Torii C - Search Results

1

Influence of MTHFR and RFC1 polymorphisms on toxicities during maintenance chemotherapy for childhood acute lymphoblastic leukemia or lymphoma.

Shimasaki N, Mori T, Torii C, Sato R, Shimada H, Tanigawara Y, Kosaki K, Takahashi T. Shimasaki N, et al. Among authors: torii c. J Pediatr Hematol Oncol. 2008 May;30(5):347-52. doi: 10.1097/MPH.0b013e318165b25d. J Pediatr Hematol Oncol. 2008. PMID: 18458567

2

Effects of methylenetetrahydrofolate reductase and reduced folate carrier 1 polymorphisms on high-dose methotrexate-induced toxicities in children with acute lymphoblastic leukemia or lymphoma.

Shimasaki N, Mori T, Samejima H, Sato R, Shimada H, Yahagi N, Torii C, Yoshihara H, Tanigawara Y, Takahashi T, Kosaki K. Shimasaki N, et al. Among authors: torii c. J Pediatr Hematol Oncol. 2006 Feb;28(2):64-8. doi: 10.1097/01.mph.0000198269.61948.90. J Pediatr Hematol Oncol. 2006. PMID: 16462575

3

Comprehensive screening of the thiopurine methyltransferase polymorphisms by denaturing high-performance liquid chromatography.

Udaka T, Torii C, Takahashi D, Mori T, Aramaki M, Kosaki R, Tanigawara Y, Takahashi T, Kosaki K. Udaka T, et al. Among authors: torii c. Genet Test. 2005 Summer;9(2):85-92. doi: 10.1089/gte.2005.9.85. Genet Test. 2005. PMID: 15943548

4

[Molecular diagnosis of multiple malformation syndrome].

Torii C, Kosaki K. Torii C, et al. Nihon Rinsho. 2005 Dec;63 Suppl 12:431-6. Nihon Rinsho. 2005. PMID: 16416829 Review. Japanese. No abstract available.

5

EFNB1 mutation at the ephrin ligand-receptor dimerization interface in a patient with craniofrontonasal syndrome.

Torii C, Izumi K, Nakajima H, Takahashi T, Kosaki K. Torii C, et al. Congenit Anom (Kyoto). 2007 Mar;47(1):49-52. doi: 10.1111/j.1741-4520.2006.00140.x. Congenit Anom (Kyoto). 2007. PMID: 17300690

6

Split hand foot malformation with whorl-like pigmentary pattern: phenotypic expression of somatic mosaicism for the p63 mutation.

Kosaki R, Naito Y, Torii C, Takahashi T, Nakajima T, Kosaki K. Kosaki R, et al. Among authors: torii c. Am J Med Genet A. 2008 Oct 1;146A(19):2574-7. doi: 10.1002/ajmg.a.32415. Am J Med Genet A. 2008. PMID: 18792980 No abstract available.

7

Survival of a male mosaic for PORCN mutation with mild focal dermal hypoplasia phenotype.

Yoshihashi H, Ohki H, Torii C, Ishiko A, Kosaki K. Yoshihashi H, et al. Among authors: torii c. Pediatr Dermatol. 2011 Sep-Oct;28(5):550-4. doi: 10.1111/j.1525-1470.2010.01209.x. Epub 2010 Dec 7. Pediatr Dermatol. 2011. PMID: 21133992

8

Branchial arch defects and 19p13.12 microdeletion: defining the critical region into a 0.8 M base interval.

Kosaki K, Saito H, Kosaki R, Torii C, Kishi K, Takahashi T. Kosaki K, et al. Among authors: torii c. Am J Med Genet A. 2011 Sep;155A(9):2212-4. doi: 10.1002/ajmg.a.33908. Epub 2011 Aug 3. Am J Med Genet A. 2011. PMID: 21815246

9

Juvenile Muscular Atrophy of a Unilateral Upper Extremity (Hirayama Disease) in a Patient with CHARGE Syndrome.

Yagihashi T, Hatori K, Ishii K, Torii C, Momoshima S, Takahashi T, Kosaki K. Yagihashi T, et al. Among authors: torii c. Mol Syndromol. 2010;1(2):91-94. doi: 10.1159/000315525. Epub 2010 Jun 30. Mol Syndromol. 2010. PMID: 21046013 Free PMC article.

10

Screening for CHARGE syndrome mutations in the CHD7 gene using denaturing high-performance liquid chromatography.

Aramaki M, Udaka T, Torii C, Samejima H, Kosaki R, Takahashi T, Kosaki K. Aramaki M, et al. Among authors: torii c. Genet Test. 2006 Winter;10(4):244-51. doi: 10.1089/gte.2006.10.244. Genet Test. 2006. PMID: 17253929

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

57 results

Search Page

Filters