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Showing articles 0 to 6 of 6

Filter Applied: inclusion bodies,intracytopasmic (Click to remove)

Clinicopathologic Conference, Primary Progressive Aphasia, Semantic Variant, due to TAR DNA Binding Protein 43 associated Frontotemporal Lobar Degen
NEJM 376:158-167, Case 1-2017, 2017

Classic & Generalized Variants of Pick's Disease, A Clinicopath, Ultrastruc & Immunocyto Study
Ann Neurol 16:467-480, Munoz-Garcia,D.,et al, 1984

Intractable Epilepsy and Progressive Cognitive Decline in a Young Man
JAMA Neurol 74:737-740, Cohen, A.L.,et al, 2017

Various Types of Hereditary Inclusion Body Myopathies Map to Chromosome 9p1-q1
Ann Neurol 41:548-551, Argov,Z.,et al, 1997

CT Scanning & Diagnosis of Adrenoleukodystrophy
Neurol 27:884, Greenberg,H.S.,et al, 1977

Polymyositis & Dermatomyositis
NEJM 292:344, 1975, 292:403975., Bohan,A.,et al, 1975



Showing articles 0 to 6 of 6