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Research 331–360 of 1000+
- Clinicopathologic and trichoscopic features of keratosis follicularis spinulosa decalvans: A case series study
- Beta thalassemia revealing hypothyroidism: A case report
- Clinical cases of Darier-White follicular dyskeratosis
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- ANALYSIS OF THE RELATION BETWEEN ALOPECIA AND RESISTANCE TO 1,25‐DIHYDROXYVITAMIN D
- Value of dermoscopy for the diagnosis of monilethrix
- Pregnancy and Skin
- Does Complement Have a Role in the Pathogenesis of Alopecia Areata?
- Folliculin, the Product of the Birt-Hogg-Dube Tumor Suppressor Gene, Interacts with the Adherens Junction Protein p0071 to Regulate Cell-Cell Adhesion
- A Kaleidoscope of Keratin Gene Expression and the Mosaic of Its Regulatory Mechanisms
- Clinical characteristics and risk factors of female precocious puberty
- Premature graying of hairs: Ayurveda perspective
- He Shou Wu (Polygonum multiflorum)-Induced Hepatocellular Hepatitis
- Dental considerations in acrodermatitis enteropathica: A report of two cases
- Efficacy and tolerability of HDMHG0401-10 in Patients with Androgenetic Alopecia: A Randomized Double-blind Placebo-controlled Trial
- A case of dyschromatosis universalis
- Structural Stability of Wild Type and Mutated α-Keratin Fragments: Molecular Dynamics and Free Energy Calculations
- Madarosis: A marker of many Maladies
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- Study of the Thyroid Profile of Patients with Alopecia
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report
- Case Report: Exceptional Association of Leydig Cell Ovarian Tumor and Primary Hyperparathyroidism in a Postmenopausal Patient
- Molecular–clinical correlations in a family with variable tissue mitochondrial DNA T8993G mutant load
- Vitamin D‐dependent rickets Type II with alopecia: two case reports and review of the literature
- Post-COVID-19 Sydrome and Decrease in Health-Related Quality of Life in Kidney Transplant Recipients after SARS-COV-2 Infection—A Cohort Longitudinal Study from the North of Poland
- Unmasking pseudopelade of Brocq in male adult: a rare case report
- A Forty-Two-Year-Old Male with Multiple Gastrointestinal Polyps, Cutaneous Manifestations, and Nail Dystrophy
- THE EFFECT OF AUTOLOGOUS PLATELET RICH PLASMA (PRP) ON PATIENTS WITH ALOPECIA AREATA