208 related articles for article (PubMed ID: 21891829)
41. 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]
42. 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]
43. Testicular failure in a patient with G6PC3 deficiency.
Yeshayahu Y; Asaf R; Dubnov-Raz G; Schiby G; Simon AJ; Lev A; Somech R
Pediatr Res; 2014 Aug; 76(2):197-201. PubMed ID: 24796372
[TBL] [Abstract][Full Text] [Related]
44. [Molecular analysis of two cases of severe congenital neutropenia].
Park J; Kim M; Lim J; Kim Y; Cho B; Park YJ; Han K
Korean J Lab Med; 2010 Apr; 30(2):111-6. PubMed ID: 20445326
[TBL] [Abstract][Full Text] [Related]
45. Mutations in the gene for the granulocyte colony-stimulating-factor receptor in patients with acute myeloid leukemia preceded by severe congenital neutropenia.
Dong F; Brynes RK; Tidow N; Welte K; Löwenberg B; Touw IP
N Engl J Med; 1995 Aug; 333(8):487-93. PubMed ID: 7542747
[TBL] [Abstract][Full Text] [Related]
46. 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]
47. A novel G6PC3 homozygous 1-bp deletion as a cause of severe congenital neutropenia.
Aróstegui JI; de Toledo JS; Pascal M; García C; Yagüe J; Díaz de Heredia C
Blood; 2009 Aug; 114(8):1718-9. PubMed ID: 19696212
[No Abstract] [Full Text] [Related]
48. Ovarian failure in HAX1-deficient patients: is there a gender-specific difference in pubertal development in severe congenital neutropenia or Kostmann disease?
Carlsson G; Kriström B; Nordenskjöld M; Henter JI; Fadeel B
Acta Paediatr; 2013 Jan; 102(1):78-82. PubMed ID: 23050867
[TBL] [Abstract][Full Text] [Related]
49. [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]
50. Severe Congenital Neutropenia Type 4: A Rare Disease Harboring a G6pc3 Gene Pathogenic Variant Particular to the Mexican Population.
López-Rodríguez L; Svyryd Y; Benítez-Alonso EO; Rivero-García P; Luna-Muñoz L; Mutchinick OM
Rev Invest Clin; 2022; 74(6):328-339. PubMed ID: 36546889
[TBL] [Abstract][Full Text] [Related]
51. Severe congenital neutropenia due to G6PC3 deficiency: Case series of five patients and literature review.
Velez-Tirado N; Yamazaki-Nakashimada MA; Lopez Valentín E; Partida-Gaytan A; Scheffler-Mendoza SC; Chaia Semerena GM; Alvarez-Cardona A; Suárez Gutiérrez MA; Medina Torres EA; Baeza Capetillo P; Hirschmugl T; Garncarz W; Espinosa-Padilla SE; Aguirre Hernández J; Klein C; Boztug K; Lugo Reyes SO
Scand J Immunol; 2022 Apr; 95(4):e13136. PubMed ID: 34964150
[TBL] [Abstract][Full Text] [Related]
52. Strong evidence for autosomal dominant inheritance of severe congenital neutropenia associated with ELA2 mutations.
Boxer LA; Stein S; Buckley D; Bolyard AA; Dale DC
J Pediatr; 2006 May; 148(5):633-6. PubMed ID: 16737875
[TBL] [Abstract][Full Text] [Related]
53. 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]
54. 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]
55. Three patients with glucose-6 phosphatase catalytic subunit 3 deficiency.
Cetinkaya PG; Cagdas D; Arikoglu T; Gumruk F; Tezcan I
J Pediatr Endocrinol Metab; 2020 Jul; 33(7):957-961. PubMed ID: 32623377
[TBL] [Abstract][Full Text] [Related]
56. A Novel Mutation in G6PC3 Gene Associated Non-syndromic Severe Congenital Neutropenia.
Khera S; Pramanik SK; Patnaik SK
Indian Pediatr; 2020 Jun; 57(6):574-575. PubMed ID: 32562405
[No Abstract] [Full Text] [Related]
57. The clinical, immunohematological, and molecular study of Iranian patients with severe congenital neutropenia.
Rezaei N; Moin M; Pourpak Z; Ramyar A; Izadyar M; Chavoshzadeh Z; Sherkat R; Aghamohammadi A; Yeganeh M; Mahmoudi M; Mahjoub F; Germeshausen M; Grudzien M; Horwitz MS; Klein C; Farhoudi A
J Clin Immunol; 2007 Sep; 27(5):525-33. PubMed ID: 17587155
[TBL] [Abstract][Full Text] [Related]
58. [Diagnosis and treatment procedures of congenital neutropenia].
Qiao M; Xue SL; Zou JY; Dai L; Liu HW; Chen Y; Sun AN; Wu DP
Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2012 Oct; 20(5):1221-4. PubMed ID: 23114152
[TBL] [Abstract][Full Text] [Related]
59. Resolution of inflammatory colitis with pegfilgrastim treatment in a case of severe congenital neutropenia due to glucose 6 phosphatase catalytic subunit-3 deficiency.
Kaya Z; Eğritaş O; Albayrak M; Göçün PU; Koçak U; Dalgiç B; Gürsel T
J Pediatr Hematol Oncol; 2014 Jul; 36(5):e316-8. PubMed ID: 24322501
[TBL] [Abstract][Full Text] [Related]
60. 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]
[Previous] [Next] [New Search]