M Michael Cohen

Summary

Affiliation: Dalhousie University
Country: Canada

Publications

  1. ncbi request reprint Beckwith-Wiedemann syndrome: historical, clinicopathological, and etiopathogenetic perspectives
    M Michael Cohen
    Department of Pediatrics, Dalhousie Univesity, Halifax, Nova Scotia B3H 3J5, Canada
    Pediatr Dev Pathol 8:287-304. 2005
  2. ncbi request reprint Proteus syndrome: an update
    M Michael Cohen
    Dalhousie University, Halifax, Nova Scotia, Canada
    Am J Med Genet C Semin Med Genet 137:38-52. 2005
  3. ncbi request reprint Role of leptin in regulating appetite, neuroendocrine function, and bone remodeling
    M Michael Cohen
    Department of Pediatrics, Dalhousie University, 5981 University Ave, Halifax, Nova Scotia
    Am J Med Genet A 140:515-24. 2006
  4. ncbi request reprint Vascular update: morphogenesis, tumors, malformations, and molecular dimensions
    M Michael Cohen
    Department of Pediatrics, Dalhousie University, 5981 University Ave, Halifax, Nova Scotia B3H 1W2
    Am J Med Genet A 140:2013-38. 2006
  5. ncbi request reprint Holoprosencephaly: clinical, anatomic, and molecular dimensions
    M Michael Cohen
    Department of Pediatrics, Dalhousie University, Halifax, Nova Scotia, Canada
    Birth Defects Res A Clin Mol Teratol 76:658-73. 2006
  6. ncbi request reprint Robert J. Gorlin, 1923-2006: a remembrance
    M Michael Cohen
    Department of Pediatrics, Dalhousie University, Nova Scotia, Canada
    Am J Med Genet A 140:2516-20. 2006
  7. ncbi request reprint The new bone biology: pathologic, molecular, and clinical correlates
    M Michael Cohen
    Department of Pediatrics, Dalhousie University, Halifax, Nova Scotia, Canada
    Am J Med Genet A 140:2646-706. 2006
  8. ncbi request reprint Hemangiomas: their uses and abuses
    M Michael Cohen
    Department of Pediatrics, Dalhousie University, Halifax, Nova Scotia, Canada
    Am J Med Genet A 143:235-40. 2007
  9. ncbi request reprint Genetic drift. Robert J. Gorlin as a humorist
    M Michael Cohen
    Department of Pediatrics, Dalhousie University, Halifax, Nova Scotia, Canada
    Am J Med Genet A 143:1131-4. 2007
  10. doi request reprint Perspectives on craniosynostosis: sutural biology, some well-known syndromes, and some unusual syndromes
    M Michael Cohen
    Department of Pediatrics, Faculty of Medicine, Dalhousie University, Halifax, Nova Scotia, Canada
    J Craniofac Surg 20:646-51. 2009

