Neudle.com: "wheelchair"

Differential
(Click to cross reference)

abdominal protrusion

acromicria

acute intermittant porphyria

adult polyglucosan body disease

advances in neurology

adverse drug reaction

alternating rapid movement

alveolar hypoventilation

amniocentesis

amphiphysin antibodies

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, differential diagnosis

anterior spinal artery

anterior spinal artery infarction

anti Hu antibody

anti mGluR1 encephalitis

anticoagulant, treatment

anticonvulsants

anticonvulsants, selection of

anticonvulsants, untoward effects of

aortic surgery

applause sign

apraxia of eye movements

ataxia telangiectasia

atrioventricular block

atypical

autoantibodies

autoimmune cerebellar ataxia

autoimmune disease

autonomic dysfunction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

benign essential tremor

biopterin deficiency

biotin

biotin deficiency

biotin deficiency, juvenile form

biotin-responsive basal ganglia disease

bulbar palsy, progressive

carcinoembryonic antigen

CAT scan, emission, abnormal

cataracts

cauda equina, enhancement

cauda equina, lesion of

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar edema

cerebellar lesion

cerebellar vermis

cerebellum, disease of

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral infarction, subcortical

cerebral palsy

cerebrospinal fluid, drainage of

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, proteincytologic dissociation

cerebrovascular accident

cerebrovascular accident, recurrent

chemotherapy, CNS treatment and complications with

chest x-ray, abnormal

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

clonus

clubfoot as related to neurologic disease

collapsin response mediator protein 5 IgG

contactin associated protein like 2 antibodies

contractures, joint

contrast agents, neurotoxicity of

conus medullaris, lesion of

copper deficiency

coprolalia

corpus callosum, atrophy of

corpus callosum, thinning

C-reactive protein, elevated

creatine phosphokinase(CPK)elevated

degenerative diseases of CNS

delay in diagnosis

dementia

dementia, familial

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, reversible

dementia, subcortical

denervation of muscle

denervation potentials

developmental milestones, loss of

developmental retardation

diabetes mellitus

diabetes mellitus, neurologic manifestations of

differential diagnosis

difficulty climbing stairs

diplopia

disability, neurological

dissociated sensory loss

distal muscle weakness

diurnal variation

dopa responsive dystonia

drug abuse, neurologic complications of

dystonia, etiology of

dystonia, painful

dystonia, treatment of

dystrophin

ears of the Lynx MR sign

ecchymoses

electrocardiogram, abnormal

electrocardiogram, LVH

electroencephalogram, abnormalities of

electroencephalogram, video monitoring with

electromyogram

emotional lability

encephalitis

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, paraneoplastic

encephalomyelitis

encephalopathy

encephalopathy, progressive

endovascular therapy

enzyme, defect

enzyme, muscle disease

eosinophilia

eosinophilic granulomatosis with polyangiitis

epidemiology of neurology

executive dysfunction

extrapyramidal movement disorder, progressive

eye movement, disorders of

face, numbness of

facial appearance, abnormal

facial weakness

facial weakness, bilateral

fine motor function, impaired

finger nose finger test

finger tapping

fingerprint bodies

fistula, arterio-venous

fistula, arterio-venous, dural

fistula, arterio-venous, dural, spinal

flaccid paralysis

fluctuate

folic acid deficiency

foot deformity

frataxin

Friedreich's ataxia

frontotemporal dementia, behavioral variant

gammaglobulin therapy, intravenous

ganglionitis

gastric partitioning

gastrocnemius muscle weakness

gaze palsy

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glutamic acid decarboxylase, antibody

