Jun Kido (J Kido)

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 32

Top Topics

Intellectual Disability

Top Venues

Journal of inherited metabolic disease

Inquiry : a journal of medical care organization, provision and financing

Human genome variation

Pediatrics international : official journal of the Japan Pediatric Society

This page only lists publications with an associated author ORCID identifier.

Publications

Mariko Nagayoshi, Mika Ogata, Nami Hirai, Jun Kido
Disaster Preparedness for Children With Food Allergies During the 2016 Kumamoto Earthquake-Observational Study. Inquiry : a journal of medical care organization, provision and financing 61 (2024)
Jun Kido, Georgios Makris, Saikat Santra, Johannes Häberle
Clinical landscape of citrin deficiency: A global perspective on a multifaceted condition. Journal of inherited metabolic disease (2024)
Mariko Nagayoshi, Mika Ogata, Nami Hirai, Jun Kido
Disaster Preparedness for Children With Food Allergies During the 2016 Kumamoto Earthquake-Observational Study. Inquiry : a journal of medical care organization, provision and financing 61 (2024)
Mariko Nagayoshi, Mika Ogata, Nami Hirai, Jun Kido
Disaster Preparedness for Children With Food Allergies During the 2016 Kumamoto Earthquake-Observational Study. Inquiry : a journal of medical care organization, provision and financing 61 (2024)
Mariko Nagayoshi, Mika Ogata, Nami Hirai, Jun Kido
Disaster Preparedness for Children With Food Allergies During the 2016 Kumamoto Earthquake-Observational Study. Inquiry : a journal of medical care organization, provision and financing 61 (2024)
Yusuke Noda, Jun Kido, Yohei Misumi, Keishin Sugawara, Sachiko Ohori, Atsushi Fujita, Naomichi Matsumoto, Mitsuharu Ueda, Kimitoshi Nakamura
Heterozygous c.175C>T variant in PURA gene causes severe developmental delay. Clinical case reports 11 (9) (2023)
Jun Kido, Johannes Häberle, Toju Tanaka, Masayoshi Nagao, Yoichi Wada, Chikahiko Numakura, Ryosuke Bo, Hiromi Nyuzuki, Sumito Dateki, Shinsuke Maruyama, Kei Murayama, Yoshida Shinichiro, Kimitoshi Nakamura
Improved sensitivity and specificity for citrin deficiency using selected amino acids and acylcarnitines in the newborn screening. Journal of inherited metabolic disease (2023)
Jun Kido, Kimiyasu Egami, Yohei Misumi, Keishin Sugawara, Naomi Tsuchida, Naomichi Matsumoto, Mitsuharu Ueda, Kimitoshi Nakamura
X-linked intellectual disability related to a novel variant of KLHL15. Human genome variation 10 (1) (2023)
Fusa Nagamatsu, Jun Kido, Yoshiko Suginohara, Toshiro Nakamura, Rie Nakamura, Nagisa Komatsu, Daisuke Miyamoto, Yasuyuki Hamada, Takafumi Kashiwagi, Shigeto Sugino, Hideo Kiyohara, Kimitoshi Nakamura, Shirou Matsumoto
Outcomes of Pediatric Obesity-Related Lifestyle Disease Screenings in Kumamoto. Pediatrics international : official journal of the Japan Pediatric Society (2022)
Jun Kido, Johannes Häberle, Keishin Sugawara, Toju Tanaka, Masayoshi Nagao, Takaaki Sawada, Yoichi Wada, Chikahiko Numakura, Kei Murayama, Yoriko Watanabe, Kanako Kojima-Ishii, Hideo Sasai, Kiyotaka Kosugiyama, Kimitoshi Nakamura
Clinical manifestation and long-term outcome of citrin deficiency: Report from a nationwide study in Japan. Journal of inherited metabolic disease 45 (3) (2022)
Nami Hirai, Mika Ogata, Jun Kido, Masashi Nakamura, Nayu Sato, Nobue Takamatsu, Naoshi Shimojo, Yuji Aoki, Kayoko Matsunaga, Tomoyuki Mizukami
Food-Dependent Exercise-Induced Anaphylaxis Caused by Carrots: A Case Report. Pediatric allergy, immunology, and pulmonology (2022)
Jun Kido, Shirou Matsumoto, Johannes Häberle, Yukihiro Inomata, Mureo Kasahara, Seisuke Sakamoto, Reiko Horikawa, Akihiro Tanemura, Hideaki Okajima, Tatsuya Suzuki, Kimitoshi Nakamura
Role of liver transplantation in urea cycle disorders: Report from a nationwide study in Japan. Journal of inherited metabolic disease 44 (6) (2021)
Takaaki Sawada, Jun Kido, Keishin Sugawara, Kimitoshi Nakamura
High-Risk Screening for Fabry Disease: A Nationwide Study in Japan and Literature Review. Diagnostics (Basel, Switzerland) 11 (10) (2021)
Rina Hama, Jun Kido, Keishin Sugawara, Toshiro Nakamura, Kimitoshi Nakamura
Hyperprolinemia type I caused by homozygous p.T466M mutation in PRODH. Human genome variation 8 (1) (2021)
Takaaki Sawada, Jun Kido, Keishin Sugawara, Ken Momosaki, Shinichiro Yoshida, Kanako Kojima-Ishii, Takahito Inoue, Shirou Matsumoto, Fumio Endo, Shouichi Ohga, Shinichi Hirose, Kimitoshi Nakamura
