Giuseppina Marra
Overview
Explore the profile of Giuseppina Marra including associated specialties, affiliations and a list of published articles.
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Articles
17
Citations
414
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0
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Recent Articles
1.
La Scola C, Marra G, Ammenti A, Pasini A, Taroni F, Bertulli C, et al.
Pediatr Nephrol
. 2020 Mar;
35(8):1483-1490.
PMID: 32211991
Background: Subjects with a congenital solitary kidney (CSK) are believed to be at risk of hypertension due to their low number of nephrons. However, as CSK is a congenital abnormality...
2.
Ammenti A, Alberici I, Brugnara M, Chimenz R, Guarino S, La Manna A, et al.
Acta Paediatr
. 2019 Aug;
109(2):236-247.
PMID: 31454101
Aim: Our aim was to update the recommendations for the diagnosis, treatment and follow-up of the first febrile urinary tract infection in young children, which were endorsed in 2012 by...
3.
Marra G, Taroni F, Berrettini A, Montanari E, Manzoni G, Montini G
J Nephrol
. 2018 Apr;
32(2):199-210.
PMID: 29680873
Nephrolithiasis is a rare disease in children. For many years children with kidney stones have been managed like "small adults", but there are significant differences between the pediatric and the...
4.
Montini G, Edefonti A, Galan Y, Diaz M, Medina Manzanarez M, Marra G, et al.
PLoS One
. 2016 May;
11(5):e0153963.
PMID: 27171479
Background: The widely recognized clinical and epidemiological relevance of the socioeconomic determinants of health-disease conditions is expected to be specifically critical in terms of chronic diseases in fragile populations in...
5.
Salice P, Ardissino G, Barbier P, Baca L, Vecchi D, Ghiglia S, et al.
J Hypertens
. 2013 Oct;
31(11):2165-75.
PMID: 24077245
Background And Objectives: Information on ambulatory blood pressure monitoring (ABPM) in children is scarce. While in adults office BP (OBP) is higher than ABP and the difference increases as OBP...
6.
Giani M, Mastrangelo A, Villa R, Turolo S, Marra G, Tirelli A, et al.
Pediatr Nephrol
. 2013 Jun;
28(9):1837-42.
PMID: 23748277
Background: Alport syndrome (AS) is a progressive hereditary glomerular disease. Recent data indicate that aldosterone promotes fibrosis mediated by the transforming growth factor-β1 (TGF-β1) pathway, which may worsen proteinuria. Spironolactone...
7.
Adenine phosphoribosyltransferase deficiency: an underdiagnosed cause of lithiasis and renal failure
Marra G, Vercelloni P, Edefonti A, Manzoni G, Pavesi M, Fogazzi G, et al.
JIMD Rep
. 2013 Feb;
5:45-8.
PMID: 23430916
We describe an infant affected by adenine phosphoribosyltransferase (APRT) deficiency diagnosed at 18 months of age with a de novo mutation that has not been previously reported. APRT deficiency is...
8.
Marra G, Vercelloni P
Pediatr Med Chir
. 2012 Nov;
34(4):202-3.
PMID: 23173414
No abstract available.
9.
Addis M, Meloni C, Tosetto E, Ceol M, Cristofaro R, Melis M, et al.
Eur J Hum Genet
. 2012 Oct;
21(6):687-90.
PMID: 23047739
Dent's disease is an X-linked renal tubulopathy caused by mutations mainly affecting the CLCN5 gene. Defects in the OCRL gene, which is usually mutated in patients with Lowe syndrome, have...
10.
Ammenti A, Cataldi L, Chimenz R, Fanos V, La Manna A, Marra G, et al.
Acta Paediatr
. 2011 Nov;
101(5):451-7.
PMID: 22122295
Unlabelled: We report the recommendations for the diagnosis, treatment, imaging evaluation and use of antibiotic prophylaxis in children with the first febrile urinary tract infection, aged 2 months to 3...