Niizuma H - Search Results

1

Ruxolitinib treatment of a patient with steroid-dependent severe autoimmunity due to STAT1 gain-of-function mutation.

Moriya K, Suzuki T, Uchida N, Nakano T, Katayama S, Irie M, Rikiishi T, Niizuma H, Okada S, Imai K, Sasahara Y, Kure S. Moriya K, et al. Among authors: niizuma h. Int J Hematol. 2020 Aug;112(2):258-262. doi: 10.1007/s12185-020-02860-7. Epub 2020 Mar 16. Int J Hematol. 2020. PMID: 32180118

2

Refractory chronic immune thrombocytopenic purpura in a child with acute lymphoblastic leukemia.

Horino S, Rikiishi T, Niizuma H, Abe H, Watanabe Y, Onuma M, Hoshi Y, Sasahara Y, Yoshinari M, Kazama T, Hayashi Y, Kumaki S, Tsuchiya S. Horino S, et al. Among authors: niizuma h. Int J Hematol. 2009 Nov;90(4):483-485. doi: 10.1007/s12185-009-0424-0. Epub 2009 Oct 10. Int J Hematol. 2009. PMID: 19816666

3

Vincristine-resistant Kasabach-Merritt phenomenon successfully treated with low-dose radiotherapy.

Watanabe Y, Onuma M, Looi CY, Saito Y, Kitazawa H, Niizuma H, Rikiishi T, Sakamoto O, Sasahara Y, Kumaki S, Watanabe M, Ushio S, Tsuchiya S. Watanabe Y, et al. Among authors: niizuma h. Int J Hematol. 2011 Jan;93(1):126-8. doi: 10.1007/s12185-010-0740-4. Epub 2010 Dec 15. Int J Hematol. 2011. PMID: 21161618 No abstract available.

4

Successful cord blood transplantation with reduced-intensity conditioning for childhood cerebral X-linked adrenoleukodystrophy at advanced and early stages.

Niizuma H, Uematsu M, Sakamoto O, Uchiyama T, Horino S, Onuma M, Matsuhashi T, Rikiishi T, Sasahara Y, Minegishi M, Tsuchiya S. Niizuma H, et al. Pediatr Transplant. 2012 Mar;16(2):E63-70. doi: 10.1111/j.1399-3046.2011.01539.x. Epub 2011 Aug 11. Pediatr Transplant. 2012. PMID: 21834803

5

Interstitial lung disease in two brothers with novel compound heterozygous ABCA3 mutations.

Kitazawa H, Moriya K, Niizuma H, Kawano K, Saito-Nanjo Y, Uchiyama T, Rikiishi T, Sasahara Y, Sakamoto O, Setoguchi Y, Kure S. Kitazawa H, et al. Among authors: niizuma h. Eur J Pediatr. 2013 Jul;172(7):953-7. doi: 10.1007/s00431-013-1977-8. Epub 2013 Feb 27. Eur J Pediatr. 2013. PMID: 23443156

6

Successful treatment with rituximab of an infant with refractory autoimmune hemolytic anemia.

Moriya K, Matsuhashi T, Onuma M, Niizuma H, Rikiishi T, Asada H, Suzuki J, Sasahara Y, Kure S. Moriya K, et al. Among authors: niizuma h. Int J Hematol. 2013 Aug;98(2):237-9. doi: 10.1007/s12185-013-1374-0. Epub 2013 May 24. Int J Hematol. 2013. PMID: 23702915

7

A case series of CAEBV of children and young adults treated with reduced-intensity conditioning and allogeneic bone marrow transplantation: a single-center study.

Watanabe Y, Sasahara Y, Satoh M, Looi CY, Katayama S, Suzuki T, Suzuki N, Ouchi M, Horino S, Moriya K, Nanjyo Y, Onuma M, Kitazawa H, Irie M, Niizuma H, Uchiyama T, Rikiishi T, Kumaki S, Minegishi M, Wada T, Yachie A, Tsuchiya S, Kure S. Watanabe Y, et al. Among authors: niizuma h. Eur J Haematol. 2013 Sep;91(3):242-248. doi: 10.1111/ejh.12151. Epub 2013 Jun 28. Eur J Haematol. 2013. PMID: 23734904

8

Selective expansion of donor-derived regulatory T cells after allogeneic bone marrow transplantation in a patient with IPEX syndrome.

Horino S, Sasahara Y, Sato M, Niizuma H, Kumaki S, Abukawa D, Sato A, Imaizumi M, Kanegane H, Kamachi Y, Sasaki S, Terui K, Ito E, Kobayashi I, Ariga T, Tsuchiya S, Kure S. Horino S, et al. Among authors: niizuma h. Pediatr Transplant. 2014 Feb;18(1):E25-30. doi: 10.1111/petr.12184. Epub 2013 Nov 7. Pediatr Transplant. 2014. PMID: 24224516

9

Somatic BRAF c.1799T>A p.V600E Mosaicism syndrome characterized by a linear syringocystadenoma papilliferum, anaplastic astrocytoma, and ocular abnormalities.

Watanabe Y, Shido K, Niihori T, Niizuma H, Katata Y, Iizuka C, Oba D, Moriya K, Saito-Nanjo Y, Onuma M, Rikiishi T, Sasahara Y, Watanabe M, Aiba S, Saito R, Sonoda Y, Tominaga T, Aoki Y, Kure S. Watanabe Y, et al. Among authors: niizuma h. Am J Med Genet A. 2016 Jan;170A(1):189-94. doi: 10.1002/ajmg.a.37376. Epub 2015 Sep 11. Am J Med Genet A. 2016. PMID: 26360803

10

Novel Compound Heterozygous RTEL1 Gene Mutations in a Patient With Hoyeraal-Hreidarsson Syndrome.

Moriya K, Niizuma H, Rikiishi T, Yamaguchi H, Sasahara Y, Kure S. Moriya K, et al. Among authors: niizuma h. Pediatr Blood Cancer. 2016 Sep;63(9):1683-4. doi: 10.1002/pbc.26030. Epub 2016 Apr 29. Pediatr Blood Cancer. 2016. PMID: 27128385 No abstract available.

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 Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

129 results

Search Page

Filters