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Journal Abstract Search

223 related items for PubMed ID: 7356407

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. 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]

  • 4. Charcot-Marie-Tooth disease associated with 'essential tremor' and normal and/or slightly diminished motor conduction velocity. Report of 7 cases.
    Salisachs P, Codina A, Gimenez-Roldan S, Zarranz JJ.
    Eur Neurol; 1979 Mar; 18(1):49-58. PubMed ID: 436863
    [Abstract] [Full Text] [Related]

  • 5. Motor and sensory conduction velocity in patients with Charcot-Marie-Tooth disease exposed to carbon disulphide.
    Florescu A, Vasilescu C.
    Neurol Psychiatr (Bucur); 1976 Mar; 14(2):97-103. PubMed ID: 968423
    [No Abstract] [Full Text] [Related]

  • 6. Charcot-Marie-Tooth's disease with severe trophic and sensory disorders. Study of a case following along a half a century with anatomical studies.
    Barraquer-Bordas L, Navarro C, Salisachs P.
    Acta Neurol Latinoam; 1981 Mar; 27(3-4):177-89. PubMed ID: 6965173
    [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 Mar; 61(3):389-99. PubMed ID: 6317809
    [Abstract] [Full Text] [Related]

  • 8. X-linked Charcot-Marie-Tooth disease with connexin 32 mutations: clinical and electrophysiologic study.
    Birouk N, LeGuern E, Maisonobe T, Rouger H, Gouider R, Tardieu S, Gugenheim M, Routon MC, Léger JM, Agid Y, Brice A, Bouche P.
    Neurology; 1998 Apr; 50(4):1074-82. PubMed ID: 9566397
    [Abstract] [Full Text] [Related]

  • 9. [Charcot-Marie-Tooth neural muscular atrophy (HMSN type I) with isolated tumerous hypertrophy of the median nerve].
    Berger W, Goth D, Ketelsen U.
    Nervenarzt; 1982 Dec; 53(12):725-8. PubMed ID: 7155235
    [No Abstract] [Full Text] [Related]

  • 10. Autosomal recessive axonal form of Charcot-Marie-Tooth Disease caused by compound heterozygous 3'-splice site and Ser130Cys mutation in the GDAP1 gene.
    Kabzińska D, Kochański A, Drac H, Ryniewicz B, Rowińska-Marcińska K, Hausmanowa-Petrusewicz I.
    Neuropediatrics; 2005 Jun; 36(3):206-9. PubMed ID: 15944907
    [Abstract] [Full Text] [Related]

  • 11. 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 31; 37(1):69-72. PubMed ID: 842296
    [Abstract] [Full Text] [Related]

  • 12. Short latency somatosensory evoked potentials in Charcot-Marie-Tooth disease. A family with an intermediate form.
    Rossi A, Paradiso C, Dell'Anna P, Mondelli M.
    Acta Neurol Scand; 1985 Feb 31; 71(2):156-63. PubMed ID: 2984874
    [Abstract] [Full Text] [Related]

  • 13. Peroneal muscular atrophy.
    Hosking G.
    Dev Med Child Neurol; 1980 Jun 31; 22(3):386-90. PubMed ID: 7390037
    [No Abstract] [Full Text] [Related]

  • 14. Charcot-Marie-Tooth disease with Leber optic atrophy.
    McLeod JG, Low PA, Morgan JA.
    Neurology; 1978 Feb 31; 28(2):179-84. PubMed ID: 563998
    [Abstract] [Full Text] [Related]

  • 15. Peroneal muscular atrophy with autosomal dominant inheritance.
    McLeod JG, Low PA.
    Clin Exp Neurol; 1977 Feb 31; 14():142-53. PubMed ID: 616594
    [Abstract] [Full Text] [Related]

  • 16. 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 31; 2(3):269-74. PubMed ID: 7341549
    [Abstract] [Full Text] [Related]

  • 17. F-wave conduction velocity in the deep peroneal nerve: Charcot-Marie-Tooth disease and dystrophia myotonica.
    Panayiotopoulos CP.
    Muscle Nerve; 1978 Aug 31; 1(1):37-44. PubMed ID: 752107
    [Abstract] [Full Text] [Related]

  • 18. 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 31; 28(1):17-40. PubMed ID: 932772
    [Abstract] [Full Text] [Related]

  • 19. [Charcot-Marie-Tooth disease. Electromyographic studies in 45 patients].
    Freitas MR, Nascimento OJ, Nevares MT, Escada TM.
    Arq Neuropsiquiatr; 1995 Sep 31; 53(3-B):552-9. PubMed ID: 8585810
    [Abstract] [Full Text] [Related]

  • 20. [Electromyography in Charcot-Marie disease].
    Zumstein V, Schneider C.
    Schweiz Arch Neurol Neurochir Psychiatr; 1982 Sep 31; 130(2):297-307. PubMed ID: 7134908
    [No Abstract] [Full Text] [Related]

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