• A Novel MGP Gene Mutation Causing Keutel Syndrome in a Brazilian Patient
• A Rare Diagnosis: Keutel Syndrome
• A Rare Genetic Disorder: Keutel Syndrome with Dermatologic Manifestation
• Assessment of MGP gene expression in cancer and contribution to prognosis
• Characterization of vitamin K-dependent carboxylase mutations that cause bleeding and nonbleeding disorders
• Deeper understanding of carboxylase
• Evaluation of MGP gene expression in colorectal cancer
• Inherited Arterial Calcification Syndromes: Etiologies and Treatment Concepts
• Keutel Syndrome, a Review of 50 Years of Literature
• Keutel syndrome: Augmentation of the nose with serial fat grafting
• Matrix Gla protein deficiency impairs nasal septum growth, causing midface hypoplasia
• New perspectives on rare connective tissue calcifying diseases
• Prevention of Arterial Elastocalcinosis: Differential Roles of the Conserved Glutamic Acid and Serine Residues of Matrix Gla Protein
• Specific heterozygous variants in MGP lead to endoplasmic reticulum stress and cause spondyloepiphyseal dysplasia
• The Role of Vitamin K and Its Related Compounds in Mendelian and Acquired Ectopic Mineralization Disorders
• Tracheobronchial calcifications in a child
• Tracheobronchial Tree Ossification in a 5-Year-Old Boy with Keutel Syndrome: A Case Report