• A case of Kindler syndrome in a young Indian female with exon deletion
• A case of Kindler syndrome with severe esophageal stenosis
• A Deep-Intronic FERMT1 Mutation Causes Kindler Syndrome: An Explanation for Genetically Unsolved Cases
• A novel frameshift mutation in the <em>FERMT1</em> gene in a Chinese patient with Kindler syndrome
• A novel large deletion mutation of FERMT1 gene in a Chinese patient with Kindler syndrome
• A novel mutation in the FERMT1 gene in Turkish siblings with Kindler syndrome
• A Novel Nonsense Mutation in Exon 5 of KIND1 Gene in an Iranian Family with Kindler Syndrome
• A novel pathogenic FERMT1 variant in four families with Kindler syndrome in Argentina
• Acral skin atrophy in an infant: an early clue to Kindler syndrome diagnosis
• Aggressive periodontitis associated with Kindler syndrome in a large Kindler syndrome pedigree
• Anesthetic management in a patient with Kindler's syndrome
• Assessment of the risk and characterization of non-melanoma skin cancer in Kindler syndrome: study of a series of 91 patients
• Breast cancer in a patient with Kindlers syndrome
• Case of Kindler syndrome resulting from mutation in the FERMT1 gene
• Clinical Characteristics and Gene Mutations in 186 Cases of Kindler Syndrome
• Clinical Snippets
• Congenital bullous poikiloderma (Kindler syndrome) - new mutation
• Corneal erosion and Kindler syndrome
• Corneal lesions in Kindler syndrome: a case report
• Cutaneous and laryngeal squamous cell carcinoma in mixed epidermolysis bullosa, kindler syndrome
• Dysphagia Due to Kindler Syndrome
• Epidemiology of inherited epidermolysis bullosa in Romania and genotype-phenotype correlations in patients with dystrophic epidermolysis bullosa
• Erosive pustular dermatosis of the scalp and Kindler syndrome: a new association
• Evaluation and treatment of the newborn with epidermolysis bullosa
• Expression of exon-8-skipped kindlin-1 does not compensate for defects of Kindler syndrome
• FERMT1 promoter mutations in patients with Kindler syndrome
• Fibroblast activation and abnormal extracellular matrix remodelling as common hallmarks in three cancer-prone genodermatoses
• First report of the c.1676G&gt;A homozygous variant in a family with Kindler syndrome
• Flightless I, a contributing factor to skin blistering in Kindler syndrome patients?
• Focal adhesions in the skin: lessons learned from skin fragility disorders
• Founder mutation c.676insC in three unrelated Kindler syndrome families belonging to a particular clan from Pakistan
• Histopathological diagnosis of inherited epidermolysis bullosa
• Induction of phenotype modifying cytokines by FERMT1 mutations
• Induction of senescence pathways in Kindler syndrome primary keratinocytes
• Inherited skin disorders presenting with poikiloderma
• Inhibition of cyclin-dependent kinase activity exacerbates H₂ O₂ -induced DNA damage in Kindler syndrome keratinocytes
• Inhibition of α₂-adrenoceptor is renoprotective in 5/6 nephrectomy-induced chronic kidney injury rats
• Invasive squamous cell carcinoma of the hand in a patient with Kindler syndrome: Case report and literature review
• Is adermatoglyphia an additional feature of Kindler Syndrome?
• Kindler epidermolysis bullosa-like skin phenotype and downregulated basement membrane zone gene expression in poikiloderma with neutropenia and a homozygous USB1 mutation
• Kindler Syndrome
• Kindler syndrome complicated by invasive squamous cell carcinoma of the palate
• Kindler syndrome in a patient with colitis and primary sclerosing cholangitis: coincidence or association?
