Neudle.com: "multisystem atrophy"

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abdominal distention

abdominal protrusion

abducens nerve paralysis

addiction, heroin

addiction, heroin-neurologic complications with

Addison's disease

adolescent medicine

adverse drug reaction

amyloid angiopathy, cerebral

amyloidosis

amyotrophic lateral sclerosis

anatomy of

anemia

angiography, cerebral

anti Tr antibodies

anticoagulant, treatment

anticonvulsants

anticonvulsants, untoward effects of

antiphospholipid antibodies

anxiety

apraxia

apraxia of eye movements

aqueduct of Sylvius, stenosis

aqueductal stenosis

areflexia

Argyll Robertson pupil

arteritic anterior ischemic optic neuropathy

ataxia telangiectasia

autoimmune cerebellar ataxia

autoimmune disease

autonomic cardiovascular reflexes

autonomic dysfunction

autonomic dysfunction, acute

autonomic dysfunction, evaluation of

autonomic nervous system

autonomic neuropathy

autonomic neuropathy, idiopathic

B 12 deficiency

B12

basal ganglia, lesion of

basal ganglia, lesion, bilateral

Behcet's syndrome

benign essential tremor

calcification, intracranial

carcinoembryonic antigen

carcinoma

cardiac surgery, neurologic complications with

cardiomyopathy

carotid artery occlusion, intracranial

CAT scan

CAT scan, abnormal

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, venography

cauda equina, lesion of

celiac disease, adult

celiac disease, childhood

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellar vermis

cerebellum, disease of

cerebral arteries

cerebral cortical atrophy

cerebral edema, vasogenic

cerebral venous infarction

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebral venous thrombosis, etiology

cerebral venous thrombosis, recurrent

cerebrospinal fluid, elevated protein of

cerebrovascular accident

cerebrovascular accident, acute management of

cerebrovascular accident, prevention of

cerebrovascular accident, prognosis in

cerebrovascular accident, recurrent

cerebrovascular accident, thrombolytic agents in treatment

cerebrovascular accident, young adult

children

chorea

choreoathetosis

chromosomal abnormality

chromosome 11

cigarette smoking

Clinical Pathologic Conference(C.P.C.)

collateral circulation

controversies in neurology

corpus callosum, lesion of

cortical-basal ganglionic degeneration

CPAP

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

craniectomy, decompressive

creatine phosphokinase(CPK)elevated

critical care unit

cryopyrin-associated periodic syndrome

degenerative diseases of CNS

dementia

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, reversible

dementia, thalamic

dementia, treatment of

demyelinating disease

depression

dermatitis herpetiformis

developmental retardation

diabetes insipidus

diabetes mellitus

diarrhea

differential diagnosis

difficulty climbing stairs

distal muscle weakness

dopamine receptor

dopamine receptor, D2

drooling

dural sinus thrombosis

electroencephalogram, abnormalities of

encephalitis, autoimmune

epidemiology of neurology

Erdheim-Chester disease

erectile dysfunction

erythema migrans

evidence-based research

extraocular muscle lesion

extrapyramidal movement disorder, progressive

eye movement, disorders of

facial appearance, abnormal

facial expression abnormality

fatal familial insomnia

fatigue

fever

fibrinolytic agents

fibrinolytic agents, intra-venous local infusion

fine motor function, impaired

fingers, abnormal

fluorescein angiography

foot drop

foot drop, bilateral

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

gammaglobulin therapy, intravenous

ganglionitis

gastrointestinal disease, neurologic complications

gastrointestinal motility

gastrointestinal perforation

gastroparesis

gaze palsy, supranuclear

genetic neurologic disorders

genetic testing

genital ulcerations

giant cell arteritis

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glutamate dehydrogenase deficiency

