194 related articles for article (PubMed ID: 24115682)
21. 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]
22. Clinical, Laboratory Features and Clinical Courses of Patients with Wiskott Aldrich Syndrome and X-linked Thrombocytopenia-A single center study.
Bildik HN; Cagdas D; Ozturk Kura A; Oskay Halacli S; Sanal O; Tezcan I
Immunol Invest; 2022 Jul; 51(5):1272-1283. PubMed ID: 34098853
[TBL] [Abstract][Full Text] [Related]
23. Novel mutations in the Wiskott-Aldrich syndrome protein gene and their effects on transcriptional, translational, and clinical phenotypes.
Lemahieu V; Gastier JM; Francke U
Hum Mutat; 1999; 14(1):54-66. PubMed ID: 10447259
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. 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]
26. 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]
27. 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]
28. 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]
29. Wiskott-Aldrich syndrome.
Notarangelo LD; Miao CH; Ochs HD
Curr Opin Hematol; 2008 Jan; 15(1):30-6. PubMed ID: 18043243
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. A case of Wiskott-Aldrich syndrome with de novo mutation at exon 4.
Doğu F; Ariga T; Ikincioğullari A; Bozdoğan G; Aytekin C; Metin A; Babacan E
Turk J Pediatr; 2006; 48(1):66-8. PubMed ID: 16562789
[TBL] [Abstract][Full Text] [Related]
32. [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]
33. 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]
34. Novel WASP mutation in a patient with Wiskott-Aldrich syndrome: Case report and review of the literature.
Eghbali M; Sadeghi-Shabestari M; Najmi Varzaneh F; Zare Bidoki A; Rezaei N
Allergol Immunopathol (Madr); 2016; 44(5):450-4. PubMed ID: 26993433
[TBL] [Abstract][Full Text] [Related]
35. Mutations of the Wiskott-Aldrich Syndrome Protein affect protein expression and dictate the clinical phenotypes.
Ochs HD
Immunol Res; 2009; 44(1-3):84-8. PubMed ID: 19082760
[TBL] [Abstract][Full Text] [Related]
36. A unique presentation of Wiskott-Aldrich syndrome in relation to platelet size.
Patel PD; Samanich JM; Mitchell WB; Manwani D
Pediatr Blood Cancer; 2011 Jul; 56(7):1127-9. PubMed ID: 21488158
[TBL] [Abstract][Full Text] [Related]
37. Identification of six novel WASP gene mutations in patients suffering from Wiskott-Aldrich syndrome.
Brooimans RA; van den Berg AJ; Tamminga RY; Revesz T; Wulffraat NM; Zegers BJ
Hum Mutat; 2000 Apr; 15(4):386-7. PubMed ID: 10737997
[TBL] [Abstract][Full Text] [Related]
38. Genetic characteristics of eighty-seven patients with the Wiskott-Aldrich syndrome.
Gulácsy V; Freiberger T; Shcherbina A; Pac M; Chernyshova L; Avcin T; Kondratenko I; Kostyuchenko L; Prokofjeva T; Pasic S; Bernatowska E; Kutukculer N; Rascon J; Iagaru N; Mazza C; Tóth B; Erdos M; van der Burg M; Maródi L;
Mol Immunol; 2011 Feb; 48(5):788-92. PubMed ID: 21185603
[TBL] [Abstract][Full Text] [Related]
39. Monozygotic twin pair showing discordant phenotype for X-linked thrombocytopenia and Wiskott-Aldrich syndrome: a role for epigenetics?
Buchbinder D; Nadeau K; Nugent D
J Clin Immunol; 2011 Oct; 31(5):773-7. PubMed ID: 21710275
[TBL] [Abstract][Full Text] [Related]
40. X-linked thrombocytopenia caused by a mutation in the Wiskott-Aldrich syndrome (WAS) gene that disrupts interaction with the WAS protein (WASP)-interacting protein (WIP).
Luthi JN; Gandhi MJ; Drachman JG
Exp Hematol; 2003 Feb; 31(2):150-8. PubMed ID: 12591280
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
