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Differential
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abortion, spontaneous

abulia

aciduria

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome, infants and children

acrocyanosis

activities of daily living scale

acute necrotizing encephalitis

adrenoleukodystrophy

adrenomyeloneuropathy

adverse drug reaction

affect, flat

aggression

agitation

Aicardi-Goutieres syndrome

alcohol

alcohol, neurologic complications with

alcoholism

Alexanders disease

algorithm

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

Alzheimer's disease

Alzheimer's disease, behavioral symptoms

Alzheimer's disease, early symptoms

Alzheimer's disease, noncognitive symptoms

Alzheimer's disease, preclinical

Alzheimer's disease, treatment of

amyotrophic lateral sclerosis

ANA

anemia

angiography, cerebral

aniridia

anomic aphasia

anorexia

anterior horn cell disease

anticholinesterase

anticonvulsants

anticonvulsants, teratogenicity of

aphasia, progressive, non-fluent

aphasia, progressive, primary

arthropathy, neuropathic

aspirin

asterixis

asterixis, causes of

asterixis, unilateral

autonomic dysfunction

autonomic nervous system

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar artery migraine

behavior

behavior, combative

behavioral disorder

behavioral disorder, acute

calcification, intracranial

callosal angle

carbon monoxide poisoning

carbonic anhydrase II deficiency

CAT scan, angiography

CAT scan, angiography, false negative

CAT scan, chest

CAT scan, emission, abnormal

CAT scan, venography

cataracts

cataracts, congenital

caudate nucleus

caudate nucleus, atrophy

caudate nucleus, infarction

caudate nucleus, lesion of, bilateral

central nervous system, infection of

cerebellar ataxia, children

cerebellar atrophy, primary

cerebellar degeneration

cerebellar hypoplasia

cerebellar vermis

cerebellum, disease of

cerebral arteries, territory of

cerebral cortical atrophy

cerebral edema

cerebral folate deficiency syndrome

cerebral palsy

cerebral palsy, work up

cerebro hepato renal syndrome

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, amonia

cerebrospinal fluid, cytology

cerebrospinal fluid, drainage of

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, glutamine

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, xanthochromia of

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, bilateral

cerebrovascular accident, complications with

cerebrovascular disease

ceruloplasmin, serum

chemotherapy, CNS treatment and complications with

chest x-ray, abnormal

chilbran skin lesions

chromosomal abnormality

chromosome 2

chromosome 6

cingulate island sign

Clinical Pathologic Conference(C.P.C.)

