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

exercise-related muscle strength increase

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 2800 to 2850 of 3776 << Previous Next >>

Clinicopath Conf
Acute Multiple Sclerosis, Case Record 42-1990, NEJM 323:1123-1135990., , 1990

Fulminant Monophasic Multiple Sclerosis, Marburg's Type
JNNP 53:918-921, Johnson,M.D.,et al, 1990

Optic Neuritis:A Prospective Study
Neurol 40:919-923, Celesia,G.G.,et al, 1990

Scleroderma, fasciitis, and Eosinophilia Associated with the Ingestion of Tryptophan
NEJM 322:874-881, 9261990., Silver,R.M.,et al, 1990

Chronic Injuries of the Spinal Cord:Assessment with MR Imaging
Radiology 175:849-854, Yamashita,Y.,et al, 1990

Established Anticonvulsants and Treatment of Refractory Epilepsy
Lancet 336:350-354, Brodie,M.J., 1990

Surgery for Epilepsy
National Institutes of Health Concensus Conference, JAMA 264:729-7331990., , 1990

Surgical Management of Complex Partial Seizures
JAMA 264:734-737, Uematsu,S., 1990

Status Epilepticus in Adults
Lancet 336:551-552, Brodie,M.J., 1990

Prenatal Prediction of Risk of the Fetal Hydantoin Syndrome
NEJM 322:1567-1572, Buehler,B.A.,et al, 1990

MR Imaging in Patients with Temporal Lobe Seizures:Correlation of Results with Pathologic Findings
AJR 155:581-586, Heinz,E.R.,et al, 1990

Diagnosis of Epilepsy
Lancet 336:291-295, Chadwick,D., 1990

Masturbation Mimicking Abdominal Pain or Seizures in Young Girls
1990., Fleisher,D.R.&Morrison.A.,J Pediatr 116:810-814, 1990

Risks Associated with Giving Benzodiazepines to Patients with Acute Neurological Injuries
BMJ 300:1189-1190, Eldridge,P.R.&Punt,J.A.G., 1990

Trigeminal Sensory Neuropathy Associated with Connective Tissue Diseases
Neurol 40:891-896, Hagen,N.A.,et al, 1990

Congenital Brain Anomalies Associated with the Hypoplastic Left Heart Syndrome
Pediatrics 85:984-990, Glauser,T.A.,et al, 1990

Syncope:Current Diagnostic Evaluation and Management
Ann Int Med 112:850-863, Manolis,A.S.,et al, 1990

Trauma of the Spine and Spinal Cord-I
BMJ 301:34-38, Swain,A.,et al, 1990

Respiratory Problems of Air Travel in Patients with Spinal Cord Injuries
BMJ 300:1498-1499, Armitage,J.M.,et al, 1990

Vision and Hearing During Deferoxamine Therapy
J Pediatr 117:326-330, Cohen,A.,et al, 1990

"Endogenous"Benzodiazepine Activity in Body Fluids of Patients with Hepatic Encephalopathy
Lancet 336:81-83, Mullen,K.D.,et al, 1990

Mitochondrial Myopathy with a Defect of Mitochondrial-Protein Transport
NEJM 323:37-42, Schapira,A.H.V.,et al, 1990

Location of Facioscapulohumeral Muscular Dystrophy Gene on Chromosome 4
Lancet 336:651-653, Wijmenga,C.,et al, 1990

Mapping of Acute (Type 1) Spinal Muscular Atrophy to Chromosome 5q12-q14
Lancet 336:271-273, Melki,J.,et al, 1990

Spinal Muscular Atrophies
Editorial, Lancet 336:280-2811990., , 1990

Paraneoplastic Motor Neuron Disease and Renal Cell Carcinoma:Improvement after Nephrectomy
Neurol 40:960-962, Evans,B.K.,et al, 1990

