Neudle.com: "progressive autonomic failure"

Differential
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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

autonomic cardiovascular reflexes

autonomic dysfunction

autonomic dysfunction, acute

autonomic dysfunction, evaluation of

autonomic nervous system

botulism immune globulin

campylobacter infection

CAT scan, emission, abnormal

cataracts

cerebellar degeneration

cerebellar lesion

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, oligoclonal IgG in

chest pain

chewing movements

chorea

cingulate island sign

Clinical Pathologic Conference(C.P.C.)

collapsin response mediator protein 5 IgG

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

dementia

dementia, familial

dementia, rapidly progressive

depression

dermatomyositis

diabetes mellitus

diabetes mellitus, chemical

dialysis

dialysis dementia

dialysis disequilibrium syndrome

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

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, 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, 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

leukoencephalopathy

life expectancy

lightheaded

light-near dissociation, causes of

memory, defect of recent

memory, impairment of

mental status, abnormal

metabolic disorder, primary

midodrine

mimics

Mini Mental Status Examination

misdiagnosis

monoamine oxidase inhibitors

mortality

Morvan's fibrillary chorea

motor neuron disease

movement disorder

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, diffusion weighted

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

nerve conduction studies

nerve growth factor

nerve growth stimulating activity

neuroblastoma

neurofibromatosis 1

neurogenic bladder

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, hereditary peripheral

neuropathy, paraneoplastic

neuropathy, sensory

neuropathy, sensory, hereditary

neuroprotective agents

neurotoxin

next-generation sequencing

NMDA antagonists

NOTCH2NLC

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

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

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

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, temperature difference

sleep pathology and physiology

SNCA duplication

spasticity

spinal cord, lesion of

stare

steroid

steroid therapy, CNS treatment and complications with

suck, poor

sweating

sweating, abnormality of

sympathetic block

sympathetic nervous system

sympathomimetic drugs

tensilon test, false positive

thermography

thymoma

tongue, impaired movements of

tongue, weakness

trauma

treatment of neurologic disorder

tremor

trinucleotide repeats

uremia

uremic encephalopathy

urinary incontinence

urine osmolality, elevated

walking, difficulty with

Watson-Schwartz reaction

weakness

weakness, acute

weakness, generalized

weakness, infant

weakness, progressive

Showing articles 0 to 50 of 3653 Next >>

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

Clinicopathologic Conference, Infant Botulism, Case 3-2024
NEJM 390:358-366, Case 3-2024, 2024

A 45-Year-Old Man with Progressive Insomia and Psychiatric and Motor Symptoms
Neurol 94:e1213-e1218, Lima, J.E.E.,et al, 2020

A 58-year-old Man with Hand Tremor and Episodes of Neck Pain
Neurol 93:557-561, Urso, D.,et al, 2019

GGC Repeat Expansion of NOTCH2NLC in Adult Patients with Leukoencephalopathy
Ann Neurol 86:962-968,809, Okubo, M.,et al, 2019

An Unusual Cause of Hypokalemic Paralysis
Neurol 87:e174-e177, Shree, R.,et al, 2016

Clinicopathologic Conference, Botulism
NEJM 372:364-372, Case 3-2015, 2015

Multiple-System Atrophy
NEJM 372:249-263, Fanciulli, A. & Wenning, G.K., 2015

Paraneoplastic Neurological Syndromes
Clin Exp Immunol 175:336-348, Leypoldt, F. & Wandinger, K.-P., 2014

Guillain-Barre Syndrome
NEJM 366:2294-2304, Yuki, N. & Hartung, H.P., 2012

Acute Intermittent Porphyria Presenting as Acute Pancreatitis and Posterior Reversible Encephalopathy Syndrome
Acta Neurol Taiwan 17:177-183, Shen, F.,et al, 2008

Neurogenic Orthostatic Hypotension
NEJM 358:615-624, Freeman,R., 2008

Clinicopath Conf, Multiple-System Atrophy
NEJM 351:912-921, Case 27-2004, 2004

Treatment of Postural Hypotension
JNNP 65:285-289, Mathias,C.J.&Kimber,J.R., 1998

Morvan's Fibrillary Chorea: A Paraneoplastic Manifestation of Thymoma
JNNP 65:857-862, Lee,E.K.,et al, 1998

Adult Botulism
Muscle & Nerve, 20:100-10297., Shapiro,B.E.,et al, 1997

Clinical and Radiologic Findings in Progressive Facial Hemiatrophy (Parry-Romberg Syndrome)
AJNR 18:751-757, Cory,R.C.,et al, 1997

Some Specific Clinical Features Differentiate Multiple System Atrophy (Striatonigral Variety) from Parkinson's Disease
Arch Neurol 52:294-298, Colosimo,C.,et al, 1995

