Terms: = Bone cancer AND WAS, P42768, 7454, ENSG00000015285, WASP, THC, IMD2 AND Diagnosis
6 results:
1. Multiplexed Proteomic Analysis for diagnosis and Screening of Five Primary Immunodeficiency Disorders From Dried Blood Spots.
Collins CJ; Yi F; Dayuha R; Whiteaker JR; Ochs HD; Freeman A; Su HC; Paulovich AG; Segundo GRS; Torgerson T; Hahn SH
Front Immunol; 2020; 11():464. PubMed ID: 32296420
[TBL] [Abstract] [Full Text] [Related]
2. 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]
3. 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
[TBL] [Abstract] [Full Text] [Related]
4. Outcomes of unrelated cord blood transplantation in pediatric recipients.
Styczynski J; Cheung YK; Garvin J; Savage DG; Billote GB; Harrison L; Skerrett D; Wolownik K; Wischhover C; Hawks R; Bradley MB; Del Toro G; George D; Yamashiro D; van de Ven C; Cairo MS
Bone Marrow Transplant; 2004 Jul; 34(2):129-36. PubMed ID: 15107815
[TBL] [Abstract] [Full Text] [Related]
5. Mixed chimera status of 12 patients with Wiskott-Aldrich syndrome (WAS) after hematopoietic stem cell transplantation: evaluation by flow cytometric analysis of intracellular WAS protein expression.
Yamaguchi K; Ariga T; Yamada M; Nelson DL; Kobayashi R; Kobayashi C; Noguchi Y; Ito Y; Katamura K; Nagatoshi Y; Kondo S; Katoh H; Sakiyama Y
Blood; 2002 Aug; 100(4):1208-14. PubMed ID: 12149199
[TBL] [Abstract] [Full Text] [Related]
6. Novel mutations, no detectable mRNA and familial genetic analysis of the Wiskott-Aldrich syndrome protein gene in six Japanese patients with Wiskott-Aldrich syndrome.
Sasahara Y; Kawai S; Kumaki S; Ohashi Y; Minegishi M; Tsuchiya S
Eur J Pediatr; 2000; 159(1-2):23-30. PubMed ID: 10653325
[TBL] [Abstract] [Full Text] [Related]
