Neudle.com: dystonic posture

Differential
(Click to cross reference)

abscess, intracerebral

abscess, intracranial

abscess, retropharyngeal

abscess, sphenoid sinus

acanthocytosis

acetazolamide

aciduria

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome-related complex

advances in neurology

adverse drug reaction

aggression

agitation

agnosia, color

Aicardi-Goutieres syndrome

airway obstruction

akathisia

akinesia of eyelid function

alcohol

alcohol, neurologic complications with

alcoholic withdrawal states, DT's, convulsions, etc.

alexia without agraphia

algorithm

alien hand syndrome

alpha-fetoprotein

alternating hemiplegia

alternating hemiplegia of childhood

alveolar hypoventilation

AMPA receptor antibodies

amphetamines, dyskinesia associated with

amphiphysin antibodies

amyloidosis

amyotrophic chorea-acanthocytosis

amyotrophic lateral sclerosis

anatomy of

anemia

anemia, hemolytic

aneurysm, intracranial

ankle edema

anoxia

anterocollis

anti basal ganglia antibodies

anti GQ1b IgG antibody

anti IgLON5

anticholinergic drugs

anticholinesterase

anticonvulsants

anticonvulsants, blood level determination of

anticonvulsants, untoward effects of

antidepressant

anti-dopamine 2 receptor antibody

antiemetic

antihistamines

antistreptolysin titer

anxiety

anxiolytic agents

aortic valve, lesion of

aphasia

aphasia, progressive, primary

aphonia

applause sign

apraxia

apraxia of eye movements

apraxia of eyelid opening

apraxia, constructional

arteriovenous malformation

arteriovenous malformation, cerebral

arthralgia

arthritis

arthrogryposis multiplex

ataxia telangiectasia

ataxic-dystonia syndromes

athetosis

athetosis, causes of

atlanto-axial subluxation

ATP1A3 gene

attention

attention deficit disorder with hyperactivity

attention span

atypical

auditory evoked brainstem potentials

autoantibodies

autoimmune basal ganglia encephalitis

autoimmune disease

automobile accidents

autonomic dysfunction

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar artery migraine

behavioral disorder

benign essential tremor

bent spine syndrome

benzodiazepine

beta adrenergic blocker

bilirubin encephalopathy

biotin deficiency, juvenile form

biotin-responsive basal ganglia disease

botulinum toxin, complications of

brainstem, dysfunction

calcification, intracranial

calcium antagonist

calcium antagonist, side effects of

camptocormia

carbamazepine

carbamazepine, toxicity

carbon monoxide poisoning

carcinoembryonic antigen

carcinoma

cardiac arrest

cardiac arrest and resuscitation

cardiomyopathy

cardiopulmonary bypass

carotid artery occlusion, neck

carpal tunnel syndrome

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, isodense lesion with acute hemorrhage

caudate nucleus, atrophy

caudate nucleus, lesion of

cavernous hemangioma

cavernous sinus

cavernous sinus, metastasis to

cavernous sinus, syndrome

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar edema

cerebellar lesion

cerebellar pontine angle

cerebellar pontine angle tumor

cerebellum

cerebral cortex

cerebral cortical atrophy

cerebral edema

cerebral embolism

cerebral embolism, cardiac origin

cerebral infarction

cerebral ischemia

cerebral palsy

cerebral palsy, adults

cerebral palsy, associated problems with

cerebral peduncle

cerebral vasculature, calcification

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, biochemical markers of CNS tumors

cerebrospinal fluid, cell count, normal

cerebrospinal fluid, elevated protein of

cerebrovascular accident

cerebrovascular accident, complications with

cerebrovascular accident, infancy and childhood

cerebrovascular accident, nonarterial territory

cerebrovascular accident, young adult

ceruloplasmin, serum

cervical spine

cervical spine injury

chilbran skin lesions

children

China

chiropractic manipulation

chiropractic manipulation, neurologic complications with

choreoathetosis, paroxysmal

chromosomal abnormality

chronic progressive external ophthalmoplegia

cinnarizine

cirrhosis

cirrhosis, causes of childhood

cisterna magna

Clinical Pathologic Conference(C.P.C.)

