Sangiuolo FC - Search Results

1

Variants in MHY7 Gene Cause Arrhythmogenic Cardiomyopathy.

Ferradini V, Parca L, Martino A, Lanzillo C, Silvetti E, Calò L, Caselli S, Novelli G, Helmer-Citterich M, Sangiuolo FC, Mango R. Ferradini V, et al. Among authors: sangiuolo fc. Genes (Basel). 2021 May 22;12(6):793. doi: 10.3390/genes12060793. Genes (Basel). 2021. PMID: 34067482 Free PMC article.

2

Polymerase chain reaction in the detection of mRNA transcripts from the slow skeletal troponin T (TNNT1) gene in myotonic dystrophy and normal muscle.

Novelli G, Gennarelli M, Zelano G, Sangiuolo F, Lo Cicero S, Samson F, Dallapiccola B. Novelli G, et al. Cell Biochem Funct. 1992 Dec;10(4):251-6. doi: 10.1002/cbf.290100407. Cell Biochem Funct. 1992. PMID: 1473264

3

Molecular characterization of a frameshift mutation in exon 19 of the CFTR gene.

Sangiuolo F, Lo Cicero S, Maceratesi P, Quattrucci S, Novelli G, Dallapiccola B. Sangiuolo F, et al. Hum Mutat. 1993;2(5):422-4. doi: 10.1002/humu.1380020517. Hum Mutat. 1993. PMID: 7504970 No abstract available.

4

A new method for direct analysis of polymerase chain reaction-amplified human papillomavirus using DNA enzyme immunoassay.

Sangiuolo F, De Santis L, Cavicchini A, Angeloni U, Romanini C, Novelli G, Dallapiccola B. Sangiuolo F, et al. Int J Clin Lab Res. 1994;24(4):223-6. doi: 10.1007/BF02592468. Int J Clin Lab Res. 1994. PMID: 7894049

5

Simultaneous detection of delta F508, G542X, N1303K, G551D, and 1717-1G-->A cystic fibrosis alleles by a multiplex DNA enzyme immunoassay.

Sangiuolo F, Maceratesi P, Mesoraca A, Botta A, Cavicchini A, Novelli G, Dallapiccola B. Sangiuolo F, et al. Int J Clin Lab Res. 1995;25(3):142-5. doi: 10.1007/BF02592555. Int J Clin Lab Res. 1995. PMID: 8562976

6

Identification of five new mutations and three novel polymorphisms in the muscle chloride channel gene (CLCN1) in 20 Italian patients with dominant and recessive myotonia congenita. Mutations in brief no. 118. Online.

Sangiuolo F, Botta A, Mesoraca A, Servidei S, Merlini L, Fratta G, Novelli G, Dallapiccola B. Sangiuolo F, et al. Hum Mutat. 1998;11(4):331. doi: 10.1002/(SICI)1098-1004(1998)11:4<331::AID-HUMU12>3.0.CO;2-3. Hum Mutat. 1998. PMID: 10215406

7

A distinctive autosomal dominant vacuolar neuromyopathy linked to 19p13.

Servidei S, Capon F, Spinazzola A, Mirabella M, Semprini S, de Rosa G, Gennarelli M, Sangiuolo F, Ricci E, Mohrenweiser HW, Dallapiccola B, Tonali P, Novelli G. Servidei S, et al. Neurology. 1999 Sep 11;53(4):830-7. doi: 10.1212/wnl.53.4.830. Neurology. 1999. PMID: 10489050

8

Fine mapping of a distinctive autosomal dominant vacuolar neuromyopathy using 11 novel microsatellite markers from chromosome band 19p13.3.

Sangiuolo F, Bruscia E, Capon F, Servidei S, Dallapiccola B, Novelli G. Sangiuolo F, et al. Eur J Hum Genet. 2000 Oct;8(10):809-12. doi: 10.1038/sj.ejhg.5200547. Eur J Hum Genet. 2000. PMID: 11039585

9

Pharmacogenetics of human androgens and prostatic diseases.

Novelli G, Margiotti K, Sangiuolo F, Reichardt JK. Novelli G, et al. Pharmacogenomics. 2001 Feb;2(1):65-72. doi: 10.1517/14622416.2.1.65. Pharmacogenomics. 2001. PMID: 11258198 Review.

10

Towards the pharmacogenomics of cystic fibrosis.

Sangiuolo F, D'Apice MR, Bruscia E, Lucidi V, Novelli G. Sangiuolo F, et al. Pharmacogenomics. 2002 Jan;3(1):75-87. doi: 10.1517/14622416.3.1.75. Pharmacogenomics. 2002. PMID: 11966405 Review.

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