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1
المؤلفون: Hiroshi Masuda, Tohru Kobayashi, Akira Hachiya, Yasutaka Nakashima, Hiroyuki Shimizu, Tomo Nozawa, Yoshihito Ogihara, Shuichi Ito, Shinichi Takatsuki, Nobuyuki Katsumata, Yasuo Suzuki, Satoshi Takenaka, Keiichi Hirono, Tomio Kobayashi, Hiroshi Suzuki, Eisuke Suganuma, Kei Takahashi, Tsutomu Saji, Satoshi Matsuzaki, Shoko Yamazaki, Kazuyuki Ikeda, Takuma Hara, Taichi Kanetaka, Toshitaka Kizawa, Masako Kikuchi, Ryoki Hara, Kentaro Fujii, Mayu Takahashi, Kaori Sonoda, Tomokuni Yoshihashi, Tomoyuki Imagawa, Kazuko Yamazaki, Takasuke Ebato, Shinji Oana, Ayako Murase, Shinichiro Sakaki, Takeshi Fujimoto, Yoshihiko Saito, Ryota Shirai, Ichiro Takeuchi, Kazuyuki Naoi, Yasushi Kenmotsu, Chiaki Goto, Hiroaki Kise, Seigo Okada, Sayuri Kishimoto, Utako Oba, Sayaka Ozawa, Mitsuru Seki, Tesshu Odagiri, Junko Shiono, Kiyoshi Nagumo, Mitsuaki Kimura, Muneo Yoshibayashi, Norihisa Horita, Tatsuo Tsuboi, Tomoyo Matsubara, Satoshi Hara, Taku Ishii, Susumu Hosokawa, Takayuki Kishi, Ryuji Fukazawa, Shunichi Ogawa, Miho Ohshima, Hideo Fukunaga, Hiroko Kouzan, Tomoko Ichihara, Kunio Hashimoto, Hirohide Tokunaga, Satoru Iwashima, Kiyoshi Hamahira, Yukiko Ishiguchi, Mayumi Kajino, Kanta Kishi, Noriko Nagai, Shigeru Ito, Hirotaro Ogino, Eriko Amaya, Hiraku Doi, Kenji Waki, Taisuke Shiraishi, Takashi Iwai, Tetsuji Sato, Katsumi Akimoto, Takashi Soga, Hiroyuki Naito, Makiko Aihara, Yutaka Fukuda, Kazuo Imagawa, Takeshi Shiba, Shigenobu Matsuki, Masaru Miura, Tooru Araki, Hideto Furuyama, Takeshi Naito, Tomoyuki Miyamoto
المصدر: The Journal of Pediatrics. 195:115-120.e3
مصطلحات موضوعية: Male, medicine.medical_specialty, Time Factors, Mucocutaneous Lymph Node Syndrome, 030204 cardiovascular system & hematology, Nationwide survey, Disease course, 03 medical and health sciences, 0302 clinical medicine, Japan, Refractory, Surveys and Questionnaires, Internal medicine, White blood cell, medicine, Humans, Blood test, 030212 general & internal medicine, Child, Adverse effect, Retrospective Studies, medicine.diagnostic_test, business.industry, Infant, medicine.disease, Infliximab, medicine.anatomical_structure, Antirheumatic Agents, Child, Preschool, Pediatrics, Perinatology and Child Health, Female, Kawasaki disease, business, medicine.drug
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2
المؤلفون: Gen Nishimura, Masahito Irie, Hiroshi Kishimoto, Kouji Masumoto, Fumitoshi Ishino, Fumiko Kato, Takeshi Utsunomiya, Masahiro Nakayama, Anne C. Ferguson-Smith, Tsutomu Ogata, Mika Noguchi, Masayo Kagami, Hiroko Kouzan, Yukichi Tanaka, Michiyo Okada, Hirofumi Ohashi, Yumiko Komatsu, Kentarou Matsuoka, Shunji Yamamori, Yoichi Sekita, Kenji Kurosawa, Kenjirou Kosaki, Tsutomu Takahashi, Yoko Tanaka
المصدر: Nature Genetics. 40:237-242
مصطلحات موضوعية: Male, Heterozygote, congenital, hereditary, and neonatal diseases and abnormalities, Molecular Sequence Data, Mothers, Regulatory Sequences, Nucleic Acid, Biology, Polymorphism, Single Nucleotide, Fathers, Genomic Imprinting, Genetics, Humans, Computer Simulation, Epigenetics, In Situ Hybridization, Fluorescence, Chromosomes, Human, Pair 14, Calcium-Binding Proteins, Membrane Proteins, Proteins, Chromosome Breakage, DNA Methylation, Uniparental Disomy, Physical Chromosome Mapping, Phenotype, Pedigree, Case-Control Studies, Mutation, Mutation (genetic algorithm), Intercellular Signaling Peptides and Proteins, DNA, Intergenic, Female, RNA, Long Noncoding, Gene Deletion
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3
المؤلفون: Toju Tanaka, Toshiyuki Fukao, Naomi Sakaguchi, Hiroko Kouzan, Tomoko Ichihara, Mika Ishige, Katsuaki Ohara, Yasutomi Kinosada, Yuka Aoyama, Toshiyuki Yamamoto
المصدر: International Journal of Molecular Medicine
مصطلحات موضوعية: Male, uniparental disomy, Biology, medicine.disease_cause, Exon, Alu Elements, Genetics, medicine, Humans, Multiplex ligation-dependent probe amplification, multiplex ligation-dependent probe amplification, Sequence Deletion, Mutation, mitochondrial 3-hydroxy-3-methylglutaryl CoA lyase, Base Sequence, Microarray analysis techniques, Chromosome, Infant, Oxo-Acid-Lyases, General Medicine, Exons, Articles, medicine.disease, Molecular biology, Uniparental disomy, 3-hydroxy-3-methylglutaryl-CoA lyase, Alu element, Uniparental Isodisomy, Chromosomes, Human, Pair 1, Female, Multiplex Polymerase Chain Reaction, microarray, Metabolism, Inborn Errors
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4دورية أكاديمية
المؤلفون: YUKA AOYAMA, TOSHIYUKI YAMAMOTO, NAOMI SAKAGUCHI, MIKA ISHIGE, TOJU TANAKA, TOMOKO ICHIHARA, KATSUAKI OHARA, HIROKO KOUZAN, YASUTOMI KINOSADA, TOSHIYUKI FUKAO
المصدر: International Journal of Molecular Medicine; 2015, Vol. 35 Issue 6, p1554-1560, 7p