チャイルドシート着用が新生児の呼吸循環機能に与える影響 : ベット状シートと椅子状シートの比較
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概要
- 論文の詳細を見る
- 2002-02-01
著者
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永瀬 裕朗
Department Of Pediatrics Kobe University School Medicine
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YONETANI MASAHIKO
Department of Pediatrics, Kobe University School Medicine
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UETANI YOSHIYUKI
Department of Pediatrics, Kobe University School Medicine
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Nakamura Hajime
Hyogo Prefectural Kobe Children's Hospital
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Nakamura H
Hyogo Prefectural Kobe Children's Hospital
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Uetani Yoshiyuki
神戸大学医学系研究科
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Uetani Yoshiyuki
Department Of Pediatrics Kobe University School Of Medicine
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Yonetani M
Kobe Univ. Graduate School Of Medicine Kobe Jpn
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Nakamura Hajime
Department Of Development And Aging Faculty Of Medicine Kobe University Graduate School Of Medicine
関連論文
- Complete skipping of exon 66 due to novel mutations of the dystrophin gene was identified in two Japanese families of Duchenne muscular dystrophy with severe mental retardation
- チャイルドシート着用が新生児の呼吸循環機能に与える影響 : ベット状シートと椅子状シートの比較
- Evaluation of mutation effects on UGT1A1 activity toward 17β-estradiol using liquid chromatography-tandem mass spectrometry
- Prenatal diagnosis of a Japanese family at risk for tay-sachs disease : application of a fluorescent competitive allele-specific polymerase chain reaction (pcr) method
- タイ国のGilbert症候群患者姉妹のUGT1A1遺伝子に認められた新しいミスセンス異変
- A prospective clinical study on inhaled nitric oxide therapy for neonates in Japan
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- Eyelid myoclonia with absences in monozygotic twins
- Clinical features of infants with subependymal germinolysis and choroid plexus cysts
- Evaluation of change of cerebral circulation by SpO_2 in preterm infants with apneic episodes using near infrared spectroscopy
- A novel cryptic exon in intron 3 of the dystrophin gene was incorporated into dystrophin mRNA with a single nucleotide deletion in exon 5
- Gly71Arg mutation of the bilirubin UDP-glucuronosyltransferase 1A1 gene is associated with neonatal hyperbilirubinemia in the Japanese population
- Molecular genetics of spinal muscular atrophy : contribution of the NAIP gene to clinical severity
- Oligonucleotides against a splicing enhancer sequence led to dystrophin production in muscle cells from a Duchenne muscular dystrophy patient
- Purine-rich exon sequences are not necessarily splicing enhancer sequence in the dystrophin gene
- End-tidal carbon monoxide is predictive for neonatal non-hemolytic hyperbilirubinemia
- Non-homologous recombination between Alu and LINE-1 repeats caused a 430-kb deletion in the dystrophin gene : a novel source of genomic instability
- A simple explanation for a case of incompatibility with the reading frame theory in Duchenne muscular dystrophy: failure to detect an aberrant restriction fragment in Southern blot analysis
- Vascular involvement in benign infantile mitochondrial myopathy caused by reversible cytochrobe c oxidase dificiency
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- Classification of Congenital Hypothyroidism Based on Scintigraphy, Ultrasonography and the Serum Thyroglobulin Level
- Preventive effects of dexamethasone on hypoxic-ischemic brain damage in the neonatal rat
- Neonatal Renal Artery Blood Flow Velocities Using Color Doppler Ultrasonography
- Factors Affecting Prognosis of Intrauterine Hydrocephalus Diagnosed in the Third Trimester : Computerized Data Analysis on Controversies in Fetal Surgery
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