152 related articles for article (PubMed ID: 7341549)
1. Progressive peroneal muscular atrophy (Charcot-Marie-Tooth disease) associated with beta-thalassemia trait and glucose-6-phosphate dehydrogenase (G-6-PD) deficiency. A clinical and nerve biopsy case.
Inzitari D; Rizzuto N; Antuono P; Sità D
Ital J Neurol Sci; 1981 Aug; 2(3):269-74. PubMed ID: 7341549
[TBL] [Abstract][Full Text] [Related]
2. Nemaline rod myopathy and Charcot-Marie-Tooth disease. Report of a case in a 10-year-old girl.
Danon MJ; Sarpel G; Manaligod JR
Arch Neurol; 1980 Feb; 37(2):123-7. PubMed ID: 7356407
[TBL] [Abstract][Full Text] [Related]
3. Charcot-Marie-Tooth disease: study of a large kinship with an intermediate form.
Rossi A; Paradiso C; Cioni R; Rizzuto N; Guazzi G
J Neurol; 1985; 232(2):91-8. PubMed ID: 4020397
[TBL] [Abstract][Full Text] [Related]
4. Peroneal muscular atrophy (PMA) and related disorders. I. Clinical manifestations as related to biopsy findings, nerve conduction and electromyography.
Buchthal F; Behse F
Brain; 1977 Mar; 100 Pt 1():41-66. PubMed ID: 861715
[No Abstract] [Full Text] [Related]
5. Focal glomerulosclerosis associated with Charcot-Marie-Tooth disease.
Gherardi R; Belghiti-Deprez D; Hirbec G; Bouche P; Weil B; Lagrue G
Nephron; 1985; 40(3):357-61. PubMed ID: 4010852
[TBL] [Abstract][Full Text] [Related]
6. Evidence that Charcot-Marie-tooth disease with tremor coincides with the Roussy-Levy syndrome.
Barbieri F; Filla A; Ragno M; Crisci C; Santoro L; Corona M; Campanella G
Can J Neurol Sci; 1984 Nov; 11(4 Suppl):534-40. PubMed ID: 6509399
[TBL] [Abstract][Full Text] [Related]
7. Peroneal muscular atrophy. Part 1. Clinical and electrophysiological study.
Bouché P; Gherardi R; Cathala HP; Lhermitte F; Castaigne P
J Neurol Sci; 1983; 61(3):389-99. PubMed ID: 6317809
[TBL] [Abstract][Full Text] [Related]
8. [Ocular findings in Charcot-Marie-Tooth disease, HMSN type I].
Bürki E
Klin Monbl Augenheilkd; 1981 Aug; 179(2):94-6. PubMed ID: 7347789
[TBL] [Abstract][Full Text] [Related]
9. Hereditary motor sensory neuropathy type I presenting as scapuloperoneal atrophy (Davidenkow syndrome) electrophysiological and pathological studies.
Ronen GM; Lowry N; Wedge JH; Sarnat HB; Hill A
Can J Neurol Sci; 1986 Aug; 13(3):264-6. PubMed ID: 3742344
[TBL] [Abstract][Full Text] [Related]
10. Peroneal muscular atrophy. Part 2. Nerve biopsy studies.
Gherardi R; Bouché P; Escourolle R; Hauw JJ
J Neurol Sci; 1983; 61(3):401-16. PubMed ID: 6655490
[TBL] [Abstract][Full Text] [Related]
11. Variability in nerve biopsy findings in a kinship with dominantly inherited Charcot-Marie-Tooth disease.
Van Weerden TW; Houthoff HJ; Sie O; Minderhoud JM
Muscle Nerve; 1982 Mar; 5(3):185-96. PubMed ID: 7088015
[No Abstract] [Full Text] [Related]
12. [Hereditary spastic paraplegia associated with peroneal muscular atrophy].
Laso FJ; Cacho J; Díez Jarilla JL; González Macías J
Med Clin (Barc); 1982 Apr; 78(8):329-31. PubMed ID: 7087602
[No Abstract] [Full Text] [Related]
13. Motor and sensory conduction velocity in patients with Charcot-Marie-Tooth disease exposed to carbon disulphide.
Florescu A; Vasilescu C
Neurol Psychiatr (Bucur); 1976; 14(2):97-103. PubMed ID: 968423
[No Abstract] [Full Text] [Related]
14. 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]
15. Leber's optic neuropathy and Charcot-Marie-Tooth disease. Report of a case.
McCluskey DJ; O'Connor PS; Sheehy JT
J Clin Neuroophthalmol; 1986 Jun; 6(2):76-81. PubMed ID: 2942573
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. [Charcot-Marie-Tooth disease associated with a pyramidal syndrome: clinical, electrophysiological, and neuropathological study of neuro-muscular biopsies in 14 cases].
Thiam A; Sene FD; Ndao AK; Ndiaye M; Ndiaye IP
Dakar Med; 2002; 47(2):182-7. PubMed ID: 15776672
[TBL] [Abstract][Full Text] [Related]
18. Focal mucoid degeneration of peripheral nerve. Light- and electronmicroscopic observation in a sural nerve biopsy of a case of progressive neural muscular atrophy (Charcot-Marie-Tooth).
Meier C; Bischoff A
Acta Neuropathol; 1977 Jan; 37(1):69-72. PubMed ID: 842296
[TBL] [Abstract][Full Text] [Related]
19. Nephropathy associated with Charcot-Marie-Tooth disease.
Hara M; Ichida F; Higuchi A; Tanizawa T; Okada T
Int J Pediatr Nephrol; 1984 Jun; 5(2):99-102. PubMed ID: 6490324
[TBL] [Abstract][Full Text] [Related]
20. Clinico-electrophysiological correlation of extensor digitorum brevis muscle atrophy in children with charcot-marie-tooth disease 1A duplication.
Berciano J; García A; Calleja J; Combarros O
Neuromuscul Disord; 2000 Aug; 10(6):419-24. PubMed ID: 10899448
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]