concentration, impaired

confusion

confusional state, acute

congenital heart disease

congenital infection, CNS

congenital infection, viral

congenital malformation

congenital malformation, dilantin therapy causing

contractures, joint

conversion reaction

copper metabolism, abnormal

cornea, opacification in infancy-causes of

cornea, opacity of

corpus callosum

corpus callosum, hypoplastic

corpus callosum, lesion of

cranial nerve palsies

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

cry, abnormal

cry, weak

crying

cryptococcal meningitis

cryptorchidism

cultured skin fibroblasts

cytomegalic inclusion disease

cytomegalovirus infection

cytomegalovirus infection, congenital

degenerative diseases of CNS

dementia, age at onset

dementia, cerebrovascular disease causing

dementia, childhood

dementia, familial

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, reversible

dementia, subcortical

dementia, thalamic

dementia, treatment of

demyelinating disease

dentate nuclei

dentate nuclei, lesion of

depression

depression, psychotic

developmental disability

developmental evaluation

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diagnostic criteria

differential diagnosis

dilantin

diplopia

disability, neurological

disconnection syndrome

disorientation

downward gaze

Dravet syndrome

dural arteriovenous malformation

dystonic reaction, acute

electroencephalogram

electroencephalogram, abnormalities of

electron microscopy

encephalitis

encephalitis, brainstem

encephalitis, human immunodeficiency virus type 1

encephalopathy

encephalopathy, delayed

encephalopathy, metabolic

endovascular therapy

enzyme, defect

epidemiology of neurology

executive dysfunction

eye movement, disorders of

eyes, sunken

facial appearance, abnormal

fatty acid, elevated plasma content

feeding disorder

fetus

fever

fine motor function, impaired

finger nose finger test

fistula, arterio-venous

fistula, arterio-venous, dural

fluctuate

fluency

fluorescein angiography

folic acid

folic acid deficiency

fracture, pathologic

frontal lobe, atrophy

frontal lobe, behavior with disease of

frontal lobe, pathologic signs of

frontotemporal dementia, behavioral variant

fundus, abnormality of

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic neurologic disorders

genetic testing

Gillespie syndrome

glaucoma

glioblastoma multiforme(astrocytoma Gr.III)

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glutamine

glycine

Gorlin-Goltz syndrome

granulomatous disease

grasp reflex

gray matter

growth retardation

Guillain Barre syndrome

gyrus, abnormal

hallucination

hallucination, visual

heavy metal intoxication

hemangioma, facial

hemangioma, leptomeningeal

hemangioma, skin

hemianopia

hemiparesis

hemiparesis, transient

hemiplegia

hemoglobin abnormality, neurologic complications of

hemophagocytic lymphohistiocytosis, cerebromeningeal

hemophagocytosis

hemophilia

hemorrhage, thalamic

hepatic encephalopathy

hepatolenticular degeneration, non-Wilsonian

hepatomegaly

hepatosplenomegaly

heralding manifestation

herpes labialis

herpes simplex encephalitis

herpes simplex encephalitis, differential diagnosis of

herpes simplex encephalitis, recurrent

herpes simplex encephalitis, treatment of

herpes simplex myelitis

herpes simplex virus

herpes simplex virus infection, immunosuppressed patient

herpes simplex virus, human nervous system and

herpes simplex virus, localization of

herpes simplex virus, malignancy with

herpes simplex virus, pathogenesis of

herpes simplex virus, pathology of

herpes simplex, neurocutaneous lesions in

herpes virus

herpes virus infection

hexosaminidase-A and B

hoarding

human immunodeficiency virus type 1

human immunodeficiency virus type 1, asymptomatic

human immunodeficiency virus type 1, infants and children

human T-lymphotropic virus type I(HTLV-I)