granular osmiphilic material

granuloma, eosinophilic

granulomatous disease

hemiplegia, progressive

heralding manifestation

high arched palate

histochemistry of muscle

H-reflex testing

human immunodeficiency virus type 1

hydrocephalus

hydrocephalus, normal pressure

hypertrophic intracranial pachymeningitis

hypotension, systemic

hypothalamus, lesion of

hypothyroidism

hypotonia

iatrogenic neurologic disorders

immunology and the nervous system

inability to stand on tiptoes

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion body myositis

incontinence, fecal

intellectual deficit

intellectual deterioration

intravenous

irritability

Isaacs syndrome

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

leg weakness, bilateral

leg weakness, unilateral

leucine rich glioma inactivated 1 antibodies

Lewy body disease, diffuse

lid closure, weakness of

lymphoma, primary of CNS

malabsorption

malabsorption syndrome

malformation, vascular, dural

malignancy screen

malignancy, occult

manganese intoxication

marche a petits pas

masked facies

memory, impairment of

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine

mimics

Mini Mental Status Examination

misdiagnosis

mitochondrial disease

mobility

mobility aids

molecular genetics

monoclonal gammopathy

mononeuritis multiplex

mononeuritis multiplex, causes of

movement disorder, drug induced

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, complications with

MRI, contraindications

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, false negative

MRI, high signal intensity of basal ganglia

MRI, spinal cord, increased intramedullary cord signal

MRI, spine

MRS

multiple system atrophy

muscle atrophy, progressive

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscle weakness, sudden onset of

