Imai K - Search Results

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. Albert MH, et al. Among authors: imai k. Blood. 2010 Apr 22;115(16):3231-8. doi: 10.1182/blood-2009-09-239087. Epub 2010 Feb 19. Blood. 2010. PMID: 20173115 Free article.

2

X-linked thrombocytopenia in a girl.

Inoue H, Kurosawa H, Nonoyama S, Imai K, Kumazaki H, Matsunaga T, Sato Y, Sugita K, Eguchi M. Inoue H, et al. Among authors: imai k. Br J Haematol. 2002 Sep;118(4):1163-5. doi: 10.1046/j.1365-2141.2002.03740.x. Br J Haematol. 2002. PMID: 12199801 Free article.

3

Clinical course of patients with WASP gene mutations.

Imai K, Morio T, Zhu Y, Jin Y, Itoh S, Kajiwara M, Yata J, Mizutani S, Ochs HD, Nonoyama S. Imai K, et al. Blood. 2004 Jan 15;103(2):456-64. doi: 10.1182/blood-2003-05-1480. Epub 2003 Sep 11. Blood. 2004. PMID: 12969986 Free article.

4

WASP (Wiskott-Aldrich syndrome protein) gene mutations and phenotype.

Imai K, Nonoyama S, Ochs HD. Imai K, et al. Curr Opin Allergy Clin Immunol. 2003 Dec;3(6):427-36. doi: 10.1097/00130832-200312000-00003. Curr Opin Allergy Clin Immunol. 2003. PMID: 14612666 Review.

5

Allogeneic hematopoietic stem cell transplantation for seven children with X-linked hyper-IgM syndrome: a single center experience.

Tomizawa D, Imai K, Ito S, Kajiwara M, Minegishi Y, Nagasawa M, Morio T, Nonoyama S, Mizutani S. Tomizawa D, et al. Among authors: imai k. Am J Hematol. 2004 May;76(1):33-9. doi: 10.1002/ajh.20044. Am J Hematol. 2004. PMID: 15114594 Free article.

6

Analysis of class switch recombination and somatic hypermutation in patients affected with autosomal dominant hyper-IgM syndrome type 2.

Imai K, Zhu Y, Revy P, Morio T, Mizutani S, Fischer A, Nonoyama S, Durandy A. Imai K, et al. Clin Immunol. 2005 Jun;115(3):277-85. doi: 10.1016/j.clim.2005.02.003. Clin Immunol. 2005. PMID: 15893695

7

Female hyper IgM syndrome type 1 with a chromosomal translocation disrupting CD40LG.

Imai K, Shimadzu M, Kubota T, Morio T, Matsunaga T, Park YD, Yoshioka A, Nonoyama S. Imai K, et al. Biochim Biophys Acta. 2006 Mar;1762(3):335-40. doi: 10.1016/j.bbadis.2005.10.003. Epub 2005 Oct 28. Biochim Biophys Acta. 2006. PMID: 16311023 Free article.

8

Impaired induction of DNA lesions during immunoglobulin class-switch recombination in humans influences end-joining repair.

Kracker S, Imai K, Gardès P, Ochs HD, Fischer A, Durandy AH. Kracker S, et al. Among authors: imai k. Proc Natl Acad Sci U S A. 2010 Dec 21;107(51):22225-30. doi: 10.1073/pnas.1012591108. Epub 2010 Dec 6. Proc Natl Acad Sci U S A. 2010. PMID: 21135220 Free PMC article.

9

Endocrine complications in primary immunodeficiency diseases in Japan.

Nozaki T, Takada H, Ishimura M, Ihara K, Imai K, Morio T, Kobayashi M, Nonoyama S, Hara T. Nozaki T, et al. Among authors: imai k. Clin Endocrinol (Oxf). 2012 Oct;77(4):628-34. doi: 10.1111/j.1365-2265.2012.04390.x. Clin Endocrinol (Oxf). 2012. PMID: 22432851

10

Clinical profile and genetic basis of Wiskott-Aldrich syndrome at Chandigarh, North India.

Suri D, Singh S, Rawat A, Gupta A, Kamae C, Honma K, Nakagawa N, Imai K, Nonoyama S, Oshima K, Mitsuiki N, Ohara O, Bilhou-Nabera C, Proust A, Ahluwalia J, Dogra S, Saikia B, Minz RW, Sehgal S. Suri D, et al. Among authors: imai k. Asian Pac J Allergy Immunol. 2012 Mar;30(1):71-8. Asian Pac J Allergy Immunol. 2012. PMID: 22523910 Free article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

5,078 results

Search Page