Neudle.com: midbrain atrophy

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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 1350 to 1400 of 2535 << Previous Next >>

Signs and Symptoms of Reflex Sympathetic Dystrophy:Prospective Study of 829 Patients
Lancet 342:1012-1016, Veldman,P.H.J.M.,et al, 1993

Communicating Hydrocephalus, Basilar Invagination, and Other Neurologic Features in Osteogenesis Imperfecta
Neurol 43:2603-2608, Charnas,L.R.&Marini,J.C., 1993

Choroid Plexus Infection in Cerebral Toxoplasmosis in AIDS Patients
Neurol 43:2035-2040, Falangola,M.F.&Petito,C.K., 1993

Neurosurgical Management of the Acquired Immunodeficiency Syndrome
West J Med 158:249-253, Andrews,B.T.&Kenefick,T.P., 1993

Poliomyelitis:Hyperintensity of the Anterior Horn Cells on MRI Images of the Spinal Cord
AJR 161:863-865, Malzberg,M.S.,et al, 1993

Hereditary Motor-Sensory Neuropathy (Charcot-Marie-Tooth Disease) with Nerve Deafness:A New Variant
J Pediatr 123:431-434, Hamiel,O.P.,et al, 1993

Charcot-Marie-Tooth Disease Type 1A:Association with a Spontaneous Point Mutation in the PMP22 Gene
NEJM 329:96-101, Roa,B.B.,et al, 1993

Magnetic Resonance Imaging of Brain and the Neuromotor Disorder in Endemic Cretinism
Ann Neurol 34:91-94, Ma,T.,et al, 1993

Leber's Hereditary Optic Neuropathy as a Cause of Severe Visual Loss in Childhood
Pediatrics 91:988-989, Moorman,C.M.&Elston,J.S., 1993

Atypical Leber's Hereditary Optic Neuropathy with Molecular Confiramtion
Arch Neurol 50:470-473, Weiner,N.C.,et al, 1993

Leber's Hereditary Optic Neuropathy, New Genetic Considerations
Arch Neurol 50:540-548, Newman,N.J., 1993

Neuropathic Findings in Oculopharyngeal Muscular Dystrophy, Seven Cases & Review of Literature
Arch Neurol 50:481-488, Hardiman,O.,et al, 1993

Pretectal Eyelid Retraction and Lag
Ann Neurol 33:554-557, Galetta,S.L.,et al, 1993

Multiple System Atrophy & Prog Supranuc Palsy, Dimin Striatal D2 Dopamine Receptor Act by SPECT
Arch Neurol 50:513-516, vanRoyen,E.,et al, 1993

TORCH Infections in the Newborn
Semin Neurol 13:106-115, Donley,D.K., 1993

Embolic Cerebral Infarction:MR Findings in the First 3 Hours AFter Onset
AJR 160:1077-1082, Shimosegawa,E.,et al, 1993

Single-Photon Emission Computed Tomographic Investigation of Patients with Motor Neuron Disease
Neurol 43:1569-1573, Abe,K.,et al, 1993

Spinal Fluid Cells and Protein in Amyotrophic Lateral Sclerosis
Arch Neurol 50:489-491, Norris,F.H.,et al, 1993

The Natural History of Amyotrophic Lateral Sclerosis
Neurol 43:1316-1322, Ringel,S.P.,et al, 1993

MRI in Acute Transverse Myelopathy
Neuroradiology 35:221-226, Holtas,S.,et al, 1993

Facial Asymmetry, Hippocampal Pathology, & Remote Symptomatic Seizures:A Temporal Lobe Epileptic Syndrome
Neurol 43:725-727, Cascino,G.D.,et al, 1993

Update on Surgical Treatment of the Epilepsies, Second Intern Palm Desert Conf on Surgical Trtm of Epilepsies (1992)
Neurol 43:1612-1617, Engel,J.Jr., 1993

Early Childhood Prolonged Febrile Convulsions, Atrophy & Sclerosis of Mesial Struc & Temporal Lobe Epilepsy:An MRI Study
Neurol 43:1083-1087, Cendes,F.,et al, 1993

Magnetic Resonance Imaging in Childhood Intractable Partial Epilepsies:Pathologic Correlations
Neurol 43:681-687, Kuzniecky,R.,et al, 1993

Detection of Hippocampal Pathology in Intractable Partial Epilepsy
Neurol 43:1793-1799, Jackson,G.D.,et al, 1993

