640 related articles for article (PubMed ID: 33942228)
21. Lymphadenopathy as the primary manifestation of malignant transformation in two patients with severe congenital neutropenia.
Gamper CJ; Takemoto CM; Schowinsky J; Borowitz MJ; Horwitz MS; Strouse JJ
Pediatr Blood Cancer; 2008 May; 50(5):1072-5. PubMed ID: 18213714
[TBL] [Abstract][Full Text] [Related]
22. Molecular screening of the neutrophil elastase gene in congenital neutropenia.
Thomas M; Jayandharan G; Chandy M
Indian Pediatr; 2006 Dec; 43(12):1081-4. PubMed ID: 17202606
[TBL] [Abstract][Full Text] [Related]
23. Screening of genetic variants in
Arunachalam AK; Suresh H; Edison ES; Korula A; Aboobacker FN; George B; Shaji RV; Mathews V; Balasubramanian P
J Clin Pathol; 2020 Jun; 73(6):322-327. PubMed ID: 31732620
[TBL] [Abstract][Full Text] [Related]
24. Mutations in the gene encoding neutrophil elastase in congenital and cyclic neutropenia.
Dale DC; Person RE; Bolyard AA; Aprikyan AG; Bos C; Bonilla MA; Boxer LA; Kannourakis G; Zeidler C; Welte K; Benson KF; Horwitz M
Blood; 2000 Oct; 96(7):2317-22. PubMed ID: 11001877
[TBL] [Abstract][Full Text] [Related]
25. Novel G6PC3 Mutations in Patients with Congenital Neutropenia: Case Reports and Review of the Literature.
Maroufi SF; Shaka Z; Mojtabavi H; Sadeghalvad M; Rayzan E; Sedighi I; Shahkarami S; Najafi M; Rohlfs M; Klein C; Rezaei N
Endocr Metab Immune Disord Drug Targets; 2021; 21(9):1660-1668. PubMed ID: 34137364
[TBL] [Abstract][Full Text] [Related]
26. Novel ELANE mutation causing severe congenital neutropenia with unpredictable fluctuations in neutrophil counts.
Cachia J; Camilleri DJ; Pace D
Pediatr Blood Cancer; 2023 Nov; 70(11):e30640. PubMed ID: 37596916
[No Abstract] [Full Text] [Related]
27. Mutation, drift and selection in single-driver hematologic malignancy: Example of secondary myelodysplastic syndrome following treatment of inherited neutropenia.
Wojdyla T; Mehta H; Glaubach T; Bertolusso R; Iwanaszko M; Braun R; Corey SJ; Kimmel M
PLoS Comput Biol; 2019 Jan; 15(1):e1006664. PubMed ID: 30615612
[TBL] [Abstract][Full Text] [Related]
28. A Truncated Granulocyte Colony-stimulating Factor Receptor (G-CSFR) Inhibits Apoptosis Induced by Neutrophil Elastase G185R Mutant: IMPLICATION FOR UNDERSTANDING CSF3R GENE MUTATIONS IN SEVERE CONGENITAL NEUTROPENIA.
Qiu Y; Zhang Y; Hu N; Dong F
J Biol Chem; 2017 Feb; 292(8):3496-3505. PubMed ID: 28073911
[TBL] [Abstract][Full Text] [Related]
29. A novel ELANE gene mutation in a patient with severe congenital neutropenia and intermittent thrombocytopenia.
Sayour EJ; Carter C; Eldjerou L
Pediatr Blood Cancer; 2015 Oct; 62(10):1870-1. PubMed ID: 25882539
[No Abstract] [Full Text] [Related]
30. Severe congenital neutropenia: a negative synergistic effect of multiple mutations of ELANE (ELA2) gene.
Lanciotti M; Caridi G; Rosano C; Pigullo S; Lanza T; Dufour C
Br J Haematol; 2009 Sep; 146(5):578-80. PubMed ID: 19594744
[No Abstract] [Full Text] [Related]
31. Hepatic hemangioendothelioma in an infant with severe congenital neutropenia.
Dinand V; Yadav SP; Bellanné-Chantelot C; Jain S; Bhargava M; Sachdeva A
J Pediatr Hematol Oncol; 2012 May; 34(4):298-300. PubMed ID: 22510773
[TBL] [Abstract][Full Text] [Related]
32. Congenital neutropenia in a newborn.
Walkovich K; Boxer LA
J Perinatol; 2011 Apr; 31 Suppl 1():S22-3. PubMed ID: 21448199
[TBL] [Abstract][Full Text] [Related]
33. Severe congenital neutropenia and chronic neutrophilic leukemia: an intriguing molecular connection unveiled by oncogenic mutations in CSF3R.
Touw IP; Beekman R
Haematologica; 2013 Oct; 98(10):1490-2. PubMed ID: 24091926
[No Abstract] [Full Text] [Related]
34. An overview of how on-call consultant paediatricians can recognise and manage severe primary immunodeficiencies.
Wekell P; Hertting O; Holmgren D; Fasth A
Acta Paediatr; 2019 Dec; 108(12):2175-2185. PubMed ID: 31278775
[TBL] [Abstract][Full Text] [Related]
35. Functional interaction between mutations in the granulocyte colony-stimulating factor receptor in severe congenital neutropenia.
Ward AC; Gits J; Majeed F; Aprikyan AA; Lewis RS; O'Sullivan LA; Freedman M; Shigdar S; Touw IP; Dale DC; Dror Y
Br J Haematol; 2008 Aug; 142(4):653-6. PubMed ID: 18513286
[TBL] [Abstract][Full Text] [Related]
36. Acquired centromeric heteromorphism of chromosome 7 yields discordant results between fluorescent in situ hybridization and karyotype analysis in a child with severe congenital neutropenia.
Farra C; Raimondi S; Abboud M
Pediatr Hematol Oncol; 2019 Oct; 36(7):432-437. PubMed ID: 31411529
[TBL] [Abstract][Full Text] [Related]
37. ELANE gene mutation-induced cyclic neutropenia manifesting as recurrent fever with oral mucosal ulcer: A case report.
Chen X; Peng W; Zhang Z; Wu Y; Xu J; Zhou Y; Chen L
Medicine (Baltimore); 2018 Mar; 97(10):e0031. PubMed ID: 29517659
[TBL] [Abstract][Full Text] [Related]
38. A patient with severe congenital neutropenia harbors a missense ELANE mutation due to paternal germline mosaicism.
Ying Y; Ye J; Chen Y; Chen Q; Chen Y; Lu X; Xi H; Gu F; Pan D; Zhao J
Clin Chim Acta; 2022 Feb; 526():14-20. PubMed ID: 34968504
[TBL] [Abstract][Full Text] [Related]
39. The many causes of severe congenital neutropenia.
Dale DC; Link DC
N Engl J Med; 2009 Jan; 360(1):3-5. PubMed ID: 19118300
[No Abstract] [Full Text] [Related]
40. A pediatric case of congenital neutropenia with SRP54 gene mutation in which monocytosis and gingival swelling were useful in differentiating from autoimmune neutropenia.
Manabe T; Taku K; Hoshina T; Higuchi N; Karakawa S; Kusuhara K
Pediatr Blood Cancer; 2022 Sep; 69(9):e29648. PubMed ID: 35253356
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
