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Items: 1 to 20 of 41

1.

TARGT Gene Therapy Platform for Correction of Anemia in End-Stage Renal Disease.

Blum S, Shapir N, Miari R, Lerner B, Koren B, Doenyas-Barak K, Efrati S, Pergola PE, Schwartz D, Chernin G, Yagil Y, Guzy S, Nyska A, Neil GA.

N Engl J Med. 2017 Jan 12;376(2):189-191. doi: 10.1056/NEJMc1606202. No abstract available.

2.

Preclinical and Preliminary Clinical Evaluation of Genetically Transduced Dermal Tissue Implants for the Sustained Secretion of Erythropoietin and Interferon α.

Shapir N, Miari R, Blum S, Schwartz D, Chernin G, Neil GA, Afik D, Panet A.

Hum Gene Ther Clin Dev. 2015 Dec;26(4):216-27. doi: 10.1089/humc.2015.125.

PMID:
26684446
3.

Preclinical and preliminary clinical evaluation of genetically transduced dermal tissue implants for the sustained secretion of erythropoietin and interferon α.

Shapir N, Miari R, Blum S, Schwartz D, Chernin G, Neil G, Afik D, Panet A.

Hum Gene Ther Clin Dev. 2015 Dec 9. [Epub ahead of print]

PMID:
26650479
4.

Target Hemoglobin May Be Achieved with Intravenous Iron Alone in Anemic Patients with Cardiorenal Syndrome: An Observational Study.

Ben-Assa E, Shacham Y, Shashar M, Leshem-Rubinow E, Gal-Oz A, Schwartz IF, Schwartz D, Silverberg DS, Chernin G.

Cardiorenal Med. 2015 Oct;5(4):246-53. doi: 10.1159/000433564.

5.

Prevention of pruritus with ethyl-chloride in skin prick test: a double-blind placebo-controlled prospective study.

Gal-Oz A, Kivity S, Shacham Y, Fiszer E, Rogowsky O, Chernin G.

Allergy Asthma Clin Immunol. 2015 Sep 4;11(1):25. doi: 10.1186/s13223-015-0091-z.

6.

High prevalence of elevated blood pressure among children with neurofibromatosis type 1.

Dubov T, Toledano-Alhadef H, Chernin G, Constantini S, Cleper R, Ben-Shachar S.

Pediatr Nephrol. 2016 Jan;31(1):131-6. doi: 10.1007/s00467-015-3191-6.

PMID:
26314566
7.

Estradiol augments while progesterone inhibits arginine transport in human endothelial cells through modulation of cationic amino acid transporter-1.

Bentur OS, Schwartz D, Chernichovski T, Ingbir M, Weinstein T, Chernin G, Schwartz IF.

Am J Physiol Regul Integr Comp Physiol. 2015 Aug 15;309(4):R421-7. doi: 10.1152/ajpregu.00532.2014.

8.

The Phosphate Binder Ferric Citrate and Mineral Metabolism and Inflammatory Markers in Maintenance Dialysis Patients: Results From Prespecified Analyses of a Randomized Clinical Trial.

Van Buren PN, Lewis JB, Dwyer JP, Greene T, Middleton J, Sika M, Umanath K, Abraham JD, Arfeen SS, Bowline IG, Chernin G, Fadem SZ, Goral S, Koury M, Sinsakul MV, Weiner DE; Collaborative Study Group..

Am J Kidney Dis. 2015 Sep;66(3):479-88. doi: 10.1053/j.ajkd.2015.03.013.

9.

Anemia and iron deficiency in COPD patients: prevalence and the effects of correction of the anemia with erythropoiesis stimulating agents and intravenous iron.

Silverberg DS, Mor R, Weu MT, Schwartz D, Schwartz IF, Chernin G.

BMC Pulm Med. 2014 Feb 24;14:24. doi: 10.1186/1471-2466-14-24.

10.

L-arginine improves endothelial function, independently of arginine uptake, in aortas from chronic renal failure female rats.

Nesher N, Frolkis I, Schwartz D, Chernichovski T, Levi S, Pri-Paz Y, Chernin G, Shtabsky A, Ben-Gal Y, Paz Y, Schwartz IF.

Am J Physiol Renal Physiol. 2014 Feb 15;306(4):F449-56. doi: 10.1152/ajprenal.00457.2013.

11.

C-reactive protein and carotid and femoral intima media thickness: predicting inflammation.

Boaz M, Chernin G, Schwartz I, Katzir Z, Schwartz D, Agbaria A, Gal-Oz A, Weinstein T.

Clin Nephrol. 2013 Dec;80(6):449-55. doi: 10.5414/CN108067.

PMID:
24131677
12.

