Neudle.com: progressive autonomic failure

Differential
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acetylcholine receptor antibody

acoustic nerve

acute intermittant porphyria

Adies pupil

adrenergic blocker

adult polyglucosan body disease

adverse drug reaction

alpha adrenergic blocker

aluminum

Alzheimer's disease

amphiphysin antibodies

amyloidosis

amyotrophic lateral sclerosis

anatomy of

anisocoria

anorexia

antibodies to voltage-gated calcium channels

antiganglioside antibodies

antineurofascin antibodies

autoimmune autonomic ganglionopathy

autoimmune disease

autonomic cardiovascular reflexes

autonomic dysfunction

autonomic dysfunction, acute

autonomic dysfunction, evaluation of

autonomic nervous system

autonomic neuropathy

autosomal dominant leukodystrophy

botulism immune globulin

campylobacter infection

CAT scan, emission, abnormal

cataracts

cerebellar degeneration

cerebellar lesion

cerebellar vermis

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, oligoclonal IgG in

cingulate island sign

Clinical Pathologic Conference(C.P.C.)

collapsin response mediator protein 5 IgG

contactin associated protein like 1 antibodies

contactin associated protein like 2 antibodies

corpus callosum

corpus callosum, lesion of

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

cyst, arachnoid, infant

deep tendon reflexes

degenerative diseases of CNS

delay in diagnosis

dementia

dementia, familial

dementia, rapidly progressive

dementia, subcortical

depression

dermatomyositis

diabetes mellitus

diabetes mellitus, chemical

dialysis

dialysis dementia

dialysis disequilibrium syndrome

differential diagnosis

diplopia

disorientation

distal muscle atrophy

distal muscle weakness

electroencephalogram, abnormalities of

electromyogram

electromyogram, incremental response

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, paraneoplastic

encephalomyelitis

encephalopathy

ephedrine

epidemiology of neurology

erectile dysfunction

exercise

exome sequencing

extrapyramidal movement disorder, progressive

facial asymmetry

facial weakness

facial weakness, bilateral

falling

familial

fasciculation

fatal familial insomnia

gammaglobulin therapy, intravenous

gammaglobulin therapy, intravenous, refractory

ganglionitis

gastroparesis

gene mutation

genetic neurologic disorders

genetic testing

glaucoma

glucose tolerance test, abnormal

glycogen storage disease

guanethidine

Guillain Barre syndrome

Guillain Barre syndrome, axonal form

Guillain Barre syndrome, complications

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, etiology of

Guillain Barre syndrome, prognosis of

Guillain Barre syndrome, variant forms of

hallucination, auditory

heralding manifestation

hypokalemic paralysis

hyponatremia

hypoosmolality of serum

hypophonia

hyporeflexia

hyposmia

hypotension, neurologic causes of

hypotension, systemic

immunology and the nervous system

immunotherapy

impotence

inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with

inattention

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intranuclear

infant, evaluation of

insight, loss

insomnia

intellectual deficit

intellectual deterioration

intrinsic hand muscles, wasting of

irritability

irritable baby

Jewish

juvenile distal and segmental muscular atrophy

laughing

laughing, pathologic

L-dopa

leg weakness, bilateral

lethargy

leucine rich glioma inactivated 1 antibodies

light-near dissociation, causes of

memory, defect of recent

memory, impairment of

mental status, abnormal

metabolic disorder, primary

middle cerebellar peduncle, lesion, bilateral

midodrine

mimics

Mini Mental Status Examination

misdiagnosis

monoamine oxidase inhibitors

mononeuritis multiplex

mortality

Morvan's fibrillary chorea

motor neuron disease

movement disorder

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, contrast enhanced

MRI, diffusion weighted

MRI, lumbosacral plexus

multiple sclerosis

multiple system atrophy

muscle atrophy, progressive

muscle cramp

muscle pain

muscle strength, testing

muscle twitching

muscle weakness

muscle weakness, proximal

muscle weakness, sudden onset of

myasthenia gravis

myasthenia gravis, paraneoplastic

myelopathy, necrotizing

nerve conduction studies

nerve growth factor

nerve growth stimulating activity

nerve root enhancement

nerve root hypertrophy

neuroblastoma

neurofibromatosis 1

neurogenic bladder

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic signs

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuromuscular junction, abnormality of

