Neudle.com: "extensor posturing"

Differential
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abdominal distention

abdominal muscle paralysis

abdominal reflex, absent

abducens nerve paralysis

abducens nerve paralysis, bilateral

abscess, intracerebral

abulia

acanthocytosis

aceruloplasminemia

acetylcholine receptor antibody

acid maltase deficiency

acid maltase deficiency, adult

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome myelopathy

acquired immunodeficiency syndrome, congenital

acquired immunodeficiency syndrome, infants and children

acquired immunodeficiency syndrome-related complex

acrocyanosis

acute disseminated encephalomyelitis

acute disseminated encephalomyelitis, multiphasic

acute respiratory distress syndrome

acyl CoA dehydrogenase deficiency

addiction, heroin

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adult polyglucosan body disease

adverse drug reaction

affect, inappropriate

agenesis of corpus callosum

aggression

agitation

Aicardi-Goutieres syndrome

altered states of consciousness

alternating rapid movement

amyotrophic chorea-acanthocytosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, juvenile

amyotrophic lateral sclerosis, misdiagnosis

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

ANA

anemia

anemia, megaloblastic

aneurysm, vertebral basilar system

angiitis, granulomatous of CNS

anterior horn cell disease

anterior tibial muscle weakness

anterocollis

anti GQ1b IgG antibody

anti Hu antibody

antibodies to voltage-gated calcium channels

anticholinergic drugs

anticoagulant, complications of

anticoagulant, treatment

anticoagulant, treatment in CVD

Argyll Robertson pupil

arm swing, reduced

arm weakness

Arnold Chiari malformation

asterixis, unilateral

atherosclerosis, generalized

atherosclerosis, premature

atrioventricular block

attention deficit disorder with hyperactivity

attention span

atypical

auditory evoked brainstem potentials

autism

autoantibodies

autoimmune disease

autonomic dysfunction

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

Babinski sign in new born

bacterial infection

bacterial infection, CNS

baldness

ballismus, bilateral

basal ganglia

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar artery occlusion

bedridden

behavior modification

behavioral disorder

behavioral disorder, acute

Behcet's syndrome

Bell's phenomenon

benign essential tremor

bent spine syndrome

Bickerstaff's brainstem encephalitis

bone marrow infarction

bone marrow necrosis

bone marrow transplantation

Borrelia burgdorferi infection

botulinum toxin

botulinum toxin, complications of

botulism

botulism immune globulin

brain biopsy, false negative

brain biopsy, stereotaxic

brain purpura

brainstem

brainstem, glioma

brainstem, glioma in children

brainstem, glioma, adult

brainstem, hemorrhage, primary

brainstem, infarction of

brainstem, ischemia

brainstem, lesion of

brainstem, neoplasms of

brucellosis

brucellosis, nervous system involvement with

bulbar palsy, childhood

bulbar palsy, progressive

calcification, intracranial

calculations

camptocormia

campylobacter infection

cardiac arrest and resuscitation

cardiomyopathy

cardiovascular disease

carnitine deficiency

carnitine deficiency myopathy

carotid angiogram

CAT scan

CAT scan, abnormal

CAT scan, angiography

CAT scan, chest

CAT scan, dense artery sign

CAT scan, emission, abnormal

CAT scan, metrizamide

CAT scan, myelogram with

cataracts

cauda equina, enhancement

central core disease

central nervous system, infection of

central pontine myelinolysis

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar degeneration

cerebellar hemangioma

cerebellar infarction

cerebellar lesion

cerebellar vermis

cerebral cortical atrophy

cerebral death

cerebral edema

cerebral edema, origin and treatment

cerebral embolism

cerebral embolism, cardiac origin

cerebral embolism, mechanical extraction

cerebral folate deficiency syndrome

cerebral infarction

cerebral palsy

cerebral peduncle

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, amonia

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, flow cytometry

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, glutamine

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, pressure increased

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, red cells in

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, acute management of

cerebrovascular accident, prognosis in

cerebrovascular accident, vascular territory involved

cerebrovascular accident, young adult

cerebrovascular disease

cerebrovascular disease, cardiovascular disease with

cerebrovascular disease, predisposed factor in

chemotherapy, CNS treatment and complications with

cherry red spot

cherry red spot-myoclonus syndrome

chilbran skin lesions

choroid plexus, tumor of

chromosomal abnormality

chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids

chronic progressive external ophthalmoplegia

claudication, intermittent of cauda equina

cleft lip

cleft palate

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

cobalamin C deficiency

coccidioidomycosis

cognition

collagen vascular disease

Collier's sign

coma

complications

comprehension, impaired

compression fracture

concentration, impaired

conduction block

confusion

congenital bilateral perisylvian syndrome

congenital heart disease

congenital malformation

congenital malformation, non CNS

congenital myopathy

congestive heart failure

consanguinity

constipation

contractures, joint

controversies in neurology

convergence, impaired

conversion reaction

copper

copper deficiency

corneomandibular reflex

coronavirus

corpus callosum

corpus callosum, infarction of

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cortical-basal ganglionic degeneration

