1. Decreased sialylation of IgA1 O‐glycans associated with pneumococcal hemolytic uremic syndrome. Issue 6 (December 2013) Authors: Aoki, Hisaaki; Shiomi, Masashi; Ikeda, Tae; Ishii, Tsubura; Shimizu, Nobuhiko; Togawa, Masao; Okamoto, Nobuhiko; Kadoya, Machiko; Wada, Yoshinao Journal: Pediatrics international Issue: Volume 55:Issue 6(2013) Page Start: e143 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Early infancy‐onset stimulation‐induced myoclonic seizures in three siblings with inherited glycosylphosphatidylinositol (GPI) anchor deficiency. Issue 1 (6th March 2018) Authors: Mogami, Yukiko; Suzuki, Yasuhiro; Murakami, Yoshiko; Ikeda, Tae; Kimura, Sadami; Yanagihara, Keiko; Okamoto, Nobuhiko; Kinoshita, Taroh Journal: Epileptic disorders Issue: Volume 20:Issue 1(2018) Page Start: 42 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Early manifestations of BPAN in a pediatric patient. Issue 12 (26th September 2014) Authors: Okamoto, Nobuhiko; Ikeda, Tae; Hasegawa, Tatsuji; Yamamoto, Yuto; Kawato, Kazumi; Komoto, Tomohiro; Imoto, Issei Journal: American journal of medical genetics Issue: Volume 164:Issue 12(2014.) Page Start: 3095 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Ictal 99mTc-Ethyl Cysteinate Dimer SPECT Findings of a Girl With Refractory Localization-Related Epilepsy Who Developed Transient Ictal Bradycardia. Issue 3 (20th July 2015) Authors: Kimizu, Tomokazu; Toshikawa, Hiromitsu; Kimura, Sadami; Ikeda, Tae; Mogami, Yukiko; Yanagihara, Keiko; Kishima, Haruhiko; Suzuki, Yasuhiro Journal: Child neurology open Issue: Volume 2:Issue 3(2015) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Loss-of-function and gain-of-function mutations in PPP3CA cause two distinct disorders. (8th February 2018) Authors: Mizuguchi, Takeshi; Nakashima, Mitsuko; Kato, Mitsuhiro; Okamoto, Nobuhiko; Kurahashi, Hirokazu; Ekhilevitch, Nina; Shiina, Masaaki; Nishimura, Gen; Shibata, Takashi; Matsuo, Muneaki; Ikeda, Tae; Ogata, Kazuhiro; Tsuchida, Naomi; Mitsuhashi, Satomi; Miyatake, Satoko; Takata, Atsushi; Miyake, Nori... Journal: Human molecular genetics Issue: Volume 27:Number 8(2018:Apr. 15) Page Start: 1421 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Targeted capture and sequencing for detection of mutations causing early onset epileptic encephalopathy. Issue 7 (10th May 2013) Authors: Kodera, Hirofumi; Kato, Mitsuhiro; Nord, Alex S.; Walsh, Tom; Lee, Ming; Yamanaka, Gaku; Tohyama, Jun; Nakamura, Kazuyuki; Nakagawa, Eiji; Ikeda, Tae; Ben‐Zeev, Bruria; Lev, Dorit; Lerman‐Sagie, Tally; Straussberg, Rachel; Tanabe, Saori; Ueda, Kazutoshi; Amamoto, Masano; Ohta, Sayaka; Nonoda, Yut... Journal: Epilepsia Issue: Volume 54:Issue 7(2013:Jul.) Page Start: 1262 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Time course of serum neuron‐specific enolase levels from infancy to early adulthood in a female patient with beta‐propeller protein‐associated neurodegeneration. Issue 5 (7th February 2023) Authors: Hirano, Shodo; Suzuki, Yasuhiro; Ikeda, Tae; Okamoto, Nobuhiko Journal: American journal of medical genetics Issue: Volume 191:Issue 5(2023) Page Start: 1384 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