Detail Information

Publications40

  1. ncbi request reprint Beckwith-Wiedemann syndrome: historical, clinicopathological, and etiopathogenetic perspectives
    M Michael Cohen
    Department of Pediatrics, Dalhousie Univesity, Halifax, Nova Scotia B3H 3J5, Canada
    Pediatr Dev Pathol 8:287-304. 2005
    ..Topics discussed in this article are organized as a series of perspectives: general, historical, epidemiologic, clinical, pathologic, genetic/molecular, diagnostic, and differential diagnostic...
  2. ncbi request reprint Proteus syndrome: an update
    M Michael Cohen
    Dalhousie University, Halifax, Nova Scotia, Canada
    Am J Med Genet C Semin Med Genet 137:38-52. 2005
    ..The etiology is unknown to date. Diagnostic criteria are emphasized because misdiagnosis of Proteus syndrome is common. Finally, evaluation and management are discussed...
  3. ncbi request reprint Role of leptin in regulating appetite, neuroendocrine function, and bone remodeling
    M Michael Cohen
    Department of Pediatrics, Dalhousie University, 5981 University Ave, Halifax, Nova Scotia
    Am J Med Genet A 140:515-24. 2006
    ..The leptin and insulin pathways may interact and may be important in the pathogenesis of the metabolic syndrome...
  4. ncbi request reprint Vascular update: morphogenesis, tumors, malformations, and molecular dimensions
    M Michael Cohen
    Department of Pediatrics, Dalhousie University, 5981 University Ave, Halifax, Nova Scotia B3H 1W2
    Am J Med Genet A 140:2013-38. 2006
    ....
  5. ncbi request reprint Holoprosencephaly: clinical, anatomic, and molecular dimensions
    M Michael Cohen
    Department of Pediatrics, Dalhousie University, Halifax, Nova Scotia, Canada
    Birth Defects Res A Clin Mol Teratol 76:658-73. 2006
    ....
  6. ncbi request reprint Robert J. Gorlin, 1923-2006: a remembrance
    M Michael Cohen
    Department of Pediatrics, Dalhousie University, Nova Scotia, Canada
    Am J Med Genet A 140:2516-20. 2006
  7. ncbi request reprint The new bone biology: pathologic, molecular, and clinical correlates
    M Michael Cohen
    Department of Pediatrics, Dalhousie University, Halifax, Nova Scotia, Canada
    Am J Med Genet A 140:2646-706. 2006
    ....
  8. ncbi request reprint Hemangiomas: their uses and abuses
    M Michael Cohen
    Department of Pediatrics, Dalhousie University, Halifax, Nova Scotia, Canada
    Am J Med Genet A 143:235-40. 2007
    ..It is concluded that the term "segmental hemangioma" is imprecise, ill-advised, misguided, and should be abandoned...
  9. ncbi request reprint Genetic drift. Robert J. Gorlin as a humorist
    M Michael Cohen
    Department of Pediatrics, Dalhousie University, Halifax, Nova Scotia, Canada
    Am J Med Genet A 143:1131-4. 2007
  10. doi request reprint Perspectives on craniosynostosis: sutural biology, some well-known syndromes, and some unusual syndromes
    M Michael Cohen
    Department of Pediatrics, Faculty of Medicine, Dalhousie University, Halifax, Nova Scotia, Canada
    J Craniofac Surg 20:646-51. 2009
    ....
  11. ncbi request reprint Major long-term factors influencing dental education in the twenty-first century
    M Michael Cohen
    Dalhousie University, Halifax, Nova Scotia, Canada
    J Dent Educ 66:360-73; discussion 380-4. 2002
    ....
  12. doi request reprint Genetic Drift. Word smithing in medical genetics
    M Michael Cohen
    Department of Pediatrics, Faculty of Medicine, Dalhousie University, 5981 University Avenue, Halifax, Nova Scotia, Canada B3H 1W2
    Am J Med Genet A 152:1-3. 2010
    ....
  13. doi request reprint Cloverleaf skulls: etiologic heterogeneity and pathogenetic variability
    M Michael Cohen
    Department of Pediatrics, Faculty of Medicine, Dalhousie University, 5981 University Avenue, Halifax, Nova Scotia B3H 1W2, Canada
    J Craniofac Surg 20:652-6. 2009
    ..Another table summarizes the relative frequencies of the cloverleaf skull syndromes...
  14. doi request reprint No man's craniosynostosis: the arcana of sutural knowledge
    M Michael Cohen
    Department of Pediatrics, Faculty of Medicine, Dalhousie University, Halifax, Nova Scotia, Canada
    J Craniofac Surg 23:338-42. 2012
    ....
  15. ncbi request reprint Malformations of the craniofacial region: evolutionary, embryonic, genetic, and clinical perspectives
    M Michael Cohen
    Dalhousie University, Halifax, Nova Scotia, Canada B3H 3J5
    Am J Med Genet 115:245-68. 2002
    ....
  16. ncbi request reprint Persistent hyperinsulinemic hypoglycemia of infancy
    M Michael Cohen
    Department of Oral and Maxillofacial Sciences, Pediatrics, Community Health and Epidemiology, Health Services Administration, and Sociology and Social Anthropology, Dalhousie University, Halifax, Nova Scotia, Canada
    Am J Med Genet A 122:351-3. 2003
    ..PHHI is caused by mutations in SUR1, which is a member of the ATP-binding cassette superfamily, and in Kir6.2, which is a member of the inwardly rectifying family of potassium channels...
  17. ncbi request reprint Some chondrodysplasias with short limbs: molecular perspectives
    M Michael Cohen
    Department of Oral and Maxillofacial Sciences, Dalhousie University, Halifax, Nova Scotia, Canada
    Am J Med Genet 112:304-13. 2002
    ..The latter group includes achondroplasia, hypochondroplasia, thanatophoric dysplasia (types 1 and 2), San Diego platyspondylic dysplasia, and SADDAN...