Measurement of Whole Temporal Lobe and Hippocampus for MR Volumetry:Normative Data
Neurol 43:2006-2010, Bhatia,S.,et al, 1993

Charact of Medial Temporal Lobe Epilepsy:Interictal & Ictal EEG, Neuropsych Test, Imaging, Surg Results & Path
Ann Neurol 34:781-787, Williamson,P.D.,et al, 1993

Hippocampal Sclerosis in Epilepsy and Childhood Febrile Seizures
Lancet 342:1391-1394, Kuks,J.B.M.,et al, 1993

Hippocampal Sclerosis in Children with Intractable Temporal Lobe Epilepsy:Detection with MR Imaging
AJR 161:1045-1048, Grattan-Smith,J.D.,et al, 1993

Diagnosis of Medial Temporal Lobe Seizure Onset:Relative Specificity and Sensitivity of Quantitative MRI
Neurol 43:2117-2124, Spencer,S.S.,et al, 1993

X-Chromosome Effects on Female Brain:A Magnetic Resonance Imaging Study of Turner's Syndrome
Lancet 342:1197-1200, Murphy,D.G.M.,et al, 1993

Functional and Magnetic Resonance Imaging Correlates of Callosal Involvement in Multiple Sclerosis
Arch Neurol 50:1077-1082, Pelletier,J.,et al, 1993

Hallervorden-Spatz Disease with Bilat Invol of Globus Pallidus & Substantia Nigra:MR Demonstra
J Comput Assist Tomogr 17:961-963, Porter-Grenn,L.,et al, 1993

MRI Pallidal Hyperintensity & Brain Atrophy in Cirrhotic Pts:2 Different MRI Patterns of Clin Deterior?
Neurol 43:2570-2573, Kulisevsky,J.,et al, 1993

Brain Imaging in Late-Onset CM2 Gangliosidosis
Neurol 43:2055-2058, Streifler,J.Y.,et al, 1993

Risk Factors for Nursing Home Placement in Advanced Parkinson's Disease
Neurol 43:2227-2229, Goetz,C.G.&Stebbins,G.T., 1993

Clinicopath Conf
Acquired Demyelinating Neuropathy, ? CIDP, ? Motor Neuropathy with Multifocal Conduction Blocks, Cas, 41-1EJM 329:1182-1190,1993., 1993

Inherited Primary Peripheral Neuropathies
JAMA 270:2326, 23301993., Lupski,J.R.,et al, 1993

Discrete Cortical Infarction with Prominent Impairment of Thumb Flexion
Stroke 24:2118-2120, Terao,Y.,et al, 1993

Funct'l Import of Ventric Enlarge & Cortical Atrophy in Healthy Subj & Alcoholics:PET, MR, & Neuropsych Testing
Radiology 186:59-65, Wang,G.,et al, 1993

Cerebellar Infarction, Clinical and Anatomic Observations in 66 Cases
Stroke 24:76-83, Kase,C.S.,et al, 1993

Magnetic Resonance Imaging in Hereditary and Idiopathic Ataxia
Neurol 43:318-325, Wullner,U.,et al, 1993

Pick's Disease Versus Alzheimer's Disease:A Comparison of Clinical Characteristics
Neurol 43:289-292, Mendez,M.F.,et al, 1993

Clinicopath Conf
Cysticercosis Involving Basal Cisterns of Brain, Case 8-1993, NEJM 328:566-573993., , 1993

Callosal Atrophy with Reduced Cortical Oxygen Metabolism in Carotid Artery Disease
Stroke 24:88-93, Yamauchi,H.,et al, 1993

The Visual Variant of Alzheimer's Disease, A Clinicopathologic Case Study
Neurol 43:305-313, Levine,D.N.,et al, 1993

Rapidly Progressive Aphasic Dementia and Motor Neuron Disease
Ann Neurol 33:200-207, Caselli,R.J.,et al, 1993

Terfenadine-Induced Tremor
Ann Neurol 33:226, Soto,J.,et al, 1993

Competent Pts with Adv States of Perm Paralysis Have the Right to Forgo Life-Sustaining Therapy
Neurol 43:224-225, Bernat,J.L.,et al, 1993

Stimulus-Specific pathological Laughter:A Case Report with Discrete Unilateral Localization
Neurol 43:229-230, Doorenbos,D.I.,et al, 1993

Showing articles 1350 to 1400 of 2535 << Previous Next >>