1.Ikegawa S, Nagano A, Nakamura K. Chondrodysplasia punctata
mimicking Blount's disease: a case report. Acta Orthop Scand 1990;61(6):580-1
2.Ikegawa S, Nakamura K, Kawai N, Nishino J. Blount's disease in a pair of identical twins. Acta Orthop Scand 1990;61(6):582
3.Ikegawa S, Nagano A, Nakamura K. A case of multiple epiphyseal dysplasia complicated by unilateral Perthes' disease. Acta Orthop Scand 1991;62(6):606-8
4.Ikegawa S, Nagano A, Matushita T, Nakamura K. Metachondromatosis: A report of two cases in a family. J Jpn Orthop Assoc 1992;66(5):460-6
5.Ikegawa S, Hoshikawa Y, Doi M. Idiopathic acro-osteolysis in an elderly woman: a 10-year follow-up. Arch Orthop Trauma Surg 1992;111:181-2
6.Ikegawa S, Nagano A, Kurokawa T. Disproportionate short stature, type E bracydactyly and exostoses of tibiae in a patient with an XYY karyotype: a 'new' syndrome? Clinical Dysmorphology 1992; 1:217-9
7.Ikegawa S, Nakamura K, Hoshino Y, Shiba M. Thoracic disc herniation in spondyloepiphyseal dysplasia. Acta Orthop Scand 1993;64(1):105-6
8.Ikegawa S, Sakaguchi R, Kimuzuka M, Yanagisako Y, Tokimura F. Recurrent dislocation of the patella in Kabuki make-up syndrome. J Pediatr Orthop 1993;13(2):265-7
9.Ikegawa S, Nagano A, Satoyoshi E.Skeletal abnormalities in Satoyoshi's syndrome Skeletal Radiol 1993;22(5):321-4
10.Ikegawa S, Iwaya T, Taniguchi K, Kimuzuka M. Retinal detachment in Spondyloepiphyseal dysplasia congenita. J Pediatr Orthop 1993;13(6):791-2,1993
11.Ikegawa S, Nagano A, Nakamura K, Kurokawa T. A case of Satoyoshi's syndrome. J Pediatr Orthop 1993;13(6):793-6
12.Ikegawa S, Hizuka N, Kurokawa T, Hoshino Y, Ohnishi I, Shizume K. Increase of serum growth-hormone binding protein in patients with ossification of the posterior longitudinal ligament of the spine. Spine 1993:18(13);1757-60
13.Ikegawa S. Spondyloepiphyseal dysplasia tarda: the autosomal recessive form in two sisters. Arch Orthop Trauma Surg 1993:113;49-52.
14.Seichi A, Hoshino Y, Ikegawa S, Tanaka T, Yanagisako Y, Kimizuka M, Kurokawa T. Cervical spinal atrophy associated with spina bifida. Paraplegia 1993:31;262-4.
15.Toda T, Ikegawa S, Okui K, Kondo E, Saito K, Fukuyama I, Kanazawa I, Nakamura Y. Refined Mapping of a gene resoonsible for Fukuyama type congenital muscular dystrophy：evidence for a strong linkage disequilibrium. Am J Hum Genet 1994:55,946-50.
16.Ikegawa S, Nagano A, Nakamura K, Nakamura S. Brachyolmia: a report of two cases. J Pediatr Orthop 1995:15(1); 105-7
17.Ikegawa S, Sudo K, Okui K, Nakamura Y. Isolation, characerization and chromosomal assignment of human colligin-2.Cytogenet Cell Genet 1995(71):182-6
18.Ikegawa S, Fukushima Y, Isomura M, Takada F, Nakamura Y. Mutation of fibroblast growth factor receptor-3 in six sporadic and one familial Japanese cases with achondroplasia. Hum Genet 1995:96(3);309-311
19.Toda T, Ikegawa S, Miyake M, Nakahori Y, Nakamura Y. Dinucleotide repeat polymorphism on chromosome 9q32. Jpn J Human Genet 1995:40, 333-4.
20.Nishimura G, Fukushima Y, Ohashi H, Ikegawa S. Mutation of fibroblast growth factor receptor-3 in achondroplasia. Am J Med Genet 1995:59; 393-5
21.Ikegawa S. Calcific tendinitis of pectoralis major insertion: A reportof two cases. Arch Orthop Traum Surg 1996;115:118-9.
22.Ikegawa S, Toda T, Okui K, Nakamura Y. Structure and chromosomal assignment of human S1-5 gene. Genomics 1996;35(3):590-2.
23.Inoue M, Isomura M, Ikegawa S, Fujiwara T, Shin S, Moriya H, Nakamura Y. Isolation and characerization ofa novel human cDNA clone homologous to a yeast transcriptional factor, GCN5. Cytogenet Cell Genet 1996:73;134-6
24.Ikegawa S, Kumano Y, Okui K, Fujiwara T, Takahashi E, Nakamura Y. Isolation, characerization and chromosomal assignment of human WNT7A gene.Cytogenet Cell Genet 1996;74:149-52
25.Ikegawa S, Nakamura K, Haga N, Nagano A, Nakamura Y. Mutation in the N-terminal globular domain of type X collagen also cause Schmid metaphyseal chondrodysplasia. Hum Mutat 1997;9:131-135
26.Ikegawa S, Nakamura Y. Structure of the gene encoding human colligin-2. Gene1997 (in press)