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Research 181–210 of 488
- Psoriasis and Related Disorders
- Acitretin for the Treatment of Psoriasis: A Case Report of Long-Lasting Alopecia
- An unusual case of increased hair pigmentation in previously grey-white hair
- [Netherton's syndrome in two sisters].
- Graft versus host disease–like: A new paraneoplastic syndrome
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Stanozolol in the Treatment of Pityriasis Rubra Pilaris
- Characterizing Disease Features and Other Medical Diagnoses in Patients With Pityriasis Rubra Pilaris
- Identification of compound heterozygous mutations in <i>AP1B1</i> leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome
- Severe, Disfiguring, Pityriasis Rubra Pilaris in a Woman in the Dominican Republic
- Abnormal Wool Growth and Alopecia of Artificially Reared Lambs
- 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
- Ichthyosis linearis circumflexa with bamboo hair: challenges in the diagnosis and management
- Netherton Syndrome
- Salt-losing tubulopathy and chronic dermatitis
- DERMATOLOJİK ACİLLER
- Ichthyosis with confetti: clinics, molecular genetics and management
- A new heterozygous frameshift variant in keratin 10 resulting in ichthyosis hystrix in a father and daughter
- Forme létale de syndrome de Netherton au sein d’une famille multiplex consanguine
- Care of the newborn with ichthyosis
- 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
- 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
- Trichoscopy in Unveiling the Triad of Netherton Syndrome