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Research 661–690 of 1000+
- Ability to cycle despite severe freezing of gait in atypical parkinsonism in Fahr's syndrome
- Comparative advantage and efficacy of natural products for polycystic ovary syndrome
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Alopecia areata: a comprehensive review of clinical, immunologic, and genetic perspectives
- JAK inhibition decreases the autoimmune burden in Down syndrome
- Diseases of Hair
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Claves diagnósticas en displasias pilosas II
- Kelulut Honey Regulates Sex Steroid Receptors in a Polycystic Ovary Syndrome Rat Model
- Novel compound heterozygous cadherin 3 mutations in hypotrichosis and juvenile macular dystrophy
- Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family
- Diseases of Hair
- Constitutive activation of Stat3 in mouse epidermis is linked to hair deficiency and cytoskeletal network damage
- Trichothiodystrophy
- Molecular Mechanisms and Targeted Therapeutics in Androgenetic Alopecia: From Signaling Pathways to Regenerative Approaches
- Association of JAK 1 and JAK 2 gene polymorphism with alopecia areata risk: a case–control genetic study
- Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review
- Role of Trichoscopy in diagnosing Genotrichosis—A Report of Two Cases
- Complete defect in PA-PLA1α secretion function leading to autosomal recessive woolly hair and hypotrichosis: insights from a novel compound heterozygous LIPH variant study in a Chinese pedigree
- Generation of the Krt24-CreERT2 Mouse Line Targeting Outer Bulge Hair Follicle Cells
- Relationship of Hypothyroidism with Alopecia Areata and Androgenetic Alopecia: Insights from a Two-Sample Mendelian Randomization Study
- The necessity of investigations to clarify sex and racial disparities in pathophysiology of Long COVID
- Keratosis Pilaris-like Eruption during Treatment of Chronic Myeloid Leukemia with Tyrosine Kinase Inhibitors: Literature Review and Report of a Case Related to Imatinib
- Bachmann–Bupp syndrome and treatment
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Rare and Underappreciated Causes of Polycystic Ovarian Syndrome
- Three Cases of Canine Dermatomyositis-Like Disease
- Molecular Genetics of Human Hair Diseases
- Current evaluation of amenorrhea