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Research 30 of 44
- Beyond the usual: a case of acrodermatitis enteropathica clinically resembling erythrokeratoderma variabilis
- Erythrokeratodermia Variabilis
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Ichthyosis
- Clinical Manifestation and Classification of Japanese patients with Inherited Keratinizing Disorders
- Dermatoses of pregnancy
- Oral retinoids-present status
- Oral Retinoids in Dermatology
- Chemotherapy of psoriasis and other skin disorders with oral retinoids
- Symmetrical acrokeratoderma: A peculiar entity in China? Clinicopathologic and immunopathologic study of 34 new cases
- Experiences From a Combined Dermatology and Rheumatology Clinic
- Congenital atrichia and hypotrichosis
- Sebaceous carcinoma arising at a chronic candidiasis skin lesion of a patient with keratitis-ichthyosis-deafness (KID) syndrome
- Vitamins
- Madarosis
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Diseases of Periocular Hair
- Subject Index
- Connexin mutations in human disease
- Genetics of Inherited Ichthyoses and Related Diseases
- Madarosis from mitochondriopathy
- Mice lacking desmocollin 1 show epidermal fragility accompanied by barrier defects and abnormal differentiation
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis
- Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3
- New developments in the molecular treatment of ichthyosis: review of the literature
- 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
- Gene-knockout mice with abnormal epidermal and hair follicular development
- Ichthyosis linearis circumflexa in a child. Response to narrowband UVB therapy.
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation