Terms: = Leukemia AND WAS, P42768, 7454, ENSG00000015285, WASP, THC, IMD2 AND Diagnosis
9 results:
1. Somatic mutations activating Wiskott-Aldrich syndrome protein concomitant with RAS pathway mutations in juvenile myelomonocytic leukemia patients.
Coppe A; Nogara L; Pizzuto MS; Cani A; Cesaro S; Masetti R; Locatelli F; Te Kronnie G; Basso G; Bortoluzzi S; Bresolin S
Hum Mutat; 2018 Apr; 39(4):579-587. PubMed ID: 29316027
[TBL] [Abstract] [Full Text] [Related]
2. [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]
3. Analyses of Genetic and Clinical Parameters for Screening Patients With Inherited Thrombocytopenia with Small or Normal-Sized Platelets.
Ouchi-Uchiyama M; Sasahara Y; Kikuchi A; Goi K; Nakane T; Ikeno M; Noguchi Y; Uike N; Miyajima Y; Matsubara K; Koh K; Sugita K; Imaizumi M; Kure S
Pediatr Blood Cancer; 2015 Dec; 62(12):2082-8. PubMed ID: 26175287
[TBL] [Abstract] [Full Text] [Related]
4. Genetic analysis and clinical picture of severe congenital neutropenia in Israel.
Lebel A; Yacobovich J; Krasnov T; Koren A; Levin C; Kaplinsky C; Ravel-Vilk S; Laor R; Attias D; Ben Barak A; Shtager D; Stein J; Kuperman A; Miskin H; Dgany O; Giri N; Alter BP; Tamary H
Pediatr Blood Cancer; 2015 Jan; 62(1):103-8. PubMed ID: 25284454
[TBL] [Abstract] [Full Text] [Related]
5. Wiskott-Aldrich syndrome presenting with a clinical picture mimicking juvenile myelomonocytic leukaemia.
Yoshimi A; Kamachi Y; Imai K; Watanabe N; Nakadate H; Kanazawa T; Ozono S; Kobayashi R; Yoshida M; Kobayashi C; Hama A; Muramatsu H; Sasahara Y; Jakob M; Morio T; Ehl S; Manabe A; Niemeyer C; Kojima S
Pediatr Blood Cancer; 2013 May; 60(5):836-41. PubMed ID: 23023736
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6. Wiskott-Aldrich syndrome with unusual clinical features similar to juvenile myelomonocytic leukemia.
Sano H; Kobayashi R; Suzuki D; Yasuda K; Nakanishi M; Nagashima T; Yamada M; Kobayashi K
Int J Hematol; 2012 Aug; 96(2):279-83. PubMed ID: 22736231
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7. [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
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8. Wiskott-Aldrich syndrome is an important differential diagnosis in male infants with juvenile myelomonocytic leukemialike features.
Watanabe N; Yoshimi A; Kamachi Y; Kawabe T; Muramatsu H; Matsumoto K; Manabe A; Kojima S; Kato K
J Pediatr Hematol Oncol; 2007 Dec; 29(12):836-8. PubMed ID: 18090932
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9. Donor and host influences in bone marrow transplantation for immunodeficiency disease and leukemia.
Kersey J; Filipovich A; McGlave P; Woods W; Weisdorf D; Neglia J; Dusenbery K; Blazar B; Nesbit M; Ramsay N
Semin Hematol; 1993 Oct; 30(4 Suppl 4):105-8; discussion 109. PubMed ID: 8303303
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