muscular dystrophy

muscular dystrophy, cardiovascular changes with

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, differential diagnosis of

muscular dystrophy, distal, Miyoshi

muscular dystrophy, Duchenne

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

mutism

myasthenia gravis, limb-girdle

myasthenia gravis, paraneoplastic

myasthenic syndrome

myelitis, longitudinal

myelomalacia

myeloneuropathy

myelopathy

myelopathy, chronic progressive

myopathy, mitochondrial

nemaline rod myopathy

nemaline rod myopathy, adult onset

neoplasm, primary of CNS

nephrogenic systemic fibrosis

nerve biopsy

nerve conduction studies

nerve root biopsy

nerve root enhancement

nerve root hypertrophy

neuritis, causes of

neurocutaneous disease

neuroendocrinology

neurogenic bladder

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic evaluation

neurolymphomatosis

neuromuscular junction

neuronal cell surface antigen

neuronal ceroid-lipofuscinosis

neuronopathy

neuronopathy, sensory

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, asymptomatic

neuropathy, diabetic

neuropathy, painful

neuropathy, paraneoplastic

neuropathy, sensory

neurotoxic

neurotoxin

next-generation sequencing

NMDA antagonists

Notch3 gene

numbness, generalized

nutritional deficiency

nystagmus

nystagmus, gaze-evoked

obsessive-compulsive disorder

ocular motility, disorders of

oculopharyngeal muscular dystrophy

old age, neurology of

onconeural antibodies

ophthalmoplegia

ophthalmoplegia, progressive external

opsoclonus-myoclonus syndrome

optic atrophy

organomegaly

orthostatic hypotension

pachymeningitis, cranial

paralysis, acute areflexic

paralysis, asymmetric

paraneoplastic cerebellar degeneration

paranoia

paraparesis

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

paraplegia

paraspinal muscle

paraspinal muscle weakness

paresthesias

paresthesias, feet

paresthesias, generalized

Parkinson disease

Parkinson disease, arteriosclerotic

Parkinson disease, axial symptoms

Parkinson disease, diagnosis

Parkinson disease, differential diagnosis of

Parkinson disease, drug induced

Parkinson disease, juvenile

Parkinson disease, L-dopa nonresponsive

Parkinson disease, misdiagnosis

Parkinson disease, tremor, absence of

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

Parkinsonism, freezing phenomena in

PAS positive

PAS positive material in the brain

pathologic reflex

pathology

penguin silhouette sign

percussion induced muscle contraction

peripheral nerve, lesion of

pleocytosis of cerebrospinal fluid

POEMS syndrome

POLG1 gene

polyglucosan body

polyglucosan body disease

polyneuritis, acute sensory

position sensation

posterior column disease

posterior leukoencephalopathy syndrome

postural abnormality

practice guidelines

pregnancy, neurologic complications in

primary lateral sclerosis

prion disease

progeria

prognosis

progressive myoclonic epilepsy

progressive neurologic disorder

progressive spinal muscular atrophy

progressive supranuclear palsy

prolactin, elevated

proprioception

proprioception, abnormal

proximal muscle atrophy

pseudoathetosis

pseudobulbar palsy

psychiatric problems in neurologic disorders

psychomotor retardation

pyramidal tract dysfunction

quadriceps atrophy

quadriparesis

quadriplegia

radiation hypersensitivity

radiation therapy, CNS treatment and complications with

ragged-red fibers

Rankin score

rapidly progressing neurologic illness

rash

Red flags

release phenomena

remote effect of cancer on the nervous system

reversible neurologic disorder

saccadic eye movements, abnormal

scoliosis, neurologic association with

scooters

screening

scurvy

sedimentation rate, elevated

seizure

sensory loss

sensory loss, patchy

sensory nerve action potentials

sensory polyneuropathy

sequencing difficulty

short stature

shunt procedure, lumboperitoneal

shunt procedure, ventricular

sinemet

skin, biopsy

skin, lesions in neurologic disorders

skin, thickened

slit lamp examination

small vessel vasculitis

small-bowel resection

snout reflex

sodium valproate

somatosensory evoked potentials

spastic ataxia

spastic paraplegia, type 11

spasticity

speech disorder

speech disorder, childhood

speech, loss of

spinal cord

spinal cord, enlargement

spinal cord, infarction of

spinal cord, lesion of

spinal cord, vascular malformation of

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 2

spinocerebellar ataxia type 7

standing difficulty

stare

status epilepticus

stem cell transplantation

stereotyped behavior

steroid therapy, CNS treatment and complications with

storage disease of CNS

striatum, lesion of

striatum, lesion of, bilateral

stridor

stuttering

sudden death

symmetric brain lesions

temporal lobe, atrophy

temporal lobe, lesion

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

thalamus, lesion of

thalamus, lesion of-bilateral

titubation

toe walking

tongue, fasciculations of

tongue, impaired movements of

treatment of neurologic disorder

tremor

tremor, intention

trinucleotide repeats

tripping

tyrosine hydroxylase deficiency

ventricular enlargement

vertigo

vibratory sensation, abnormal

vision, blurred

visual acuity, decreased

vitamin supplementation

vitamin, multiple

walking

walking frame

walking, difficulty with

weakness

weakness, acute

weakness, generalized

weakness, progressive

weakness, proximal

weakness, rapidly progressive

weaning from respirator, failure to

Showing articles 0 to 50 of 65 Next >>

A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
JAMA Neurol 81:83-84, Hua,L.,et al, 2024

A 60-Year-Old Woman with Rapidly Progressive Muscle Weakness and Ophthalmoparesis
Neurol 103:e209708, Wannarong,T.,et al, 2024

Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
JAMA Neurol 80:107-108, Bernaola,M.T.,et al, 2023

A 60-Year Old Man with Asymmetric Weakness and Persistent Fever
Neurol 100:530-536, Zheng,Y.,et al, 2023

A 6-Year-Old Girl with Progressive Toe Walking
Neurol 98:e769-e773, Libdeh, A.A. & Ibrahim, A., 2022

Paraneoplastic Myeloneuropathies
Neurol 96:e632-e639, Shah, S.,et al, 2021

A Middle-aged Woman with Severe Scoliosis and Encephalopathy
JAMA Neurol 78:251-252, Mohan, G.,et al, 2021

Clinicopathologic Conference, Normal Pressure Hydrocephalus
NEJM 384:1350-1358, Case 10-2021, 2021

A 72-year-old Man with a Progressive Cognitive and Cerebellar Syndrome
Neurol 95:e2707-e2710, Lad, M. & Griffiths, T.D., 2020

Clinical features, prognostic factors, and antibody effects in anti-mGluR1 encephalitis
Neurol 95:e3012-e3025, Spatola, M.,et al, 2020

Neuropathy, Encephalopathy, Status Epilepticus, and Acute Intermittent Porphyria
Lancet 395:e101, Ahmed, M.A.,et al, 2020

Ears of the Lynx Magnetic Resonance Imaging Sign
Ann Neurol 88:16-17, Baghbanian, S.M.,et al, 2020

Clinical Characteristics, Risk Factors, and Outcomes of POEMS Syndrome
Neurol 95:e268-e279, Keddie, S.,et al, 2020

Toxic Diffuse Isolated Cerebellar Edema from Over-the-Counter Health Supplements
Neurol 92:965-966, Kim, D.D.,et al, 2019

Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019

Clinicopathologic Conference, Vitamin C Deficiency (Scurvey), Vitamin B6 & Folate Deficiencies
NEJM 379:282-289, Case 22-2018, 2018

Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
Front Neurol doi:10.3389/fneur.2017.00472, Velazquez-Perez, L.C.,et al, 2017

Cerebellar Ataxia and Hearing Impairment
JAMA Neurol 74:243-244, Lin, C.Y. & Kuo, S.H., 2017

