Disease: Amelogenesis imperfecta nephrocalcinosis
- Abnormal teeth and renal calcifications: Answers
- Abnormal teeth and renal calcifications: Questions
- Distal renal tubular acidosis, autoimmune thyroiditis, enamel hypomaturation, and tooth agenesis caused by homozygosity of a novel double-nucleotide substitution in SLC4A4
- Enamel and dentin in Enamel renal syndrome: A confocal Raman microscopy view
- Enamel Renal Gingival Syndrome in an Adolescent
- Enamel Renal Syndrome: A Case History Report
- Enamel renal syndrome: A case report with calcifications in pulp, gingivae, dental follicle and kidneys
- Enamel renal syndrome: A case report with review of literature
- Enamel renal syndrome: A novel homozygous FAM20A founder mutation in 5 new Brazilian families
- Enamel Renal Syndrome: A Systematic Review
- Enamel Renal Syndrome: Protocol for a Scoping Review
- Enamel-renal syndrome in 2 patients with a mutation in FAM20 A and atypical hypertrichosis and hearing loss phenotypes
- Enamel-renal syndrome with congenital heart defects and asthma: a rare association in a Moroccan child
- Enamel-Renal-Syndrome: case report
- FAM20A mutations and transcriptome analyses of dental pulp tissues of enamel renal syndrome
- First characterization of LTBP3 variants in two Moroccan families with hypoplastic amelogenesis imperfecta
- Genetic evaluation of paediatric nephrocalcinosis: phenotype-driven genetic panels reveal a rare diagnosis
- Hypoplastic amelogenesis imperfecta, bilateral nephrolithiasis and FGF-23-mediated hypophosphataemia: a triad of FAM20A-related enamel renal syndrome
- In-depth investigation of FAM20A insufficiency effects on deciduous dental pulp cells: Altered behaviours, osteogenic differentiation, and inflammatory gene expression
- Kohlschütter-Tönz syndrome: Case report with novel feature and detailed review of features associated with ROGDI variants
- Nephrocalcinosis associated with continuous enamel hypoplasia and severe alveolar bone loss: a case report and literature review
- Nephrocalcinosis in Amelogenesis Imperfecta Caused by the FAM20A Mutation
- Pathogenesis of Enamel-Renal Syndrome Associated Gingival Fibromatosis: A Proteomic Approach
- Physicochemical analysis of human pulpal mineralization secondary to FAM20A mutations
- Prosthetic Rehabilitation of a Patient with Rare and Severe Enamel Renal Syndrome
- Renal tubular estrogen ß receptors are expressed at high levels in small vessel vasculitis and are primarily localized in the distal tubule
- The ABCs of the atypical Fam20 secretory pathway kinases
- The emerging roles and therapeutic potential of cyclin M/CorC family of Mg<sup>2+</sup> transporters
- Transcriptome analysis of gingival tissues of enamel-renal syndrome
- Two new families with enamel renal syndrome: A novel FAM20A gene mutation and review of literature