Neudle.com: midbrain atrophy

Neurology Specific Literature Search

Differential
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abducens nerve paralysis

alien hand syndrome

alpha-fetoprotein

alternating rapid movement

angiography, cerebral

ankle reflex, absent

anterior tibial muscle weakness

anti Yo antibody

antiviral agents

apnea, primary central

apraxia of eyelid opening

aqueduct of Sylvius, enlargement

aqueduct of Sylvius, obstruction

aqueduct of Sylvius, stenosis

aqueductal obstruction

arm swing, reduced

ataxia telangiectasia

ataxia, cerebellar

ataxia, progressive

ataxia, sensory

ataxia, truncal

attention deficit disorder with hyperactivity

autonomic dysfunction

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

B 12 deficiency

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

Behcet's syndrome

biologic markers

blinking, reduced

brain biopsy, false negative

brainstem, atrophy

brainstem, deformity of

brainstem, glioma

brainstem, glioma in children

brainstem, hemorrhage, primary

brainstem, lesion of

brainstem, neoplasms of

calcification, intracranial

carcinoma of lung

CAT scan, abnormal

CAT scan, emission, abnormal

cauda equina, enhancement

cauda equina, lesion of

cavernous sinus

cavernous sinus, metastasis to

central nervous system, infection of

cerebellar ataxia, autosomal recessive

cerebellar ataxia, hereditary

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar disease, eye movement disorder in

cerebellar hypoplasia

cerebellar lesion

cerebellar tonsils

cerebellum, disease of

cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortical atrophy

cerebral infarction

cerebral infarction, subcortical

cerebral peduncle

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, biochemical markers of CNS tumors

cerebrospinal fluid, cytology

cerebrospinal fluid, enzymes in

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrovascular accident

chest x-ray, abnormal

Clinical Pathologic Conference(C.P.C.)

cogwheel rigidty

controversies in neurology

convergence, impaired

Cornelia de Lange syndrome

corpus callosum, lesion of

corpus callosum, thinning

cortical-basal ganglionic degeneration

cranial neuropathy, multiple

cysticercosis, cerebral

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia, frontotemporal

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diagnostic criteria

difficulty going down stairs

distal muscle weakness

down-beat nystagmus, primary position of gaze

downward gaze, paralysis of

dysdiadochokinesia

dystonia, focal

ectopic pinealoma

emergencies, neurologic

epidemiology of neurology

exome sequencing

eye movement, disorders of

eyelid opening, difficulty with

facial weakness

facial weakness, bilateral

fine motor function, impaired

finger nose finger test

fingerprint bodies

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

Friedreich's ataxia

frontotemporal brain sagging syndrome

gastrointestinal perforation

gaze palsy, supranuclear

gaze palsy, vertical

genetic neurologic disorders

genetic testing

glioma, low-grade

globus pallidus, infarction

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

granular osmiphilic material

growth retardation

headache, severe

heel-knee-shin test

hemorrhage, thalamic

hepatic failure

hepatolenticular degeneration, non-Wilsonian

heralding manifestation

high arched feet

Horner's syndrome

human chorionic gonadotropin, elevated

hummingbird sign

hydrocephalus, non-communicating(obstructive)

