191 related articles for article (PubMed ID: 29348920)
1. Wiskott-Aldrich syndrome that was initially diagnosed as immune thrombocytopenic purpura secondary to a cytomegalovirus infection.
Kaneko R; Yamamoto S; Okamoto N; Akiyama K; Matsuno R; Toyama D; Hoshino A; Imai K; Isoyama K
SAGE Open Med Case Rep; 2018; 6():2050313X17753788. PubMed ID: 29348920
[TBL] [Abstract][Full Text] [Related]
2. When
Jin YY; Wu J; Chen TX; Chen J
Front Immunol; 2019; 10():1549. PubMed ID: 31354712
[No Abstract] [Full Text] [Related]
3. A rare case of Wiskott-Aldrich Syndrome with normal platelet size: a case report.
Baharin MF; Dhaliwal JS; Sarachandran SV; Idris SZ; Yeoh SL
J Med Case Rep; 2016 Jun; 10(1):188. PubMed ID: 27356510
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. Wiskott-Aldrich Syndrome Misdiagnosed as Immune Thrombocytopenic Purpura: A Case Report.
Karalexi MA; Tzanoudaki M; Fryganas A; Gkergki A; Spyropoulou D; Papadopoulou A; Papaevangelou V; Petrocheilos I
J Pediatr Hematol Oncol; 2018 Apr; 40(3):240-242. PubMed ID: 28859046
[TBL] [Abstract][Full Text] [Related]
7. Acquired Thrombotic Thrombocytopenic Purpura in a 5-Year-old Child With Wiskott-Aldrich Syndrome.
Özdemir Ö; Orhan MF; Büyükavcı M; Görükmez O
J Pediatr Hematol Oncol; 2022 Mar; 44(2):e434-e437. PubMed ID: 33769392
[TBL] [Abstract][Full Text] [Related]
8. Identification of a novel WAS mutation in a South African patient presenting with atypical Wiskott-Aldrich syndrome: a case report.
Glanzmann B; Möller M; Schoeman M; Urban M; van Helden PD; Frigati L; Grewal R; Pieters H; Loos B; Hoal EG; Glashoff RH; Cornelissen H; Rabie H; Esser MM; Kinnear CJ
BMC Med Genet; 2020 Jun; 21(1):124. PubMed ID: 32503528
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. [Identification of two novel WASP gene mutations in 3 boys with Wiskott-Aldrich syndrome].
Jiang LP; Xu YH; Yang XQ; Liu EM; Wang LJ; Lau YL; Chan KW
Zhonghua Er Ke Za Zhi; 2003 Aug; 41(8):590-3. PubMed ID: 14744380
[TBL] [Abstract][Full Text] [Related]
11. Lentiviral haemopoietic stem/progenitor cell gene therapy for treatment of Wiskott-Aldrich syndrome: interim results of a non-randomised, open-label, phase 1/2 clinical study.
Ferrua F; Cicalese MP; Galimberti S; Giannelli S; Dionisio F; Barzaghi F; Migliavacca M; Bernardo ME; Calbi V; Assanelli AA; Facchini M; Fossati C; Albertazzi E; Scaramuzza S; Brigida I; Scala S; Basso-Ricci L; Pajno R; Casiraghi M; Canarutto D; Salerio FA; Albert MH; Bartoli A; Wolf HM; Fiori R; Silvani P; Gattillo S; Villa A; Biasco L; Dott C; Culme-Seymour EJ; van Rossem K; Atkinson G; Valsecchi MG; Roncarolo MG; Ciceri F; Naldini L; Aiuti A
Lancet Haematol; 2019 May; 6(5):e239-e253. PubMed ID: 30981783
[TBL] [Abstract][Full Text] [Related]
12. Confirming or excluding the diagnosis of Wiskott-Aldrich syndrome in children with thrombocytopenia of an unknown etiology.
Ariga T; Nakajima M; Yoshida J; Yamato K; Nagatoshi Y; Yanai F; Caviles AP; Nelson DL; Sakiyama Y
J Pediatr Hematol Oncol; 2004 Jul; 26(7):435-40. PubMed ID: 15218418
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Assessment of Immature Platelet Fraction in the Diagnosis of Wiskott-Aldrich Syndrome.
Sokolic R; Oden N; Candotti F
Front Pediatr; 2015; 3():49. PubMed ID: 26082919
[TBL] [Abstract][Full Text] [Related]
15. [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]
16. 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]
17. 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]
18. A Novel WASP Gene Mutation in a Chinese Boy with Wiskott-Aldrich Syndrome.
Wu H; Hu C; Dang D; Guo YJ
Indian J Hematol Blood Transfus; 2014 Sep; 30(Suppl 1):353-5. PubMed ID: 25332617
[TBL] [Abstract][Full Text] [Related]
19. Wiskott-Aldrich syndrome with possible congenital
Sobouti B; Bahrami A; Rahmani F; Talebi S; Sherafati V; Vafapour M; Rezaei N
Natl Med J India; 2021; 34(1):24-26. PubMed ID: 34397000
[TBL] [Abstract][Full Text] [Related]
20. [The Wiskott-Aldrich syndrome in adulthood].
Matzdorff A; Meindl A; Pralle H
Dtsch Med Wochenschr; 2000 Feb; 125(6):147-50. PubMed ID: 10700878
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
