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Items: 43

1.

Effect of Peritoneal Dialysis on Serum Fibrosis Biomarkers in Patients with Refractory Congestive Heart Failure.

Kunin M, Carmon V, Beckerman P, Dinour D.

Int J Mol Sci. 2019 May 28;20(11). pii: E2610. doi: 10.3390/ijms20112610.

2.

Intraperitoneal antibiotic administration for prevention of postoperative peritoneal catheter-related infections.

Kunin M, Dinour D, Rosin D.

Clin Exp Nephrol. 2018 Apr;22(2):448-452. doi: 10.1007/s10157-017-1476-8. Epub 2017 Sep 14.

PMID:
28913721
3.

Hyponatremia in refractory congestive heart failure patients treated with icodextrin-based peritoneal dialysis: A case series.

Kunin M, Ganon L, Holtzman EJ, Dinour D.

Nefrologia. 2018 Jan - Feb;38(1):87-91. doi: 10.1016/j.nefro.2017.05.010. Epub 2017 Jul 29. English, Spanish.

4.

High Normal Uric Acid Levels Are Associated with an Increased Risk of Diabetes in Lean, Normoglycemic Healthy Women.

Shani M, Vinker S, Dinour D, Leiba M, Twig G, Holtzman EJ, Leiba A.

J Clin Endocrinol Metab. 2016 Oct;101(10):3772-3778. Epub 2016 Aug 17.

PMID:
27533308
5.

Loss of function of NaPiIIa causes nephrocalcinosis and possibly kidney insufficiency.

Dinour D, Davidovits M, Ganon L, Ruminska J, Forster IC, Hernando N, Eyal E, Holtzman EJ, Wagner CA.

Pediatr Nephrol. 2016 Dec;31(12):2289-2297. Epub 2016 Jul 4.

6.

Inflammatory Biomarkers in Refractory Congestive Heart Failure Patients Treated with Peritoneal Dialysis.

Kunin M, Carmon V, Arad M, Levin-Iaina N, Freimark D, Holtzman EJ, Dinour D.

Biomed Res Int. 2015;2015:590851. doi: 10.1155/2015/590851. Epub 2015 Oct 11.

7.

Uric acid levels within the normal range predict increased risk of hypertension: a cohort study.

Leiba A, Vinker S, Dinour D, Holtzman EJ, Shani M.

J Am Soc Hypertens. 2015 Aug;9(8):600-9. doi: 10.1016/j.jash.2015.05.010. Epub 2015 May 16.

PMID:
26101171
8.

Evaluation of an infant with hypercalcemia.

Dinour D, Ganon L.

Pediatr Nephrol. 2015 Mar;30(3):537. doi: 10.1007/s00467-014-2993-2. Epub 2014 Dec 19. No abstract available.

PMID:
25523476
9.

Maternal and infantile hypercalcemia caused by vitamin-D-hydroxylase mutations and vitamin D intake.

Dinour D, Davidovits M, Aviner S, Ganon L, Michael L, Modan-Moses D, Vered I, Bibi H, Frishberg Y, Holtzman EJ.

Pediatr Nephrol. 2015 Jan;30(1):145-52. doi: 10.1007/s00467-014-2889-1. Epub 2014 Sep 7.

PMID:
25194629
10.

Wild-type uromodulin prevents NFkB activation in kidney cells, while mutant uromodulin, causing FJHU nephropathy, does not.

Dinour D, Ganon L, Nomy LI, Ron R, Holtzman EJ.

J Nephrol. 2014 Jun;27(3):257-64. doi: 10.1007/s40620-014-0079-7. Epub 2014 Mar 20.

PMID:
24648000
11.

Chronic hypercalcaemia from inactivating mutations of vitamin D 24-hydroxylase (CYP24A1): implications for mineral metabolism changes in chronic renal failure.

Colussi G, Ganon L, Penco S, De Ferrari ME, Ravera F, Querques M, Primignani P, Holtzman EJ, Dinour D.

Nephrol Dial Transplant. 2014 Mar;29(3):636-43. doi: 10.1093/ndt/gft460. Epub 2013 Nov 13.

PMID:
24235083
12.

Familial Mediterranean fever (FMF) with proteinuria: clinical features, histology, predictors, and prognosis in a cohort of 25 patients.

Kukuy O, Livneh A, Ben-David A, Kopolovic J, Volkov A, Shinar Y, Holtzman E, Dinour D, Ben-Zvi I.

J Rheumatol. 2013 Dec;40(12):2083-7. doi: 10.3899/jrheum.130520. Epub 2013 Oct 15.

PMID:
24128782
13.

Peritoneal dialysis in patients with refractory congestive heart failure: potential prognostic factors.

Kunin M, Arad M, Dinour D, Freimark D, Holtzman EJ.

Blood Purif. 2013;35(4):285-94. doi: 10.1159/000351202. Epub 2013 May 24.