Guillain Barre syndrome, differential diagnosis of

hallucination

hallucination, visual

head injury

headache

headache, intermittent

headache, severe

hemiparesis

hepatitis

heralding manifestation

histiocytosis

HLA

Horner's syndrome

Horner's syndrome, childhood

hypotension, systemic

hypotonia

iatrogenic neurologic disorders

inclusion bodies, eosinophilic cytoplasmic

incontinence, fecal

infraorbital nerve

intellectual deficit

intellectual deterioration

intestinal pseudoobstruction

intracerebral hemorrhage

intracranial hypertension, benign

intracranial pressure, increased

intrathecal medication

iritis

Jakob-Creutzfeldt disease

lacrimal gland enlargement

L-dopa

leg numbness

leg weakness, bilateral

lenticular nucleus, lesion of

lenticular nucleus, lesion of, bilateral

level of consciousness, decreased

Lewy body

Lewy body disease, diffuse

lymphoma involving CNS

lymphoma, primary of CNS

memory, impairment of

meningeal biopsy

meningeal enhancement

mental status, abnormal

methylmalonic aciduria

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

mimics

Mini Mental Status Examination

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

MNGIE syndrome

monoclonal gammopathy

mononeuritis multiplex

movement disorder, extrapyramidal

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, functional

MRI, gradient-echo

MRI, hypointense signal foci on

multiple organ failure

multiple sclerosis

multiple system atrophy

muscle biopsy

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

myasthenic syndrome

myelopathy

myelopathy, necrotizing

myoclonic jerks

myoclonus

myoclonus, stimulus sensitive

myopathy

myopathy, inclusion body

myopathy, inclusion body with Paget's disease

nausea and vomiting

neurocutaneous disease

neuroendocrinology

neurologic complications of, surgery

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic examination, focal

neurologic signs

neuromyelitis optica (Devic's disease)

