Neudle.com: subcortical white matter disease

Differential
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abulia

aciduria

acquired immunodeficiency syndrome

acute disseminated encephalomyelitis

addiction, heroin

adrenoleukodystrophy

adrenomyeloneuropathy

advances in neurology

AMPA receptor antibodies

amyloid angiopathy, cerebral

amyloid angiopathy, cerebral, Boston criteria

amyloid angiopathy, cerebral, inflammatory type

amyloid beta protein

amyloid-related imaging abnormalities

anemia

aneurysm

aneurysm, intracranial

angiitis, granulomatous of CNS

angiitis, isolated of CNS

angiography, cerebral

antibodies to measles

anticoagulant, treatment

autoimmune basal ganglia encephalitis

autonomic dysfunction

B 12 deficiency

basal ganglia

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

behavioral disorder, acute

border zone hypoperfusion

border zone infarct

border zone infarct, internal

calcification, intracranial

calcification, intraventricular

calcification, periventricular

Canavan's disease

carbon monoxide poisoning

carcinoma

carotid angiogram

carotid artery

carotid artery disease

carotid artery occlusion, intracranial

carotid artery occlusion, neck

carotid artery stenosis

CAT scan

CAT scan, abnormal

CAT scan, cerebrovascular disease

catatonia

central nervous system, infection of

central pontine myelinolysis

centrum semiovale

cerebellar hypoplasia

cerebellar infarction

cerebellar infarction, bilateral

cerebellar lesion

cerebellar peduncle

cerebellar vermis

cerebral atherosclerosis

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy

cerebral blood flow

cerebral cortex

cerebral cortical atrophy

cerebral embolism

cerebral embolism, cardiac origin

cerebral infarction

cerebral infarction, hemorrhagic

cerebral infarction, small, deep

cerebral infarction, subcortical

cerebral ischemia

cerebral palsy

cerebral peduncle

cerebral venous thrombosis

cerebrospinal fluid, elevated protein of

cerebrovascular accident

cerebrovascular accident, atrial myxoma

cerebrovascular accident, familial occurrence

cerebrovascular accident, genetic

cerebrovascular accident, location of

cerebrovascular accident, multiple

cerebrovascular accident, non atherosclerotic cause of

cerebrovascular accident, pathophysiology

cerebrovascular accident, recurrent

cerebrovascular accident, silent

cerebrovascular accident, topographic pattern

cerebrovascular accident, young adult

cerebrovascular disease

cerebrovascular disease, rapidly progressive

cerebrovascular disease, risk factors in

chemotherapy, CNS treatment and complications with

children

chorea

choreoathetosis

chromosomal abnormality

chromosome 19

circle of Willis

Clinical Pathologic Conference(C.P.C.)

cognition

collapsin response mediator protein 5 IgG

coma

complications

confusion

confusional state, acute

congenital infection, CNS

congenital infection, viral

corpus callosum

corpus callosum, infarction of

corpus callosum, lesion of

cytomegalic inclusion disease

cytomegalovirus infection

cytomegalovirus infection, congenital

dementia, cerebrovascular disease causing

dementia, rapidly progressive

dementia, subcortical

demyelinating disease

differential diagnosis

digital subtraction angiography

disability rating scale, neurological

disability, neurological

disseminated intravascular coagulation(DIC)