  18. ncbi request reprint Unclassifiable craniosynostosis phenotypes, FGFR2 Trp290 mutations, acanthosis nigricans, and unpaired cysteine mutations
    M Michael Cohen
    Department of Oral and Maxillofacial Sciences, Dalhousie University, Halifax, Nova Scotia, Canada
    Am J Med Genet 113:1-3. 2002
  19. ncbi request reprint Craniofacial anomalies: Clinical and molecular perspectives
    M Michael Cohen
    Departments of Oral and Maxillofacial Sciences, Pediatrics, Community Health and Epidemiology, Health Services Administration, and Sociology and Social Anthropology, Dalhousie University, Halifax, Nova Scotia, Canada
    Ann Acad Med Singapore 32:244-51. 2003
    ....
  20. ncbi request reprint Mental deficiency, alterations in performance, and CNS abnormalities in overgrowth syndromes
    M Michael Cohen
    Dalhousie University, Halifax, B3H 3J5 Nova Scotia, Canada
    Am J Med Genet C Semin Med Genet 117:49-56. 2003
    ....
  21. ncbi request reprint Craniofacial sutures. Development, disease and treatment. Foreword
    M Michael Cohen
    Dalhousie University, Halifax, Canada
    Front Oral Biol 12:vii-ix. 2008
  22. doi request reprint Holoprosencephaly: A mythologic and teratologic distillate
    M Michael Cohen
    Department of Pediatrics, Dalhousie University, Halifax, Nova Scotia, Canada
    Am J Med Genet C Semin Med Genet 154:8-12. 2010
    ..quot;..
  23. ncbi request reprint Vasculogenesis, angiogenesis, hemangiomas, and vascular malformations
    M Michael Cohen
    Department of Oral and Maxillofacial Sciences, Dalhousie University, Halifax, Nova Scotia, Canada
    Am J Med Genet 108:265-74. 2002
  24. ncbi request reprint The hedgehog signaling network
    M Michael Cohen
    Department of Oral and Maxillofacial Sciences, Dalhousie University, Halifax, Nova Scotia, Canada
    Am J Med Genet A 123:5-28. 2003
    ..Many more factors that are essential for the hedgehog signaling network are also discussed: Megalin, Rab23, Hip, GAS1, PKA, GSK3, CK1, Slimb, SAP18, and CBP...
  25. ncbi request reprint Molecular dimensions of gastrointestinal tumors: some thoughts for digestion
    M Michael Cohen
    Department of Oral and Maxillofacial Sciences, Pediatrics, Community Health and Epidemiology, Health Services Administration, and Sociology and Social Anthropology, Dalhousie University, Halifax, Nova Scotia, Canada
    Am J Med Genet A 122:303-14. 2003
    ....
  26. doi request reprint Hedgehog signaling update
    M Michael Cohen
    Department of Pediatrics, Faculty of Medicine, Dalhousie University, Halifax, Nova Scotia, Canada
    Am J Med Genet A 152:1875-914. 2010
    ....
  27. doi request reprint Genetic drift. Overview of German, Nazi, and Holocaust medicine
    M Michael Cohen
    Department of Pediatrics, Faculty of Medicine, Dalhousie University, Halifax, Nova Scotia, Canada
    Am J Med Genet A 152:687-707. 2010
    ....
  28. ncbi request reprint Teratogenesis of holoprosencephaly
    M Michael Cohen
    Department of Oral and Maxillofacial Sciences, Dalhousie University, Halifax, Nova Scotia, Canada
    Am J Med Genet 109:1-15. 2002
    ....
  29. ncbi request reprint Proteus syndrome: misdiagnosis with PTEN mutations
    M Michael Cohen
    Am J Med Genet A 122:323-4. 2003
  30. ncbi request reprint More on vascular malformations
    M Michael Cohen
    Plast Reconstr Surg 109:2591-4; author reply 2594-5. 2002
  31. ncbi request reprint Bone morphogenetic proteins with some comments on fibrodysplasia ossificans progressiva and NOGGIN
    M Michael Cohen
    Am J Med Genet 109:87-92. 2002
  32. ncbi request reprint Editorial: perspectives on craniosynostosis
    M Michael Cohen
    Am J Med Genet A 136:313-26. 2005
  33. ncbi request reprint Autosomal recessive alobar holoprosencephaly with essentially normal faces
    Mason Barr
    Department of Pediatrics, University of Michigan, Ann Arbor, Michigan 48109, USA
    Am J Med Genet 112:28-30. 2002
    ..A similar family was reported by Khan et al. [1970: Dev Med Child Neurol 12:71-76]. Alobar holoprosencephaly with essentially normal faces has also been observed in infants of diabetic mothers [Barr et al., 1983: J Pediatr 102:565-568]...
  34. ncbi request reprint TGF beta/Smad signaling system and its pathologic correlates
    M Michael Cohen
    Am J Med Genet A 116:1-10. 2003
  35. doi request reprint Segmental hemangioma: the misuse of a term
    M Michael Cohen
    Am J Med Genet A 146:672-3. 2008
  36. ncbi request reprint Neoplasms associated with alterations in fibroblast growth factor receptors
    M Michael Cohen
    Am J Med Genet A 119:97-100. 2003
  37. ncbi request reprint Clinical and molecular diagnosis should be consistent
    Karen W Gripp
    Am J Med Genet A 121:188-9. 2003
  38. ncbi request reprint Infants of diabetic mothers and neonatal small left colon
    M Michael Cohen
    Am J Med Genet A 122:301-2. 2003
  39. ncbi request reprint Reassessment of the Proteus syndrome literature: application of diagnostic criteria to published cases
    Joyce T Turner
    Genetic Diseases Research Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland 20892, USA
    Am J Med Genet A 130:111-22. 2004
    ..This article contains supplementary material, which may be viewed at the American Journal of Medical Genetics website at http://www.interscience.wiley.com/jpages/0148-7299/suppmat/index.html...
  40. ncbi request reprint Seven letters to the editor reporting new findings in patients with holoprosencephaly
    M Michael Cohen
    Am J Med Genet A 136:343-4. 2005