BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

348 related articles for article (PubMed ID: 12661054)

  • 21. Demyelinating polyneuropathy with focally folded myelin sheaths in a family of Miniature Schnauzer dogs.
    Vanhaesebrouck AE; Couturier J; Cauzinille L; Mizisin AP; Shelton GD; Granger N
    J Neurol Sci; 2008 Dec; 275(1-2):100-5. PubMed ID: 18809183
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Limb girdle muscular dystrophy due to LAMA2 mutations: diagnostic difficulties due to associated peripheral neuropathy.
    Chan SH; Foley AR; Phadke R; Mathew AA; Pitt M; Sewry C; Muntoni F
    Neuromuscul Disord; 2014 Aug; 24(8):677-83. PubMed ID: 24957499
    [TBL] [Abstract][Full Text] [Related]  

  • 23. MRI of peripheral nerves and pathology of sural nerves in hereditary motor and sensory neuropathy type III.
    Tachi N; Kozuka N; Ohya K; Chiba S; Naganuma M
    Neuroradiology; 1995 Aug; 37(6):496-9. PubMed ID: 7477868
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Immunohistochemical evaluation of merosin deficiency in congenital muscular dystrophies.
    Brett FM; Loring P; Caesar A; Burke M; Brennan RP; King M; Farrell MA
    Arch Pathol Lab Med; 1998 Jan; 122(1):69-71. PubMed ID: 9448020
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Severe infantile neuropathy with diaphragmatic weakness and its relationship to SMARD1.
    Pitt M; Houlden H; Jacobs J; Mok Q; Harding B; Reilly M; Surtees R
    Brain; 2003 Dec; 126(Pt 12):2682-92. PubMed ID: 14506069
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Congenital neuropathy caused by hypomyelination].
    Pagès M; Voisin M; Echenne B; Pagés AM; Dumas R; Jean R
    Arch Fr Pediatr; 1983; 40(7):557-60. PubMed ID: 6314923
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Muscular dystrophies due to alterations at extracellular space level: congenital muscular dystrophy caused by merosin deficiency].
    Smeyers P
    Rev Neurol; 1999 Jan 16-31; 28(2):141-9. PubMed ID: 10101782
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A case of severe congenital chronic inflammatory demyelinating polyneuropathy with complete spontaneous remission.
    Majumdar A; Hartley L; Manzur AY; King RH; Orrell RW; Muntoni F
    Neuromuscul Disord; 2004 Dec; 14(12):818-21. PubMed ID: 15564039
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A Japanese family with early-onset ataxia with motor and sensory neuropathy.
    Kobayashi S; Takuma H; Murayama S; Sakurai M; Kanazawa I
    J Neurol Sci; 2007 Mar; 254(1-2):44-8. PubMed ID: 17258771
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Congenital muscular dystrophy: use of brain MR imaging findings to predict merosin deficiency.
    Lamer S; Carlier RY; Pinard JM; Mompoint D; Bagard C; Burdairon E; Estournet B; Barois A; Vallée C
    Radiology; 1998 Mar; 206(3):811-6. PubMed ID: 9494506
    [TBL] [Abstract][Full Text] [Related]  

  • 31. MR spectroscopy and diffusion tensor imaging of the brain in congenital muscular dystrophy with merosin deficiency: metabolite level decreases, fractional anisotropy decreases, and apparent diffusion coefficient increases in the white matter.
    Sijens PE; Fock JM; Meiners LC; Potze JH; Irwan R; Oudkerk M
    Brain Dev; 2007 Jun; 29(5):317-21. PubMed ID: 17113260
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Thin axons relative to myelin spiral length in hereditary motor and sensory neuropathy, type I.
    Nukada H; Dyck PJ; Karnes JL
    Ann Neurol; 1983 Dec; 14(6):648-55. PubMed ID: 6316837
    [TBL] [Abstract][Full Text] [Related]  

  • 33. EMG and nerve conduction studies in children with congenital muscular dystrophy.
    Quijano-Roy S; Renault F; Romero N; Guicheney P; Fardeau M; Estournet B
    Muscle Nerve; 2004 Feb; 29(2):292-9. PubMed ID: 14755496
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Demyelinating peripheral neuropathy in merosin-deficient congenital muscular dystrophy.
    Shorer Z; Philpot J; Muntoni F; Sewry C; Dubowitz V
    J Child Neurol; 1995 Nov; 10(6):472-5. PubMed ID: 8576559
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Dejerine-sottas disease with a novel de novo dominant mutation, Ser 149 Arg, of the peripheral myelin protein 22.
    Ohnishi A; Yamamoto T; Izawa K; Yamamori S; Takahashi K; Mega H; Jinnai K
    Acta Neuropathol; 2000 Mar; 99(3):327-30. PubMed ID: 10663978
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Ultrastructural changes in peripheral nerve in hereditary motor and sensory neuropathy-Lom.
    King RH; Tournev I; Colomer J; Merlini L; Kalaydjieva L; Thomas PK
    Neuropathol Appl Neurobiol; 1999 Aug; 25(4):306-12. PubMed ID: 10476047
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Minimal pathologic expression of a mutant gene for hereditary motor and sensory neuropathy.
    Dyck PJ; Karnes JL; Windebank AJ; Sparks M; Stevens JC; O'Brien PC
    Mayo Clin Proc; 1983 Jul; 58(7):419-25. PubMed ID: 6865475
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Clinical report of hereditary motor and sensory neuropathy with proximal dominance in Shiga prefecture].
    Takahashi M; Mitsui Y; Yorifuji S; Nakamura Y; Tsukamoto Y; Nishimoto K
    Rinsho Shinkeigaku; 2007 Sep; 47(9):571-6. PubMed ID: 18018614
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths: clinical, electrophysiologic, and genetic aspects of a large family.
    Quattrone A; Gambardella A; Bono F; Aguglia U; Bolino A; Bruni AC; Montesi MP; Oliveri RL; Sabatelli M; Tamburrini O; Valentino P; Van Broeckhoven C; Zappia M
    Neurology; 1996 May; 46(5):1318-24. PubMed ID: 8628474
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Decreased axon caliber and neurofilaments in hereditary motor and sensory neuropathy, type I.
    Nukada H; Dyck PJ
    Ann Neurol; 1984 Aug; 16(2):238-41. PubMed ID: 6541018
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 18.