• Allogeneic bone marrow transplantation in craniometaphyseal dysplasia
• Biopsy-proven multiple sclerosis in an adult patient with atypical craniometaphyseal dysplasia
• Cardiopulmonary arrest caused by craniometaphyseal dysplasia
• Chiari type I malformation caused by craniometaphyseal dysplasia
• Cochlear Implantation in Craniometaphyseal Dysplasia
• Craniometaphyseal dysplasia
• Craniometaphyseal Dysplasia Mutations in ANKH Negatively Affect Human Induced Pluripotent Stem Cell Differentiation into Osteoclasts
• Craniometaphyseal dysplasia unnoticed until 19 years of age: First diagnosed from facial nerve paralysis
• Craniometaphyseal dysplasia with obvious biochemical abnormality and rickets-like features
• Craniometaphyseal dysplasia-induced hearing loss
• Dental abnormalities in a mouse model for craniometaphyseal dysplasia
• Dental Anomalies Associated with Craniometaphyseal Dysplasia
• Dietary phosphate supplement does not rescue skeletal phenotype in a mouse model for craniometaphyseal dysplasia
• Differences in intracellular localisation of ANKH mutants that relate to mechanisms of calcium pyrophosphate deposition disease and craniometaphyseal dysplasia
• Enabling an unimpeded surgical approach to the skull base in patients with cranial hyperostosis, exemplarily demonstrated for craniometaphyseal dysplasia
• Induced pluripotent stem cell reprogramming by integration-free Sendai virus vectors from peripheral blood of patients with craniometaphyseal dysplasia
• Infant with persistent nasal obstruction. Craniometaphyseal dysplasia (CMD)
• Intracranial hypertension in two cases of craniometaphyseal dysplasia: differing surgical options
• Maternal mosaicism of an ANKH mutation in a family with craniometaphyseal dysplasia
• Metaphyseal dysplasia, epiphyseal dysplasia, diaphyseal dysplasia, and related conditions. I. Familial metaphyseal dysplasia and craniometaphyseal dysplasia; their relation to leontiasis ossea and osteopetrosis; disorders of bone remodeling
• Middle cranial fossa facial nerve decompression before two years of age
• Miscellaneous Bone Disorders
• Novel COL4A2 variant in a large pedigree: Consequences and dilemmas
• Otological aspects and surgical outcome in a consanguineous family with a novel ANKH gene mutation
• Rapid degradation of progressive ankylosis protein (ANKH) in craniometaphyseal dysplasia
• Restriction of Dietary Phosphate Ameliorates Skeletal Abnormalities in a Mouse Model for Craniometaphyseal Dysplasia
• Rice diversity panel provides accurate genomic predictions for complex traits in the progenies of biparental crosses involving members of the panel
• Simultaneous LeFort III and LeFort I Osteotomies in Craniometaphyseal Dysplasia
• Transmastoid Facial Nerve Decompression for Craniometaphyseal Dysplasia
• Turbinoplasty surgery for nasal obstruction in craniometaphyseal dysplasia: A case report and review of the literature
• Two novel large ANKH deletion mutations in sporadic cases with craniometaphyseal dysplasia