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 *

121 related articles for article (PubMed ID: 15395775)

  • 61. Clinical and genetic description of a family with Charcot-Marie-Tooth disease type 1B from a transmembrane MPZ mutation.
    Eggers SD; Keswani SC; Melli G; Cornblath DR
    Muscle Nerve; 2004 Jun; 29(6):867-9. PubMed ID: 15170620
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Lipid abnormalities in hereditary neuropathy. Part 3. Plasma and erythrocyte lipids of HMSN-III (Dejerine-Sottas disease).
    Yao JK; Dyck PJ
    J Neurol Sci; 1978 Aug; 38(1):59-65. PubMed ID: 702184
    [TBL] [Abstract][Full Text] [Related]  

  • 63. [Isolated paralysis of the external popliteal sciatic nerve. Moneneuritis form of Déjerine-Sottas disease].
    May V; Glowinski J; Beraneck L
    Rev Rhum Mal Osteoartic; 1978 Apr; 45(4):301-4. PubMed ID: 675117
    [No Abstract]   [Full Text] [Related]  

  • 64. Charcot-Marie-Tooth disease associated with "essential tremor": Report of 7 cases and a review of the literature.
    Salisachs P
    J Neurol Sci; 1976 May; 28(1):17-40. PubMed ID: 932772
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Subarachnoid block and enlargement of the spinal canal in hypertrophic neuritis.
    De León GA; Hodges FJ
    J Neurol Sci; 1976 Jun; 28(2):139-46. PubMed ID: 1271079
    [TBL] [Abstract][Full Text] [Related]  

  • 66. [Neural muscular atrophy and hypertrophic neuritis; clinical and genealogical data in relation to a family of Bern canton].
    LUBAN B
    Schweiz Arch Neurol Psychiatr; 1951; 68(1):34-63. PubMed ID: 14876368
    [No Abstract]   [Full Text] [Related]  

  • 67. Occurrence of Optic Neuritis and Cervical Cord Schwannoma with Charcot-Marie-Tooth Type 4B1 Disease.
    Scott P; Bruwer Z; Al-Kharusi K; Meftah D; Al-Murshedi F
    Oman Med J; 2016 May; 31(3):227-30. PubMed ID: 27162595
    [TBL] [Abstract][Full Text] [Related]  

  • 68. The pathology of charcot-marie-tooth disease and related disorders.
    Thomas PK; King RH; Small JR; Robertson AM
    Neuropathol Appl Neurobiol; 1996 Aug; 22(4):269-84. PubMed ID: 8875461
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Clinical phenotypes of different MPZ (P0) mutations may include Charcot-Marie-Tooth type 1B, Dejerine-Sottas, and congenital hypomyelination.
    Warner LE; Hilz MJ; Appel SH; Killian JM; Kolodry EH; Karpati G; Carpenter S; Watters GV; Wheeler C; Witt D; Bodell A; Nelis E; Van Broeckhoven C; Lupski JR
    Neuron; 1996 Sep; 17(3):451-60. PubMed ID: 8816708
    [TBL] [Abstract][Full Text] [Related]  

  • 70. New mutation of the MPZ gene in a family with the Dejerine-Sottas disease phenotype.
    Floroskufi P; Panas M; Karadima G; Vassilopoulos D
    Muscle Nerve; 2007 May; 35(5):667-9. PubMed ID: 17143884
    [TBL] [Abstract][Full Text] [Related]  

  • 71. [Charcot-Marie-Tooth neural amyotrophy].
    Khurmatulina TI; Obichkina LA; Belogolovykh EN; Baliuk II
    Med Sestra; 1987 May; 46(5):31-4. PubMed ID: 3669966
    [No Abstract]   [Full Text] [Related]  

  • 72. Clinical and electrophysiological phenotype of a homozygously duplicated Charcot-Marie-Tooth (type 1A) disease.
    Sturtz FG; Latour P; Mocquard Y; Cruz S; Fenoll B; LeFur JM; Mabin D; Chazot G; Vandenberghe A
    Eur Neurol; 1997; 38(1):26-30. PubMed ID: 9252795
    [TBL] [Abstract][Full Text] [Related]  

  • 73. [Contribution of morphological studies of the peripheral nerve to a better comprehension of Charcot-Marie-Tooth atrophy and Roussy-Levy hereditary areflexic dystaxia].
    Lapresle J
    Acquis Med Recent; 1980; ():91-6. PubMed ID: 7395444
    [No Abstract]   [Full Text] [Related]  

  • 74. [Polymorphism of Charcot-Marie-Tooth neural amyotrophy in uniovular twins].
    Popov'ian MD; Dubinskaia EE; Ageeva TS
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1977; 77(10):1446-8. PubMed ID: 563155
    [TBL] [Abstract][Full Text] [Related]  

  • 75. [Effect of pregnancy on the course of Charcot-Marie-Tooth neural amyotrophy].
    Badalian LO; Temin PA; Mukhin KIu; Arkhipov BA; Avakian GN
    Akush Ginekol (Mosk); 1986 Jun; (6):70-1. PubMed ID: 2944428
    [No Abstract]   [Full Text] [Related]  

  • 76. A de novo duplication in 17p11.2 and a novel mutation in the Po gene in two Déjérine-Sottas syndrome patients.
    Silander K; Meretoja P; Nelis E; Timmerman V; Van Broeckhoven C; Aula P; Savontaus ML
    Hum Mutat; 1996; 8(4):304-10. PubMed ID: 8956034
    [TBL] [Abstract][Full Text] [Related]  

  • 77. Argyll-Robertson-like pupils in the neural type of Charcot-Marie-Tooth disease.
    Salisachs P; Lapresle J
    Eur Neurol; 1977; 16(1-6):172-5. PubMed ID: 615709
    [TBL] [Abstract][Full Text] [Related]  

  • 78. Quantitation of Meissner's corpuscles in hereditary neurologic disorders. Charcot-Marie-Tooth disease, Roussy-Levy syndrome, Dejerine-Sottas disease, hereditary sensory neuropathy, spinocerebellar degenerations, and hereditary spastic paraplegia.
    Dyck PJ; Winkelmann RK; Bolton CF
    Neurology; 1966 Jan; 16(1):10-7. PubMed ID: 5948001
    [No Abstract]   [Full Text] [Related]  

  • 79. Non-hypertrophic familial neuropathy associated with intention tremor. A variety of Charcot-Marie-Tooth disease?
    Delwaide PJ; Schoenen J
    J Neurol Sci; 1976 Jan; 27(1):59-69. PubMed ID: 175133
    [TBL] [Abstract][Full Text] [Related]  

  • 80. Molecular genetics of Charcot-Marie-Tooth disease and related neuropathies.
    Chance PF; Fischbeck KH
    Hum Mol Genet; 1994; 3 Spec No():1503-7. PubMed ID: 7849745
    [TBL] [Abstract][Full Text] [Related]  

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