235 related articles for article (PubMed ID: 19398129)
61. Extended spectrum of human glucose-6-phosphatase catalytic subunit 3 deficiency: novel genotypes and phenotypic variability in severe congenital neutropenia.
Boztug K; Rosenberg PS; Dorda M; Banka S; Moulton T; Curtin J; Rezaei N; Corns J; Innis JW; Avci Z; Tran HC; Pellier I; Pierani P; Fruge R; Parvaneh N; Mamishi S; Mody R; Darbyshire P; Motwani J; Murray J; Buchanan GR; Newman WG; Alter BP; Boxer LA; Donadieu J; Welte K; Klein C
J Pediatr; 2012 Apr; 160(4):679-683.e2. PubMed ID: 22050868
[TBL] [Abstract][Full Text] [Related]
62. Severe congenital neutropenia and the unfolded protein response.
Xia J; Link DC
Curr Opin Hematol; 2008 Jan; 15(1):1-7. PubMed ID: 18043239
[TBL] [Abstract][Full Text] [Related]
63. [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]
64. Is pegfilgrastim safe and effective in congenital neutropenia? An analysis of the French Severe Chronic Neutropenia registry.
Beaupain B; Leblanc T; Reman O; Hermine O; Vannier JP; Suarez F; Lutz P; Bordigoni P; Jourdain A; Schoenvald M; Ouachee M; François S; Kohser F; Jardin F; Devouassoux G; Bertrand Y; Nove-Josserand R; Donadieu J;
Pediatr Blood Cancer; 2009 Dec; 53(6):1068-73. PubMed ID: 19618456
[TBL] [Abstract][Full Text] [Related]
65. Bone marrow necrosis preceding infantile acute lymphoblastic leukaemia.
Eusni RM; Hamidah Hussin N; Zarina AL; Rahman J
Malays J Pathol; 2007 Dec; 29(2):113-7. PubMed ID: 19108404
[TBL] [Abstract][Full Text] [Related]
66. Candida norvegensis fungaemia in a neutropenic patient with acute non-lymphoblastic leukaemia.
Kiraz N; Akay OM; Sen Y; Aslan V; Akgun Y; Gulbas Z
Mycoses; 2010 Sep; 53(5):460-2. PubMed ID: 19496937
[TBL] [Abstract][Full Text] [Related]
67. Isolated asymptomatic severe neutropenia as the presentation of myeloid/natural killer cell acute leukemia.
Rubio-Batllés M; de La Mata AC; Romero Macias JR; Vitaller AR
Haematologica; 2000 Mar; 85(3):322-4. PubMed ID: 10702827
[No Abstract] [Full Text] [Related]
68. Successful treatment of hepatic encephalopathy in a patient with acute lymphoblastic leukemia.
Dada R; Wilop S; Jost E; Galm O; Gassler N; Osieka R
Acta Haematol; 2009; 122(4):216-20. PubMed ID: 19887778
[TBL] [Abstract][Full Text] [Related]
69. 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]
70. Clinical spectrum and long-term follow-up of 14 cases with G6PC3 mutations from the French Severe Congenital Neutropenia Registry.
Desplantes C; Fremond ML; Beaupain B; Harousseau JL; Buzyn A; Pellier I; Roques G; Morville P; Paillard C; Bruneau J; Pinson L; Jeziorski E; Vannier JP; Picard C; Bellanger F; Romero N; de Pontual L; Lapillonne H; Lutz P; Chantelot CB; Donadieu J
Orphanet J Rare Dis; 2014 Dec; 9():183. PubMed ID: 25491320
[TBL] [Abstract][Full Text] [Related]
71. Genetic and molecular diagnosis of severe congenital neutropenia.
Ward AC; Dale DC
Curr Opin Hematol; 2009 Jan; 16(1):9-13. PubMed ID: 19057199
[TBL] [Abstract][Full Text] [Related]
72. [Collection of hematopoietic progenitor cells from healthy donors].
Bojanić I; Cepulić BG; Mazić S
Acta Med Croatica; 2009 Jun; 63(3):237-44. PubMed ID: 19827352
[TBL] [Abstract][Full Text] [Related]
73. 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]
74. HAX-1 deficiency: Characteristics of five cases including an asymptomatic patient.
Aydogmus C; Cipe F; Tas M; Akinel A; Öner Ö; Keskindemirci G; Bornaun H; Kutluk G; Hocaoglu AB
Asian Pac J Allergy Immunol; 2016 Mar; 34(1):73-6. PubMed ID: 26994629
[TBL] [Abstract][Full Text] [Related]
75. A molecular classification of congenital neutropenia syndromes.
Boxer LA; Newburger PE
Pediatr Blood Cancer; 2007 Oct; 49(5):609-14. PubMed ID: 17584878
[TBL] [Abstract][Full Text] [Related]
76. A case of syndromic neutropenia and mutation in G6PC3.
Gatti S; Boztug K; Pedini A; Pasqualini C; Albano V; Klein C; Pierani P
J Pediatr Hematol Oncol; 2011 Mar; 33(2):138-40. PubMed ID: 21285905
[TBL] [Abstract][Full Text] [Related]
77. A novel G6PC3 gene mutation in severe congenital neutropenia: pancytopenia and variable bone marrow phenotype can also be part of this syndrome.
Arikoglu T; Kuyucu N; Germeshausen M; Kuyucu S
Eur J Haematol; 2015 Jan; 94(1):79-82. PubMed ID: 24750412
[TBL] [Abstract][Full Text] [Related]
78. Granulocyte colony-stimulating factor receptor mutations in a patient with acute lymphoblastic leukemia secondary to severe congenital neutropenia.
Germeshausen M; Ballmaier M; Schulze H; Welte K; Flohr T; Beiske K; Storm-Mathisen I; Abrahamsen TG
Blood; 2001 Feb; 97(3):829-30. PubMed ID: 11227095
[No Abstract] [Full Text] [Related]
79. Alport syndrome. Molecular genetic aspects.
Hertz JM
Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
[TBL] [Abstract][Full Text] [Related]
80. Congenital neutropenia syndromes.
Boztug K; Welte K; Zeidler C; Klein C
Immunol Allergy Clin North Am; 2008 May; 28(2):259-75, vii-viii. PubMed ID: 18424332
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]