hyperhomocysteinemia

hyperpigmentation of skin

hypopituitarism

hypothalamus, disturbance of

hypotonia, infants

iatrogenic neurologic disorders

ideomotor apraxia

imbalance, postural

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

infant, evaluation of

infantile tremor syndrome

intellectual deterioration

interpeduncular cistern, compressed

intracranial pressure, increased

Klinefelter's syndrome

Krabbe's disease

lactic acidemia

leg weakness, bilateral

Leigh's disease

lenticular nucleus, lesion of, bilateral

leukoencephalopathy

level of consciousness, decreased

life expectancy

light-near dissociation, causes of

lysosomal storage disease

mammillary bodies

memory, impairment of

meningeal enhancement

meningitis, carcinomatous

metabolic disorder, primary

methylmalonic acidemia

microhemorrhage, intracerebral

midbrain, atrophy

midbrain, compression

midbrain, hemorrhage

midbrain, infarction of

midbrain, lesion of

midbrain, neoplasm of

midbrain, swollen

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

molecular genetics

morning glory sign

movement disorder

MRI, contrast enhanced

MRI, contrast enhanced, subependymal

MRI, diffusion weighted

MRI, spinal cord

multiple sclerosis, differential diagnosis of

multiple system atrophy

myoclonus, epilepsy

nausea and vomiting

neoplasm, germ cell

neoplasm, intracranial with metastasis extracranially

neoplasm, metastatic to CNS

neoplasm, primary intracerebral

neoplasm, primary intracranial-treatment of

neoplasm, primary of CNS

neoplasm, primary of CNS-children

neoplasm, primary of CNS-survival

neoplasm, primary of CNS-treatment of

nerve conduction studies

nerve root enhancement

nerve root, lumbar, lesion of

neuroendocrinology

neurologic disease, diagnoses of

neurologic signs

neuronal ceroid-lipofuscinosis

neuroophthalmology

neuropathology, brain

neuropathy, demyelinating

neuropathy, peripheral

neuropathy, sensory

nutritional deficiency

nystagmus, primary position of gaze

nystagmus, retractorius

nystagmus, rotary

nystagmus, upbeating-in primary position of gaze

obsessive-compulsive disorder

ophthalmoplegia

optic neuropathy

optic neuropathy, bilateral

Parkinson disease

Parkinson disease, atypical

Parkinson disease, axial symptoms

Parkinson disease, L-dopa nonresponsive

Parkinson disease, tremor, absence of

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

PAS positive material in the brain

penguin silhouette sign

periaqueductal lesion

personality change

pineal, calcification of

pineal, neoplasm

pituitary stalk, lesion of

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

pons, flattened

pons, lesion of

positional head-hanging test

precocious puberty

prepontine cistern, effaced

pretectal syndrome

primary intracranial hypotension

progressive neurologic disorder

progressive supranuclear palsy

pseudobulbar palsy

psychomotor retardation

pupil, abnormality in neurologic disorders

pupil, light reflex, abnormal

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadrigeminal plate

quality of life

radiation therapy, CNS treatment and complications with

reading disorder, acquired

reading problem, causes of

remote effect of cancer on the nervous system

respiratory failure

reversible neurologic disorder

rigidity, axial

root lesion, nerve

saccadic eye movements

saccadic eye movements, abnormal

sagging of the brain

sarcoidosis, CNS

seizure, children

sequencing difficulty

serum tumor markers

setting sun phenomena

shunt procedure, lumboperitoneal

shunt procedure, lumboperitoneal-complications of

shunt procedure, ventricular

shunt procedure, ventricular-complications of

shunt procedure, ventriculo-peritoneal

Shy-Drager syndrome

skin, lesions in neurologic disorders

skull x-ray, abnormal

speech disorder

speech disorder, childhood

speech disorder, non aphasic

speech, delayed development of

speech, loss of

spinal cord, lesion of

spinocerebellar ataxia

spinocerebellar ataxia type 12

splenium of corpus callosum

splenium of corpus callosum, displaced

status epilepticus

steroid therapy, CNS treatment and complications with

storage disease of CNS

striatonigral degeneration

striatonigral degeneration, infantile

striatum, lesion of

striatum, lesion of, bilateral

subcortical U fibers

substantia nigra

subthalamic nucleus

superior colliculus

suprasellar lesion

symmetric brain lesions

tandem gait, ataxic

thalamic tumors

third ventricle, enlargement of

third ventricle, wall

tonsillar herniation of cerebellum

treatment of neurologic disorder

tremor, cerebellar

tremor, intention

tremor, writing

trinucleotide repeats

trochlear nerve

trochlear nerve palsy

uncal herniation

upgaze, paralysis of

urinary incontinence

vibratory sensation, abnormal

vision, blurred

visual field defect

visual symptoms

vitamin deficiency

vitamin E deficiency

voice, abnormality of

walking, delayed

walking, difficulty with

Wernicke's encephalopathy

white matter disease

white matter disease, periventricular

wide based gait

Wolfram syndrome

Showing articles 2050 to 2100 of 2535 << Previous Next >>

Bilateral Optic Neuropathy with Remission in Young Men, Variation on a Theme by Leber
Arch Neurol 40:2-6, Lessell,S.,et al, 1983

