Detalhe da pesquisa
1.
Biallelic hypomorphic variants in CAD cause uridine-responsive macrocytic anaemia with elevated haemoglobin-A2.
Br J Haematol
; 204(3): 1067-1071, 2024 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-37984840
2.
Genetic backgrounds and clinical characteristics of congenital neutropenias in Israel.
Eur J Haematol
; 2024 Apr 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-38600884
3.
Excellent response to treatment with hydroxychloroquine in pediatric patients with SLE-related immune thrombocytopenia.
Pediatr Blood Cancer
; 71(5): e30911, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38348516
4.
A Need for a Novel Survival Risk Scoring System for Intensive Care Admissions Due to Sepsis in Pediatric Hematology/Oncology Patients.
J Intensive Care Med
; 39(5): 484-492, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-37981801
5.
Symptomatic corpus luteum hemorrhage in adolescent females with ITP.
Eur J Pediatr
; 2024 Apr 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-38602530
6.
Cellular and metabolic characteristics of pre-leukemic hematopoietic progenitors with GATA2 haploinsufficiency.
Haematologica
; 108(9): 2316-2330, 2023 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36475518
7.
Cytopenias in pediatric kidney transplant recipients: preceding factors and clinical consequences.
Pediatr Nephrol
; 38(10): 3445-3454, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37079102
8.
Neonatal Thrombocytopenia: Differing Characteristics of NAIT Versus Non-NAIT.
J Pediatr Hematol Oncol
; 45(6): e728-e732, 2023 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37027241
9.
[GENETIC PANELS FOR THE DIAGNOSIS OF RARE CONGENITAL HEMATOLOGICAL DISORDERS].
Harefuah
; 162(1): 52-56, 2023 Jan.
Artigo
em Hebraico
| MEDLINE | ID: mdl-36714943
10.
Novel manifestations of immune dysregulation and granule defects in gray platelet syndrome.
Blood
; 136(17): 1956-1967, 2020 10 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-32693407
11.
Syndromes predisposing to leukemia are a major cause of inherited cytopenias in children.
Haematologica
; 107(9): 2081-2095, 2022 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35295078
12.
Cerebral sinus venous thrombosis in children with inherited bleeding disorders: A case series.
Pediatr Blood Cancer
; 69(10): e29902, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35880957
13.
Congenital thrombocytopenia associated with a heterozygous variant in the MEIS1 gene encoding a transcription factor essential for megakaryopoiesis.
Platelets
; 33(4): 645-648, 2022 May 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-35130804
14.
Characterization of Fanconi Anemia Patients with Head and Neck Squamous Cell Carcinoma: Israel Fanconi Registry.
Isr Med Assoc J
; 24(8): 491-496, 2022 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-35971997
15.
Incorporation of somatic panels for the detection of haematopoietic transformation in children and young adults with leukaemia predisposition syndromes and with acquired cytopenias.
Br J Haematol
; 193(3): 570-580, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33368157
16.
Pediatric myelodysplastic syndrome with inflammatory manifestations: Diagnosis, genetics, treatment, and outcome.
Pediatr Blood Cancer
; 68(10): e29138, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34019335
17.
Mechanism for survival of homozygous nonsense mutations in the tumor suppressor gene BRCA1.
Proc Natl Acad Sci U S A
; 115(20): 5241-5246, 2018 05 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29712865
18.
Splenectomy in childhood for non-malignant haematologic disorders - long-term follow-up shows minimal adverse effects.
Br J Haematol
; 190(6): 909-915, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32342506
19.
Characterization and genotype-phenotype correlation of patients with Fanconi anemia in a multi-ethnic population.
Haematologica
; 105(7): 1825-1834, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31558676
20.
Congenital neutropenia with variable clinical presentation in novel mutation of the SRP54 gene.
Pediatr Blood Cancer
; 67(6): e28237, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32277798