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Journal Abstract Search

164 related items for PubMed ID: 5724670

  • 41. [Anaesthesia in juvenile muscular atrophy (Kugelberg-Welander syndrome) (author's transl)].
    Götz E, Bogosyan S.
    Anasth Intensivther Notfallmed; 1980 Aug; 15(4):360-2. PubMed ID: 7053118
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  • 42. [The importance of studying stimulation parameters in amyotrophic lateral sclerosis and Charcot-Marie-Tooth neural amyotrophy].
    Kyral V, Pára F.
    Sb Ved Pr Lek Fak Karlovy Univerzity Hradci Kralove Suppl; 1980 Aug; 23(4):415-22. PubMed ID: 6971479
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  • 43. [Does the pseudomyopathic form of ankylosing spondylitis exist?].
    Jorgensen C, Haguenau M, Assouline E, Mikol J.
    Rev Rhum Mal Osteoartic; 1989 Mar 15; 56(4):341-2. PubMed ID: 2711114
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  • 44. [Pseudomyopathic spinal muscular atrophy (Wohlfahrt-Kugelberg-Welander syndrome). Clinical case contribution].
    Flügel KA, Fritsch HB.
    Munch Med Wochenschr; 1969 May 16; 111(20):1169-75. PubMed ID: 5819287
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  • 46. [Familial amyotrophic lateral sclerosis. Critic of its classification and analysis of 14 families of Spanish origin].
    Giménez-Roldán S, Esteban A.
    Rev Clin Esp; 1978 Jan 31; 148(2):167-73. PubMed ID: 635269
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  • 53. Dissociated small hand muscle atrophy in amyotrophic lateral sclerosis: frequency, extent, and specificity.
    Kuwabara S, Sonoo M, Komori T, Shimizu T, Hirashima F, Inaba A, Misawa S, Hatanaka Y, Tokyo Metropolitan Neuromuscular Electrodiagnosis Study Group.
    Muscle Nerve; 2008 Apr 31; 37(4):426-30. PubMed ID: 18236469
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  • 55. Proximal neurogenic muscular atrophy in adolescence and adulthood with X-linked recessive inheritance. Kugelberg-Welander disease and its variant of late onset in one pedigree.
    Tsukagoshi H, Shoji H, Furukawa T.
    Neurology; 1970 Dec 31; 20(12):1188-93. PubMed ID: 5529907
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  • 57. [PSEUDOMYOPATHIC SPINAL MUSCULAR ATROPHY. HEREDITARY NEUROGENIC PROXIMAL AMYOTROPHY OF KUGELBERG AND WELANDER].
    BECKER PE.
    Z Mensch Vererb Konstitutionsl; 1963 Dec 17; 37():193-220. PubMed ID: 14112868
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  • 59. Progressive muscle atrophy with hypokalemic periodic paralysis and calcium channel mutation.
    Meyer T, Jurkat-Rott K, Huebner A, Lehmann-Horn F, Linke P, Van Landeghem F, Dullinger JS, Spuler S.
    Muscle Nerve; 2008 Jan 17; 37(1):120-4. PubMed ID: 17587224
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