neuronopathy, sensory

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, amyloid

neuropathy, peripheral

nicotine

non-arteritic antererior ischemic optic neuropathy

nutritional deficiency

nystagmus

ocular motility, disorders of

old age, neurology of

Onufrowicz nucleus

ophthalmoplegia

ophthalmoplegia, painful

ophthalmoplegia, total

optic atrophy

optic atrophy, bilateral

optic nerve, blood supply of

optic nerve, infarction of

optic neuropathy

optic neuropathy, bilateral

optic neuropathy, ischemic

optic neuropathy, ischemic, anterior

optic neuropathy, ischemic, posterior

oral contraceptives

oral contraceptives, cerbrovascular disease and

oral ulcerations

orbit, fat

orbit, inflammation in

orbit, lesions of

orbit, pseudotumor of

orbit, tomograms of

orthostatic hypotension

orthostatic hypotension, idiopathic

parasympathetic nervous system

paresthesias

paresthesias, hands

Parkinson disease

Parkinson disease, arteriosclerotic

Parkinson disease, atypical

Parkinson disease, dementia with

Parkinson disease, diagnosis

Parkinson disease, differential diagnosis of

Parkinson disease, drug induced

Parkinson disease, L-dopa nonresponsive

Parkinson disease, misdiagnosis

Parkinson disease, rapid progression

Parkinson disease, treatment of

Parkinson disease, tremor, absence of

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

pleocytosis of cerebrospinal fluid

POEMS syndrome

polymerase chain reaction

polyneuropathy

polyneuropathy, critically ill

pons, atrophy

postoperative neurologic complications

postural abnormality

practice guidelines

pregnancy, neurologic complications in

prethrombotic state

prevention of neurologic disorders

progressive neurologic disorder

progressive supranuclear palsy

psychiatric problems in neurologic disorders

psychomotor retardation

pupil, abnormality in neurologic disorders

pure autonomic failure

purple glove syndrome

purple hands

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract dysfunction

radiation hypersensitivity

ragged-red fibers

rapidly progressing neurologic illness

rash

remote effect of cancer on the nervous system

renal failure

respirations in CNS disease

respirator

respiratory failure

respiratory tract infection

retinal vasculopathy with cerebral leukodystrophy

retinopathy

retroperitoneal mass

reversible neurologic disorder

sedimentation rate, elevated

seizure

sensorineural hearing loss

sensory loss

septicemia

serologic testing

sexual behavior, disorder of

sexual dysfunction in neurologic disease

short stature

Shy-Drager syndrome

sinemet

single photon emission computed tomography

skin, biopsy

skin, lesions in neurologic disorders

spinal cord, injury of

spinal cord, injury, sexual dysfunction in

spinal cord, lesion of

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 2

spinocerebellar ataxia type 7

spinocerebellar ataxia type 8

spinocerebellar degeneration

spirochete infection

stare

stem cell transplantation

steppage gait

steroid therapy, CNS treatment and complications with

striatonigral degeneration

superior sagittal sinus thrombosis

sympathetic nervous system

tissue plasminogen activator, intravenous

Tolosa Hunt syndrome

tongue, ulcer

tracheostomy

treatment of neurologic disorder

tremor

tremor, cerebellar

trigeminal nerve, hypertrophy

trigeminal neuralgia

trinucleotide repeats

trochlear nerve palsy

vascular endothelial growth factor

vibratory sensation, abnormal

visual acuity, decreased, monocular

visual field defect

visual field defect, altitudinal

visual loss

visual loss, progressive

visual loss, slow

visual loss, sudden-unilateral

vitamin deficiency

vitiligo

walking, difficulty with

Wallerian degeneration

weakness

weakness, generalized

weakness, progressive

weaning from respirator, failure to

word-finding difficulty

Showing articles 0 to 50 of 2366 Next >>

Reversible Cortical and Basal Ganglia Lesions in Late-Onset Methylmalonic Aciduria
JAMA Neurol 81:1-82, Chu,X.C.,et al, 2024

IgG4-Related Orbital Inflammation
https://EyeWiki.org, Oct, Chelnis,J. & Gervasio,K.A., 2023

Cutaneous a-Synuclein Signatures in Patients with MultipleSystem Atrophy and Parkinson Disease
Neurol 100:e1529-e1539, Gibbons,C.,et al, 2023

Complete Evaluation of Dementia: PET and MRI Correlation and Diagnosis for the Neuroradiologist
AJNR 42:998-1007, Oldan, J.D.,et al, 2021

Vitamin B12 Deficiency in a 29-Year-Old Woman
Neurol 97:e643-e646, Huddar, A.,et al, 2021

A 22-Year-Old Man with Progressive Bilateral Visual Loss
Neurol 94:625-630, Yang, S.L.,et al, 2020

A 47-year-old Man with Rapidly Progressive Ataxia and Vitiligo
Neurol 94:e1664-e1669, Han, F.,et al, 2020

Central Nervous System Involvement in Erdheim-Chester Disease
Neurol 95:e2746-e2754, Aubart,F.C.,et al, 2020

Bilateral Middle Cerebellar Peduncle Lesions:Neuroimaging Features and Differential Diagnoses
Brain Behav 10:e01778, Jiang,J.,et al, 2020

Intrathecal Administration of Autologous Mesenchymal Stem Cells in Multiple System Atrophy
Neurol 93:e77-e87, Singer, W.,et al, 2019

Stridor in Multiple System Atrophy
Neurol 93:630-639, Cortelli, P.,et al, 2019

Progressive Proximal Weakness in a 56-year-old Man with Bone Pain
Neurol 93:939-944, Torabi,T.,et al, 2019

Atypical Parkinsonian Syndromes: A General Neurologists Perspective
Eur J Neurol 25:41-58, Deutschlander, A.B.,et al, 2018

Neuropsychiatric Involvement of Behcets Disease
www.SMGEbooks.com Dec, Soyak, M., 2017

Purple Hands in Multiple System Atrophy
Neurol 86:2314, Coon, E.A.,et al, 2016

A 44-Year-Old Man with Eye, Kidney, and Brain Dysfunction
Ann Neurol 79:507-519, Vodopivec, I.,et al, 2016

Extraintestinal Manifestations of Coeliac Disease
Nat Rev Gastroenterol Hepatol 12:561-571, Leffler, D.A.,et al, 2015

A 48-year-old Man with Walking Difficulty
Neurol 85:e165-e169, Kalladka, D.,et al, 2015

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

Ischemic Optic Neuropathies
NEJM 372:2428-2436, Biousse, V. & Newman, N.J., 2015

Degenerative Diseases of the Nervous System, Multiple System Atrophy
Adams & Victors Principles of Neurology, Chp 39, pg 1095, Ropper, A.H.,et al, 2014

Facial Bradykinesia
JNNP 84:681-685, Bologna, M.,et al, 2013

Incidence and Pathology of Synucleinopathies and Tauopathies Related to Parkinsonism
JAMA Neurol 70:859-866, Savica, R.,et al, 2013