DPPX, antibodies, encephalitis

drug abuse

drug abuse, neurologic complications of

electrical fields, alternating

electroencephalogram, abnormalities of

electroencephalogram, pediatric patients

electroencephalogram, periodic complexes

electron microscopy

emotional lability

encephalitis

encephalitis, autoimmune

encephalitis, etiology

encephalitis, human immunodeficiency virus type 1

encephalitis, viral

encephalopathy

encephalopathy, delayed

exercise

external capsule

Fabry's disease

faciobrachial dystonic seizure

falling

false negative

familial

familial hemiplegic migraine

ferritinemia

fever

finger nose finger test

fluorescein angiography

fundus, abnormality of

gamma amino butyric acid receptor antibody

gaze palsy, supranuclear

genetic neurologic disorders

genetic screening

genetic testing

gliomatosis cerebri

granular osmiphilic material

hemianopia, homonymous

hemiparesis

hemophagocytic lymphohistiocytosis

hemophagocytosis

hemosiderosis of CNS, superficial

herpes simplex encephalitis

HTRA1 gene

human immunodeficiency virus type 1

hydrocephalus

hydrocephalus, normal pressure

hyperekplexia

hyperglycemia

hyperglycemia, neurologic dysfunction associated with

hyperglycemia, nonketotic

hyperglycemic hemianopia

hyperreflexia

hypersomnia

hypertension

hypertension, cerebrovascular disease with

hypertensive encephalopathy

hypomyelination

hyponatremia

hypoxic encephalopathy

imbalance

imbalance, postural

immune reconstitution inflammatory syndrome

immunosuppression

immunosuppressive agents

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intranuclear

insomnia

intellectual deficit

intellectual deterioration

internal capsule

intracerebral hemorrhage

intracerebral hemorrhage, lobar

intracerebral hemorrhage, multiple

intracerebral hemorrhage, multiple simultaneous

intracerebral hemorrhage, small

iron, serum

iron, serum, elevated

leg weakness, bilateral

lesions too numerous to count

lethargy

leucine rich glioma inactivated 1 antibodies

leuko-araiosis

leukodystrophy

leukoencephalopathy

leukoencephalopathy, differential diagnosis

leukoencephalopathy, toxic

level of consciousness, decreased

life expectancy

limbic encephalitis

liver function enzymes

low back pain

lupus anticoagulant

lymphoma

lymphoma involving CNS

lymphoma, primary of CNS

macrocephaly

magnetic susceptibility

memory, defect of recent

memory, impairment of

meningitis, aseptic

meningitis, noninfectious

mental status, abnormal

mesial temporal lobe

metabolic acidosis

metachromatic leukodystrophy

methylmalonic aciduria

microangiopathy, brain

microangiopathy, retina

microcephaly

microemboli

microhemorrhage, intracerebral

midbrain, lesion of

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

middle cerebral artery, occlusion of

middle cerebral artery, stenosis of

Mini Mental Status Examination

misdiagnosis

mitochondrial disease

monoclonal antibodies

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, cortical enhancement

MRI, diffusion weighted

MRI, FLAIR

MRI, gradient-echo

MRI, gray matter enhancement

MRI, high signal foci on

MRI, hypointense signal foci on

MRI, negative

MRI, punctate pattern

MRI, ring sign

MRI, susceptibility weighted

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, familial

multiple sclerosis, misdiagnosis

myasthenic syndrome

myelitis, transverse, recurrent

myelopathy

myoclonus

neoplasm, primary of CNS

neoplastic angioendotheliosis

neurexin-3 alpha antibodies

neurologic disease, diagnoses of

neurologic examination, focal

neurologic symptoms

neuronal cell surface antigen

neuronal intranuclear inclusion disease

neuropathology

neuropathology, brain

neuropathy

neuropathy, demyelinating

neuroradiology

neurotoxic

next-generation sequencing

old age, neurology of

opportunistic infection, CNS

Parkinson disease, arteriosclerotic

Parkinson disease, L-dopa nonresponsive

Parkinsonism syndrome

paroxysmal neurologic deficits

PAS positive

PAS positive material in the brain

Pelizaeus Merzbacher

persistent vegetative state

personality change

pes cavus

phenylketonuria

pleocytosis of cerebrospinal fluid

polymerase chain reaction

polymerase chain reaction, false negative

pons, lesion of

posterior leukoencephalopathy syndrome

postpartum

precipitating factors

pregnancy, neurologic complications in

prevention of neurologic disorders

prognosis

progressive multifocal leucoencephalopathy

progressive neurologic disorder

propionic aciduria

