Zelikovic I - Search Results

1

A novel missense mutation in SLC5A2 encoding SGLT2 underlies autosomal-recessive renal glucosuria and aminoaciduria.

Magen D, Sprecher E, Zelikovic I, Skorecki K. Magen D, et al. Among authors: zelikovic i. Kidney Int. 2005 Jan;67(1):34-41. doi: 10.1111/j.1523-1755.2005.00053.x. Kidney Int. 2005. PMID: 15610225 Free article.

2

Autosomal recessive renal proximal tubulopathy and hypercalciuria: a new syndrome.

Magen D, Adler L, Mandel H, Efrati E, Zelikovic I. Magen D, et al. Among authors: zelikovic i. Am J Kidney Dis. 2004 Apr;43(4):600-6. doi: 10.1053/j.ajkd.2003.12.024. Am J Kidney Dis. 2004. PMID: 15042536

3

A loss-of-function mutation in NaPi-IIa and renal Fanconi's syndrome.

Magen D, Berger L, Coady MJ, Ilivitzki A, Militianu D, Tieder M, Selig S, Lapointe JY, Zelikovic I, Skorecki K. Magen D, et al. Among authors: zelikovic i. N Engl J Med. 2010 Mar 25;362(12):1102-9. doi: 10.1056/NEJMoa0905647. N Engl J Med. 2010. PMID: 20335586 Free article.

4

Mutations in GALNT3, encoding a protein involved in O-linked glycosylation, cause familial tumoral calcinosis.

Topaz O, Shurman DL, Bergman R, Indelman M, Ratajczak P, Mizrachi M, Khamaysi Z, Behar D, Petronius D, Friedman V, Zelikovic I, Raimer S, Metzker A, Richard G, Sprecher E. Topaz O, et al. Among authors: zelikovic i. Nat Genet. 2004 Jun;36(6):579-81. doi: 10.1038/ng1358. Epub 2004 May 9. Nat Genet. 2004. PMID: 15133511

5

Clinical quiz. Maternal chronic bilateral nephropathy.

Magen D, Blazer S, Zelikovic I. Magen D, et al. Among authors: zelikovic i. Pediatr Nephrol. 2002 Aug;17(8):695-8. doi: 10.1007/s00467-002-0856-8. Pediatr Nephrol. 2002. PMID: 12214597 No abstract available.

6

An infant with polydactyly and renal anomalies: early diagnosis of a rare syndrome.

Magen D, Ish-Shalom N, Lorber A, Khoury A, Zelikovic I. Magen D, et al. Among authors: zelikovic i. Nephrol Dial Transplant. 2002 Dec;17(12):2261-4. doi: 10.1093/ndt/17.12.2261. Nephrol Dial Transplant. 2002. PMID: 12454245 No abstract available.

7

A novel mutation in the chloride channel gene, CLCNKB, as a cause of Gitelman and Bartter syndromes.

Zelikovic I, Szargel R, Hawash A, Labay V, Hatib I, Cohen N, Nakhoul F. Zelikovic I, et al. Kidney Int. 2003 Jan;63(1):24-32. doi: 10.1046/j.1523-1755.2003.00730.x. Kidney Int. 2003. PMID: 12472765 Free article.

8

MPGN type I induced by granulocyte colony stimulating factor.

Magen D, Mandel H, Berant M, Ben-Izhak O, Zelikovic I. Magen D, et al. Among authors: zelikovic i. Pediatr Nephrol. 2002 May;17(5):370-2. doi: 10.1007/s00467-002-0847-9. Pediatr Nephrol. 2002. PMID: 12042897

9

Early performance of voiding cystourethrogram after urinary tract infection in children.

Kassis I, Kovalski Y, Magen D, Berkowitz D, Zelikovic I. Kassis I, et al. Among authors: zelikovic i. Isr Med Assoc J. 2008 Jun;10(6):453-6. Isr Med Assoc J. 2008. PMID: 18669146 Free article.

10

Fanconi-Bickel syndrome and autosomal recessive proximal tubulopathy with hypercalciuria (ARPTH) are allelic variants caused by GLUT2 mutations.

Mannstadt M, Magen D, Segawa H, Stanley T, Sharma A, Sasaki S, Bergwitz C, Mounien L, Boepple P, Thorens B, Zelikovic I, Jüppner H. Mannstadt M, et al. Among authors: zelikovic i. J Clin Endocrinol Metab. 2012 Oct;97(10):E1978-86. doi: 10.1210/jc.2012-1279. Epub 2012 Aug 3. J Clin Endocrinol Metab. 2012. PMID: 22865906 Free PMC article.

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