Neudle.com: midbrain atrophy

Neurology Specific Literature Search

Differential
(Click to cross reference)

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 1150 to 1200 of 2433 << Previous Next >>

Some Specific Clinical Features Differentiate Multiple System Atrophy (Striatonigral Variety) from Parkinson's Disease
Arch Neurol 52:294-298, Colosimo,C.,et al, 1995

Clinical/Metabolic Correlations in Multiple System Atrophy, A PET Study
Arch Neurol 52:179-185, Perani,D.,et al, 1995

Different of Multi Syst Atrophy from Idiopathic Parkinson's Disease Using Proton MR Spectroscopy
Ann Neurol 37:204-210, Davie,C.A.,et al, 1995

Parkinsonism-Recognition and Differential Diagnosis
BMJ 310:447-452, Quinn,N., 1995

Classic Neurogenic Thoracic Outlet Syndrome in a Competitive Swimmer:A True Scalenus Anticus Syndrome
Muscle & Nerve 18:229-233995., Katirji,B.&Hardy,R.W., 1995

Paraneoplastic Cerebellar Degeneeration with Anti-Yo Antibody in a Man
Neurol 45:1226-1227, Felician,O.,et al, 1995

Pineal Parenchymal Tumors:CT and MR Features
J Comput Assist Tomogr 19:509-517, Chiechi,M.V.,et al, 1995

High Resolution MRI of Anterior Visual Pathway in Pts with Optic Neuropathies Using Fast Spin Echo & Phased Array Local Coils
JNNP 58:562-569, Gass,A.,et al, 1995

Multiple System Atrophy presenting as Parkinsonism:Clinical Features and Diagnostic Criteria
JNNP 59:144-151, Albanese,A.,et al, 1995

Stereotactic Ventral Pallidotomy for Parkinson's Disease
Neurol 45:753-761, Dogali,M.,et al, 1995

Bilateral Ulnar Handcuff Neuropathies with Segmental Conduction Block
Muscle & Nerve 18:1021-1023995., Satkunam,L.&Zochodne,D., 1995

Complications with Shunts in Adults with Spina Bifida
BMJ 311:286-287, Tomlinson,P.&Sugarman,I.D., 1995

The Predictive Value of CSF Dynamic Tests in Patients with the Idiopathic Adult Hydrocephalus Syndrome
Arch Neurol 52:783-789, Malm,J.,et al, 1995

PET Studies on the Dopaminergic Sys & Striatal Opioid Binding in the OPCA Variant of Multiple System Atrophy
Ann Neurol 37:568-573, Rinne,J.O.,et al, 1995

Juvenile Huntington Disease:CT and MR Features
AJNR 16:1405-1412, Ho,V.B.,et al, 1995

Surgical Treatment of Temporal Lobe Epilepsy:Clinical, Radiological and Histopathological Findings in 178 Patients
JNNP 58:666-673, Zentner,J.,et al, 1995

Bilaterally Symmetric Hippocampi and Surgical Outcome, Jack
Neurol 45:1353-1358, Jr,C.R.,et al, 1995

Hippocampal Volumetrics Differentiate Pts with Temporal Lobe Epilepsy & Extratemporal Lobe Epil
Arch Neurol 52:819-824, Gilmore,R.L.,et al, 1995

Preoperative MRI Predicts Outcome of Temporal Lobectomy:An Actuarial Analysis
Neurol 45:1358-1363, 12481995., Berkovic,S.F.,et al, 1995

Comparison of Ictal SPECT and Interictal PET in the Presurgical Evaluation of Temporal Lobe Epielspy
Ann Neurol 37:738-745, Ho,S.S.,et al, 1995

Neurologic Abnormalities in Murderers
Neurol 45:1641-1647, Blake,P.Y.,et al, 1995

Genetic Homogeneity Between Childhood-Onset and Adult-Onset Autosomal Recessive Spinal Muscular Atrophy
Lancet 346:741-742, Brahe,C.,et al, 1995

Cataplexy Associated with Midbrain Lesion
Neurol 45:393-394, Fernandez,J.M.,et al, 1995

Third Nerve Palsy as a Presentign Sign of Acquired Immune Deficiency Syndrome
J Clin Neuro-ophthalmol 7:125-128, Antworth,M.V.,et al, 1995

Brainstem Ocular Motility Defects and AIDS
Am J Ophthalmol 106:437-442, Hamed,L.M.,et al, 1995

