Sekido K - Search Results

1

Possible linkage between specific histological structures and aberrant reactivation of the Wnt pathway in adamantinomatous craniopharyngioma.

Kato K, Nakatani Y, Kanno H, Inayama Y, Ijiri R, Nagahara N, Miyake T, Tanaka M, Ito Y, Aida N, Tachibana K, Sekido K, Tanaka Y. Kato K, et al. Among authors: sekido k. J Pathol. 2004 Jul;203(3):814-21. doi: 10.1002/path.1562. J Pathol. 2004. PMID: 15221941

2

Nasal chondromesenchymal hamartoma of infancy: the first Japanese case report.

Kato K, Ijiri R, Tanaka Y, Hara M, Sekido K. Kato K, et al. Among authors: sekido k. Pathol Int. 1999 Aug;49(8):731-6. doi: 10.1046/j.1440-1827.1999.00933.x. Pathol Int. 1999. PMID: 10504541 Review.

3

Concurrent Ewing sarcoma family of tumors and fibrous dysplasia: possible diagnostic pitfall.

Kato K, Hayashi T, Tabuchi K, Okuzumi N, Kigasawa H, Abe Y, Toyoda Y, Aida N, Sekido K, Sato H, Tanaka M, Tanaka Y. Kato K, et al. Among authors: sekido k. J Pediatr Hematol Oncol. 2007 Jan;29(1):15-8. doi: 10.1097/MPH.0b013e31803076bb. J Pediatr Hematol Oncol. 2007. PMID: 17230061

4

Spinal cartilaginous meningioma in a child: a case report.

Ijiri R, Hara M, Tanaka Y, Kato K, Sekido K. Ijiri R, et al. Among authors: sekido k. Childs Nerv Syst. 2000 Feb;16(2):80-3. doi: 10.1007/PL00007284. Childs Nerv Syst. 2000. PMID: 10663811

5

Primary orbital melanoma in a child.

Ijiri R, Tanaka Y, Kato K, Sekido K, Sato H, Ito D. Ijiri R, et al. Among authors: sekido k. Med Pediatr Oncol. 2000 Aug;35(2):142-3. doi: 10.1002/1096-911x(200008)35:2<142::aid-mpo14>3.0.co;2-n. Med Pediatr Oncol. 2000. PMID: 10918242 No abstract available.

6

Ossifying fibromyxoid tumor of soft parts in a child: a case report.

Ijiri R, Tanaka Y, Misugi K, Sekido K, Nishi T. Ijiri R, et al. Among authors: sekido k. J Pediatr Surg. 1999 Aug;34(8):1294-6. doi: 10.1016/s0022-3468(99)90175-6. J Pediatr Surg. 1999. PMID: 10466619 Review.

7

Radiation-associated xanthomatous meningioma in a child.

Ijiri R, Tanaka Y, Hara M, Sekido K. Ijiri R, et al. Among authors: sekido k. Childs Nerv Syst. 2000 May;16(5):304-8. doi: 10.1007/s003810050519. Childs Nerv Syst. 2000. PMID: 10883374 Review.

8

Phenotypic diversity in patients with craniosynostoses unrelated to Apert syndrome: the role of fibroblast growth factor receptor gene mutations.

Ito S, Sekido K, Kanno H, Sato H, Tanaka M, Yamaguchi K, Yamamoto I. Ito S, et al. Among authors: sekido k. J Neurosurg. 2005 Jan;102(1 Suppl):23-30. doi: 10.3171/ped.2005.102.1.0023. J Neurosurg. 2005. PMID: 16206730

9

Cytologic features of desmoplastic infantile ganglioglioma: a report of two cases.

Hasegawa Y, Hayabuchi Y, Namba I, Watanabe T, Kato K, Ijiri R, Tanaka Y, Sekido K, Kigasawa H, Hara M. Hasegawa Y, et al. Among authors: sekido k. Acta Cytol. 2001 Nov-Dec;45(6):1037-42. doi: 10.1159/000328351. Acta Cytol. 2001. PMID: 11726100

10

Trigonocephaly in a boy with paternally inherited deletion 22q11.2 syndrome.

Yamamoto T, Sameshima K, Sekido K, Aida N, Matsumoto N, Naritomi K, Kurosawa K. Yamamoto T, et al. Among authors: sekido k. Am J Med Genet A. 2006 Jun 15;140(12):1302-4. doi: 10.1002/ajmg.a.31297. Am J Med Genet A. 2006. PMID: 16691595

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