103 related articles for article (PubMed ID: 29896746)
1. [Diagnose of a neonate with X-linked thrombocytopenia by next generation sequencing].
Gao M; Kang L; Liu Y; Gai Z
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Jun; 35(3):422-425. PubMed ID: 29896746
[TBL] [Abstract][Full Text] [Related]
2. Identification of a Novel Gene Mutation in a Chinese Pedigree with X-linked Thrombocytopenia.
Zhang JW; Luo YX; Yang YL; Long B; Lu Y; Zhang XZ
Clin Lab; 2018 Oct; 64(11):. PubMed ID: 30549999
[TBL] [Abstract][Full Text] [Related]
3. Clinical and genetic analysis of 2 rare cases of Wiskott-Aldrich syndrome from Chinese minorities: Two case reports.
Liu H; Wang Y; Li Y; Tao L; Zhang Y; He X; Zhou Y; Liu X; Wang Y; Li L
Medicine (Baltimore); 2021 Apr; 100(16):e25527. PubMed ID: 33879693
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. [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]
6. 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]
7. 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]
8. 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]
9. 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]
10. [Clinical features and genotype analysis of 132 patients with Wiskott-Aldrich syndrome].
Li W; Liu D; Zhang X; Ding Y; Zhao X
Zhonghua Er Ke Za Zhi; 2015 Dec; 53(12):925-30. PubMed ID: 26887548
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. [Genetic screening in early diagnosis of neonatal WAS gene-related disorders].
Liu X; Yang L; Wang XC; Wu BB; Wang HJ; Wang HS; Qian XW; Cheng GQ; Cao Y; Sun JQ; Zhou WH
Zhonghua Er Ke Za Zhi; 2019 Jun; 57(6):429-433. PubMed ID: 31216799
[No Abstract] [Full Text] [Related]
13. 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]
14. Hematopoietic Stem Cell Transplantation for X-Linked Thrombocytopenia With Mutations in the WAS gene.
Oshima K; Imai K; Albert MH; Bittner TC; Strauss G; Filipovich AH; Morio T; Kapoor N; Dalal J; Schultz KR; Casper JT; Notarangelo LD; Ochs HD; Nonoyama S
J Clin Immunol; 2015 Jan; 35(1):15-21. PubMed ID: 25388447
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. A novel Wiskott-Aldrich syndrome protein mutation in an infant with thrombotic thrombocytopenic purpura.
Kawasaki Y; Toyoda H; Otsuki S; Iwasa T; Iwamoto S; Azuma E; Itoh-Habe N; Wada H; Fujimura Y; Morio T; Imai K; Mitsuiki N; Ohara O; Komada Y
Eur J Haematol; 2013 Feb; 90(2):164-8. PubMed ID: 23237501
[TBL] [Abstract][Full Text] [Related]
17. Two cases of Wiskott-Aldrich syndrome in neonates due to gene mutations.
Zhang S; Zhang R; Chen C; Sun J
Fetal Pediatr Pathol; 2013 Jul; 32(4):312-5. PubMed ID: 23301916
[TBL] [Abstract][Full Text] [Related]
18. [Novel mutations of GLB1 gene identified in a Chinese pedigree affected with GM1 gangliosidosis].
Gao M; Jin R; Zhang K; Li Z; Gai Z; Liu Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Feb; 36(2):128-131. PubMed ID: 30703229
[TBL] [Abstract][Full Text] [Related]
19. [Target gene sequence capture and next generation sequencing technology to diagnose four children with Alagille syndrome].
Gao ML; Zhong XM; Ma X; Ning HJ; Zhu D; Zou JZ
Zhonghua Er Ke Za Zhi; 2016 Jun; 54(6):441-5. PubMed ID: 27256232
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]