124 related articles for article (PubMed ID: 4406308)
1. Charcot-Marie-Tooth disease. A diagnostic problem.
Siegel IM
JAMA; 1974 May; 228(7):873. PubMed ID: 4406308
[No Abstract] [Full Text] [Related]
2. [Proceedings: Enzymology of the muscular myelopathic atrophies: enzymologic and ultrastructural study on Charcot-Marie-Tooth disease].
Rizzoli AA
Quad Sclavo Diagn; 1973 Mar; 9(1):166-75. PubMed ID: 4788705
[No Abstract] [Full Text] [Related]
3. The differential diagnosis of scapuloperoneal amyotrophy.
Spalke G; Hökendorf H; von Roques P
J Neurol; 1976 Jun; 212(3):253-69. PubMed ID: 58977
[TBL] [Abstract][Full Text] [Related]
4. [Early diagnosis and differentiation of Charcot-Marie neural atrophy].
Lobzin VS; Saĭkova LA; Poliakova LA; Kosachev VD
Zh Nevropatol Psikhiatr Im S S Korsakova; 1984; 84(11):1601-5. PubMed ID: 6524176
[TBL] [Abstract][Full Text] [Related]
5. [Charcot-Marie-Tooth disease with late appearance: clinical and electromyographic study].
Amici R; Avanzini G; Caccia MR; Negri S
Riv Patol Nerv Ment; 1968 Aug; 89(4):281-300. PubMed ID: 5760424
[No Abstract] [Full Text] [Related]
6. A case of scapulo-tibio-peroneal syndrome. Electromyographic and histoenzymologic considerations.
Negri S; Caraceni T; Cornelio F
Eur Neurol; 1973; 10(1):31-40. PubMed ID: 4269485
[No Abstract] [Full Text] [Related]
7. [Sporadic distal myopathy].
Il'ina NA; Aver'ianov IuN; Nechkina NP; Potomskaia LZ; Sokolina NA
Zh Nevropatol Psikhiatr Im S S Korsakova; 1983; 83(11):1620-3. PubMed ID: 6675357
[TBL] [Abstract][Full Text] [Related]
8. [Relationships between genotype and phenotype in Charcot-Marie-Tooth disease].
Câmpeanu E; Morariu M
Rev Roum Neurol; 1970; 7(1):47-56. PubMed ID: 5527990
[No Abstract] [Full Text] [Related]
9. 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]
10. 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]
11. Spinal muscular atrophy with autosomal dominant inheritance. Report of a new kindred.
Zellweger H; Simpson J; McCormick WF; Ionasescu V
Neurology; 1972 Sep; 22(9):957-63. PubMed ID: 4673381
[No Abstract] [Full Text] [Related]
12. [Neurophysiological, histological and chromosome study of Charcot-Marie-Tooth disease].
Messina C; Fiorillo A; Caliri F
Acta Neurol (Napoli); 1968; 23(1):21-33. PubMed ID: 5739560
[No Abstract] [Full Text] [Related]
13. Chronic proximal spinal muscular atrophy.
Namba T; Aberfeld DC; Grob D
J Neurol Sci; 1970 Nov; 11(5):401-23. PubMed ID: 5503267
[No Abstract] [Full Text] [Related]
14. [Electromyography in Charcot-Marie disease].
Zumstein V; Schneider C
Schweiz Arch Neurol Neurochir Psychiatr; 1982; 130(2):297-307. PubMed ID: 7134908
[No Abstract] [Full Text] [Related]
15. Non-hypertrophic familial neuropathy associated with intention tremor. A variety of Charcot-Marie-Tooth disease?
Delwaide PJ; Schoenen J
J Neurol Sci; 1976 Jan; 27(1):59-69. PubMed ID: 175133
[TBL] [Abstract][Full Text] [Related]
16. [Type II proximal spinal muscular atrophy. Clinical, electrophysiological, histopathological and histochemical studies].
Tangheroni W; Cao A; Cianchetti C; Calisti L
Minerva Pediatr; 1974 Jun; 26(22):1125-45. PubMed ID: 4276719
[No Abstract] [Full Text] [Related]
17. [Familial neurogenic amyotrophy, similar to Charcot-Marie-Tooth disease. Clinical and ultrastructural study].
Vital C; Julien J; Vallat JM; Le Blanc M
Rev Neurol (Paris); 1970 Jan; 122(1):15-28. PubMed ID: 5433253
[No Abstract] [Full Text] [Related]
18. F-wave conduction velocity in the deep peroneal nerve: Charcot-Marie-Tooth disease and dystrophia myotonica.
Panayiotopoulos CP
Muscle Nerve; 1978; 1(1):37-44. PubMed ID: 752107
[TBL] [Abstract][Full Text] [Related]
19. Hereditary hypertrophic neuropathy with facial and trigeminal involvement. Report of a case and comments on its possible identity with Hellsing syndrome.
Kalyanaraman K; Smith BH; Schlagenhauff RE
Arch Neurol; 1974 Jul; 31(1):15-7. PubMed ID: 4834537
[No Abstract] [Full Text] [Related]
20. Neurogenic scapuloperoneal syndrome in childhood.
Mercelis R; Demeester J; Martin JJ
J Neurol Neurosurg Psychiatry; 1980 Oct; 43(10):888-96. PubMed ID: 7441268
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]