Sugawara H - Search Results

1

A novel gene is disrupted at a 14q13 breakpoint of t(2;14) in a patient with mirror-image polydactyly of hands and feet.

Kondoh S, Sugawara H, Harada N, Matsumoto N, Ohashi H, Sato M, Kantaputra PN, Ogino T, Tomita H, Ohta T, Kishino T, Fukushima Y, Niikawa N, Yoshiura K. Kondoh S, et al. Among authors: sugawara h. J Hum Genet. 2002;47(3):136-9. doi: 10.1007/s100380200015. J Hum Genet. 2002. PMID: 11954550

2

Duplication of 8p23.2: a benign cytogenetic variant?

Harada N, Takano J, Kondoh T, Ohashi H, Hasegawa T, Sugawara H, Ida T, Yoshiura K, Ohta T, Kishino T, Kajii T, Niikawa N, Matsumoto N. Harada N, et al. Among authors: sugawara h. Am J Med Genet. 2002 Aug 15;111(3):285-8. doi: 10.1002/ajmg.10584. Am J Med Genet. 2002. PMID: 12210324

3

Preferential paternal origin of microdeletions caused by prezygotic chromosome or chromatid rearrangements in Sotos syndrome.

Miyake N, Kurotaki N, Sugawara H, Shimokawa O, Harada N, Kondoh T, Tsukahara M, Ishikiriyama S, Sonoda T, Miyoshi Y, Sakazume S, Fukushima Y, Ohashi H, Nagai T, Kawame H, Kurosawa K, Touyama M, Shiihara T, Okamoto N, Nishimoto J, Yoshiura K, Ohta T, Kishino T, Niikawa N, Matsumoto N. Miyake N, et al. Among authors: sugawara h. Am J Hum Genet. 2003 May;72(5):1331-7. doi: 10.1086/375166. Epub 2003 Apr 9. Am J Hum Genet. 2003. PMID: 12687502 Free PMC article.

4

Breakpoint analysis of a familial balanced translocation t(2;8)(q31;p21) associated with mesomelic dysplasia.

Sugawara H, Egashira M, Harada N, Jakobs TC, Yoshiura K, Kishino T, Ohta T, Niikawa N, Matsumoto N. Sugawara H, et al. J Med Genet. 2002 Jul;39(7):E34. doi: 10.1136/jmg.39.7.e34. J Med Genet. 2002. PMID: 12114491 Free PMC article. No abstract available.

5

Complex low-copy repeats associated with a common polymorphic inversion at human chromosome 8p23.

Sugawara H, Harada N, Ida T, Ishida T, Ledbetter DH, Yoshiura K, Ohta T, Kishino T, Niikawa N, Matsumoto N. Sugawara H, et al. Genomics. 2003 Aug;82(2):238-44. doi: 10.1016/s0888-7543(03)00108-3. Genomics. 2003. PMID: 12837273

6

A rapid diagnostic method for a retrotransposal insertional mutation into the FCMD gene in Japanese patients with Fukuyama congenital muscular dystrophy.

Kato R, Kawamura J, Sugawara H, Niikawa N, Matsumoto N. Kato R, et al. Among authors: sugawara h. Am J Med Genet A. 2004 May 15;127A(1):54-57. doi: 10.1002/ajmg.a.20669. Am J Med Genet A. 2004. PMID: 15103718

7

Condition of microcephaly, growth retardation, joint contractures, atopic dermatitis, and mental retardation in two Japanese sisters: a new autosomal recessive MCA/MR syndrome?

Kondoh T, Yamamoto T, Kono Y, Matsumoto T, Sugawara H, Matsumoto N, Moriuchi H. Kondoh T, et al. Among authors: sugawara h. Am J Med Genet. 2001 Jul 22;102(1):63-7. doi: 10.1002/1096-8628(20010722)102:1<63::aid-ajmg1415>3.0.co;2-u. Am J Med Genet. 2001. PMID: 11471174

8

Spontaneous bubble domain formation in a layered ferromagnetic crystal.

Fukumura T, Sugawara H, Hasegawa T, Tanaka K, Sakaki H, Kimura T, Tokura Y. Fukumura T, et al. Among authors: sugawara h. Science. 1999 Jun 18;284(5422):1969-71. doi: 10.1126/science.284.5422.1969. Science. 1999. PMID: 10373110

9

[Evaluation of a synthetic thrombin inhibitor MD 805 as an anticoagulant after open heart and vascular surgery].

Sugawara H, Kumon K, Tanaka K, Ego Y, Naito Y, Fujita T. Sugawara H, et al. Kyobu Geka. 1983;36(7):533-7. Kyobu Geka. 1983. PMID: 6620752 Japanese. No abstract available.

10

A case of Cushing's syndrome in a pregnant woman associated with hypertension, hypokalemia, and gestational diabetes mellitus.

Sugawara H, Wada N, Baba S, Miyoshi A, Obara S, Yamazaki Y, Sasano H. Sugawara H, et al. Diabetol Int. 2024 Jul 23;15(4):845-849. doi: 10.1007/s13340-024-00745-2. eCollection 2024 Oct. Diabetol Int. 2024. PMID: 39469560

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