coumarin

COVID-19

cranial nerve enhancement

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

C-reactive protein, elevated

creatine kinase

creatine phosphokinase MB isoenzyme elevation

creatine phosphokinase(CPK)elevated

cryptococcal meningitis

cultured skin fibroblasts

cyclic vomiting

cyst, epidermoid of CNS

decerebrate Posture, unilateral

decompressive spinal cord surgery

decorticate posture

deep gray nuclei

deep tendon reflexes

degenerative diseases of CNS

Dejerine's sign

Dejerine-Sottas syndrome

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, subcortical

demyelinating disease

denervation of muscle

denervation potentials

dense basilar artery sign

dense middle cerebral artery sign

dental procedure, neurologic complications with

dentate nuclei

dentate nuclei, lesion of

developmental abnormality of brain

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes mellitus

diagnostic criteria

diaphragmatic paralysis

diaphragmatic paralysis, causes of

diarrhea

diet

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

digiti quinti sign

diplegia, brachial

diplopia

disability, neurological

disorientation

distal muscle atrophy

distal muscle weakness

dizziness

doll's head maneuver

dopa responsive dystonia

Dravet syndrome

drooling

dropped head syndrome

drowsiness

drug abuse

drug abuse, inhalation

drug abuse, neurologic complications of

drug induced neurologic disorders

dyskinesia, buccal lingual facial

dystonia musculorum deformens

dystonia, cervical

dystonia, children

dystonia, drug induced

dystonia, face

dystonia, focal

dystonia, post traumatic

dystonia, treatment of

dystrophic calcification

ear, abnormal

ears of the Lynx MR sign

efficacy

electrical sensation

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, triphasic delta waves

electromyogram

electromyogram, decremental response

electromyogram, incremental response

embolism, paradoxical

embolism, vertebral-basilar artery

emergencies, neurologic

emergencies, neurosurgical

Emery-Dreifuss muscular dystrophy

emotional lability

Emperor's clothes syndrome

empyema, epidural-spinal

encephalitis

encephalitis lethargica

encephalitis, brainstem

encephalitis, viral

encephalomyelitis

encephalopathy

encephalopathy, acute

encephalopathy, Hashimoto's

encephalopathy, metabolic

encephalopathy, progressive

endocarditis, subacute bacterial

endovascular therapy

enzyme, defect

enzyme, muscle disease

eosinophilia

ependymal

ependymoma

epidemiology of neurology

epileptic encephalopathy

episodic disorders

episodic neurologic deficits

evoked potentials

executive dysfunction

exercise

exercise intolerance

exercise-induced neurologic dysfunction

exercise-related muscle strength increase

exome sequencing

extensor digitorum brevis

eye closure

eye movement, disorders of

face, elongated

face, numbness of

facial anomalies

facial appearance, abnormal

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

fatal familial insomnia

fetal alcohol syndrome

fever

fibrillations

fine motor function, impaired

finger nose finger test

folic acid deficiency

Friedreich's ataxia, late onset

frontal balding

