors: gennarelli m. Biomed Pharmacother. 1993;47(8):321-30. doi: 10.1016/0753-3322(93)90081-u. Biomed Pharmacother. 1993. PMID: 8061254 Review. No abstract available.

8

Male hypogonadism in myotonic dystrophy is related to (CTG)n triplet mutation.

Mastrogiacomo I, Pagani E, Novelli G, Angelini C, Gennarelli M, Menegazzo E, Bonanni G, Dallapiccola B. Mastrogiacomo I, et al. Among authors: gennarelli m. J Endocrinol Invest. 1994 May;17(5):381-3. doi: 10.1007/BF03349005. J Endocrinol Invest. 1994. PMID: 8077624

9

(CTG)n triplet mutation and phenotype manifestations in myotonic dystrophy patients.

Novelli G, Gennarelli M, Menegazzo E, Mostacciuolo ML, Pizzuti A, Fattorini C, Tessarolo D, Tomelleri G, Giacanelli M, Danieli GA, et al. Novelli G, et al. Among authors: gennarelli m. Biochem Med Metab Biol. 1993 Aug;50(1):85-92. doi: 10.1006/bmmb.1993.1049. Biochem Med Metab Biol. 1993. PMID: 8373638

10

Failure in detecting mRNA transcripts from the mutated allele in myotonic dystrophy muscle.

Novelli G, Gennarelli M, Zelano G, Pizzuti A, Fattorini C, Caskey CT, Dallapiccola B. Novelli G, et al. Among authors: gennarelli m. Biochem Mol Biol Int. 1993 Feb;29(2):291-7. Biochem Mol Biol Int. 1993. PMID: 8495213

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