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

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概要

• 論文の詳細を見る
• 2010-06-01

著者

• Matsumoto Tadashi

  Department Of Pediatrics Nagasaki University School Of Medicine

• Masuzaki Hideaki

  Department Of Gynecology School Of Medicine Nagasaki University

• Ishimaru Tadayuki

  Genetic Counseling Unit Nagasaki University Hospital

• Ishimaru Tadayuki

  Department Of Obsterics And Gynecology Atomic Bomb Disease Institute Nagasaki University School Of M

• Matsuzaka Tetsuo

  Division Of Pediatrics Nagasaki Prefectural Center Of Medicine And Welfare For Children

• Matsuzaka Tetsuo

  Department Of Pediatrics Nagasaki University School Of Medicine

• Minematsu Toshio

  Institute Of Disease Control Aisenkai Nichinan Hospital

• Moriuchi Hiroyuki

  Department Of Pediatrics Nagasaki University Graduate School Of Biomedical Sciences

• Moriuchi Hiroyuki

  Department Of Pediatrics Nagasaki University Hospital

• Matsumoto Tadashi

  Genetic Counseling Unit Nagasaki University Hospital

• Tagawa Masato

  Department Of Pediatrics Nagasaki University Hospital

• 田川 正人

  Department Of Pediatrics Nagasaki University Hospital

• Minematsu Toshio

  Institute For Disease Control Aiseikai-nichinan Hospital

• Moriuchi Hiroyuki

  Department Of Molecular Microbiology And Immunology Nagasaki University Graduate School Of Biomedica

• Masuzaki Hideaki

  Department Of Obstetrics And Gynecology Nagasaki University Hospital

• Matsumoto Tadashi

  Division Of Pediatrics Nagasaki Prefectural Center Of Medicine And Welfare For Children

• Matsumoto Tadashi

  長崎大学 看

• Matsumoto Hiroshi

  Department Of Pediatrics National Defense Medical College

• Matsumoto Tadashi

  School Of Allied Medical Sciences Nagasaki University

• Moriuchi Hiroyuki

  Department Of Pediatrics Kumamoto University Graduate School Of Medical Science

• Tsuda Masayoshi

  Department Of Human Genetics Nagasaki University Graduate School Of Biomedical Sciences

• 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
• Demographic and Reproductive Factors for High Seroprevalence of Chlamydia Trachomatis among Pregnant Women in Japan
• 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
• Fetal Diagnosis
• Microarray comparative genomic hybridization (CGH)-based prenatal diagnosis for chromosome abnormalities using cell-free fetal DNA in amniotic fluid
• 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
• Laparoscopic Diagnosis of Adenomyosis : a Case Report
• The gene for mesomelic dysplasia Kantaputra type is mapped to chromosome 2q24-q32
• Pediatric CT scan usage in Japan : results of a hospital survey
• Rapid Change in the Uterine Cervix During Transvaginal Ultrasonographic Assessment
• Involvement of Parathyroid Hormone-Related Peptide in Cell Proliferation Activity of Human Uterine Leiomyomas
• Does increased nuchal translucency indicate a fetal abnormality? A retrospective study to clarify the clinical significance of nuchal translucency in Japan
• Congenital diaphragmatic hernia : an evaluation of the prognostic value of the lung-to-head ratio
• Repeat-directed isolation of a novel gene preferentially expressed from the maternal allele in human placenta
• Fetal Arterial Blood Flow Waveforms in Premature Labor and Effect of Ritodrine Infusion
• Expression of the arylhydrocarbon receptor in the peri-implantation period of the mouse uterus and the impact of dioxin on mouse implantation
• 6-26.Targeting Toll-like receptor 4 (TLR4) Suppresses Cytokine Production and Growth of Endometriosis(Session 8 Reproduction 2)
• IS-38 Immunoexpression of Hepatocyte Growth Factor and c-Met Receptor in Eutopic Endometrium Predicts the Activity of Ectopic Endometrium
• 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)
• IS-96 Midpregnancy maternal serum leptin levels and the subsequent development of gestational hypertension
• Mutation Spectrum Induced by Dihydropyrazines in Escherichia coli(Molecular and Cell Biology)
• IA-21 Identification of estrogen receptor b positive intraepithelial lymphocytes and their possible roles in the normal and tubal pregnancy oviducts(THE 46TH ANNUAL MEETING OF THE JAPAN SOCIETY OF HISTOCHEMISTRY AND CYTOCHEMISTRY)
• Increases in Serum Nitrite and Nitrate of a New-Fold Adversely Affect the Outcome of Pregnancy in Rats
• 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
• First case of liposarcoma arising from the fallopian tube: Case report and review of the literature
• A Hhal/BstUl polymorphism in a novel gene at human chromosome 11p15.5
• A New Approach to Methotrexate and Lipiodol Suspensions for Ectopic Pregnancy : Preliminary in vitro and Animal Experiments
• P-IS-55 Identification and characterization of estrogen receptorβ positive intraepithelial lymphocytes in the normal oviduct and oviduct during tubal pregnancy(Reproduction 1,Group 102,International Session)
• 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
• Placental multiple chorionic cysts in maternal scleroderma
• Fetal response to induced maternal emotions.
• 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
• Immunohistochemical Expression of P-Glycoprotein in Cases of Uterine Cervical Cancer
• Miller syndrome with novel dihydroorotate dehydrogenase gene mutations
• Identification of chromosome 15q26 terminal deletion with telomere sequences and its bearing on genotype-phenotype analysis
• Human Papillomavirus Infection and Its Possible Correlation with p63 Expression in Cervical Cancer in Japan, Mongolia, and Myanmar
• Clinical application of array-based comparative genomic hybridization by two-stage screening for 536 patients with mental retardation and multiple congenital anomalies
• Epidemiology of human papillomavirus genotypes in pregnant Japanese women
• Clinical application of fetal sex determination using cell-free fetal DNA in pregnant carriers of X-linked genetic disorders
• 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
• Meta-analysis of genome-wide association scans for genetic susceptibility to endometriosis in Japanese population
• Increases in Serum Nitrite and Nitrate of a Few-Fold Adversely Affect the Outcome of Pregnancy in Rats
• T cell subsets in normal pregnancy and spontaneous abortion
• Multiple Immune Abnormalities in a Patient with Idiopathic CD4+ T-Lymphocytopenia
• Population based cohort study for Pediatric Infectious Diseases research in Vietnam
• Copy number variation of the antimicrobial-gene, defensin beta 4, is associated with susceptibility to cervical cancer
• An elderly patient with chronic active Epstein-Barr virus infection with mixed cryoglobulinemia and review of the literature

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