collapsin response mediator protein 5 IgG

colloid cyst of third ventricle

coma

coma, causes of

coma, episodic

coma, unknown etiology

comorbidities

complications

compression fracture

compression neuropathy

computers, neurologic diagnosis and

confusion

conjugate gaze, forced

copper metabolism, abnormal

cornea, opacity of

Cornelia de Lange syndrome

cortical blindness

cortical-basal ganglionic degeneration

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

C-reactive protein, elevated

creatine phosphokinase(CPK)elevated

crying, pathologic

cultured skin fibroblasts

degenerative diseases of CNS

dementia, treatment of

dental procedure, neurologic complications with

dentate nuclei, lesion of

depression

dermatomyositis

developmental milestones, loss of

developmental retardation

differential diagnosis

disability, neurological

discectomy

discectomy, cervical

disease modifying agents

distal muscle atrophy

dopa responsive dystonia

dopamine

dopamine agonist

dopamine antagonist

dopamine depleting agents

dopamine receptor, D2

dorsal column stimulator

DPPX, antibodies, encephalitis

drooling

droperidol

drug abuse

drug abuse, neurologic complications of

drug induced neurologic disorders

drug overdose

drug overdose, accidental

drug withdrawal

dural sinus thrombosis

dying

dysarthria

dysarthria-clumsy hand syndrome

dysdiadochokinesia

dyskinesia

dyskinesia, buccal lingual facial

dyskinesia, causes of

dyskinesia, drug induced

dystonia musculorum deformens

dystonia musculorum deformens, carrier

dystonia, axial

dystonia, cervical

dystonia, children

dystonia, classification

dystonia, delayed onset

dystonia, drug induced

dystonia, etiology of

dystonia, evaluation of

dystonia, face

dystonia, focal

dystonia, focal lesion causing

dystonia, focal task specific

dystonia, post traumatic

dystonia, prevalence of

dystonia, psychogenic

dystonia, segmental

dystonia, symptomatic

dystonia, tongue

dystonia, treatment of

dystonia, truncal

dystonic lipidosis

dystonic reaction, acute

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electromyogram

electron microscopy

ELISA

emergencies, neurologic

emotional lability

employment

empyema, epidural

empyema, epidural-spinal

empyema, subdural

encephalitis

encephalitis lethargica

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, clinical picture and treatment of

