Neudle.com: "midbrain atrophy"

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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

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)

hypopituitarism

hypothalamus, disturbance of

hypotonia, infants

iatrogenic neurologic disorders

ideomotor apraxia

imbalance, postural

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

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, 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

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 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 0 to 50 of 2398 Next >>

Reversible Parkinsonism Caused by Lumboperitoneal Shunt Overdrainage
Neurol 99:486-488, Takeuchi, H.,et al, 2022

Clinicopathologic Conference, Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome
NEJM 385:165-175, Case 20-2021, 2021

Complex Ataxia
Neurol 95:136-141, Abkur, T.,et al, 2020

Pes Cavus and Neuropathy
Neurol 93:e823-e826, Alderson,J.,& Ghosh,P.S., 2019

Action Tremor, Impaired Balance, and Executive Dysfunction in Midlife
JAMA Neurol 74:603-604, Birch, R.C. & Trollor, J.N., 2017

Advances in Progressive Supranuclear Palsy: New Diagnostic Criteria, Biomarkers, and Therapeutic Approaches
Lancet Neurol 16:552-563, Boxer, A.L.,et al, 2017

MRI Characteristics of Globus Pallidus Infarcts in Isolated Methylmalonic Acidemia
AJNR 36:194-201, Baker, E.H.,et al, 2015

Characyeristic features and progression of abnormalities on MRI for CARASIL
Neurol 85:459-463, Sekine, Y., etal, 2015

Disturbances of Cerebrospinal Fluid, Including Hydrocephalus, Pseudotumor Cerebri, and Low-Pressure Syndromes, Parkinsonism and Midbrain Syndromes with Hydrocephalus and Shunting
Adams & Victors Principles of Neurology, Chp 30, pg 627, Ropper, A.H.,et al, 2014

The Autosomal Recessive Cerebellar Ataxias
NEJM 366:636-646, Anheim,M.,et al, 2012

Basal Ganglia Involvement in Wernicke Encephalopathy: Report of 2 Cases
AJNR 32:E129-E131, Zuccoli, G.,et al, 2011

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

Frontotemporal brain sagging syndrome
Neurol 76:1377-1382, Wicklund, M.R.,et al, 2011

A 75-Year-Old Woman with Progressive Right-Hand Tremor and Inability to Use Her Right Side
Neurol 73:1399-1405, Kertesz,A.,et al, 2009

Imaging-Pathologic Correlation in Corticobasal Degeneration
AJNR 30:1884-1892, Tokumaru,A.,et al, 2009

Progressive Supranuclear Palsy: A Current Review
The Neurologist 14:79-88, Lubarsky,M. &Juncos,J.L., 2008

New and Reliable MRI Diagnosis for Progressive Supranuclear Palsy
Neurol 64:2050-2055, Oba,H.,et al, 2005

Morning Glory Sign: A Particular MR Finding in Progressive Supranuclear Palsy
Magn Reson Med Sci 3:125-132, Adachi, M., et al, 2004

SCA-12: Tremor with Cerebellar and Cortical Atrophy is Associated with a CAG Repeat Expansion
Neruol 56:299-303,287, O'Hearn,E.,et al, 2001

Tectal Gliomas: Natural History of an Indolent Lesion in Pediatric Patients
Pediatr Neurosurg 32:24-29, Bowers,D.C.,et al, 2000

Clinicopath Conf
Progressive Supranuclear Palsy, Case 26, 1997, NEJM 337:549-55697., , 1997

Paraneoplastic Cerebellar Degeneration
Arch Int Med 157:1258-1262, Bolla,L.&Palmer,R.M., 1997

Wolfram Syndrome:Hereditary Diabetes Mellitus with Brainstem and Optic Atrophy
Ann Neurol 39:352-360, Scolding,N.J.,et al, 1996

MR of Sarcoidosis in the Head and Spine:Spectrum of Manifestations and Radiographic Response to Steroid Therapy
AJNR 15:973-982, Lexa,F.J.&Grossman,R.I., 1994

Focal Tectal Tumors:Management and Prognosis
Neurol 44:953-956, Squires,L.A.,et al, 1994

The Motor Disorder of Multiple System Atrophy
JNNP 56:1239-1242, Quinn,N.P.&Marsden,C.D., 1993

Clinicopath Conf
Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992

Chronic Acquired Hepatic Failure:MR Imaging of the Brain at 1. 5 T
AJR 157:1111-1116, Brunberg,J.A.,et al, 1991

MRI Findings in Neuro-Behcet's Disease
Neurol 41:405-408, AlKawi,M.Z.,et al, 1991

Non-Neoplastic Pineal Cysts
Neurol 41:1034-1040, Fetell,M.R.,et al, 1991

Central Nervous System Germinomas, A Review
Arch Neurol 48:652-657, Horowitz,M.B.&Hall,W.A., 1991

MR Imaging of Pineal Tumors
AJR 155:143-151, Tien,R.D.,et al, 1990

The Pretectal Syndrome:206 Patients
Neurol 40:684-690, Keane,J.R., 1990

Wernicke Encephalopathy:MR Findings in Five Patients
AJR 155:1309-1314, Gallucci,M.,et al, 1990

MR Imaging in Progressive Suupranuclear Palsy and Shy-Drager Syndrome
J Comput Assist Tomogr 13:555-560, Savoiardo,M.,et al, 1989

Clinicopath Conf
Adenocarcinoma of Lung, with Metastasis to Meninges of Brain, Spinal Cord & Optic Nerves, Case Recor, 14-1EJM 318:903-915,1988., 1988

Partial Dorsal Mesencephalic Hemorrhages:Report of Three Cases
Neurol 36:529-533, Sand,J.J.,et al, 1986

Mesencephalic Hemorrhages:Clinical & Computed Tomographic Correlations
Weisberg. L. A. , Neurol 36:713-7166., , 1986

Death from Cysticercosis
West J Med 140:787-789, Keane,J.R., 1984

Clin. Path. Conference
Pineocytoma, Case Record 35-1983, NEJM 309:542-549983., , 1983

Human Cerebellar Hypoplasia, A Syndrome of Diverse Causes
Arch Neurol 37:300-305, Sarnatt,H.B.,et al, 1980

Pineal Tumors
Arch Neurol 35:736-740, Donat,J.F.,et al, 1978

Encephalomyelopathy of Leigh
Editorial BMJ 238, 1971, May., , 1971

An 81-Year-Old Man with Imbalance and Memory Impairment
, Golbe,L.I.,et al,

A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
JAMA Neurol 81:83-84, Hua,L.,et al, 2024

Reversible Cortical and Basal Ganglia Lesions in Late-Onset Methylmalonic Aciduria
JAMA Neurol 81:1-82, Chu,X.C.,et al, 2024

Neurovascular Complications of Iatrogenic Fusarium solani Meningitis
NEJM 390:522-529, Strong, N.,et al, 2024

A 51-Year-Old Woman with Abnormal Corups Callosum Signal
JAMA Neurol 81:192-193, Xie,N. & Sun, Q, 2024

Clinicopathologic Conference, Myeloperoxidase antineutrophil cytoplasmic antibody-associated vasculitis
NEJM 390:843-851, Case 7-2024, 2024

Showing articles 0 to 50 of 2398 Next >>