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Differential
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Addison's disease
adrenoleukodystrophy
adrenomyeloneuropathy
agnosia
agnosia, visual
albinism
Alexanders disease
Alzheimer's disease
anomic aphasia
aphasia
aphasia, progressive, primary
apraxia
apraxia of eye movements
areflexia
astrocytoma
autonomic nervous system
bacterial infection
basal ganglia, degeneration
basal ganglia, lesion of
bat bite
blindness
brain biopsy
brain scan, abnormal
brainstem, lesion of
carcinoma
CAT scan, abnormal
CAT scan, contrast enhanced
CAT scan, demyelinating disease
CAT scan, emission, abnormal
cataracts
cerebellar lesion
cerebral cortical atrophy
cerebro hepato renal syndrome
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
Chediak-Higashi syndrome
cherry red spot
cherry red spot-myoclonus syndrome
chromosome 9
Clinical Pathologic Conference(C.P.C.)
collagen vascular disease
confusion
conjunctival biopsy
cornea, opacity of
deep gray nuclei
degenerative diseases of CNS
delusion
dementia
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
demyelinating disease
dentate nuclei
dentate nuclei, lesion of
dermatomyositis
distal muscle weakness
DNA probes
dysmorphic
dysphasia
dyspraxia
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
electron microscopy
encephalitis
encephalitis, viral
encephalopathy
encephalopathy, progressive
enzyme, defect
familial
fever
frontal lobe, atrophy
gadolinium
gait disorder
Gaucher's disease
gene
gene mutation
genetic neurologic disorders
genetic testing
GFAP gene
glabellar sign
hallucination
hallucination, visual
hippocampus
Hirschprung's disease
hyperpigmentation of skin
hypotonia
immunohistochemistry
immunologic disease
immunosuppressive agents
impotence
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, intracytopasmic
inclusion bodies, intranuclear
inclusion bodies, location of
insular cortex
intellectual deterioration
Lafora body
Lafora's disease
language disorder in adults
lethargy
leukocyte peroxidase
leukodystrophy
leukoencephalopathy
Lewy body
Lewy body disease, diffuse
lipid storage disorder of CNS
lissencephaly
liver transplantation
lobar atrophy
malformation, CNS, congenital
mesial temporal sclerosis
methotrexate
micropolygyria
misdiagnosis
molecular genetics
mortality
MRI
MRI, abnormal
MRI, contrast enhanced
muscle biopsy
muscle weakness
muscular dystrophy, facioscapulohumeral
myoclonic jerks
myoclonus
myopathy
myopathy, inclusion body
myopathy, inclusion body, hereditary
myopathy, steroid induced
myopathy, vacuolar
myositis
Negri bodies
neoplasm, primary intracerebral
neoplasm, primary of CNS
neuraminidase deficiency
neurologic complications of, systemic cancer
neurologic disease, diagnoses of
neuropathology
neuropathy, peripheral
nystagmus
ophthalmoplegia
optic atrophy
optic nerve
optic nerve, hypoplasia of
organ transplantation
osteopetrosis
pachygyria
Parkinson disease
Parkinsonism syndrome
PAS positive
PAS positive material in the brain
photophobia
Pick's disease
polycystic kidneys
polymyositis
polyneuropathy
posterior fossa, lesion of
prognosis
progressive myoclonic epilepsy
progressive neurologic disorder
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
rabies, nervous system involvement with
rash
release phenomena
renal transplantation
retinal degeneration
review article
RFLPs
Rosenthal fibers
seizure
seizure, children
seizure, intractable
seizure, teenager
semantic dementia
skin, biopsy
skin, darkening of
skin, lesions in neurologic disorders
spinocerebellar degeneration
steroid therapy, CNS treatment and complications with
symmetric brain lesions
temporal lobe
temporal lobe, atrophy
testicular biopsy
viral infection
viral infection, CNS
visual evoked response
visual loss
visual loss, slow
weakness, progressive
weight loss
white matter disease
word-finding difficulty
Showing articles 0 to 50 of 1902 Next >>

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

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

Neuropathology of the Neuroradiologist: Rosenthal Fibers
AJNR 27:958-961, Wippold,F., II,et al, 2006

Unusual Variants of Alexander's Disease
Ann Neurol 57:327-338, van der Knaap,M.S., et al, 2005

Transmission of Rabies Virus from an Organ Donor to Four Transplant Recipients
NEJM 352:1103-11, Srinivasan,A., et al, 2005

Most Cases of Dementia with Hippocampal Sclerosis May Represent Frontotemporal Dementia
Neurol 63:538-542, Hatanpaa,K.J.,et al, 2004

Clinicopath Conf
Dementia with Lewy Bodies, Anaplastic Astrocytoma of Right Insular Region, Case 7-1998, NEJM 338:603, 61098., 1998

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

Lewy Body Disease and Dementia
Arch Int Med 156:487-493, Kalra,S.,et al, 1996

Infantile Gaucher's Disease:A Case with Neuronal Storage
Ann Neurol 23:300-303, Grafe,M.,et al, 1988

Parkinson's Disease & Megacolon:Concentric Hyaline Inclusions (Lewy Bodies) in Enteric Ganglion Cells
Neurol 37:1253-1255, Kupsky,W.J.,et al, 1987

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

Chediak-Higashi Syndrome
Arch Neurol 41:1001-1002, Pettit,R.E.,et al, 1984

Infantile Osteopetrosis & Neuronal Storage Disease
Neurol 33:437-441, Ambler,M.W.,et al, 1983