encephalitis, etiology

encephalitis, focal

encephalitis, paraneoplastic

encephalitis, viral

encephalomyelitis, postinfectious

encephalopathy

encephalopathy, metabolic

encephalopathy, neonatal

encephalopathy, post anoxic

encephalopathy, progressive

endocarditis

entrapment neuropathy

enuresis

enzyme, defect

ependymoma

epidemiology of neurology

epileptic encephalopathy

episodic disorders

episodic neurologic deficits

epsilon sarcoglycan gene

executive dysfunction

exercise

exercise intolerance

exercise-induced neurologic dysfunction

exome sequencing

extralimbic encephalitis

extrapyramidal movement disorder, progressive

eye color

eye movement, disorders of

face, contractions

facial expression abnormality

facial nerve palsy

faciobrachial dystonic seizure

fine motor function, impaired

fourth ventricle, enlargement of

fourth ventricle, neoplasm of

frontal behavioral spatial syndrome

frontal lobe, pathologic signs of

fungal infection, CNS

gait disorder

gait, apraxic

galactorrhea

gamma amino butyric acid

gamma amino butyric acid receptor antibody

gamma hydroxybutyric acid

gammaglobulin therapy, intravenous

GAMT gene

gangliosidosis GM1

gangliosidosis, generalized

gaze deviation

gaze palsy

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic testing

gests antagoniste

Gilles de la Tourette syndrome

glabellar sign

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

globus pallidus, stimulation

GLUT1

GLUT1 deficiency syndrome

glutamic acid decarboxylase, antibody

glutaric acidemia

glutaric aciduria

glycine receptor antibodies

Guillain Barre syndrome

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

hallucination

hallucination, visual

head injury, pediatric

hemianopia, homonymous

hemiparesis, transient

hemiplegia

hepatic encephalopathy

hepatic encephalopathy, treatment of

hepatic failure

hepatitis

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

hepatolenticular degeneration(Wilson's disease), screening for

hepatomegaly

hepatosplenomegaly

heralding manifestation

herniated disc, cervical

human immunodeficiency virus type 1

Huntington's chorea

Huntington's chorea, genetic counselling

Huntington's disease, children

hydrocephalus

hyperbilirubinemia

hyperbilirubinemia, CNS abnormality after

hyperekplexia

hyperhidrosis

hyperpyrexia, CNS disorder causing

hypotension, systemic

hypoxic encephalopathy

iatrogenic neurologic disorders

immunosuppressive agents

immunotherapy

inappropriate antidiuretic(A.D.H.)hormone

inattention

inborn errors of metabolism

inclusion bodies, intranuclear

incontinence, fecal

incoordination

infantile bilateral striatal necrosis

intellectual deterioration

interferon alpha

internal capsule

internal cerebral vein

internet

intestinal pseudoobstruction

intracerebral hemorrhage

intracranial pressure, increased

intrathecal antispasticity drugs

Jakob-Creutzfeldt disease

jaundice

jaw jerk, abnormal

jugular foramen syndrome

karyotyping

Kayser-Fleischer ring

Kearns-Sayre syndrome

kernicterus

ketoacidosis

ketogenic diet

Klinefelter's syndrome

klippel feil syndrome

laryngismus stridulus

laterocollis

laughing, pathologic

L-dopa

L-dopa, drug interactions with and side effects of

L-dopa, enteral infusion, continuous

Leber's hereditary optic neuropathy

left handedness

leg spasms

leg spasms, painful

leg weakness, bilateral

Leigh's disease

Leigh's disease, adult variety

lenticular nucleus, lesion of

lenticular nucleus, lesion of, bilateral

leucine rich glioma inactivated 1 antibodies

level of consciousness, decreased

levitation

Lewy body disease, diffuse

lipid storage disorder of CNS

liver function enzymes

liver transplantation

lysosomal storage disease

malformation, vascular

malformation, vascular, cerebral

manganese intoxication

masked facies

mastoiditis

mediastinum, mass of

medical-legal aspects of neurology

MELAS syndrome

memory

memory, defect of recent

memory, impairment of

meningismus

meningitis

meningitis, carcinomatous

mental retardation

mental retardation, etiology of

mental status, abnormal

MERRF syndrome

metabolic acidosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

metachromatic leukodystrophy, juvenile

methylmalonic acidemia

midbrain, infarction of

migraine, treatment of

mimics

mineralization

Mini Mental Status Examination

miosis

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

mongolism

monoamines

monoclonal antibodies

movement disorder, delayed onset

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, extrapyramidal-treatment of

movement disorder, hyperkinetic

movement disorder, paroxysmal

movement disorder, psychogenic

movement disorder, treatment of

MRI, CAT scan compared to

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, eye of tiger sign

MRI, FLAIR

MRI, gradient-echo

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, mouse ears

MRI, negative

MRI, paramagnetic effect

MRI, susceptibility weighted

MRI, T1 weighted high signal foci

MRS

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple sclerosis, paroxysmal symptoms in

