Neudle.com: inclusion bodies cytoplasmic

Differential
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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 350 to 400 of 652 << Previous Next >>

Use of the Polymerase Chain Reaction in the Diagnosis of Herpes Simplex Encephalitis:A Decision Analysis Model
Am J Med 105:287-295, Tebas,P.,et al, 1998

A 6-Year-Old Child with Vacant Episodes and Unilateral Convulsions
Lancet 352:1750, Burgner,D.,et al, 1998

Diagnosis of Cytomegalovirus Encephalitis in Pts with AIDS by Cytomegalovirus Genomes in Cells of Cerebrospinal Fluid
Neurol 50:693-697, Wildemann,B.,et al, 1998

Acute Leukoencephalopathies:Differential Diagnosis and Investigation
The Neurologist 4:148-166, Weinshenker,B.G.,et al, 1998

Clinicopath Conf
Subacute Sclerosing Panencephalitis, Case 15-1998, NEJM 338:1448-1456998., , 1998

A 35-Year-Old Bricklayer with Hemimyoclonic Jerks
Lancet 351:1926, Grunewald,T.,et al, 1998

Atypical Herpes Simplex Virus Encephalitis Diagnosed by PCR Amplification of Viral DNA from CSF
Neurol 51:554-559, Fodork,P.A.,et al, 1998

Poliomyelitis-Like Illness Due to Japanese Encephalitis Virus
lancet 351:1094-1097, Solomon,T.,et al, 1998

Sporadic Incusion-Body Myositis and hereditary Inclusion-Body Myopathies
Arch Neurol 55:915-920, Askanas,V.&Engel,W.K., 1998

Inclusion Body Myositis in Twins
Neurol 51:598-600, Amato,A.A.&Shebert,R.T., 1998

Clinicopath Conf
Wegener's Granulomatosis Involving Sinuses, Skull, and Cranial Nerves, Case 28-1998, NEJM 339:755-76, , 199, 1998

PCR on CSF to Show Influenza-Associated Acute Encephalopathy or Encephalitis
Lancet 352:873-875, Fujimoto,S.,et al, 1998

Meningoencephalomyelitis Caused by Herpes Simplex Virus-1 in Pt with Idiopathic T CD4+Lymphocytopenia
Neurol 50:569-570, Tumbarello,M.,et al, 1998

Neuroradiographic Manifestations of Encephalitis
NEJM 337:1393-1394, Pfister,H-W.,et al, 1997

Cognitive Recovery Instead of Decline After Acute Encephalitis:A Prospective Follow Up Study
JNNP 63:222-227, Hokkanen,L.&Launes,J., 1997

Treatment of Inflammatory Myopathies
Muscle & Nerve 20:651-664997., Mastaglia,F.L.,et al, 1997

Magnetic Resonance Imaging of the Forearm as a Diagnostic Aid in Pts with Sporadic Inclusion Body Myositis
Neurol 48:863-866, Sekul,E.A.,et al, 1997

Anterior Opercular Syndrome, Caused by Herpes Simplex Encephalitis
Neurol 49:494-497, McGrath,M.N.,et al, 1997

Clinical and Neuroradiographic Manifestations of Eastern Equine Encephalitis
NEJM 336:1867-1874, Deresiewicz,R.L.,et al, 1997

Epstein-Barr Virus Encephalomyelitis Diagnosed by Polymerase Chain Reaction:Detection of the Genome in the CSF
Neurol 48:1351-1355, Tselis,A.,et al, 1997

HIV Infection-1
BMJ 314:487-491, 579-5831997., Cohn,J.A., 1997

The Therapeutic Dilemma of Inclusion Body Myositis
Neurol 48:567-568, Barohn,R.J., 1997

Herpes Simplex Encephalitis Treated with Acyclovir:Diagnosis and Long Term Outcome
JNNP 63:321-326, McGrath,N.,et al, 1997

Small-Vessel Vasculitis
NEJM 337:1512-1523, Jennette,J.C.&Falk,R.J., 1997

Adult-Onset Temporal Lobe Epilepsy Associated with Smoldering Herpes Simplex 2 Infection
Neurol 48:425-430, Cornford,M.E.&McCormick,G.F., 1997

