Nii E - Search Results

1

Molecular characterization of two novel VEGFR3 mutations in Japanese families with Milroy's disease.

Futatani T, Nii E, Obata M, Ichida F, Okabe Y, Kanegane H, Miyawaki T. Futatani T, et al. Among authors: nii e. Pediatr Int. 2008 Feb;50(1):116-8. doi: 10.1111/j.1442-200X.2007.02505.x. Pediatr Int. 2008. PMID: 18279219 No abstract available.

2

Acrodysostosis with unusual iridal color changing with age.

Nii E, Urawa M, Nshimura T, Kitou H, Ikegawa S, Shimizu S, Taneda H, Uchida A, Niikawa N. Nii E, et al. Am J Med Genet B Neuropsychiatr Genet. 2007 Sep 5;144B(6):824-5. doi: 10.1002/ajmg.b.30492. Am J Med Genet B Neuropsychiatr Genet. 2007. PMID: 17440934

3

GC79/TRPS1 and tumorigenesis in humans.

Kobayashi H, Hino M, Inoue T, Nii E, Ikeda K, Son C, Iwakura T, Ishihara T, Ogawa Y. Kobayashi H, et al. Among authors: nii e. Am J Med Genet A. 2005 Apr 30;134(3):341-3. doi: 10.1002/ajmg.a.30596. Am J Med Genet A. 2005. PMID: 15690404 No abstract available.

4

Proximal tibiofibular synostosis with 49,XXXXY syndrome, a rare congenital bone anomaly.

Nishimura T, Nii E, Urawa M, Nishiyama M, Taki S, Uchida A. Nishimura T, et al. Among authors: nii e. J Orthop Sci. 2008 Jul;13(4):390-5. doi: 10.1007/s00776-008-1230-x. Epub 2008 Aug 13. J Orthop Sci. 2008. PMID: 18696202 No abstract available.

5

Limb-lengthening and angular correction for dysplasia epiphysealis hemimelica.

Nishiyama M, Nii E, Akeda K, Uchida A. Nishiyama M, et al. Among authors: nii e. J Orthop Sci. 2001;6(4):358-61. doi: 10.1007/s007760100032. J Orthop Sci. 2001. PMID: 11479766

6

Heterozygous mutations in cyclic AMP phosphodiesterase-4D (PDE4D) and protein kinase A (PKA) provide new insights into the molecular pathology of acrodysostosis.

Kaname T, Ki CS, Niikawa N, Baillie GS, Day JP, Yamamura K, Ohta T, Nishimura G, Mastuura N, Kim OH, Sohn YB, Kim HW, Cho SY, Ko AR, Lee JY, Kim HW, Ryu SH, Rhee H, Yang KS, Joo K, Lee J, Kim CH, Cho KH, Kim D, Yanagi K, Naritomi K, Yoshiura K, Kondoh T, Nii E, Tonoki H, Houslay MD, Jin DK. Kaname T, et al. Among authors: nii e. Cell Signal. 2014 Nov;26(11):2446-59. doi: 10.1016/j.cellsig.2014.07.025. Epub 2014 Jul 24. Cell Signal. 2014. PMID: 25064455 Clinical Trial.

7

Ischio-spinal dysostosis: a previously unrecognised combination of malformations.

Nishimura G, Kimizuka M, Shiro R, Nii E, Nishiyama M, Kawano T, Kaku T, Kawada Y. Nishimura G, et al. Among authors: nii e. Pediatr Radiol. 1999 Mar;29(3):212-7. doi: 10.1007/s002470050574. Pediatr Radiol. 1999. PMID: 10201042

8

[Four cases of cancer of unknown primary site that manifested as mediastinal metastatic lesions].

Chen F, Tatsumi A, Nii E, Tanaka H, Muguruma H, Doi H, Nakayama T. Chen F, et al. Among authors: nii e. Nihon Kokyuki Gakkai Zasshi. 1999 Dec;37(12):1003-7. Nihon Kokyuki Gakkai Zasshi. 1999. PMID: 10707543 Japanese.

9

[Pulmonary infarction diagnosed by transbronchial lung biopsy].

Doi H, Nii E, Muguruma H, Nakayama T, Terasawa M. Doi H, et al. Among authors: nii e. Nihon Kokyuki Gakkai Zasshi. 1999 Dec;37(12):974-8. Nihon Kokyuki Gakkai Zasshi. 1999. PMID: 10707537 Japanese.

10

[Medullary sponge kidney associated with congenital total hemihypertrophy (author's transl)].

Komeda Y, Hoshina A, Sugimura Y, Saito K, Nii E. Komeda Y, et al. Among authors: nii e. Rinsho Hoshasen. 1982 Apr;27(4):477-80. Rinsho Hoshasen. 1982. PMID: 7109277 Japanese. No abstract available.

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