multiple system atrophy

Munchausen syndrome

muscle biopsy

muscle cramp

muscle diseases, characteristics of

muscle weakness, proximal

muscle, metabolic disorders of

muscular dystrophy

muscular dystrophy, Duchenne

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

myasthenia gravis, drug induced

myasthenia gravis, unmasked

myasthenic crisis

mycoplasma

mycoplasma pneumoniae

mycotoxin

myelogram

myelopathy

myelopathy, chronic progressive

myopathy, carcinomatous

myopathy, metabolic

myopathy, mitochondrial

myopathy, thyroid disease causing

neoplasm, intracranial

neoplasm, intracranial with metastasis extracranially

neoplasm, metastatic to CNS

neoplasm, peripheral nerve

neoplasm, posterior fossa

neoplasm, primary intracerebral

neoplasm, primary intracranial-treatment of

neoplasm, primary of CNS

neoplasm, primary of CNS-children

neoplasm, primary of CNS-infants

neoplasm, primary of CNS-survival

neoplasm, primary of CNS-treatment of

nerve biopsy

nerve conduction studies

neuritis, causes of

neurochemistry

neurocutaneous disease

neurodegeneration with brain iron accumulation

neuroendocrinology

neurofibrillary degeneration

neuroleptic

neuroleptic malignant syndrome

neuroleptic, atypical

neurologic complications

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic disease, diagnoses of, clinical bedside

neurologic disease, multifocal

neurologic disease, tempo

neurologic evaluation

neurologic examination

neurologic examination, focal

neurologic signs

neurologic symptoms

neurologic symptoms, unexplained

neurologic testing

neuromyotonia

neuronal intranuclear inclusion disease

neuronopathy

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, diabetic

neuropathy, peripheral

next-generation sequencing

nonsteroidal anti-inflammatory drug

norepinephrine

numb clumsy hands syndrome

nystagmus

nystagmus, congenital

obsessive-compulsive disorder

occipital lobe, lesion of

occupational neurologic disorders

occupational neuropathies

ocular motility, disorders of

ocular myopathy

ocular myopathy, differential diagnosis

Oculinum

oculogyric crisis

old age, neurology of

opened mouth

ophelia syndrome

ophthalmoplegia

ophthalmoplegia, progressive external

optokinetic nystagmus, abnormal

oral contraceptives

oral contraceptives, choreiform movements with

organomegaly

orthostatic hypotension

osteomyelitis

osteomyelitis, skull

osteomyelitis, spinal

otitis, neurologic complications with

paraspinal muscle weakness

Parkinson disease

Parkinson disease, axial symptoms

Parkinson disease, differential diagnosis of

Parkinson disease, drug induced

Parkinson disease, dystonia with

Parkinson disease, familial

Parkinson disease, fluctuations in

Parkinson disease, freezing phenomena in

Parkinson disease, juvenile

Parkinson disease, L-dopa nonresponsive

Parkinson disease, mode of onset

Parkinson disease, on-off phenomena in

Parkinson disease, postencephalitic

Parkinson disease, prognosis of

Parkinson disease, progression

Parkinson disease, psychogenic

Parkinson disease, rapid onset

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinson disease, tremor, absence of

