Successful Treatment of Metachromatic Leukodystrophy Using Bone Marrow Transplantation of HoxB4 Overexpressing Cells

von Miyake, Noriko, Miyake, Koichi, Karlsson, Stefan, Shimada, Takashi
Veröffentlicht 2010

Intracellular mRNA cleavage by 3′ tRNase under the direction of 2′-O-methyl RNA heptamers

von Tamura, Masato, Nashimoto, Chikako, Miyake, Noriko, Daikuhara, Yasushi, Ochi, Kozo, Nashimoto, Masayuki
Veröffentlicht 2003

TMEM67 mutations found in a case of Joubert syndrome with renal hypodysplasia

von Komatsu, Yumiko, Suzuki, Toshifumi, Tsurusaki, Yoshinori, Miyake, Noriko, Matsumoto, Naomichi, Yan, Kunimasa
Veröffentlicht in CEN Case Rep (2016)

Recent Advances in the Pathophysiology of Musculocontractural Ehlers-Danlos Syndrome

von Kosho, Tomoki, Mizumoto, Shuji, Watanabe, Takafumi, Yoshizawa, Takahiro, Miyake, Noriko, Yamada, Shuhei
Veröffentlicht in Genes (Basel) (2019)

Childhood Nephrotic Syndrome Complicated by Catastrophic Multiple Arterial Thrombosis Requiring Bilateral Above-Knee Amputation

von Togashi, Hayato, Shimosato, Yuko, Saida, Ken, Miyake, Noriko, Nakamura, Takeshi, Ito, Shuichi
Veröffentlicht in Front Pediatr (2020)

Two novel CHN1 mutations in two families with Duane’s retraction syndrome

von Chan, Wai-Man, Miyake, Noriko, Zhu-Tam, Lily, Andrews, Caroline, Engle, Elizabeth C.
Veröffentlicht 2011

CHN1 Mutations are not a Common Cause of Sporadic Duane’s Retraction Syndrome

von Miyake, Noriko, Andrews, Caroline, Fan, Wen, He, Wei, Chan, Wai-Man, Engle, Elizabeth C.
Veröffentlicht 2010

Helicobacter cinaedi Bacteremia Mimicking a Flare of Systemic Lupus Erythematosus

von Nishida, Ruriko, Shimono, Nobuyuki, Miyake, Noriko, Chong, Yong, Shimoda, Shinji, Tsukamoto, Hiroshi, Akashi, Koichi
Veröffentlicht in Intern Med (2017)

Incomplete recovery of the fecal flora of hematological patients with neutropenia and repeated fluoroquinolone prophylaxis

von Chong, Yong, Shimoda, Shinji, Miyake, Noriko, Aoki, Takatoshi, Ito, Yoshikiyo, Kamimura, Tomohiko, Shimono, Nobuyuki
Veröffentlicht in Infect Drug Resist (2017)

A novel 8-bp duplication in ADAT3 causes mild intellectual disability

von Salehi Chaleshtori, Ahmad Reza, Miyake, Noriko, Ahmadvand, Mohammad, Bashti, Oranous, Matsumoto, Naomichi, Noruzinia, Mehrdad
Veröffentlicht in Hum Genome Var (2018)

Performance Comparison of Bench-Top Next Generation Sequencers Using Microdroplet PCR-Based Enrichment for Targeted Sequencing in Patients with Autism Spectrum Disorder

von Koshimizu, Eriko, Miyatake, Satoko, Okamoto, Nobuhiko, Nakashima, Mitsuko, Tsurusaki, Yoshinori, Miyake, Noriko, Saitsu, Hirotomo, Matsumoto, Naomichi
Veröffentlicht 2013

Adeno-associated virus type 8 vector–mediated expression of siRNA targeting vascular endothelial growth factor efficiently inhibits neovascularization in a murine choroidal neovasc...

von Igarashi, Tsutomu, Miyake, Noriko, Fujimoto, Chiaki, Yaguchi, Chiemi, Iijima, Osamu, Shimada, Takashi, Takahashi, Hiroshi, Miyake, Koichi
Veröffentlicht 2014

‘Cortical cerebellar atrophy' dwindles away in the era of next-generation sequencing

von Yoshida, Kunihiro, Miyatake, Satoko, Kinoshita, Tomomi, Doi, Hiroshi, Tsurusaki, Yoshinori, Miyake, Noriko, Saitsu, Hirotomo, Matsumoto, Naomichi
Veröffentlicht in J Hum Genet (2014)

MicroRNA cluster miR-17-92 regulates multiple functionally related voltage-gated potassium channels in chronic neuropathic pain

von Sakai, Atsushi, Saitow, Fumihito, Maruyama, Motoyo, Miyake, Noriko, Miyake, Koichi, Shimada, Takashi, Okada, Takashi, Suzuki, Hidenori
Veröffentlicht in Nat Commun (2017)

Nephron development and extrarenal features in a child with congenital nephrotic syndrome caused by null LAMB2 mutations

von Kino, Jiro, Tsukaguchi, Hiroyasu, Kimata, Takahisa, Nguyen, Huan Thanh, Nakano, Yorika, Miyake, Noriko, Matsumoto, Naomichi, Kaneko, Kazunari
Veröffentlicht in BMC Nephrol (2017)

Erratum to: Nephron development and extrarenal features in a child with congenital nephrotic syndrome caused by null LAMB2 mutations

von Kin, Jiro, Tsukaguchi, Hiroyasu, Kimata, Takahisa, Nguyen, Huan Thanh, Nakano, Yorika, Miyake, Noriko, Matsumoto, Naomichi, Kaneko, Kazunari
Veröffentlicht in BMC Nephrol (2017)

A novel DARS2 mutation in a Japanese patient with leukoencephalopathy with brainstem and spinal cord involvement but no lactate elevation

von Shimojima, Keiko, Higashiguchi, Takafumi, Kishimoto, Kanako, Miyatake, Satoko, Miyake, Noriko, Takanashi, Jun-ichi, Matsumoto, Naomichi, Yamamoto, Toshiyuki
Veröffentlicht in Hum Genome Var (2017)

Independent occurrence of de novo HSPD1 and HIP1 variants in brothers with different neurological disorders – leukodystrophy and autism

von Yamamoto, Toshiyuki, Yamamoto-Shimojima, Keiko, Ueda, Yuki, Imai, Katsumi, Takahashi, Yukitoshi, Imagawa, Eri, Miyake, Noriko, Matsumoto, Naomichi
Veröffentlicht in Hum Genome Var (2018)

Short-lasting unilateral neuralgiform headache attacks with ispilateral facial flushing is a new variant of paroxysmal extreme pain disorder

von Imai, Noboru, Miyake, Noriko, Saito, Yoshiaki, Kobayashi, Emiko, Ikawa, Masako, Manaka, Shinya, Shiina, Masaaki, Ogata, Kazuhiro, Matsumoto, Naomichi
Veröffentlicht in J Headache Pain (2015)

Risk Factors Associated with Stenotrophomonas maltophilia Bacteremia: A Matched Case-Control Study

von Sumida, Kosuke, Chong, Yong, Miyake, Noriko, Akahoshi, Tomohiko, Yasuda, Mitsuhiro, Shimono, Nobuyuki, Shimoda, Shinji, Maehara, Yoshihiko, Akashi, Koichi
Veröffentlicht in PLoS One (2015)