PMID:
23712042
14.

Severe and long-lasting hypotension occuring immediately after parathyroidectomy in hypertensive hemodialysis patients: a case series.

Leiba A, Cohen MS, Dinour D, Holtzman EJ.

J Hum Hypertens. 2013 Jun;27(6):399-401. doi: 10.1038/jhh.2012.49. No abstract available.

PMID:
23652769
15.

Loss-of-function mutations of CYP24A1, the vitamin D 24-hydroxylase gene, cause long-standing hypercalciuric nephrolithiasis and nephrocalcinosis.

Dinour D, Beckerman P, Ganon L, Tordjman K, Eisenstein Z, Holtzman EJ.

J Urol. 2013 Aug;190(2):552-7. doi: 10.1016/j.juro.2013.02.3188. Epub 2013 Mar 5.

PMID:
23470222
16.

[What a dentist should know about renal insufficiency: Part B].

Littner M, Littner D, Barenboim SF, Dinour D.

Refuat Hapeh Vehashinayim (1993). 2012 Oct;29(4):14-22, 71. Hebrew.

PMID:
23367723
17.

[What a dentist should know about renal insufficiency: Part A].

Littner M, Littner D, Barenboim SF, Dinour D.

Refuat Hapeh Vehashinayim (1993). 2012 Oct;29(4):7-13, 71. Hebrew.

PMID:
23367722
18.

Nephrotic range proteinuria and resistant hypertension--is it the egg that came first?

Leiba A, Capua M, Dinour D, Adir EH, Sela BA, Holtzman EJ.

Kidney Int. 2012 Sep;82(5):612. doi: 10.1038/ki.2012.121. No abstract available.

19.

Renal disease with OCRL1 mutations: Dent-2 or Lowe syndrome?

Levin-Iaina N, Dinour D.

J Pediatr Genet. 2012 Mar;1(1):3-5. doi: 10.3233/PGE-2012-002. No abstract available.

20.

Urinary organic anion transporter protein profiles in AKI.

Kunin M, Holtzman EJ, Melnikov S, Dinour D.

Nephrol Dial Transplant. 2012 Apr;27(4):1387-95. doi: 10.1093/ndt/gfr541. Epub 2011 Sep 26.

PMID:
21945944
21.

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.

Nephrol Dial Transplant. 2012 Mar;27(3):1035-41. doi: 10.1093/ndt/gfr419. Epub 2011 Aug 2.

PMID:
21810765
22.

Molecular study of proteinuria in patients treated with B₁₂ supplements: do not forget megaloblastic anemia type 1.

Levin-Iaina N, Dinour D, Morduchowicz G, Ganon L, Holtzman EJ.

Nephron Clin Pract. 2011;118(2):c67-71. doi: 10.1159/000320391. Epub 2010 Dec 8.

PMID:
21150213
23.

URAT1 mutations cause renal hypouricemia type 1 in Iraqi Jews.

Dinour D, Bahn A, Ganon L, Ron R, Geifman-Holtzman O, Knecht A, Gafter U, Rachamimov R, Sela BA, Burckhardt G, Holtzman EJ.

Nephrol Dial Transplant. 2011 Jul;26(7):2175-81. doi: 10.1093/ndt/gfq722. Epub 2010 Dec 9.

PMID:
21148271
24.

Homozygous SLC2A9 mutations cause severe renal hypouricemia.

Dinour D, Gray NK, Campbell S, Shu X, Sawyer L, Richardson W, Rechavi G, Amariglio N, Ganon L, Sela BA, Bahat H, Goldman M, Weissgarten J, Millar MR, Wright AF, Holtzman EJ.

J Am Soc Nephrol. 2010 Jan;21(1):64-72. doi: 10.1681/ASN.2009040406. Epub 2009 Nov 19.

25.

Dent's disease manifesting as focal glomerulosclerosis: Is it the tip of the iceberg?

Frishberg Y, Dinour D, Belostotsky R, Becker-Cohen R, Rinat C, Feinstein S, Navon-Elkan P, Ben-Shalom E.

Pediatr Nephrol. 2009 Dec;24(12):2369-73. doi: 10.1007/s00467-009-1299-2.

PMID:
19806368
26.

Truncating mutations in the chloride/proton ClC-5 antiporter gene in Seven Jewish Israeli families with Dent's 1 disease.

Dinour D, Davidovitz M, Levin-Iaina N, Lotan D, Cleper R, Weissman I, Knecht A, Holtzman EJ.

Nephron Clin Pract. 2009;112(4):c262-7. doi: 10.1159/000224793. Epub 2009 Jun 16.

PMID:
19546586
27.

Late diagnosis of primary hyperoxaluria type 2 in the adult: effect of a novel mutation in GRHPR gene on enzymatic activity and molecular modeling.