Treatment of Multiple System Atrophy Using Intravenous Immunoglobulin
BMC Neurol 12:131, Novak, P.,et al, 2012

Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
Brain 134:3326-3332, Garone, C.,et al, 2011

Diagnosis and Management of Cerebral Venous Thrombosis: A Statement for Healthcare Professionals From the American Heart Association/American Stroke Association
Stroke 42:1158-1192, Saposnik,G.,et al, 2011

A Hereditary Moyamoya Syndrome With Multisystemic Manifestations
Neurol 75:259-264, Herv�,D., et al, 2010

Clinicopath Conf, Neuro-Behcets Disease
NEJM 360:2341-2351, Case 17-2009, 2009

The Hot Cross Bun Sign in the Patients with Spinocerebellar Ataxia
Eur J Neurol 16:513-516, Lee, Y.-C.,et al, 2009

Second Consensus Statement on the Diagnosis of Multiple System Atrophy
Neurol 71:670-676, Gilman,S.,et al., 2008

Sexual Function in Men and Women With Neurological Disorders
Lancet 369:512-525, Rees,P.M.,et al, 2007

Pupil Findings in a Consecutive Series of 150 Patients with Generalised Autonomic Neuropathy
JNNP 77:1163-1168, Bremner,F. &Smith,S., 2006

Clinicopath Conf., Degoss Disease
NEJM 355:2575-2584, Case 38-2006, 2006

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

Morning Glory Sign: A Particular MR Finding in Progressive Supranuclear Palsy
Magn Reson Med Sci 3:125-132, Adachi, M., et al, 2004

Constipation in Neurological Diseases
JNNP 74:13-19, Winge,K.,et al, 2003

Diffusion-Weighted Imaging Discriminates Progressive Supranuclear Palsy from PD, But Not From the Parkinson Variant of Multiple System Atrophy
Neurol 60:922-927, Seppi,K.,et al, 2003

Diffusion-weighted MRI Differentiates the Parkinson Variant of Multiple System Atrophy from PD
Neurol 58:575-580, Schocke,M.F.H.,et al, 2002

T2-weighted MRI Differentiates Multiple System Atrophy from Parkinson's Disease
Neurol 59;1265-1267, Kraft,E.,et al, 2002

Fragile X Premutation Carriers: Characteristic MR Imaging Findings of Adult Male Patients with Progressive Cerebellar and Cognitive Dysfunction.
AJNR 23:1757-1766, Brunberg,J.A.,et al, 2002

Improved Accuracy of Clinical Diagnosis of Lewy Body Parkinson's Disease
Neurol 57:1497-1499, Hughes,A.J.,et al, 2001

Evolution of Sporadic Olivopontocerebellar Atrophy Into Multiple System Atrophy
Neurol 55:527-532, Gilman,S. et al, 2000

Prevalence of Progressive Supranuclear Palsy and Multiple System Atrophy:A Cross-Sectional Study
Lancet 354:1771-1775, Schrag,A.,et al, 1999

Magnetic Resonance Imaging-Based Volumetry Differentiates Idiopathic Parkinson's Syndrome from Multiple System Atrophy and Progressive Supranuclear Palsy
Ann Neurol 45:65-74, Schulz,J.B.,et al, 1999

Clinical Usefulness of Magnetic Resonance Imaging in Multiple System Atrophy
JNNP 65:65-71, Schrag,A.,et al, 1998

Multiple-System Atrophy is Genet Distinct from Ident Inherited Causes of Spinocerebellar Degen
Neurol 49:1598-1604, Brandmann,O.,et al, 1997

Sympathetic Cardioneuropathy in Dysautonomias
NEJM 336:696-702, 7211997., Goldstein,D.S.,et al, 1997

Survival of Patients with Pathologically Proven Multiple System Atrophy:A Meta-Analysis
Neurol 48:384-393, Ben-Shlomo,Y.,et al, 1997

Neuro-Ophthalmic Manifestations of Lyme Disease
J Neuro-Ophthalmol 17:108-121, Balcer,L.J.,et al, 1997

Showing articles 0 to 50 of 2366 Next >>