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Page 1
Modifiers of Autosomal Dominant Polycystic Kidney Disease Severity: The Role of PKD1 Hypomorphic Alleles.
Genes (Basel). 2023 Jun 7;14(6):1230. doi: 10.3390/genes14061230.
Genes (Basel). 2023.
PMID: 37372410
Free PMC article.
Review.
Identification of a serum and urine extracellular vesicle signature predicting renal outcome after kidney transplant.
Burrello J, Monticone S, Burrello A, Bolis S, Cristalli CP, Comai G, Corradetti V, Grange C, Orlando G, Bonafè M, La Manna G, Barile L, Bussolati B.
Burrello J, et al. Among authors: cristalli cp.
Nephrol Dial Transplant. 2023 Feb 28;38(3):764-777. doi: 10.1093/ndt/gfac259.
Nephrol Dial Transplant. 2023.
PMID: 36073758
Free PMC article.
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DNAJB11 Mutation in ADPKD Patients: Clinical Characteristics in a Monocentric Cohort.
Aiello V, Ciurli F, Conti A, Cristalli CP, Lerario S, Montanari F, Sciascia N, Vischini G, Fabbrizio B, Di Costanzo R, Olivucci G, Pietra A, Lopez A, Zambianchi L, La Manna G, Capelli I.
Aiello V, et al. Among authors: cristalli cp.
Genes (Basel). 2023 Dec 19;15(1):3. doi: 10.3390/genes15010003.
Genes (Basel). 2023.
PMID: 38275584
Free PMC article.
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Gene Panel Analysis in a Large Cohort of Patients With Autosomal Dominant Polycystic Kidney Disease Allows the Identification of 80 Potentially Causative Novel Variants and the Characterization of a Complex Genetic Architecture in a Subset of Families.
Mantovani V, Bin S, Graziano C, Capelli I, Minardi R, Aiello V, Ambrosini E, Cristalli CP, Mattiaccio A, Pariali M, De Fanti S, Faletra F, Grosso E, Cantone R, Mancini E, Mencarelli F, Pasini A, Wischmeijer A, Sciascia N, Seri M, La Manna G.
Mantovani V, et al. Among authors: cristalli cp.
Front Genet. 2020 May 7;11:464. doi: 10.3389/fgene.2020.00464. eCollection 2020.
Front Genet. 2020.
PMID: 32457805
Free PMC article.
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Pleiotropic genes in psychiatry: Calcium channels and the stress-related FKBP5 gene in antidepressant resistance.
Fabbri C, Corponi F, Albani D, Raimondi I, Forloni G, Schruers K, Kasper S, Kautzky A, Zohar J, Souery D, Montgomery S, Cristalli CP, Mantovani V, Mendlewicz J, Serretti A.
Fabbri C, et al. Among authors: cristalli cp.
Prog Neuropsychopharmacol Biol Psychiatry. 2018 Feb 2;81:203-210. doi: 10.1016/j.pnpbp.2017.10.005. Epub 2017 Oct 6.
Prog Neuropsychopharmacol Biol Psychiatry. 2018.
PMID: 28989100
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A novel compound heterozygous mutation in an adolescent with insulin-dependent diabetes: The challenge of characterizing Wolfram syndrome.
Maltoni G, Minardi R, Cristalli CP, Nardi L, D'Alberton F, Mantovani V, Zucchini S.
Maltoni G, et al. Among authors: cristalli cp.
Diabetes Res Clin Pract. 2016 Nov;121:59-61. doi: 10.1016/j.diabres.2016.08.020. Epub 2016 Sep 8.
Diabetes Res Clin Pract. 2016.
PMID: 27657458
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