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 *

327 related articles for article (PubMed ID: 32298515)

  • 1. Molecular analysis and clinical diversity of distal hereditary motor neuropathy.
    Liu X; Duan X; Zhang Y; Sun A; Fan D
    Eur J Neurol; 2020 Jul; 27(7):1319-1326. PubMed ID: 32298515
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Genetic distribution in Chinese patients with hereditary peripheral neuropathy].
    Liu XX; Duan XH; Zhang S; Sun AP; Zhang YS; Fan DS
    Beijing Da Xue Xue Bao Yi Xue Ban; 2022 Oct; 54(5):874-883. PubMed ID: 36241230
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Distal hereditary motor neuropathies: Mutation spectrum and genotype-phenotype correlation.
    Frasquet M; Rojas-García R; Argente-Escrig H; Vázquez-Costa JF; Muelas N; Vílchez JJ; Sivera R; Millet E; Barreiro M; Díaz-Manera J; Turon-Sans J; Cortés-Vicente E; Querol L; Ramírez-Jiménez L; Martínez-Rubio D; Sánchez-Monteagudo A; Espinós C; Sevilla T; Lupo V
    Eur J Neurol; 2021 Apr; 28(4):1334-1343. PubMed ID: 33369814
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Further evidence for genetic heterogeneity of distal HMN type V, CMT2 with predominant hand involvement and Silver syndrome.
    Rohkamm B; Reilly MM; Lochmüller H; Schlotter-Weigel B; Barisic N; Schöls L; Nicholson G; Pareyson D; Laurà M; Janecke AR; Miltenberger-Miltenyi G; John E; Fischer C; Grill F; Wakeling W; Davis M; Pieber TR; Auer-Grumbach M
    J Neurol Sci; 2007 Dec; 263(1-2):100-6. PubMed ID: 17663003
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular genetics and mechanisms of disease in distal hereditary motor neuropathies: insights directing future genetic studies.
    Drew AP; Blair IP; Nicholson GA
    Curr Mol Med; 2011 Nov; 11(8):650-65. PubMed ID: 21902652
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Heat shock protein 27 R127W mutation: evidence of a continuum between axonal Charcot-Marie-Tooth and distal hereditary motor neuropathy.
    Solla P; Vannelli A; Bolino A; Marrosu G; Coviello S; Murru MR; Tranquilli S; Corongiu D; Benedetti S; Marrosu MG
    J Neurol Neurosurg Psychiatry; 2010 Sep; 81(9):958-62. PubMed ID: 20660910
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Distal hereditary motor neuropathies.
    Tazir M; Nouioua S
    Rev Neurol (Paris); 2024 Dec; 180(10):1031-1036. PubMed ID: 38702287
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mitochondrial dynamics and inherited peripheral nerve diseases.
    Pareyson D; Saveri P; Sagnelli A; Piscosquito G
    Neurosci Lett; 2015 Jun; 596():66-77. PubMed ID: 25847151
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Charcot-Marie-Tooth type 2 and distal hereditary motor neuropathy: Clinical, neurophysiological and genetic findings from a single-centre experience.
    Luigetti M; Fabrizi GM; Bisogni G; Romano A; Taioli F; Ferrarini M; Bernardo D; Rossini PM; Sabatelli M
    Clin Neurol Neurosurg; 2016 May; 144():67-71. PubMed ID: 26989944
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Clinical features of a family with late-onset distal hereditary motor neuropathy harboring p.Pro39Leu variant of HSPB1.
    Naruse H; Okubo S; Sudo A; Mitsui J; Mikata T; Ishiura H; Morishita S; Tsuji S; Toda T
    J Peripher Nerv Syst; 2023 Sep; 28(3):518-521. PubMed ID: 37249095
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The distal hereditary motor neuropathies.
    Rossor AM; Kalmar B; Greensmith L; Reilly MM
    J Neurol Neurosurg Psychiatry; 2012 Jan; 83(1):6-14. PubMed ID: 22028385
    [TBL] [Abstract][Full Text] [Related]  

  • 13. ALS5/SPG11/KIAA1840 mutations cause autosomal recessive axonal Charcot-Marie-Tooth disease.
    Montecchiani C; Pedace L; Lo Giudice T; Casella A; Mearini M; Gaudiello F; Pedroso JL; Terracciano C; Caltagirone C; Massa R; St George-Hyslop PH; Barsottini OG; Kawarai T; Orlacchio A
    Brain; 2016 Jan; 139(Pt 1):73-85. PubMed ID: 26556829
    [TBL] [Abstract][Full Text] [Related]  

  • 14. HSJ1-related hereditary neuropathies: novel mutations and extended clinical spectrum.
    Gess B; Auer-Grumbach M; Schirmacher A; Strom T; Zitzelsberger M; Rudnik-Schöneborn S; Röhr D; Halfter H; Young P; Senderek J
    Neurology; 2014 Nov; 83(19):1726-32. PubMed ID: 25274842
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Assessment of Targeted Next-Generation Sequencing as a Tool for the Diagnosis of Charcot-Marie-Tooth Disease and Hereditary Motor Neuropathy.
    Lupo V; García-García F; Sancho P; Tello C; García-Romero M; Villarreal L; Alberti A; Sivera R; Dopazo J; Pascual-Pascual SI; Márquez-Infante C; Casasnovas C; Sevilla T; Espinós C
    J Mol Diagn; 2016 Mar; 18(2):225-34. PubMed ID: 26752306
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mutations in heat shock protein beta-1 (HSPB1) are associated with a range of clinical phenotypes related to different patterns of motor neuron dysfunction: A case series.
    Katz M; Davis M; Garton FC; Henderson R; Bharti V; Wray N; McCombe P
    J Neurol Sci; 2020 Jun; 413():116809. PubMed ID: 32334137
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Frequent genes in rare diseases: panel-based next generation sequencing to disclose causal mutations in hereditary neuropathies.
    Dohrn MF; Glöckle N; Mulahasanovic L; Heller C; Mohr J; Bauer C; Riesch E; Becker A; Battke F; Hörtnagel K; Hornemann T; Suriyanarayanan S; Blankenburg M; Schulz JB; Claeys KG; Gess B; Katona I; Ferbert A; Vittore D; Grimm A; Wolking S; Schöls L; Lerche H; Korenke GC; Fischer D; Schrank B; Kotzaeridou U; Kurlemann G; Dräger B; Schirmacher A; Young P; Schlotter-Weigel B; Biskup S
    J Neurochem; 2017 Dec; 143(5):507-522. PubMed ID: 28902413
    [TBL] [Abstract][Full Text] [Related]  

  • 18. HSPB1 and HSPB8 in inherited neuropathies: study of an Italian cohort of dHMN and CMT2 patients.
    Capponi S; Geroldi A; Fossa P; Grandis M; Ciotti P; Gulli R; Schenone A; Mandich P; Bellone E
    J Peripher Nerv Syst; 2011 Dec; 16(4):287-94. PubMed ID: 22176143
    [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.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 17.