neuromyotonia

neuronal cell surface antigen

neuronal intranuclear inclusion disease

neuronopathy, sensory

neuropathology

neuropathy

neuropathy, amyloid

neuropathy, autoimmune

neuropathy, hereditary peripheral

neuropathy, painful

neuropathy, paraneoplastic

neuropathy, peripheral

neuropathy, sensory

neuropathy, sensory, hereditary

neuroprotective agents

neurotoxin

next-generation sequencing

NMDA antagonists

node of Ranvier

nodopathy, autoimmune

nonresponsive

NOTCH2NLC

ocular dysmetria

onconeural antibodies

ophthalmoplegia

ophthalmoplegia, acute

ophthalmoplegia, bilateral, acute

ophthalmoplegia, total

opsoclonus-myoclonus syndrome

optic neuropathy

oral contraceptives

orthostatic hypotension

orthostatic hypotension, idiopathic

orthostatic hypotension, treatment of

paralysis, acute areflexic

paraneoplastic cerebellar degeneration

paresthesias

Parkinson disease

Parkinson disease, atypical

Parkinson disease, differential diagnosis of

Parkinson disease, familial

Parkinson disease, L-dopa nonresponsive

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

paroxysmal neurologic deficits

peripheral nerve, lesion of

pheochromocytoma

physical therapy

plasmapheresis

pleocytosis of cerebrospinal fluid

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polyneuropathy

polyneuropathy, uremic

porphyria

posterior leukoencephalopathy syndrome

postural abnormality

posturography

prevention of neurologic disorders

prion disease

prognosis

progressive hemifacial atrophy

progressive neurologic disorder

progressive supranuclear palsy

pruritus

pseudobulbar palsy

psychiatric problems in neurologic disorders

psychological testing

pupil, abnormality in neurologic disorders

pupil, dilated and fixed, bilateral

pupil, dilated, bilateral

pupil, light reflex, abnormal

pupil, oval

pupil, tonic

pure autonomic failure

pyramidal tract

pyramidal tract dysfunction

reflex sympathetic dystrophy

reflex sympathetic dystrophy, children

remote effect of cancer on the nervous system

renal failure

renal transplantation

renal tubular acidosis

repetitive nerve stimulation

salivation, excessive

schizophrenia

scleroderma

scleroderma, neurologic involvement with

screening

seizure

sensory ganglia

serum lipase, elevated

shoulder, pain in

Shy-Drager syndrome

sicca syndrome

single-fiber electromyography

Sjogren's syndrome

skin, biopsy

skin, temperature difference

sleep pathology and physiology

SNCA duplication

spasticity

spinal cord, lesion of

stare

steroid

steroid therapy, CNS treatment and complications with

subcortical U fibers

suck, poor

sweating

sweating, abnormality of

sympathetic block

sympathetic nervous system

sympathomimetic drugs

tensilon test, false positive

thalamus, lesion of-bilateral

thermography

thymoma

tongue, impaired movements of

tongue, weakness

trauma

treatment of neurologic disorder

tremor

trinucleotide repeats

uremia

uremic encephalopathy

urinary frequency

urinary incontinence

urinary retention

urine osmolality, elevated

walking, difficulty with

Watson-Schwartz reaction

weakness

weakness, acute

weakness, generalized

weakness, infant

weakness, progressive

Showing articles 3350 to 3400 of 3776 << Previous Next >>

Progressive Hemifacial Atrophy
Arch Neurol 39:44-46, Asher,S.W.,et al, 1982

Ipecac-induced Myopathy Simulating Dermatomyositis
Neurol 32:91-94, Bennett,H.S.,et al, 1982

Slowly Progressive Aphasia Without Generalized Dementia
Ann Neurol 11:592-598, Mesulam,M.M., 1982

Cerebral Embolism as the Initial Manifestation of Peripartum Cardiomyopathy
Neurol 32:668-671, Hodgman,M.T.,et al, 1982

Cardiomyopathy Associated with the Syndrome of Amyotrophic Chorea & Acanthocytosis
Ann Int Med 96:616-617, Faillace,R.T.,et al, 1982

Classic Amyotrophic Lateral Sclerosis With Dementia
Arch Neurol 39:681-683, Wilkstrom,J.,et al, 1982

Trigeminal Neuropathy in Progressive Systemic Sclerosis
Am J Med 73:57-62, Farrell,D.A.,et al, 1982

Neurogenic Arthrogryposis in One Identical Twin, Sul
Arch Neurol 39:717-718, Yi,C.,et al, 1982

Neurologic Complications of Primary Sjogren's Syndrome
Medicine 61:247-257, Alexander,E.L.,et al, 1982

Progressive Multifocal Leukoencephalopathy In A Male Homosexual With T-Cell Immune Deficiency
NEJM 307:1436-1438, Miller,J.R.,et al, 1982

Brainstem Encephalitis & The Syndrome Of Miller Fisher
Brain 105:481-495, Al-Din,A.N.,et al, 1982

Clin. Path. Conference
Mucormycosis Involving Left Nasal & paranasal Sinuses & Orbit, & Diabetes Mellitus, Case Record 38-1, 82, NEJM814,1982., 1982

Motor Spastic Paraplegia & Unilateral Infra-nuclear Facial Palsy Complicating Tetanus
BMJ 285:477-478, Jain,M.K.,et al, 1982

The Female Carrier of Duchenne Muscular Dystrophy
BMJ 284:1423-1424, Dubowitz,V., 1982

Progressive Muscle Disease in a Young Woman With Family History of Duchenne's Muscular Dystrophy
Arch Neurol 39:378-380, Olson,B.J.,et al, 1982

Serial Two-dimensional Echocardiography in Duchenne Muscular Dystrophy
Neurol 32:1101-1105, Goldberg,S.J.,et al, 1982