frontal lobe, atrophy

frontal lobe, behavior with disease of

frontal lobe, pathologic signs of

frontotemporal dementia, behavioral variant

gadolinium

gag reflex, depressed

gait disorder

gait, apraxic

gait, spastic

gammaglobulin therapy, intravenous

ganglionitis

gangliosidosis GM2

gastric dilatation, acute

gastric partitioning

gastrocnemius muscle weakness

gaze deviation

gaze palsy

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic neurologic disorders

genetic screening

genetic testing

Gerstmann-Straussler-Scheinker disease

giant axonal neuropathy

girdle sensation

glabellar sign

glioblastoma multiforme(astrocytoma Gr.III)

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glutamate dehydrogenase deficiency

glutamic acid decarboxylase, antibody

glutamine

GM1 ganglioside antibodies

Google

granular osmiphilic material

grasp reflex

grasping

Guillain Barre syndrome

Guillain Barre syndrome, axonal form

Guillain Barre syndrome, pharyngeal-cervical-brachial variant

Guillain Barre syndrome, variant forms of

Hallervorden Spatz disease

hallucination

hallucination, olfactory

hematoma, epidural-spinal

hemifacial spasm

hemiparesis

hemiplegia

hemiplegia, progressive

hemoglobin abnormality, neurologic complications of

hemosiderosis of CNS, superficial

hepatic encephalopathy

hepatic encephalopathy, acute

hepatic failure

hepatic failure, acute

hepatitis B virus

hepatolenticular degeneration, non-Wilsonian

hepatomegaly

hepatosplenomegaly

heralding manifestation

herniated disc

herniated disc, cervical

highly active antiretroviral therapy

hip flexor weakness

Hispanics

histochemistry of muscle

history of neurology

HMGcoA reductase inhibitors

human immunodeficiency virus type 1

Huntington's chorea

hydrocephalus

hydroxychloroquine

hyperammonemic encephalopathy

hyperbilirubinemia

hypercalcemia

hypercapnia

hypereosinophilic syndrome(HES)

hyperhidrosis

hyperhomocysteinemia

hyperintense vessel sign

hyperparathyroidism

hyperpigmentation of skin

hyperpyrexia, CNS disorder causing

hypoglycorrhachia, causes of

hypomyelination

hyponatremia

hyponatremia with cerebral disorders

hyponatremic encephalopathy

hypophonia

hyporeflexia

hypothalamus

hypothalamus, disturbance of

hypothermia

hypothermia, causes of

iatrogenic neurologic disorders

ileus, paralytic

imbalance

imbalance, postural

immune checkpoint inhibitors

immune-related adverse events

immunosuppression

immunosuppressive agents

immunotherapy

impotence

inability to stand on tiptoes

inattention

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intranuclear

inclusion body myositis

incontinence, fecal

incoordination

infant, evaluation of

infection

infectious mononucleosis

infectious mononucleosis, neurologic findings with

intellectual deterioration

interferon alpha

internal capsule

internet

internuclear ophthalmoplegia

interobserver agreement

interstitial pulmonary fibrosis

intestinal biopsy

intestinal pseudoobstruction

intracranial pressure, increased

intracranial pressure, increased, treatment of

intrauterine

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

lactic dehydrogenase(LDH)

