Neudle.com: inclusion bodies cytoplasmic

Differential
(Click to cross reference)

abdominal protrusion

acquired immunodeficiency syndrome

Addison's disease

adrenoleukodystrophy

adrenomyeloneuropathy

adult polyglucosan body disease

adverse drug reaction

alternating rapid movement

Alzheimer's disease

amyloid

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, guamian type of

amyotrophic lateral sclerosis, misdiagnosis

animal bite

animal exposure

anomic aphasia

anterior horn cell disease

anti DNA agent

antibodies to measles

antimalarials

antiviral agents

aphasia

aphasia, progressive, primary

apraxia

apraxia of eye movements

areflexia

arthralgia

arthritis

arthrogryposis multiplex

autonomic dysfunction

autonomic nervous system

axonal degeneration

Babinski sign

basal ganglia

basal ganglia, lesion of

basal ganglia, lesion, bilateral

CAT scan, demyelinating disease

CAT scan, emission, abnormal

CAT scan, false negative

cataracts

CD4 counts

central core disease

central nervous system, infection of

central nervous system, infection, cancer patient

cerebellar atrophy, primary

cerebellar lesion

cerebral cortex

cerebral cortical atrophy

cerebral infarction, hemorrhagic

cerebro hepato renal syndrome

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cell count, normal

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, oligoclonal IgG in

cerebrovascular accident

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

Clinical Pathologic Conference(C.P.C.)

creatine phosphokinase(CPK)elevated

cytomegalovirus infection

cytosine arabinoside

deep gray nuclei

degenerative diseases of CNS

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, thalamic

demyelinating disease

depression

diagnostic criteria

differential diagnosis

difficulty climbing stairs

disorientation

distal muscle atrophy

distal muscle weakness

electroencephalogram, abnormalities of

electroencephalogram, periodic complexes

encephalitis, brainstem

encephalitis, episodic

encephalopathy, progressive

enzyme, muscle disease

epidemiology of neurology

epilepsia partialis continua

executive dysfunction

extrapyramidal movement disorder, progressive

face, numbness of

facial weakness

facial weakness, bilateral

Fazio-Londe's disease

fever

fingerprint bodies

foot drop

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

frontal lobe, atrophy

frontal lobe, behavior with disease of

frontotemporal dementia, behavioral variant

fundus, abnormality of

gait disorder

gait, spastic

gait, waddling

gammaglobulin therapy, intravenous

genetic neurologic disorders

genetic testing

GFAP gene

glabellar sign

glioblastoma multiforme(astrocytoma Gr.III)

