153 related articles for article (PubMed ID: 37193639)
21. Delayed Puberty and Gonadal Failure in Patients with HAX1 Mutation.
Cekic S; Saglam H; Gorukmez O; Yakut T; Tarim O; Kilic SS
J Clin Immunol; 2017 Aug; 37(6):524-528. PubMed ID: 28681255
[TBL] [Abstract][Full Text] [Related]
22. Severe congenital neutropenia.
Welte K; Zeidler C; Dale DC
Semin Hematol; 2006 Jul; 43(3):189-95. PubMed ID: 16822461
[TBL] [Abstract][Full Text] [Related]
23. Severe developmental delay and epilepsy in a Japanese patient with severe congenital neutropenia due to HAX1 deficiency.
Matsubara K; Imai K; Okada S; Miki M; Ishikawa N; Tsumura M; Kato T; Ohara O; Nonoyama S; Kobayashi M
Haematologica; 2007 Dec; 92(12):e123-5. PubMed ID: 18055975
[TBL] [Abstract][Full Text] [Related]
24. Severe congenital neutropenia in 2 siblings of consanguineous parents. The role of HAX1 deficiency.
Mamishi S; Esfahani SA; Parvaneh N; Diestelhorst J; Rezaei N
J Investig Allergol Clin Immunol; 2009; 19(6):500-3. PubMed ID: 20128427
[TBL] [Abstract][Full Text] [Related]
25. Central nervous system involvement in severe congenital neutropenia: neurological and neuropsychological abnormalities associated with specific HAX1 mutations.
Carlsson G; van't Hooft I; Melin M; Entesarian M; Laurencikas E; Nennesmo I; Trebińska A; Grzybowska E; Palmblad J; Dahl N; Nordenskjöld M; Fadeel B; Henter JI
J Intern Med; 2008 Oct; 264(4):388-400. PubMed ID: 18513342
[TBL] [Abstract][Full Text] [Related]
26. In vitro study of HAX1 gene therapy by retro viral transduction as a therapeutic target in severe congenital neutropenia.
Farajifard H; Zavvar M; Rajaei T; Noorbakhsh F; Nikougoftar-Zarif M; Azadmanesh K; Kompani F; Rezaei N
Eur Cytokine Netw; 2018 Nov; 29(4):146-152. PubMed ID: 30698159
[TBL] [Abstract][Full Text] [Related]
27. Compound heterozygous HAX1 mutations in a Swedish patient with severe congenital neutropenia and no neurodevelopmental abnormalities.
Carlsson G; Elinder G; Malmgren H; Trebinska A; Grzybowska E; Dahl N; Nordenskjöld M; Fadeel B
Pediatr Blood Cancer; 2009 Dec; 53(6):1143-6. PubMed ID: 19499579
[TBL] [Abstract][Full Text] [Related]
28. Impact of different genetic mutations on granulocyte development and G-CSF responsiveness in congenital neutropenia.
Meng X; Zhang H; Dong L; Min Q; Yu M; Li Y; Liu L; Wang W; Ying W; Sun J; Wang JY; Hou J; Wang X
Blood Adv; 2024 Apr; 8(7):1667-1682. PubMed ID: 38286463
[TBL] [Abstract][Full Text] [Related]
29. Homozygous HAX1 mutations in severe congenital neutropenia patients with sporadic disease: a novel mutation in two unrelated British kindreds.
Smith BN; Ancliff PJ; Pizzey A; Khwaja A; Linch DC; Gale RE
Br J Haematol; 2009 Mar; 144(5):762-70. PubMed ID: 19036076
[TBL] [Abstract][Full Text] [Related]
30. HAX1 mutation in an infant with severe congenital neutropenia.
Eghbali A; Eshghi P; Malek F; Abdollahpour H; Rezaei N
Turk J Pediatr; 2010; 52(1):81-4. PubMed ID: 20402072
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. Cyclic manner of neutropenia in a patient with
Cipe FE; Celiksoy MH; Erturk B; Aydogmus Ç
Pediatr Hematol Oncol; 2018 Apr; 35(3):181-185. PubMed ID: 30346863
[No Abstract] [Full Text] [Related]
33. 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]
34. Severe congenital neutropenia.
Welte K; Zeidler C
Hematol Oncol Clin North Am; 2009 Apr; 23(2):307-20. PubMed ID: 19327585
[TBL] [Abstract][Full Text] [Related]
35. [Neurological findings in severe congenital neutropenia with HAX1 mutations].
Ishikawa N; Kobayashi M
No To Hattatsu; 2009 Nov; 41(6):415-9. PubMed ID: 19928538
[TBL] [Abstract][Full Text] [Related]
36. Coexistence of Gaucher Disease and severe congenital neutropenia.
Kose MD; Canda E; Kağnıcı M; Uçar SK; Onay H; Yıldırım Sozmen E; Karapınar D; Özkınay F; Çoker M
Blood Cells Mol Dis; 2019 May; 76():1-6. PubMed ID: 30473482
[TBL] [Abstract][Full Text] [Related]
37. A novel compound heterozygous HAX1 mutation in a Chinese patient with severe congenital neutropenia and chronic myelomonocytic leukemia transformation but without neurodevelopmental abnormalities.
Xue SL; Li JL; Zou JY; Su J; Chen SN; Wu DP
Haematologica; 2012 Feb; 97(2):318-20. PubMed ID: 22102707
[No Abstract] [Full Text] [Related]
38. Kostmann syndrome and severe congenital neutropenia.
Zeidler C; Welte K
Semin Hematol; 2002 Apr; 39(2):82-8. PubMed ID: 11957189
[TBL] [Abstract][Full Text] [Related]
39. Risk of myelodysplastic syndrome and acute myeloid leukemia in congenital neutropenias.
Freedman MH; Alter BP
Semin Hematol; 2002 Apr; 39(2):128-33. PubMed ID: 11957196
[TBL] [Abstract][Full Text] [Related]
40. [Genetic diagnosis of a patient with non-syndromic variants of congenital neutropenia].
Xue SL; Chen Y; Qiu QC; Feng YF; Dai L; Qiao M; Wu DP
Zhonghua Nei Ke Za Zhi; 2011 Nov; 50(11):922-5. PubMed ID: 22333123
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]