Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Hidehito Kondo"'
Autor:
Hiroshi Sakuma, Jun-ichi Takanashi, Kazuhiro Muramatsu, Hidehito Kondo, Takashi Shiihara, Motomasa Suzuki, Kazuo Okanari, Mariko Kasai, Osamu Mitani, Tomoyuki Nakazawa, Taku Omata, Konomi Shimoda, Yuichi Abe, Yoshihiro Maegaki, Kei Murayama, Yuka Murofushi, Hiroaki Nagase, Akihisa Okumura, Yasunari Sakai, Hiroko Tada, Masashi Mizuguchi, Japanese Pediatric Neuro-COVID-19 Study Group, Tsuyoshi Matsuoka, Hiroshi Oakada, Tatsuharu Sato, Kenjiro Kikuchi, Satoshi Akamine, Nanako Kawata, Shinichiro Morichi, Hideyuki Iwayama, Ryuta Tanaka, Yoshiyuki Hanaoka, Yuki Minamisawa, Tatsuya Ema, Mitsuo Motobayashi, Tomoshiro Ito, Fumikazu Sano
Publikováno v:
Frontiers in Neuroscience, Vol 17 (2023)
Background and objectivesTo clarify whether severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection cause acute encephalopathy in children and which are the most common syndromes that cause them and what are the outcomes.MethodsA natio
Externí odkaz:
https://doaj.org/article/d27b86d3fea846ce99dd9d7559309e79
Autor:
Yoshinori Satomura, Kazuhiko Bessho, Nobutoshi Nawa, Hidehito Kondo, Shogo Ito, Takao Togawa, Masanao Yano, Yuki Yamano, Taisuke Inoue, Miho Fukui, Shinsuke Onuma, Tomoya Fukuoka, Kie Yasuda, Takeshi Kimura, Makiko Tachibana, Taichi Kitaoka, Shin Nabatame, Keiichi Ozono
Publikováno v:
Journal of Medical Case Reports, Vol 16, Iss 1, Pp 1-6 (2022)
Abstract Background Arthrogryposis, renal dysfunction, and cholestasis syndrome (ARCS) is a rare autosomal recessive disorder caused by mutations in VPS33B (ARCS1) and VIPAS39 (ARCS2). As per literature, most patients with ARCS died of persistent inf
Externí odkaz:
https://doaj.org/article/ac1143801be74e5f85e9d7f8ee61ab4c
Autor:
Hiroaki Hanafusa, Hiroshi Yamaguchi, Hidehito Kondo, Miwako Nagasaka, Ming Juan Ye, Shizuka Oikawa, Shoichi Tokumoto, Kazumi Tomioka, Masahiro Nishiyama, Naoya Morisada, Masafumi Matsuo, Kandai Nozu, Hiroaki Nagase
Publikováno v:
Brain and Development. 45:317-323
Publikováno v:
Forensic Science, Medicine and Pathology. 18:474-477
Alpha-ketoadipic acid is one of the metabolic intermediates of lysine and tryptophan, and it is known as the biochemical hallmark of alpha-ketoadipic aciduria (α-KA). α-KA is a rare autosomal recessive disorder. Its pathophysiology is reduced alpha
Autor:
Satoshi Ekuni, Kei Hirayama, Miwako Nagasaka, Keita Osumi, Hidehito Kondo, Erina Nakahara, Keiko Shimojima Yamamoto, Hitoshi Kanno, Yoshinori Katayama
Publikováno v:
American Journal of Case Reports. 24
Autor:
Sachiko Nakaoka, Yusuke Hamada, Takanobu Otomo, Hidehito Kondo, Keiichi Ozono, Keiko Matsuoka, Norio Sakai, Toko Shibuya, Kenichi Sakamoto
Publikováno v:
Brain and Development. 43:867-872
In mucopolysaccharidoses (MPS), spinal cord compression (SCC) resulting from glycosaminoglycan (GAG) accumulation is a critical complication that can cause significant neurological and respiratory morbidities. However, clinically similar disorders su
Publikováno v:
Pediatrics international : official journal of the Japan Pediatric SocietyREFERENCES. 64(1)
Autor:
Hidehito Kondo, Daisuke Uda, Koichi Tanda, Zenro Kizaki, Masashi Nishida, Hongmei Dai, Masayuki Itoh
Publikováno v:
Neuropediatrics.
Joubert syndrome (JS) is a genetic neurodevelopmental disorder characterized by lower brainstem dysplasia and cerebellar vermis agenesis termed molar tooth sign (MTS), psychomotor retardation, abnormal respiratory pattern in infancy, and oculomotor a
Autor:
Zenro Kizaki, Yasushi Okazaki, Hidehito Kondo, Tomohiro Chiyonobu, Takenori Tozawa, Akira Ohtake, Yoshihito Kishita, Rei Takada, Kei Murayama
Publikováno v:
Brain and Development. 42:69-72
Background The mitochondrial DNA MT-ATP6 gene encodes the ATP6 subunit of the mitochondrial ATP synthase. The m.9185 T > C variant in MT-ATP6 has been reported to cause various neurological disorders including late-onset Leigh syndrome (LS). To our k
Publikováno v:
International heart journal. 61(5)
A Japanese girl with polycystic kidney disease (PKD) developed normally, but at 8 months of age, she was hospitalized for acute onset dyspnea. On the day after admission to hospital, her general condition suddenly became worse. An echocardiogram show