Neudle.com: midbrain atrophy

Differential
(Click to cross reference)

abducens nerve paralysis

accommodation

alien hand syndrome

alopecia

alpha-fetoprotein

alternating rapid movement

aminoacidurias

anemia

angiography, cerebral

anisocoria

ankle reflex, absent

anosmia

anterior tibial muscle weakness

apnea, primary central

applause sign

apraxia of eyelid opening

aqueduct of Sylvius, enlargement

aqueduct of Sylvius, obstruction

aqueduct of Sylvius, stenosis

aqueductal obstruction

ataxia telangiectasia

attention deficit disorder with hyperactivity

autoantibodies

autonomic dysfunction

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

B 12 deficiency

Babinski sign

basal ganglia

basal ganglia, lesion of

basal ganglia, lesion, bilateral

brain biopsy, false negative

brainstem

brainstem, atrophy

brainstem, deformity of

brainstem, glioma

brainstem, glioma in children

brainstem, hemorrhage, primary

brainstem, lesion of

brainstem, neoplasms of

breast feeding

CAG repeats

calcification, intracranial

CAT scan, emission, abnormal

cauda equina

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

children

cirrhosis

Clinical Pathologic Conference(C.P.C.)

controversies in neurology

convergence

convergence, impaired

Cornelia de Lange syndrome

corpus callosum, lesion of

corpus callosum, thinning

cortical-basal ganglionic degeneration

cough

cranial neuropathy, multiple

cysticercosis

cysticercosis, cerebral

deafness

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia

dementia, frontotemporal

depression

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diagnostic criteria

diarrhea

difficulty going down stairs

diplopia

distal muscle weakness

dizziness

down-beat nystagmus, primary position of gaze

downward gaze

downward gaze, paralysis of

emergencies, neurologic

epidemiology of neurology

exome sequencing

eye movement, disorders of

eyelid opening, difficulty with

facial weakness

facial weakness, bilateral

falling

familial

fine motor function, impaired

finger nose finger test

fingerprint bodies

foot deformity

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

Friedreich's ataxia

frontotemporal brain sagging syndrome

gadolinium

gait disorder

gait, apraxic

gastrointestinal perforation

gaze palsy

gaze palsy, supranuclear

gaze palsy, vertical

gene

gene mutation

genetic neurologic disorders

genetic testing

glioma

glioma, low-grade

globus pallidus, infarction

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

granular osmiphilic material

hepatolenticular degeneration, non-Wilsonian

hepatomegaly

heralding manifestation

high arched feet

Horner's syndrome

human chorionic gonadotropin, elevated

hummingbird sign

hydrocephalus

hydrocephalus, non-communicating(obstructive)