Current status of newborn screening for Pompe disease in Japan. Orphanet journal of rare diseases 16 (1) (2021)
Jun Kido, Shirou Matsumoto, Johannes Häberle, Yoko Nakajima, Yoichi Wada, Narutaka Mochizuki, Kei Murayama, Tomoko Lee, Hiroshi Mochizuki, Yoriko Watanabe, Reiko Horikawa, Mureo Kasahara, Kimitoshi Nakamura
Long-term outcome of urea cycle disorders: Report from a nationwide study in Japan. Journal of inherited metabolic disease 44 (4) (2021)
Jun Kido, Hiroshi Mitsubuchi, Takehisa Watanabe, Keishin Sugawara, Hideo Sasai, Toshiyuki Fukao, Kimitoshi Nakamura
A female patient with GSD IXc developing multiple and recurrent hepatocellular carcinoma: a case report and literature review. Human genome variation 8 (1) (2021)
Jun Kido, Shirou Matsumoto, Keishin Sugawara, Takaaki Sawada, Kimitoshi Nakamura
Variants associated with urea cycle disorders in Japanese patients: Nationwide study and literature review. American journal of medical genetics. Part A 185 (7) (2021)
Mika Ogata, Jun Kido, Kimitoshi Nakamura
Oral Immunotherapy for Children with Cow's Milk Allergy. Pathogens (Basel, Switzerland) 10 (10) (2021)
Shinichiro Yoshida, Jun Kido, Takaaki Sawada, Ken Momosaki, Keishin Sugawara, Shirou Matsumoto, Fumio Endo, Kimitoshi Nakamura
Fabry disease screening in high-risk populations in Japan: a nationwide study. Orphanet journal of rare diseases 15 (1) (2020)
Jun Kido, Shirou Matsumoto, Kimitoshi Nakamura
Carglumic Acid Contributes to a Favorable Clinical Course in a Case of Severe Propionic Acidemia. Case reports in pediatrics 2020 (2020)
Takaaki Sawada, Jun Kido, Keishin Sugawara, Shirou Matsumoto, Fumio Takada, Kazuya Tsuboi, Akira Ohtake, Fumio Endo, Kimitoshi Nakamura
Detection of novel Fabry disease-associated pathogenic variants in Japanese patients by newborn and high-risk screening. Molecular genetics & genomic medicine 8 (11) (2020)
Ken Momosaki, Jun Kido, Shirou Matsumoto, Shiro Ozasa, Kimitoshi Nakamura
Adrenocorticotropic Hormone Therapy Improved Spasms and Sleep Disturbance in Smith-Magenis Syndrome: A Case Report. Pediatric reports 12 (3) (2020)
Takaaki Sawada, Jun Kido, Kimitoshi Nakamura
Newborn Screening for Pompe Disease. International journal of neonatal screening 6 (2) (2020)
Shirou Matsumoto, Johannes Häberle, Jun Kido, Hiroshi Mitsubuchi, Fumio Endo, Kimitoshi Nakamura
Urea cycle disorders-update. Journal of human genetics 64 (9) (2019)
Ken Momosaki, Jun Kido, Shinichiro Yoshida, Keishin Sugawara, Tatsuki Miyamoto, Takahito Inoue, Toshika Okumiya, Shirou Matsumoto, Fumio Endo, Shinichi Hirose, Kimitoshi Nakamura
Newborn screening for Pompe disease in Japan: report and literature review of mutations in the GAA gene in Japanese and Asian patients. Journal of human genetics 64 (8) (2019)
Jun Kido, Shirou Matsumoto, Takaaki Sawada, Fumio Endo, Kimitoshi Nakamura
Rhabdomyolysis in organic acidemia patients manifesting with metabolic decompensation. Hemodialysis international. International Symposium on Home Hemodialysis 23 (4) (2019)
Jun Kido, Shirou Matsumoto, Hiroshi Mitsubuchi, Fumio Endo, Kimitoshi Nakamura
Early liver transplantation in neonatal-onset and moderate urea cycle disorders may lead to normal neurodevelopment. Metabolic brain disease 33 (5) (2018)
Jun Kido, Takanobu Yoshida, Hiroshi Mitsubuchi, Shirou Matsumoto, Kimitoshi Nakamura
Impact of the 2016 Kumamoto Earthquake on a female patient with ornithine transcarbamoylase deficiency. Pediatrics international : official journal of the Japan Pediatric Society 59 (11) (2018)
Jun Kido, Shirou Matsumoto, Rieko Sakamoto, Hiroshi Mitsubuchi, Yukihiro Inomata, Kimitoshi Nakamura
Recovery of severe acute liver failure without transplantation in patients with Wilson disease. Pediatric transplantation 22 (8) (2018)
K Nonaka, Y Kajiura, M Bando, E Sakamoto, Y Inagaki, J H Lew, Koji Naruishi, T Ikuta, K Yoshida, T Kobayashi, H Yoshie, T Nagata, Jun Kido
Advanced glycation end-products increase IL-6 and ICAM-1 expression via RAGE, MAPK and NF-κB pathways in human gingival fibroblasts. Journal of periodontal research 53 (3) (2017)
Jun Kido, Shirou Matsumoto, Ken Momosaki, Rieko Sakamoto, Hiroshi Mitsubuchi, Fumio Endo, Kimitoshi Nakamura
Liver transplantation may prevent neurodevelopmental deterioration in high-risk patients with urea cycle disorders. Pediatric transplantation 21 (6) (2017)