Disease: KID syndrome
- A Case Report on Copper Beaten Skull Appearance: A Forgotten Entity
- Antibody gene transfer treatment drastically improves epidermal pathology in a keratitis ichthyosis deafness syndrome model using male mice
- Are patients with syndromic craniosynostosis at greater risk for epilepsy than patients with non-syndromic craniosynostosis?
- Cochlear implantation in child with keratitis-ichthyosis-deafness syndrome: A case report
- Conformational changes and CO<sub>2</sub>-induced channel gating in connexin26
- Connexin hemichannel inhibition ameliorates epidermal pathology in a mouse model of keratitis ichthyosis deafness syndrome
- Disparity in neonatal abstinence syndrome by race/ethnicity, socioeconomic status, and geography, in neonates ≥ 35 weeks gestational age
- Effect of tracheostomy timing in pediatric patients with traumatic brain injury
- Emergence of multiple revertant keratinocyte clones in a patient with KID syndrome
- Expression of KID syndromic mutation Cx26S17F produces hyperactive hemichannels in supporting cells of the organ of Corti
- Genome Sequences of Two Pseudomonas aeruginosa Isolates with Defects in Type III Secretion System Gene Expression from a Chronic Ankle Wound Infection
- Hyperkeratotic Nodule on the Knee in a Patient With KID Syndrome
- Ichthyosis follicularis syndromes in patients with mutations in GJB2
- Incidence, Characteristics, and Outcomes of Robin Sequence: A Population-Based Analysis in the United States
- Inherited ichthyosis and fungal infection: an update on pathogenesis and treatment strategies
- Keratitis-ichthyosis-deafness syndrome and hidradenitis suppurativa
- Keratitis-ichthyosis-deafness Syndrome with Heterozygous p.D50N in the <em>GJB2</em> Gene in Two Serbian Adult Patients
- Keratitis-ichthyosis-deafness syndrome with lethal p.Ala88Val variant and severe hypercalcemia
- Keratitis-ichthyosis-deafness syndrome: A comprehensive review of cutaneous and systemic manifestations
- KID Syndrome and Hidradenitis Suppurativa: A Rare Association Responding to Surgical Treatment
- KID syndrome in a Malaysian child with identification of novel heterozygous missense mutation GJB2 c.581T>A(p. 194Phe>Tyr)
- KID Syndrome: A Rare Congenital Ichthyosiform Disorder
- Ocular phenotype and therapeutic interventions in keratitis-ichthyosis-deafness (KID) syndrome
- Oral Nodular Chronic Hyperplastic Candidiasis of the Tongue: A Case Report
- Otological problems in ichthyosis: A literature review
- Parental mosaic cutaneous-gonadal GJB2 mutation: From epidermal nevus to inherited ichthyosis-deafness syndrome
- Phenotypic spectrum of autosomal recessive Keratitis-Ichthyosis-Deafness Syndrome (KIDAR) due to mutations in AP1B1
- Protozoan Parasites in Adult Dairy Small Ruminants and Potential Predictors for Their Presence in Faecal Samples
- Severe atopic eczema treated by dupilumab in a child with keratitis-ichthyosis-deafness syndrome
- The Clinical Manifestation of p.Asp50Asn Heterozygous Mutation of <em>GJB2</em> Gene in 3 Members of a Family Is Similar to That of Clouston Syndrome
- The Effects of Orofacial Myofunctional Therapy on Children with OSAHS's Craniomaxillofacial Growth: A Systematic Review
- TP53 in AML and MDS: The new (old) kid on the block
- Use of Systemic Mycophenolate Mofetil Therapy in Ocular Surface Inflammatory Pathologies at the Initiative and Responsibility of the Ophthalmologist