Rezaei N - Search Results

1

HAX1-dependent control of mitochondrial proteostasis governs neutrophil granulocyte differentiation.

Fan Y, Murgia M, Linder MI, Mizoguchi Y, Wang C, Łyszkiewicz M, Ziȩtara N, Liu Y, Frenz S, Sciuccati G, Partida-Gaytan A, Alizadeh Z, Rezaei N, Rehling P, Dennerlein S, Mann M, Klein C. Fan Y, et al. Among authors: rezaei n. J Clin Invest. 2022 May 2;132(9):e153153. doi: 10.1172/JCI153153. J Clin Invest. 2022. PMID: 35499078 Free PMC article.

2

HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease).

Klein C, Grudzien M, Appaswamy G, Germeshausen M, Sandrock I, Schäffer AA, Rathinam C, Boztug K, Schwinzer B, Rezaei N, Bohn G, Melin M, Carlsson G, Fadeel B, Dahl N, Palmblad J, Henter JI, Zeidler C, Grimbacher B, Welte K. Klein C, et al. Among authors: rezaei n. Nat Genet. 2007 Jan;39(1):86-92. doi: 10.1038/ng1940. Epub 2006 Dec 24. Nat Genet. 2007. PMID: 17187068

3

The clinical, immunohematological, and molecular study of Iranian patients with severe congenital neutropenia.

Rezaei N, Moin M, Pourpak Z, Ramyar A, Izadyar M, Chavoshzadeh Z, Sherkat R, Aghamohammadi A, Yeganeh M, Mahmoudi M, Mahjoub F, Germeshausen M, Grudzien M, Horwitz MS, Klein C, Farhoudi A. Rezaei N, et al. J Clin Immunol. 2007 Sep;27(5):525-33. doi: 10.1007/s10875-007-9106-y. Epub 2007 Jun 21. J Clin Immunol. 2007. PMID: 17587155

4

Association of HAX1 deficiency with neurological disorder.

Rezaei N, Chavoshzadeh Z, R Alaei O, Sandrock I, Klein C. Rezaei N, et al. Neuropediatrics. 2007 Oct;38(5):261-3. doi: 10.1055/s-2008-1062704. Neuropediatrics. 2007. PMID: 18330843

5

Novel HAX1 mutations in patients with severe congenital neutropenia reveal isoform-dependent genotype-phenotype associations.

Germeshausen M, Grudzien M, Zeidler C, Abdollahpour H, Yetgin S, Rezaei N, Ballmaier M, Grimbacher B, Welte K, Klein C. Germeshausen M, et al. Among authors: rezaei n. Blood. 2008 May 15;111(10):4954-7. doi: 10.1182/blood-2007-11-120667. Epub 2008 Mar 12. Blood. 2008. PMID: 18337561 Free article.

6

Necrosis of nasal cartilage due to mucormycosis in a patient with severe congenital neutropenia due to HAX1 deficiency.

Fahimzad A, Chavoshzadeh Z, Abdollahpour H, Klein C, Rezaei N. Fahimzad A, et al. Among authors: rezaei n. J Investig Allergol Clin Immunol. 2008;18(6):469-72. J Investig Allergol Clin Immunol. 2008. PMID: 19123440 Free article.

7

Neutropenia and primary immunodeficiency diseases.

Rezaei N, Moazzami K, Aghamohammadi A, Klein C. Rezaei N, et al. Int Rev Immunol. 2009;28(5):335-66. doi: 10.1080/08830180902995645. Int Rev Immunol. 2009. PMID: 19811314 Review.

8

JAGN1 deficiency causes aberrant myeloid cell homeostasis and congenital neutropenia.

Boztug K, Järvinen PM, Salzer E, Racek T, Mönch S, Garncarz W, Gertz EM, Schäffer AA, Antonopoulos A, Haslam SM, Schieck L, Puchałka J, Diestelhorst J, Appaswamy G, Lescoeur B, Giambruno R, Bigenzahn JW, Elling U, Pfeifer D, Conde CD, Albert MH, Welte K, Brandes G, Sherkat R, van der Werff Ten Bosch J, Rezaei N, Etzioni A, Bellanné-Chantelot C, Superti-Furga G, Penninger JM, Bennett KL, von Blume J, Dell A, Donadieu J, Klein C. Boztug K, et al. Among authors: rezaei n. Nat Genet. 2014 Sep;46(9):1021-7. doi: 10.1038/ng.3069. Epub 2014 Aug 17. Nat Genet. 2014. PMID: 25129144 Free PMC article.

9

Preference of Genetic Diagnosis of CXCR4 Mutation Compared with Clinical Diagnosis of WHIM Syndrome.

Aghamohammadi A, Abolhassani H, Puchalka J, Greif-Kohistani N, Zoghi S, Klein C, Rezaei N. Aghamohammadi A, et al. Among authors: rezaei n. J Clin Immunol. 2017 Apr;37(3):282-286. doi: 10.1007/s10875-017-0387-5. Epub 2017 Mar 28. J Clin Immunol. 2017. PMID: 28353164 No abstract available.

10

A novel VPS13B mutation in Cohen syndrome: a case report and review of literature.

Momtazmanesh S, Rayzan E, Shahkarami S, Rohlfs M, Klein C, Rezaei N. Momtazmanesh S, et al. Among authors: rezaei n. BMC Med Genet. 2020 Jun 30;21(1):140. doi: 10.1186/s12881-020-01075-1. BMC Med Genet. 2020. PMID: 32605629 Free PMC article. Review.

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