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Journals / Balkan Medical Journal / 2022 / Cilt: 39 - Sayı: 1

Clinical and Genetic Survey for Charcot-Marie-Tooth Neuropathy Based on the Findings in Turkey, a Country with a High Rate of Consanguineous Marriages

Ayşe CANDAYAN
Yeşim PARMAN
Esra BATTALOĞLU
Pages
3–11
Publication Date
2022-10-11
DOI
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CANDAYAN, A., PARMAN, Y., BATTALOĞLU, E. (2022). Clinical and Genetic Survey for Charcot-Marie-Tooth Neuropathy Based on the Findings in Turkey, a Country with a High Rate of Consanguineous Marriages. Balkan Medical Journal, Cilt: 39 - Sayı: 1, 3–11. https://ajindex.com/articles/460767

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References (16)

  1. Pisciotta C, Shy ME. Neuropathy. Handb Clin Neurol. 2018
  2. [CrossRef] 2. De Jonghe P, Timmerman V, Nelis E, Martin JJ, Van Broeckhoven C. Charcot-Marie Tooth disease and related peripheral neuropathies. J Peripher Nerv Syst. 1997
  3. [CrossRef] 3. Laurá M, Pipis M, Rossor AM, Reilly MM. Charcot-marie-Tooth disease and related disorders: An evolving landscape. Curr Opin Neurol. 2019
  4. [CrossRef] 4. Timmerman V, Strickland AV, Züchner S. Genetics of Charcot-Marie-Tooth (CMT) disease within the frame of the human genome project success. Genes (Basel). 2014
  5. [CrossRef] 5. Parman Y, Battaloǧlu E. Recessively transmitted predominantly motor neuropathies. Handb Clin Neurol. 2013
  6. [CrossRef] 6. Rossor AM, Evans MRB, Reilly MM. A practical approach to the genetic neuropathies. Pract Neurol. 2015
  7. [CrossRef] 7. Skre H. Genetic and clinical aspects of Charcot-Marie-Tooth’s disease. Clin Genet. 1974
  8. [CrossRef] 8. Barreto LC, Oliveira FS, Nunes PS, et al. Epidemiologic Study of Charcot-Marie Tooth Disease: A Systematic Review. Neuroepidemiology. 2016
  9. [CrossRef] 9. Bird TD, Ott J, Giblett ER. Evidence for linkage of Charcot-Marie-Tooth neuropathy to the Duffy locus on chromosome 1. Am J Hum Genet. 1982
  10. [CrossRef] 10. Lupski JR, de Oca-Luna RM, Slaugenhaupt S, et al. DNA duplication associated with Charcot-Marie-Tooth disease type 1A. Cell. 1991
  11. [CrossRef] 11. Parman Y, Battaloǧlu E, Baris I, Bilir B, et al. Clinicopathological and genetic study of early-onset demyelinating neuropathy. Brain. 2004
  12. [CrossRef] 12. Pareyson D, Scaioli, Laurà M. Clinical and Electrophysiological Aspects of Charcot Marie-Tooth Disease. Neuromolecular Med. 2006
  13. [CrossRef] 13. Davis CJ, Bradley WG, Madrid R. The peroneal muscular atrophy syndrome: clinical, genetic, electrophysiological and nerve biopsy studies. I. Clinical, genetic and electrophysiological findings and classification. J Genet Hum. 1978
  14. [CrossRef] 14. Nave KA, Sereda MW, Ehrenreich H. Mechanisms of disease: Inherited demyelinating neuropathies - From basic to clinical research. Nat Clin Pract Neurol. 2007
  15. [CrossRef] 15. Siskind CE, Panchal S, Smith CO, et al. A review of genetic counseling for Charcot Marie Tooth disease (CMT). J Genet Couns. 2013
  16. [CrossRef] 16. Brennan KM, Bai Y, Shy ME. Demyelinating CMT -- what’s known, what’s new and what’s in store? Neurosc