glycogen storage disease

granular osmiphilic material

grasp reflex

gray matter

Guillain Barre syndrome

Guillain Barre syndrome, steroid treatment in

hallucination

hallucination, visual

hand weakness

headache

heavy metal intoxication

hemianopia

hemianopia, homonymous

hemiparesis

hepatosplenomegaly

herpes labialis

herpes simplex encephalitis

herpes simplex encephalitis, atypical

herpes simplex encephalitis, diagnosis of

herpes simplex virus

herpes simplex virus infection, immunosuppressed patient

herpes simplex virus, human nervous system and

herpes simplex, neurocutaneous lesions in

herpes virus

herpes virus infection

herpes zoster

herpes zoster, disseminated

highly active antiretroviral therapy

hippocampus

Hirschprung's disease

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

Horner's syndrome

human immunodeficiency virus type 1

hydrocephalus

hydrocephalus, communicating

hydrophobia

hyperpigmentation of skin

hyperreflexia

hypophonia

hypotension, systemic

hypotonia

iatrogenic neurologic disorders

immunosuppressive agents

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

inclusion bodies, location of

inclusion bodies, ubiquitin

inclusion body myositis

intellectual deterioration

intracerebral hemorrhage

intrinsic hand muscles, wasting of

iododeoxyuridine

JC virus

Jewish

Kugelberg-Welander syndrome

lactic acidemia

Lafora body

Lafora's disease

language disorder in adults

laughing

laughing, pathologic

leg weakness, bilateral

leg weakness, unilateral

lethargy

leukemia

leukemia, neurologic findings assoc.with

leukoencephalitis

leukoencephalopathy

leukoencephalopathy, differential diagnosis

level of consciousness, decreased

Lewy body

Lewy body disease, diffuse

lissencephaly

liver biopsy

liver transplantation

lobar atrophy

locus ceruleus, lesion of

logopenia

loss of sympathy

lymphoma

lymphoma involving CNS

lymphoma, primary of CNS

malformation, CNS, congenital

marche a petits pas

memory, defect of recent

memory, impairment of

mesial temporal sclerosis

micropolygyria

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

Mini Mental Status Examination

misdiagnosis

mitochondrial disease

molecular genetics

Montreal cognitive assessment

movement disorder, extrapyramidal

MPTP

MRI

MRI, abnormal

MRI, diffusion weighted

MRI, mass effect on

MRI, serial

MRS

multiple system atrophy

muscle atrophy, progressive

muscle biopsy

muscle culture

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

myopathy, distal, vacuolar

myopathy, inclusion body

myopathy, inclusion body with Paget's disease

myopathy, inclusion body, hereditary

neoplasm, primary intracerebral

neoplasm, primary of CNS

nerve biopsy

nerve conduction studies

nerve culture

neurofibrillary degeneration

neurogenic bladder

neuroleptic

neuroleptic sensitivity

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuropathology

neuropathology, brain

neuropathy

neuropathy, peripheral

neuropathy, sensory

neurotoxin

nystagmus

obsessive-compulsive disorder

oculogyric crisis

ophthalmoplegia

opportunistic infection

opportunistic infection, CNS

optic atrophy

optic nerve

optic nerve, hypoplasia of

oral contraceptives

organ donor

organ transplantation

orthostatic hypotension

Parkinson disease, drug induced

Parkinson disease, L-dopa nonresponsive

Parkinson disease, misdiagnosis

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

PAS positive

PAS positive material in the brain

pathognomonic

pathologic reflex

perseveration

persistent vegetative state

pleocytosis of cerebrospinal fluid

pleurisy

poison, mercury

poison, neurologic problems with

polycystic kidneys

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polymerase chain reaction, false negative

polyneuropathy

postural abnormality

pregnancy, neurologic complications in

prevention of neurologic disorders

prognosis

progressive multifocal leucoencephalopathy

progressive myoclonic epilepsy

progressive neurologic disorder

proximal muscle atrophy

pseudobulbar palsy

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

psychosis

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

rabies, nervous system involvement with

radiation therapy, CNS treatment and complications with

renal transplantation

research

respiratory distress syndrome, neurologic status with

respiratory failure

respiratory tract infection

rubeola, encephalitis

salivation, excessive

serologic testing of cerebrospinal fluid

serologic testing, false negative

skin, biopsy

skin, darkening of

skin, lesions in neurologic disorders

sleep pathology and physiology

slow virus infection of CNS

spasticity

spinocerebellar ataxia

spongy degeneration of brain

stare

steroid therapy, CNS treatment and complications with

storage disease of CNS

stuttering

subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease

subacute sclerosing panencephalitis, acute

symmetric brain lesions

synucleinopathy

systemic illness

systemic lupus erythematosus

systemic lupus erythematosus, drug induced

systemic lupus erythematosus, neurologic complications with

tandem gait, ataxic

tangential

tapetoretinal degeneration

tau protein

tauopathy

temporal lobe

temporal lobe, atrophy

testicular biopsy

thalamus, lesion of

thymus and neuromuscular function

treatment of neurologic disorder

tremor

tremor, intention

tricresylphosphate

trinucleotide repeats

tuberculosis

ubiquitin

urinary incontinence

varicella zoster virus

varicella zoster virus, encephalitis

varicella zoster virus, vasculopathy

vasculitides

vasculopathy

vincristine neurotoxicity

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visual loss

visual loss, progressive

visual loss, slow

visuospatial disturbance

walking, difficulty with

weakness

weakness, generalized

weakness, progressive

weight loss

Werdnig-Hoffman disease

wheelchair

white matter disease

white matter disease, subcortical

wide based gait

word-finding difficulty

Showing articles 0 to 50 of 652 Next >>

A 60-Year-Old Man with Weakness and Gait Dysfunction
JAMA Neurol 82:305-306, Jones,F.J.S.,et al, 2025

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

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

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

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

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

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

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

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

Neuronal Intranuclear Inclusion Disease Cases with Leukoencephalopathy Diagnosed via Skin Biopsy
JNNP 85:354-356, Sone, J.,et al, 2014

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Rabies
Adams & Victors Principles of Neurology, Chp 33, pg 753, Ropper, A.H.,et al, 2014