lacunar infarction

laminectomy, cervical

laminectomy, lumbar

language disorder in adults

left-right orientation

leg spasms, painful

leg weakness, bilateral

Leigh's disease

lenticular nucleus, lesion of, bilateral

leptospirosis

lethargy

leukemia

leukemia, neurologic findings assoc.with

leuko-araiosis

leukocyte enzyme abnormality

leukodystrophy

leukoencephalopathy

level of consciousness, decreased

Lhermitte's sign

lid closure, weakness of

lipid storage disorder of CNS

lipid storage myopathy

liver biopsy

liver disease

liver function enzymes

liver transplantation

lymphadenopathy, hilar

lymphoma

lymphoma involving CNS

lysosomal storage disease

magnetic stimulation

magnetic stimulation, brain

malformation, CNS, congenital

malformation, vascular

manganese intoxication

masseter muscle wasting

meconium staining

mediastinum, lymph-node biopsy

mediastinum, mass of

mediastinum, widening

medical-legal aspects of neurology

MEK inhibitor

melanoma, malignant

memory, defect of recent

memory, impairment of

meningeal biopsy

meningeal enhancement

meningeal gliomatosis

meningitis

meningitis, actinomycotic

meningitis, aseptic

meningitis, bacterial

meningitis, blastomyces

meningitis, brucellosis

meningitis, candida

meningitis, carcinomatous

meningitis, chronic

meningitis, chronic benign lymphocytic

meningitis, cladosporium

meningitis, coenurosis

meningitis, CSF cell count-normal

meningitis, cysticercosis

meningitis, echinococcal

meningitis, eosinophilic

meningitis, fungal

meningitis, helminthic

meningitis, histoplasma

meningitis, leptospira

meningitis, lymphomatous

meningitis, Mollaret's

meningitis, neutrophilic

meningitis, nocardia

meningitis, paracoccidioides

meningitis, pneumococcal

meningitis, post myelography

meningitis, recurrent

meningitis, syphilitic

meningitis, TB

meningitis, toxoplasma

meningoencephalitis

meningoencephalitis, toxoplasma

mental retardation

mental retardation, familial

mental status, abnormal

MERCI trial

metabolic acidosis

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, late-infantile

methyl benzene

methylmalonic acid, serum

methylmalonic acidemia

microcephaly

micrognathia

microhemorrhage, intracerebral

midbrain, lesion of

middle cerebellar peduncle, lesion

mitochondrial disease

mitral valve lesion

mixed connective tissue disease

molecular genetics

monoclonal antibodies

monoclonal gammopathy

monomelic myositis

Montreal cognitive assessment

mortality

motor dysfunction

motor neuron disease

motor neuron disease, spontaneous recovery

movement disorder

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, psychogenic

movement disorder, treatment of

MRI

MRI, abnormal

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, contrast enhanced, high dose

MRI, diffusion tensor

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, FLAIR

MRI, FLAIR, hyperintense vessels

MRI, gradient-echo

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, hypointense signal foci on

