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Research 211–240 of 1000+
- PSAT097 Patient Preference Research: Preferred Adjunctive Medication Attributes of Adult Patients with Classic Congenital Adrenal Hyperplasia
- Diffuse congenital hypotrichosis simplex with associated hair shaft fragility
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- BH15 Nonsyndromic hypotrichosis: a rare case of congenital hypotrichosis 15 and management with minoxidil
- Giant Congenital Melanocytic Nevus Correction: A Case Report
- Nonclassic Congenital Adrenal Hyperplasia: An Overview
- Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- A gene for pachyonychia congenita is closely linked to the keratin gene cluster on 17q12-q21.
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- Pachyonychia Congenita-Associated Alopecia. A Microscopic Analysis Using Transverse Section Technique
- A new type of pachyonychia congenita.
- Delayed-onset pachyonychia congenita caused by a novel mutation in the V2 domain of keratin 6b
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- KERATIN 17-related recessive atypical pachyonychia congenita with variable hair and tooth anomalies
- Resolution of the plantar hyperkeratosis of pachyonychia congenita during chemotherapy for Ewing sarcoma
- Pachyonychia congenita: Sporadic onset with mutation analysis
- Hypotrichosis congenita (KRT71 mutation) in Hereford cattle in Uruguay
- A rare cause of irrevocable childhood alopecia feigning alopecia universalis: Atrichia congenita with papular lesions
- Hypotrichosis congenita of Marie Unna
- Non-classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency revisited: an update with a special focus on adolescent and adult women
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- Non-classic congenital adrenal hyperplasia
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- Treatment of unilateral congenital ptosis
- Management of the Female With Non-classical Congenital Adrenal Hyperplasia (NCCAH): A Patient-Oriented Approach
- Ulerythema ophryogenes with multiple congenital anomalies
- Identification of a novel<i>PNPLA1</i>mutation in a Spanish family with autosomal recessive congenital ichthyosis
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction
- Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II