• A case of ichthyosis linearis circumflexa successfully treated with topical tacrolimus
• A case of netherton syndrome: successful treatment with omalizumab and pulse prednisolone and its effects on cytokines and immunoglobulin levels
• A case of Netherton's syndrome with cerebral infarction
• A clinical and immunological study of Netherton's syndrome
• A compound heterozygous mutation of the SPINK5 gene in a Taiwanese boy with Netherton syndrome
• A Japanese infant with localized ichthyosis linearis circumflexa on the palms and soles harbouring a compound heterozygous mutation in the SPINK5 gene
• A novel mutation in <em>SPINK5</em> gene underlies a case of atypical Netherton syndrome
• An additional case of ichthyosis linearis circumflexa
• Biological treatments for pediatric Netherton syndrome
• Clearance of ichthyosis linearis circumflexa with balneophototherapy
• Clinical and genetic characterization of Netherton syndrome due to SPINK5 founder variant in Latvian population
• Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype-phenotype correlation
• Comèl-Netherton syndrome
• Comel's ichthyosis linearis circumflexa: treatment with Ro 10-9359. Electron microscopic study
• Comel's linear circumflex ichthyosis and Netherton's syndrome. General conceptions based on study of 4 cases (author's transl)
• Considerations in surgical management of a Buschke-Lowenstein tumor in Netherton syndrome: A case report
• CONTRIBUTION TO THE PATHOGENESIS OF ICHTHYOSIS LINEARIS CIRCUMFLEXA (COM'EL)
• Desquamating Rash in a Patient with Undiagnosed Netherton Syndrome
• Explorations of antimitotic agents in the treatment of a congenital disease, ichthyosis linearis circumflexa
• Hair anomalies in Comel's linear circumflex ichthyosis
• Ichthyosis linearis circumflex Comel with bullous variation
• Ichthyosis linearis circumflexa
• Ichthyosis linearis circumflexa
• Ichthyosis linearis circumflexa
• Ichthyosis linearis circumflexa
• Ichthyosis linearis circumflexa
• Ichthyosis linearis circumflexa [proceedings]
• Ichthyosis linearis circumflexa and Netherton's syndrome with idiopathic dwarfism
• Ichthyosis Linearis Circumflexa as the Only Clinical Manifestation of Netherton Syndrome
• Ichthyosis linearis circumflexa Comel and Netherton's syndrome; an ultrastructural study
• Ichthyosis linearis circumflexa Comel with Trichorrhexis invaginata (Netherton's Syndrom): an ultrastructural study of the skin changes
• Ichthyosis linearis circumflexa comel with trichorrhexis invaginata (Netherton's syndrome). A light microscopical study of the skin changes
• Ichthyosis linearis circumflexa comel. A clinico-statistical approach to its relationship with Netherton's syndrome
• Ichthyosis linearis circumflexa in a child. Response to narrowband UVB therapy
• Ichthyosis linearis circumflexa with bamboo hair: challenges in the diagnosis and management
• Ichthyosis linearis circumflexa with sub-corneum blisters
• Ichthyosis linearis circumflexa: morphological and biochemical studies
• ICHTHYOSIS LINEARIS CIRCUMFLEXA: NOT ALWAYS A PART OF NETHERTON SYNDROME
• Ichthyosis linearis circumflexa. Description of 2 clinical cases
• Ichthyosis linearis circumflexa. Description of a case
• Ichthyosis: etiology, diagnosis, and management
• Ichtryosis Linearis Circumflexa
• LINEAR CIRCUMFLEX ICHTHYOSIS OF COM'EL
• Long-term dupilumab therapy in Netherton syndrome with severe atopic manifestations: Case report and review of the literature
• Multiple defects of the hair shaft in Netherton's disease. Association with ichthyosis linearis circumflexa
• Nertherton's syndrome
• Neterton's syndrome and ichthyosis linearis circumflexa
• Netherton syndrome
• Netherton syndrome
• Netherton syndrome caused by compound heterozygous mutation, c.80A&gt;G mutation in SPINK5 and large-sized genomic deletion mutation, and successful treatment of intravenous immunoglobulin