ARHGDIA mutations cause nephrotic syndrome via defective RHO GTPase signaling.

Gee HY, Saisawat P, Ashraf S, Hurd TW, Vega-Warner V, Fang H, Beck BB, Gribouval O, Zhou W, Diaz KA, Natarajan S, Wiggins RC, Lovric S, Chernin G, Schoeb DS, Ovunc B, Frishberg Y, Soliman NA, Fathy HM, Goebel H, Hoefele J, Weber LT, Innis JW, Faul C, Han Z, Washburn J, Antignac C, Levy S, Otto EA, Hildebrandt F.

J Clin Invest. 2013 Aug;123(8):3243-53. doi: 10.1172/JCI69134.

13.

Cyclosporine attenuates arginine transport, in human endothelial cells, through modulation of cationic amino acid transporter-1.

Grupper A, Shashar M, Bahry D, Pri-Paz Y, Ben Tur O, Levi S, Chernichovski T, Chernin G, Schwartz IF.

Am J Nephrol. 2013;37(6):613-9. doi: 10.1159/000350614.

PMID:
23796541
14.

When the chimney is blocked: malignant renovascular hypertension after endovascular repair of abdominal aortic aneurysm.

Gal-Oz A, Wolf YG, Rosen G, Sharon H, Schwartz IF, Chernin G.

BMC Nephrol. 2013 Mar 26;14:71. doi: 10.1186/1471-2369-14-71.

15.

Care of undocumented-uninsured immigrants in a large urban dialysis unit.

Chernin G, Gal-Oz A, Schwartz IF, Shashar M, Schwartz D, Weinstein T.

BMC Nephrol. 2012 Sep 19;13:112. doi: 10.1186/1471-2369-13-112.

16.

Attenuated glomerular arginine transport prevents hyperfiltration and induces HIF-1α in the pregnant uremic rat.

Schwartz IF, Grupper A, Soetendorp H, Hillel O, Laron I, Chernichovski T, Ingbir M, Shtabski A, Weinstein T, Chernin G, Shashar M, Hershkoviz R, Schwartz D.

Am J Physiol Renal Physiol. 2012 Aug 1;303(3):F396-404. doi: 10.1152/ajprenal.00488.2011.

17.

Secondary prevention of hyperkalemia with sodium polystyrene sulfonate in cardiac and kidney patients on renin-angiotensin-aldosterone system inhibition therapy.

Chernin G, Gal-Oz A, Ben-Assa E, Schwartz IF, Weinstein T, Schwartz D, Silverberg DS.

Clin Cardiol. 2012 Jan;35(1):32-6. doi: 10.1002/clc.20987.

18.

Exome sequencing reveals cubilin mutation as a single-gene cause of proteinuria.

Ovunc B, Otto EA, Vega-Warner V, Saisawat P, Ashraf S, Ramaswami G, Fathy HM, Schoeb D, Chernin G, Lyons RH, Yilmaz E, Hildebrandt F.

J Am Soc Nephrol. 2011 Oct;22(10):1815-20. doi: 10.1681/ASN.2011040337.

19.

COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness.

Heeringa SF, Chernin G, Chaki M, Zhou W, Sloan AJ, Ji Z, Xie LX, Salviati L, Hurd TW, Vega-Warner V, Killen PD, Raphael Y, Ashraf S, Ovunc B, Schoeb DS, McLaughlin HM, Airik R, Vlangos CN, Gbadegesin R, Hinkes B, Saisawat P, Trevisson E, Doimo M, Casarin A, Pertegato V, Giorgi G, Prokisch H, Rötig A, Nürnberg G, Becker C, Wang S, Ozaltin F, Topaloglu R, Bakkaloglu A, Bakkaloglu SA, Müller D, Beissert A, Mir S, Berdeli A, Varpizen S, Zenker M, Matejas V, Santos-Ocaña C, Navas P, Kusakabe T, Kispert A, Akman S, Soliman NA, Krick S, Mundel P, Reiser J, Nürnberg P, Clarke CF, Wiggins RC, Faul C, Hildebrandt F.

J Clin Invest. 2011 May;121(5):2013-24. doi: 10.1172/JCI45693.

20.

Screening for NPHS2 mutations may help predict FSGS recurrence after transplantation.

Jungraithmayr TC, Hofer K, Cochat P, Chernin G, Cortina G, Fargue S, Grimm P, Knueppel T, Kowarsch A, Neuhaus T, Pagel P, Pfeiffer KP, Schäfer F, Schönermarck U, Seeman T, Toenshoff B, Weber S, Winn MP, Zschocke J, Zimmerhackl LB.

J Am Soc Nephrol. 2011 Mar;22(3):579-85. doi: 10.1681/ASN.2010010029.

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