Manabe N - Search Results

1

Benign form of congenital angulation of long bones associated with shortening of soft tissues.

Nakamura K, Haga N, Manabe N, Iizuka T. Nakamura K, et al. Among authors: manabe n. Clin Dysmorphol. 1998 Jan;7(1):1-10. Clin Dysmorphol. 1998. PMID: 9546823

2

A mild form of pseudoachondroplasia: minimal epi-metaphyseal involvement of long bones.

Manabe N, Nakamura K, Ikegawa S, Kimizuka M. Manabe N, et al. Eur J Radiol. 1998 Sep;28(2):155-9. doi: 10.1016/s0720-048x(97)00116-2. Eur J Radiol. 1998. PMID: 9788021

3

Swelling of the dorsum of the hand and/or foot can be a first sign of Maffucci syndrome.

Nakamura K, Matsushita T, Haga N, Manabe N, Ishida T, Kurokawa T. Nakamura K, et al. Among authors: manabe n. Arch Orthop Trauma Surg. 1999;119(7-8):470-3. doi: 10.1007/s004020050024. Arch Orthop Trauma Surg. 1999. PMID: 10613243

4

Spondylar dysplasia in type X collagenopathy.

Nishimura G, Manabe N, Kosaki K, Haga N, Ohashi H, Nakamura K, Ikegawa S. Nishimura G, et al. Among authors: manabe n. Pediatr Radiol. 2001 Feb;31(2):76-80. doi: 10.1007/s002470000394. Pediatr Radiol. 2001. PMID: 11214689

5

Novel mutation in exon 18 of the cartilage oligomeric matrix protein gene causes a severe pseudoachondroplasia.

Mabuchi A, Haga N, Ikeda T, Manabe N, Ohashi H, Takatori Y, Nakamura K, Ikegawa S. Mabuchi A, et al. Among authors: manabe n. Am J Med Genet. 2001 Nov 22;104(2):135-9. doi: 10.1002/ajmg.10067. Am J Med Genet. 2001. PMID: 11746044

6

Novel types of COMP mutations and genotype-phenotype association in pseudoachondroplasia and multiple epiphyseal dysplasia.

Mabuchi A, Manabe N, Haga N, Kitoh H, Ikeda T, Kawaji H, Tamai K, Hamada J, Nakamura S, Brunetti-Pierri N, Kimizuka M, Takatori Y, Nakamura K, Nishimura G, Ohashi H, Ikegawa S. Mabuchi A, et al. Among authors: manabe n. Hum Genet. 2003 Jan;112(1):84-90. doi: 10.1007/s00439-002-0845-9. Epub 2002 Oct 29. Hum Genet. 2003. PMID: 12483304

7

Stature and severity in multiple epiphyseal dysplasia.

Haga N, Nakamura K, Takikawa K, Manabe N, Ikegawa S, Kimizuka M. Haga N, et al. Among authors: manabe n. J Pediatr Orthop. 1998 May-Jun;18(3):394-7. J Pediatr Orthop. 1998. PMID: 9600570

8

Independent impairment of osteoblast and osteoclast differentiation in klotho mouse exhibiting low-turnover osteopenia.

Kawaguchi H, Manabe N, Miyaura C, Chikuda H, Nakamura K, Kuro-o M. Kawaguchi H, et al. Among authors: manabe n. J Clin Invest. 1999 Aug;104(3):229-37. doi: 10.1172/JCI5705. J Clin Invest. 1999. PMID: 10430604 Free PMC article.

9

Cellular and molecular mechanism of low-turnover osteopenia in the klotho-deficient mouse.

Kawaguchi H, Manabe N, Chikuda H, Nakamura K, Kuroo M. Kawaguchi H, et al. Among authors: manabe n. Cell Mol Life Sci. 2000 May;57(5):731-7. doi: 10.1007/s000180050037. Cell Mol Life Sci. 2000. PMID: 10892339 Free PMC article.

10

Novel and recurrent mutations clustered in the von Willebrand factor A domain of MATN3 in multiple epiphyseal dysplasia.

Mabuchi A, Haga N, Maeda K, Nakashima E, Manabe N, Hiraoka H, Kitoh H, Kosaki R, Nishimura G, Ohashi H, Ikegawa S. Mabuchi A, et al. Among authors: manabe n. Hum Mutat. 2004 Nov;24(5):439-40. doi: 10.1002/humu.9286. Hum Mutat. 2004. PMID: 15459972

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

458 results

Search Page

Filters