Corso G - Search Results

1

Slc7a7 disruption causes fetal growth retardation by downregulating Igf1 in the mouse model of lysinuric protein intolerance.

Sperandeo MP, Annunziata P, Bozzato A, Piccolo P, Maiuri L, D'Armiento M, Ballabio A, Corso G, Andria G, Borsani G, Sebastio G. Sperandeo MP, et al. Among authors: corso g. Am J Physiol Cell Physiol. 2007 Jul;293(1):C191-8. doi: 10.1152/ajpcell.00583.2006. Epub 2007 Mar 21. Am J Physiol Cell Physiol. 2007. PMID: 17376816 Free article.

2

Clinical and biochemical screening for Smith-Lemli-Opitz syndrome. Italian SLOS Collaborative Group.

Guzzetta V, De Fabiani E, Galli G, Colombo C, Corso G, Lecora M, Parenti G, Strisciuglio P, Andria G. Guzzetta V, et al. Among authors: corso g. Acta Paediatr. 1996 Aug;85(8):937-42. doi: 10.1111/j.1651-2227.1996.tb14190.x. Acta Paediatr. 1996. PMID: 8863875

3

Lathosterolosis, a novel multiple-malformation/mental retardation syndrome due to deficiency of 3beta-hydroxysteroid-delta5-desaturase.

Brunetti-Pierri N, Corso G, Rossi M, Ferrari P, Balli F, Rivasi F, Annunziata I, Ballabio A, Russo AD, Andria G, Parenti G. Brunetti-Pierri N, et al. Among authors: corso g. Am J Hum Genet. 2002 Oct;71(4):952-8. doi: 10.1086/342668. Epub 2002 Aug 20. Am J Hum Genet. 2002. PMID: 12189593 Free PMC article.

4

Characterization of liver involvement in defects of cholesterol biosynthesis: long-term follow-up and review.

Rossi M, Vajro P, Iorio R, Battagliese A, Brunetti-Pierri N, Corso G, Di Rocco M, Ferrari P, Rivasi F, Vecchione R, Andria G, Parenti G. Rossi M, et al. Among authors: corso g. Am J Med Genet A. 2005 Jan 15;132A(2):144-51. doi: 10.1002/ajmg.a.30426. Am J Med Genet A. 2005. PMID: 15580635 Review.

5

Vitamin D status in patients affected by Smith-Lemli-Opitz syndrome.

Rossi M, Federico G, Corso G, Parenti G, Battagliese A, Frascogna AR, Della Casa R, Dello Russo A, Strisciuglio P, Saggese G, Andria G. Rossi M, et al. Among authors: corso g. J Inherit Metab Dis. 2005;28(1):69-80. doi: 10.1007/s10545-005-3676-8. J Inherit Metab Dis. 2005. PMID: 15702407

6

Clinical phenotype of lathosterolosis.

Rossi M, D'Armiento M, Parisi I, Ferrari P, Hall CM, Cervasio M, Rivasi F, Balli F, Vecchione R, Corso G, Andria G, Parenti G. Rossi M, et al. Among authors: corso g. Am J Med Genet A. 2007 Oct 15;143A(20):2371-81. doi: 10.1002/ajmg.a.31929. Am J Med Genet A. 2007. PMID: 17853487

7

A Targeted Mass Spectrometry Approach to Identify Peripheral Changes in Metabolic Pathways of Patients with Alzheimer's Disease.

Reveglia P, Paolillo C, Angiolillo A, Ferretti G, Angelico R, Sirabella R, Corso G, Matrone C, Di Costanzo A. Reveglia P, et al. Among authors: corso g. Int J Mol Sci. 2023 Jun 4;24(11):9736. doi: 10.3390/ijms24119736. Int J Mol Sci. 2023. PMID: 37298687 Free PMC article.

8

A rare case of sterol-C4-methyl oxidase deficiency in a young Italian male: Biochemical and molecular characterization.

Frisso G, Gelzo M, Procopio E, Sica C, Lenza MP, Dello Russo A, Donati MA, Salvatore F, Corso G. Frisso G, et al. Among authors: corso g. Mol Genet Metab. 2017 Aug;121(4):329-335. doi: 10.1016/j.ymgme.2017.06.013. Epub 2017 Jun 27. Mol Genet Metab. 2017. PMID: 28673550

9

Serum lipids and apolipoproteins in children with the Smith-Lemli-Opitz syndrome.

Behúlová D, Bzdúch V, Skodová J, Dello Russo A, Corso G, Ponec J, Kasanická A. Behúlová D, et al. Among authors: corso g. J Inherit Metab Dis. 2000 Jun;23(4):413-5. doi: 10.1023/a:1005668305864. J Inherit Metab Dis. 2000. PMID: 10896307 No abstract available.

10

Effects of sample storage on 7- and 8-dehydrocholesterol levels analysed on whole blood spots by gas chromatography-mass spectrometry-selected ion monitoring.

Corso G, Rossi M, De BD, Rossi I, Parenti G, Dello RA. Corso G, et al. J Chromatogr B Analyt Technol Biomed Life Sci. 2002 Jan 25;766(2):365-70. doi: 10.1016/s0378-4347(01)00520-5. J Chromatogr B Analyt Technol Biomed Life Sci. 2002. PMID: 11824824

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