Huntington's chorea

Huntington's disease, children

hydrocephalus

hydrocephalus, congenital

hydrocephalus, fetal

hydrocephalus, normal pressure

hydrocephalus, normal pressure, etiology

hydroxyglutaric aciduria

hyperglycinemia

hyperglycinemia, nonketotic

hyperpigmentation of skin

hyperpyrexia, CNS disorder causing

hyperreflexia

hypersomnia

hypertensive encephalopathy, venous

hypothermia, causes of

immunofluorescent exam of CSF cells

immunologic disease

immunosuppression

immunosuppressive agents

impulsivity

inappropriate behavior

inattention

inborn errors of metabolism

inclusion bodies

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

incontinence, fecal

incontinentia pigmenti

infantile hemiplegia

infantile spasm

infection, recurrent

infectious mononucleosis

inflexibility, mental

initiative, lack of

insomnia

intellectual deficit

intellectual deterioration

intelligence quotient

intracerebral hemorrhage

intracerebral hemorrhage, recurrent

intracranial hemorrhage

intracranial pressure, increased

intrauterine

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

intraventricular hemorrhage

iododeoxyuridine

iris, abnormal

irritability

Jakob-Creutzfeldt disease

jaundice

Kleine-Levin syndrome

lacunar infarction

language disorder in adults

L-dopa

leg weakness, unilateral

Leigh's disease

lens, dislocation of

lenticular nucleus, lesion of, bilateral

lethargy

leukodystrophy

leukoencephalopathy

leukoencephalopathy, toxic

leukotrienes

levamisole

level of consciousness, decreased

Lewy body disease, diffuse

limbic encephalitis

limbic system

lipid storage disorder of CNS

lumbar puncture, complications of

lung biopsy

lymphadenopathy

lymphadenopathy, hilar

lymphoma

lymphoma involving CNS

lymphoma, primary of CNS

lysosomal storage disease

macrocephaly

malformation, CNS, congenital

masked facies

memantine

memory, defect of recent

memory, impairment of

meningeal enhancement

meningitis, granulomatous

meningitis, neurologic aspects and complications of

meningitis, rheumatoid

meningoencephalitis

mental retardation

mental status, abnormal

metabolic acidosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

methylglutaconic aciduria

microaneurysm, retinal

microangiopathy, brain

microcephaly

micrographia

microhemorrhage, intracerebral

mild cognitive impairment

mimics

misdiagnosis

mitochondrial disease

molybdenum cofactor deficiency

monoamines

monoamines, brain

mononeuropathy

mononeuropathy multiplex

Montreal cognitive assessment

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, angiography

MRI, angiography, false negative

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, cortical enhancement

MRI, diffusion weighted

MRI, flow void, blood

MRI, gray matter enhancement

multinucleated giant cell

myxedema, neurologic manifestations of

nasal bridge, wide

nausea and vomiting

necrotizing granuloma

neoplasm, primary intracerebral

neoplasm, primary of CNS

neurocutaneous disease

neuroleptic

neuroleptic, atypical

neurolipidosis IV

neurologic complications

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic disease, tempo

neurologic examination

neurologic examination, focal

neurologic testing

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, peripheral

newborn, evaluation of

nose, abnormal

nutritional deficiency

nystagmus

obsessive-compulsive disorder

ocular motility, disorders of

olanzapine

old age, neurology of

ophthalmoplegia

opisthotonus

opportunistic infection

opportunistic infection, CNS

optic atrophy

optic nerve

optic nerve, hypoplasia of

optic neuropathy

osteoporosis

pachygyria

pain, increased response

parietal lobe, atrophy

Parkinson disease, axial symptoms

Parkinson disease, tremor, absence of

Parkinsonism syndrome

patent ductus arteriosus

pathologic reflex

Pelizaeus Merzbacher

penguin silhouette sign

perceptual-motor dysfunction

photosensitivity, skin

Pick bodies

picking at skin

Pick's disease

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

poison, mercury

poison, neurologic problems with

polycystic kidneys

polyinosinic cytidic acid(poly IC)

polymerase chain reaction

port wine nevus

posterior cortical atrophy

pregnancy, neurologic complications in

premature infant

prenatal

prenatal diagnosis by amniocentesis

prognosis

progressive infantile poliodystrophy

progressive multifocal leucoencephalopathy

progressive neurologic disorder

progressive supranuclear palsy

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychomotor retardation

psychosis

pulmonary infiltrates

pulmonary nodules

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

rapidly progressing neurologic illness

rehabilitation for neurologic disorders

release phenomena

REM sleep behavior disorder

remote effect of cancer on the nervous system

renal failure

renal tubular acidosis

repetitive questioning

retina, abnormal

retinal artery occlusion

retinal branch artery occlusion

retinal degeneration

retinal dysplasia

retinal microvascular disease

retinopathy

retrocollis

retrovirus

reversible neurologic disorder

review article

rheumatoid arthritis

rheumatoid arthritis factor(R.A.factor)

