Anthony Bleyer to Biopsy
This is a "connection" page, showing publications Anthony Bleyer has written about Biopsy.
Connection Strength
0.334
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Devuyst O, Olinger E, Weber S, Eckardt KU, Kmoch S, Rampoldi L, Bleyer AJ. Autosomal dominant tubulointerstitial kidney disease. Nat Rev Dis Primers. 2019 09 05; 5(1):60.
Score: 0.158
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Gupta K, Iskandar SS, Daeihagh P, Ratliff HL, Bleyer AJ. Distribution of pathologic findings in individuals with nephrotic proteinuria according to serum albumin. Nephrol Dial Transplant. 2008 May; 23(5):1595-9.
Score: 0.070
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Murray SL, Dorman A, Benson KA, Connaughton DM, Stapleton CP, Fennelly NK, Kennedy C, McDonnell CA, Kidd K, Cormican SM, Ryan LA, Lavin P, Little MA, Bleyer AJ, Doyle B, Cavalleri GL, Hildebrandt F, Conlon PJ. Utility of Genomic Testing after Renal Biopsy. Am J Nephrol. 2020; 51(1):43-53.
Score: 0.040
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Yu SM, Bleyer AJ, Anis K, Herlitz L, Živná M, Hulková H, Markowitz GS, Jim B. Autosomal Dominant Tubulointerstitial Kidney Disease Due to MUC1 Mutation. Am J Kidney Dis. 2018 04; 71(4):495-500.
Score: 0.035
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Bolar NA, Golzio C, Živná M, Hayot G, Van Hemelrijk C, Schepers D, Vandeweyer G, Hoischen A, Huyghe JR, Raes A, Matthys E, Sys E, Azou M, Gubler MC, Praet M, Van Camp G, McFadden K, Pediaditakis I, Pristoupilová A, Hodanová K, Vyletal P, Hartmannová H, Stránecký V, Hulková H, Barešová V, Jedlicková I, Sovová J, Hnízda A, Kidd K, Bleyer AJ, Spong RS, Vande Walle J, Mortier G, Brunner H, Van Laer L, Kmoch S, Katsanis N, Loeys BL. Heterozygous Loss-of-Function SEC61A1 Mutations Cause Autosomal-Dominant Tubulo-Interstitial and Glomerulocystic Kidney Disease with Anemia. Am J Hum Genet. 2016 Jul 07; 99(1):174-87.
Score: 0.032