• Netherton syndrome in one Chinese adult with a novel mutation in the SPINK5 gene and immunohistochemical studies of LEKTI
• Netherton syndrome previously misdiagnosed as hyper IgE syndrome caused by a probable mutation in SPINK5 C
• Netherton syndrome subtypes share IL-17/IL-36 signature with distinct IFN-α and allergic responses
• Netherton Syndrome with a Novel Likely Pathogenic Variant c.420del (p.Ser141ProfsTer5) in SPINK5 Gene: A Case Report
• Netherton syndrome with ichthyosis linearis circumflexa and trichorrhexis invaginatum
• Netherton syndrome-A therapeutic challenge in childhood
• Netherton Syndrome: A Case Report and Review of Literature
• Netherton syndrome: a type of infantile erythroderma with failure to thrive, immune deficiency, rickets. Report of 3 cases
• Netherton Syndrome: Case Report and Review of the Literature
• Netherton syndrome: disease expression and spectrum of SPINK5 mutations in 21 families
• Netherton syndrome: report of two Taiwanese siblings with staphylococcal scalded skin syndrome and mutation of SPINK5
• Netherton syndrome: successful use of topical tacrolimus and pimecrolimus in four siblings
• Netherton syndrome: weakened immunity, generalized verrucosis and carcinogenesis
• Netherton-Comel's syndrome
• Netherton's disease and ichthyosis linearis circumflexa
• Netherton's disease and ichthyosis linearis circumflexa. Report of a case and review of the literature
• Netherton's Syndrome
• Netherton's syndrome and ichthyosis linearis circumflexa
• Netherton's syndrome in two sisters
• Netherton's Syndrome: A Case of Two Male Siblings Diagnosed in Adulthood
• Netherton's syndrome: a syndrome of elevated IgE and characteristic skin and hair findings
• Netherton's syndrome: an electronmicroscopic study
• Netherton's syndrome: the importance of eyebrow hair
• Netherton's syndrome: ultrastructure of the active lesion under retinoid therapy
• On ichthyosis linearis circumflexa
• Oral Tofacitinib Therapy for the Effective Management of Netherton Syndrome
• Outcomes of Systemic Treatment in Children and Adults With Netherton Syndrome: A Systematic Review
• Persistent methicillin-resistant Staphylococcus aureus bacteremia in an adult patient with Netherton's syndrome: A case report
• Rapid and easy diagnosis of Netherton syndrome with dermoscopy
• Retinoids in disorders of keratinization: their use in adults
• Secukinumab use in the treatment of Netherton's syndrome
• Serum parathyroid hormone level is elevated in some patients with disorders of keratinization
• Severe congenital generalized exfoliative erythroderma in newborns and infants: a possible sign of Netherton syndrome
• Significant response to Pembrolizumab for metastatic cutaneous squamous cell carcinoma in patient with Netherton syndrome
• Skin barrier lipid enzyme activity in Netherton patients is associated with protease activity and ceramide abnormalities
• Successful retinoid therapy of Netherton syndrome
• Successful therapy of ichthyosis linearis circumflexa with PUVA
• Successful treatment of Netherton's syndrome with topical calcipotriol
• Symptomatology of Comel's linear circumflex ichthyosis (a case associated with genito-anal papillomatosis)
• Tacrolimus in dermatology-pharmacokinetics, mechanism of action, drug interactions, dosages, and side effects: part I
• The Arid Melancholy-Netherton Syndrome With Protein Energy Malnutrition
• The syndrome of Comel-Netherton (trichorrhexis invaginata, ichthyosis linearis circumflexa and atopic eczema)
• Topical tacrolimus Protopic
• Trichoscopy as a diagnostic tool in trichorrhexis invaginata and Netherton syndrome
• Two siblings affected by Netherton/Comèl syndrome. Diagnostic pathology and description of a new SPINK5 variant