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Research 271–300 of 1000+
- Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma
- First Symposium of Ichthyosis Experts
- Parry–Romberg Syndrome: Radioclinical Dissociation in a Paucisymptomatic Form and a Proposed Diagnostic Framework
- Molecular Genetic Characteristics of the Hoxc13 Gene and Association Analysis of Wool Traits
- Subject Index
- Hair fragility (trichorrhexis nodosa) in alopecic Pomeranian dogs
- Berardinelli–Seip syndrome
- Hair loss.
- Secondary Cicatricial and other Permanent Alopecias
- Congenital goiter in sibling goat kids
- Eyelash trichomegaly: review of congenital, acquired, and drug‐associated etiologies for elongation of the eyelashes
- 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
- NIPAL4 mutation c.527C˃A identified in Romanian patients with autosomal recessive congenital ichthyosis
- Identification of a novel<i>PNPLA1</i>mutation in a Spanish family with autosomal recessive congenital ichthyosis
- A Rare Case of Keratosis Follicularis Spinulosa Decalvans Affecting a Female Child
- Unveiling the Potential of Dermoscopy in Diagnosing Netherton Syndrome
- Hair Shaft Abnormalities – Clues to Diagnosis and Treatment
- P142 – 3046: Encephalocraniocutaneous lipomatosis, a rare neurocutaneous disorder: Report of additional three cases
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- Congenital atrichia with papular lesions: a rare cause of irreversible childhood alopecia
- Epicardial Fat Thickness in Children with Classic Congenital Adrenal Hyperplasia
- Neuroimaging Findings in Congenital Biotinidase Deficiency: A Case Report
- Atrichia congenita with papular lesions: A rare cause of pediatric alopecia
- Congenital Atrichia: A Case Report
- Epicardial fat thickness in children with classic congenital adrenal hyperplasia
- A rare cause of irrevocable childhood alopecia feigning alopecia universalis: Atrichia congenita with papular lesions
- “Case Report : Early Congenital Syphilis”
- Hypothyroidism in Dogs
- Androgen excess and post-reproductive health
- <i>NIPAL4</i> deletion identified in an American Bully with autosomal recessive congenital ichthyosis and response to topical therapy