Pupil Sparing in Oculomotor Palsy:A Brief Review
Ann Neurol 13:143-148, Nadeau,S.E.,et al, 1983

Clin. Path. Conference
Multiple-System Atrophy with Parkinsonism, Case 28-13, NEJM 308:1406-1414983., , 1983

Neurodegenerative Disease of Infancy & Childhood
Ann Neurol 13:351-364, Dyken,P.,et al, 1983

Familial Porencephaly
Arch Neurol 40:567-569, Berg,R.A.,et al, 1983

Evoked Potentials in Olivopontocerebellar Atrophy
Arch Neurol 40:366-369, Hammond,E.J.,et al, 1983

Corpus Callosotomy for Control of Intractable Epilepsy in Children
Neurol 33:891-897, Geoffroy,G.,et al, 1983

Preoperative CT Diagnosis of Mesial Temporal Sclerosis for Surgical Treatment of Epilepsy
Ann Neurol 13:59-64, Wyler,A.R.,et al, 1983

Unilateral Cerebellar Hypoplasia
J Comput Assist Tomogr 7:1077-1078, Mendelsohn,D.B.,et al, 1983

Oligoclonal IgG Bands in Cerebrospinal Fluid in Various Neurological Diseases
Ann Neurol 13:434-439, Chu,A.B.,et al, 1983

Ruptured Aneurysms
BMJ 286:1299-1300, Hitchock,E.R., 1983

Dominant Spinopontine Atrophy
Arch Neurol 40:259-260, Pogacar,S.,et al, 1983

Boxers-Computed Tomography, EEG, & Neurological Evaluation
JAMA 249:211-213, Ross,R.J.,et al, 1983

Reflex Sympathetic Dystrophy (Causalgia) Treatment with Guanethidine
Arch Neurol 40:430-432, Tabira,T.,et al, 1983

Sclerosteosis:Neurogenetic & Pathophysiologic Analysis of an American Kinship
Neurol 33:267-277, Stein,S.A.,et al, 1983

Adult Polyglucosan Body Disease:Clinical & Nerve Biopsy Findings in Two Cases
Ann Neurol 13:440-444, Vos,A.L.M.,et al, 1983

Neuro-Ophthalmologic Signs in the Angiitic Form of Neurosarcoidosis
Neurol 33:1130-1135, Caplan,L.,et al, 1983

Fungal Meningitis Manifesting as Hydrocephalus
Arch Int Med 143:728-731, Mangham,D.,et al, 1983

Quadriceps Myopathy:A Varient of the Limb-Girdle Dystrophy Syndrome
JNNP 46:355-357, Swash,M.,et al, 1983

Acute Respiratory Failure in Motor Neuron Disease
Arch Neurol 40:30-32, Hill,R.,et al, 1983

Effect on Weakness & Spasticity in Amyotrophic Lateral Sclerosis of Thyrotropin-Releasing Hormone
Lancet 2:73-75, Engel,W.K.,et al, 1983

Syndromes of Amytrophic Lateral Sclerosis & Dementia:Relation to Transmissible Creutzfeldt-Jakob Disease
Ann Neurol 14:17-26, Salazar,A.M.,et al, 1983

Conjugal Amyotrophic Lateral Sclerosis
Ann Neurol 14:699, Paolino,E.,et al, 1983

Multifocal Central Nervous System Damage Caused by Toluene Abuse
Neurol 33:1337-1340, Lazar,R.B.,et al, 1983

