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Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations.
Am J Hum Genet. 2017 Nov 2;101(5):789-802. doi: 10.1016/j.ajhg.2017.09.018.
Am J Hum Genet. 2017.
PMID: 29100090
Free PMC article.
Copy-number disorders are a common cause of congenital kidney malformations.
Sanna-Cherchi S, Kiryluk K, Burgess KE, Bodria M, Sampson MG, Hadley D, Nees SN, Verbitsky M, Perry BJ, Sterken R, Lozanovski VJ, Materna-Kiryluk A, Barlassina C, Kini A, Corbani V, Carrea A, Somenzi D, Murtas C, Ristoska-Bojkovska N, Izzi C, Bianco B, Zaniew M, Flogelova H, Weng PL, Kacak N, Giberti S, Gigante M, Arapovic A, Drnasin K, Caridi G, Curioni S, Allegri F, Ammenti A, Ferretti S, Goj V, Bernardo L, Jobanputra V, Chung WK, Lifton RP, Sanders S, State M, Clark LN, Saraga M, Padmanabhan S, Dominiczak AF, Foroud T, Gesualdo L, Gucev Z, Allegri L, Latos-Bielenska A, Cusi D, Scolari F, Tasic V, Hakonarson H, Ghiggeri GM, Gharavi AG.
Sanna-Cherchi S, et al. Among authors: goj v.
Am J Hum Genet. 2012 Dec 7;91(6):987-97. doi: 10.1016/j.ajhg.2012.10.007. Epub 2012 Nov 15.
Am J Hum Genet. 2012.
PMID: 23159250
Free PMC article.
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Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations.
Sanna-Cherchi S, Khan K, Westland R, Krithivasan P, Fievet L, Rasouly HM, Ionita-Laza I, Capone VP, Fasel DA, Kiryluk K, Kamalakaran S, Bodria M, Otto EA, Sampson MG, Gillies CE, Vega-Warner V, Vukojevic K, Pediaditakis I, Makar GS, Mitrotti A, Verbitsky M, Martino J, Liu Q, Na YJ, Goj V, Ardissino G, Gigante M, Gesualdo L, Janezcko M, Zaniew M, Mendelsohn CL, Shril S, Hildebrandt F, van Wijk JAE, Arapovic A, Saraga M, Allegri L, Izzi C, Scolari F, Tasic V, Ghiggeri GM, Latos-Bielenska A, Materna-Kiryluk A, Mane S, Goldstein DB, Lifton RP, Katsanis N, Davis EE, Gharavi AG.
Sanna-Cherchi S, et al. Among authors: goj v.
Am J Hum Genet. 2017 Dec 7;101(6):1034. doi: 10.1016/j.ajhg.2017.11.003.
Am J Hum Genet. 2017.
PMID: 29220675
Free PMC article.
No abstract available.
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Severe prolonged neutropenia following administration of tocilizumab in a patient affected by COVID-19: a case report and brief review of the literature.
Bernardo L, Del Sesto S, Giordano L, Benincaso AR, Biondi P, Goj V, Ferrara F, Talenti A, Grisolia A, Ascierto PA.
Bernardo L, et al. Among authors: goj v.
Drugs Ther Perspect. 2020;36(12):568-572. doi: 10.1007/s40267-020-00777-z. Epub 2020 Sep 14.
Drugs Ther Perspect. 2020.
PMID: 32952393
Free PMC article.
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Best practice guidelines for idiopathic nephrotic syndrome: recommendations versus reality.
Pasini A, Aceto G, Ammenti A, Ardissino G, Azzolina V, Bettinelli A, Cama E, Cantatore S, Crisafi A, Conti G, D'Agostino M, Dozza A, Edefonti A, Fede C, Groppali E, Gualeni C, Lavacchini A, Lepore M, Maringhini S, Mariotti P, Materassi M, Mencarelli F, Messina G, Negri A, Piepoli M, Ravaglia F, Simoni A, Spagnoletta L, Montini G; NefroKid Study Group.
Pasini A, et al.
Pediatr Nephrol. 2015 Jan;30(1):91-101. doi: 10.1007/s00467-014-2903-7. Epub 2014 Aug 17.
Pediatr Nephrol. 2015.
PMID: 25127916
Free PMC article.
Clinical Trial.
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Persistent tubular resistance to aldosterone in infants with congenital hydronephrosis corrected neonatally.
Marra G, Goj V, Appiani AC, Dell Agnola CA, Tirelli SA, Tadini B, Nicolini U, Cavanna G, Assael BM.
Marra G, et al. Among authors: goj v.
J Pediatr. 1987 Jun;110(6):868-72. doi: 10.1016/s0022-3476(87)80398-0.
J Pediatr. 1987.
PMID: 3295159
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Early childhood hyperkalemia: variety of pseudohypoaldosteronism.
Claris Appiani A, Marra G, Tirelli SA, Goj V, Romeo L, Cavanna G, Assael BM.
Claris Appiani A, et al. Among authors: goj v.
Acta Paediatr Scand. 1986 Nov;75(6):970-4. doi: 10.1111/j.1651-2227.1986.tb10325.x.
Acta Paediatr Scand. 1986.
PMID: 3551490
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Renal tubular acidosis in a case of Shwachman's syndrome.
Marra G, Claris Appiani A, Romeo L, Marzorati D, Valade A, Goj V, Assael BM.
Marra G, et al. Among authors: goj v.
Acta Paediatr Scand. 1986 Jul;75(4):682-4. doi: 10.1111/j.1651-2227.1986.tb10273.x.
Acta Paediatr Scand. 1986.
PMID: 3751564
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