162 related articles for article (PubMed ID: 23018568)
41. Successful use of empagliflozin to treat neutropenia in two G6PC3-deficient children: Impact of a mutation in SGLT5.
Boulanger C; Stephenne X; Diederich J; Mounkoro P; Chevalier N; Ferster A; Van Schaftingen E; Veiga-da-Cunha M
J Inherit Metab Dis; 2022 Jul; 45(4):759-768. PubMed ID: 35506446
[TBL] [Abstract][Full Text] [Related]
42. Phenotypic heterogeneity and evidence of a founder effect associated with G6PC3 mutations in patients with severe congenital neutropenia.
Smith BN; Evans C; Ali A; Ancliff PJ; Hayee B; Segal AW; Hall G; Kaya Z; Shakoori AR; Linch DC; Gale RE
Br J Haematol; 2012 Jul; 158(1):146-9. PubMed ID: 22469094
[No Abstract] [Full Text] [Related]
43. Heterozygous M1V variant of ELA-2 gene mutation associated with G-CSF refractory severe congenital neutropenia.
Setty BA; Yeager ND; Bajwa RP
Pediatr Blood Cancer; 2011 Sep; 57(3):514-5. PubMed ID: 21618407
[TBL] [Abstract][Full Text] [Related]
44. Chronic neutropenic colitis with complete colonic obstruction in a patient with severe congenital neutropenia associated with G6PC3 mutations.
Nikolouzakis TK; Spyridakis K; Tzardi M; Tsaknakis G; Ximeri M; Klimiankou M; Chrysos E; Skokowa J; Papadaki HA
Ann Hematol; 2022 Jul; 101(7):1583-1585. PubMed ID: 35084551
[No Abstract] [Full Text] [Related]
45. Neutrophil dysfunction triggers inflammatory bowel disease in G6PC3 deficiency.
Goenka A; Doherty JA; Al-Farsi T; Jagger C; Banka S; Cheesman E; Fagbemi A; Hughes SM; Wynn RF; Hussell T; Arkwright PD
J Leukoc Biol; 2021 Jun; 109(6):1147-1154. PubMed ID: 32930428
[TBL] [Abstract][Full Text] [Related]
46. Further delineation of the phenotype of severe congenital neutropenia type 4 due to mutations in G6PC3.
Banka S; Chervinsky E; Newman WG; Crow YJ; Yeganeh S; Yacobovich J; Donnai D; Shalev S
Eur J Hum Genet; 2011 Jan; 19(1):18-22. PubMed ID: 20717171
[TBL] [Abstract][Full Text] [Related]
47. 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]
48. 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]
49. Congenital neutropenia.
Klein C
Hematology Am Soc Hematol Educ Program; 2009; ():344-50. PubMed ID: 20008220
[TBL] [Abstract][Full Text] [Related]
50. Adult siblings with homozygous G6PC3 mutations expand our understanding of the severe congenital neutropenia type 4 (SCN4) phenotype.
Fernandez BA; Green JS; Bursey F; Barrett B; MacMillan A; McColl S; Fernandez S; Rahman P; Mahoney K; Pereira SL; Scherer SW; Boycott KM; Woods MO;
BMC Med Genet; 2012 Nov; 13():111. PubMed ID: 23171239
[TBL] [Abstract][Full Text] [Related]
51. Glucose-6-phosphatase-β, implicated in a congenital neutropenia syndrome, is essential for macrophage energy homeostasis and functionality.
Jun HS; Cheung YY; Lee YM; Mansfield BC; Chou JY
Blood; 2012 Apr; 119(17):4047-55. PubMed ID: 22246029
[TBL] [Abstract][Full Text] [Related]
52. A rare case of syndromic severe congenital neutropenia: JAGN1 mutation.
Çipe FE; Aydoğmuş Ç; Baskın K; Keskindemirci G; Garncarz W; Boztuğ K
Turk J Pediatr; 2020; 62(2):326-331. PubMed ID: 32419428
[TBL] [Abstract][Full Text] [Related]
53. Granulocyte colony-stimulating factor, congenital neutropenia, and acute myeloid leukemia.
Naparstek E
N Engl J Med; 1995 Aug; 333(8):516-8. PubMed ID: 7542748
[No Abstract] [Full Text] [Related]
54. [Congenital neutropenia type IV: case report].
Peruffo MV; Nainsztein G; Salvaneschi Quiña V; Samaruga C; Cuello MF; Romano S; Caferri H
Arch Argent Pediatr; 2022 Oct; 120(5):e213-e217. PubMed ID: 36190223
[TBL] [Abstract][Full Text] [Related]
55. Leukocytoclastic vasculitis in patients with severe congenital neutropenia.
Kilic SS; Mustafayeva S; Ipek K; Adim SB
J Trop Pediatr; 2010 Oct; 56(5):359-62. PubMed ID: 20100783
[TBL] [Abstract][Full Text] [Related]
56. Genetics and pathophysiology of severe congenital neutropenia syndromes unrelated to neutrophil elastase.
Boztug K; Klein C
Hematol Oncol Clin North Am; 2013 Feb; 27(1):43-60, vii. PubMed ID: 23351987
[TBL] [Abstract][Full Text] [Related]
57. Prevention and control of infections in patients with severe congenital neutropenia; a follow up study.
Salehi T; Fazlollahi MR; Maddah M; Nayebpour M; Tabatabaei Yazdi M; Alizadeh Z; Eshghi P; Chavoshzadeh Z; Movahedi M; Hamidieh AA; Cheraghi T; Pourpak Z; Moin M
Iran J Allergy Asthma Immunol; 2012 Mar; 11(1):51-6. PubMed ID: 22427476
[TBL] [Abstract][Full Text] [Related]
58. Mutations in the G6PC3 gene cause Dursun syndrome.
Banka S; Newman WG; Ozgül RK; Dursun A
Am J Med Genet A; 2010 Oct; 152A(10):2609-11. PubMed ID: 20799326
[TBL] [Abstract][Full Text] [Related]
59. Failure to eliminate a phosphorylated glucose analog leads to neutropenia in patients with G6PT and G6PC3 deficiency.
Veiga-da-Cunha M; Chevalier N; Stephenne X; Defour JP; Paczia N; Ferster A; Achouri Y; Dewulf JP; Linster CL; Bommer GT; Van Schaftingen E
Proc Natl Acad Sci U S A; 2019 Jan; 116(4):1241-1250. PubMed ID: 30626647
[TBL] [Abstract][Full Text] [Related]
60. Acute lymphoblastic leukemia following severe congenital neutropenia or de novo ALL?
Valera ET; Brassesco MS; Germeshausen M; Silveira Vda S; Queiroz RG; Roxo P; Scrideli CA; de Menezes UP; Ferriani V; Tone LG
Leuk Res; 2009 Sep; 33(9):e139-42. PubMed ID: 19398129
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
