「Congenital Dysfibrinogenemia Presented with Massive Hematomas Formed after Hysterectomy」の関連論文
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Screening method for congenital dysfibrinogenemia using clot waveform analysis with the Clauss method
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Automated screening procedure for the phenotypes of congenital fibrinogen disorders using novel parameters, |min1|c and Ac/|min1|c, obtained from clot waveform analysis using the Clauss method
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Acquired dysfibrinogenemia: monoclonal λ-type IgA binding to fibrinogen caused lower functional plasma fibrinogen level and abnormal clot formation
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Hereditary Congenital Methemoglobinemia Diagnosed at the Age of 79 Years: A Case Report
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Combined Hypophysitis and Type 1 Diabetes Mellitus Related to Immune Checkpoint Inhibitors
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Case report: Late middle-aged features of FAM111A variant, Kenny–Caffey syndrome type 2-suggestive symptoms during a long follow-up
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Clinical Significance of Serum Galectin-9 and Soluble CD155 Levels in Patients with Systemic Sclerosis
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Clinical and genetic features of cystic fibrosis in Japan
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Usefulness of interleukin-18 as a diagnostic biomarker to differentiate adult-onset Still’s disease with/without macrophage activation syndrome from other secondary hemophagocytic lymphohistiocytosis in adults
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Lack of association between seropositivity of vasculopathy-related viruses and moyamoya disease
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Clinical and genetic investigation of 136 Japanese patients with congenital hypothyroidism
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Prenatal diagnosis of severe mitochondrial disease caused by nuclear gene defects: a study in Japan
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Steroid profiling for assessing adrenal hepatic syndrome in canine hepatocellular carcinoma
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Paraproteinemia and neuropathy
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A case of eosinophilic polyangiitis with granulomatosis that evolved to cardiac arrest due to advanced atrioventricular block
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Beneficial screening of Fabry disease in patients with hypohidrosis
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Analysis of immunologic comorbidities in ulcerative colitis patients: a tool to prevent exacerbations in ulcerative colitis cases
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Risk factors for cisplatin-induced acute kidney injury: A pilot study on the usefulness of genetic variants for predicting nephrotoxicity in clinical practice
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Genetic screening for malignant hyperthermia and comparison of clinical symptoms in Japan
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Genetic screening for malignant hyperthermia and comparison of clinical symptoms in Japan
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Clinical characteristics and outcomes of the right congenital diaphragmatic hernia compared to the left: a 10-year single-center experience
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Rescue of recurrent deep intronic mutation underlying cell type-dependent quantitative NEMO deficiency
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Paraneoplastic Pemphigus Mimicking Toxic Epidermal Necrolysis Associated with Follicular Lymphoma: Possible Pathological Role of CD8 T Cells.
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Gestational psittacosis: A case report and literature review.
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Regulation of Angiopoietin-2 before and after Mechanical Circulatory Support Therapy
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Failure of internal fixation for ankle joint Charcot neuroarthropathy with beta(2)-microglobulin amyloidosis: a case report
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Neonatal Pseudohypoaldosteronism Type-1 in Japan
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Circulatory C-type natriuretic peptide reduces mucopolysaccharidosis-associated craniofacial hypoplasia in vivo
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FKRP mutations cause congenital muscular dystrophy 1C and limb-girdle muscular dystrophy 2I in Asian patients
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A proteome signature of umbilical cord serum associated with congenital diaphragmatic hernia
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A case of Erdheim–Chester disease with the BRAF V600E mutation diagnosed via endoscopic sinus surgery
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Molecular genetic study of the FMR1 CGG repeat configurations in the Japanese population and patients with Fragile X-Associated Tremor/Ataxia Syndrome
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A cerebrospinal fluid microRNA analysis: Progressive supranuclear palsy
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Systematic Review of Clinical Characteristics and Genotype-Phenotype Correlation in LAMB2-Associated Disease
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Genome-wide association study of IgA nephropathy using 23 465 microsatellite markers in a Japanese population
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A clinical and genetic study of SPG31 in Japan
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Case report : Vascular graft infection due to Aspergillus species presenting with recurrent vascular occlusion
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Illustrative review of cardiac amyloidosis by multimodality imaging
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The prevalence and characteristics of hypouricemia: a descriptive study of medical check-up and administrative claims data
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Studies on the molecular pathogenesis and the novel disease-associated genes in dogs with inflammatory colorectal polyps [an abstract of entire text]
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The association between chronic deciduitis and preeclampsia.
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An autopsy case of primary gliosarcoma with multiple extracranial metastases: pathology after administration of bevacizumab and genetic profile
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2型糖尿病の病態把握における平均血小板容積MPVの有用性に関する検討
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A case of Cockayne syndrome with unusually mild clinical manifestations
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4q25 Microdeletion with Axenfeld-Rieger Syndrome and Developmental Delay
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Paraneoplastic isolated adrenocorticotropic hormone deficiency revealed after immune checkpoint inhibitors therapy: new insights into anti-corticotroph antibody
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Development of highly efficient methods for comprehensive pathogen detection using next generation sequencing
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Decreased serum phosphate levels are a useful biomarker to predict occurrence and severity of cytokine release syndrome in chimeric antigen receptor T-cell therapy
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Simple, Frequent Indicator for Personal Identification-Postmortem and Antemortem Abdominal Computed Tomography Findings of a Charred Body.
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Kynurenic acid is a potential overlapped biomarker between diagnosis and treatment response for depression from metabolome analysis