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 3450 to 3500 of 3776 << Previous Next >>

Trichlorethylene
In Vinken PJ, Bruyn GW, Eds, Handbook of Clin Neurol, Vol 36, North-Holland Publ Co, 457, Feldman,R.G., 1979

Cluster Headaches from Isosorbide Dinitrate
Ann Neurol 6:554-555, Bernar,J.L., 1979

Dialysis Encephalopathy Treated with Clonazepan
Ann Neurol 6:555-556, Trauner,D.,et al, 1979

Familial Fatal Parkinsonism with Alveolar Hypoventilation & Mental Depression
Ann Neurol 6:523-531, Purdy,A.,et al, 1979

Gyrate Atrophy of the Choroid & Retina with Hyperornithinemia:Tubular Aggreg. & Type 2 Fiber Atrophy
Neurol 29:966, Sipila,I.,et al, 1979

Chronic Progressive Myelopathy:Investigation with CSF Electrophoresis, Evoked Potentials, & CT Scan
Ann Neurol 6:419-424, Patty,D.W.,et al, 1979

Reversal of Incipient Brain Death From Head-Injury Apnea At the Scene Of Accidents
NEJM 301:109, Levine,J.E.,et al, 1979

Creatine Phosphokinase MB Band In Oculopharyngeal Muscular Dystrophy
(Letter) NEJM 301:270979., Diskin,C.J., 1979

Extraocular Muscle Biopsy in Chronic Progressive External Ophthalmoplegia
Ann Neurol 6:326-339, Ringel,S.P.,et al, 1979

Subacute Motor Neuronopathy:A Remote Effect of Lymphoma
Ann Neurol 5:271-287, Schold,S.C.,et al, 1979

Bilateral Rhinocerebral Phycomycosis
Ann Neurol 6:131-133, Kasper,L.H.,et al, 1979

Haemophilic Neuromyopathy
JNNP 42:600-605, Defaria,C.R.,et al, 1979

Paraparesis in Hereditary Multiple Exostoses:Case Report
Neurol 29:973-977, Ferrari,G.,et al, 1979

A Familial Mitochondrial Myopathy With Central Defect in Neural Transmission
Arch Neurol 36:553-556, Barron,S.A.,et al, 1979

Eosinophilic Polymyositis
Arch Neurol 36:721-722, 1979, Stark,R.J., 1979

Lymphocyte Capping in Muscular Dystrophy
Neurol 29:1419-1421, Hauser,S.L.,et al, 1979

Reversibility of Human Myopathy Caused by Vitamin E Deficiency
Neurol 29:1182-1186, Tomasi,L.G., 1979

Muscular Dystrophy in Six Young Girls
Neurol 29:1486-1491, Hazama,R.,et al, 1979

Amyotrophic Lateral Sclerosis With Ophthalmoplegia; A Cliniocopathologic Study
Arch Neurol 36:615-617, Harvey,D.G.,et al, 1979

Remission of a Syndrome Indistinguishable from Motor Neuron Disease after Resection of Bronchial Carcinoma
BMJ 2:176-177, , 1979

Clinical Pathological Conference
Amyotrophic Lateral Sclerosis, Case Record 46-1979, NEJM 301:1104-1111979., , 1979

Familial Subacute Necrotizing Encephalomyelopathy of the Adult Form (Adult Leigh Syndrome)
Ann Neurol 6:200-206, Kalimo,H.,et al, 1979

Disorders of Neuromuscular Transmission Caused by Drugs
NEJM 301:409-413, Argov,Z.,et al, 1979

Familial Kearns-Sayre syndrome
Neurol 29:1172-1174, Schnitzler,E.R.,et al, 1979

Basal Ganglia Calcification in Kearns-Sayre Syndrome
Arch Neurol 36:711-713, Robertson,W.C.Jr., 1979

Nephrotoxic Effects of Computerized Tomographic Brain Scan
NEJM 300:45-46, 1979. (Letter), Theerman,M.R.,et al, 1979

Acute Hepatic Failure Associated with the Use of Sodium Valproate
NEJM 300:962-966, Suchy,F.J.,et al, 1979

Abnormalties In Cultured Muscle & Periphral Nerve Of A Patient With Adrenomyeloneuropathy
NEJM 301:588-590, Askanas,V.,et al, 1979

Presenile Dementia With Motor Neuron Disease in Japan, A New Entity
Arch Neurol 36:592-593, Mitsuyama,Y.,et al, 1979

Brainstem Auditory Evoked Responses in Progressive Supranuclear Palsy
Ann Neurol 6:369, Tolosa,E.S.,et al, 1979

Progressive Supranuclear Palsy & Normal-pressure Hydrocephalus
Neurol 29:1544-1546, Morariu,M.A., 1979

'Locked-in Coma'in Postinfective Polyneuropathy
Arch Neurol 36:46-47, Carroll,W.M.,et al, 1979

Emery-Dreifuss Muscular Dystrophy
Ann Neurol 5:111-117, Rowland,L.P.,et al, 1979

Use of the ECG in the Diagnosis of Childhood Spinal Muscular Atrophy
Arch Neurol 36:317-318, Russman,B.S.,et al, 1979

Age & Cerebrospinal-Fluid Protein in Motor-Neuron Disease
NEJM 300:437-438, Guiloff,R.J.,et al, 1979

Double-Blind Study of Modified Neurotoxin in Motor Neuron Disease
Neurol 29:77-81, Tyler,H.R., 1979

Diazepam & Dialysis Encephalopathy
Neurol 29:414-415, Snider,W.D.,et al, 1979

Uraemic Myoclonus:An Example of Reticular Reflex Myoclonus
JNNP 42:52-55, Chadwick,D.,et al, 1979

Headache
In Clinical Neurology, Baker & Baker Editor. In Vol. II, Harper & Row, Publishers 1979, Chap. 13, p., 38-43. n,A.P., 1979

Quadriceps Myopathy in Two Brothers
Rhode Island Med J 62:125, Finelli,P.F., 1979

Linear Scleroderma as a Cause for Hemiatrophy
Ann Neurol 5:307, Rosenberg,R.,et al, 1979

Progressive Myelopathy Due to Extramedullary Hematopoiesis:Case Report & Review of the Literature
Ann Neurol 5:485-489, Stahl,S.M.,et al, 1979

Marfan Syndrome
NEJM 300:772-777, Pyeritz,R.E.,et al, 1979

Isolated Trigeminal Sensory Neuropathy:Early Manifestation of Mixed Connective Tissue Disease
Neurol 28:1286-1289, Searles,R.P.,et al, 1978

Carnitine Deficiency Acute Postpartum Crisis
Ann Neurol 4:558-561, Angelini,C.,et al, 1978

A Case of Schwartz-Jampel Syndrome with Unusual Muscle Biopsy Findings
Ann Neurol 3:93, Fariello,R.,et al, 1978

Computerized Cranial Tomography in Cerebral Diseases of White Matter
Neurol 28:534, Lane,B.,et al, 1978

The Cervical Myelopathy Associated with Rheumatoid Arthritis:Analysis of 32 Patients, with Two Post-mortem Cases
Ann Neurol 3:144, Nakano,K.K.,et al, 1978

Myoglobinuria & Renal Failure after Status Epilepticus
Neurol 28:200, Singhal,P.C.,et al, 1978

Celiac Sprue & Refractory Sprue
Gastroenter. 75:3071978., Trier,J.S.,et al, 1978

Showing articles 3450 to 3500 of 3776 << Previous Next >>