NaserEddin A - Search Results

1

Two decades of stem cell transplantation in patients with Fanconi anemia: Analysis of factors affecting transplant outcomes.

Fink O, Even-Or E, Avni B, Grisariu S, Zaidman I, Schejter YD, NaserEddin A, Najajreh M, Stepensky P. Fink O, et al. Among authors: nasereddin a. Clin Transplant. 2023 Jan;37(1):e14835. doi: 10.1111/ctr.14835. Epub 2022 Nov 23. Clin Transplant. 2023. PMID: 36259220 Free PMC article.

2

Enteroviral Infection in a Patient with BLNK Adaptor Protein Deficiency.

NaserEddin A, Shamriz O, Keller B, Alzyoud RM, Unger S, Fisch P, Prus E, Berkun Y, Averbuch D, Shaag A, Wahadneh AM, Conley ME, Warnatz K, Elpeleg O, Stepensky P. NaserEddin A, et al. J Clin Immunol. 2015 May;35(4):356-60. doi: 10.1007/s10875-015-0164-2. Epub 2015 Apr 17. J Clin Immunol. 2015. PMID: 25893637

3

Deep intronic mis-splicing mutation in JAK3 gene underlies T-B+NK- severe combined immunodeficiency phenotype.

Stepensky P, Keller B, Shamriz O, NaserEddin A, Rumman N, Weintraub M, Warnatz K, Elpeleg O, Barak Y. Stepensky P, et al. Among authors: nasereddin a. Clin Immunol. 2016 Feb;163:91-5. doi: 10.1016/j.clim.2016.01.001. Epub 2016 Jan 6. Clin Immunol. 2016. PMID: 26769277

4

The use of whole exome sequencing for the diagnosis of autosomal recessive malignant infantile osteopetrosis.

Shamriz O, Shaag A, Yaacov B, NaserEddin A, Weintraub M, Elpeleg O, Stepensky P. Shamriz O, et al. Among authors: nasereddin a. Clin Genet. 2017 Jul;92(1):80-85. doi: 10.1111/cge.12804. Epub 2016 Jun 2. Clin Genet. 2017. PMID: 27187610

5

Mutations in EFL1, an SBDS partner, are associated with infantile pancytopenia, exocrine pancreatic insufficiency and skeletal anomalies in aShwachman-Diamond like syndrome.

Stepensky P, Chacón-Flores M, Kim KH, Abuzaitoun O, Bautista-Santos A, Simanovsky N, Siliqi D, Altamura D, Méndez-Godoy A, Gijsbers A, Naser Eddin A, Dor T, Charrow J, Sánchez-Puig N, Elpeleg O. Stepensky P, et al. J Med Genet. 2017 Aug;54(8):558-566. doi: 10.1136/jmedgenet-2016-104366. Epub 2017 Mar 22. J Med Genet. 2017. PMID: 28331068

6

Successful hematopoietic stem cell transplantation for osteopetrosis using reduced intensity conditioning.

Shadur B, Zaidman I, NaserEddin A, Lokshin E, Hussein F, Oron HC, Avni B, Grisariu S, Stepensky P. Shadur B, et al. Among authors: nasereddin a. Pediatr Blood Cancer. 2018 Jun;65(6):e27010. doi: 10.1002/pbc.27010. Epub 2018 Feb 22. Pediatr Blood Cancer. 2018. PMID: 29469225

7

Respiratory manifestations in LPS-responsive beige-like anchor (LRBA) protein-deficient patients.

Shamriz O, Shadur B, NaserEddin A, Zaidman I, Simanovsky N, Elpeleg O, Kerem E, Reiter J, Stepensky P. Shamriz O, et al. Among authors: nasereddin a. Eur J Pediatr. 2018 Aug;177(8):1163-1172. doi: 10.1007/s00431-018-3171-5. Epub 2018 May 18. Eur J Pediatr. 2018. PMID: 29777306

8

T⁺ NK⁺ IL-2 Receptor γ Chain Mutation: a Challenging Diagnosis of Atypical Severe Combined Immunodeficiency.

Stepensky P, Keller B, Shamriz O, von Spee-Mayer C, Friedmann D, Shadur B, Unger S, Fuchs S, NaserEddin A, Rumman N, Amro S, Molho Pessach V, Abuzaitoun O, Somech R, Elpeleg O, Ehl S, Warnatz K. Stepensky P, et al. Among authors: nasereddin a. J Clin Immunol. 2018 May;38(4):527-536. doi: 10.1007/s10875-018-0514-y. Epub 2018 Jun 9. J Clin Immunol. 2018. PMID: 29948574

9

Management of XLP-1 and ITK deficiency: The challenges posed by PID with an unpredictable spectrum of disease manifestations.

Shadur B, Abuzaitoun O, NaserEddin A, Even-Or E, Zaidman I, Stepensky P. Shadur B, et al. Among authors: nasereddin a. Clin Immunol. 2019 Jan;198:39-45. doi: 10.1016/j.clim.2018.12.016. Epub 2018 Dec 17. Clin Immunol. 2019. PMID: 30572125

10

Successful treatment with daratumumab for post-HSCT refractory hemolytic anemia.

Even-Or E, Naser Eddin A, Shadur B, Dinur Schejter Y, Najajreh M, Zelig O, Zaidman I, Stepensky P. Even-Or E, et al. Pediatr Blood Cancer. 2020 Jan;67(1):e28010. doi: 10.1002/pbc.28010. Epub 2019 Sep 22. Pediatr Blood Cancer. 2020. PMID: 31544339

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