Levin-Iaina N, Dinour D, Romero L, Ron R, Brady RL, Cramer SD, Holtzman EJ.

J Urol. 2009 May;181(5):2146-51. doi: 10.1016/j.juro.2009.01.045. Epub 2009 Mar 17.

PMID:
19296982
28.

Non-urate transporter 1-related renal hypouricemia and acute renal failure in an Israeli-Arab family.

Bahat H, Dinour D, Ganon L, Feldman L, Holtzman EJ, Goldman M.

Pediatr Nephrol. 2009 May;24(5):999-1003. doi: 10.1007/s00467-008-1093-6. Epub 2009 Feb 3.

PMID:
19189137
29.

Mutations in the familial Mediterranean fever gene of patients with IgA nephropathy and other forms of glomerulonephritis.

Kukuy OL, Kopolovic J, Blau A, Ben-David A, Lotan D, Shaked M, Shinar Y, Dinour D, Langevitz P, Livneh A.

Clin Genet. 2008 Feb;73(2):146-51. doi: 10.1111/j.1399-0004.2007.00945.x. Epub 2007 Dec 19.

PMID:
18177471
30.

Familial pure proximal renal tubular acidosis--a clinical and genetic study.

Katzir Z, Dinour D, Reznik-Wolf H, Nissenkorn A, Holtzman E.

Nephrol Dial Transplant. 2008 Apr;23(4):1211-5. Epub 2007 Sep 19.

PMID:
17881426
31.

A novel missense mutation in the sodium bicarbonate cotransporter (NBCe1/SLC4A4) causes proximal tubular acidosis and glaucoma through ion transport defects.

Dinour D, Chang MH, Satoh J, Smith BL, Angle N, Knecht A, Serban I, Holtzman EJ, Romero MF.

J Biol Chem. 2004 Dec 10;279(50):52238-46. Epub 2004 Oct 7.

32.

Progressive nephropathy associated with mitochondrial tRNA gene mutation.

Dinour D, Mini S, Polak-Charcon S, Lotan D, Holtzman EJ.

Clin Nephrol. 2004 Aug;62(2):149-54.

PMID:
15356973
33.

Acute myeloid leukemia associated with nephrotic syndrome: case report and literature review.

Levi I, Dinour D, Ben-Bassat I, Raanani P.

Leuk Lymphoma. 2002 May;43(5):1133-6. Review.

PMID:
12148897
34.

Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family.

Schlingmann KP, Weber S, Peters M, Niemann Nejsum L, Vitzthum H, Klingel K, Kratz M, Haddad E, Ristoff E, Dinour D, Syrrou M, Nielsen S, Sassen M, Waldegger S, Seyberth HW, Konrad M.

Nat Genet. 2002 Jun;31(2):166-70. Epub 2002 May 28.

PMID:
12032568
35.

Lithium intoxication due to carbamazepine-induced renal failure.

Mayan H, Golubev N, Dinour D, Farfel Z.

Ann Pharmacother. 2001 May;35(5):560-2.

PMID:
11346062
36.

Disparate effects of adenosine A1- and A2-receptor agonists on intrarenal blood flow.

Agmon Y, Dinour D, Brezis M.

Am J Physiol. 1993 Dec;265(6 Pt 2):F802-6.

PMID:
8285213
37.

Adenosine: an emerging role in the control of renal medullary oxygenation?

Dinour D, Agmon Y, Brezis M.

Exp Nephrol. 1993 May-Jun;1(3):152-7. Review. No abstract available.

PMID:
8081964
38.

Splenic infarction: a complication of cardiac catheterization.

Rose M, Dinour D, Chisin R.

Clin Cardiol. 1992 Sep;15(9):697-8.

39.

Effects of adenosine on intrarenal oxygenation.

Dinour D, Brezis M.

Am J Physiol. 1991 Nov;261(5 Pt 2):F787-91.

PMID:
1951710
40.

Role of nitric oxide in renal medullary oxygenation. Studies in isolated and intact rat kidneys.

Brezis M, Heyman SN, Dinour D, Epstein FH, Rosen S.

J Clin Invest. 1991 Aug;88(2):390-5.

41.

Susceptibility of Henle's loop to hypoxic and toxic insults.

Brezis M, Dinour D, Greenfeld Z, Rosen S.

Adv Nephrol Necker Hosp. 1991;20:41-56. Review. No abstract available.

PMID:
2063721
42.

Postpartum renal failure in systemic lupus erythematosus.

Dinour D, Yinnon AM, Slotki IN, Rosenmann E, Brezis M.

Clin Nephrol. 1990 Oct;34(4):152-6.

PMID:
2257700
43.

Megaesophagus and recurrent apnea in an adult patient with familial dysautonomia.

Maayan C, Oren A, Goldin E, Dinour D, Goldberg M, Mogle P.

Am J Gastroenterol. 1990 Jun;85(6):729-32.

PMID:
2353694

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