Search
for
Sort by
Research 331–360 of 507
- 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
- The urine as a diagnostic key for a homozygous EGFR mutation
- Netherton Syndrome
- 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
- 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
- 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
- Disorders of Keratinization
- Ichthyosis and Trichothiodystrophy: the Tay and PIBI(D)S Syndromes
- A General Paediatric Approach to Ankyloblepharon–Ectodermal Dysplasia–Cleft Lip/Palate Syndrome in Infancy: A Case Report
- Unveiling the Potential of Dermoscopy in Diagnosing Netherton Syndrome
- Combination of Netherton Syndrome and Hypopituitarism with Isolated Somatotropin Deficiency: Case Study
- Netherton's syndrome: A syndrome of elevated IgE and characteristic skin and hair findings
- Miscellaneous conditions