D'Alessandro MM - Search Results

1

Primary hyperoxaluria in Italy: the past 30 years and the near future of a (not so) rare disease.

Mandrile G, Pelle A, Sciannameo V, Benetti E, D'Alessandro MM, Emma F, Montini G, Peruzzi L, Petrarulo M, Romagnoli R, Vitale C, Cellini B, Giachino D. Mandrile G, et al. Among authors: d alessandro mm. J Nephrol. 2022 Apr;35(3):841-850. doi: 10.1007/s40620-022-01258-4. Epub 2022 Feb 26. J Nephrol. 2022. PMID: 35218550 Free PMC article.

2

Lumasiran treatment in pediatric patients with PH1: real-world data within a compassionate use program in Italy.

Taroni F, Peruzzi L, Longo G, Becherucci F, Malgieri G, D'Alessandro MM, Montini G. Taroni F, et al. Among authors: d alessandro mm. Clin Kidney J. 2024 Mar 28;17(5):sfae090. doi: 10.1093/ckj/sfae090. eCollection 2024 May. Clin Kidney J. 2024. PMID: 38742209 Free PMC article.

3

[Severe renal failure in a child].

Maringhini S, D'Alessandro MM, Di Martino A, Stella M, Raiata F, Marangella M. Maringhini S, et al. G Ital Nefrol. 2004 Nov-Dec;21(6):581-6. G Ital Nefrol. 2004. PMID: 15593027 Italian.

4

Mutational Spectrum of CYP24A1 Gene in a Cohort of Italian Patients with Idiopathic Infantile Hypercalcemia.

Gigante M, Santangelo L, Diella S, Caridi G, Argentiero L, D''Alessandro MM, Martino M, Stea ED, Ardissino G, Carbone V, Pepe S, Scrutinio D, Maringhini S, Ghiggeri GM, Grandaliano G, Giordano M, Gesualdo L. Gigante M, et al. Nephron. 2016;133(3):193-204. doi: 10.1159/000446663. Epub 2016 Jul 9. Nephron. 2016. PMID: 27394135

5

Fourier Transform Infrared Analysis of Urinary Calculi and Metabolic Studies in a Group of Sicilian Children.

D'Alessandro MM, Gennaro G, Tralongo P, Maringhini S. D'Alessandro MM, et al. Iran J Kidney Dis. 2017 May;11(3):209-216. Iran J Kidney Dis. 2017. PMID: 28575881 Free article.

6

Renal angiomyolipomatosis and bleeding aneurysms in a tuberous sclerosis context: selective artery embolization in a girl with end-stage renal failure.

Pelizzo G, Vallone MG, Milazzo M, Rosone G, Amoroso S, Pavone G, D'Alessandro MM, Unti E, Calcaterra V. Pelizzo G, et al. Pediatr Rep. 2020 Aug 6;12(2):8352. doi: 10.4081/pr.2020.8352. eCollection 2020 Aug 6. Pediatr Rep. 2020. PMID: 32922707 Free PMC article.

7

Autosomal recessive polycystic kidney disease: case report of a newborn with rare PKHD1 mutation, rapid renal enlargement and early fatal outcome.

Serra G, Corsello G, Antona V, D'Alessandro MM, Cassata N, Cimador M, Giuffrè M, Schierz IAM, Piro E. Serra G, et al. Ital J Pediatr. 2020 Oct 15;46(1):154. doi: 10.1186/s13052-020-00922-4. Ital J Pediatr. 2020. PMID: 33059727 Free PMC article.

8

[Nephrocalcinosis in children].

D'Alessandro MM, Pavone G, Castiglione MC, Tranchida AM, Sapia MC, Cusumano R, Corrado C, Mongiovì R, Maringhini S. D'Alessandro MM, et al. G Ital Nefrol. 2015 Dec;35(Suppl 71):2018-supp71. G Ital Nefrol. 2015. PMID: 29710439 Italian.

9

[Atypical Hemolytic Uremic Syndrome: experience of a pediatric center].

Cusumano R, Sapia MC, Corrado C, La Barba E, D'Alessandro MM, Pavone G, Maringhini S. Cusumano R, et al. G Ital Nefrol. 2015 Dec;35(Suppl 71):2018-supp71. G Ital Nefrol. 2015. PMID: 29710440 Italian.

10

Novel SCNN1A gene splicing-site mutation causing autosomal recessive pseudohypoaldosteronism type 1 (PHA1) in two Italian patients belonging to the same small town.

Serra G, Antona V, D'Alessandro MM, Maggio MC, Verde V, Corsello G. Serra G, et al. Among authors: d alessandro mm. Ital J Pediatr. 2021 Jun 16;47(1):138. doi: 10.1186/s13052-021-01080-x. Ital J Pediatr. 2021. PMID: 34134742 Free PMC article.

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