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Items: 22

1.

A 57 kB Genomic Deletion Causing CTNS Loss of Function Contributes to the CTNS Mutational Spectrum in the Middle East.

Najafi M, Tamandani DMK, Azarfar A, Bakey Z, Behjati F, Antony D, Schüle I, Sadeghi-Bojd S, Karimiani EG, Schmidts M.

Front Pediatr. 2019 Mar 21;7:89. doi: 10.3389/fped.2019.00089. eCollection 2019.

2.

Mimicry and well known genetic friends: molecular diagnosis in an Iranian cohort of suspected Bartter syndrome and proposition of an algorithm for clinical differential diagnosis.

Najafi M, Kordi-Tamandani DM, Behjati F, Sadeghi-Bojd S, Bakey Z, Karimiani EG, Schüle I, Azarfar A, Schmidts M.

Orphanet J Rare Dis. 2019 Feb 13;14(1):41. doi: 10.1186/s13023-018-0981-5.

3.

Long non-coding RNA PAX8-AS1 polymorphisms increase the risk of childhood acute lymphoblastic leukemia.

Bahari G, Hashemi M, Naderi M, Sadeghi-Bojd S, Taheri M.

Biomed Rep. 2018 Feb;8(2):184-190. doi: 10.3892/br.2017.1028. Epub 2017 Dec 13.

4.

FHIT promoter DNA methylation and expression analysis in childhood acute lymphoblastic leukemia.

Bahari G, Hashemi M, Naderi M, Sadeghi-Bojd S, Taheri M.

Oncol Lett. 2017 Oct;14(4):5034-5038. doi: 10.3892/ol.2017.6796. Epub 2017 Aug 23.

5.

Association of Endothelin-1 rs5370 G>T gene polymorphism with the risk of nephrotic syndrome in children.

Hashemi M, Sadeghi-Bojd S, Aryanezhad S, Rezaei M.

J Nephropathol. 2017 Jul;6(3):138-143. doi: 10.15171/jnp.2017.24. Epub 2016 Dec 17.

6.

Evaluation of functional RAGE gene polymorphisms in childhood acute lymphoblastic leukemia-A case-control study from Iran.

Eskandari-Nasab E, Hashemi M, Hasani SS, Naderi M, Sadeghi-Bojd S, Taheri M.

Nucleosides Nucleotides Nucleic Acids. 2017 Mar 4;36(3):170-180. doi: 10.1080/15257770.2016.1243716. Epub 2017 Jan 3.

PMID:
28045617
7.

Association of lnc-LAMC2-1:1 rs2147578 and CASC8 rs10505477 Polymorphisms with Risk of Childhood Acute Lymphoblastic Leukemia

Hashemi M, Bahari G, Naderi M, Sadeghi Bojd S, Taheri M.

Asian Pac J Cancer Prev. 2016 Nov 1;17(11):4985-4989.

8.

Pri-miR-34b/c rs4938723 polymorphism is associated with the risk of childhood acute lymphoblastic leukemia.

Hashemi M, Bahari G, Naderi M, Sadeghi-Bojd S, Taheri M.

Cancer Genet. 2016 Nov;209(11):493-496. doi: 10.1016/j.cancergen.2016.09.009. Epub 2016 Sep 30.

PMID:
27886674
9.

Postnatal Evaluation and Outcome of Prenatal Hydronephrosis.

Sadeghi-Bojd S, Kajbafzadeh AM, Ansari-Moghadam A, Rashidi S.

Iran J Pediatr. 2016 Mar 5;26(2):e3667. doi: 10.5812/ijp.3667. eCollection 2016 Apr.

10.

Analysis of the IL-10, IL-12, and TNF-α Gene Polymorphisms in Patients With Vesicoureteral Reflux Among the Southeast Iranian Population.

Kordi Tamandani DM, Naeimi N, Ghasemi A, Baranzahi T, Sadeghi-Bojd S.

Nephrourol Mon. 2016 Mar 12;8(2):e34061. doi: 10.5812/numonthly.34061. eCollection 2016 Mar.