pseudobulbar palsy

pseudoxanthoma elasticum

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychomotor retardation

psychosis

psychotic behavior

pyramidal tract

pyramidal tract dysfunction

quadriparesis

radiation therapy, CNS treatment and complications with

retinal branch artery occlusion

sedimentation rate, elevated

seizure

seizure, children

seizure, complications following

seizure, febrile

seizure, hyperglycemia causing

seizure, prolonged

seizure, visual loss with

sensorineural hearing loss

serologic testing

serologic testing, false negative

single photon emission computed tomography

skin, biopsy

slow virus infection of CNS

small vessel disease

small vessel disease, cerebral

snout reflex

spinal cord, infarction of

splenomegaly

spondylolysis

spondylosis

steroid therapy, CNS treatment and complications with

Still's disease

striatal encephalitis

striatum, lesion of

striatum, lesion of, bilateral

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

subarachnoid hemorrhage

subarachnoid hemorrhage, cerebral convexity

subcortical hemorrhage

subcortical U fibers

Susac's syndrome

symmetric brain lesions

syncope

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

temporal lobe, lesion

temporal lobe, lesion, bilateral

transient ischemic attack

transient neurologic deficit

treatment of neurologic disorder

treatment resistant

tremor

trinucleotide repeats

urea-cycle enzymopathies

urinary frequency

urinary incontinence

Van der Knaap disease

Virchow-Robin spaces, dilated

virus, slow

visual acuity, decreased

visual field defect

visual loss

walking, difficulty with

white matter disease, location

white matter disease, periventricular

white matter disease, subcortical

white matter disease, unilateral

white matter hyperintensities

wide based gait

workup

Showing articles 1950 to 2000 of 2058 << Previous Next >>

Phosphorylase Deficiency
In Englel & Banker, Myology, McGraw-Hill Book Co, Ch 52, 1585-1601, DiMauro,S.&Bresolin,N., 1986

Acid Maltase Deficiency
Engel, A. G. in Engel and Banker, Myology, McGraw-Hill Co, New York, Ch 55, p. 1629-1651, , 1986

GM1 Gangliosidosis:Clinical and Laboratory Findings in Eight Families
Hum Genet 70:347-354, Giugliani,R.,et al, 1985

Intraparenchymal Hemorrhages
In Neurosurgery, Wilkins RH and Regachary SS, McGraw Hill Book Co, New York 155285., McCormick,W.F., 1985

Aphasia & Agraphia in Lesions of the Posterior Internal Capsule & Putamen
Neurol 35:1797-1801, Tanridag,O.&Kirshner,H.S., 1985

Amnestic Syndrome & Vertical Gaze Palsy:Early Detection of Bilateral Thalamic Infarction by CT & NMR
Stroke 16:823-827, Swanson,R.A.&Schmidley,J.W., 1985

Clinicopathological Conference
Angiitis of Central Nervous System, Case 35-1985, NEJM 313:566-575985., , 1985

Hallervorden-Spatz Disease:Cysteine Accumulation & Cysteine Dioxygenase Deficiency in the Globus Palladus
Ann Neurol 18:482-489, Perry,T.L.,et al, 1985

Carbonic Anhydrase II Deficiency in 12 Families with Osteopetrosis with Renal Tubular Acidosis & Cerebral Calcification
NEJM 313:139-181, Sly,W.S.,et al, 1985

Developmental Dyslexia:Four Consecutive Patients with Cortical Anomalies
Ann Neurol 18:222-233, Galaburda,A.M.,et al, 1985

Cerebral Lateralization, Biological Mechanisms, Associations, & Pathology:I
Arch Neurol 42:428-459, 4271985., Geschwind,N.&Galaburda,A.M., 1985

Biotinidase Deficiency:Initial Clinical Features & Rapid Diagnosis
Ann Neurol 18:614-617, Wolf,B.,et al, 1985

Presentation of Bilateral Thalamic Infarction on CT, MRI & PET
Neuroradiology 27:414-419, Bewermeyer,H.,et al, 1985

Takayasu Arteritis, A Study of 32 North American Patients
Medicine 64:89-99, Hall,S.,et al, 1985

Pure Psychic Akinesia with Bilateral Lesions of Basal Ganglia
JNNP 47:377-385, Laplane,D.,et al, 1984

Computed Tomographic Findings in Wernicke-Korsakoff Syndrome
Arch Neurol 41:453-454, McDowell,J.R.,et al, 1984

Neurologic Outcome in Children with Inborn Errors of Urea Synthesis
NEJM 310:1500-1505, Msall,M.,et al, 1984

Treatment of Episodic Hyperammonemia in Children with Inborn Errors of Urea Synthesis
NEJM 310:1630-1634, Brushlow,S.W.,et al, 1984

Neurological Disorders Associated with Deficiency of Glutamate Dehydrogenase
Ann Neurol 15:144-153, Plaitakis,A.,et al, 1984

Aphasia after Left Thalamic Infarction
Arch Neurol 41:1296-1298, Gorelick,P.B.,et al, 1984

Subcortical Dementia
Arch Neurol 41:874-879, Cummings,J.L.,et al, 1984

Detection of Urea Cycle Enzymopathies in Childhood
Arch Neurol 41:758-760, Trauner,D.A.,et al, 1984