rheumatoid arthritis, neurologic complications of

saccadic eye movements, abnormal

seizure, psychomotor-temporal lobe

seizure, tonic-clonic

self-mutilation

semantic dementia

semialdehyde dehydrogenase deficiency

sensorineural hearing loss

sequencing difficulty

sexual behavior, disorder of

sexual dysfunction in neurologic disease

shadowing

short stature

short steps

shunt procedure, lumboperitoneal

shunt procedure, ventricular

shunt procedure, ventricular-complications of

sickle cell trait

sinemet

single photon emission computed tomography

skin, biopsy

skin, lesions in neurologic disorders

sleep pathology and physiology

snout reflex

sodium channel dysfunction

somnolence

spasticity

speech disorder, childhood

splenomegaly

spongy degeneration of brain

startle reaction

status epilepticus

stereotyped behavior

steroid therapy, CNS treatment and complications with

Sturge-Weber syndrome

subacute myelo-opticoneuropathy(S.M.O.N.)complex

subarachnoid hemorrhage

subdural hematoma

subtemporal decompression

syphilis, diagnosis and treatment

systemic illness

systemic lupus erythematosus

temporal lobe, atrophy

thalamus, infarction of

thalamus, lesion of

thalamus, lesion of-bilateral

toxoplasmosis, acquired

toxoplasmosis, CNS

transient ischemic attack

transient ischemic attack, venous

transient neurologic deficit

transplacental virus infections

treatment of neurologic disorder

treatment, non-pharmacologic

tremor

trichopoliodystrophy

trigeminal neuralgia

trinucleotide repeats

twitching

ultrasonography

ultrasonography, head, fetus-neonate

urine test for metabolic disorders

urine test in toxic screen

vaccinia

varicella zoster virus

ventricular enlargement

vision, failure of in childhood

visual acuity, decreased

Walker-Warburg syndrome

walking frame

walking, difficulty with

word-finding difficulty

workup

Showing articles 0 to 50 of 96 Next >>

Clinicopathologic Conference, Diffuse Large B-Cell Lymphoma
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Neuroimaging Biomarkers in a Patient with Probable Psychiatric-Onset Prodromal Dementia with Lewy Bodies
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Rapidly Progressive Thalamic Dementia
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Clinicopathologic Conference, Normal Pressure Hydrocephalus
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Cocaine and Levamisole Cerebral Toxicity
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Vitamin B12 Deficiency in a 29-Year-Old Woman
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A 72-year-old Man with a Progressive Cognitive and Cerebellar Syndrome
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Clinicopathologic conference, Frontotemporal Lobar Degeneration with tau-positive inclusions consistent with Picks disease
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A 12-year-old girl with headache and change in mental status
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Pyruvate Dehydrogenase Deficiency (PDCD)
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Clinical and Neuroimaging Features in Gorlin-Goltz Syndrome
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Precipitous Deterioration of Motor Function, Cognition, and Behavior
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A 55-year-old Man with Rapidly Progressive Dementia and Parkinsonism
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Huntington Disease: Clinical Features and Diagnosis
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A Young Man with Progressive Language Difficulty and Early-Onset Dementia
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Molybdenum Cofactor Deficiency
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Non-Alzheimers Dementia 1 Frontotemporal Dementia
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"Noncognitive" Symptoms of Early Alzheimer Disease
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Assessment and Management of Behavioral and Psychological Symptoms of Dementia
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Kleine-Levin Syndrome in 120 Patients: Differential Diagnosis and Long Episodes
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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
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Neuropsychiatric Changes Precede Classic Motor Symptoms in ALS and Do Not Affect Survival
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A 14-Year-Boy with Spells of Somnolence and Cognitive Changes
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The Acquired Metabolic Disorders of the Nervous System, Uremic Encephalopathy
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The Acquired Metabolic Disorders of the Nervous System, Hypothyroidism
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Disturbances of Cerebrospinal Fluid, Including Hydrocephalus, Pseudotumor Cerebri, and Low-Pressure Syndromes, Normal Pressure Hydrocephalus
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Inherited Metabolic Diseases of the Nervous System, Galactosemia
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Inherited Metabolic Diseases of the Nervous System, Lipogranulomatosis (Farber Disease)
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Inherited Metabolic Diseases of the Nervous System, Subacute Necrotizing Encephalopathy (Leigh Disease)
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Frontotemporal Dementia
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Cognitive Delay in a 7-year-old Girl
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Sturge-Weber Syndrome
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3-Methylglutaconic Aciduria Type I Redefined: A Syndrome With Late-Onset Leukoencephalopathy
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Autoantibodies to Folate Receptors in the Cerebral Folate Deficiency Syndrome
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Natural History of Nonketotic Hyperglycinemia in 65 Patients
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Rapidly Reversible Dementia
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Clinical Spectrum of Succinic Semialdehyde Dehydrogenase Deficiency
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