Landau D - Search Results

1

Familial autosomal recessive renal tubular acidosis: importance of early diagnosis.

Vivante A, Lotan D, Pode-Shakked N, Landau D, Svec P, Nampoothiri S, Verma I, Abu-Libdeh A, Bockenhauer D, Dekel B, Anikster Y. Vivante A, et al. Among authors: landau d. Nephron Physiol. 2011;119(3):p31-9. doi: 10.1159/000329668. Epub 2011 Aug 18. Nephron Physiol. 2011. PMID: 21849803

2

Renal hypodysplasia associates with a WNT4 variant that causes aberrant canonical WNT signaling.

Vivante A, Mark-Danieli M, Davidovits M, Harari-Steinberg O, Omer D, Gnatek Y, Cleper R, Landau D, Kovalski Y, Weissman I, Eisenstein I, Soudack M, Wolf HR, Issler N, Lotan D, Anikster Y, Dekel B. Vivante A, et al. Among authors: landau d. J Am Soc Nephrol. 2013 Mar;24(4):550-8. doi: 10.1681/ASN.2012010097. Epub 2013 Mar 21. J Am Soc Nephrol. 2013. PMID: 23520208 Free PMC article.

3

Clinical Approach to Proximal Renal Tubular Acidosis in Children.

Finer G, Landau D. Finer G, et al. Among authors: landau d. Adv Chronic Kidney Dis. 2018 Jul;25(4):351-357. doi: 10.1053/j.ackd.2018.05.006. Adv Chronic Kidney Dis. 2018. PMID: 30139461 Review.

4

Effect of growth hormone therapy on IGF-I, bone GLA-protein and bone mineral content in short children with and without chronic renal failure.

Zadik Z, Vaisman N, Lotan D, Vaisman E, Landau D, Blachar Y, Katz A, Drukker A. Zadik Z, et al. Among authors: landau d. Horm Res. 1992;38(3-4):145-9. doi: 10.1159/000182530. Horm Res. 1992. PMID: 1306846

5

Two novel homozygous SLC2A9 mutations cause renal hypouricemia type 2.

Dinour D, Gray NK, Ganon L, Knox AJ, Shalev H, Sela BA, Campbell S, Sawyer L, Shu X, Valsamidou E, Landau D, Wright AF, Holtzman EJ. Dinour D, et al. Among authors: landau d. Nephrol Dial Transplant. 2012 Mar;27(3):1035-41. doi: 10.1093/ndt/gfr419. Epub 2011 Aug 2. Nephrol Dial Transplant. 2012. PMID: 21810765

6

Hemolytic Uremic Syndrome: A Contemporary Pediatric Experience.

Alfandary H, Rinat C, Gurevich E, Eisenstein I, Goldberg O, Kropach N, Landau D. Alfandary H, et al. Among authors: landau d. Nephron. 2020;144(3):109-117. doi: 10.1159/000505401. Epub 2020 Jan 14. Nephron. 2020. PMID: 31935726

7

Is the prognosis of congenital single functioning kidney benign? A population-based study.

Alfandary H, Haskin O, Goldberg O, Dagan A, Borovitz Y, Levi S, Davidovits M, Erlich T, Landau D, Pleniceanu O. Alfandary H, et al. Among authors: landau d. Pediatr Nephrol. 2021 Sep;36(9):2837-2845. doi: 10.1007/s00467-021-04980-6. Epub 2021 Feb 22. Pediatr Nephrol. 2021. PMID: 33619660

8

Incidence of Impaired Kidney Function Among Adolescent Patients Hospitalized With Anorexia Nervosa.

Gurevich E, Steiling S, Landau D. Gurevich E, et al. Among authors: landau d. JAMA Netw Open. 2021 Nov 1;4(11):e2134908. doi: 10.1001/jamanetworkopen.2021.34908. JAMA Netw Open. 2021. PMID: 34807260 Free PMC article.

9

[NEPHROTIC SYNDROME RECURRENCE POST-RENAL TRANSPLANTATION: 10 YEARS' EXPERIENCE AT SCHNEIDER CHILDREN'S MEDICAL CENTER IN ISRAEL].

Fisher D, Borovitz Y, Alfandari H, LEvi S, Hamdani G, Dagan A, Davidovits M, Landau D, Haskin O. Fisher D, et al. Among authors: landau d. Harefuah. 2021 Dec;160(12):786-792. Harefuah. 2021. PMID: 34957712 Hebrew.

10

[Genetic and phenotypic aspects of autosomal recessive polycystic kidney disease in southern Israel].

Finer G, Birk O, Landau D. Finer G, et al. Among authors: landau d. Harefuah. 2004 Jul;143(7):466-70, 552. Harefuah. 2004. PMID: 15669417 Hebrew.

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