Epidemiological and clinical studies of West syndrome in Nagasaki
スポンサーリンク
概要
- 論文の詳細を見る
- 2001-10-01
著者
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Matsumoto Tadashi
Department Of Pediatrics Nagasaki University School Of Medicine
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MORIUCHI Hiroyuki
Department of Pediatrics, Nagasaki University School of Medicine
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TSURU Akira
Department of Pediatrics, Nagasaki University School of Medicine
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Tsuru Akira
Department Of Pediatrics Nagasaki University School Of Medicine
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Matsuo Atsuko
Department of Neurosurgery, Asahikawa Medical College
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MATSUZAKA Tetsuo
Department of Pediatrics, Nagasaki University School of Medicine
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Matsuzaka Tetsuo
Division Of Pediatrics Nagasaki Prefectural Center Of Medicine And Welfare For Children
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Matsuzaka Tetsuo
Department Of Pediatrics Nagasaki University School Of Medicine
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Moriuchi Hiroyuki
Department Of Pediatrics Nagasaki University School Of Medicine
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Moriuchi Hiroyuki
Department Of Pediatrics Nagasaki University Graduate School Of Biomedical Sciences
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Matsumoto Tadashi
Genetic Counseling Unit Nagasaki University Hospital
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Nakashita Yoshio
Division Of Pediatrics Sasebo City General Hospital
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TANAKA Shigeki
Division of Pediatrics, National Nagasaki-Chuo Hospital
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BABA Chikako
Division of Pediatrics, Japanese Red Cross Nagasaki Atomic Bomb Hospital
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TOMIMASU Kunio
Division of Pediatrics, Nagasaki Municipal Hospital
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Matsuo Atsuko
Department Of Neurosurgery Asahikawa Medical College
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Matsuo Atsuko
Department Of Pediatrics Nagasaki University School Of Medicine
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Baba Chikako
Division Of Pediatrics Japanese Red Cross Nagasaki Atomic Bomb Hospital
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Tagawa Masato
Department Of Pediatrics Nagasaki University Hospital
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Tomimasu Kunio
Division Of Pediatrics Nagasaki Municipal Hospital
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Tanaka Shigeki
Division Of Pediatrics National Nagasaki-chuo Hospital
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Moriuchi Hiroyuki
Department Of Molecular Microbiology And Immunology Nagasaki University Graduate School Of Biomedica
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Tsujihata Mitsuhiro
Nagasaki Laboratory Mitsubishi Chemical Medience Corporation
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Matsumoto Tadashi
Division Of Pediatrics Nagasaki Prefectural Center Of Medicine And Welfare For Children
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Matsumoto Tadashi
長崎大学 看
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Matsumoto Hiroshi
Department Of Pediatrics National Defense Medical College
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Matsumoto Tadashi
School Of Allied Medical Sciences Nagasaki University
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Matsuzaka Tetsuo
Department Of Pediatrics Graduate School Of Biomedical Sciences Nagasaki University
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Moriuchi Hiroyuki
Department Of Pediatrics Kumamoto University Graduate School Of Medical Science
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Tsuda Masayoshi
Department Of Human Genetics Nagasaki University Graduate School Of Biomedical Sciences
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MORIUCHI Hiroyuki
Department of Pediatrics, Kumamoto University Graduate School of Medical Science
関連論文
- Activation-dependent T cell expression of the X-linked lymphoproliferative disease gene product SLAM-associated protein and its assessment for patient detection
- Probable Noonan syndrome in a boy without PTPN11 mutation, manifesting unusual complications.
- Mirror duplication of chromosome 21 with complete phenotype of Down syndrome.
