Restagno G - Search Results

1

Inferring biallelism of two FSH receptor mutations associated with spontaneous ovarian hyperstimulation syndrome by evaluating FSH, LH and HCG cross-activity.

Lazzaretti C, Riccetti L, Sperduti S, Anzivino C, Brigante G, De Pascali F, Potì F, Rovei V, Restagno G, Mari C, Lussiana C, Benedetto C, Revelli A, Casarini L. Lazzaretti C, et al. Among authors: restagno g. Reprod Biomed Online. 2019 May;38(5):816-824. doi: 10.1016/j.rbmo.2018.12.021. Epub 2018 Dec 23. Reprod Biomed Online. 2019. PMID: 30910395

2

Mutations and polymorphisms of the FSH receptor (FSHR) gene: clinical implications in female fecundity and molecular biology of FSHR protein and gene.

Lussiana C, Guani B, Mari C, Restagno G, Massobrio M, Revelli A. Lussiana C, et al. Among authors: restagno g. Obstet Gynecol Surv. 2008 Dec;63(12):785-95. doi: 10.1097/OGX.0b013e31818957eb. Obstet Gynecol Surv. 2008. PMID: 19017414 Review.

3

Ovarian hyper-stimulation syndrome after spontaneous conception.

Lussiana C, Guani B, Restagno G, Rovei V, Menato G, Revelli A, Massobrio M. Lussiana C, et al. Among authors: restagno g. Gynecol Endocrinol. 2009 Jul;25(7):455-9. doi: 10.1080/09513590902898213. Gynecol Endocrinol. 2009. PMID: 19499413

4

FSH-receptor Ala307Thr polymorphism is associated to polycystic ovary syndrome and to a higher responsiveness to exogenous FSH in Italian women.

Dolfin E, Guani B, Lussiana C, Mari C, Restagno G, Revelli A. Dolfin E, et al. Among authors: restagno g. J Assist Reprod Genet. 2011 Sep;28(10):925-30. doi: 10.1007/s10815-011-9619-4. Epub 2011 Jul 27. J Assist Reprod Genet. 2011. PMID: 21792664 Free PMC article.

5

Application of pyrosequencing to the identification of sequence variations in the cystic fibrosis transmembrane conductance regulator gene.

Mari C, Bruno F, Galbiati S, Torri A, Lombardo F, Seia M, Ferrari M, Restagno G, Cremonesi L. Mari C, et al. Among authors: restagno g. Clin Chem Lab Med. 2009;47(9):1051-4. doi: 10.1515/CCLM.2009.262. Clin Chem Lab Med. 2009. PMID: 19728845

6

Integrated strategy for fast and automated molecular characterization of genes involved in craniosynostosis.

Stenirri S, Restagno G, Ferrero GB, Alaimo G, Sbaiz L, Mari C, Genitori L, Maurizio F, Cremonesi L. Stenirri S, et al. Among authors: restagno g. Clin Chem. 2007 Oct;53(10):1767-74. doi: 10.1373/clinchem.2007.089292. Epub 2007 Aug 10. Clin Chem. 2007. PMID: 17693524

7

The IVS1 +319 t>a of SOD1 gene is not an ALS causing mutation.

Restagno G, Gomez A, Lombardo F, Cocco E, Calvo A, Ghiglione P, Mutani R, Chiò A. Restagno G, et al. Amyotroph Lateral Scler Other Motor Neuron Disord. 2005 Mar;6(1):45-9. doi: 10.1080/14660820410021276. Amyotroph Lateral Scler Other Motor Neuron Disord. 2005. PMID: 16036425

8

Low renin-angiotensin system activity gene polymorphism and dysplasia associated with posterior urethral valves.

Peruzzi L, Lombardo F, Amore A, Merlini E, Restagno G, Silvestro L, Papalia T, Coppo R. Peruzzi L, et al. Among authors: restagno g. J Urol. 2005 Aug;174(2):713-7. doi: 10.1097/01.ju.0000164739.13408.e2. J Urol. 2005. PMID: 16006956

9

Analysis of CA/GT microsatellite polymorphism in IVS8 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene: a study of Italian CF families.

Restagno G, Garnerone S, Gennaro C, Ferrone M, Carbonara A. Restagno G, et al. Clin Genet. 1992 Dec;42(6):309-13. doi: 10.1111/j.1399-0004.1992.tb03262.x. Clin Genet. 1992. PMID: 1283566

10

delta F508 deletion in cystic fibrosis in Italian families.

Restagno G, Garnerone S, Gennaro C, Varetto O, Ansaldi N, Castello D, Santini B, Carbonara AO. Restagno G, et al. Hum Genet. 1990 Sep;85(4):422-3. doi: 10.1007/BF02428293. Hum Genet. 1990. PMID: 1976596

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