Neudle.com: arm atrophy

Differential
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abducens nerve paralysis

abducens nerve paralysis, bilateral

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, heralded by neurologic invol

addiction, heroin

addiction, heroin-neurologic complications with

Addison's disease

Adies pupil

adult polyglucosan body disease

advances in neurology

alien hand syndrome

allodynia

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

amyotrophic lateral sclerosis-like syndrome

anatomy of

anemia

angiography, neurologic complications with

anterior horn cell disease

anterior spinal artery infarction

anticoagulant, complications of

anticoagulant, treatment

anticonvulsants, untoward effects of

antiviral agents

applause sign

apraxia

apraxia of eye movements

arterial dissection, vertebral

asthma

asthma, poliomyelitis-like syndrome with

autonomic dysfunction

basement membrane thickening

basophilic stippling of red blood cells

brachial neuritis, acute

brachial neuritis, bilateral

brachial neuritis, prognosis of

brachial plexus

brachial plexus injury

brachial plexus neuropathy

brachial plexus neuropathy, bilateral

brachial plexus neuropathy, familial

brachial plexus neuropathy, recurrent

brachial plexus, lesion of

bulbar palsy, progressive

cardiac catheterization, neurologic complications

cardiomyopathy

carotid artery disease

cashew nut sign

CAT scan, abnormal

CAT scan, emission, abnormal

cataracts

CD4 counts

central nervous system, infection of

cerebellar ataxia, hereditary

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebral cortical atrophy

cerebral embolism

cerebral embolism, artery to artery

cerebral embolism, cardiac origin

cerebral infarction

cerebral venous thrombosis

cerebrovascular accident

cerebrovascular accident, etiology

cerebrovascular accident, location of

cerebrovascular accident, mimics

cerebrovascular accident, vascular territory involved

Clinical Pathologic Conference(C.P.C.)

cognition

cold temperature

compartment syndrome

compartment syndrome, medial brachial fascial

complications

compression neuropathy

conduction block

confusion

corona radiata

corpus callosum, infarction of

corpus callosum, lesion of

cortical hand knob

cortical hand knob infarct

cortical hemorrhage

cortical infarction

cortical infarction, small

cortical muscular atrophy

cortical topography

cortical-basal ganglionic degeneration

cough

cranial neuropathy

cranial neuropathy, multiple

Creutzfeldt-Jakob disease, genetic

degenerative diseases of CNS

delay in diagnosis

dementia

dementia, frontotemporal

denervation of muscle

denervation potentials

developmental milestones, loss of

diabetes mellitus

diabetes mellitus, neurologic manifestations of

differential diagnosis

diplegia, atonic

diplegia, brachial

diplopia

disability, neurological

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

drug abuse, neurologic complications of

drug induced neurologic disorders

dural sinus thrombosis

dying

dysarthria

dysdiadochokinesia

dyskinesia, buccal lingual facial

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electroencephalogram, inflammatory disease