hyperhomocysteinemia

hyperpigmentation of skin

hyperreflexia

hypophonia

hypopituitarism

hypothalamus, disturbance of

hypotonia

hypotonia, infants

iatrogenic neurologic disorders

ideomotor apraxia

imbalance

imbalance, postural

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

incoordination

infant, evaluation of

infantile tremor syndrome

intellectual deterioration

interpeduncular cistern, compressed

intracranial pressure, increased

Klinefelter's syndrome

Krabbe's disease

lactic acidemia

L-dopa

leg weakness, bilateral

Leigh's disease

lenticular nucleus, lesion of, bilateral

lethargy

leukodystrophy

leukoencephalopathy

level of consciousness, decreased

life expectancy

light-near dissociation, causes of

liver disease

low back pain

lysosomal storage disease

mammillary bodies

masked facies

memory, impairment of

meningeal enhancement

meningioma

meningitis, carcinomatous

metabolic disorder, primary

methylmalonic acidemia

Mexican

Mexico

microhemorrhage, intracerebral

midbrain

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

MRI, contrast enhanced

MRI, contrast enhanced, subependymal

MRI, diffusion weighted

MRI, negative

MRI, serial

MRI, spinal cord

multiple sclerosis, differential diagnosis of

multiple system atrophy

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

neuropathology, brain

neuropathy

neuropathy, demyelinating

neuropathy, peripheral

neuropathy, sensory

nutritional deficiency

nystagmus

nystagmus, primary position of gaze

nystagmus, retractorius

nystagmus, rotary

nystagmus, upbeating-in primary position of gaze

obesity

obsessive-compulsive disorder

optic neuropathy, bilateral

pain, back

papilledema

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

PAS positive material in the brain

past pointing

penguin silhouette sign

periaqueductal lesion

personality change

pes cavus

pineal

pineal, calcification of

pituitary stalk, lesion of

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

pons, flattened

pons, lesion of

positional head-hanging test

preclinical

precocious puberty

prepontine cistern, effaced

pretectal area

pretectal syndrome

primary intracranial hypotension

prognosis

progressive neurologic disorder

progressive supranuclear palsy

pseudobulbar palsy

psychomotor retardation

pupil

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

quadriparesis

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

retrocollis

reversible neurologic disorder

saccadic eye movements

saccadic eye movements, abnormal

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

sinemet

skew deviation

skin, lesions in neurologic disorders

skull x-ray, abnormal

spasticity

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

steroid therapy, CNS treatment and complications with

storage disease of CNS

striatonigral degeneration

striatonigral degeneration, infantile

striatum, lesion of

striatum, lesion of, bilateral

symmetric brain lesions

third ventricle, enlargement of

third ventricle, wall

titubation

toe walking

tonsillar herniation of cerebellum

treatment of neurologic disorder

trinucleotide repeats

tripping

trochlear nerve

trochlear nerve palsy

vibratory sensation, abnormal

voice, abnormality of

walking frame

walking, delayed

walking, difficulty with

Wernicke's encephalopathy

wheelchair

white hair

white matter disease

white matter disease, periventricular

Showing articles 300 to 350 of 2433 << Previous Next >>

Pseudoradial Nerve Palsy Caused by Acute Ischemic Stroke
J Invest Med Case Report doi:10.1177/2324709616658310, Tahir, H.,et al, 2016

SPG7 Mutations Explain a Significant Proportion of French Canadian Spastic Ataxia Cases
Eur J Hum Genet 24:1016-1021, Choquet,K.,et al, 2016

Differential Diagnosis
Thoracic Key, Southerland,A.W.,et al, 2016

Emerging Cases of Powassan Virus Encephalitis in New England:Clinical Presentation, Imaging, and Review of the Literature
CID 62:707-713, Piantadosi,A.,et al, 2016

Ocular Manifestations in Systemic Lupus Erythematosus
Br J Ophthalmol 100:135-144, Silpa-Archa,S.,et al, 2016

MRI Characteristics of Neuromyelitis Optica Spectrum Disorder
Neurol 84:1165-1173, Jin Kim, H.,et al, 2015

Extraintestinal Manifestations of Coeliac Disease
Nat Rev Gastroenterol Hepatol 12:561-571, Leffler, D.A.,et al, 2015

Practice Guideline: Idiopathic Normal Pressure Hydrocephalus: Response to Shunting and Predictors of Response
Neurol 85:2063-2071, Halperin, J.J.,et al, 2015

A 48-year-old Man with Walking Difficulty
Neurol 85:e165-e169, Kalladka, D.,et al, 2015

A Case of Hirayama Disease Presenting with Polymyoclonus
Neurol 85:e156, Ong, J.J.Y.,et al, 2015

Brain Abnormalities in Newly Diagnosed Neuropsychiatric Lupus: Systematic MRI Approach and Correlation with Clinical and Laboratory Data in a Large Multicenter Cohort
Autoimmun Rev 14:153-159, Sarbu, N.,et al, 2015

Stent-Retriever Thrombectomy after Intravenous t-PA vs. t-PA Alone in Stroke
NEJM 372:2285-2295,2347, Saver, J.L.,et al, 2015

Ischemic Optic Neuropathies
NEJM 372:2428-2436, Biousse, V. & Newman, N.J., 2015

Parry Romberg Syndrome: 7 Cases and Literature Review
AJNR 36:1355-1361, Wong, M.,et al, 2015

Responsibilities of Health Care PRofessionals in Counseling and Educating Patients with Incurable Neurological Diseases Regarding "Stem Cell Tourism"
JAMA Neurol 72:1342-1345, Bowman, M.,et al, 2015

A 56-year-old Man with Cognitive Impairment and Difficulty Tying his Necktie
Neurol 85:e116-e122, Baker, J.M.,et al, 2015

Non-Alzheimers Dementia 1 Frontotemporal Dementia
Lancet 386:1672-1682, Bang, Jee.,et al, 2015

Non-Alzheimers Dementia 2 Lewy Body Dementias
Lancet 386:1683-1697, Walker, Z.,et al, 2015

Autopsy Case of Severe Generalized Dystonia and Static Ataxia with Marked Cerebellar Atrophy
Neurol 85:1522-1524, Miyamoto, R.,et al, 2015

Clinicopathologic Conference, Frontotemporal Lobar Degeneration with Tau-positive Inclusions (Picks Disease Subtype) Due to a Gly389Arg MAPT Mutation, Resulting in the Behavioral Variant of Frontotemporal Dementia with Parkinsonism
NEJM 372:1151-1162, Miller, B.L.,et al, 2015

Owls Eye Sign
Neurol 84:1500, Kumar, S.,et al, 2015

Comparing 3T and 1.5T MRI for Mapping Hippocampal Atrophy in the Alzheimers Disease Neuroimaging Initiative
AJNR 36:653-660, Chow, N.,et al, 2015

Clinicopathologic Conference, Primitive Neuroectodermal Tumor of CNS, with Involvement of Thalamus, Medial Cerebral Cortex, Brainstem, Cerebellum and Subarachnoid Space
NEJM 372:1550-1562, Case 12-2015, 2015