- A Japanese patient with a mild Lenz-Majewski syndrome
- The Jewish-type Cohen syndrome complicated with refractory bronchial asthma and depression
- Two infantile cases of congenital myotonic dystrophy with cholelithiasis/cholestasis
- Genotype-phenotype correlation of 5p- syndrome : pitfall of diagnosis
- Renal tubular dysgenesis complicated with severe cranium hypoplasia
- Mutation analysis of the ALD gene in seven Japanese families with X-linked adrenoleukodystrophy
- Protein-losing enteropathy complicated with recurrent convulsions and developmental delay in a 4-month-old boy
- Genetic Counseling System in Nagasaki University Hospital and Genetic Services in Nagasaki Prefecture-Now and Future
- Special Report A Genetic Counseling System in Nagasaki Prefecture: The Course and Current Status of the Genetic Counseling Unit in Nagasaki University Hospital
- Differential T-cell response in a young child and neonates with toxic shock syndrome
- The gene for mesomelic dysplasia Kantaputra type is mapped to chromosome 2q24-q32
- Pediatric CT scan usage in Japan : results of a hospital survey
- IV G6 Antieptic effect of unilateral suppression of the subthalamic nucleus for focal neocortical seizures
- III G3 Changes in glucose metabolism during high-frequency stimulation of the subthalamic nucleus(STN)in kainic acid-induced seizures.
- A case of Schinzel-Giedion syndrome complicated with progressive severe gingival hyperplasia and progressive brain atrophy
- A case of megalocornea-mental retardation syndrome complicated with bilateral sensorineural hearing impairment
- Autosomal dominant onychodystrophy and congenital sensorineural deafness
- A severe case of Moebius syndrome with calcification on the fourth ventricular floor
- New radiological finding by magnetic resonance imaging examination of the brain in Coffin-Lowry syndrome
- A NAGER ACROFACIAL DYSOSTOSIS SYNDROME PATIENT WITH SEVERE RESPIRATORY DISTRESS SYNDROME (RDS)
- Neuropsychological and MRI Assessment of Young Adults with Hemiplegic Cerebral Palsy
- Epidemiological and clinical studies of West syndrome in Nagasaki
- Developmental Assessment-Based Surgical Intervention for Intractable Epilepsies in Infants and Young Children
- A case of achondroplasia with severe respiratory failure, profound developmental delay and hypercreatine phosphokinasemia
- Quantitative EEG Analyses and Surgical Outcome After Corpus Callosotomy
- Acute pancreatitis associated with systemic lupus erythematosus: Successful treatment with plasmapheresis followed by aggressive immunosuppressive therapy.
- Novel germline mutation in the RB1 gene with multifocal bone tumors following retinoblastoma
- Miller Fisher syndrome with transient coma : comparison with Bickerstaff brainstem encephalitis
- The calming effect of a maternal breast milk odor on the human newborn infant
- Severe subaortic stenosis that progressed over a 12-year period after cardiac surgery
- Case with Small Testes Associated with Skeletal Dysplasia
- PROP1 Abnormality
- Detection of cytomegalovirus in preserved umbilical cord from a boy with autistic disorder
- 長崎県妊婦におけるサイトメガロウイルス感染の血清疫学的調査
- Miller syndrome with novel dihydroorotate dehydrogenase gene mutations
- Identification of chromosome 15q26 terminal deletion with telomere sequences and its bearing on genotype-phenotype analysis
- Clinical application of array-based comparative genomic hybridization by two-stage screening for 536 patients with mental retardation and multiple congenital anomalies
- Novel mutations in the SIL1 gene in a Japanese pedigree with the Marinesco-Sjogren syndrome
- A type of familial cleft of the soft palate maps to 2p24.2–p24.1 or 2p21–p12
- Japanese map of the earwax gene frequency : a nationwide collaborative study by Super Science High School Consortium
- Molecular karyotyping in 17 patients and mutation screening in 41 patients with Kabuki syndrome
- Multiple Immune Abnormalities in a Patient with Idiopathic CD4+ T-Lymphocytopenia
- Population based cohort study for Pediatric Infectious Diseases research in Vietnam
- An elderly patient with chronic active Epstein-Barr virus infection with mixed cryoglobulinemia and review of the literature