selected scholarly activity
-
conferences
- Skin prick test responses with commercial sesame extract and raw tahini as predictors of sesame allergy in children. Allergy. European Journal of Allergy and Clinical Immunology. 494-495. 2018
-
journal articles
- Insights into Hospitalized Children with Urinary Tract Infections: Epidemiology and Antimicrobial Resistance Patterns in Israel-A Single Center Study.. Children. 11:1142. 2024
- Dual novel variants in CD40 leading to hyper IgM syndrome: a case report of a school-aged female with new-onset recurrent pneumonia. LymphoSign Journal. 11:1-6. 2024
- 58 Expanding the Phenotype of BCL11B Variants: A Novel Canadian Case Series. Clinical Immunology. 262:110000-110000. 2024
- Corrigendum: A novel variant in RUNX1 in a patient with refractory eosinophilic gastrointestinal disease and long-term clinical response to ketotifen. LymphoSign Journal. 10:77-77. 2023
- Deep phenotypic characterization of the retinal dystrophy in patients with RNU4ATAC-associated Roifman syndrome. Eye. 37:3734-3742. 2023
- The impact of COVID-19 infection in pediatric and adult patients with primary immunodeficiency: a single center analysis. LymphoSign Journal. 10:71-76. 2023
-
Favorable outcome of
COVID ‐19 in pediatric patients with primary immunodeficiency. Pediatric Allergy and Immunology. 34:e13928. 2023 - Magnetic resonance findings may aid in diagnosis of protracted febrile myalgia syndrome: a retrospective, multicenter study. Orphanet Journal of Rare Diseases. 17:15. 2022
- A novel variant in RUNX1 in a patient with refractory eosinophilic gastrointestinal disease and long-term clinical response to ketotifen. LymphoSign Journal. 9:72-76. 2022
- Case series of COVID-19 outcomes in adult patients with inborn errors of immunity. LymphoSign Journal. 9:62-66. 2022
- An unusual presentation of DiGeorge syndrome. LymphoSign Journal. 9:52-56. 2022
- CTLA4 haploinsufficiency caused by a novel heterozygous splice site mutation. LymphoSign Journal. 9:40-44. 2022
- Novel heterozygous FOXN1 mutation identified following newborn screening for severe combined immunodeficiency is associated with improving immune parameters. LymphoSign Journal. 9:45-51. 2022
- A novel mutation in TRAC in a patient with abnormal newborn screening for severe combined immunodeficiency. LymphoSign Journal. 9:5-10. 2022
- Novel mutation in PIK3CD affecting the Ras-binding domain. LymphoSign Journal. 9:11-16. 2022
- Case Report: Eosinophilic Esophagitis in a Patient With a Novel STAT1 Gain-of-Function Pathogenic Variant. Frontiers in Immunology. 13:801832. 2022
- DNA‐Binding domain mutations confer severe outcome at an early age among STAT1 gain‐of‐function patients. Pediatric Allergy and Immunology. 33:e13694. 2022
- Wiskott-Aldrich syndrome caused by a novel mutation in the WAS gene and presenting with a mild phenotype. LymphoSign Journal. 8:94-98. 2021
- Chronic mucocutaneous Candidiasis caused by a novel STAT1 mutation: a report of 4 patients. LymphoSign Journal. 8:64-67. 2021
- A novel splice site variant in FOXN1 in a patient with abnormal newborn screening for severe combined immunodeficiency and congenital lymphopenia. LymphoSign Journal. 8:1-4. 2021
- Homozygous NF-kB1 mutation causing combined immunodeficiency: a histopathological analysis. LymphoSign Journal. 8:11-18. 2021
- The Sesame-Peanut Conundrum in Israel: Reevaluation of Food Allergy Prevalence in Young Children. Journal of Allergy and Clinical Immunology: In Practice. 9:200-205. 2021
- Using skin prick test to sesame paste in the diagnosis of sesame seed allergy. Journal of Allergy and Clinical Immunology: In Practice. 8:1456-1458. 2020
- Metabolic assessment of Merkel cell carcinoma. Nuclear Medicine Communications. 37:865-873. 2016
- Novel variant in IGHM gene in a patient with agammaglobulinemia: A case report of a preschool child presenting with recurrent pneumonia. LymphoSign Journal. 00:1-5.