Parkinson disease, unilateral

Parkinson disease, young onset

Parkinsonism syndrome

paroxysmal dystonic choreoathetosis

paroxysmal exertion-induced dyskinesia

paroxysmal hemiplegia

paroxysmal hypnogenic dyskinesia

paroxysmal kinesigenic dyskinesia

paroxysmal neurologic deficits

paroxysmal neurologic disorder

paroxysmal nonkinesigenic dyskinesia

parsidol

pathognomonic

pathology

patient information and support

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection

pediatric opioid use associated neurotoxicity

penguin silhouette sign

penicillamine

perineural invasion

peripheral nerve, lesion of

peroxisomal disease

personality change

personality disorder

phencyclidine poisoning

phenothiazine

phenothiazine, dyskinesia associated with

phenylketonuria

photophobia

pigmentary retinopathy

Pisa syndrome

pitfalls

pituitary, adenoma

pituitary, microadenoma

pleocytosis of cerebrospinal fluid

pleural effusion

poison, neurologic problems with

POLG1 gene

poliomyelitis

polycythemia, primary

polycythemia, secondary

posterior cerebral artery

posterior cerebral artery embolism

posterior cerebral artery territory infarction

postoperative neurologic complications

postural abnormality

potassium channel antibodies

practice guidelines

precipitating factors

pregnancy, neurologic complications in

premature infant

prenatal

pretectal syndrome

prevention of neurologic disorders

primary episodic ataxia

primary familial brain calcification

progressive neurologic disorder

progressive supranuclear palsy

proprioception, abnormal

pseudoathetosis

pseudobulbar palsy

pseudochorea

pseudohypoparathyroidism

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

psychosis

psychosis, acute

psychosomatic disease

pupil, abnormality in neurologic disorders

pupil, tonic

pure sensory stroke

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

radial nerve, palsy of

radiation hypersensitivity

radiation therapy, CNS treatment and complications with

radiculopathy

ragged-red fibers

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

rectal biopsy

recurrent

Red flags

reflex sympathetic dystrophy

release phenomena

remote effect of cancer on the nervous system

renal failure

renal stones

repetition strain injury

repetitive nerve stimulation

reserpine treatment in movement disorder

respirator

respiratory failure

respiratory tract infection

restless leg syndrome

reversible neurologic disorder

saccadic eye movements, abnormal

safety

salivation, excessive

sedimentation rate, elevated

seizure

seizure, adult onset

seizure, children

seizure, differential diagnosis of

seizure, dystonic

seizure, laughing as manifestation

seizure, neonatal

seizure, psychomotor-temporal lobe

seizure, stimulus sensitive

seizure, unknown origin

selective serotonin reuptake inhibitors

self harm

self-mutilation

semialdehyde dehydrogenase deficiency

sensorineural hearing loss

sensory loss

sensory loss, cortical

sensory tricks

sequencing difficulty

serologic testing

serologic testing, false negative

seronegative

sexual behavior, disorder of

single photon emission computed tomography

sinusitis

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, lesions in neurologic disorders

sleep apnea, obstructive

sleep pathology and physiology

slit lamp examination

spasticity, treatment of

speech disorder

speech disorder, childhood

speech disorder, non aphasic

spinal cord

spinal cord, compression of

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, neoplasm, infants and children

