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22. [Variant of the facial-scapular-humeral-gluteal-femoral form of primary myopathy in children]. Grinio LP Zh Nevropatol Psikhiatr Im S S Korsakova; 1979; 79(10):1338-41. PubMed ID: 494906 [TBL] [Abstract][Full Text] [Related]
23. Facioscapulohumeral muscular dystrophy with congenital absence of sternocleidomastoid muscles. Penchaszadeh V Birth Defects Orig Artic Ser; 1971 Feb; 7(2):116-7. PubMed ID: 5173120 [No Abstract] [Full Text] [Related]
24. [Ocular myopathy. A familial case of oculo-pharyngeal and skeletal muscular dystrophy with late onset]. Manigand G; Lucsko M; Deparis M Sem Hop; 1969 Nov; 45(45):2803-8. PubMed ID: 4312491 [No Abstract] [Full Text] [Related]
25. [Serum aldolase activity in patients with myopathies and in their close reltives]. Dzhuraev A Zh Nevropatol Psikhiatr Im S S Korsakova; 1971; 71(8):1159-63. PubMed ID: 5136820 [No Abstract] [Full Text] [Related]
26. [Muscle innervation in Werdnig-Hoffmann spinal amyotrophy and several other atrophies in children]. Olenev SN; Savel'eva-Vasil'eva ; Zav'ialova NS Zh Nevropatol Psikhiatr Im S S Korsakova; 1972; 72(10):1445-9. PubMed ID: 4660417 [No Abstract] [Full Text] [Related]
27. Quantifying Labial Strength and Function in Facial Paralysis: Effect of Targeted Lip Injection Augmentation. Starmer H; Lyford-Pike S; Ishii LE; Byrne PA; Boahene KD JAMA Facial Plast Surg; 2015; 17(4):274-8. PubMed ID: 26086151 [TBL] [Abstract][Full Text] [Related]
28. [Birth and metamorphosis of Landouzy-Dejerine progressive atrophic myopathy]. Sorrel-Dejerine Y; Fardeau M Rev Neurol (Paris); 1982; 138(12):1041-51. PubMed ID: 6763289 [TBL] [Abstract][Full Text] [Related]
29. [Rapidly progressing facio-scapulo-humero-femoro-peroneal muscular dystrophy with sensorineural deafness]. Badalian LO; Temin PA; Mukhin KIu; Nikanorova MIu; Bulaeva NV; Kret LA; Lysov VL Zh Nevropatol Psikhiatr Im S S Korsakova; 1991; 91(9):5-8. PubMed ID: 1664615 [TBL] [Abstract][Full Text] [Related]
30. Landouzy-Dejerine disease: a progressive metameric muscular dystrophy of autosomal dominant inheritance with a variable intrafamilial phenotype expression. Rossi A; Giannini F; D'Amore I; Guazzi GC Acta Neurol (Napoli); 1985 Apr; 7(2):93-111. PubMed ID: 4013841 [No Abstract] [Full Text] [Related]
31. [Malate dehydrogenase activity in children with myopathy]. Gil'manov VKh Zh Nevropatol Psikhiatr Im S S Korsakova; 1973; 73(6):829-31. PubMed ID: 4753593 [No Abstract] [Full Text] [Related]
32. [Functional study of a gene candidate for Landouzy-Dejerine muscular dystrophy]. Belayew A Bull Mem Acad R Med Belg; 2004; 159(5-6):343-8; discussion 348-9. PubMed ID: 15693543 [TBL] [Abstract][Full Text] [Related]
33. Axonal motor and sensory neuropathy in myotonic dystrophy. Mondelli M; Rossi A; Malandrini A; Della Porta P; Guzaai GC Acta Neurol Scand; 1993 Aug; 88(2):141-8. PubMed ID: 8213059 [TBL] [Abstract][Full Text] [Related]
35. [Histopathological aspects of progressive muscular dystrophies. The place of classical histological techniques in their diagnosis]. Escourolle R; Fardeau M Ann Anat Pathol (Paris); 1973; 18(1):109-37. PubMed ID: 4577474 [No Abstract] [Full Text] [Related]
36. Familial muscular dystrophy of late onset. Bacon PA; Smith B J Neurol Neurosurg Psychiatry; 1971 Feb; 34(1):93-7. PubMed ID: 5551698 [TBL] [Abstract][Full Text] [Related]
37. [MYOPATHY OF THE LANDOUZY-D'EJERINE TYPE. REPORT OF A HISTORICAL CASE]. JUSTIN BESANCON L; PEQUIGNOT H; CONTAMIN F; DELAVIERRE P; ROLLAND P Sem Hop; 1964 Dec; 40():2990-9. PubMed ID: 14257214 [No Abstract] [Full Text] [Related]
38. [Various epidemiologic and genetic aspects of the basic neurohereditary diseases]. Skudarnova ZA; Sakharov LN; Makeenkova LI; Torbochkina MD; Filonova AV Zh Nevropatol Psikhiatr Im S S Korsakova; 1973; 73(6):848-53. PubMed ID: 4270984 [No Abstract] [Full Text] [Related]
39. New type of X-linked progressive muscular dystrophy involving shoulder girdle and back. Ji XW; Tan J; Chen XY; Yi SX; Liang H Am J Med Genet; 1990 Oct; 37(2):209-12. PubMed ID: 2248287 [TBL] [Abstract][Full Text] [Related]
40. Facioscapulohumeral dystrophy presenting in infancy with facial diplegia and sensorineural deafness. Korf BR; Bresnan MJ; Shapiro F; Sotrel A; Abroms IF Ann Neurol; 1985 May; 17(5):513-6. PubMed ID: 4004175 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]