M J Aldred

Summary

Country: Australia

Publications

  1. ncbi request reprint Clinical and radiographic features of a family with autosomal dominant amelogenesis imperfecta with taurodontism
    M J Aldred
    Department of Dentistry, Royal Children s Hospital, Melbourne, Australia
    Oral Dis 8:62-8. 2002
  2. pmc Amelogenesis imperfecta
    Peter J M Crawford
    Paediatric Dentistry, Division of Child Dental Health, Dental School, Lower Maudlin St, Bristol BS1 2LY, UK
    Orphanet J Rare Dis 2:17. 2007
  3. ncbi request reprint Oral medicine and oral pathology--the impact of electronic information
    Michael J Aldred
    Faculty of Oral Pathology, Royal College of Pathologists of Australasia, Surry Hills, New South Wales
    Ann R Australas Coll Dent Surg 16:60-2. 2002
  4. ncbi request reprint It's only teeth - are there limits to genetic testing?
    M Aldred
    Department of Dentistry, Royal Children s Hospital, Melbourne, Australia
    Clin Genet 63:333-9. 2003
  5. ncbi request reprint Amelogenesis imperfecta: a classification and catalogue for the 21st century
    M J Aldred
    Department of Dentistry, Royal Children s Hospital, Melbourne, Australia
    Oral Dis 9:19-23. 2003
  6. ncbi request reprint Molecular analysis for genetic counselling in amelogenesis imperfecta
    M J Aldred
    Department of Dentistry, Royal Children s Hospital, Melbourne, Australia
    Oral Dis 8:249-53. 2002
  7. ncbi request reprint Identification of a locus on chromosome 2q11 at which recessive amelogenesis imperfecta and cone-rod dystrophy cosegregate
    Louise M Downey
    Molecular Medicine Unit, CSB, St James s University Hospital, Leeds University, Leeds LS9 7TF UK
    Eur J Hum Genet 10:865-9. 2002
  8. ncbi request reprint Enamel defects and Lyonization in focal dermal hypoplasia
    Richard Balmer
    Leeds Dental Institute, Leeds, United Kingdom
    Oral Surg Oral Med Oral Pathol Oral Radiol Endod 98:686-91. 2004
  9. ncbi request reprint DLX3 mutation associated with autosomal dominant amelogenesis imperfecta with taurodontism
    Juan Dong
    Department of Pediatric Dentistry, Dental School, University of Texas Health Science Center at San Antonio, 7703 Floyd Curl Drive, MC 7888, San Antonio, TX 78229, USA
    Am J Med Genet A 133:138-41. 2005
  10. ncbi request reprint Dental findings in a family with hyperparathyroidism-jaw tumor syndrome and a novel HRPT2 gene mutation
    Michael J Aldred
    Dorevitch Pathology, Victoria 3084, Australia
    Oral Surg Oral Med Oral Pathol Oral Radiol Endod 101:212-8. 2006

Collaborators

Detail Information

Publications10

  1. ncbi request reprint Clinical and radiographic features of a family with autosomal dominant amelogenesis imperfecta with taurodontism
    M J Aldred
    Department of Dentistry, Royal Children s Hospital, Melbourne, Australia
    Oral Dis 8:62-8. 2002
    ....
  2. pmc Amelogenesis imperfecta
    Peter J M Crawford
    Paediatric Dentistry, Division of Child Dental Health, Dental School, Lower Maudlin St, Bristol BS1 2LY, UK
    Orphanet J Rare Dis 2:17. 2007
    ..In infancy, the primary dentition may be protected by the use of preformed metal crowns on posterior teeth. The longer-term care involves either crowns or, more frequently these days, adhesive, plastic restorations...
  3. ncbi request reprint Oral medicine and oral pathology--the impact of electronic information
    Michael J Aldred
    Faculty of Oral Pathology, Royal College of Pathologists of Australasia, Surry Hills, New South Wales
    Ann R Australas Coll Dent Surg 16:60-2. 2002
    ..Without doubt these mechanisms will be further developed and refined in the present century...
  4. ncbi request reprint It's only teeth - are there limits to genetic testing?
    M Aldred
    Department of Dentistry, Royal Children s Hospital, Melbourne, Australia
    Clin Genet 63:333-9. 2003
    ..The questions we pose are whether these approaches are appropriate. We hope that this review will stimulate debate on these issues...
  5. ncbi request reprint Amelogenesis imperfecta: a classification and catalogue for the 21st century
    M J Aldred
    Department of Dentistry, Royal Children s Hospital, Melbourne, Australia
    Oral Dis 9:19-23. 2003
    ..We argue that this system is of more benefit to these individuals and families than previous classifications...
  6. ncbi request reprint Molecular analysis for genetic counselling in amelogenesis imperfecta
    M J Aldred
    Department of Dentistry, Royal Children s Hospital, Melbourne, Australia
    Oral Dis 8:249-53. 2002
    ..To use molecular genetics to establish the mode of inheritance in a family with amelogenesis imperfecta...
  7. ncbi request reprint Identification of a locus on chromosome 2q11 at which recessive amelogenesis imperfecta and cone-rod dystrophy cosegregate
    Louise M Downey
    Molecular Medicine Unit, CSB, St James s University Hospital, Leeds University, Leeds LS9 7TF UK
    Eur J Hum Genet 10:865-9. 2002
    ..It remains to be established whether this pedigree is segregating two closely linked mutations causing disparate phenotypes or whether a single defect is causing pathology in both teeth and eyes...
  8. ncbi request reprint Enamel defects and Lyonization in focal dermal hypoplasia
    Richard Balmer
    Leeds Dental Institute, Leeds, United Kingdom
    Oral Surg Oral Med Oral Pathol Oral Radiol Endod 98:686-91. 2004
    ..This supports the proposal that focal dermal hypoplasia is X-linked. The authors conclude that the pattern of dental defects in focal dermal hypoplasia is consistent with Lyonization...
  9. ncbi request reprint DLX3 mutation associated with autosomal dominant amelogenesis imperfecta with taurodontism
    Juan Dong
    Department of Pediatric Dentistry, Dental School, University of Texas Health Science Center at San Antonio, 7703 Floyd Curl Drive, MC 7888, San Antonio, TX 78229, USA
    Am J Med Genet A 133:138-41. 2005
    ..Previous studies have shown a DLX3 mutation outside the homeodomain associated with tricho-dento-osseous syndrome (TDO) suggesting TDO and some forms of AIHHT are allelic...
  10. ncbi request reprint Dental findings in a family with hyperparathyroidism-jaw tumor syndrome and a novel HRPT2 gene mutation
    Michael J Aldred
    Dorevitch Pathology, Victoria 3084, Australia
    Oral Surg Oral Med Oral Pathol Oral Radiol Endod 101:212-8. 2006
    ..Cemento-ossifying fibroma is the preferred term to better reflect the pathologies found in most individuals and families,and to emphasize the significance of the jaw lesions in the diagnosis of the syndrome...