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 3750 to 3776 of 3776 << Previous

Uremic Polyneuropathy
Arch Neurol 8:413, Asbury,A.,et al, 1963

Course & Prognosis in Amyotrophic Lateral Sclerosis
Arch Neurol 8:17, Mackay,R., 1963

Angiokeratoma Corporis Diffusum
Quart J Med 31:177, 1962 April., Wise,D.,et al, 1962

Facial Pain:A Diagnostic Headache Group Practice, Apr, 1973, P 17-21, Anatomic Pathways Related to Pain in Face & Neck
J Neurosurg 19:116, Taren,J.,et al, 1962

Candida Endocarditis-Clinical & Pathologic Studies
Am J Med 32:251-285, 1962, Andriole,V.T.,et al, 1962

Neuro CPC of MGH
Meningioma at Thoracic Cord, NEJM 264:824-8271961., , 1961

Painful Ophthalmoplegia
Neurol 11:56, Hunt,W.,et al, 1961

Neuro CPC of MGH
Reticulum Cell Sarcoma of Brain & Meninges, NEJM 265:1205-121061., , 1961

Basilar Artery Migraine
Lancet 1:15-17, Bickerstaff,E.R., 1961

Amyotrophic Lateral Sclerosis:Clinical Syndrome Differential Diagnosis
Med Clin North Am 44:1013, Mulder,D.W., 1960

Myasthenic Syndrome in Patients with ALS
et al Neurol 9:627, Mulder,D.W., 1959

Increased Spinal Fluid Protein in Hyperparathyroidism & Other Hypercalcemic States
Arch Int Med 104:29, Edwards,G.,et al, 1959

Neuro CPC of MGH
Cervical Spondylosis with Protruded Disk, NEJM 261:715-7201959., , 1959

Neuro CPC of MGH
Congenital Vascular Malfor. of Spinal Cord, NEJM 258:949-954958., , 1958

Bilateral Loss of Vision from Cerebral Infarction
Brain 80:28, Symonds,C.,et al, 1957

The Significance of Nonbacterial Thrombotic Endocarditis:An Autopsy & Clinical Study of 78 Cases
Ann Int Med 46:255, MacDonald,R.A.,et al, 1957

Compression of the Thoracic Spinal Cord in a Patient with Scleroderma
Bull Hosp Joint Dis 18:98, 1957, Kaplan,A.,et al, 1957

Neurologic Manifestations of Chronic Pulmonary Insufficiency
NEJM 257:579-590, Austen,F.K.,et al, 1957

An Unusual Variant of Acute Idiopathic Polyneuritis (Syndrome of Ophthalmoplegia, Ataxia, & Areflexia)
NEJM 255:57, Fisher,C.M., 1956

Localization of Lesions Causing Horner's Syndrome
Arch Ophthamol 44:710, Jaffe,N., 1950

Five Types of Dystrophy
Together with Other Conditions Producing Insidious Muscle Weakness-Table 1-Hospital Med p. 60., , 1850

Failure of Vision in Childhood
Proc Royal Soc Medicine, pp 494-500., , 1850

Clinical Pathological Conference, Scleroderma, Spastic Paraparesis & Chronic Myelogenous Leukemia
Prov. VAH, Dec. 12, 77., Finelli,P.F., 1850

An 81-Year-Old Man with Imbalance and Memory Impairment
, Golbe,L.I.,et al,

Electric Shocks and Weakness of the Right Hand in a Young Man:Hirayama Disease
, Witiw,C.D.&OToole,J.E.,

Degenerative Diseases of the Nervous System, Primary Lateral Sclerosis
Adams & Victors Principles of Neurology, Chp 39, pg 1112, Ropper, A.H.,et al,

Clinical Study of Nine Patients with ReNU Syndrome
, Okamoto,N.,et al,

Showing articles 3750 to 3776 of 3776 << Previous