Severe Encephalitis with Rapid Recovery
Lancet 349:470, Tong,C.Y.W.,et al, 1997

Neuroradiographic Findings in Newborn Period & Outcome in Children with Sympt Congen CMV Infection
Pediatrics 99:409-414, Boppana,S.B.,et al, 1997

Brainstem CMV Encephalitis in AIDS:Clinical Case and MRI Features
Neurol 48:529-530, Pierelli,F.,et al, 1997

Craniectomy:An Aggressive Treatment Approach in Severe Encephalitis
Neurol 48:412-417, Schwab,S.,et al, 1997

Diagnosis of Viral Infections of the Central Nervous System:Clinical Interpretation of PCR Results
Lancet 349:313-317, Jeffery,K.J.M.,et al, 1997

Hypomanic Symptoms Caused by Herpes Simplex Encephalitis
Neurol 47:1374-1378, Fisher,C.M., 1996

Acute Lumbosacral Polyradiculopathy Due to Cytomegalovirus in Advanced HIV Disease:CSF Findings in 17 Patients
JNNP 61:456-460, Miller,R.F.,et al, 1996

Investigation of Muscle Disease
JNNP 60:256-274, Mastaglia,F.L.&Laing,N.G., 1996

Amnesia in Acute Herpetic and Nonherpetic Encephalitis
Arch Neurol 53:972-978, Hokkanen,L.,et al, 1996

Ocular Manifestations of AIDS
JAMA 275:142-144, 1491996., Whitcup,S.M., 1996

Prognosis and Response of Cytomegalovirus Encepyhalitis and Meningomyelitis in AIDS
Neurol 46:444-450, Cohen,B.A., 1996

The Role of Lab Investig in the Dx & Management of Pts with Suspected Herpes Simplex Encephalitis:A Consensus Rpt
JNNP 61:339-345, Clinque,P.,et al, 1996

Cytomegalovirus Encephalitis
Ann Int Med 125:577-578, Arribas,J.R.,et al, 1996

Treatment of Rasmussen's Syndrome with Ganciclovir
Neurol 47:925-928, McLachlan,R.S.,et al, 1996

Herpes Encephalitis is a Disease of Middle Aged & Elderly People:PCR for Detection of HSV in CSF of 516 Pts with Encephalitis
JNNP 60:174-178, Koskiniemi,M.,et al, 1996

Neuroimaging Findings in Patients with AIDS
Clin Inf Dis 22:906-919, Walot,I.,et al, 1996

Intravenous Immunoglobulin Treatment of Neurological Disease
JNNP 60:359-361, Otten,A.,et al, 1996

Pure Motor Hand Weakness
Semin Neurol 16:75-81, Lewis,R.A., 1996

Cytomegalovirus Infection and Guillain-Barre Syndrome:The Clinical, Electrophysiologic, and Prognostic Features
Neurol 47:668-673, Visser,L.H.,et al, 1996

Re-emergence of Epidemic Venezuelan Equine Encephalomyelitis in South America
Lancet 348:436-440, Weaver,S.C.,et al, 1996

Multiple Mitochondrial DNA Deletions in Sporadic Inclusion Body Myositis:A Study of 56 Patients
Ann Neurol 39:789-795, Santorelli,F.M.,et al, 1996

Bilateral Brachial Plexus Neuritis Following Parvovirus B19 and Cytomegalovirus Infection
Ann Neurol 40:928-932, Maas,J.J.,et al, 1996

Inclusion Body Myositis:Clinical and Pathological Boundaries
Ann Neurol 40:581-586, Amato,A.A.,et al, 1996

Evaluation of the Polymerase Chain Reaction for Diagnosis of Herpes Simplex Virus Encephalitis
Arch Int Med 31:146-148, Puchhammer-Stockl,E.,et al, 1995

Apolipoprotein E E4 in Inclusion Body Myositis
Ann Neurol 38:957-959, Garlepp,M.J.,et al, 1995

Showing articles 350 to 400 of 652 << Previous Next >>