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Research 721–750 of 1000+
- P-18 THREE BODY PROBLEM PATIENT: EHLER DANLOS SYNDROME COMBINED WITH HYPOPHOSPHATASIA AND FATTY ACID OXIDATION DEFECT
- Compound glycyrrhizin promotes hair growth in C57BL/6 mice by regulating the Wnt/β-catenin pathway
- Ankyloblepharon-ectodermal dysplasia-clefting syndrome: Surgical and medical management in an infant with bilateral corneal perforations
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- Monilethrix: a typical case report with microscopic and dermatoscopic findings
- Treatment of Keratosis Pilaris With 810-nm Diode Laser
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa
- The function of TRPS1 in the development and differentiation of bone, kidney, and hair follicles.
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- CPC14 Blaschko-linear trichoepitheliomas: unveiling type 1 segmental mosaicism
- Characterization of Bsk mice: I. The Bsk mutation does not involve a recombination of cornea-specific keratin 12 and skin-specific hair keratin genes.
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Male polycystic ovarian syndrome phenotype: a meta-analysis of endocrine-metabolic dysregulation in fathers and brothers of PCOS-affected women
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Nagashima-Type Palmoplantar Keratosis: A Common Asian Type Caused by SERPINB7 Protease Inhibitor Deficiency
- Epidermal expression of the truncated prelamin A causing Hutchinson-Gilford progeria syndrome: effects on keratinocytes, hair and skin
- Transgenic Kallikrein 14 Mice Display Major Hair Shaft Defects Associated with Desmoglein 3 and 4 Degradation, Abnormal Epidermal Differentiation, and IL-36 Signature
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- P latelet rich plasma application by dermapen microneedling and intradermal point‐by‐point injection methods, and their comparison with clinical findings and trichoscan in patients with androgenetic alopecia
- Studies on basal cell carcinoma with emphasis on the role of the human homologue of the Drosophila patched gene
- Unleashing the Furry Beast: Exploring the Fascinating World of Hypertrichosis Lanuginosa
- Ashwagandha root in the treatment of non-classical adrenal hyperplasia
- Causes and Management of Hypertrichosis
- Central centrifugal cicatricial alopecia: challenges and solutions
- Congenital atrichia associated with situs inversus and mesocardia
- Presence of Uterine Leiomyomas Has No Significant Impact on Gene Expression Profile in the Scalp of Patients with Central Centrifugal Cicatricial Alopecia
- Ehlers-Danlos syndrome: From bedside to bench
- Long-term Prophylaxis with Androgens in the management of Hereditary Angioedema (HAE) in emerging countries
- Effectiveness of Rosmarinus officinalis for Androgenetic Alopecia: A Literature Review