1. Worldwide trends in diabetes since 1980: a pooled analysis of 751 population-based studies with 4·4 million participants. Issue 10027 (9th April 2016) Authors: Zhou, B; Lu, Y; Hajifathalian, K; Bentham, J; Di Cesare, M; Danaei, G; Bixby, H; Cowan, MJ; Ali, MK; Taddei, C; Lo, WC; Reis-Santos, B; Stevens, GA; Riley, LM; Miranda, JJ; Bjerregaard, P; Rivera, JA; Fouad, HM; Ma, G; Mbanya, JC Journal: Lancet Issue: Volume 387:Issue 10027(2016) Page Start: 1513 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Correlation between a specific Wilms tumour suppressor gene (WT1) mutation and the histological findings in Wilms tumour (WT). Issue 12 (1st December 2002) Authors: Shibata, R; Hashiguchi, A; Sakamoto, J; Yamada, T; Umezawa, A; Hata, J Journal: Journal of medical genetics Issue: Volume 39:Issue 12(2002) Page Start: e83 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Identification of carriers of Duchenne/Becker muscular dystrophy by a novel method based on detection of junction fragments in the dystrophin gene. Issue 12 (December 1996) Authors: Yamagishi, H; Kato, S; Hiraishi, Y; Ishihara, T; Hata, J; Matsuo, N; Takano, T Journal: Journal of medical genetics Issue: Volume 33:Issue 12(1996) Page Start: 1027 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Axonal and perikaryal involvement in chronic inflammatory demyelinating polyneuropathy. Issue 6 (1st June 1999) Authors: Nagamatsu, M; Terao, S; Misu, K; Li, M; Hattori, N; Ichimura, M; Sakai, M; Yamamoto, H; Watanabe, H; Riku, S; Ikeda, E; Hata, J; Oda, M; Satake, M; Nakamura, N; Matsuya, S; Hashizume, Y; Sobue, G Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 66:Issue 6(1999) Page Start: 727 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Do intronic mutations affecting splicing of WT1 exon 9 cause Frasier syndrome?. Issue 1 (January 1998) Authors: Kikuchi, H; Takata, A; Akasaka, Y; Fukuzawa, R; Yoneyama, H; Kurosawa, Y; Honda, M; Kamiyama, Y; Hata, J Journal: Journal of medical genetics Issue: Volume 35:Issue 1(1998) Page Start: 45 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Sex reversal in a child with a 46, X, Yp+ karyotype: support for the existence of a gene(s), located in distal Xp, involved in testis formation. Issue 4 (April 1992) Authors: Ogata, T; Hawkins, J R; Taylor, A; Matsuo, N; Hata, J; Goodfellow, P N Journal: Journal of medical genetics Issue: Volume 29:Issue 4(1992) Page Start: 226 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Impaired male sex development in an infant with molecularly defined partial 9p monosomy: implication for a testis forming gene(s) on 9p. Issue 4 (April 1997) Authors: Ogata, T; Muroya, K; Matsuo, N; Hata, J; Fukushima, Y; Suzuki, Y Journal: Journal of medical genetics Issue: Volume 34:Issue 4(1997) Page Start: 331 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Ten year recurrence after first ever stroke in a Japanese community: the Hisayama study. Issue 3 (16th February 2005) Authors: Hata, J; Tanizaki, Y; Kiyohara, Y; Kato, I; Kubo, M; Tanaka, K; Okubo, K; Nakamura, H; Oishi, Y; Ibayashi, S; Iida, M Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 76:Issue 3(2005) Page Start: 368 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