Disease: Keutel syndrome
- 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