144 related articles for article (PubMed ID: 23689198)
1. X-linked thrombocytopenia in a female with a complex familial pattern of X-chromosome inactivation.
Daza-Cajigal V; Martínez-Pomar N; Garcia-Alonso A; Heine-Suñer D; Torres S; Vega AK; Molina IJ; Matamoros N
Blood Cells Mol Dis; 2013 Aug; 51(2):125-9. PubMed ID: 23689198
[TBL] [Abstract][Full Text] [Related]
2. Wiskott-Aldrich syndrome/X-linked thrombocytopenia in China: Clinical characteristic and genotype-phenotype correlation.
Liu DW; Zhang ZY; Zhao Q; Jiang LP; Liu W; Tu WW; Song WX; Zhao XD
Pediatr Blood Cancer; 2015 Sep; 62(9):1601-8. PubMed ID: 25931402
[TBL] [Abstract][Full Text] [Related]
3. Two novel mutations identified in the Wiskott-Aldrich syndrome protein gene cause Wiskott-Aldrich syndrome and thrombocytopenia.
Andreu N; Matamoros N; Escudero A; Fillat C
Int J Mol Med; 2007 May; 19(5):777-82. PubMed ID: 17390083
[TBL] [Abstract][Full Text] [Related]
4. Intermittent X-linked thrombocytopenia with a novel WAS gene mutation.
Wada T; Itoh M; Maeba H; Toma T; Niida Y; Saikawa Y; Yachie A
Pediatr Blood Cancer; 2014 Apr; 61(4):746-8. PubMed ID: 24115682
[TBL] [Abstract][Full Text] [Related]
5. Mutations of the WASP gene in 10 Japanese patients with Wiskott-Aldrich syndrome and X-linked thrombocytopenia.
Itoh S; Nonoyama S; Morio T; Imai K; Okawa H; Ochs HD; Shimadzu M; Yata J
Int J Hematol; 2000 Jan; 71(1):79-83. PubMed ID: 10729999
[TBL] [Abstract][Full Text] [Related]
6. Detection of 28 novel mutations in the Wiskott-Aldrich syndrome and X-linked thrombocytopenia based on multiplex PCR.
Proust A; Guillet B; Picard C; de Saint Basile G; Pondarré C; Tamary H; Dreyfus M; Tchernia G; Fischer A; Delaunay J
Blood Cells Mol Dis; 2007; 39(1):102-6. PubMed ID: 17400488
[TBL] [Abstract][Full Text] [Related]
7. Hematopoietic stem cell transplantation for X-linked thrombocytopenia from a mild symptomatic carrier.
Okuya M; Kurosawa H; Kubota T; Endoh K; Ogiwara A; Nonoyama S; Hagisawa S; Sato Y; Matsushita T; Fukushima K; Sugita K; Sato T; Arisaka O
Bone Marrow Transplant; 2010 Mar; 45(3):607-9. PubMed ID: 19684625
[No Abstract] [Full Text] [Related]
8. Intermittent low platelet counts hampering diagnosis of X-linked thrombocytopenia in children: report of two unrelated cases and a novel mutation in the gene coding for the Wiskott-Aldrich syndrome protein.
Medina SS; Siqueira LH; Colella MP; Yamaguti-Hayakawa GG; Duarte BKL; Dos Santos Vilela MM; Ozelo MC
BMC Pediatr; 2017 Jun; 17(1):151. PubMed ID: 28641574
[TBL] [Abstract][Full Text] [Related]
9. X-linked thrombocytopenia in three males with normal sized platelets due to novel WAS gene mutations.
Mantadakis E; Sawalle-Belohradsky J; Tzanoudaki M; Kanariou M; Chatzimichael A; Albert MH
Pediatr Blood Cancer; 2014 Dec; 61(12):2305-6. PubMed ID: 25154619
[TBL] [Abstract][Full Text] [Related]
10. [WASP gene mutation analysis of a family of X-linked thrombocytopenia].
Shi RM; Liu ZG; Yang YH
Zhongguo Dang Dai Er Ke Za Zhi; 2010 Oct; 12(10):784-7. PubMed ID: 20959042
[TBL] [Abstract][Full Text] [Related]
11. Disruption of hSWI/SNF complexes in T cells by WAS mutations distinguishes X-linked thrombocytopenia from Wiskott-Aldrich syndrome.
