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Showing articles 0 to 7 of 7

Filter Applied: histochemistry of muscle (Click to remove)

The Wide Spectrum of Myofibrillar Myopathy Suggests a Multifactorial Etiology and Pathogenesis
Neurol 51:1646-1655, Amato,A.A.,et al, 1998

Congenital Muscular Dystrophy:Clinical & Pathologic Study of 50 Pts with Classical (Occidental) Merosin-Positive Form
Neurol 46:815-818, Kobayashi,O.,et al, 1996

Late Denervation in Patients with Antecedent Paralytic Poliomyelitis
NEJM 317:7-12, Cashman,N.R.,et al, 1987

Cytochrome c Oxidase Deficiency in Leigh Syndrome
Ann Neurol 22:498-506, DiMauro,S.,et al, 1987

Quadriceps Myopathy:A Varient of the Limb-Girdle Dystrophy Syndrome
JNNP 46:355-357, Swash,M.,et al, 1983

Acridine Orange-Nucleic Acid Fluorescence
Arch Neurol 37:641-644, Perl,D.P.,et al, 1980

Adult Onset Nemaline Myopathy
Neurol 28:1306-1309, Brownell,A.K.W.,et al, 1978



Showing articles 0 to 7 of 7