Parenti G - Search Results

1

Long-term monitoring for short/branched-chain acyl-CoA dehydrogenase deficiency: A single-center 4-year experience and open issues.

Rossi A, Turturo M, Albano L, Fecarotta S, Barretta F, Crisci D, Gallo G, Perfetto R, Uomo F, Vallone F, Villani G, Strisciuglio P, Parenti G, Frisso G, Ruoppolo M. Rossi A, et al. Among authors: parenti g. Front Pediatr. 2022 Sep 6;10:895921. doi: 10.3389/fped.2022.895921. eCollection 2022. Front Pediatr. 2022. PMID: 36147814 Free PMC article.

2

Clinical variability of cardio-facio-cutaneous syndrome: report of two additional cases.

Ghezzi M, Parenti G, de Franchis R, Farina V, de Leva F, Guarino A, Canani RB, Strisciuglio P. Ghezzi M, et al. Among authors: parenti g. Clin Genet. 1992 Oct;42(4):206-9. doi: 10.1111/j.1399-0004.1992.tb03239.x. Clin Genet. 1992. PMID: 1358488 Review.

3

Echo-Doppler abnormalities in mucopolysaccharide storage diseases.

Farina V, de Leva F, Caso P, Scippa L, Parenti G, Strisciuglio P. Farina V, et al. Among authors: parenti g. Acta Paediatr. 1992 Sep;81(9):702-4. doi: 10.1111/j.1651-2227.1992.tb12339.x. Acta Paediatr. 1992. PMID: 1421914 No abstract available.

4

Dietary treatment of liver glycogenosis.

Andria G, Parenti G, Strisciuglio P, Tinello C. Andria G, et al. Among authors: parenti g. Beitr Infusionsther. 1991;27:161-9. Beitr Infusionsther. 1991. PMID: 1713097 Review. No abstract available.

5

Evidence of polyglandular involvement in Niemann-Pick disease type B.

Strisciuglio P, Di Maio S, Parenti G, Franzese A, Lubrano P, Mariano A, Andria G. Strisciuglio P, et al. Among authors: parenti g. Eur J Pediatr. 1987 Jul;146(4):431-3. doi: 10.1007/BF00444957. Eur J Pediatr. 1987. PMID: 2820735

6

The presence of a reduced amount of 32-kd "protective" protein is a distinct biochemical finding in late infantile galactosialidosis.

Strisciuglio P, Parenti G, Giudice C, Lijoi S, Hoogeveen AT, d'Azzo A. Strisciuglio P, et al. Among authors: parenti g. Hum Genet. 1988 Nov;80(3):304-6. doi: 10.1007/BF01790104. Hum Genet. 1988. PMID: 3142815

7

Lysinuric protein intolerance characterized by bone marrow abnormalities and severe clinical course.

Parenti G, Sebastio G, Strisciuglio P, Incerti B, Pecoraro C, Terracciano L, Andria G. Parenti G, et al. J Pediatr. 1995 Feb;126(2):246-51. doi: 10.1016/s0022-3476(95)70552-x. J Pediatr. 1995. PMID: 7844671 Review.

8

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: parenti g. Acta Paediatr. 1996 Aug;85(8):937-42. doi: 10.1111/j.1651-2227.1996.tb14190.x. Acta Paediatr. 1996. PMID: 8863875

9

Pulmonary manifestations of Gaucher disease: an increased risk for L444P homozygotes?

Santamaria F, Parenti G, Guidi G, Filocamo M, Strisciuglio P, Grillo G, Farina V, Sarnelli P, Rizzolo MG, Rotondo A, Andria G. Santamaria F, et al. Among authors: parenti g. Am J Respir Crit Care Med. 1998 Mar;157(3 Pt 1):985-9. doi: 10.1164/ajrccm.157.3.9706057. Am J Respir Crit Care Med. 1998. PMID: 9517621

10

HHH syndrome (hyperornithinaemia, hyperammonaemia, homocitrullinuria), with fulminant hepatitis-like presentation.

Fecarotta S, Parenti G, Vajro P, Zuppaldi A, Della Casa R, Carbone MT, Correra A, Torre G, Riva S, Dionisi-Vici C, Santorelli FM, Andria G. Fecarotta S, et al. Among authors: parenti g. J Inherit Metab Dis. 2006 Feb;29(1):186-9. doi: 10.1007/s10545-006-0120-7. J Inherit Metab Dis. 2006. PMID: 16601889

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

401 results

Search Page