Clinicopathological Conference
Maroteaux-Lamy Syndrome, Case 44-1983, NEJM 309:1109-1117983., , 1983

Peduncular Hallucinations Caused by Brainstem Compression
Neurol 33:1360-1361, Dunn,D.W.,et al, 1983

Downbeating Nystagmus
Arch Neurol 40:777-784, Halmagyi,G.M.,et al, 1983

Cerebellar Degeneration Caused by High-Dose Cytosine Arabinoside:A Clinicopathological Study
Ann Neurol 14:520-527, Winkelman,M.D.,et al, 1983

Arachnoid Cyst of the Fourth Ventricle Manifesting Normal Pressure Hydrocephalus
Neurosurgery 12:108-110, Korosue,K.,et al, 1983

Acute Hydrocephalus in Tuberculous Meningitis in Adults
Sem Hop 59:1687-1688, Tasseau,F., 1983

Nonfamilial Amyotrophy with Dementia, etc
Advances in Neurology, Human Motor Neuron Diseases, Ed. Rowland, Raven Press, NY 1982 vol 36, p 173., Tyler,H.R., 1982

Intraventricular Hemorrhage In The Premature Infant
NEJM 306:1464-1468, Molteni,R.A.,et al, 1982

Clin. Path. Conference
Osteopetrosis, Malignant Juvenile Form, Case Record 37-1982, NEJM 307:735-74382., , 1982

Cranial Computed Tomography in the Diagnosis of Multiple Sclerosis
JNNP 45:905-912, Loizou,L.A.,et al, 1982

Cerebellar Atrophy in Epilepsy & Headache:Lack of Relationship to Phenytoin
Neurol 32:910-912, Ballenger,C.E.,et al, 1982

Clin. Path. Conference
Tuberculous Meningitis, Case Record 2-1982, NEJM 306:91-97982., , 1982

Progressive Hemifacial Atrophy
Arch Neurol 39:44-46, Asher,S.W.,et al, 1982

A Prospective Study of Lacunar Infarction Using Computerized Tomography
Neurol 32:49-56, Donnan,G.A.,et al, 1982

Chlorpropamide-Induced Optic Neuropathy
Arch Int Med 142:381, Wymore,J.,et al, 1982

Abnormal Brainstem Auditory Evoked Potentials in Chronic Paint Sniffers
Ann Neurol 12:553-556, Metrick,S.A.,et al, 1982

Treatment of Adult-Onset Obstructive Hydrocephalus with Low-or Medium-Pressure CSF Shunts
Neurol 32:1057-1061, McQuarrie,I.G.,et al, 1982

Neurological Aspect of Hyponatraemia
Postgrad Med J 58:737-740, Daggett,P.,et al, 1982

Computed Tomography in Pick's Disease:Findings in a Family Affected in Three Consecutive Generations
J Comput Assist Tomogr 6:907-911, Groen,J.J.,et al, 1982

Cysticercosis Cerebri, Review of 127 Cases
Arch Neurol 39:534-539, McCormick,G.F.,et al, 1982

Santavuori Disease:Diagnosis by Leukocyte Ultrastructure
Neurol 32:1277-1281, Baumann,R.J.,et al, 1982

Pure Motor Hemiplegia Due to Infarction of the Cerebral Peduncle
Arch Neurol 39:524-526, Ho,K-L., 1982

Cerebellar Strokes:Mortality, Surgical Indications, & Results Of Ventricular Drainage
Lancet 2:429-432, Shenkin,H.A.,et al, 1982

Cardiomyopathy Associated with the Syndrome of Amyotrophic Chorea & Acanthocytosis
Ann Int Med 96:616-617, Faillace,R.T.,et al, 1982

Neurotransmitters & CNS Disease, Basal Ganglia Disease
Lancet 2:1141-1147, Marsden,C.D., 1982

Classic Amyotrophic Lateral Sclerosis With Dementia
Arch Neurol 39:681-683, Wilkstrom,J.,et al, 1982

Showing articles 2050 to 2100 of 2535 << Previous Next >>