Lower Motor Neuron Disease in a Patient with Autoantibodies Against Gangliosides GM1 and GD1b:Improvement with Immunotherapy
Neurol 40:842-844, Shy,M.E.,et al, 1990

Polyclonal IgM Anti-GM1 Ganglioside Antibody in Patients with Motor Neuron Disease and Variants
Ann Neurol 27:558-563, Salazar-Grueso,E.F.,et al, 1990

Immunologic Reactivity Against Borrelia Burgdorfi in Patients with Motor Neuron Disease
Arch Neurol 47:586-594, Halperin,J.J.,et al, 1990

2-Amino-3- (methylamino) -Propanoic Acid (BMAA) in Cycad Flour:An Unlikely Cause of ALS & Parkinsonism-Dementia of Guam
Neurol 40:767-772, Duncan,M.W.,et al, 1990

Anderson-Fabry Disease
Editorial, Lancet 336:24-251990., , 1990

Perineural Spread of Cutaneous Head and Neck Cancer
Arch Neurol 47:73-77, Clouston,P.D.,et al, 1990

PET Study in Progressive Supranuclear Palsy, Hypometabolic Pattern
Arch Neurol 47:747-752, Blin,J.,et al, 1990

Excessive Muscular Fatigue in Patients with Spastic Paraparesis
Neurol 40:1271-1274, Miller,R.G.,et al, 1990

Avoidable Factors Contributing to Death of Children with Head Injury
BMJ 300:87-91, Sharples,P.M.,et al, 1990

Seizures in Relation to Shunt Dysfunction in Children with Meningomyelocele
J Pediatr 116:57-60, Hack,C.H.,et al, 1990

Follow-up MR STudies in Hallervorden-Spatz Disease
J Comput Assist Tomogr 14:118-120, Gallucci,M.,et al, 1990

Cerebral Ventriculitis:MR Findings
J Comput Assist Tomogr 14:272-275, Barloon,T.J.,et al, 1990

Patterns of Disease Activity in Multiple Sclerosis:Clinical and Magnetic Resonance Imaging Study
BMJ 300:631-634, Thompson,A.J.,et al, 1990

Attitudes of Mothers to Neonatal Screening for Duchenne Muscular Dystrophy
BMJ 300:1112, Smith,R.A.,et al, 1990

Molecular Genetics of Duchenne and Becker Muscular Dystrophy
J Pediatr 117:1-15, Darras,B.T., 1990

Dantrolene Sodium and Hepatic Injury
Neurol 40:1427-1432, Chan,C.H., 1990

Autoantibodies to Gaba-Ergic Neurons & Pancreatic Beta Cells in Stiff-Man Syndrome
NEJM 322:1555-1560, Solimena,M.,et al, 1990

Van Gogh Had Meniere's Disease and Not Epilepsy
JAMA 264:491-493, Kaufman Arenberg,I.,et al, 1990

Mitochondrial Myopathy Caused by Long-Term Ziduvudine Therapy
NEJM 322:1098-1105, Dalakas,M.C.,et al, 1990

A Patient with Progressive Myelopathy and Antibodies to HTLV-I & HIV Type I in Serum and Cerebrospinal Fluid
Arch Neurol 47:477-479, Aboulafia,D.M.,et al, 1990

Transvrse Myelitis and Spastic Paraparesis in a Patient with HIV Infection
NEJM 322:1322, Dodson,D., 1990

Nationwide Survey of HTLV-I-Associated Myelopathy in Japan:Ass with Blood Transufsion
Ann Neurol 28:50-56, Osame,M.,et al, 1990

Familial Spastic Paraparesis Syndrome Associated with HTLV-I Infection
NEJM 323:732-737, Salazar-Grueso,E.F.,et al, 1990

Multiple Sclerosis or HTLV-I Myelitis
Neurol 40:1020-1022, Poser,C.M.,et al, 1990

Showing articles 2800 to 2850 of 3776 << Previous Next >>