1. A simple, refined approach to diagnosing renovascular hypertension in children: A 10‐year study. Issue 8 (23rd July 2020) Authors: Saida, Ken; Kamei, Koichi; Hamada, Riku; Yoshikawa, Takahisa; Kano, Yuji; Nagata, Hiroko; Sato, Mai; Ogura, Masao; Harada, Ryoko; Hataya, Hiroshi; Miyazaki, Osamu; Nosaka, Shunsuke; Ito, Shuichi; Ishikura, Kenji Journal: Pediatrics international Issue: Volume 62:Issue 8(2020) Page Start: 937 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Ampicillin‐ and ampicillin/sulbactam‐resistant Escherichia coli infection in a neonatal intensive care unit in Japan. Issue 6 (20th June 2016) Authors: Saida, Ken; Ito, Yukako; Shima, Yosuke; Kasuga, Eriko; Kusakari, Mai; Miyosawa, Yukihide; Baba, Atsushi Journal: Pediatrics international Issue: Volume 58:Issue 6(2016) Page Start: 537 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Ampicillin‐ and ampicillin/sulbactam‐resistant Escherichia coli infection in a neonatal intensive care unit in Japan. Issue 6 (June 2016) Authors: Saida, Ken; Ito, Yukako; Shima, Yosuke; Kasuga, Eriko; Kusakari, Mai; Miyosawa, Yukihide; Baba, Atsushi Journal: Pediatrics international Issue: Volume 58:Issue 6(2016) Page Start: 537 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Coagulopathy as a complication of kidney biopsies in paediatric systemic lupus erythematosus patients with antiphospholipid syndrome. Issue 6 (10th June 2018) Authors: Nagata, Hiroko; Sato, Mai; Ogura, Masao; Yoshikawa, Takahisa; Yamamoto, Kazuna; Matsumura, Sohshi; Kano, Yuji; Saida, Ken; Sako, Mayumi; Kamei, Koichi; Yoshioka, Takako; Ogata, Kentaro; Ito, Shuichi; Ishikura, Kenji Journal: Nephrology Issue: Volume 23:Issue 6(2018) Page Start: 592 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Diversity of renal phenotypes in patients with WDR19 mutations: Two case reports. Issue 7 (July 2017) Authors: Yoshikawa, Takahisa; Kamei, Koichi; Nagata, Hiroko; Saida, Ken; Sato, Mai; Ogura, Masao; Ito, Shuichi; Miyazaki, Osamu; Urushihara, Maki; Kondo, Shuji; Sugawara, Noriko; Ishizuka, Kiyonobu; Hamasaki, Yuko; Shishido, Seiichiro; Morisada, Naoya; Iijima, Kazumoto; Nagata, Michio; Yoshioka, Takako; O... Journal: Nephrology Issue: Volume 22:Issue 7(2017) Page Start: 566 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Efficient detection of copy‐number variations using exome data: Batch‐ and sex‐based analyses. Issue 1 (11th November 2020) Authors: Uchiyama, Yuri; Yamaguchi, Daisuke; Iwama, Kazuhiro; Miyatake, Satoko; Hamanaka, Kohei; Tsuchida, Naomi; Aoi, Hiromi; Azuma, Yoshiteru; Itai, Toshiyuki; Saida, Ken; Fukuda, Hiromi; Sekiguchi, Futoshi; Sakaguchi, Tomohiro; Lei, Ming; Ohori, Sachiko; Sakamoto, Masamune; Kato, Mitsuhiro; Koike, Taka... Journal: Human mutation Issue: Volume 42:Issue 1(2021) Page Start: 50 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Neuronal intranuclear inclusion disease presenting with an MELAS-like episode in chronic polyneuropathy. (December 2020) Authors: Ishihara, Tasuku; Okamoto, Tomoko; Saida, Ken; Saitoh, Yuji; Oda, Shinji; Sano, Terunori; Yoshida, Takuhiro; Morita, Yuki; Fujita, Atsushi; Fukuda, Hiromi; Miyake, Noriko; Mizuguchi, Takeshi; Saito, Yuko; Sekijima, Yoshiki; Matsumoto, Naomichi; Takahashi, Yuji Journal: Neurology Issue: Volume 6:Number 6(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Pathogenic variants in the survival of motor neurons complex gene GEMIN5 cause cerebellar atrophy. Issue 6 (7th October 2021) Authors: Saida, Ken; Tamaoki, Junya; Sasaki, Masayuki; Haniffa, Muzhirah; Koshimizu, Eriko; Sengoku, Toru; Maeda, Hiroki; Kikuchi, Masahiro; Yokoyama, Haruna; Sakamoto, Masamune; Iwama, Kazuhiro; Sekiguchi, Futoshi; Hamanaka, Kohei; Fujita, Atsushi; Mizuguchi, Takeshi; Ogata, Kazuhiro; Miyake, Noriko; Miy... Journal: Clinical genetics Issue: Volume 100:Issue 6(2021) Page Start: 722 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Recurrent de novo missense variants in GNB2 can cause syndromic intellectual disability. Issue 5 (28th June 2021) Authors: Tan, Natalie B; Pagnamenta, Alistair T; Ferla, Matteo P; Gadian, Jonathan; Chung, Brian HY; Chan, Marcus CY; Fung, Jasmine LF; Cook, Edwin; Guter, Stephen; Boschann, Felix; Heinen, Andre; Schallner, Jens; Mignot, Cyril; Keren, Boris; Whalen, Sandra; Sarret, Catherine; Mittag, Dana; Demmer, Laurie... Journal: Journal of medical genetics Issue: Volume 59:Issue 5(2022) Page Start: 511 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. SOFT syndrome in a patient from Chile. Issue 3 (20th December 2018) Authors: Saida, Ken; Silva, Sebastian; Solar, Benjamin; Fujita, Atsushi; Hamanaka, Kohei; Mitsuhashi, Satomi; Koshimizu, Eriko; Mizuguchi, Takeshi; Miyatake, Satoko; Takata, Atsushi; Miyake, Noriko; Matsumoto, Naomichi Journal: American journal of medical genetics Issue: Volume 179:Issue 3(2019) Page Start: 338 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