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]