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المؤلفون: Kobayashi, Satoru, Mizuno, Nana, Yokoi, Kyoko, Mori, Takayasu, Sohara, Eisei, Uchida, Shinichi
المصدر: Medicine
مصطلحات موضوعية: Male, Hypernatremia, Polyuria, Osmolar Concentration, Infant, Diabetes Insipidus, Nephrogenic, Syndrome, Magnetic Resonance Imaging, nephrogenic diabetes insipidus, AVPR2, Humans, Clinical Case Report, Child, osmotic demyelination syndrome, Research Article, Demyelinating Diseases
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::c34f7c36ba7275531e82658e8e67c540
http://europepmc.org/articles/PMC8772767 -
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المؤلفون: Noda, Shohei, Mandai, Shintaro, Oda, Takashi, Shinoto, Tomoko, Sato, Hidehiko, Sato, Keiko, Hirokawa, Katsuiku, Noda, Yumi, Uchida, Shinichi
المصدر: Medicine
مصطلحات موضوعية: Male, Nephrotic Syndrome, nephrotic syndrome, Glomerulonephritis, Membranoproliferative, sinusitis, Diagnosis, Differential, Asymptomatic Diseases, Humans, Clinical Case Report, Sinusitis, Tomography, X-Ray Computed, glomerulonephritis, Research Article, asymptomatic infection, Aged
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::bc66021e83400afc8ed151386457a1af
http://europepmc.org/articles/PMC7310930 -
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المؤلفون: Yamazaki, Kimihiro, Ochi, Masayuki, Ogura, Daisuke, Kuroki, Kazuhiko, Eisaki, Hiroshi, Uchida, Shinichi, Aoki, Hideo
مصطلحات موضوعية: Condensed Matter::Superconductivity, Condensed Matter - Superconductivity
URL الوصول: https://explore.openaire.eu/search/publication?articleId=arXiv_______::3d3cf84ecb54189d9f9114787752e451
http://arxiv.org/abs/2003.04015 -
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المؤلفون: Yamazaki, Kimihiro, Ochi, Masayuki, Ogura, Daisuke, Kuroki, Kazuhiko, Eisaki, Hiroshi, Uchida, Shinichi, Aoki, Hideo
مصطلحات موضوعية: Superconductivity (cond-mat.supr-con), Condensed Matter::Superconductivity, FOS: Physical sciences
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::d9068006d5fcec522f8a1a731a811364
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المؤلفون: Masayuki Yamanouchi, Uchida Shinichi, Kenmei Takaichi, Hiroki Mizuno, Noriko Hayami, Takashi Sakoh, Eiko Hasegawa, Tatsuya Suwabe, Yoshifumi Ubara, Naoki Sawa, Takuya Fujimaru, Masahiro Kawada, Takayasu Mori, Rikako Hiramatsu, Akinari Sekine, Junichi Hoshino, Eisei Sohara
المصدر: Molecular Genetics & Genomic Medicine, Vol 7, Iss 6, Pp n/a-n/a (2019)
Molecular Genetics & Genomic Medicineمصطلحات موضوعية: 0301 basic medicine, Adult, medicine.medical_specialty, Trichlormethiazide, Hyperkalemia, lcsh:QH426-470, Pseudohypoaldosteronism, Amino Acid Motifs, Mutation, Missense, Anion gap, 030105 genetics & heredity, Protein Serine-Threonine Kinases, Excretion, 03 medical and health sciences, pseudohypoaldosteronism type II, D564N, WNK4, Internal medicine, Genetics, medicine, Missense mutation, Humans, Diuretics, Molecular Biology, Genetics (clinical), Antihypertensive Agents, Kidney, business.industry, Original Articles, medicine.disease, Urinary calcium, Pedigree, lcsh:Genetics, 030104 developmental biology, Endocrinology, medicine.anatomical_structure, Phenotype, Female, Original Article, medicine.symptom, business, familial case, medicine.drug
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المؤلفون: Uchida, Shinichi, Asai, Yoshiyuki, Kariya, Yoshiaki, Tsumoto, Kunichika, Hibino, Hiroshi, Honma, Masashi, Abe, Takeshi, Nin, Fumiaki, Kurata, Yasutaka, Furutani, Kazuharu, Suzuki, Hiroshi, Kitano, Hiroaki, Inoue, Ryuji, Kurachi, Yoshihisa
المصدر: The journal of physiological sciences : JPS, vol 69, iss 3
مصطلحات موضوعية: Software platform, Physiology, Systems Biology, Research, Medical Physiology, Computational Biology, Computer simulation, Good Health and Well Being, Japan, Physiological experiments, Animals, Humans, Disease, Generic health relevance, Omics study, Software
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::5d81d28c01e09b7ef45028be0c6b3c91
https://escholarship.org/uc/item/2wq5w18z -
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المؤلفون: Kusuda, Takeshi, Hosoya, Tadashi, Mori, Takayasu, Ihara, Katsuhito, Nishida, Hidenori, Chiga, Motoko, Sohara, Eisei, Rai, Tatemitsu, Koike, Ryuji, Uchida, Shinichi, Kohsaka, Hitoshi
المصدر: Internal Medicine
مصطلحات موضوعية: Adult, Diagnosis, Differential, SLC12A3 mutation, Antibodies, Antinuclear, Gitelman syndrome, Humans, Case Report, Sjögren's syndrome, Female, Genetic Predisposition to Disease, Solute Carrier Family 12, Member 3
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::2a1214d61e8e2a6222ce618988eb4100
http://europepmc.org/articles/PMC5140875