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Research 31–60 of 520
- Immunomodulators in the treatment of cutaneous lymphoma
- Severe, Disfiguring, Pityriasis Rubra Pilaris in a Woman in the Dominican Republic
- Abnormal Wool Growth and Alopecia of Artificially Reared Lambs
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- Human T‐lymphotropic virus 1 (HTLV‐1)‐associated lichenoid dermatitis induced by CD8<sup>+</sup> T cells in HTLV‐1 carrier, HTLV‐1‐associated myelopathy/tropical spastic paraparesis and adult T‐cell leukemia/lymphoma
- Missense mutation Y449H of the K10 gene in a patient with severe epidermolytic ichthyosis
- Ichthyosis linearis circumflexa with bamboo hair: challenges in the diagnosis and management
- The urine as a diagnostic key for a homozygous EGFR mutation
- Psoriasis and Related Disorders
- Netherton Syndrome
- Severe pityriasis rubra pilaris complicated with Kaposi's varicelliform eruption and cutaneous MRSA infection case report
- Omenn syndrome in a 10-month-old male with athymia and VACTERL association
- Mucocutaneous presentations of consultant critical and non-critical cases of admitted COVID-19 patients, outpatients and vaccine-associated dermatoses: a large original study of a general COVID-19 centers from Iran
- Salt-losing tubulopathy and chronic dermatitis
- Acitretin for the Treatment of Psoriasis: A Case Report of Long-Lasting Alopecia
- DERMATOLOJİK ACİLLER
- An unusual case of increased hair pigmentation in previously grey-white hair
- Forme létale de syndrome de Netherton au sein d’une famille multiplex consanguine
- Care of the newborn with ichthyosis
- Ichthyosis with confetti: clinics, molecular genetics and management
- A novel mutation in the connexin 26 gene (<i>GJB2</i>) in a child with clinical and histological features of keratitis–ichthyosis–deafness (KID) syndrome
- Severe form of keratitis–ichthyosis–deafness (KID) syndrome associated with septic complications
- [The Netherton syndrome with alopecia and prolinuria].
- Vulvovaginal involvement in Netherton syndrome: A case report
- A new heterozygous frameshift variant in keratin 10 resulting in ichthyosis hystrix in a father and daughter
- Netherton Syndrome
- The keratins and their disorders
- KERATINS AND SKIN DISORDERS
- Ichthyosis with confetti: a rare diagnosis and treatment plan
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation