266 related articles for article (PubMed ID: 7477868)
21. Dominantly inherited motor and sensory neuropathy with excessive myelin folding complex.
Umehara F; Takenaga S; Nakagawa M; Takahashi K; Izumo S; Matsumuro K; Sakota S; Nishimura T; Yoshikawa H; Osame M
Acta Neuropathol; 1993; 86(6):602-8. PubMed ID: 8310815
[TBL] [Abstract][Full Text] [Related]
22. Congenital hypomyelination neuropathy in a newborn.
Hakamada S; Kumagai T; Hara K; Miyazaki S; Miyazaki K; Watanabe K
Neuropediatrics; 1983 Aug; 14(3):182-3. PubMed ID: 6312355
[TBL] [Abstract][Full Text] [Related]
23. MR imaging of the cauda equina in hereditary motor sensory neuropathies: correlations with sural nerve biopsy.
Cellerini M; Salti S; Desideri V; Marconi G
AJNR Am J Neuroradiol; 2000; 21(10):1793-8. PubMed ID: 11110529
[TBL] [Abstract][Full Text] [Related]
24. Sensory-motor chronic neuropathy in two siblings: atypical presentation of tomaculous neuropathy.
Malandrini A; Guazzi GC; Federico A
Clin Neuropathol; 1992; 11(6):318-22. PubMed ID: 1473315
[TBL] [Abstract][Full Text] [Related]
25. Congenital demyelinating motor and sensory neuropathy with focally folded myelin sheaths.
Gabreëls-Festen AA; Joosten EM; Gabreëls FJ; Stegeman DF; Vos AJ; Busch HF
Brain; 1990 Dec; 113 ( Pt 6)():1629-43. PubMed ID: 2276038
[TBL] [Abstract][Full Text] [Related]
26. Hereditary motor and sensory neuropathy of neuronal type with onset in early childhood.
Ouvrier RA; McLeod JG; Morgan GJ; Wise GA; Conchin TE
J Neurol Sci; 1981 Aug; 51(2):181-97. PubMed ID: 6268756
[TBL] [Abstract][Full Text] [Related]
27. Protein zero (P0)-deficient mice show myelin degeneration in peripheral nerves characteristic of inherited human neuropathies.
Martini R; Zielasek J; Toyka KV; Giese KP; Schachner M
Nat Genet; 1995 Nov; 11(3):281-6. PubMed ID: 7581451
[TBL] [Abstract][Full Text] [Related]
28. Clinicopathologic analysis of 124 biopsy-proven peripheral nerve diseases.
Hong SM; Ha H; Suh JH; Kim KK; Khang SK; Ro JY; Park SH
J Korean Med Sci; 2000 Apr; 15(2):211-6. PubMed ID: 10803700
[TBL] [Abstract][Full Text] [Related]
29. Congenital hypomyelinating neuropathy: two patients with long-term follow-up.
Phillips JP; Warner LE; Lupski JR; Garg BP
Pediatr Neurol; 1999 Mar; 20(3):226-32. PubMed ID: 10207934
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. Expression of P0 protein in sural nerve of a patient with hereditary motor and sensory neuropathy type III.
Tachi N; Kasai K; Chiba S; Naganuma M; Uyemura K; Hayasaka K
J Neurol Sci; 1994 Jun; 124(1):67-70. PubMed ID: 7523605
[TBL] [Abstract][Full Text] [Related]
32. Novel missense mutation in the early growth response 2 gene associated with Dejerine-Sottas syndrome phenotype.
Timmerman V; De Jonghe P; Ceuterick C; De Vriendt E; Löfgren A; Nelis E; Warner LE; Lupski JR; Martin JJ; Van Broeckhoven C
Neurology; 1999 Jun; 52(9):1827-32. PubMed ID: 10371530
[TBL] [Abstract][Full Text] [Related]
33. Sensory action potentials and biopsy of the sural nerve in neuropathy.
Behse F; Buchthal
Brain; 1978 Sep; 101(3):473-93. PubMed ID: 213163
[TBL] [Abstract][Full Text] [Related]
34. 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]
35. [Hereditary neuropathy with liability to pressure palsies (tomaculous neuropathy). Clinical, electrophysical and molecular study of two affected families].
Eirís-Punal J; Vidal-Lijó M; Barros-Angueira F; Lopez-Fernández MJ; Pintos-Martínez E; Beiras-Iglesias A; Castro-Gago M
Rev Neurol; 2000 Sep 16-30; 31(6):506-10. PubMed ID: 11055050
[TBL] [Abstract][Full Text] [Related]
36. The status of HMSN type III.
Gabreëls-Festen AA; Gabreëls FJ; Jennekens FG; Janssen-van Kempen TW
Neuromuscul Disord; 1994 Jan; 4(1):63-9. PubMed ID: 8173353
[TBL] [Abstract][Full Text] [Related]
37. MR imaging of Dejerine-Sottas disease.
Maki DD; Yousem DM; Corcoran C; Galetta SL
AJNR Am J Neuroradiol; 1999 Mar; 20(3):378-80. PubMed ID: 10219400
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. Sensory nerve pathology in multifocal motor neuropathy.
Corse AM; Chaudhry V; Crawford TO; Cornblath DR; Kuncl RW; Griffin JW
Ann Neurol; 1996 Mar; 39(3):319-25. PubMed ID: 8602750
[TBL] [Abstract][Full Text] [Related]
40. Hereditary motor and sensory neuropathy with optic atrophy. Ultrastructural and morphometric observations on nerve fibers, mitochondria, and dense-cored vesicles.
Sommer C; Schröder JM
Arch Neurol; 1989 Sep; 46(9):973-7. PubMed ID: 2775013
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
