Search details
1.
Hematologically important mutations: Leukocyte adhesion deficiency (second update).
Blood Cells Mol Dis
; 99: 102726, 2023 03.
Article
in English
| MEDLINE | ID: mdl-36696755
2.
MKL1 deficiency results in a severe neutrophil motility defect due to impaired actin polymerization.
Blood
; 135(24): 2171-2181, 2020 06 11.
Article
in English
| MEDLINE | ID: mdl-32128589
3.
Clinical and Immunological Characteristics of 63 Patients with Chronic Granulomatous Disease: Hacettepe Experience.
J Clin Immunol
; 41(5): 992-1003, 2021 07.
Article
in English
| MEDLINE | ID: mdl-33629196
4.
Hematologically important mutations: X-linked chronic granulomatous disease (fourth update).
Blood Cells Mol Dis
; 90: 102587, 2021 09.
Article
in English
| MEDLINE | ID: mdl-34175765
5.
Hematologically important mutations: The autosomal forms of chronic granulomatous disease (third update).
Blood Cells Mol Dis
; 92: 102596, 2021 12.
Article
in English
| MEDLINE | ID: mdl-34547651
6.
Genetic Characteristics, Infectious, and Noninfectious Manifestations of 32 Patients with Chronic Granulomatous Disease.
Int Arch Allergy Immunol
; 181(7): 540-550, 2020.
Article
in English
| MEDLINE | ID: mdl-32512560
7.
Identification of genetic biomarkers for alloimmunization in sickle cell disease.
Br J Haematol
; 186(6): 887-899, 2019 09.
Article
in English
| MEDLINE | ID: mdl-31168801
8.
Genetic variation of human neutrophil Fcγ receptors and SIRPα in antibody-dependent cellular cytotoxicity towards cancer cells.
Eur J Immunol
; 48(2): 344-354, 2018 02.
Article
in English
| MEDLINE | ID: mdl-28952147
9.
Defective AP-3-dependent VAMP8 trafficking impairs Weibel-Palade body exocytosis in Hermansky-Pudlak Syndrome type 2 blood outgrowth endothelial cells.
Haematologica
; 104(10): 2091-2099, 2019 10.
Article
in English
| MEDLINE | ID: mdl-30630984
10.
Genetic Analysis of 13 Iranian Families With Leukocyte Adhesion Deficiency Type 1.
J Pediatr Hematol Oncol
; 41(1): e3-e6, 2019 01.
Article
in English
| MEDLINE | ID: mdl-29750748
11.
A false-carrier state for the c.579G>A mutation in the NCF1 gene in Ashkenazi Jews.
J Med Genet
; 55(3): 166-172, 2018 03.
Article
in English
| MEDLINE | ID: mdl-29331982
12.
Approach to Molecular Diagnosis of Chronic Granulomatous Disease (CGD): an Experience from a Large Cohort of 90 Indian Patients.
J Clin Immunol
; 38(8): 898-916, 2018 11.
Article
in English
| MEDLINE | ID: mdl-30470980
13.
Analysis of Chronic Granulomatous Disease in the Kavkazi Population in Israel Reveals Phenotypic Heterogeneity in Patients with the Same NCF1 mutation (c.579G>A).
J Clin Immunol
; 38(2): 193-203, 2018 02.
Article
in English
| MEDLINE | ID: mdl-29411231
14.
Retrotransposable genetic elements causing neutrophil defects.
Eur J Clin Invest
; 48 Suppl 2: e12953, 2018 Nov.
Article
in English
| MEDLINE | ID: mdl-29774526
15.
Characterization of 4 New Mutations in the CYBB Gene in 10 Iranian Families With X-linked Chronic Granulomatous Disease.
J Pediatr Hematol Oncol
; 40(5): e268-e272, 2018 07.
Article
in English
| MEDLINE | ID: mdl-29702544
16.
Hermansky-Pudlak syndrome type 2: Aberrant pre-mRNA splicing and mislocalization of granule proteins in neutrophils.
Hum Mutat
; 38(10): 1402-1411, 2017 10.
Article
in English
| MEDLINE | ID: mdl-28585318
17.
Diagnosis of Interstitial Lung Disease Caused by Possible Hypersensitivity Pneumonitis in a Child: Think CGD.
J Clin Immunol
; 37(3): 269-272, 2017 Apr.
Article
in English
| MEDLINE | ID: mdl-28224353
18.
Mutation in an exonic splicing enhancer site causing chronic granulomatous disease.
Blood Cells Mol Dis
; 66: 50-57, 2017 07.
Article
in English
| MEDLINE | ID: mdl-28886419
19.
Chronic granulomatous disease: Clinical, functional, molecular, and genetic studies. The Israeli experience with 84 patients.
Am J Hematol
; 92(1): 28-36, 2017 Jan.
Article
in English
| MEDLINE | ID: mdl-27701760
20.
Early Complement Component Deficiency in a Single-Centre Cohort of Pediatric Onset Lupus.
J Clin Immunol
; 35(8): 777-85, 2015 Nov.
Article
in English
| MEDLINE | ID: mdl-26563161