Editorial: Cell-to-cell communications in tissue homeostasis and repair
Frontiers in Cell and Developmental Biology, 2023 Osamu Shimmi, Osamu Shimmi, Esko Kankuri
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Dental Management of a Child with Dentinogenesis Imperfecta: A Case Report
Frontiers in Dentistry, 2016 Dentinogenesis imperfecta (DI) is a hereditary dentin defect caused by an autosomal dominant mutation in dentin sialophosphoprotein gene. Defective dentin development results in discolored teeth that are prone to wear and fracture.
Najmeh Akhlaghi +2 more
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<i>Dentinogenesis Imperfecta</i> in Primary Dentition: Case Report. [PDF]
Reports (MDPI)Petrova L, Ustiča J, Čēma I.
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Osteogenesis Imperfecta Type 4 With COL1A2 c.1135G>A (p.Gly379Arg) Variant: Unmodified by Concurrent ALPL c.1559delT (p.Leu520ArgfsTer86) Carrier Status: A Case Report. [PDF]
CureusNomura K +4 more
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Diagnosis complexity of dentinogenesis imperfecta involving <i>DSPP</i> genetic variants. [PDF]
J Med GenetCaravello G +11 more
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Dentin Autograft as a Pulp Capping Material: A Systematic Review. [PDF]
J Pharm Bioallied SciChaudhari WA +5 more
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Management of Osteogenesis Imperfecta Complicated by Severe Pneumonia in a Resource-Limited Setting: A Case Report. [PDF]
Case Rep PediatrShah BK +6 more
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Wnt/β-Catenin Pathway and Hydraulic Calcium Silicate-Based Cements: A Narrative Review. [PDF]
Dent J (Basel)Del Giudice C +6 more
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Functional and Aesthetic Treatment of Patients With Tooth Structure Anomalies: A Narrative Review. [PDF]
CureusReuter AK, Ehlers V.
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