Solitary Midbrain Toxoplasmosis and Olivary Hypertrophy in a Patient with Acquired Immunodeficiency Syndrome
Clin Neuropath 8:35-40, Kure,K.,et al, 1995

"Rubral"Tremor due to Midbrain Toxoplasma Abscess
Movement Disorders 5:254-256, Koppel,B.S.&Daras,M., 1995

Clinicopath Conf
Multiple Myeloma with Bilateral Carpal Tunnel Syndrome Probably Due to Secondary Amyloid Deposit, Ca, e38-1995,NEJM 333:1625-1630,1995., 1995

The Hippocampus in Status Epilept:Signal Intensity & Morph Changes with Sequent Fast Spin-Echo MR Imaging
Radiology 194:249-256, Tien,R.D.&Felsberg,G.J., 1995

Clinical, Neuropath & Genetic Studies of Large Spinocerebellar Ataxia Type 1 (SCA1) Kindred: (CAG) n Early Premonitory Signs & Symp
Neurol 45:24-30, Genis,D.,et al, 1995

Autosomal Dominant Cerebellar Phenotypes:The Genotype has Settled the Issue
Neurol 45:1-5, Rosenberg,R.N., 1995

Magnetic Resonance Angiography in the Diagnosis of Deep Cerebral Venous Thrombosis
J Stroke Cerebrovasc Dis 5:29-32, Finelli,P.F.,et al, 1995

Cranial MRI in Ataxia-Telangiectasia
Neuroradiology 37:77-82, Sardanelli,F.,et al, 1995

On Politics and Health:An Epidemic of Neurologic Disease in Cuba
Ann Int Med 122:530-533, Roman,G.C., 1995

Gadolinium-Enhanced MR Findings in a Pediatric Case of Wernicke Encephalopathy
AJNR 16:700-702, Harter,S.B.&Nokes,S.R., 1995

Neurofibromatosis Type 1:Pathologic Substrate of High-Signal-Intensity Foci in the Brain
Radiology 195:721-724, DiPaolo,D.P.,et al, 1995

MR Findings in Adult-Onset Adrenoleukodystrophy
AJNR 16:1227-1237, Kumar,A.J.,et al, 1995

Posterior Cerebral Artery Stenosis with Midbrain Infarction
Stroke 26:900-902, Duncan,G.W.&Weindling,S.M., 1995

Neurosurgical Management of Cerebellar Haematoma and Infarct
JNNP 59:287-292, Mathew,P.,et al, 1995

Thalamic Hemorrhage:A Prospective Study of 100 Patients
Stroke 26:964-970, Kumral,E.,et al, 1995

Binswanger's Disease-Revisited
Neurol 45:626-633, Caplan,L.R., 1995

Double-Blind Study with Levorotatory form of Hydroxytryptophan in Pts with Degen Cerebellar Dis
Arch Neurol 52:451-455, 4401995., Wessel,K.,et al, 1995

MRI of the Brain in Wilson Disease:T2 Signal Loss Under Therapy
J Comput Assist Tomogr 19:635-638, Engelbrecht,V.,et al, 1995

Multiple Sclerosis in the Spinal Cord, MR Appearance and Correlation with Clinical Parameters
Radiology 195:725-732, Tartaglino,L.M.,et al, 1995

Clinical and Genetic Studies of Fatal Familial Insomnia
Neurol 45:1068-1075, Reder,A.T.,et al, 1995

Dentatorubral-Pallidoluysian Atrophy:Clin Features Closely Related to Unstable Expansion of Trinucleotide (CAG) Repeat
Ann Neurol 37:769-775, Ikeuchi,T.,et al, 1995

Apolipoprotein E Genotype in Diverse Neurodegenerative Disorders
Ann Neurol 38:131-135, Schneider,J.A.,et al, 1995

Reflex Sympathetic Dystrophy
BMJ 310:1645-1648, Paice,E., 1995

Reflex Sympathetic Dystrophy in Children
BMJ 310:1648-1649, Lloyd-Thomas,A.R.&Lauder,G., 1995

Encephalopathy with Parkinsonian Features in Children Following Bone Marrow Transplantations and High-Dose Amphotericin B
Ann Neurol 37:810-814, Mott,S.H.,et al, 1995

Showing articles 1150 to 1200 of 2433 << Previous Next >>