「Myelodysplastic syndrome with trisomy 8 presenting periodic fever and multiple MEFV gene variants outside exon 10: a case report」の関連論文
-
Dupilumab suppresses relapsing chronic eosinophilic pneumonia with severe asthma
-
Clinical, radiological, and pathological features of idiopathic and secondary interstitial pneumonia cases with pleuroparenchymal fibroelastosis undergoing lung transplantation
-
Congenital Dysfibrinogenemia Presented with Massive Hematomas Formed after Hysterectomy
-
Genomic analysis for the prediction of prognosis in small-bowel cancer
-
Genomic analysis for the prediction of prognosis in small-bowel cancer
-
Tumour-immune microenvironment in duodenal-type follicular lymphoma
-
The ocular involvement did not accompany with the genital ulcer or the gastrointestinal symptoms at the early stage Behcet’s disease
-
The association of thyroglobulin single nucleotide polymorphism with miniature dachshunds-specific inflammatory colorectal polyps and its involvement in interleukin-6 amplifier induced chronic inflammation
-
Complete resection and untethering of the cervical and thoracic spinal dermal sinus tracts in adult patients
-
The role of inflammatory biomarkers in predicting primary acquired nasolacrimal duct obstruction and postoperative recurrence
-
Hereditary Mucoepithelial Dysplasia and Autosomal-Dominant IFAP Syndrome Is a Clinical Spectrum Due to SREBF1 Variants
-
Genome-wide association study of IgA nephropathy using 23 465 microsatellite markers in a Japanese population
-
GOS2 regulates innate immunity of Kawasaki disease via IncRNA RP1-280 10.1
-
A systemic form chronic active Epstein-Barr virus infection diagnosed from erythema nodosum-like skin lesions
-
An extremely rare missense mutation of the androgen receptor gene in a Vietnamese family with complete androgen insensitivity syndrome
-
Progression of Recurrent Pancreatitis to Chronic Pancreatitis within 3 Years due to SPINK1 Mutation IVS3+2T>C
-
Gestational psittacosis: A case report and literature review.
-
Identification of a novel causative mutation in KRT1 in diffuse palmoplantar keratoderma, facilitated by whole-exome sequencing
-
Case report: Severe non-pigmenting fixed drug eruption showing general symptoms caused by chondroitin sulfate sodium
-
Comparison of clinical features between patients with acute exacerbation of idiopathic interstitial pneumonia and collagen vascular disease-associated interstitial pneumonia
-
Case of osteopetrosis with multiple impacted primary and permanent teeth diagnosed at eight years old
-
Successful Management of Refractory Autoimmune Hemolytic Anemia with Cold Agglutinin Disease with Splenectomy: A Case Report with Review of Literature
-
Normocomplementemic urticarial vasculitis with laryngeal and intestinal tract edema
-
UBAP1 mutations cause juvenile-onset hereditary spastic paraplegias (SPG80) and impair UBAP1 targeting to endosomes
-
A case of chronic eosinophilic pneumonia associated with rheumatoid arthritis in glucocorticoid-free remission with JAK inhibitor: A case report
-
Effectiveness of Profiling Serum IL-18 and Neopterin in Diagnosis of Adult-Onset Still's Disease Complicated by Pulmonary Tuberculosis: A Case Report
-
聴力障害で発症した高安動脈炎:症例報告とその臨床背景
-
Rituximab in combination with cyclosporine and steroid pulse therapy for childhood-onset multidrug-resistant nephrotic syndrome: a multicenter single-arm clinical trial (JSKDC11 trial)
-
α-Synuclein BAC transgenic mice exhibit RBD-like behaviour and hyposmia: a prodromal Parkinson’s disease model
-
Segmental cutaneous leukocytoclastic vasculitis associated with herpes zoster: a case report and literature review
-
Molecular genetic study of the FMR1 CGG repeat configurations in the Japanese population and patients with Fragile X-Associated Tremor/Ataxia Syndrome
-
Pathological gait in Rett syndrome: Quantitative evaluation using three-dimensional gait analysis
-
Characteristics of cortical spreading depression and c-Fos expression in transgenic mice having a mutation associated with familial hemiplegic migraine 2 (本文)
-
A case of localized tracheobronchial relapsing polychondritis with positive matrilin-1 staining.
-
TNFRSF11A-Associated Dysosteosclerosis: A Report of the Second Case and Characterization of the Phenotypic Spectrum
-
思春期早発症の9歳女児に急性発症した上腸間膜動脈症候群の1例
-
Examination of risk factors for postoperative vestibular symptoms in patients with cholesteatoma
-
Rescue of recurrent deep intronic mutation underlying cell type-dependent quantitative NEMO deficiency
-
Interactions of amyloid coaggregates with biomolecules and its relevance to neurodegeneration
-
A case of systemic lupus erythematosus/systemic sclerosis overlap syndrome successfully treated with belimumab
-
Efficacy and Safety of Adalimumab Therapy for the Treatment of Non-infectious Uveitis: Efficacy comparison among Uveitis Aetiologies
-
Efficacy and Safety of Adalimumab Therapy for the Treatment of Non-infectious Uveitis: Efficacy comparison among Uveitis Aetiologies
-
Minor hallucinations in isolated rapid eye movement sleep behavior disorder indicative of early phenoconversion : A preliminary study.
-
Clinical significance of seasonal human coronaviruses in immunocompromised host
-
Time‐resolved 3D cine phase‐contrast magnetic resonance imaging (4D‐flow MRI) can quantitatively assess portosystemic shunt severity and confirm normalization of portal flow after embolization of large portosystemic shunts
-
Elderly patient with 5q spinal muscular atrophy type 4 markedly improved by Nusinersen
-
Potential roles of gastroesophageal reflux in patients with superficial esophageal squamous cell carcinoma without major causative risk factors
-
Unique reticular hyperkeratotic eruptions seen in a patient with Darier's disease and attention deficit hyperactivity disorder
-
Real-world efficacy of adalimumab and infliximab for refractory intestinal Behçet's disease
-
A case of Erdheim–Chester disease with the BRAF V600E mutation diagnosed via endoscopic sinus surgery