「Paraproteinemia and neuropathy」の関連論文
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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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Successful treatment of a novel type I interferonopathy due to a de novo PSMB9 gene mutation with a Janus kinase inhibitor
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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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Genome-wide association study of IgA nephropathy using 23 465 microsatellite markers in a Japanese population
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Combined Hypophysitis and Type 1 Diabetes Mellitus Related to Immune Checkpoint Inhibitors
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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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Lack of association between seropositivity of vasculopathy-related viruses and moyamoya disease
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Human induced pluripotent stem cells generated from a patient with idiopathic basal ganglia calcification
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Biclonal Gammopathy as a Misleading Indicator to Diagnose POEMS Syndrome: An Autopsy Case Report and a Review of the Literature
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Studies on the pathological mechanism of alopecia areata in C3H/HeJ mouse model
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Tumour-immune microenvironment in duodenal-type follicular lymphoma
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Fatal Dieulafoy lesion with IgG4-related disease: An autopsy case report
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Myelodysplastic syndrome with trisomy 8 presenting periodic fever and multiple MEFV gene variants outside exon 10: a case report
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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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Congenital Dysfibrinogenemia Presented with Massive Hematomas Formed after Hysterectomy
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Study on the function of fermented rice bran and its indole compounds in animal and cell-based inflammatory models
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Labyrinthine calcification in ears with otitis media and antineutrophil cytoplasmic antibody-associated vasculitis (OMAAV): A report of two cases
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Amyloidosis of the Respiratory System: 16 Patients with Amyloidosis Initially Diagnosed Ante-mortem by Pulmonologists
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Case report: Severe non-pigmenting fixed drug eruption showing general symptoms caused by chondroitin sulfate sodium
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A clinical and genetic study of SPG31 in Japan
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Interactions of amyloid coaggregates with biomolecules and its relevance to neurodegeneration
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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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Aseptic meningitis as an initial presentation of Sjögren syndrome: a report of two cases and literature review
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Morphea in a Crohn's disease patient undergoing ustekinumab treatment
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A case of localized tracheobronchial relapsing polychondritis with positive matrilin-1 staining.
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Suppression of Systemic Lupus Erythematosus in NZBWF1 mice infected with Hymenolepis microstoma
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Beneficial screening of Fabry disease in patients with hypohidrosis
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Identification of anti-citrullinated osteopontin antibodies and increased inflammatory response by enhancement of osteopontin binding to fibroblast-like synoviocytes in rheumatoid arthritis
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Efficacy of Recombinant Human – Soluble Thrombomodulin for Severe Acute Pancreatitis in a Rat Experimental Model
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Clinical efficacy of the combined treatment of anti-PD-L1 rat-bovine chimeric antibody with a COX-2 inhibitor in calves infected with Mycoplasma bovis
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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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Characteristics of cortical spreading depression and c-Fos expression in transgenic mice having a mutation associated with familial hemiplegic migraine 2 (本文)
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Rescue of recurrent deep intronic mutation underlying cell type-dependent quantitative NEMO deficiency
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Development of highly efficient methods for comprehensive pathogen detection using next generation sequencing
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Inactivation of the PD-1-dependent immunoregulation in mice exacerbates contact hypersensitivity resembling immune-related adverse events
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GOS2 regulates innate immunity of Kawasaki disease via IncRNA RP1-280 10.1
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UBAP1 mutations cause juvenile-onset hereditary spastic paraplegias (SPG80) and impair UBAP1 targeting to endosomes
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Optimized sonoreactor for accelerative amyloid-fibril assays through enhancement of primary nucleation and fragmentation
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Circulatory C-type natriuretic peptide reduces mucopolysaccharidosis-associated craniofacial hypoplasia in vivo
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Studies on Cytotoxic Effects of Tumor Necrosis Factor-Related Apoptosis Inducing Ligand (TRAIL) to Canine Cell Lines Derived from Hemangiosarcoma and Mammary Epithelial Tumor
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Mechanisms of HIV-induced peripheral neuropathic pain by focusing on Schwann cell-macrophage interaction
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Immunohistochemical assessment of sex-determining region Y (SRY)-related high mobility group (HMG)-box 2 (Sox2) and Krüppel-like factor 4 (Klf4) in ameloblastomas
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The ocular involvement did not accompany with the genital ulcer or the gastrointestinal symptoms at the early stage Behcet’s disease
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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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Implications of interleukin-17 in psoriatic lesions as Koebner phenomenon caused by recurrent occupational burns
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Endothelial cell malfunction in unruptured intracranial aneurysm lesions revealed using a 3D-casted mold
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Illustrative review of cardiac amyloidosis by multimodality imaging
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Clinical Significance of Serum Galectin-9 and Soluble CD155 Levels in Patients with Systemic Sclerosis
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Case report : Vascular graft infection due to Aspergillus species presenting with recurrent vascular occlusion
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An autopsy case of primary gliosarcoma with multiple extracranial metastases: pathology after administration of bevacizumab and genetic profile