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「"Kono M "[Author]」の検索結果

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[Fourteen Cases of Implanted Central Venous Access Port-Related Bloodstream Infection].

Distinctive characteristics and prognostic significance of interstitial pneumonia with autoimmune features in patients with chronic fibrosing interstitial pneumonia.

Bilateral striatal necrosis and dyschromatosis symmetrica hereditaria: A-I editing efficiency of ADAR1 mutants and phenotype expression.

Case of mild X-linked ichthyosis complicated with paroxysmal supraventricular tachycardia and anemia.

ANCA-Negative Granulomatosis with Polyangiitis Presenting with Hypertrophic Cranial Pachymeningitis, Abducens Nerve Palsy, and Stenosis of the Internal Carotid Artery.

Anti-PL-7 Antisynthetase Syndrome with Eosinophilic Pleural Effusion.

Intramuscular haemorrhage in a patient with dermatomyositis and anti-TIF1γ antibodies.

Discovery of [cis-3-({(5R)-5-[(7-fluoro-1,1-dimethyl-2,3-dihydro-1H-inden-5-yl)carbamoyl]-2-methoxy-7,8-dihydro-1,6-naphthyridin-6(5H)-yl}carbonyl)cyclobutyl]acetic acid (TAK-828F) as a Potent, Selective, and Orally Available Novel Retinoic Acid Receptor-Related Orphan Receptor γt Inverse Agonist.

Quantification of hand synovitis in rheumatoid arthritis: Arterial mask subtraction reinforced with mutual information can improve accuracy of pixel-by-pixel time-intensity curve shape analysis in dynamic MRI.

Transcriptional factor ICER promotes glutaminolysis and the generation of Th17 cells.

An infant with generalized pustular psoriasis and geographic tongue had a heterozygous IL36RN mutation and IgG2 deficiency.

Effects of Processing Conditions During Manufacture on Retronasal-Aroma Compounds from a Milk Coffee Drink.

Sunlight is merely a temporary modifier of dyschromatosis symmetrica hereditaria.

Mild case of Hailey-Hailey disease caused by a novel ATP2C1 mutation.

Usefulness of Early Plate Removal in Patients With Occlusal Discrepancies After Sagittal Split Ramus Osteotomy.

Neutrophil gelatinase-associated lipocalin in patients with sarcoidosis.

Pharmacological inhibitory profile of TAK-828F, a potent and selective orally available RORγt inverse agonist.

Filaggrin gene mutations may influence the persistence of food allergies in Japanese primary school children.

Identification of novel quinazolinedione derivatives as RORγt inverse agonist.

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