An Autosomal-dominant Dystrophy with Humeropelvic Distribution & Cardiomyopathy
Neurol 32:1399-1401, Fenichel,G.M.,et al, 1982

Myotonic Dystrophy, Mitral Valve Prolapse, and Cerebral Embolism
Stroke 13:93-94, Morris,L.K.,et al, 1982

Misdiagnosis of Stroke
Lancet 1:328-331, Norris,J.W.&Hachinski,V.C., 1982

Conjugate Deviation of Gaze in Hepatic Encephalopathy
JNNP 45:1168, Sandyk, R.et al, 1982

Amyotrophic Lateral Sclerosis & its Association with Dementia, Parkinsonism & Other Neurological Disorders:A Review
Brain 104:217-247, Hudson,A.J., 1981

Correlation of CT Scanning and Pathologic Features of Ophthalmic Graves'Disease
Ophthalmol 88:553-564, Trokel,S.L.&Jakobiec,F.A., 1981

Vitamin E Deficiency in Werdnig-Hoffmann Disease
Ann Neurol 10:266-268, Shapira,Y.,et al, 1981

Primary Lateral Sclerosis
Arch Neurol 38:630-633, Beal,M.F.,et al, 1981

Treatment Of Early Stages Of Dialysis Encephalopathy By Aluminium Depletion
Lancet 2:1344-1345, Ackrill,P.,et al, 1981

Ocular Skew Deviation in Hepatic Coma
(Letter) , JNNP 44:45881., , 1981

Changes in the Basal Ganglia Following Cyanide Poisoning
J Comput Assist Tomogr 5:755-756, Finelli,P.F., 1981

Association Of Spinocerebellar Disorders With Cystic Fibrosis Or Chronic Childhood Cholestasis & Very Low Serum Vit. E
Lancet 2:1319-1321, Elias,E.,et al, 1981

Improvement of Stiff-man Syndrome with Sodium Valproate
Neurol 31:1162-1163, Spehlmann,R.,et al, 1981

Circulating Immune Complexes in Neurologic Disease
Neurol 31:1402-1407, Noronha,A.B.C.,et al, 1981

Emergencies in the Home, Neurological Rmergencies
BMJ 283:473-474, Lister,T.P., 1981

Clonazepam:Effective Treatment for Restless Legs Syndrome in Uraemia
BMJ 283:885-886, Matthews,W.B.,et al, 1981

Respiratory & Bulbar Paralysis with Relapsing Hyperthyroidism
BMJ 283:275-276, Edelman,J.,et al, 1981

Cholesterol Embolism as a Cause of Transient Ischemic Attacks & Cerebral Infarction
Neurol 31:860-865, Beal,M.F.,et al, 1981

Progressive Supranuclear Palsy, Computed Tomography, & Response to Antiparkinsonian Drugs
Neurol 31:442-445, Haldeman,S.,et al, 1981

Progressive Pontobulbar Palsy With Deafness
Arch Neurol 38:186-190, Brucher,J.M.,et al, 1981

Familial Spastic Paraplg, Peroneal Neuropathy, & Crural Hypopig, A New Neurocut Synd
Neurol 31:754-757, Stewart,R.M.,et al, 1981

Respiratory Distress & Arnold-Chiari Malformation
Neurol 31:97-100, Papasozomenos,S.,et al, 1981

Baclofen in the Treatment of Stiff-Man Syndrome
Ann Neurol 9:511-512, Miller,F.,et al, 1981

Progressive Supranuclear Palsy:Functional Analysis of the Response to Methysergide & Antiparkinsonian Agents
Neurol 31:1507-1518, Rafal,R.D.,et al, 1981

The Hot Bath Test in the Diagnosis of Multiple Sclerosis
JAMA 246:1113-1114, Malhotra,A.S.,et al, 1981

Transient Bilateral Visual Reduction & Mydriasis After Propranolol Treatment
Ann Neurol 10:583, Parrish,D.O.,et al, 1981

Motor Neuron Disease:Decremental Responses to Repetitive Nerve Stimulation
Neurol 31:202-204, Bernstein,L.P.,et al, 1981

Preservation of the Phrenic Motorneurons in Werdnig-Hoffman Disease
Ann Neurol 9:506-510, Kuzuhara,S.,et al, 1981

An Ultramicroscopic Study of Skin & Conjunctival Biopsies in Chronic Neuro. Disorders of Childhood
Ann Neurol 9:163-173, Arsenio-Nunes,M.L.,et al, 1981

Chronic Paroxysmal Hemicrania
Am J Med 71:169-170, Hochman,M.S., 1981

A Progressive Neurologic Syndrome In Children With Chronic Liver Disease
NEJM 304:503-508, Rosenblum,J.L.,et al, 1981

Management of Hepatic Encephalopathy
Editorial, BMJ 282:171-1721981., , 1981

Abrupt Neurological Deterioration in Children With Kearns-Sayre Syndrome
Arch Neurol 38:247-250, Coulter,D.L.,et al, 1981

Ophthalmoplegia-Plus
Arch Neurol 38:423-426, Okamoto,T.,et al, 1981

Showing articles 3350 to 3400 of 3776 << Previous Next >>