|1.||Hearing Loss (Hearing Impairment)
|1.||Simmer, James P: 5 articles (12/2011 - 05/2007)|
|2.||Hu, Jan C-C: 4 articles (12/2011 - 05/2007)|
|3.||Kim, Jung-Wook: 2 articles (12/2011 - 12/2008)|
|4.||Yamakoshi, Yasuo: 2 articles (01/2011 - 01/2011)|
|5.||Yamakoshi, Fumiko: 2 articles (01/2011 - 01/2011)|
|6.||Aggarwal, Sonia: 1 article (11/2014)|
|7.||Sahoo, Sujit Ranjan: 1 article (11/2014)|
|8.||Gupta, Dheeraj: 1 article (05/2014)|
|9.||Khandelwal, Suneet: 1 article (05/2014)|
|10.||Likhyani, Lalit: 1 article (05/2014)|
|1.||Protein Sorting Signals (Signal Peptide)IBA
08/01/2013 - "Dentin dysplasia is a rare autosomal dominant genetic disease characterized by defect of dentin development and the causal gene is DSPP (Dentin Sialophosphoprotein gene). "
06/01/2012 - "Families with nonsyndromic dentinogenesis imperfecta (DGI) and the milder, dentin dysplasia (DD), have mutations in one allele of the dentin sialophosphoprotein (DSPP) gene. "
06/01/2012 - "Rough endoplasmic reticulum trafficking errors by different classes of mutant dentin sialophosphoprotein (DSPP) cause dominant negative effects in both dentinogenesis imperfecta and dentin dysplasia by entrapping normal DSPP."
12/01/2011 - "Dentin sialophosphoprotein (DSPP) mutations cause dentin dysplasia type II (DD-II) and dentinogenesis imperfecta types II and III (DGI-II and DGI-III, respectively). "
01/01/1998 - "Refined mapping of the human dentin sialophosphoprotein (DSPP) gene within the critical dentinogenesis imperfecta type II and dentin dysplasia type II loci."
|3.||type 1 Dentin dysplasiaIBA
10/01/2013 - "Rootless teeth: Dentin dysplasia type I."
01/01/2013 - "Dentin dysplasia is a rare inherited autosomal dominant disorder characterized by rootless teeth. "
05/01/1994 - "Other causes of rootless teeth such as odontodysplasia, dentin dysplasia, trauma, infection, radiation therapy, and neoplasia were excluded from her history and clinical and radiographic findings. "
|4.||coronal Dentin dysplasiaIBA
07/01/1989 - "Dentin Dysplasia Type II is a rare heritable dentin defect, of radiopaque foci resembling free pulp stones. "
12/01/1974 - "Dentin dysplasia, type II, or dentin dysplasia, coronal type."
10/01/1997 - "However, unlike dentinogenesis imperfecta, the permanent teeth in dentin dysplasia, type II are normal in color and, on radiographs, have a thistle-tube pulp chamber configuration with pulp stones. "
03/01/2014 - "We report a rare case of hereditary enamel defect with taurodontism associated with interradicular dentin dysplasia. "
03/01/2014 - "Interradicular dentin dysplasia associated with amelogenesis imperfecta with taurodontism or trichodentoosseous syndrome: a diagnostic dilemma."
09/01/2007 - "Patients with CS may present oral defects, such as cleft soft palate, hypodontia, hyperdontia, and delayed tooth eruption, but also unusual associations of major dental anomalies such as taurodontism, microdontia, multiple dens invaginatus, and dentin dysplasia. "
03/01/2014 - "Dental anomalies were divided into four types: (a) shape (including fusion, taurodontism, and dens invagination); (b) number (including hypodontia, oligodontia, and hyperdontia); (c) structure (including amelogenesis imperfecta, dentinogenesis imperfecta, and dentin dysplasia); and (d) position (including displacement, impaction, and dilacerations). "
06/01/1999 - "Dentin dysplasia, type II, is an inherited autosomal dominant disorder in which primary teeth are amber and translucent, with pulp chambers obliterated by abnormal dentin. "
02/01/2003 - "Dentinogenesis imperfecta (DI), which is sometimes an accompanying symptom of OI, belongs to a group of genetically conditioned dentin dysplasias and is characterized clinically by an opalescent amber appearance of the dentin. "
10/01/1992 - "It is suggested that an inherited collagen abnormality in a component common to dentin, skin, ligament and tendon probably explains both EDS I and the dentin dysplasia."
04/06/2001 - "Dentin extracellular matrix components such as type I and III collagens are increased and deposited abnormally in the dental pulp, similar to the hereditary human tooth disorders such as dentin dysplasia and dentinogenesis imperfecta. "
|8.||Collagen Type III (Type III Collagen)IBA
|9.||RNA Splice SitesIBA
|10.||Dental Implants (Dental Implant)IBA
|1.||Crowns (Crown, Dental)
01/01/2013 - "Dentin dysplasia type I is a rare hereditary disturbance of dentin formation characterised clinically by nearly normal appearing crowns and hypermobility of teeth that affects one in every 100,000 individuals and manifests in both primary and permanent dentitions. "
07/01/2004 - "Dentin dysplasia type I is a rare hereditary disturbance of dentin formation characterized clinically by nearly normal appearing crowns and severe hypermobility of teeth. "
11/01/2014 - "Dentin dysplasia is a rare hereditary disturbance of dentin formation characterized by a defective dentin development with clinically normal-appearing crowns, severe hypermobility of teeth and spontaneous dental abscesses or cysts. "
01/01/2010 - "Dentin dysplasia is a rare hereditary disturbance of dentin formation characterized by defective dentin development with clinically normal appearing crowns, severe hypermobility of teeth and spontaneous dental abscesses or cysts. "
|2.||Bone Transplantation (Bone Grafting)
09/01/2006 - "In this report, we present a case of a young girl affected by dentin dysplasia type I, treated with a combination of onlay bone grafting and a sinus lift technique to accomplish implant placement. "
09/01/2006 - "Dentin dysplasia type I treated with onlay bone grafting, sinus augmentation, and osseointegrated implants."
05/01/2014 - "A Case of Dentin Dysplasia with Full Mouth Rehabilitation: A 3-year Longitudinal Study. "
05/01/2014 - "Although literature reports suggest general guidelines for treatment planning, the present case report describes a full mouth rehabilitation of an 8-year-old female patient with dentin dysplasia. "
05/01/2014 - "A Case of Dentin Dysplasia with Full Mouth Rehabilitation: A 3-year Longitudinal Study."