These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

97 related articles for article (PubMed ID: 10586231)

  • 1. Distal hereditary motor neuropathy type II (distal HMN type II): phenotype and molecular genetics.
    Timmerman V; Beuten J; Irobi J; De Jonghe P; Martin JJ; Van Broeckhoven C
    Ann N Y Acad Sci; 1999 Sep; 883():60-4. PubMed ID: 10586231
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Distal Hereditary Motor Neuropathy Type II (Distal HMN Type II): Phenotype and Molecular Genetics.
    Timmerman V; Beuten J; Irobi J; De Jonghe P; Martin JJ; VAN Broeckhoven C
    Ann N Y Acad Sci; 1999 Oct; 883(1):60-64. PubMed ID: 29086966
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Distal hereditary motor neuropathy type II (distal HMN II): mapping of a locus to chromosome 12q24.
    Timmerman V; De Jonghe P; Simokovic S; Löfgren A; Beuten J; Nelis E; Ceuterick C; Martin JJ; Van Broeckhoven C
    Hum Mol Genet; 1996 Jul; 5(7):1065-9. PubMed ID: 8817349
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Exclusion of 5 functional candidate genes for distal hereditary motor neuropathy type II (distal HMN II) linked to 12q24.3.
    Irobi J; Nelis E; Meuleman J; Venken K; De Jonghe P; Van Broeckhoven C; Timmerman V
    Ann Hum Genet; 2001 Nov; 65(Pt 6):517-29. PubMed ID: 11851982
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutation analysis of the human pancreatic phospholipase A2 gene in a family with distal hereditary motor neuropathy type II linked to 12q24.
    Beuten J; De Vriendt E; De Jonghe P; Martin JJ; Van Broeckhoven C; Timmerman V
    Neurosci Lett; 1997 Feb; 223(1):69-71. PubMed ID: 9058425
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Linkage analysis of distal hereditary motor neuropathy type II (distal HMN II) in a single pedigree.
    Timmerman V; Raeymaekers P; Nelis E; De Jonghe P; Muylle L; Ceuterick C; Martin JJ; Van Broeckhoven C
    J Neurol Sci; 1992 May; 109(1):41-8. PubMed ID: 1517763
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A clone contig of 12q24.3 encompassing the distal hereditary motor neuropathy type II gene.
    Irobi J; Tissir F; De Jonghe P; De Vriendt E; Van Broeckhoven C; Timmerman V; Beuten J
    Genomics; 2000 Apr; 65(1):34-43. PubMed ID: 10777663
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular genetics of distal hereditary motor neuropathies.
    Irobi J; De Jonghe P; Timmerman V
    Hum Mol Genet; 2004 Oct; 13 Spec No 2():R195-202. PubMed ID: 15358725
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic epidemiology of Charcot-Marie-Tooth disease.
    Braathen GJ
    Acta Neurol Scand Suppl; 2012; (193):iv-22. PubMed ID: 23106488
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Phenotypic and genotypic heterogeneity in hereditary motor neuronopathy type V: a clinical, electrophysiological and genetic study.
    Auer-Grumbach M; Löscher WN; Wagner K; Petek E; Körner E; Offenbacher H; Hartung HP
    Brain; 2000 Aug; 123 ( Pt 8)():1612-23. PubMed ID: 10908191
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [The genetics of type 1 Charcot-Marie-Tooth disease, the hereditary focal neuropathies and the hereditary distal motor neuropathies].
    Sevilla T
    Rev Neurol; 2000 Jan 1-15; 30(1):71-9. PubMed ID: 10743001
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mutation analysis of 12 candidate genes for distal hereditary motor neuropathy type II (distal HMN II) linked to 12q24.3.
    Irobi J; Nelis E; Verhoeven K; De Vriendt E; Dierick I; De Jonghe P; Van Broeckhoven C; Timmerman V
    J Peripher Nerv Syst; 2002 Jun; 7(2):87-95. PubMed ID: 12090300
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Expanding the spectrum of genes responsible for hereditary motor neuropathies.
    Previtali SC; Zhao E; Lazarevic D; Pipitone GB; Fabrizi GM; Manganelli F; Mazzeo A; Pareyson D; Schenone A; Taroni F; Vita G; Bellone E; Ferrarini M; Garibaldi M; Magri S; Padua L; Pennisi E; Pisciotta C; Riva N; Scaioli V; Scarlato M; Tozza S; Geroldi A; Jordanova A; Ferrari M; Molineris I; Reilly MM; Comi G; Carrera P; Devoto M; Bolino A
    J Neurol Neurosurg Psychiatry; 2019 Oct; 90(10):1171-1179. PubMed ID: 31167812
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Unraveling the genetics of distal hereditary motor neuronopathies.
    Irobi J; Dierick I; Jordanova A; Claeys KG; De Jonghe P; Timmerman V
    Neuromolecular Med; 2006; 8(1-2):131-46. PubMed ID: 16775372
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Construction of a PAC contig within the distal hereditary motor neuropathy type II candidate region at 12q24.
    Irobi J; Timmerman V; De Jonghe P; De Vriendt E; Van Broeckhoven C; Beuten J
    Ann N Y Acad Sci; 1999 Sep; 883():463-5. PubMed ID: 10586274
    [No Abstract]   [Full Text] [Related]  

  • 16. [Genetics of peripheral neuropathies and hereditary ataxias].
    Palau F; Sevilla T
    Neurologia; 1995 Dec; 10 Suppl 1():32-43. PubMed ID: 8838557
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2F) maps to chromosome 7q11-q21.
    Ismailov SM; Fedotov VP; Dadali EL; Polyakov AV; Van Broeckhoven C; Ivanov VI; De Jonghe P; Timmerman V; Evgrafov OV
    Eur J Hum Genet; 2001 Aug; 9(8):646-50. PubMed ID: 11528513
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genotypes & sensory phenotypes in 2 new X-linked neuropathies (CMTX3 and dSMAX) and dominant CMT/HMN overlap syndromes.
    Nicholson G; Kennerson M; Brewer M; Garbern J; Shy M
    Adv Exp Med Biol; 2009; 652():201-6. PubMed ID: 20225027
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Molecular genetics of inherited neuropathies].
    Takashima H
    Rinsho Shinkeigaku; 2006 Jan; 46(1):1-18. PubMed ID: 16541790
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Assignment of a second Charcot-Marie-Tooth type II locus to chromosome 3q.
    Kwon JM; Elliott JL; Yee WC; Ivanovich J; Scavarda NJ; Moolsintong PJ; Goodfellow PJ
    Am J Hum Genet; 1995 Oct; 57(4):853-8. PubMed ID: 7573046
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.