Parkinsonism & Basal Ganglia Infarcts
Neurol 34:1516-1518, Tolosa,E.S.,et al, 1984

Early Computed Tomographic Abnormalities Following Profound Cerebral Hypoxia
Arch Neurol 41:1098-1100, Tippin,J.,et al, 1984

Cerebellar Hemorrhage Complication Methylmalonic & Propionic Acidemia
Arch Neurol 41:1293-1296, Dave,P.,et al, 1984

Ataxia-Telangiectasia:A Multisystem Hereditary Disease with Immunodeficiency
Ann Int Med 99:367-379, Waldmann,T.A.,et al, 1983

Sphenoid Sinusitis
NEJM 309:1149-1154, Lew,D.,et al, 1983

Is"Subcortical Dementia"a Recognizable Clinical Entity
Ann Neurol 14:278-283, Mayeux,R.,et al, 1983

Symmetric Bithalamic & Striatal Hemorrhage Following Peri-natal Hypoxia in a Term Infant
J Comput Assist Tomogr 7:353-355, Kotagal,S.,et al, 1983

Enhancing Mass on CT:Neoplasm or Recent Infarction
Neurol 33:836-840, Masdeu,J.C., 1983

Nuclear Magnetic Resonance (NRM) Imaging in White Matter Dis. of the Brain Using Spin-Echo Sequences
J Comput Assist Tomogr 7:290-294, Young,I.R.,et al, 1983

Acute Neurological Dysfunction Associated with Destructive Lesions of the Basal Ganglia in Children
Ann Neurol 12:328-332, Goutieres,F.,et al, 1982

Ischemic Cerebrovascular Complications of Haemophilus Influenzae Meningitis
Arch Neurol 39:650-652, Dunn,D.W.,et al, 1982

Carbamazepine & Hematological Monitoring
Ann Neurol 11:309-312, Hart,R.G.,et al, 1982

Aphasia With Predominantly Subcortical Lesion Sites
Arch Neurol 39:2-14, Naeser,M.A.,et al, 1982

Aphasia With Nonhemorrhagic Lesions in the Basal Ganglia & Internal Capsule
Arch Neurol 39:15-20, Damasio,A.R.,et al, 1982

Hypomelanosis of Ito (incontinentia pigmenti achromians) :Macrocephaly & Gray Matter Heterotopias
Neurol 32:1013-1016, Ross,D.L.,et al, 1982

Aphasia After Right Thalamic Hemorrhage
Arch Neurol 39:667-669, Kirshner,H.S.,et al, 1982

Progressive Dyskinesia Due to Internal Cerebral Vein Thrombosis
Neurol 32:769-772, Solomon,G.E.,et al, 1982

Brain Abnormalities in Infants with Fotter Syndrome (oligohydramnios tetrad)
Neurol 31:1571-1574, Grunnet,M.L.,et al, 1981

Computed Tomography of the Brain in Severe Hypoglycaemia
J Comput Assist Tomogr 5:757-759, Kaiser,M.C.,et al, 1981

Biochemical Evidence Of Dysfunction Of Brain Neurotransmitters In The Lesch-Nyhan Syndrome
NEJM 305:1106-1111, Lloyd,K.G.,et al, 1981

Computed Tomography of Disseminated Meningeal & Ependymal Malignant Neoplasms
Jr. , et al, Neurol 31:567-57481., Ascherl,G.F., 1981

Computerized Tomographic Enhancement Patterns in Cerebral Infarction
Arch Neurol 37:21-24, Weisberg,L.A., 1980

Gray Matter Enhancement:A Computerized Tomographic Sign of Cerebral Hypoxia
Neurol 30:810-819, Kinkel,W.R.,et al, 1980

Status Epilepticus
Am J Med 69:657-665, Aminoff,M.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

Amelioration Of Neurologic Abnormalities After"Enzyme Replacement"In Adenosine Deaminase Deficiency
NEJM 303:377-380, Hirschhorn,R.,et al, 1980

Cerebellar Calcification on Computerized Tomography
Ann Neurol 7:193-194, Koller,W.C.,et al, 1980

Intracranial Calcification in Hyperparathyroidism Associated with Gait Apraxia & Parkinsonism
Neurol 30:1005-1007, Margolin,D.,et al, 1980

Showing articles 1950 to 2000 of 2058 << Previous Next >>