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Subacute Sclerosing Panencephalitis
Adams & Victors Principles of Neurology, Chp 33, pg 766, Ropper, A.H.,et al, 2014

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Progressive Multifocal Leukoencephalopathy
Adams & Victors Principles of Neurology, Chp 33, pg 767, Ropper, A.H.,et al, 2014

Subacute Sclerosing Panencephalitis
www.MedLink.com, February, Auwaeter,P.G.&Johnson,R.T., 2013

Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis
NEJM 364:1062-1074, Case 8-2011, 2011

A 63-Year-Old Woman with Urinary Incontinence and Progressive Gait Disorder
Neurol 72:1607-1613, Lossos,A.,et al, 2009

Fragile X-Associated Tremor/Ataxia Syndrome: An Aging Face of the Fragile X Gene
Arch Neurol 65:19-25, Amiri,K.,et al, 2008

A 23-Year-Old Man With Seizures and Visual Deficit
Neurol 70:73-78, Boustany,R.-M.,et al, 2008

Frontotemporal Lobar Degeneration with Motor Neuron Disease
Arch Neurol 63:489-490, Clark,C.M. &Forman,M.S., 2006

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

Frontotemporal Dementia: Clinicopathological Correlations
Ann Neurol 59:952-962, Forman,M.S.,et al, 2006

Fragile X Premutation With Atypical Symptoms at Onset
Arch Neurol 63:1135-1138, Cellini,E.,et al, 2006

Rabies Encephalomyelitis
Arch Neurol 62:873-882,855, Burton,E.C.,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, Multiple-System Atrophy
NEJM 351:912-921, Case 27-2004, 2004

Serial Proton MR Spectroscopy and Diffusion Imaging Findings in HIV-Related Herpes Simplex Encephalitis
AJNR 24:2015-2019, S�mann,P.G., et al, 2003

Subacute Sclerosing Panencephalitis
Postgrad Med J 78:63-70, Garg, R.K.,et al, 2002

Diagnosing Dementia with Lewy Bodies
Lancet 354:1227-1228, McKeith,I.G.,et al, 1999

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

Herpes Simplex Encephalitis (HSE) and the Immunocompromised: A Clinical and Autopsy Study of HSE in the Settings of Cancer and Human Immunodeficiency Virus-Type 1 Infection
Hum Pathol 29:215-222, Schiff,D. &Rosenblum,M.K., 1998

Herpes Simplex Virus Infections of the Central Nervous System in Human Immunodeficiency Virus-Infected Patients: Clinical Management by Polymerase Chain Reaction Assay of Cerebrospinal Fluid
CID 27:303-309, Cinque,P., et al, 1998

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

Gene Locus for Autosomal Recessive Distal Myopathy with Rimmed Vacuoles Maps to Chromosome 9
Ann Neurol 41:432-437, Ikeuchi,T.,et al, 1997

Subacute Measles Virus Encephalitis:A New & Fatal Opportunistic Infection in a Pt with AIDS
Neurol 46:586-587, Budka,H.,et al, 1996

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

Inclusion Body Myositis
JNNP 60:251-255, Garlepp,M.J.&Mastaglia,F.L., 1996

Clinicopath Conf
Varicella-Zoster Leukoencephalitis with Hemorrhage and Large-Vessel Vasculopathy, AIDS, Case 36-1996, NE335:1587-1595,1996., 1996

Inclusion Body Myositis and Myopathies
Ann Neurol 38:705-713, Griggs,R.C.,et al, 1995

Treatment of Inclusion-Body Myositis with High-Dose Intravenous Immunoglobulin
Neurol 43:876-879, Soueidan,S.A.&Dalakas,M.C., 1993

Neuronal Intranuclear Inclusion Disease in a Child:Diagnosis by Rectal Biopsy
Ann Neurol 27:103-106, Goutieres,F.,et al, 1990

Diffuse Lewy Body Disease and Progressive Dementia
Neurol 38:1520-1528, Burkhardt,C.R.,et al, 1988

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

Spectrum of Inclusion Body Myositis
Arch Neurol 44:1154-1157, Ringel,S.P.,et al, 1987

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

Locus Ceruleus Lesions & Eosinophilic Inclusions in MPTP-Treated Monkeys
Ann Neurol 20:449-455, Forno,L.S.,et al, 1986

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

Showing articles 0 to 50 of 652 Next >>