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 *

153 related articles for article (PubMed ID: 10933475)

  • 1. Hereditary motor and sensory neuropathy type II (HMSN-II) and neurogenic muscle hypertrophy: a case report and literature review.
    Maurelli M; Candeloro E; Egitto MT; Alfonsi E
    Ital J Neurol Sci; 1998 Jun; 19(3):184-8. PubMed ID: 10933475
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Hereditary motor and sensory neuropathies in Swedish children. I. Prevalence and distribution by disability groups.
    Hagberg B; Westerberg B
    Acta Paediatr Scand; 1983 May; 72(3):379-83. PubMed ID: 6576612
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The hypertrophic forms of hereditary motor and sensory neuropathy. A study of hypertrophic Charcot-Marie-Tooth disease (HMSN type I) and Dejerine-Sottas disease (HMSN type III) in childhood.
    Ouvrier RA; McLeod JG; Conchin TE
    Brain; 1987 Feb; 110 ( Pt 1)():121-48. PubMed ID: 3467805
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Response to immunosuppressive therapy in patients with hereditary motor and sensory neuropathy and associated dysimmune neuromuscular disorders.
    Mitchell GW; Bosch EP; Hart MN
    Eur Neurol; 1987; 27(3):188-96. PubMed ID: 3476306
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Visual evoked responses in hereditary motor and sensory neuropathies.
    Gjerstad L; Nyberg-Hansen R; Ganes T
    Acta Neurol Scand; 1988 Mar; 77(3):215-9. PubMed ID: 3163873
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hereditary motor-sensory neuropathy (HMSN): possible X-linked dominant inheritance.
    Phillips LH; Kelly TE; Schnatterly P; Parker D
    Neurology; 1985 Apr; 35(4):498-502. PubMed ID: 3856757
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mitochondrial abnormalities in human sural nerves: fine structural evaluation of cases with mitochondrial myopathy, hereditary and non-hereditary neuropathies, and review of the literature.
    Schröder JM; Sommer C
    Acta Neuropathol; 1991; 82(6):471-82. PubMed ID: 1785260
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Duffy blood groups and HLA antigens in hereditary motor-sensory neuropathy].
    Nevsímalová S; Prazák J; Herzog P; Seemanová E
    Cesk Neurol Neurochir; 1989 Oct; 52(6):409-16. PubMed ID: 2635080
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Autosomal recessive forms of hereditary motor and sensory neuropathy.
    Harding AE; Thomas PK
    J Neurol Neurosurg Psychiatry; 1980 Aug; 43(8):669-78. PubMed ID: 7431027
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic heterogeneity of hereditary motor and sensory neuropathy type VI.
    Ippel EF; Wittebol-Post D; Jennekens FG; Bijlsma JB
    J Child Neurol; 1995 Nov; 10(6):459-63. PubMed ID: 8576556
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Hereditary neuropathy with dominant inheritance, giant axons and cardiac involvement].
    Gabriel M; Vogel P; Goebel HH
    Klin Padiatr; 1986; 198(1):17-20. PubMed ID: 3007857
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Oral manifestations, dental management, and a rare homozygous mutation of the PRDM12 gene in a boy with hereditary sensory and autonomic neuropathy type VIII: a case report and review of the literature.
    Elhennawy K; Reda S; Finke C; Graul-Neumann L; Jost-Brinkmann PG; Bartzela T
    J Med Case Rep; 2017 Aug; 11(1):233. PubMed ID: 28807049
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Ulcero-mutilating neuropathy in an Austrian kinship without linkage to hereditary motor and sensory neuropathy IIB and hereditary sensory neuropathy I loci.
    Auer-Grumbach M; Wagner K; Timmerman V; De Jonghe P; Hartung HP
    Neurology; 2000 Jan; 54(1):45-52. PubMed ID: 10636124
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Hereditary motor and sensory neuropathy. Clinical, genetic and electrodiagnostic studies.
    Vasilescu C
    Rom J Neurol Psychiatry; 1993; 31(3-4):207-19. PubMed ID: 8011484
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Spanish toxic oil syndrome neuropathy in three patients with hereditary motor and sensory neuropathy type I.
    de Pablos C; Calleja J; Combarros O; Berciano J
    Arch Neurol; 1989 Feb; 46(2):202-4. PubMed ID: 2916959
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Hereditary motor and sensory neuropathy Okinawa type mimicking proximal myopathy.
    Braga VL; Tamanini JVG; Gama SM; Fraiman PHA; Silva TYT; Santos-Neto D; Barsottini OGP; Pedroso JL
    Clin Neurol Neurosurg; 2024 Apr; 239():108213. PubMed ID: 38479034
    [TBL] [Abstract][Full Text] [Related]  

  • 17. X-linked motor-sensory neuropathy type-II with deafness and mental retardation: a new disorder.
    Cowchock FS; Duckett SW; Streletz LJ; Graziani LJ; Jackson LG
    Am J Med Genet; 1985 Feb; 20(2):307-15. PubMed ID: 3856385
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutation in FAM134B causing hereditary sensory neuropathy with spasticity in a Turkish family.
    Ilgaz Aydinlar E; Rolfs A; Serteser M; Parman Y
    Muscle Nerve; 2014 May; 49(5):774-5. PubMed ID: 24327336
    [No Abstract]   [Full Text] [Related]  

  • 19. [Clinical practice of hereditary motor neuropathy (HMN) and hereditary sensory and autonomic neuropathy (HSAN)].
    Takashima H
    Rinsho Shinkeigaku; 2014; 54(12):957-9. PubMed ID: 25672680
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Autosomal recessive hereditary motor and sensory neuropathy with mental retardation, optic atrophy and pyramidal signs.
    MacDermot KD; Walker RW
    J Neurol Neurosurg Psychiatry; 1987 Oct; 50(10):1342-7. PubMed ID: 3479531
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.