Sarkar K; Sadhukhan S; Han SS; Vyas YM
Blood; 2014 Nov; 124(23):3409-19. PubMed ID: 25253772
[TBL] [Abstract][Full Text] [Related]
12. IVS6+5G>A found in Wiskott-Aldrich syndrome and X-linked thrombocytopenia in a Korean family.
Yoon SH; Cho T; Kim HJ; Kim SY; Ko JH; Baek HS; Lee HJ; Lee CH
Pediatr Blood Cancer; 2012 Feb; 58(2):297-9. PubMed ID: 22038941
[TBL] [Abstract][Full Text] [Related]
13. X-linked thrombocytopenia in a girl.
Inoue H; Kurosawa H; Nonoyama S; Imai K; Kumazaki H; Matsunaga T; Sato Y; Sugita K; Eguchi M
Br J Haematol; 2002 Sep; 118(4):1163-5. PubMed ID: 12199801
[TBL] [Abstract][Full Text] [Related]
14. Diagnosis of Wiskott-Aldrich syndrome by analysis of the X chromosome inactivation patterns in maternal leucocyte populations using the hypervariable DXS255 locus.
Hendriks RW; De Weers M; Mensink RG; Kraakman ME; Mollee-Versteegde IF; Veerman AJ; Sandkuyl LA; Schuurman RK
Clin Exp Immunol; 1991 May; 84(2):219-22. PubMed ID: 1709069
[TBL] [Abstract][Full Text] [Related]
15. Wiskott-Aldrich syndrome in a female with skewed X-chromosome inactivation.
Andreu N; Pujol-Moix N; Martinez-Lostao L; Oset M; Muñiz-Diaz E; Estivill X; Volpini V; Fillat C
Blood Cells Mol Dis; 2003; 31(3):332-7. PubMed ID: 14636648
[TBL] [Abstract][Full Text] [Related]
16. Mutation spectrum in patients with Wiskott-Aldrich syndrome and X-linked thrombocytopenia: identification of twelve different mutations in the WASP gene.
Schwartz M; Békássy A; Donnér M; Hertel T; Hreidarson S; Kerndrup G; Stormorken H; Stokland T; Tranebjaerg L; Orstavik KH; Skovby F
Thromb Haemost; 1996 Apr; 75(4):546-50. PubMed ID: 8743175
[TBL] [Abstract][Full Text] [Related]
17. Wiskott-Aldrich syndrome in a girl caused by heterozygous WASP mutation and extremely skewed X-chromosome inactivation: a novel association with maternal uniparental isodisomy 6.
Takimoto T; Takada H; Ishimura M; Kirino M; Hata K; Ohara O; Morio T; Hara T
Neonatology; 2015; 107(3):185-90. PubMed ID: 25633059
[TBL] [Abstract][Full Text] [Related]
18. Combined de-novo mutation and non-random X-chromosome inactivation causing Wiskott-Aldrich syndrome in a female with thrombocytopenia.
Boonyawat B; Dhanraj S; Al Abbas F; Zlateska B; Grunenbaum E; Roifman CM; Steele L; Meyn S; Blanchette V; Scherer SW; Swierczek S; Prchal J; Zhu Q; Torgerson TR; Ochs HD; Dror Y
J Clin Immunol; 2013 Oct; 33(7):1150-5. PubMed ID: 23943155
[TBL] [Abstract][Full Text] [Related]
19. Wiskott-Aldrich syndrome in a female.
Lutskiy MI; Sasahara Y; Kenney DM; Rosen FS; Remold-O'Donnell E
Blood; 2002 Oct; 100(8):2763-8. PubMed ID: 12351383
[TBL] [Abstract][Full Text] [Related]
20. Defective actin polymerization in EBV-transformed B-cell lines from patients with the Wiskott-Aldrich syndrome.
Facchetti F; Blanzuoli L; Vermi W; Notarangelo LD; Giliani S; Fiorini M; Fasth A; Stewart DM; Nelson DL
J Pathol; 1998 May; 185(1):99-107. PubMed ID: 9713366
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
