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Research 31–60 of 1000+
- Congenital Triangular Alopecia: A Case of Effective Response with 5% Topical Minoxidil in a Male Adolescent
- Rare Association of Congenital Triangular Alopecia with Vitiligo
- A case of unilateral congenital triangular alopecia
- Congenital Triangular Alopecia
- Regrowth of hair in congenital triangular alopecia induced by sublingual minoxidil
- Alopecia in congenital hidrotic ectodermal dysplasia responding to treatment with a combination of topical minoxidil and tretinoin
- Study of Human Leukocyte Antigen ( HLA ) in 13 cases of familial frontal fibrosing alopecia: CYP 21A2 gene p.V281L mutation from congenital adrenal hyperplasia linked to HLA class I haplotype HLA ‐ A*33:01 ; B*14:02; C*08:02 as a genetic marker
- Congenital atrichia with papular lesions: a rare cause of irreversible childhood alopecia
- Congenital Combined Melanocytic Nevus of the Scalp With Associated Alopecia Areata
- Pachyonychia Congenita-Associated Alopecia. A Microscopic Analysis Using Transverse Section Technique
- Non-classical Congenital Adrenal Hyperplasia Presenting With Severe Androgenic Alopecia: A Case Report
- 152 Alopecia patterns in patients with autosomal receesive congenital ichthyosis
- Alopecia triangularis congenita in combination with androgenetic alopecia
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- A rare cause of irrevocable childhood alopecia feigning alopecia universalis: Atrichia congenita with papular lesions
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- ALOPECIA TRIANGULAR CONGÉNITA BILATERAL EN UN NEONATO: REPORTE DE CASO
- Platelet-rich Plasma Injection and Lipofilling-assisted Hair Transplantation on Residual Scalp Alopecia Post Aplasia Cutis Congenita Verticis (ACCV)
- Alopecia patterns and trichoscopic findings in patients with autosomal recessive congenital ichthyosis
- Hereditary, Congenital, and Acquired Alopecias
- AUTOSOMAL DOMINANT INHERITANCE OF ALOPECIA CONGENITA WITH KERATOSIS PALMO-PLANTARIS
- 321 Deletion of hypoxia-inducible factor prolyl 4-hydroxylase 2 in FoxD1-lineage mesenchymal cells leads to congenital truncal alopecia
- Deletion of hypoxia-inducible factor prolyl 4-hydroxylase 2 in <i>FoxD1</i>-lineage mesenchymal cells leads to congenital truncal alopecia
- Deletion of hypoxia-inducible factor prolyl 4-hydroxylase 2 in FoxD1-lineage mesenchymal cells leads to congenital truncal alopecia
- Alopecia: A Pathologist's View
- Clinical relevance of hair microscopy in alopecia
- Molecular basis of congenital atrichia in humans and mice.
- Congenital atrichia and hypotrichosis
- Alopecia in children
- RECENT DEVELOPMENTS IN ALOPECIAS