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Research 151–180 of 307
- Symptomatic hypercalcemia and scarring alopecia as presenting features of sarcoidosis
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- A Case of Premature Hair Graying Treated with Ferrous Sulfate
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Comparison of Ischemia-modified Albumin and Exercise Stress Test in Stable Angina Pectoris
- Guidelines for perioperative antithrombotic therapy in hair restoration surgery: management of patients with coronary heart disease, mechanical heart valve, and atrial fibrillation
- Muscle weakness of the lower limbs after epidural anesthesia in a pregnant woman with undiscovered systemic lupus erythematosus
- Efficacy of exosomes in acute kidney injury treatment and the associated mechanism (Review)
- ADULT (acro–dermato–ungual–lacrimal–tooth) syndrome: A case report from India
- Werner's syndrome: incidental finding during pregnancy
- Cutaneous changes in hypothyroidism
- SMC-specific IGF1 suppresses a 45 kDa LAMP2 isoform to mediate the anti-atherosclerotic effect of ferulic acid
- Micropore-forming photocurable tissue adhesive promotes cell infiltration for wound healing
- Biomedical engineering approaches for the delivery of JAGGED1 as a potential tissue regenerative therapy
- Androphenotypic features in patients with coronary artery disease
- Trichothiodystrophy in a child with occult learning disorder
- 鍼灸療法에 의한 발모관련 인자들의 발현에 대한 실험적 연구
- Survey of alimentary radiological findings.
- Rectal Bezoar: A Rare Cause of Intestinal Obstruction
- RECONSTRUCTION OF INTESTINAL TRANSIT WITH MODIFIED KONO-S ANASTOMOSIS (ILEO-CECAL) IN A PATIENT WITH CROHN'S DISEASE
- The Rotterdam Study: objectives and design update
- Mesenchymal Stem Cells for Regenerative Medicine
- Wnt/β-catenin signalling: function, biological mechanisms, and therapeutic opportunities
- Cutaneous and Mucosal Lichen Planus: A Comprehensive Review of Clinical Subtypes, Risk Factors, Diagnosis, and Prognosis
- Budesonide for maintenance of remission in Crohn's disease
- Cantú Syndrome Is Caused by Mutations in ABCC9
- WNT Signaling in Disease
- Netherton's syndrome: A syndrome of elevated IgE and characteristic skin and hair findings
- Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations
- Peripheral Arterial Disease: Diagnosis and Management