MRI, linear enhancement

MRI, muscle

MRI, negative

MRI, nodular enhancement

MRI, paramagnetic effect

MRI, perfusion

MRI, ring sign

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, spine

MRI, susceptibility weighted

MRS

multicore myopathy

multinucleated giant cell

multiple sclerosis

multiple sclerosis, diagnosis of

multiple sclerosis, differential diagnosis of

multiple system atrophy

muscle atrophy, focal

muscle atrophy, progressive

muscle strength, testing

muscle tenderness

muscle twitching

muscle wasting, diffuse

muscle weakness

muscle weakness, insidious onset of

muscle weakness, proximal

muscle weakness, sudden onset of

muscular dystrophy

muscular dystrophy, cardiovascular changes with

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, differential diagnosis of

muscular dystrophy, distal, Miyoshi

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

mutism

myasthenia gravis

myasthenia gravis, distal weakness

myasthenia gravis, drug induced

myasthenia gravis, limb-girdle

myasthenia gravis, paraneoplastic

myasthenia gravis, presenting manifestations

myasthenic syndrome

mycoplasma

mycoplasma pneumoniae

myelitis

myelitis, longitudinal

myelitis, post infectious

myelopathy, chronic progressive

myopathy, centronuclear

myopathy, critically ill

myopathy, distal

myopathy, distal Laing

myopathy, distal, vacuolar

myopathy, drug-induced

myopathy, focal

myopathy, genetic

myopathy, inflammatory

myopathy, metabolic

myopathy, mitochondrial

myopathy, necrotizing

myopathy, necrotizing, immune-mediated

myopathy, proximal

myopathy, radiation-induced

myopathy, steroid induced

myositis, eosinophilic

myositis, focal

myositis, fungal

myositis, granulomatous

myotonia dystrophica, classification

myxedema, neurologic manifestations of

nemaline rod myopathy

nemaline rod myopathy, adult onset

neoplasm, metastatic to CNS

neoplasm, primary intracerebral

neoplasm, primary of CNS

neoplasm, primary of CNS-classification

neoplasm, primary of CNS-intraventricular

neoplasm, primary of CNS-metastasizing to subarachnoid space

neoplasm, primary of CNS-treatment of

nerve biopsy

nerve conduction studies

nerve root enhancement

nerve root hypertrophy

neuroendocrinology

neurofibrillary degeneration

neurogenic bladder

neurologic complications of, chronic pulmonary disease

neurologic complications of, surgery

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic examination

neurologic examination, focal

neurologic signs

neurologic symptoms

neurological intensive care

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction, abnormality of

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuronopathy

neuronopathy, sensory

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, iatrogenic

neuropathy, medication induced

neuropathy, motor, multifocal

neuropathy, multifocal

neuropathy, peripheral

next-generation sequencing

nutritional deficiency

nystagmus

nystagmus, gaze-evoked

nystagmus, rotary

nystagmus, upbeating on upgaze

ocular motility, disorders of

ocular myopathy

oculogyric crisis

oculopharyngeal muscular dystrophy

old age, neurology of

operculum syndrome, bilateral

ophthalmoplegia

ophthalmoplegia, plus syndrome

ophthalmoplegia, progressive external

ophthalmoplegia, total

opisthotonus

opsoclonus

optic atrophy

optic chiasm, enlarged

optic nerve

optic nerve, enlarged

optic nerve, lesion of

optic neuropathy

oral contraceptives

organ transplantation

oropharyngeal weakness

orthostatic hypotension

oscillopsia

osteomyelitis

osteomyelitis, spinal

palpebromandibular synkinesia

pancytopenia

papilledema

paralysis

paraneoplastic ganglionopathy

paranoia

paraparesis

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, familial spastic, variants

