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Results: 1 to 20 of 104

Similar articles for PubMed (Select 20173115)

1.

X-linked thrombocytopenia (XLT) due to WAS mutations: clinical characteristics, long-term outcome, and treatment options.

Albert MH, Bittner TC, Nonoyama S, Notarangelo LD, Burns S, Imai K, Espanol T, Fasth A, Pellier I, Strauss G, Morio T, Gathmann B, Noordzij JG, Fillat C, Hoenig M, Nathrath M, Meindl A, Pagel P, Wintergerst U, Fischer A, Thrasher AJ, Belohradsky BH, Ochs HD.

Blood. 2010 Apr 22;115(16):3231-8. doi: 10.1182/blood-2009-09-239087. Epub 2010 Feb 19.

2.

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 Apr 30. doi: 10.1002/pbc.25559. [Epub ahead of print]

PMID:
25931402
3.

DOCK8 deficiency: clinical and immunological phenotype and treatment options - a review of 136 patients.

Aydin SE, Kilic SS, Aytekin C, Kumar A, Porras O, Kainulainen L, Kostyuchenko L, Genel F, Kütükcüler N, Karaca N, Gonzalez-Granado L, Abbott J, Al-Zahrani D, Rezaei N, Baz Z, Thiel J, Ehl S, Marodi L, Orange JS, Sawalle-Belohradsky J, Keles S, Holland SM, Sanal Ö, Ayvaz DC, Tezcan I, Al-Mousa H, Alsum Z, Hawwari A, Metin A, Matthes-Martin S, Hönig M, Schulz A, Picard C, Barlogis V, Gennery A, Ifversen M, van Montfrans J, Kuijpers T, Bredius R, Dückers G, Al-Herz W, Pai SY, Geha R, Notheis G, Schwarze CP, Tavil B, Azik F, Bienemann K, Grimbacher B, Heinz V, Gaspar HB, Aydin R, Hagl B, Gathmann B, Belohradsky BH, Ochs HD, Chatila T, Renner ED, Su H, Freeman AF, Engelhardt K, Albert MH; inborn errors working party of EBMT.

J Clin Immunol. 2015 Feb;35(2):189-98. doi: 10.1007/s10875-014-0126-0. Epub 2015 Jan 28.

PMID:
25627830
4.

[Clinical characteristics and treatment responses of X-linked thrombocytopenia].

Zhang X, Liu D, Luo G, Du H, Wu J, Zou L, Zhao X.

Zhonghua Er Ke Za Zhi. 2014 Dec;52(12):890-5. Chinese.

PMID:
25619343
5.

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. 2014 Nov 12. [Epub ahead of print]

PMID:
25388447
6.

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 27;124(23):3409-19. doi: 10.1182/blood-2014-07-587642. Epub 2014 Sep 24.

PMID:
25253772
7.

Successful long-term outcome of kidney transplantation in a patient with X-linked thrombocytopenia: 9-year follow-up.

Garnier AS, Augusto JF, Pellier I, Subra JF, Sayegh J.

Transplantation. 2014 Sep 27;98(6):e57-8. doi: 10.1097/TP.0000000000000338. No abstract available.

PMID:
25221901
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. doi: 10.1002/pbc.25196. Epub 2014 Aug 23.

PMID:
25154619
9.

Allogeneic bone marrow transplantation appears to ameliorate IgA nephropathy in a patient with X-linked thrombocytopenia.

Hoshino A, Shimizu M, Matsukura H, Sakaki-Nakatsubo H, Nomura K, Miyawaki T, Kanegane H.

J Clin Immunol. 2014 Jan;34(1):53-7. doi: 10.1007/s10875-013-9964-4. Epub 2013 Nov 12.

PMID:
24217816
10.

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. doi: 10.1002/pbc.24787. Epub 2013 Sep 21.

PMID:
24115682
11.

Novel GATA1 mutation in residue D218 leads to macrothrombocytopenia and clinical bleeding problems.

Hermans C, De Waele L, Van Geet C, Freson K.

Platelets. 2014;25(4):305-7. doi: 10.3109/09537104.2013.815339. Epub 2013 Aug 23. No abstract available.

PMID:
23971719
12.

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. doi: 10.1016/j.bcmd.2013.04.004. Epub 2013 May 18.

PMID:
23689198
13.

Wiskott-Aldrich syndrome: a comprehensive review.

Massaad MJ, Ramesh N, Geha RS.

Ann N Y Acad Sci. 2013 May;1285:26-43. doi: 10.1111/nyas.12049. Epub 2013 Mar 25. Review.

PMID:
23527602
14.

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. doi: 10.3109/15513815.2012.754530. Epub 2013 Jan 10.

PMID:
23301916
15.

Characteristics and outcome of early-onset, severe forms of Wiskott-Aldrich syndrome.

Mahlaoui N, Pellier I, Mignot C, Jais JP, Bilhou-Nabéra C, Moshous D, Neven B, Picard C, de Saint-Basile G, Cavazzana-Calvo M, Blanche S, Fischer A.

Blood. 2013 Feb 28;121(9):1510-6. doi: 10.1182/blood-2012-08-448118. Epub 2012 Dec 20.

16.

Detection of six novel mutations in WASP gene in fifteen Iranian Wiskott-Aldrich patients.

Safaei S, Fazlollahi MR, Houshmand M, Hamidieh AA, Bemanian MH, Alavi S, Mousavi F, Pourpak Z, Moin M.

Iran J Allergy Asthma Immunol. 2012 Dec;11(4):345-8. doi: 011.04/ijaai.345348.

17.

Aberrant glycosylation of IgA in Wiskott-Aldrich syndrome and X-linked thrombocytopenia.

Shimizu M, Kanegane H, Wada T, Motoyoshi Y, Morio T, Candotti F, Yachie A.

J Allergy Clin Immunol. 2013 Feb;131(2):587-90.e1-3. doi: 10.1016/j.jaci.2012.08.040. Epub 2012 Oct 26. No abstract available.

18.

Clinical and molecular characterization of Thai patients with Wiskott-Aldrich syndrome.

Amarinthnukrowh P, Ittiporn S, Tongkobpetch S, Chatchatee P, Sosothikul D, Shotelersuk V, Suphapeetiporn K.

Scand J Immunol. 2013 Jan;77(1):69-74. doi: 10.1111/sji.12004.

PMID:
23033889
19.

Wiskott-Aldrich syndrome; an x-linked primary immunodeficiency disease with unique and characteristic features.

Ariga T.

Allergol Int. 2012 Jun;61(2):183-9. doi: 10.2332/allergolint.11-RAI-0412. Epub 2012 Feb 25. Review.

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. doi: 10.1002/pbc.23377. Epub 2011 Oct 28.

PMID:
22038941
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