Otukesh H - Search Results

1

Characterising the spectrum of autosomal recessive hereditary hearing loss in Iran.

Sloan-Heggen CM, Babanejad M, Beheshtian M, Simpson AC, Booth KT, Ardalani F, Frees KL, Mohseni M, Mozafari R, Mehrjoo Z, Jamali L, Vaziri S, Akhtarkhavari T, Bazazzadegan N, Nikzat N, Arzhangi S, Sabbagh F, Otukesh H, Seifati SM, Khodaei H, Taghdiri M, Meyer NC, Daneshi A, Farhadi M, Kahrizi K, Smith RJ, Azaiez H, Najmabadi H. Sloan-Heggen CM, et al. Among authors: otukesh h. J Med Genet. 2015 Dec;52(12):823-9. doi: 10.1136/jmedgenet-2015-103389. Epub 2015 Oct 7. J Med Genet. 2015. PMID: 26445815 Free PMC article.

2

Investigation of ATP6V1B1 and ATP6V0A4 genes causing hereditary hearing loss associated with distal renal tubular acidosis in Iranian families.

Zeinali F, Mohseni M, Fadaee M, Fattahi Z, Najmabadi H, Otukesh H, Kahrizi K. Zeinali F, et al. Among authors: otukesh h. J Laryngol Otol. 2014 Dec;128(12):1056-9. doi: 10.1017/S0022215114002540. J Laryngol Otol. 2014. PMID: 25498251

3

Exome sequencing utility in defining the genetic landscape of hearing loss and novel-gene discovery in Iran.

Mohseni M, Babanejad M, Booth KT, Jamali P, Jalalvand K, Davarnia B, Ardalani F, Khoshaeen A, Arzhangi S, Ghodratpour F, Beheshtian M, Jahanshad F, Otukesh H, Bahrami F, Seifati SM, Bazazzadegan N, Habibi F, Behravan H, Mirzaei S, Keshavarzi F, Nikzat N, Mehrjoo Z, Thiele H, Nothnagel M, Azaiez H, Smith RJ, Kahrizi K, Najmabadi H. Mohseni M, et al. Among authors: otukesh h. Clin Genet. 2021 Jul;100(1):59-78. doi: 10.1111/cge.13956. Epub 2021 Mar 24. Clin Genet. 2021. PMID: 33713422 Free PMC article.

4

Whole exome sequencing revealed a novel homozygous variant in the DGKE catalytic domain: a case report of familial hemolytic uremic syndrome.

Gholizad-Kolveiri S, Hooman N, Alizadeh R, Hoseini R, Otukesh H, Talebi S, Akouchekian M. Gholizad-Kolveiri S, et al. Among authors: otukesh h. BMC Med Genet. 2020 Aug 24;21(1):169. doi: 10.1186/s12881-020-01097-9. BMC Med Genet. 2020. PMID: 32838746 Free PMC article.

5

Histopathologic and clinical findings of congenital nephrotic syndrome in Iranian children: a study of two centers.

Mehrazma M, Otukesh H, Madani A, Hooman N, Bedayat A, Dianati Maleki N, Ehteshami Afshar A, Hoseini R. Mehrazma M, et al. Among authors: otukesh h. Iran J Kidney Dis. 2012 Nov;6(6):426-31. Iran J Kidney Dis. 2012. PMID: 23146979 Free article.

6

Prevalence and outcome of focal segmental glomerulosclerosis in Iranian children with nephrotic syndrome.

Hoseini R, Otukesh H, Fereshtehnejad SM, Tahoori A, Hooman N, Rahimzadeh N, Sadr S. Hoseini R, et al. Among authors: otukesh h. Iran J Kidney Dis. 2012 Jan;6(1):18-24. Iran J Kidney Dis. 2012. PMID: 22218115 Free article.

7

Outcome of pediatric renal transplantation in Labfi Nejad Hospital, Tehran, Iran.

Otukesh H, Basiri A, Simfrosh N, Hoseini R, Sharifian M, Sadigh N, Golnari P, Rezai M, Fereshtenejad M. Otukesh H, et al. Pediatr Nephrol. 2006 Oct;21(10):1459-63. doi: 10.1007/s00467-006-0184-5. Epub 2006 Jul 4. Pediatr Nephrol. 2006. PMID: 16819642

8

Prognosis of acute renal failure in children.

Otukesh H, Hoseini R, Hooman N, Chalian M, Chalian H, Tabarroki A. Otukesh H, et al. Pediatr Nephrol. 2006 Dec;21(12):1873-8. doi: 10.1007/s00467-006-0240-1. Epub 2006 Sep 8. Pediatr Nephrol. 2006. PMID: 16960713

9

Hyperostosis with hyperphosphatemia and tumoral calcinosis: a case report.

Otukesh H, Hoseini R, Chalian H, Chalian M, Safarzadeh AE, Shakiba M, Poorian A. Otukesh H, et al. Pediatr Nephrol. 2007 Aug;22(8):1235-7. doi: 10.1007/s00467-007-0476-4. Epub 2007 Apr 17. Pediatr Nephrol. 2007. PMID: 17437133

10

Urine macrophage migration inhibitory factor in pediatric systemic lupus erythematosus.

Otukesh H, Chalian M, Hoseini R, Chalian H, Hooman N, Bedayat A, Yazdi RS, Sabaghi S, Mahdavi S. Otukesh H, et al. Clin Rheumatol. 2007 Dec;26(12):2105-2107. doi: 10.1007/s10067-007-0632-z. Epub 2007 May 4. Clin Rheumatol. 2007. PMID: 17479310

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