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Differential
(Click to cross reference)
acquired immunodeficiency syndrome
acridine orange-RNA fluorescence
Alzheimer's disease
amyloid
amyloid plaques
arteritides
ataxia
autoantibodies
axonal degeneration
axonal spheroid
axonal transection
boxing
brain biopsy
brain biopsy, complications of
brainstem, lesion of
calf hypertrophy
carcinoma
cardiomyopathy
CAT scan
CAT scan, abnormal
central nervous system, infection of
cerebellar degeneration
cerebral cortical atrophy
cerebrospinal fluid, abnormal
cerebrospinal fluid, cytology
cerebrospinal fluid, elevated protein of
children
contractures, joint
creatine phosphokinase(CPK)elevated
cultured skin fibroblasts
cytochrome c oxidase
cytochrome c oxidase, deficiency
cytomegalovirus infection
dementia
denervation of muscle
denervation potentials
desmin
developmental disability
developmental milestones
developmental retardation
disability, neurological
distal muscle weakness
DNA probes
dystrophin
electromyogram
electron microscopy
ELISA
emerin
Emery-Dreifuss muscular dystrophy
Emery-Dreifuss muscular dystrophy, carrier
enzyme, defect
facial weakness
fatigue
fetal movements, reduced
fetus
floppy infant
gadolinium
genetic counselling
genetic neurologic disorders
gliomatosis cerebri
head injury
headache
histochemistry
histochemistry of muscle
histopathology
human immunodeficiency virus type 1
hydrocephalus
hypertrophic intracranial pachymeningitis
hypertrophic intracranial pachymeningitis, etiology
hypertrophic pachymeningitis, IgG4 related disease
hypertrophic spinal pachymeningitis
hypotonia
hypotonia, infants
iatrogenic neurologic disorders
IgG4-related disease
immunohistochemistry
immunoperoxidase staining
in situ hybridization
intellectual deterioration
JC virus
Leigh's disease
lumbar puncture
lumbar puncture, complications of
meningeal biopsy
meningeal gliomatosis
meningoencephalitis
meningoencephalitis, toxoplasma
mental retardation
merosin
microglial nodules
misdiagnosis
mitochondrial disease
MRI
MRI, abnormal
MRI, contrast enhanced
MRS
multinucleated giant cell
multiple sclerosis
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle pain
muscle weakness
muscular dystrophy
muscular dystrophy, Becker, carrier
muscular dystrophy, central nervous system abnormality
muscular dystrophy, congenital
muscular dystrophy, congenital, Fukuyama type
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
myelopathy, vacuolar
myopathy
myopathy, critically ill
myopathy, desmin
myopathy, myofibrillar
myotonia dystrophica
N-acetyl-L-aspartic acid
neoplasm, primary of CNS
neoplasm, primary of CNS-treatment of
nerve biopsy
neurofibrillary degeneration
neurogenic atrophy
neurogenic vs.myopathic atrophy
neurologic disease, diagnoses of
neuropathology
neuropathology, brain
neuropathology, peripheral nerves
neuropathy
neuropathy, peripheral
neuropathy, vasculitic, systemic
nystagmus
old age, neurology of
ophthalmoplegia
opportunistic infection
opportunistic infection, CNS
optic atrophy
pain
papovavirus
peripheral nerve, lesion of
pleocytosis of cerebrospinal fluid
poliomyelitis
polymerase chain reaction
polymyositis
polymyositis, infantile
polyneuropathy, critically ill
post polio syndrome
prognosis
progressive multifocal leucoencephalopathy
remote effect of cancer on the nervous system
respiratory failure
review article
single-fiber electromyography
skin, biopsy
slow virus infection of CNS
spinal cord, pathologic exam of
suck, poor
toxoplasmosis, CNS
treatment of neurologic disorder
vasculitides
viral infection
viral infection, CNS
viral isolation
walking, difficulty with
weakness
weakness, congenital
weakness, generalized
Western immunoblot test
Showing articles 0 to 26 of 26

IgG4-Related Disease and Hypertrophic Pachymeningitis
Medicine 92:206-216, Wallace, Z.,et al, 2013

Toxoplasmosis Manifesting as Hydroephalus on Computed Tomography
Infect Dis Clin Practice 9:390-392, Finelli,P.F. &Uphoff,D.F., 2000

Axonal Transection in the Lesions of Multiple Sclerosis
NEJM 338:278-285, 3231998., Trapp,B.D.,et al, 1998

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

X-Linked Emery-Dreifuss Muscular Dystrophy Can Be Diagnosed from Skin Biopsy or Blood Sample
Ann Neurol 42:249-253, Mora,M.,et al, 1997

Acute Type II Myofiber Atrophy in Critical Illness
Neurol 46:819-821, 6001996., Gutman,L.,et al, 1996

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

Congenital Muscular Dystrophy Syndromes Distinguished by Alkaline and Acid Phosphatase, Merosin, & Dystrophin Staining
Neurol 46:810-814, Connolly,A.M.,et al, 1996

Congenital Muscular Dystrophy with Primary Laminin a2 (Merosin) Deficiency Presenting as Inflammatory Myopathy
Ann Neurol 40:782-791, Pegoraro,E.,et al, 1996

Early Viral Brain Invasion in Iatrogenic Human Immunodeficiency Virus Infection
Neurol 42:1736-1739, Davis,L.E.,et al, 1992

Mosaic Express of Dystrophin in Carriers of Becker's Muscular Dyst & X-Linked Synd of Myalgia & Cramps
NEJM 327:1100, Minetti,C.&Bonilla,E., 1992

Diagnosis and Management of Gliomatosis Cerebri:Recent Trends
Surg Neurol 36:431-440, Ross,I.B.,et al, 1991

JC Virus Detection by In Situ Hybridization in Brain Tissue from Elderly Patients
Ann Neurol 29:428-432, Mori,M.,et al, 1991

BA4 Amyloid Protein Deposition in Brain After Head Trauma
Lancet 338:1422-1423, Roberts,G.W.,et al, 1991

AIDS-Assoc Progressive Multifocal Leukoencephalopathy (PML) :Comparison to Non-AIDS PML
Neurol 40:1073-1078, Aksamit,A.J.,et al, 1990

The Widening Spectrum of Infectious Neurological Disease
JNNP 53:629-632, Kennedy,P.G., 1990

Mosaic Expression of Dystrophic in Symptomatic Carriers of Duchenne's Muscular Dystrophy
NEJM 320:138-142, Arahata,K.,et al, 1989

Necrotizing Vasculitis and HIV Replication in Peripheral Nerves
NEJM 321:685-686, Gherardi,R.,et al, 1989

Spinal Cord and Peripheral Nerve Pathology in AIDS:The Roles of CMV & HIV
Ann Neurol 25:561-566, Grafe,M.R.&Wiley,C.A., 1989

Antineural Autoantibodies in Patients with Paraneoplastic Cerebellar Degeneration
Arch Neurol 46:1225-1229, Tsukamoto,T.,et al, 1989

Immunocytochemistry of Neurofibrillary Tangles in Dementia Pugilistica and Alzheimer's Disease:Evidence for Common Genesis
Lancet 2:1456-1458, Roberts,G.W., 1988

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

Meningeal Gliomatosis with"Negative"CSF Cytology:The Value of GFAP Staining
Neurol 34:1611-1615, Wechsler,L.R.,et al, 1984

Congenital Myotonic Dystrophy
Arch Neurol 37:693-696, Argov,Z.,et al, 1980

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



Showing articles 0 to 26 of 26