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Research 631–660 of 1000+
- Congenital insensitivity to pain with anhidrosis and progressing acro-osteolysis: a case report with 7-year follow-up
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Rare Association of Congenital Triangular Alopecia with Vitiligo
- Tissue engineering strategies combining molecular targets against inflammation and fibrosis, and umbilical cord blood stem cells to improve hampered muscle and skin regeneration following cleft repair
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Congenital triangular alopecia - A case report
- Giant congenital cerebriform pigmented nevus of scalp: case report
- Blank Spots in the Map of Human Skin: The Challenge for Xenotransplantation
- Advances in regenerative medicine-based approaches for skin regeneration and rejuvenation
- Hair diseases: a big problem on a small surface
- Expression and Function of Group IIE Phospholipase A2 in Mouse Skin
- Leveraging deep neural networks to uncover unprecedented levels of precision in the diagnosis of hair and scalp disorders
- Proteomic Analysis of Two Stem Cell Secretomes Used in Combination in a Topical Skin Care Product That Has Demonstrated Efficacy in a Double-Blinded, Vehicle-Controlled Clinical Trial
- Tanshinone IIA pretreatment protects free flaps against hypoxic injury by upregulating stem cell-related biomarkers in epithelial skin cells
- Severe impact of late diagnosis of congenital adrenal hyperplasia on gender identity, sexual orientation and function: case report and review of the literature
- Current Genetics in Hair Diseases
- Dercum Disease: Exploratory Therapeutic Approaches in the Absence of Standardized Medical Treatment—A Single Center Case Series
- Dietary Influences on Skin Health in Common Dermatological Disorders
- Congenital Trichomegaly of the Eyelashes
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- Advancing skin model development: A focus on a self-assembled, induced pluripotent stem cell-derived, xeno-free approach
- Congenital atrichia associated with situs inversus and mesocardia
- Diagnostic imaging in congenital adrenal hyperplasia – how does it help?
- The distribution of Preputial vessels in different severity of rat congenital hypospadias model: imaging study using micro-computerized tomography
- Delayed Diagnosis of Congenital Adrenal Hyperplasia Due to 3β-Hydroxysteroid Dehydrogenase Type 2 Deficiency
- BH15 Nonsyndromic hypotrichosis: a rare case of congenital hypotrichosis 15 and management with minoxidil
- Alopecia patterns and trichoscopic findings in patients with autosomal recessive congenital ichthyosis
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Tissue engineering of skin and regenerative medicine for wound care
- TRP Channels in Skin Biology and Pathophysiology