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Items: 10

1.

Acute kidney injury promotes development of papillary renal cell adenoma and carcinoma from renal progenitor cells.

Peired AJ, Antonelli G, Angelotti ML, Allinovi M, Guzzi F, Sisti A, Semeraro R, Conte C, Mazzinghi B, Nardi S, Melica ME, De Chiara L, Lazzeri E, Lasagni L, Lottini T, Landini S, Giglio S, Mari A, Di Maida F, Antonelli A, Porpiglia F, Schiavina R, Ficarra V, Facchiano D, Gacci M, Serni S, Carini M, Netto GJ, Roperto RM, Magi A, Christiansen CF, Rotondi M, Liapis H, Anders HJ, Minervini A, Raspollini MR, Romagnani P.

Sci Transl Med. 2020 Mar 25;12(536). pii: eaaw6003. doi: 10.1126/scitranslmed.aaw6003.

PMID:
32213630
2.

Reverse Phenotyping after Whole-Exome Sequencing in Steroid-Resistant Nephrotic Syndrome.

Landini S, Mazzinghi B, Becherucci F, Allinovi M, Provenzano A, Palazzo V, Ravaglia F, Artuso R, Bosi E, Stagi S, Sansavini G, Guzzi F, Cirillo L, Vaglio A, Murer L, Peruzzi L, Pasini A, Materassi M, Roperto RM, Anders HJ, Rotondi M, Giglio SR, Romagnani P.

Clin J Am Soc Nephrol. 2020 Jan 7;15(1):89-100. doi: 10.2215/CJN.06060519. Epub 2019 Dec 12.

PMID:
31831576
3.

Molecular Mechanisms of the Acute Kidney Injury to Chronic Kidney Disease Transition: An Updated View.

Guzzi F, Cirillo L, Roperto RM, Romagnani P, Lazzeri E.

Int J Mol Sci. 2019 Oct 6;20(19). pii: E4941. doi: 10.3390/ijms20194941. Review.

4.

Favorable course of previously undiagnosed Methylmalonic Aciduria with Homocystinuria (cblC type) presenting with pulmonary hypertension and aHUS in a young child: a case report.

De Simone L, Capirchio L, Roperto RM, Romagnani P, Sacchini M, Donati MA, de Martino M.

Ital J Pediatr. 2018 Aug 13;44(1):90. doi: 10.1186/s13052-018-0530-9.

5.

A propensity-matched comparison of hard outcomes in children on chronic dialysis.

Vidal E, Chesnaye NC, Paglialonga F, Minale B, Leozappa G, Giordano M, Gianoglio B, Corrado C, Roperto RM, Chimenz R, Mencarelli F, Ratsch IM, Murer L, Verrina E; Italian Registry for Paediatric Chronic Dialysis.

Eur J Pediatr. 2018 Jan;177(1):117-124. doi: 10.1007/s00431-017-3040-7. Epub 2017 Nov 16.

PMID:
29143935
6.

Role of eculizumab in a pediatric refractory gemcitabine-induced thrombotic microangiopathy: a case report.

Facchini L, Lucchesi M, Stival A, Roperto RM, Melosi F, Materassi M, Farina S, Tintori V, de Martino M, Sardi I.

J Med Case Rep. 2017 Jul 27;11(1):209. doi: 10.1186/s13256-017-1373-5.

7.

The genetic and clinical spectrum of a large cohort of patients with distal renal tubular acidosis.

Palazzo V, Provenzano A, Becherucci F, Sansavini G, Mazzinghi B, Orlandini V, Giunti L, Roperto RM, Pantaleo M, Artuso R, Andreucci E, Bargiacchi S, Traficante G, Stagi S, Murer L, Benetti E, Emma F, Giordano M, Rivieri F, Colussi G, Penco S, Manfredini E, Caruso MR, Garavelli L, Andrulli S, Vergine G, Miglietti N, Mancini E, Malaventura C, Percesepe A, Grosso E, Materassi M, Romagnani P, Giglio S.

Kidney Int. 2017 May;91(5):1243-1255. doi: 10.1016/j.kint.2016.12.017. Epub 2017 Feb 21.

PMID:
28233610
8.

Chronic kidney disease in children.

Becherucci F, Roperto RM, Materassi M, Romagnani P.

Clin Kidney J. 2016 Aug;9(4):583-91. doi: 10.1093/ckj/sfw047. Epub 2016 Jun 5.

9.

Human Urine-Derived Renal Progenitors for Personalized Modeling of Genetic Kidney Disorders.

Lazzeri E, Ronconi E, Angelotti ML, Peired A, Mazzinghi B, Becherucci F, Conti S, Sansavini G, Sisti A, Ravaglia F, Lombardi D, Provenzano A, Manonelles A, Cruzado JM, Giglio S, Roperto RM, Materassi M, Lasagni L, Romagnani P.

J Am Soc Nephrol. 2015 Aug;26(8):1961-74. doi: 10.1681/ASN.2014010057. Epub 2015 Jan 7.

10.

Heterogeneous genetic alterations in sporadic nephrotic syndrome associate with resistance to immunosuppression.

Giglio S, Provenzano A, Mazzinghi B, Becherucci F, Giunti L, Sansavini G, Ravaglia F, Roperto RM, Farsetti S, Benetti E, Rotondi M, Murer L, Lazzeri E, Lasagni L, Materassi M, Romagnani P.

J Am Soc Nephrol. 2015 Jan;26(1):230-6. doi: 10.1681/ASN.2013111155. Epub 2014 Jul 24.

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