11.

Evaluation of oxidant-antioxidant balance and total antioxidant capacity of serum in children with urinary tract infection.

Soleimani G, Sadeghi-Bojd S, Teimouri A, Nakhaee A, Sheikhhosseini A.

Niger Med J. 2016 Mar-Apr;57(2):114-8. doi: 10.4103/0300-1652.182073.

12.

Clinical characteristics and mortality risk prediction in children with acute kidney injury.

Sadeghi-Bojd S, Noori NM, Mohammadi M, Teimouri A.

Niger Med J. 2015 Sep-Oct;56(5):327-32. doi: 10.4103/0300-1652.170381.

13.

Urine Neutrophil Gelatinase Associated Lipocalin to Creatinine Ratio: A Novel Index for Steroid Response in Idiopathic Nephrotic Syndrome.

Nickavar A, Safaeian B, Sadeghi-Bojd S, Lahouti Harah dashti A.

Indian J Pediatr. 2016 Jan;83(1):18-21. doi: 10.1007/s12098-015-1809-0. Epub 2015 Jun 23.

PMID:
26096867
14.

A multivariate analysis of factors associated with infant mortality in South-East of Iran.

Ansari-Moghaddam A, Sadeghi-Bojd S, Imani M, Movahedinia S, Pourrashidi A, Mohammadi M.

J Pak Med Assoc. 2014 Oct;64(10):1123-6.

15.

Chronological variations of children poisoning causes in zahedan, South of iran.

Sadeghi-Bojd S, Khajeh A.

Int J High Risk Behav Addict. 2014 Jul 5;3(3):e19223. doi: 10.5812/ijhrba.19223. eCollection 2014 Sep.

16.

Association between NPHS1 and NPHS2 gene variants and nephrotic syndrome in children.

Hashemi M, Sadeghi-Bojd S, Rahmania K, Eskandari-Nasab E.

Iran J Kidney Dis. 2015 Jan;9(1):25-30.

17.

Evaluation of paraoxonase activity in children with nephrotic syndrome.

Hashemi M, Sadeghi-Bojd S, Raeisi M, Moazeni-Roodi A.

Nephrourol Mon. 2013 Nov;5(5):978-82. doi: 10.5812/numonthly.12606. Epub 2013 Nov 13.

18.

Effect of pro-inflammatory cytokine (IFN-γ +874, IL-18-137 G/C,-607 C/A) genes in relation to risk of vesico-ureteral reflux.

Sadeghi-Bojd S, Kordi-Tamandani DM, Hashemi M.

Ren Fail. 2014 Feb;36(1):1-4. doi: 10.3109/0886022X.2013.789959. Epub 2013 Oct 29.

PMID:
24168677
19.

A prospective study of tubular dysfunction in pediatric patients with Beta thalassemia major receiving deferasirox.

Naderi M, Sadeghi-Bojd S, Valeshabad AK, Jahantigh A, Alizadeh S, Dorgalaleh A, Tabibian S, Bamedi T.

Pediatr Hematol Oncol. 2013 Nov;30(8):748-54. doi: 10.3109/08880018.2013.823470.

PMID:
24134694
20.

IL-19 and IL-20 genes polymorphisms and haplotype analysis in a vesicoureteral reflux population.

Kordi-Tamandani DM, Sadeghi-Bojd S, Torkamanzehi A.

Hum Immunol. 2013 Jan;74(1):131-4. doi: 10.1016/j.humimm.2012.09.005. Epub 2012 Sep 19.

PMID:
23000500
21.

Kidney function tests in children with beta-thalassemia minor in Zahedan, southeast of Iran.

Sadeghi-Bojd S, Hashemi M, Naderi M, Shikhani S.

Iran J Kidney Dis. 2011 Jul;5(3):201-3.

22.

Hypercalciuria and recurrent urinary tract infections among children in Zahedan, Iran.

Sadeghi-Bojd S, Hashemi M.

J Pak Med Assoc. 2008 Nov;58(11):624-6.

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