These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
8. Characteristic clinical findings in some neurogenic myopathies and in some myogenic myopathies causing muscular weakness, hypotonia and atrophy in infancy and early childhood. Gamstorp I Birth Defects Orig Artic Ser; 1971 Feb; 7(2):72-81. PubMed ID: 5173129 [TBL] [Abstract][Full Text] [Related]
9. [Spinal facioscapulo-peroneal (or facioscapulo-crural) muscular atrophy and facioscapulo-peroneal muscular dystrophy]. Kazakov VM; Skoromets AA; Mikhaĭlov EP; Barantsevich ER Zh Nevropatol Psikhiatr Im S S Korsakova; 1986; 86(5):662-7. PubMed ID: 3739474 [TBL] [Abstract][Full Text] [Related]
10. Early muscular dystrophy: differential patterns of weakness in duchenne, limb-girdle and facioscapulohumeral types. Chyatte SB; Vignos PJ; Watkins M Arch Phys Med Rehabil; 1966 Aug; 47(8):499-503. PubMed ID: 5914825 [No Abstract] [Full Text] [Related]
11. Studies of the innervation of muscles in muscular and neuromuscular diseases. An attempt of diagnosis by comparing biopsy and end plate studies with clinical and electromyographic findings. Reske-Nielsen E; Dalby A; Dalby M Acta Neurol Scand Suppl; 1965; 13 Pt 1():289-96. PubMed ID: 4284451 [No Abstract] [Full Text] [Related]