Reversible Gait Ataxia
Neurol 88:e145-e149, Abkur, T.M. & Bede, P., 2017

Clinicopathologic Conference, Diffuse Large B-Cell Lymphoma Consistent with Neurolymphomatosis
NEJM 376:2471-2481, Case 19-2017, 2017

Clinicopathologic Conference, Copper Deficiency Myelopathy
NEJM 377:1977-1984, Case 35-2017, 2017

An 82-year-old man with Worsening Gait
Neurol 89:e246-e252, Chew, S.,et al, 2017

Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3
NEJM 377:2376-2385, Case 38-2017, 2017

A 64-year-old Man with Progressive Paraspinal Muscle Weakness
Neurol 86:e4-e9, Schneider, R.,et al, 2016

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

A 40-year old Woman with Difficulty Going Down Stairs in High-Heeled Shoes
Ann Neurol 77:1-7, Scripko, P.,et al, 2015

Clinicopathologic Conference, Frontotemporal Lobar Degeneration with Tau-positive Inclusions (Picks Disease Subtype) Due to a Gly389Arg MAPT Mutation, Resulting in the Behavioral Variant of Frontotemporal Dementia with Parkinsonism
NEJM 372:1151-1162, Miller, B.L.,et al, 2015

Evaluation of a Patient with Spinal Cord Infarction after a Hypotensive Episode
Stroke 45:e203-e205, Vongveeranonchai, N.,et al, 2014

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

Mystery Case: A Young Boy with Myoclonic Jerks
Neurol 81:e130-e134, Musleh, C.,et al, 2013

Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis
NEJM 364:1062-1074, Case 8-2011, 2011

Redefining Dysferlinopathy Phenotypes Based on Clinical Findings and Muscle Imaging Studies
Neurol 75:316-323,298, Paradas,C., et al, 2010

New Aspects on Patients Affected by Dysferlin Deficient Muscular Dystrophy
JNNP 81:946-953, Klinge,L.,et al, 2010

A 63-Year-Old Woman with Urinary Incontinence and Progressive Gait Disorder
Neurol 72:1607-1613, Lossos,A.,et al, 2009

Clinical Spectrum of Ataxia-Telangiectasia in Adulthood
Neurol 73:430-437, Verhagen,M.M.M.,et al, 2009

Progressive Supranuclear Palsy: A Current Review
The Neurologist 14:79-88, Lubarsky,M. &Juncos,J.L., 2008

A Parkinsonian Syndrome in Methcathinone Users and the Role of Manganese
NEJM 358:1009-1017, Stepens,A.,et al, 2008

Curable Cause of Paraplegia: Spinal Dural Arteriovenous Fistulae
Stroke 39:2756-2759, Aghakhani,N.,et al, 2008

Gadolinium-Based MR Contrast Agents and Nephrogenic Systemic Fibrosis
Radiology 242:647-649, Kuo,P.H.,et al, 2007

Clinicopath Conf., Gliomatosis Cerebri
Neurol 69:600-606, Fleming,J.O.,et al, 2007

Clinicopath Conf, Dopamine-Responsive-Dystonia Caused by a Mutation in the GCH1 Gene
NEJM 355:831-839, Case 26-2006, 2006

Delayed Neurotoxicity in Primary Central Nervous System Lymphoma
Arch Neurol 62:1595-1600, Omuro,A.M.P.,et al, 2005

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

Silent Infarcts Demonstrated by Diffusion-Weighted MRI in CADASIL
Eur Neurol 49: 178-180, Moon,S.Y.,et al, 2003

Desmin Myopathy, a Skeletal Myopathy with Cardiomyopathy Caused by Mutations in the Desmin Gene
NEJM 342:770-780, Dalakas,M.C.,et al, 2000

Progressive Dementia and Gait Disorder in a 78 Year Old Woman
JNNP 68:526-531, Tagliati,M.,et al, 2000

Disease Progression in Sporadic Inclusion Body Myositis: Observations in 78 Patients
Neurol 55:296-198, Peng,A. et al, 2000

A 44-Year-Old Woman with Difficulty Walking
JAMA 284:2632-2639, Iezzoni,L.I., 2000

A Woman Who Left Her Wheelchair
Lancet 353:806, Mingrone,G.,et al, 1999

Showing articles 0 to 50 of 65 Next >>