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1
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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2
المؤلفون: Shuji Kondo, Tomoko Takahashi, Aya Goji, Natsuko Kishi, Kenichi Suga, Zenichi Sakaguchi, Takanori Sekiguchi, Katsuaki Ohara, Shoji Kagami, Maki Urushihara, Sato Matsuura, Hiroko Kozan, Maki Shimizu, Yukiko Kinoshita
المصدر: Clinical and experimental nephrology. 15(4)
مصطلحات موضوعية: Nephrology, medicine.medical_specialty, Physiology, Prednisolone, urologic and male genital diseases, Methylprednisolone, Proinflammatory cytokine, Antibodies, Antineutrophil Cytoplasmic, Glomerulonephritis, Physiology (medical), Internal medicine, medicine, Rapidly progressive glomerulonephritis, Humans, Child, Cyclophosphamide, Autoantibodies, Kidney, Proteinuria, business.industry, Autoantibody, Plasmapheresis, medicine.disease, medicine.anatomical_structure, Pulse Therapy, Drug, Pauci-immune, Immunology, Drug Therapy, Combination, Female, medicine.symptom, business, medicine.drug
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3
المؤلفون: Nobuyasu Bandou, Hiroshi Akita, Atsuko Asano, Okamoto T, Hiide Yoshino, Katsuaki Ohara, Hiroko Kozan, Masao Ise, Sekiguchi T
المصدر: Pediatrics international : official journal of the Japan Pediatric Society. 41(6)
مصطلحات موضوعية: Male, Pathology, medicine.medical_specialty, Thin layer, Bulbar Palsy, Progressive, Enzyme-Linked Immunosorbent Assay, Blood Sedimentation, Gangliosides, medicine, Humans, Miller-Fisher syndrome, Child, Bulbar palsy, Autoantibodies, Miller Fisher Syndrome, biology, business.industry, Bulbar paralysis, Electrophysiology, Pediatrics, Perinatology and Child Health, Immunology, biology.protein, Chromatography, Thin Layer, Antibody, medicine.symptom, business
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4
المؤلفون: Katsuaki Ohara, Tsuyako Iwai, Takeshi Suzue, Okamoto T, Hiroko Kozan, Takanori Sekiguchi, Koji Yasutomo, Atsuko Nishioka, Shoichi Endo
المصدر: Acta paediatrica Japonica : Overseas edition. 35(4)
مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, Trisomy, Marfan Syndrome, Arachnodactyly, Gene duplication, Medicine, Humans, Abnormalities, Multiple, Hypertelorism, Ear, External, Low-set ears, Genetics, business.industry, Infant, Newborn, Chromosome, Brain, Karyotype, Laryngostenosis, Anatomy, medicine.disease, Magnetic Resonance Imaging, Hypotonia, Chromosome Banding, Phenotype, Karyotyping, Pediatrics, Perinatology and Child Health, dup, Chromosomes, Human, Pair 5, Muscle Hypotonia, Female, medicine.symptom, business
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5دورية 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
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6
المؤلفون: Katsuaki Ohara, Junji Suzue, Yoshiko Kobayashi, Shoichi Endo, Nobour Kawano, Kuniaki Fukuda, Kyoichi Hiura, Tamio Kokawa, Toshiaki Hashimoto, Masuhide Miyao
المصدر: Pediatrics International. 20:1-7
مصطلحات موضوعية: medicine.medical_specialty, Physical medicine and rehabilitation, business.industry, Pediatrics, Perinatology and Child Health, Medicine, business, Psychiatry, Non-rapid eye movement sleep, Sleep in non-human animals, Rapid Eye Movements
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7
المؤلفون: Hiroe Minato, Yashuhiro Kuroda, Katsuaki Ohara, Kenji Toshima, Toshiaki Hashimoto, Masuhide Miyao
المصدر: Archives of Neurology. 35:689
مصطلحات موضوعية: Male, Arylsulfatase A, Infant, Physiology, Leukodystrophy, Metachromatic, Twins, Monozygotic, Urine, Biology, medicine.disease, complex mixtures, digestive system diseases, Metachromatic leukodystrophy, surgical procedures, operative, Arts and Humanities (miscellaneous), Pregnancy, Immunology, Diseases in Twins, medicine, Humans, Female, Neurology (clinical), Sulfatases, Cerebroside-Sulfatase
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00783a9dc2c14057459976033f46cb3b
https://doi.org/10.1001/archneur.1978.00500340065013