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 16

spinocerebellar ataxia type 28

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar degeneration

splenomegaly

spondylosis

spongy degeneration of brain

sports medicine, neurology of

status epilepticus, intractable

stem cell transplantation

stereotaxic surgery

stereotypy

steroid

steroid therapy, CNS treatment and complications with

stiff man syndrome

stimulation, deep brain

stimulation, deep brain, bilateral

stimulation, thalamic

stooped posture

strabismus

streptococcal infection

streptococcus pyogens

striatal encephalitis

striatum, lesion of

striatum, lesion of, bilateral

stridor

striopallidodentate calcifications, familial idiopathic

strokelike episodes

subarachnoid hemorrhage

symmetric brain lesions

tardive dyskinesia, treatment of

thalamus, infarction of

thalamus, lesion of

thalamus, lesion of-bilateral

thoracic outlet syndromes

tongue, protrusion of

tonic foot response

tonic spasms

torticollis

torticollis, acute infectious

torticollis, benign paroxysmal

torticollis, familial

torticollis, infants and children

torticollis, natural history

torticollis, ocular

torticollis, post traumatic

toxic encephalopathy

toxins, nervous system

toxoplasmosis, CNS

transcutaneous electrical nerve stimulation

transient neurologic deficit

transient paroxysmal dystonia in infancy

trauma

treatment failure

treatment of neurologic disorder

tremor, post traumatic

tricyclic antidepressant

trientine dihydrochloride

trigeminal neuralgia

trinucleotide repeats

tripping

typing

typist cramp

tyrosine hydroxylase deficiency

urea-cycle enzymopathies

uric acid, low

urinary incontinence

urinary sulfatidase excretion

urine test for metabolic disorders

urine test in toxic screen

visual evoked response

visual field defect

visual impairment

visual symptoms

visuospatial disturbance

vitamin E deficiency

walking

walking frame

walking, difficulty with

weakness

weakness, generalized

weakness, progressive

weight loss

Werdnig-Hoffman disease

wheelchair

Whipple's disease

white matter disease

whole genome sequencing

X-linked dystonia-parkinsonism syndrome

x-linked mental retardation

yips

zinc

Showing articles 350 to 400 of 816 << Previous Next >>

Tetrabenazine & Movement Disorders
Neurol 31:1051-1054, Asher,S.W., 1981

Prolonged Relief of Dystonic Movements with Diazepam
Neurol 31:1457-1458, Ziegler,D.K., 1981

Dystonia With Droperidol Therapy
NEJM 305:227, Arrowsmith,J.,et al, 1981

Chronic GM1 Gangliosidosis Presenting as Dystonia:I. Clinical & Pathological Features
Ann Neurol 9:465-475, Goldman,J.E.,et al, 1981

Benign Paroxysmal Torticollis in Infancy
Arch Dis Child 56:956-959, Deonna,T.,et al, 1981

Phencyclidine:The New American Street Drug
Editorial, BMJ 281:1511-15121980., , 1980

L-Dopa in Children with Progressive Neurological Disorders
Ann Neurol 7:93, Bugiani,O.,et al, 1980

Delayed-onset Dystonia in Patients with"Static"Encephalopathy
JNNP 43:789-797, Burke,R.E.,et al, 1980

Alternating Hemiplegia in Infants:Report of Five Cases
Dev Med Child Neurol 22:784-791, Krageloh,I.&Aicardi,J., 1980

Early-Morning Dystonia-A Late Side Effect of Long-Term Levodopa Therapy
Arch Neurol 36:308-310, Melamed,E., 1979

Drug Therapy, Bromocriptine
NEJM 301:873-878, Parkes,D., 1979

Diagnosis of Treatable Wilson's Disease
NEJM 298:1347, Cartwright,G.E., 1978

Autosomal Dominant System Degeneration in Portugese Families of the Azores Islands
Neurol 28:703, Coutinho,P.,et al, 1978

Clinical Aspects of Spasmodic Dysphonia
JNNP 41:361, Aminoff,M.J.,et al, 1978

Onset & End-of-dose Levodopa-induced Dyskinesias
Arch Neurol 35:261, Lhermitte,F.,et al, 1978

Effects of Learning on Visceral Functions-Biofeedback
NEJM 296:1274, Miller,N.E.,et al, 1977

Familial Paroxysmal Dystonic Choreoathetosis & its Differentiation From Related Syndromes
Ann Neurol 2:285, Lance,J.W., 1977

Familial Spasmodic Torticollis
Neurol 27:11, Gilbert,G.J., 1977

Blepharospasm-oromandibular Dystonia Dyndrome (Brueghel's syndrome) :A Variant of Adult-onset Torsion Dystonia
JNNP 39:1204, Marsden,C.D., 1976

Dystonia & Choreoathetosis in Multiple Sclerosis
Arch Neurol 33:590, Bachman,D.S.,et al, 1976

Neurological Complications of Infections of the Head & Neck
Otolaryng Clin North Am 9:729, Kaplan,R.J., 1976

Anticonvulsant-induced Dyskinesias:A Comparison with Dyskinesias Induced by Neuroleptics
JNNP 39:1210, Chadwick,D.,et al, 1976

Acute Dystonia, An Unusual Reaction to Diphenhydramine
JAMA 236:291, Lavenstein,B.L.&Cantor,F.K., 1976

Progressive Supranuclear Palsy-Case Study
NEJM 293:346, Richardson,E.P., 1975

Catecholamines & Neurologic Diseases
NEJM 293:274, Moskowitz,M.A.,et al, 1975

Neurologic Syndrome Associated with Antipsychotic Drug Use
NEJM 289:20, 1973, 290:110974., , 1974

