BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

1053 related articles for article (PubMed ID: 10962051)

  • 1. Neurophysiology and molecular genetics of Charcot-Marie-Tooth type 1 neuropathy in Croatian children: follow-up study.
    Barisić N; Mihatov I
    Croat Med J; 2000 Sep; 41(3):306-13. PubMed ID: 10962051
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Patients homozygous for the 17p11.2 duplication in Charcot-Marie-Tooth type 1A disease.
    LeGuern E; Gouider R; Mabin D; Tardieu S; Birouk N; Parent P; Bouche P; Brice A
    Ann Neurol; 1997 Jan; 41(1):104-8. PubMed ID: 9005872
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Neurophysiologic abnormalities in children with Charcot-Marie-Tooth disease type 1A.
    Yiu EM; Burns J; Ryan MM; Ouvrier RA
    J Peripher Nerv Syst; 2008 Sep; 13(3):236-41. PubMed ID: 18844790
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2): phenotype-genotype correlations in 13 Moroccan families.
    Bouhouche A; Birouk N; Azzedine H; Benomar A; Durosier G; Ente D; Muriel MP; Ruberg M; Slassi I; Yahyaoui M; Dubourg O; Ouazzani R; LeGuern E
    Brain; 2007 Apr; 130(Pt 4):1062-75. PubMed ID: 17347251
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clinical and pathological phenotype of the original family with Charcot-Marie-Tooth type 1B: a 20-year study.
    Bird TD; Kraft GH; Lipe HP; Kenney KL; Sumi SM
    Ann Neurol; 1997 Apr; 41(4):463-9. PubMed ID: 9124803
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Screening of dominantly inherited Charcot-Marie-Tooth neuropathies.
    Ionasescu VV; Ionasescu R; Searby C
    Muscle Nerve; 1993 Nov; 16(11):1232-8. PubMed ID: 8413376
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Gene dosage is a mechanism for Charcot-Marie-Tooth disease type 1A.
    Lupski JR; Wise CA; Kuwano A; Pentao L; Parke JT; Glaze DG; Ledbetter DH; Greenberg F; Patel PI
    Nat Genet; 1992 Apr; 1(1):29-33. PubMed ID: 1301995
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Duplication of the PMP22 gene in 17p partial trisomy patients with Charcot-Marie-Tooth type-1 neuropathy.
    Roa BB; Greenberg F; Gunaratne P; Sauer CM; Lubinsky MS; Kozma C; Meck JM; Magenis RE; Shaffer LG; Lupski JR
    Hum Genet; 1996 May; 97(5):642-9. PubMed ID: 8655146
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Is the duplication present in all family members affected with Charcot-Marie-Tooth neuropathy type 1 A?
    Ionăşescu V; Ionăşescu G; Searby C; Barker DF
    Rom J Neurol Psychiatry; 1993; 31(3-4):179-87. PubMed ID: 8011481
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Overview of Charcot-Marie-Tooth disease type 1A.
    Thomas PK
    Ann N Y Acad Sci; 1999 Sep; 883():1-5. PubMed ID: 10586223
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Charcot-Marie-Tooth type 1A duplication appears to arise from recombination at repeat sequences flanking the 1.5 Mb monomer unit.
    Pentao L; Wise CA; Chinault AC; Patel PI; Lupski JR
    Nat Genet; 1992 Dec; 2(4):292-300. PubMed ID: 1303282
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Charcot-Marie-Tooth disease type 1A: a family study with microsatellites.
    Qu Y; Carpenter NJ; Whetsell L; Smith SP; Say B
    J Okla State Med Assoc; 1996 Nov; 89(11):395-9. PubMed ID: 8972170
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Charcot-Marie-Tooth type X: A novel mutation in the Cx32 gene with central conduction slowing.
    Seeman P; Mazanec R; Ctvrtecková M; Smilková D
    Int J Mol Med; 2001 Oct; 8(4):461-8. PubMed ID: 11562788
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Hereditary motor and sensory neuropathy type I: clinical and neurographical features of the 17p duplication subtype.
    Hoogendijk JE; De Visser M; Bolhuis PA; Hart AA; Ongerboer de Visser BW
    Muscle Nerve; 1994 Jan; 17(1):85-90. PubMed ID: 8264707
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genotype/phenotype correlations in X-linked dominant Charcot-Marie-Tooth disease.
    Hahn AF; Bolton CF; White CM; Brown WF; Tuuha SE; Tan CC; Ainsworth PJ
    Ann N Y Acad Sci; 1999 Sep; 883():366-82. PubMed ID: 10586261
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Severe vincristine neuropathy in Charcot-Marie-Tooth disease type 1A.
    Graf WD; Chance PF; Lensch MW; Eng LJ; Lipe HP; Bird TD
    Cancer; 1996 Apr; 77(7):1356-62. PubMed ID: 8608515
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Studies of electromyography and genetics in children with Charcot-Marie-Tooth disease type 1].
    Pan XL; Zhang NN; Ye HL; Zhao YF; Gao H
    Zhongguo Dang Dai Er Ke Za Zhi; 2011 Aug; 13(8):647-50. PubMed ID: 21849115
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A patient with both Charcot-Marie-Tooth disease (CMT 1A) and mild spinal muscular atrophy (SMA 3).
    Jedrzejowska M; Ryniewicz B; Kabzińska D; Drac H; Hausmanowa-Petrusewicz I; Kochański A
    Neuromuscul Disord; 2008 Apr; 18(4):339-41. PubMed ID: 18337101
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A large family with Charcot-Marie-Tooth Type 1a and Type 2 diabetes mellitus.
    Koç F; Sarica Y; Yerdelen D; Baris I; Battaloglu E; Sert M
    Int J Neurosci; 2006 Feb; 116(2):103-14. PubMed ID: 16393877
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [A family of early childhood-onset Charcot-Marie-Tooth disease type 2].
    Hinuma Y; Aoki M; Takahashi T; Tateyama M; Nagai M; Yoshioka M; Itoyama Y
    Rinsho Shinkeigaku; 2001 Jan; 41(1):64-7. PubMed ID: 11433771
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 53.