336 related articles for article (PubMed ID: 19775295)
1. Prevalence of mutations in ELANE, GFI1, HAX1, SBDS, WAS and G6PC3 in patients with severe congenital neutropenia.
Xia J; Bolyard AA; Rodger E; Stein S; Aprikyan AA; Dale DC; Link DC
Br J Haematol; 2009 Nov; 147(4):535-42. PubMed ID: 19775295
[TBL] [Abstract][Full Text] [Related]
2. Screening for ELANE, HAX1 and GFI1 gene mutations in children with neutropenia and clinical characterization of two novel mutations in ELANE gene.
Komvilaisak P; Yudhasompop N; Kanchanakamhaeng K; Hongeng S; Pakakasama S; Anurathapan U; Pongphitcha P; Songdej D; Sasanakul W; Sirachainan N
BMC Pediatr; 2023 Nov; 23(1):592. PubMed ID: 37993852
[TBL] [Abstract][Full Text] [Related]
3. Novel genetic etiologies of severe congenital neutropenia.
Boztug K; Klein C
Curr Opin Immunol; 2009 Oct; 21(5):472-80. PubMed ID: 19782549
[TBL] [Abstract][Full Text] [Related]
4. Genetic analysis and clinical picture of severe congenital neutropenia in Israel.
Lebel A; Yacobovich J; Krasnov T; Koren A; Levin C; Kaplinsky C; Ravel-Vilk S; Laor R; Attias D; Ben Barak A; Shtager D; Stein J; Kuperman A; Miskin H; Dgany O; Giri N; Alter BP; Tamary H
Pediatr Blood Cancer; 2015 Jan; 62(1):103-8. PubMed ID: 25284454
[TBL] [Abstract][Full Text] [Related]
5. Different pattern of gene mutations in Iranian patients with severe congenital neutropenia (including 2 new mutations).
Alizadeh Z; Fazlollahi MR; Houshmand M; Maddah M; Chavoshzadeh Z; Hamidieh AA; Shamsian BS; Eshghi P; Bolandghamat Pour S; Sadaaie Jahromi H; Mansouri M; Movahedi M; Nayebpour M; Pourpak Z; Moin M
Iran J Allergy Asthma Immunol; 2013 Mar; 12(1):86-92. PubMed ID: 23454784
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Mutations in the ELANE gene are associated with development of periodontitis in patients with severe congenital neutropenia.
Ye Y; Carlsson G; Wondimu B; Fahlén A; Karlsson-Sjöberg J; Andersson M; Engstrand L; Yucel-Lindberg T; Modéer T; Pütsep K
J Clin Immunol; 2011 Dec; 31(6):936-45. PubMed ID: 21796505
[TBL] [Abstract][Full Text] [Related]
8. Genetic insights into congenital neutropenia.
Klein C; Welte K
Clin Rev Allergy Immunol; 2010 Feb; 38(1):68-74. PubMed ID: 19440858
[TBL] [Abstract][Full Text] [Related]
9. Digenic mutations in severe congenital neutropenia.
Germeshausen M; Zeidler C; Stuhrmann M; Lanciotti M; Ballmaier M; Welte K
Haematologica; 2010 Jul; 95(7):1207-10. PubMed ID: 20220065
[TBL] [Abstract][Full Text] [Related]
10. Congenital neutropenia.
Klein C
Hematology Am Soc Hematol Educ Program; 2009; ():344-50. PubMed ID: 20008220
[TBL] [Abstract][Full Text] [Related]
11. The Clinical and Molecular Assessment of Iranian Families with Severe Congenital Neutropenia, Identification of HYOU1 and SHOC2 as Potential Novel Gene Defects.
Arab F; Rezaei N; Taheri F; Kouhpeikar H; Rayzan E; Mirbeyk M; Zare-Abdollahi D; Ghadami M
Iran J Allergy Asthma Immunol; 2022 Jun; 21(3):344-354. PubMed ID: 35822684
[TBL] [Abstract][Full Text] [Related]
12. Homozygous c.130-131 ins A (pW44X) mutation in the HAX1 gene as the most common cause of congenital neutropenia in Turkey: Report from the Turkish Severe Congenital Neutropenia Registry.