paraparesis, flaccid

paraparesis, spastic

paraplegia

paraplegia, in flexion

paraplegia, progressive

paraspinal muscle

paraspinal muscle weakness

Parkinson disease, arteriosclerotic

Parkinson disease, asymmetric onset

Parkinson disease, hemiparesis in

Parkinson disease, L-dopa nonresponsive

Parkinson disease, postencephalitic

Parkinson disease, tremor, absence of

Parkinson disease, unilateral

Parkinson disease, young onset

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

paroxysmal neurologic disorder

PAS positive

PAS positive material in the brain

past pointing

patent foramen ovale

pathologic reflex

patient information and support

pediatric neurology

pembrolizumab

Penumbra System

perivascular enhancement

pernicious anemia

peroneal nerve

peroneal nerve palsy

peroneal nerve, lesion of

peroxisomal disease

perseveration

Persistent postural-perceptual dizziness

persistent vegetative state

pituitary stalk, lesion of

plantar reflex

pleocytosis of cerebrospinal fluid

pneumonia

poison, neurologic problems with

poison, organophosphate

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polymicrogyria

polymyositis

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, familial

position sensation, abnormal

positive sharp waves

posterior column disease

posterior inferior cerebellar artery syndrome

posterior leukoencephalopathy syndrome

postictal neurologic deficits

postoperative neurologic complications

postural abnormality

precipitating factors

precocious puberty

prenatal

prenatal diagnosis by amniocentesis

primary lateral sclerosis

prion disease

prisoner

prognosis

progressive encephalomyelitis with rigidity syndrome

progressive myoclonic epilepsy

progressive neurologic disorder

proprioception, abnormal

proximal muscle atrophy

proximal myotonic myopathy

pseudobulbar palsy

pseudomyotonia

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

pupil, abnormality in neurologic disorders

pupil, light reflex, abnormal

pure dysarthria

pursuit eye movements, abnormal

pyramidal

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriparesis

quadriparesis, progressive

quadriplegia

radiation therapy, CNS treatment and complications with

remote effect of cancer on the nervous system

renal failure

renal stones

repetition, impaired

repetitive nerve stimulation

respirator

respiratory dyskinesias

respiratory failure

respiratory tract infection

reversible neurologic disorder

review article

rhabdomyolysis

rheumatic heart disease

rubella encephalitis, progressive

saccadic eye movements, abnormal

scleroderma, neurologic involvement with

sedimentation rate, elevated

seizure, tonic-clonic

selective serotonin reuptake inhibitors

sensory loss, cutaneous

sensory symptoms

serologic testing

serologic testing of cerebrospinal fluid

serotonin norepinephrine reuptake inhibitors

severe acute respiratory syndrome

shunt procedure, ventricular

sickle cell disease

single photon emission computed tomography

single-fiber electromyography

Sjogren's syndrome

skew deviation

skin, lesions in neurologic disorders

skin, temperature difference

skull x-ray, abnormal

sleep pathology and physiology

slow virus infection of CNS

slurred speech

sneeze

snout reflex

sodium channel dysfunction

somatosensory evoked potentials

spastic paraplegia, type 11

spastic paraplegia, type 7

spasticity

speech disorder

speech disorder, childhood

speech, loss of

spinal cord

spinal cord, compression of

spinal cord, lesion of

spinal cord, pathologic exam of

spinal reflexes

spinal stenosis

spinal stenosis, familial

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar ataxia type 7

spinocerebellar degeneration

spongy degeneration of brain

spontaneous movements

spontaneous remission

steroid therapy, CNS treatment and complications with

stooped posture

strabismus

striatonigral degeneration

striatonigral degeneration, infantile

striopallidodentate calcifications, familial idiopathic

subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease

subarachnoid hemorrhage

superior cerebellar artery infarction

superior sagittal sinus thrombosis

swallowing

symmetric brain lesions

syncope

syringomyelia

systemic illness

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

temporal lobe, lesion

temporal lobe, lesion, bilateral

temporalis muscle wasting

tensilon test, false positive

testicular atrophy

testicular enlargement

thalamus, lesion of

thalamus, lesion of-bilateral

tone, muscle, increased

tongue, atrophy

tongue, enlarged

tongue, fasciculations of

tongue, impaired movements of

tongue, weakness

tonic cerebellar fits

tonic foot response

torticollis

torticollis, post traumatic

toxoplasmosis, acquired

toxoplasmosis, CNS

transient neurologic deficit

trauma

treatment of neurologic disorder

tremor

tremor, cerebellar

tremor, intention

trinucleotide repeats

vaccination, neurologic complications with

valsalva maneuver

vecuronium

vegetarianism

ventricular enlargement

vertebral infarction

vertigo

vertigo, episodic

very long chain fatty acids

vibratory sensation, abnormal

visual acuity, decreased

visual evoked response

visual fields, constricted

Vogt-Koyanagi-Harada syndrome

Waldenstrom's macroglobulinemia

walking frame

walking, delayed

walking, difficulty with

Wallerian degeneration

weakness, fluctuating

weakness, generalized

weakness, progressive

weakness, proximal

weaning from respirator, failure to

weight loss

Western immunoblot test

wheelchair

white matter disease

white matter disease, periventricular

x-linked mental retardation

x-ray, spine

x-ray, thoracic spine

zinc

zoonoses

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Neurol 93:e823-e826, Alderson,J.,& Ghosh,P.S., 2019

Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019

FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance
Mol Genet Metab 125:281-291, Almannai, M.,et al, 2018

