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 *

139 related articles for article (PubMed ID: 9631399)

  • 41. Hereditary motor and sensory neuropathy type 2C is genetically distinct from types 2B and 2D.
    Nagamatsu M; Jenkins RB; Schaid DJ; Klein DM; Dyck PJ
    Arch Neurol; 2000 May; 57(5):669-72. PubMed ID: 10815132
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Chronic inflammatory demyelinating polyneuropathy or hereditary motor and sensory neuropathy? Diagnostic value of morphological criteria.
    Gabreëls-Festen AA; Gabreëls FJ; Hoogendijk JE; Bolhuis PA; Jongen PJ; Vingerhoets HM
    Acta Neuropathol; 1993; 86(6):630-5. PubMed ID: 8310819
    [TBL] [Abstract][Full Text] [Related]  

  • 43. A new type of hereditary motor and sensory neuropathy linked to chromosome 3.
    Takashima H; Nakagawa M; Nakahara K; Suehara M; Matsuzaki T; Higuchi I; Higa H; Arimura K; Iwamasa T; Izumo S; Osame M
    Ann Neurol; 1997 Jun; 41(6):771-80. PubMed ID: 9189038
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Absence of linkage of hereditary motor and sensory neuropathy type I to chromosome 1 markers.
    Middleton-Price HR; Harding AE; Berciano J; Pastor JM; Huson SM; Malcolm S
    Genomics; 1989 Feb; 4(2):192-7. PubMed ID: 2737679
    [TBL] [Abstract][Full Text] [Related]  

  • 45. PMP-22 gene duplications and deletions identified in archival, paraffin-embedded sural nerve biopsy specimens: correlation to structural changes.
    Thiex R; Schröder JM
    Acta Neuropathol; 1998 Jul; 96(1):13-21. PubMed ID: 9678509
    [TBL] [Abstract][Full Text] [Related]  

  • 46. 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]  

  • 47. The TRK-fused gene is mutated in hereditary motor and sensory neuropathy with proximal dominant involvement.
    Ishiura H; Sako W; Yoshida M; Kawarai T; Tanabe O; Goto J; Takahashi Y; Date H; Mitsui J; Ahsan B; Ichikawa Y; Iwata A; Yoshino H; Izumi Y; Fujita K; Maeda K; Goto S; Koizumi H; Morigaki R; Ikemura M; Yamauchi N; Murayama S; Nicholson GA; Ito H; Sobue G; Nakagawa M; Kaji R; Tsuji S
    Am J Hum Genet; 2012 Aug; 91(2):320-9. PubMed ID: 22883144
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Clinical and electrodiagnostic findings, nerve biopsy and blood group markers in a family with hereditary neuropathy with liability to pressure palsies.
    Leblhuber F; Reisecker F; Willeit J; Windhager E; Witzmann A; Mayr WR
    Acta Neurol Scand; 1991 Mar; 83(3):166-71. PubMed ID: 1827702
    [TBL] [Abstract][Full Text] [Related]  

  • 49. [Screening for hereditary neuromuscular disorders with molecular genetic methods in the Roma population of Hungary].
    Herczegfalvi A; Pikó H; Karcagi V
    Ideggyogy Sz; 2008 Nov; 61(11-12):426-30. PubMed ID: 19070320
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Coexistence of hereditary motor and sensory neuropathy type Ia and IgM paraproteinemic neuropathy.
    Gregory R; Thomas PK; King RH; Hallam PL; Malcolm S; Hughes RA; Harding AE
    Ann Neurol; 1993 Jun; 33(6):649-52. PubMed ID: 8498845
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Demyelinating hereditary neuropathies in children: a morphometric and ultrastructural study.
    Guzzetta F; Rodríguez J; Deodato M; Guzzetta A; Ferrière G
    Histol Histopathol; 1995 Jan; 10(1):91-104. PubMed ID: 7756749
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Gene for hereditary motor and sensory neuropathy (proximal dominant form) mapped to 3q13.1.
    Takashima H; Nakagawa M; Suehara M; Saito M; Saito A; Kanzato N; Matsuzaki T; Hirata K; Terwilliger JD; Osame M
    Neuromuscul Disord; 1999 Oct; 9(6-7):368-71. PubMed ID: 10545038
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Gene for hereditary neuropathy with liability to pressure palsies (HNPP) maps to chromosome 17 at or close to the locus for HMSN type 1.
    Mariman EC; Gabreëls-Festen AA; van Beersum SE; Jongen PJ; Ropers HH; Gabreëls FJ
    Hum Genet; 1993 Aug; 92(1):87-90. PubMed ID: 8396068
    [TBL] [Abstract][Full Text] [Related]  

  • 54. A new variant of sensory ataxic neuropathy with autosomal dominant inheritance.
    van Dijk GW; Wokke JH; Oey PL; Franssen H; Ippel PF; Veldman H
    Brain; 1995 Dec; 118 ( Pt 6)():1557-63. PubMed ID: 8595484
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Sural nerve pathology in TFG-associated motor neuron disease with sensory neuropathy.
    Li J; Meng L; Wu R; Xie Z; Gang Q; Zhang W; Wang Z; Yuan Y
    Neuropathology; 2019 Jun; 39(3):194-199. PubMed ID: 30957313
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Motor-sensory neuropathy without minifascicles in a patient with 46XY gonadal dysgenesis.
    Malandrini A; Gambelli S; Muglia M; Berti G; Gaudiano C; Patitucci A; Sugie K; Umehara F; Quattrone A; Dotti MT; Federico A
    Brain Dev; 2008 Apr; 30(4):291-4. PubMed ID: 17768021
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Hereditary motor and sensory neuropathy with deafness, mental retardation, and absence of sensory large myelinated fibers: confirmation of a new entity.
    Sabatelli M; Mignogna T; Lippi G; Servidei S; Zollino M; Padua L; Lo Monaco M; De Armas L; Mereu ML; Tonali P
    Am J Med Genet; 1998 Jan; 75(3):309-13. PubMed ID: 9475604
    [TBL] [Abstract][Full Text] [Related]  

  • 58. [Hereditary neuropathy with liability to pressure palsy].
    Eisenberg E; Baron S; Ludicer R
    Harefuah; 1989 Apr; 116(7):345-7. PubMed ID: 2737556
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Identification of novel TFG mutation in HMSN-P pedigree: Emphasis on variable clinical presentations.
    Khani M; Shamshiri H; Alavi A; Nafissi S; Elahi E
    J Neurol Sci; 2016 Oct; 369():318-323. PubMed ID: 27653917
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Early clinical and electrophysiologic features of the two most common autosomal recessive forms of Charcot-Marie-Tooth disease in the Roma (Gypsies).
    Guergueltcheva V; Tournev I; Bojinova V; Hantke J; Litvinenko I; Ishpekova B; Shmarov A; Petrova J; Jordanova A; Kalaydjieva L
    J Child Neurol; 2006 Jan; 21(1):20-5. PubMed ID: 16551448
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.