Reflex Sympathetic Dystrophy in Children
BMJ 310:1648-1649, Lloyd-Thomas,A.R.&Lauder,G., 1995

Growth Factors:Potential Therapeutic Applications in Neurology
JNNP 54:1445-1450, Drago,J.,et al, 1994

Clinicopath Conf
Small Cell CA (of lung) with Lambert-Eaton Myasthenic Syndr, Case 32-1994, NEJM 331:528-5354., , 1994

Autonomic Dysfunction in Systemic Sclerosis:Sympathetic Overactivity and Instability
Am J Med 93:143-150, Dessein,P.H.,et al, 1992

Physical Manoeuvres for Combating Orthostatis Dizziness in Autonomic Failure
Lancet 339:897-898, VanLieshout,J.J.,et al, 1992

Neurological Paraneoplastic Syndromes in Patients with Small Cell Lung Cancer, A Prospective Survey of 150 Pts
JNNP 54:764-767, Elrington,G.M.,et al, 1991

Autonomic Nervous Function in Progressive Supranuclear Palsy
Arch Neurol 48:1083-1084, vanDijk,J.G.,et al, 1991

Nervous System Complications in Uremia
Ann Int Med 109:143-153, Frasser,C.L.&Arieff,A.I., 1988

The Lambert-Eaton Myasthenic Syndrome, A Review of 50 Cases
Brain 111, 577-5961988., O'Neill,J.H.,et al, 1988

Disorders of the Autonomic Nervous System:Part 1. Pathophysiology & Clinical Features
Ann Neurol 21:419-430, McLeod,J.G.&Tuck,R.R., 1987

Midodrine, A New Agent in the Management of Idiopathic Orthostatic Hypotension & Shy-Drager Syndrome
Mayo Clin Proc 56:429-433, Schirger,A.,et al, 1981

Juvenile Type of Distal & Segmental Muscular Atrophy of Upper Extremities
Ann Neurol 3:429, Sobue,I.,et al, 1978

The Sympathetic-Nervous-System Defect in Primary Orthostatic Hypotension
NEJM 296:293, Ziegler,M.G.,et al, 1977

Fisher's Syndrome:A Pharmacological Study of the Pupils
Ann Neurol 2:63, Okajima,T.,et al, 1977

Postural Hypotension:Adrenergic Responsivity, & Levodopa Therapy
Neurol 27:921, Corder,C.N.,et al, 1977

Tonic Pupils with Acute Ophthalmoplegic Polyneuritis
Ann Neurol 2:393, Keane,J.R., 1977

Nerve Growth Factor (three parts)
NEJM 297:1096, 1149, 1211977., Mobley,W.C.,et al, 1977

Case Records of the MassGeneral Hospital, Case 41-1975, Acute Intermittent Porphyria
NEJM 293:817, Woods,B., 1975

Hemifacial Atrophy
Brit J Oral Surg 9:102, Vickery,I.M., 1971

A 56-Year-Old Woman with New-Onset Hoarsement and Dysphagia
Neurol 104:e213363, McAree,M. & Frontera, J.A., 2025

Congenital Titinopathy:Comprehensive Characterization of the Most Severe End of the Disease Spectrum
Ann Neurol 97:611-628, Coppens,S.,et al, 2025

A 19-Year-Old Woman with Progressive Weakness and Numbness in Her Arms and Legs
Neurol 104:e213495, Alsabah,A-A.,et al, 2025

Clinicopathologic Conference, Cryptococcal Meningoencephalitis
NEJM 391:2361-2369, Case 40-2024, 2024

A 24-Year-Old Man with Gait Impairment, Hearing Loss, and Recurrent Fever
Neurol 102:e209358, Barbosa,A.R.,et al, 2024

A 22-Year-Old Woman with Episodic Weakness and Jaundice
Neurol 103:e210018, Rathinasbapathi,M.,et al, 2024

Clinicopathologic Conference, Myasthenia Gravis
NEJM 391:1441-1450, Case 32-2024, 2024

Neuroleptic Malignant Syndrome
NEJM 391:1130-1138, Wijdicks,E.F.M. & Ropper,A.H., 2024

Clinicopathologic Conference, Infective Endocarditis Due to Haemophilus Parainfluenza
NEJM 391:2148-2157, Case 38-2024, 2024

Glucose Hypermetabolism in the Basal Ganglia
Neurol 101:90-91, Kim,Y.E.,et al, 2023

Clinicopathologic Conference, Systemic Immunoglobulin Light-Chain (AL) Amyloidosis
NEJM 389:166-175, Case 21-2023, 2023

A Young Adult Man with Cognitive Changes, Gait Difficulty, and Renal Insufficiency
Neurol 100:206-212, Stamm,B.,et al, 2023

Showing articles 0 to 50 of 3653 Next >>