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Research 601–630 of 1000+
- 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
- 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
- Alopecia in children
- Congenital hypotrichosis in a French bulldog
- A Review on-Types and Treatment of Alopecia
- Secondary cicatricial and other permanent alopecias
- Temporal triangular alopecia
- Fixed focal alopecia for 20 years
- Alopecia areata - probing the deforestation
- ‘Black dots’ seen under trichoscopy are not specific for alopecia areata
- A Homozygous Nonsense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia
- Congenital adrenal hyperplasia
- The diagnosis of androgenetic alopecia in children: Considerations of pathophysiological plausibility
- RECENT DEVELOPMENTS IN ALOPECIAS
- Congenital dyserythropoietic anaemia and dyskeratosis in Australian Poll Hereford calves
- [Congenital hereditary hypotrychosis. Generalized autosomal dominant hypotrichosis with pili torti (hypotrichosis congenita hereditaria Marie Unna)].
- Acquired 11β-hydroxylase Deficiency by Inhaled Etomidate and its Analogues: A Mimic of Congenital Adrenal Hyperplasia