Disease: Ichthyosis hystrix- Curth Macklin type
- A female pioneer--doubly recognized
- A novel frameshift truncation mutation in the V2 tail domain of KRT1 causes mild ichthyosis hystrix of Curth-Macklin
- A novel mutation and large size polymorphism affecting the V2 domain of keratin 1 in an African-American family with severe, diffuse palmoplantar keratoderma of the ichthyosis hystrix Curth-Macklin type
- A severe familial phenotype of Ichthyosis Curth-Macklin caused by a novel mutation in the KRT1 gene
- A Sporadic Case of Ichthyosis Curth Macklin: Rare Presentation of a Rare Disease
- A Sporadic Case of Ichthyosis Hystrix: Curth and Macklin Type
- A unique pattern of dyskeratosis characterizes epidermolytic hyperkeratosis and epidermolytic palmoplantar keratoderma
- Case of unilateral epidermal nevi without extracutaneous anomalies
- Follow-up of a family group suffering from ichthyosis hystrix type Curth-Macklin
- Helen Ollendorff Curth: A dermatologist's lasting legacy
- Helen Ollendorff-Curth: A dermatologist's lasting legacy
- Ichthyosis hystrix Curth-Macklin type in an African girl
- Ichthyosis hystrix Lambert type and Curth-Macklin type are a single entity with affected (KRT1 mutation) or unaffected (KRT10 mutation) palms and soles?
- Ichthyosis hystrix, Curth-Macklin type: a new sporadic case with a novel mutation of keratin 1
- Inherited disorders of corneocyte proteins
- Lessons from disorders of epidermal differentiation-associated keratins
- Mitotic Langerhans cell as a possible sign of activation in ichthyosis
- Role of the keratin 1 and keratin 10 tails in the pathogenesis of ichthyosis hystrix of Curth Macklin
- Seborrheic distributed papules with palmoplantar hyperkeratosis--quiz case. Diagnosis: Ichthyosis hystrix, Curth-Macklin type
- Systematized linear epidermolytic hyperkeratosis
- Transcriptomic analysis of skin in a case of ichthyosis Curth-Macklin caused by a KRT1 mutation
- Ultrastructural features of ichthyosis hystrix strongly resembling Lambert type
- Ultrastructural identification of basic abnormalities as clues to genetic disorders of the epidermis
- Ultrastructure of inborn errors of keratinization. II. Ichthyosis hystrix type Curth-Macklin