Clinical Diagnosis of the Dyskinesias
Med Clin of North Am 56:1321, Duvoisin,R., 1972

Medical Treatment of Spasmodic Torticollis
Arch Neurol 27:503, Gilbert,G., 1972

Drug-Induced Movement Disorders
Postgrad Med 180, 1971, Sept., North,R., 1971

Infantile Nystagmus:A Prospec. Study of Spasmus Nutans, Congen. Nystag, & Unclass. Nystagmus of Infancy
J Pediatr 77:177, Jayalakshuni,R.,et al, 1970

Corticodentatonigral Degeneration with Neuronal Achromasia
Arch Neurol 18:20-33, Rebeiz,J.J.,et al, 1968

Diseases of Muscles-Clinical Manifestations & Differential Diagnosis
The New Physic 263, 1967, Oct., Boshes,L., 1967

Orthopaedic Aspects of Intraspinal Tumors in Infants & Children
J Bone & Joint Surg 47A:223965., Tachdjian,M.&Matson,D., 1965

Neuro CPC of MGH
Metachromatic Leukodystrophy, NEJM 267:1198-12041962., , 1962

A 67-Year-Old Man with Exercise Intolerance nd Progressive Weakness
Neurol 106:e214830, Gosset,A.,et al, 2026

Progressive Quadriparesis and Falls in a 66-Year-Old Man With Longstanding Human Immunodeficiency Virus
Neurol 106:e214621, Ong,B.A. & Carlson,A.K., 2026

A Randomized Trial of Shunting for Idiopathic Normal-Pressure Hydrocephalus
NEJM 393:2198-2209, 2264, Luciano,M.G.,et al, 2025

A 50-Year-Old Male Patient With Acute Severe Sensory Deafferentation and Bilateral Ptosis with Rapid Recovery
Neurol 106:e214435, Pseruk,F.,et al, 2025

A 60-Year-Old Man with Weakness and Gait Dysfunction
JAMA Neurol 82:305-306, Jones,F.J.S.,et al, 2025

A 67 YEar-Old Woman with Progressive Headache, Visual Hallucinations, and Seizures
Neurol 104:e213496, Gheihman,G.,et al, 2025

A 57-Year-Old Man With Chronic Gait Unsteadiness and Diminished Lower Extremity Sensation
Neurol 104:e213713, Rawat,R.,et al, 2025

A 62-Year-Old Woman with Progressive Spasticity, Weakness,and Gait Instability
Neurol 104:e210290, Voloshyna-Farber, E.Y.,et al, 2025

A 59-Year-Old Man with Progressive Dysarthria and Gait Instability
Neurol 104:e213729, Shen,D.,et al, 2025

A 63-Year-Old Female Patient Presenting with Orthostatic Hypotension and Ataxia
Neurol 105:e213993, Shen,F.,et al, 2025

A 72-Year-Old Man with Progressive Pan-Dysautonomia
Neurol 105:e213994, Zelikovich,A.S.,et al, 2025

A 73-Year-Old Man With Progressive Proximal Muscle Weakness and Binocular Diplopia
Neurol 105:e214173, Wold,K.J.,et al, 2025

Gait Analysis in Neurologic Disorders, Methodology, Applications and Clinical Considerations
Neurol 105:e214154, Ali,F.,et al, 2025

A 38-Year-Old Man With Involuntary Jerk-Like Movements and Ataxia
Neurol 105:e214381, Gomez,A.C.et al, 2025

A 24-Year-Old Man With Persistent Spontaneous Dizziness
Neurol 105:e214337, Isaza-Pierotti,D.F., et al, 2025

Clinical Manifestations and Diagnostic Challenges in a 16-Year-Old With Early-Onset Ataxia
Neurol 104:e210253, Chadha,D.,et al, 2024

Showing articles 350 to 400 of 816 << Previous Next >>