Persistent Postural-Perceptual Dizziness (PPPD): A Common, Characteristic and Treatable Cause of Chronic Dizziness
Pract Neurol 18:5-13, Popkirov, S.,et al, 2018

Subacute Paresis in a 28-year-old man with HIV
Neurol 90:432-435, Harada, Y.,et al, 2018

A young woman with symmetric weakness and behavioral disturbance
Neurol 90:e1442-e1447, Rosenberg, J.,et al, 2018

Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy
Neurol 90:e1827-e1831, Xiao, F.,et al, 2018

Progressive Weakness and Memory Impairment in a Middle-aged Man
JAMA 320:197-198, DeFilippis, E.M.,et al, 2018

A Curable Myopathy Manifesting as Exercixe Intolerance and Respirtory Failure
Neurol 91:187-190, Silva,A.M.S.,et al, 2018

Immune Checkpoint Inhibitor-Related Myositis and Myocarditis in Patients with Cancer
Neurol 91:e985-e994, Touat, M.,et al, 2018

Young Adult with Dysphagia and Severe Weight Loss
Neurol 91:e1083-e1086, Irumudomon, O. & Ghosh, P.S., 2018

Pembrolizumab-Induced Myasthenia Gravis
Neurol 91:e1365-e1367, Algaeed, M.,et al, 2018

A 35-year-old Woman with Diplopia, Ataxia, and Altered Mental Status
Neurol 91:e1942-e1946, Bauer, Z.,et al, 2018

Man with Recurrent Paralysis and Cerebral White Matter Lesions
JAMA Neurol 74:599-600, Xiao, F., 2017

A Case of Fulminant Encephalopathy in a 69-year-old Woman
Neurol 89:e109-e114, Lamotte, G. and Williams, C, 2017

A 27-year-old man with unsteady gait
Neurol 89:e120-e123, Fernandez, D.,et al, 2017

A 34-Year-Old Man with Headache, Diploplia, and Hemiparesis
Neurol 86:e28, Lincoln, M.R.,et al, 2016

Finger Clonus
Neurol 86:e118-e119, Moccia,M.,et al, 2016

A Young Man with Acute Encephalopathy Loss of Vision, and Upper Motor Neuron Signs
Neurol 86:e173-e176, Elkhider, H.,et al, 2016

Clinicopathologic Conference, Fulminant Liver Failure Associated with Hepatitis B Virus Infection
NEJM 375:163-171, Case 21-2016, 2016

A 30-year-old Man with Progressive Weakness and Atrophy
Neurol 87:e227-e230, Quinn, C.,et al, 2016

Idiopathic Thoracic Spontaneous Spinal Epidural Hematoma
Case Reports Surg doi:10.1155/2016/5430708, Aycan, A.,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

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

A 73-year-old Man with Diplopia and Ataxia
Neurol 85:e96-e100, Gupta, H.V.,et al, 2015

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

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Progressive Rubella Panencephalitis
Adams & Victors Principles of Neurology, Chp 33, pg 766, Ropper, A.H.,et al, 2014

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Gertsmann-Straussler Schneinker Syndrome
Adams & Victors Principles of Neurology, Chp 33, pg 773, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Adrenoleukodystrophy
Adams & Victors Principles of Neurology, Chp 37, pg 988, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Machado-Joseph-Azorean Disease
Adams & Victors Principles of Neurology, Chp 39, pg 1107, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Amyotrophic Lateral Sclerosis
Adams & Victors Principles of Neurology, Chp 39, pg 1109, Ropper, A.H.,et al, 2014

Pharyngeal-Cervical-Brachial Variant of Guillain-Barr� Syndrome
JNNP 85:339-344, Wakerley, B.R. & Yuki, N., 2014

Clinical Case Conference: A 41-Year-Old Woman with Progressive Weakness and Sensory Loss
Ann Neurol 75:9-19, Stephen, C.D.,et al, 2014

Clinicopathologic Conference, Tay-Sacks Disease (GM2, Gangliosidosis)
NEJM 370:1830-1841, Case 14-2014, 2014

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