Mamishi S - Search Results

1

Novel mutations of NP in two patients with purine nucleoside phosphorylase deficiency.

Parvaneh N, Teimourian S, Jacomelli G, Badalzadeh M, Bertelli M, Zakharova E, Tabatabaei P, Parvaneh L, Pourakbari B, Yeganeh M, Tamizifar B, Mamishi S, Micheli V. Parvaneh N, et al. Among authors: mamishi s. Clin Biochem. 2008 Mar;41(4-5):350-2. doi: 10.1016/j.clinbiochem.2007.11.007. Epub 2007 Nov 21. Clin Biochem. 2008. PMID: 18067860 No abstract available.

2

Adverse drug reactions in hospitalized children in a department of infectious diseases.

Fattahi F, Pourpak Z, Moin M, Kazemnejad A, Khotaei GT, Mamishi S, Siadati A, Tabatabaei P. Fattahi F, et al. Among authors: mamishi s. J Clin Pharmacol. 2005 Nov;45(11):1313-8. doi: 10.1177/0091270005281205. J Clin Pharmacol. 2005. PMID: 16239365 No abstract available.

3

Invasive aspergillosis in chronic granulomatous disease: report of 7 cases.

Mamishi S, Parvaneh N, Salavati A, Abdollahzadeh S, Yeganeh M. Mamishi S, et al. Eur J Pediatr. 2007 Jan;166(1):83-4. doi: 10.1007/s00431-006-0205-1. Epub 2006 Jun 28. Eur J Pediatr. 2007. PMID: 16804696 No abstract available.

4

Hydatid disease in Iranian children.

Mamishi S, Sagheb S, Pourakbari B. Mamishi S, et al. J Microbiol Immunol Infect. 2007 Oct;40(5):428-31. J Microbiol Immunol Infect. 2007. PMID: 17932603

5

Novel BTK mutation presenting with vaccine-associated paralytic poliomyelitis.

Mamishi S, Shahmahmoudi S, Tabatabaie H, Teimourian S, Pourakbari B, Gheisari Y, Yeganeh M, Salavati A, Esteghamati AR, Gooya MM, Nategh R, Parvaneh N. Mamishi S, et al. Eur J Pediatr. 2008 Nov;167(11):1335-8. doi: 10.1007/s00431-008-0674-5. Epub 2008 Mar 4. Eur J Pediatr. 2008. PMID: 18317803

6

Molecular diagnosis of X-linked chronic granulomatous disease in Iran.

Teimourian S, Rezvani Z, Badalzadeh M, Kannengiesser C, Mansouri D, Movahedi M, Zomorodian E, Parvaneh N, Mamishi S, Pourpak Z, Moin M. Teimourian S, et al. Among authors: mamishi s. Int J Hematol. 2008 May;87(4):398-404. doi: 10.1007/s12185-008-0060-0. Int J Hematol. 2008. PMID: 18322777

7

Analysis of RAB27A gene in griscelli syndrome type 2: novel mutations including a deletion hotspot.

Mamishi S, Modarressi MH, Pourakbari B, Tamizifar B, Mahjoub F, Fahimzad A, Alyasin S, Bemanian MH, Hamidiyeh AA, Fazlollahi MR, Ashrafi MR, Isaeian A, Khotaei G, Yeganeh M, Parvaneh N. Mamishi S, et al. J Clin Immunol. 2008 Jul;28(4):384-9. doi: 10.1007/s10875-008-9192-5. Epub 2008 Mar 19. J Clin Immunol. 2008. PMID: 18350256

8

Severe congenital neutropenia in 2 siblings of consanguineous parents. The role of HAX1 deficiency.

Mamishi S, Esfahani SA, Parvaneh N, Diestelhorst J, Rezaei N. Mamishi S, et al. J Investig Allergol Clin Immunol. 2009;19(6):500-3. J Investig Allergol Clin Immunol. 2009. PMID: 20128427 Free article.

9

Functional characterization of two RAB27A missense mutations found in Griscelli syndrome type 2.

Ohbayashi N, Mamishi S, Ishibashi K, Maruta Y, Pourakbari B, Tamizifar B, Mohammadpour M, Fukuda M, Parvaneh N. Ohbayashi N, et al. Among authors: mamishi s. Pigment Cell Melanoma Res. 2010 Jun;23(3):365-74. doi: 10.1111/j.1755-148X.2010.00705.x. Epub 2010 Apr 3. Pigment Cell Melanoma Res. 2010. PMID: 20370853

10

Characterization of 11 new cases of leukocyte adhesion deficiency type 1 with seven novel mutations in the ITGB2 gene.

Parvaneh N, Mamishi S, Rezaei A, Rezaei N, Tamizifar B, Parvaneh L, Sherkat R, Ghalehbaghi B, Kashef S, Chavoshzadeh Z, Isaeian A, Ashrafi F, Aghamohammadi A. Parvaneh N, et al. Among authors: mamishi s. J Clin Immunol. 2010 Sep;30(5):756-60. doi: 10.1007/s10875-010-9433-2. Epub 2010 Jun 12. J Clin Immunol. 2010. PMID: 20549317

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