Yılmaz Karapınar D; Patıroğlu T; Metin A; Çalışkan Ü; Celkan T; Yılmaz B; Karakaş Z; Karapınar TH; Akıncı B; Özkınay F; Onay H; Yeşilipek MA; Akar HH; Tüysüz G; Tokgöz H; Özdemir GN; Aslan Kıykım A; Karaman S; Kılınç Y; Oymak Y; Küpesiz A; Olcay L; Keskin Yıldırım Z; Aydoğan G; Gökçe M; İleri T; Aral YZ; Bay A; Atabay B; Kaya Z; Söker M; Özdemir Karadaş N; Özbek U; Özsait Selçuk B; Özdemir HH; Uygun V; Tezcan Karasu G; Yılmaz Ş
Pediatr Blood Cancer; 2019 Oct; 66(10):e27923. PubMed ID: 31321910
[TBL] [Abstract][Full Text] [Related]
13. PML-controlled responses in severe congenital neutropenia with ELANE-misfolding mutations.
Olofsen PA; Bosch DA; Roovers O; van Strien PMH; de Looper HWJ; Hoogenboezem RM; Barnhoorn S; Mastroberardino PG; Ghazvini M; van der Velden VHJ; Bindels EMJ; de Pater EM; Touw IP
Blood Adv; 2021 Feb; 5(3):775-786. PubMed ID: 33560392
[TBL] [Abstract][Full Text] [Related]
14. Spectrum of
Arun AK; Senthamizhselvi A; Hemamalini S; Edison ES; Korula A; Fouzia NA; George B; Mathews V; Balasubramanian P
J Clin Pathol; 2018 Dec; 71(12):1046-1050. PubMed ID: 30171085
[TBL] [Abstract][Full Text] [Related]
15. Severe congenital neutropenia in a multigenerational family with a novel neutrophil elastase (ELANE) mutation.
van de Vosse E; Verhard EM; Tool AJ; de Visser AW; Kuijpers TW; Hiemstra PS; van Dissel JT
Ann Hematol; 2011 Feb; 90(2):151-8. PubMed ID: 20803142
[TBL] [Abstract][Full Text] [Related]
16. Inducible expression of a disease-associated
Garg B; Mehta HM; Wang B; Kamel R; Horwitz MS; Corey SJ
J Biol Chem; 2020 May; 295(21):7492-7500. PubMed ID: 32299910
[TBL] [Abstract][Full Text] [Related]
17. ELANE mutations in cyclic and severe congenital neutropenia: genetics and pathophysiology.
Horwitz MS; Corey SJ; Grimes HL; Tidwell T
Hematol Oncol Clin North Am; 2013 Feb; 27(1):19-41, vii. PubMed ID: 23351986
[TBL] [Abstract][Full Text] [Related]
18. Four novel ELANE mutations in patients with congenital neutropenia.
Kurnikova M; Maschan M; Dinova E; Shagina I; Finogenova N; Mamedova E; Polovtseva T; Shagin D; Shcherbina A
Pediatr Blood Cancer; 2011 Aug; 57(2):332-5. PubMed ID: 21425445
[TBL] [Abstract][Full Text] [Related]
19. Two cases of syndromic neutropenia with a report of novel mutation in G6PC3.
Alizadeh Z; Fazlollahi MR; Eshghi P; Hamidieh AA; Ghadami M; Pourpak Z
Iran J Allergy Asthma Immunol; 2011 Sep; 10(3):227-30. PubMed ID: 21891829
[TBL] [Abstract][Full Text] [Related]
20. Cyclic neutropenia and severe congenital neutropenia in patients with a shared ELANE mutation and paternal haplotype: evidence for phenotype determination by modifying genes.
Newburger PE; Pindyck TN; Zhu Z; Bolyard AA; Aprikyan AA; Dale DC; Smith GD; Boxer LA
Pediatr Blood Cancer; 2010 Aug; 55(2):314-7. PubMed ID: 20582973
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]