• Kindler syndrome protein Kindlin-1 is mainly expressed in adult tissues originating from ectoderm/endoderm
• Kindler syndrome with a novel mutation and gynaecological complication
• Kindler syndrome with palmoplantar hyperhidrosis and blonde hair
• Kindler syndrome with severe intestinal involvement: a 31-year follow-up
• Kindler syndrome with severe mucosal involvement in a large Palestinian pedigree
• Kindler syndrome with severe mucosal involvement in childhood
• Kindler syndrome with unique ocular findings
• Kindler Syndrome: A Multidisciplinary Management Approach
• Kindler syndrome: a rare case report from Greece
• Kindler syndrome: a rare case report from Syria
• Kindler syndrome: clinical and ultra-structural particularities, a propos of three cases
• Kindler syndrome: extension of FERMT1 mutational spectrum and natural history
• Kindler syndrome: report of two cases
• Kindler syndrome: the case of two Iranian sisters
• Kindler's syndrome with long thick cuticles and mottled hyperpigmentation
• Kindler's Syndrome with Recurrent Neutropenia: Report of Two Cases from Saudi Arabia
• Kindler'S syndrome: a case series of three Indian children
• Kindler's syndrome: A rare case report
• Kindler's syndrome: a report of five cases in a family
• Kindler's Syndrome: A Tale of Two Siblings
• Kindlin-1 and -2 have overlapping functions in epithelial cells implications for phenotype modification
• Kindlin-1 controls Wnt and TGF-β availability to regulate cutaneous stem cell proliferation
• Kindlin-1 protects cells from oxidative damage through activation of ERK signalling
• Kindlin-1 Regulates Epidermal Growth Factor Receptor Signaling
• Kindlin-1 regulates integrin dynamics and adhesion turnover
• Kindlin-1 Regulates Keratinocyte Electrotaxis
• Management of a rare presentation of Kindler disease with digital constriction bands-Case report
• Mild clinical phenotype of Kindler syndrome associated with late diagnosis and skin cancer
• Natural history of Kindler syndrome and propensity for skin cancer - case report and literature review
• Novel and recurrent FERMT1 gene mutations in Kindler syndrome
• Ocular manifestations in Kindler syndrome
• Ocular manifestations of genetic skin disorders
• Oral Care in Kindler Syndrome: 7-Year Follow-up of 2 Brothers
• Oral manifestations in Kindler syndrome: case report and discussion of literature findings
• Oxidative stress and mitochondrial dysfunction in Kindler syndrome
• Partial loss of epithelial phenotype in kindlin-1-deficient keratinocytes
• Rare in the scarce: ocular involvement in kindler syndrome
• Realm of revertant mosaicism expanding
• Recessive mutation in tetraspanin CD151 causes Kindler syndrome-like epidermolysis bullosa with multi-systemic manifestations including nephropathy
• Recurrent pyoderma in Kindler syndrome
• Revertant mosaicism in a human skin fragility disorder results from slipped mispairing and mitotic recombination
• Revertant mosaicism in Kindler syndrome
• Secrets of the cutaneous basement membrane
• Sequence variants in nine different genes underlying rare skin disorders in 10 consanguineous families
• Severe epidermolysis bullosa/Kindler syndrome-like phenotype of an autoinflammatory syndrome in a child
• Single Amino Acid Deletion in Kindlin-1 Results in Partial Protein Degradation Which Can Be Rescued by Chaperone Treatment
• Skin fragility and blister formation
• Sporadic Kindler syndrome with a novel mutation
• Synchronous bilateral breast cancer in a patient with kindler syndrome
• Syndactyly repair in Kindler syndrome
• The Kindler syndrome: a spectrum of FERMT1 mutations in Iranian families
• The missense mutation p.R1303Q in type XVII collagen underlies junctional epidermolysis bullosa resembling Kindler syndrome
• Two novel mutations in KIND1 in Indian patients with Kindler syndrome
• Urological Manifestations of Kindler Syndrome: A Case Report
• Using immunofluorescence (antigen) mapping in the diagnosis and classification of epidermolysis bullosa: a first report from Iran
• UV-B-induced cutaneous inflammation and prospects for antioxidant treatment in Kindler syndrome
• What is Kindler syndrome?