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Journal Abstract Search


129 related items for PubMed ID: 29877907

  • 1. Heterozygosity for CMT Type 4 Predicts a Severe Vincristine-induced Polyneuropathy Phenotype: A Case Report and Review of Literature.
    Sy A, Cheng J, Cooper R, Mueller L.
    J Pediatr Hematol Oncol; 2019 Jan; 41(1):e41-e43. PubMed ID: 29877907
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  • 4. Vincristine neuropathy in type I and type II Charcot-Marie-Tooth disease (hereditary motor sensory neuropathy).
    Igarashi M, Thompson EI, Rivera GK.
    Med Pediatr Oncol; 1995 Aug; 25(2):113-6. PubMed ID: 7603395
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  • 5. Charcot-Marie-Tooth disease type I diagnosed in a 5-year-old boy after vincristine neurotoxicity, resulting in maternal diagnosis.
    Olek MJ, Bordeaux B, Leshner RT.
    J Am Osteopath Assoc; 1999 Mar; 99(3):165-7. PubMed ID: 10217912
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  • 11. Vincristine treatment revealing asymptomatic hereditary motor sensory neuropathy type 1A.
    Mercuri E, Poulton J, Buck J, Broadbent V, Bamford M, Jungbluth H, Manzur AY, Muntoni F.
    Arch Dis Child; 1999 Nov; 81(5):442-3. PubMed ID: 10519723
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  • 15. Acute vincristine neurotoxicity in the presence of hereditary motor and sensory neuropathy type I.
    McGuire SA, Gospe SM, Dahl G.
    Med Pediatr Oncol; 1989 Nov; 17(6):520-3. PubMed ID: 2685529
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  • 16. Genetic epidemiology of Charcot-Marie-Tooth disease.
    Braathen GJ.
    Acta Neurol Scand Suppl; 2012 Nov; (193):iv-22. PubMed ID: 23106488
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