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Journal Abstract Search
103 related items for PubMed ID: 1332322
21. Facioscapulohumeral dystrophy presenting as infantile facial diplegia and late-onset limb-girdle myopathy in members of the same family. Felice KJ, Jones JM, Conway SR. Muscle Nerve; 2005 Sep; 32(3):368-72. PubMed ID: 15880682 [Abstract] [Full Text] [Related]
22. [Oculopharyngeal muscular dystrophy. Clinical, electromyography and muscle biopsy findings in 2 cases]. Klostermann W, Wessel K, Reusche E, Kessler C, Kömpf D. Nervenarzt; 1990 Jun; 61(6):351-5. PubMed ID: 2377260 [No Abstract] [Full Text] [Related]
24. [Landouzy-Dejerine syndrome. Evolution of the concept of facio-scapulo-humeral amyotrophia]. Schmitt J, Barrucand D, Schmidt C. Rev Neurol (Paris); 1977 Apr; 133(4):279-82. PubMed ID: 929032 [Abstract] [Full Text] [Related]
25. [A familial form of progressive muscular dystrophy with multiple contractures of the major joints]. Iadgarov IS, Badalian LO, Temin PA, Arkhipov BA, Bulaeva NV, Amanova ZA. Zh Nevropatol Psikhiatr Im S S Korsakova; 1991 Apr; 91(9):89-93. PubMed ID: 1664624 [Abstract] [Full Text] [Related]
30. [Identification of primary and secondary forms of progressive muscular dystrophy, from data of clinico-genetic and biochemical studies]. Bondarenko ES, Tamarkina AD, Zakoshchikova LV. Vestn Akad Med Nauk SSSR; 1973 Apr; 28(7):38-44. PubMed ID: 4786657 [No Abstract] [Full Text] [Related]