• A homozygous cathepsin C mutation associated with Haim-Munk syndrome
• Cathepsin C gene: First compound heterozygous patient with Papillon-Lefèvre syndrome and a novel symptomless mutation
• Cathepsin C in health and disease: from structural insights to therapeutic prospects
• Cathepsin-C mutation in an individual with phenotypic features of Haim-Munk syndrome: a case report
• CTSC and Papillon-Lefèvre syndrome: detection of recurrent mutations in Hungarian patients, a review of published variants and database update
• Cysteine proteases as disease markers
• Dermatologic, periodontal, and skeletal manifestations of Haim-Munk syndrome in two siblings
• Destructive arthritis in a patient with Haim-munk syndrome
• Exome sequencing identifies a novel missense variant in CTSC causing nonsyndromic aggressive periodontitis
• Genetic studies of syndromes with severe periodontitis and palmoplantar hyperkeratosis
• Haim Munk syndrome and Papillon Lefevre syndrome--allelic mutations in cathepsin C with variation in phenotype
• Haim Munk syndrome: report of two siblings of northern India treated with acitretin
• Haim-Munk syndrome
• Haim-Munk syndrome and Papillon-Lefevre syndrome are allelic mutations in cathepsin C
• Heterozygous Ile453Val codon mutation in exon 7, homozygous single nucleotide polymorphisms in intron 2 and 5 of cathepsin C are associated with Haim-Munk syndrome
• Identification of putative genetic modifying factors that influence the development of Papillon-Lefevre or Haim-Munk syndrome phenotypes
• Localisation of a gene for prepubertal periodontitis to chromosome 11q14 and identification of a cathepsin C gene mutation
• New syndrome of hypotrichosis, striate palmoplantar keratoderma, acro-osteolysis and periodontitis not due to mutations in cathepsin C
• Olmsted syndrome: clinical, molecular and therapeutic aspects
• One mutation, two phenotypes: a single nonsense mutation of the CTSC gene causes two clinically distinct phenotypes
• Palmoplantar keratoderma, oral involvement, and homozygous CTSC mutation in two brothers from Cambodia
• Papillon-Lefevre or Haim-Munk Syndrome? Report on Two Sisters in a Consanguineous Family
• Periodontal manifestations in a patient with haim-munk syndrome
• Processing and Maturation of Cathepsin C Zymogen: A Biochemical and Molecular Modeling Analysis
• Salim Haim and the syndrome that bears his name
• Structure of human dipeptidyl peptidase I (cathepsin C): exclusion domain added to an endopeptidase framework creates the machine for activation of granular serine proteases
• Subsiding of Periodontitis in the Permanent Dentition in Individuals with Papillon-Lefèvre Syndrome through Specific Periodontal Treatment: A Systematic Review
• The first case report of Haim Munk disease with neurological manifestations and literature review