Disease: Peeling skin syndrome- acral type
- 'Double trouble': diagnostic challenges in genetic skin disorders
- Acanthosis nigricans: A review
- Acral peeling in Nagashima type palmo-plantar keratosis patients reveals the role of serine protease inhibitor B 7 in keratinocyte adhesion
- Acral peeling skin syndrome
- Acral peeling skin syndrome associated with a novel CSTA gene mutation
- Acral peeling skin syndrome resulting from a novel homozygous mutation in the CSTA gene-A report of two cases
- Acral peeling skin syndrome resulting from mutations in TGM5
- Acral Peeling Skin Syndrome: A Case Report and Literature Review
- Acral peeling skin syndrome: An underdiagnosed skin disorder
- Acral Peeling Skin Syndrome: Two Unusual Cases and the Therapeutic Potential of Botulinum Toxin
- Activography reveals aberrant proteolysis in desquamating diseases of differing backgrounds
- Adult-onset acral peeling skin syndrome in a non-identical twin: a case report in South Africa
- Coincidence of acral peeling skin syndrome and Nagashima-type palmoplantar keratosis in a Japanese pedigree with acral skin peeling
- Enhanced Proteolytic Activities in Acral Peeling Skin Syndrome: A Role of Transglutaminase 5 in Epidermal Homeostasis
- Exome-based search for recurrent disease-causing alleles in Russian population
- Hypercalciuria in a child with acral peeling skin syndrome: a case report
- Novel TGM5 mutations in acral peeling skin syndrome
- PLACK syndrome: the penny dropped
- Transglutaminase diseases: from biochemistry to the bedside
- Under-recognition of acral peeling skin syndrome: 59 new cases with 15 novel mutations