Complex Regional Pain Syndrome
Neurol 84:89-96, Birklein, F.,et al, 2015

MRI Findings in Children with Acute Flaccid Paralysis and Cranial Nerve Dysfunction Occurring during the 2014 Enterovirus D68 Outbreak
AJNR 36:245-250, Maloney, J.A.,et al, 2015

Clinical Laboratory and Findings of 21 Patients with Radiation-Induced Myopathy
JNNP 86:152-158, Ghosh, P.S. & Milone M., 2015

Multiple-System Atrophy
NEJM 372:249-263, Fanciulli, A. & Wenning, G.K., 2015

A 40-year old Woman with Difficulty Going Down Stairs in High-Heeled Shoes
Ann Neurol 77:1-7, Scripko, P.,et al, 2015

Imaging Findings after Methanol Intoxication (Cohort of 46 Patients)
Neuro Endocrinol Lett 36:101-108, Vaneckova, M.,et al, 2015

Using Diffusion-Weighted Magnetic Resonance Imaging to Confirm a Diagnosis of Posterior Ischaemic Optic Neuropathy
Neuro-Ophthalmol 39:161-165, Quddus, A.,et al, 2015

Ocular Sarcoidosis
Clin Chest Med 36:669-683, Pasadhika,S. & Rosenbaum,J.T., 2015

IVth Ventricular Neurocysticercal Cyst
Neurol 83:1990, Jauhari, P.,et al, 2014

A 75-year-old man with 3 years of Visual Difficulties
Neurol 83:e160-e165, Berkowitz, A.L.,et al, 2014

Sturge-Weber Syndrome
UptoDate , Nov, Bodensteiner, J.B., 2014

The Acquired Metabolic Disorders of the Nervous System, Ischemic-Hypoxic Encephalopathy
Adams & Victors Principles of Neurology Chp 40, pg 1133, Ropper, A.H.,et al, 2014

The Acquired Metabolic Disorders of the Nervous System, Carbon Monoxide Poisoning
Adams & Victors Principles of Neurology Chp 40, pg 1138, Ropper, A.H.,et al, 2014

Diseases of the Nervous System Caused by Nutritional Deficiency, Vitamin B12 (Cobalamin) Deficiency (Subacute Combined Degeneration)
Adams & Victors Principles of Neurology Chp 41, pg 1172, Ropper, A.H.,et al, 2014

Diseases of the Nervous System Caused by Nutritional Deficiency, Nutritional Optic and Peripheral Neuropathy, Tobacco-Alcohol Amblyopia, and Strochan Syndrome
Adams & Victors Principles of Neurology Chp 41, pg 1177, Ropper, A.H.,et al, 2014

Diseases of the Nervous System Caused by Nutritional Deficiency, "Alcoholic" Cerebellar Degeneration
Adams & Victors Principles of Neurology Chp 41, pg 1178, Ropper, A.H.,et al, 2014

Alcohol and Alcoholism
Adams & Victors Principles of Neurology Chp 42, pg 1186, Ropper, A.H.,et al, 2014

Disturbances of Cerebrospinal Fluid, Including Hydrocephalus, Pseudotumor Cerebri, and Low-Pressure Syndromes, Hydrocephalus
Adams & Victors Principles of Neurology, Chp 30, pg 622, Ropper, A.H.,et al, 2014

Infections of the Nervous System, (Bacterial, Fungal, Spirochetal, Parasitic) and Sarcoidosis, Septic Thrombosis of the Superior Sagittal Sinus
Adams & Victors Principles of Neurology, Chp 32, pg 713, Ropper, A.H.,et al, 2014

Infections of the Nervous System, (Bacterial, Fungal, Spirochetal, Parasitic) and Sarcoidosis, Sarcoidosis
Adams & Victors Principles of Neurology, Chp 32, pg 721, Ropper, A.H.,et al, 2014

Infections of the Nervous System, (Bacterial, Fungal, Spirochetal, Parasitic) and Sarcoidosis, Neurosyphilis
Adams & Victors Principles of Neurology, Chp 32, pg 723, Ropper, A.H.,et al, 2014

Intracranial Neoplasms and Paraneoplastic Disorders, Ependymoma
Adams & Victors Principles of Neurology, Chp 31, pg 655, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Tay Sachs Disease
Adams & Victors Principles of Neurology, Chp 37, pg 957, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Globoid Cell Leukodystrophy (Krabbe Disease, Galactocerebrosidase)
Adams & Victors Principles of Neurology, Chp 37, pg 959, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Neuroaxonal Dystrophy
Adams & Victors Principles of Neurology, Chp 37, pg 972, Ropper, A.H.,et al, 2014

Neuropsychiatric Changes Precede Classic Motor Symptoms in ALS and Do Not Affect Survival
Neurol 82:149-155, Mioshi, E.,et al, 2014

Cerebral Abnormalities in Adults with Ataxia-Telangiectasia
AJNR 35:119-123, Lin, D.D.M.,et al, 2014

Showing articles 300 to 350 of 2433 << Previous Next >>