Skin & Conjunctival Nerve Biopsies in Adreno-leukodystrophy & Its Variants
Ann Neurol 8:291-295, Martin,J.J.,et al, 1980

Peripheral Neuropathy in the Cherry-Red Spot-Myoclonus Syndrome (Sialidosis Type I)
Ann Neurol 7:450-456, Steinman,L.,et al, 1980

Clinical Pathological Conference
Adrenoleukodystrophy, with Peripheral Neuropathy, Case Record 18-1979, NEJM 300:1037-104579., , 1979

Globoid cells, Glial nodules, & Peculiar Fibrillary Changes in the cerebro-hepato-renal Syndrome of Zellweger
Ann Neurol 2:473, deLeon,G.A.,et al, 1977

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

MR Imaging Patterns and Prognosis in Powassan Virus Encephalitis
Neurologist doi.10.1097/NRI.0000000000000533, Finelli,P.F., 2023

Epidemiology, Survival, and Clinical Characteristics of Inclusion Body Myositis
Ann Neurol 92:201-212, Lindgren, U.,et al, 2022

Neuroimaging Findings in Parechovirus Encephalitis: A Case Series of Pediatric Patients
Pediatr Neurol 130:41-45, Tierradentro-Garcia, L.O.,et al, 2022

Confused About Confusion
NEJM 386:80-87, Spanjaart, A.M.,et al, 2022

A Triad of Tremor, Ataxia, and Cognitive Impairment
Neurol 96:e1802-e1803, Au, L.W.C.,et al, 2021

A 65-Year-Old Woman with Tremor
Neurol 97:e1257-e1261, Ye, J.,et al, 2021

Anti-cN1A Antibodies are Associated with More Severe Dysphagia in Sporadic Inclusion Body Myositis
Cells 10:1146, Lucchini,M.,et al, 2021

Bornavirus Encephalitis Shows a Characteristic Magnetic Resonance Phenotype in Humans
Ann Neurol 88:723-735, Finck, T.,et al, 2020

Clinicopathologic conference, Frontotemporal Lobar Degeneration with tau-positive inclusions consistent with Picks disease
NEJM 383:2666-2675, Case 41-2020, 2020

Progressive Proximal Weakness in a 56-year-old Man with Bone Pain
Neurol 93:939-944, Torabi,T.,et al, 2019

GGC Repeat Expansion of NOTCH2NLC in Adult Patients with Leukoencephalopathy
Ann Neurol 86:962-968,809, Okubo, M.,et al, 2019

Clinicopathologic Conference, Powassan Virus Encephalitis
NEJM 380:380-387, Case 3-2019, 2019

A 40-Year-Old Woman Presenting with Distal Leg Weakness
Neurol 92:242-247, Fam, D.,et al, 2019

Acute Encephalitis in Immunocompetent Adults
Lancet 393:702-716, Venkatesan, A.,et al, 2019

Cerebral Atrophy and Leukoencephalopathy in a Young Man Presenting with Encephalitic Episodes
JAMA Neurol 75:1563-1564, Xiao, F.,et al, 2018

Neuronal Intranuclear Inclusion Disease Showing Intranuclear Inclusions in Renal Biopsy 12 Years Earlier
Neurol 91:884-886, Motoki, M.,et al, 2018

Hemorrhagic Encephalitis Associated with H3N2 Influenza A Viral Pneumonia
Neurol 90:336-337, AbdelRazek, M.A.,et al, 2018

Clinicopathologic Conference, Human Herpesvirus 6-Related Meningoencephalitis
NEJM 378:659-669, Case 5-2018, 2018

Antibody-Mediated Encephalitis
NEJM 378:840-851, Dalmau, J.,et al, 2018

A 42-year-old man with unilateral leg weakness
Neurol 90:e1085-e1090, Schneider, R.,et al, 2018

A 22-year-old postpartum woman with new-onset seizures and headache
Neurol 90:1631-1635, McGehrin, K.,et al, 2018

Acute Viral Encephalitis
NEJM 379:357-366, Tyler,K.L., 2018

A Man with Rapidly Progressive Weakness and Respiratory Failure
Neurol 91:e686-e691, Xu,D.,et al, 2018

Human Parechovirus: An Increasingly Recognized Cause of Sepsis-Like Illness in Young Infants
Clin Microbiol Reviews 31:1-17, Olijve, L.,et al, 2018

Powassan Virus-A New Reemerging Tick-Borne Disease
Front Public Health 5:342, Fatmi,S.S., et al, 2017

Emerging Cases of Powassan Virus Encephalitis in New England:Clinical Presentation, Imaging, and Review of the Literature
CID 62:707-713, Piantadosi,A.,et al, 2016

Hepatitis C Virus Infection in Inclusion Body Myositis
Neurol 86:211-217, Uruha, A.,et al, 2016

The Spectrum of Acute Encephalitis
Neurol 84:359-366, Singh, T.D.,et al, 2015

Clinicopathologic Conference, Frontotemporal Lobar Degeneration with Tau-positive Inclusions (Picks Disease Subtype) Due to a Gly389Arg MAPT Mutation, Resulting in the Behavioral Variant of Frontotemporal Dementia with Parkinsonism
NEJM 372:1151-1162, Miller, B.L.,et al, 2015



Showing articles 0 to 50 of 1902 Next >>