electromyogram

emotional lability

encephalitis

entrapment neuropathy

enzyme, muscle disease

epidemiology of neurology

episodic neurologic deficits

facial weakness, bilateral

fine motor function, impaired

Friedreich's ataxia, late onset

gaze palsy, supranuclear

genetic neurologic disorders

genetic testing

girdle sensation

granular osmiphilic material

heavy metal intoxication

hemiparesis

hemiplegia

heralding manifestation

herpes zoster

highly active antiretroviral therapy

hip flexor weakness

Hispanics

hospice

human immunodeficiency virus type 1

iatrogenic neurologic disorders

intellectual deterioration

intracerebral hemorrhage

intrinsic hand muscles, wasting of

introverted

irritability

Jakob-Creutzfeldt disease

Jewish

juvenile distal and segmental muscular atrophy

juxtacortical hemorrhage

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

Leber's hereditary optic neuropathy

leg atrophy

leg numbness

leg weakness, bilateral

leg weakness, unilateral

life support, withdrawal of

linear lesion

livedo reticularis

lumbosacral plexopathy

lumbosacral plexus, neuritis

Man-In-The-Barrel syndrome

masked facies

median nerve

median nerve, lesion of

median neuropathy

memory, impairment of

mental status, abnormal

microangiopathy, brain

midbrain

midbrain, atrophy

middle cerebral artery territory infarction

middle cerebral artery, emboli to

middle cerebral artery, occlusion of

Minamata disease

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

mitochondrial recessive ataxic syndrome

molecular genetics

monoclonal gammopathy

monomelic amyotrophy

mononeuropathy

mononeuropathy chronic inflammatory demyelinating

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, lumbosacral plexus

MRI, muscle

MRI, peripheral nerve

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, spine

MRI, susceptibility weighted

multifocal acquired demyelinating sensory motor neuropathy

multiple myeloma

multiple system atrophy

muscle atrophy, focal

muscle atrophy, progressive

muscle atrophy, static

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

myasthenia gravis

myasthenia gravis, distal weakness

myelin protein zero gene

myelitis, longitudinal

myelomalacia

myeloneuropathy

myelopathy

myocardial infarction

myoclonic jerks

myoclonus

myoclonus, cortical

myoclonus, stimulus sensitive

neck pain

neck weakness

neoplasm, intracranial

neoplasm, primary intracranial

neoplasm, primary of CNS

nerve biopsy

nerve conduction studies

nerve conduction studies, sensory

nerve enlargement

nerve injury

nerve root hypertrophy

neuritis, heavy metals causing

neuroendocrinology

neurogenic bladder

neurologic disease, diagnoses of

neurologic examination

neurologic signs

neurologic symptoms

neuromuscular disease, electrodiagnosis of

neuronal ceroid-lipofuscinosis

neuronopathy, sensory

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, multifocal

neuropathy, onion bulb

neuropathy, painful

neuropathy, peripheral

neuropathy, sensory

neuropathy, toxic

neuroprotective agents

occupational neurologic disorders

occupational neuropathies

ophthalmoplegia

opportunistic infection, CNS

optic atrophy

optic neuropathy

optic neuropathy, hereditary

orthostatic hypotension

osteoporosis

owl's eye sign of spinal cord

paralysis, asymmetric

parietal lobe, lesion of

parietal lobe, syndromes of

Parkinson disease, axial symptoms

Parkinson disease, tremor, absence of

Parkinsonism syndrome

penguin silhouette sign

peripheral blood smear

pleocytosis of cerebrospinal fluid

POEMS syndrome

poison, mercury

poliomyelitis-like illness

polyglucosan body

polyglucosan body disease

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

polyradiculoneuropathy

position sensation

positive sharp waves

posterior column disease

posterior fossa

posterior fossa, lesion of

postpartum

precentral gyrus

precipitating factors

pregnancy, neurologic complications in

primary lateral sclerosis

prion disease

prognosis

progressive multifocal leucoencephalopathy

progressive myoclonic epilepsy

progressive neurologic disorder

progressive supranuclear palsy

proprioception

proprioception, abnormal

proximal muscle atrophy

pseudoathetosis

pseudobulbar palsy

pseudoperipheral palsy

pseudoulnar palsy

psychological testing

psychomotor retardation

pupil, dilated and fixed, bilateral

pyramidal tract

pyramidal tract dysfunction

quadriceps atrophy

radial nerve

rapidly progressing neurologic illness

rash

real-time quaking-induced conversion

recruitment

recruitment, reduced

recurrent

reflex sympathetic dystrophy

reflex sympathetic dystrophy, children

Refsum's disease

remote effect of cancer on the nervous system

reverse split hand sign

reversible neurologic disorder

saccadic eye movements, abnormal

scalenus anticus syndrome

sensorineural hearing loss

sensory loss

sensory loss, cortical

sensory loss, cutaneous

sensory loss, leg

sensory loss, patchy

sensory loss, pseudoradicular

sensory loss, truncal

sensory nerve action potentials

sensory symptoms

sensory testing, quantitative

sequencing difficulty

shoulder-hand syndrome

sinemet

skin, discoloration

skin, temperature difference

sleep

sleep pathology and physiology

spinal cord, cervical

spinal cord, compression of

spinal cord, enlargement

spinal cord, infarction of

spinal cord, ischemic lesion of

spinal cord, lesion of

spinocerebellar ataxia

spinocerebellar ataxia type 6

spinocerebellar degeneration

splenium of corpus callosum

spontaneous muscle activity

sports medicine, neurology of

stellate-ganglion block

stem cell transplantation

steppage gait

strokelike episodes

sudden death

superior sagittal sinus thrombosis

suprascapular nerve

suprascapular neuropathy

supraspinatus muscle

sweating, abnormality of

thoracic outlet syndromes

thrombocytopenia

tomaculous neuropathy

tongue, atrophy

trauma

treatment of neurologic disorder

tremor

trinucleotide repeats

vascular endothelial growth factor

vasculopathy

vestibular areflexia

vibratory sensation, abnormal

visual fields, constricted

walking, difficulty with

walking, difficulty with in dark

weakness, generalized

weakness, progressive

word-finding difficulty

workup

wrist drop

zinc

Showing articles 1050 to 1100 of 2428 << Previous Next >>

Sympathetic Cardioneuropathy in Dysautonomias
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Hereditary Frontotemporal Dementia is Linked to Chromosome 17q21-q22:Genetic & Clinicopath Study of 3 Dutch Families
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Frontotemporal Dementia is on the MAP
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Alteration of White Matter MR Signal Intensity in Frontotemporal Dementia
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CT and MR Findings of Neuroacanthocytosis
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What Are the Obstacles for an Accurate Clinical Diagnosis of Pick's Disease
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X Linked Adrenoleukodystrophy:Clinical Presentation, Diagnosis, and Therapy
JNNP 63:4-14, vanGeel,B.M.,et al, 1997

A 36-Year-Old Woman Recuperating From a Stroke
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Cysticercosis, Clinical Classification Based on Imaging Studies
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Paramedian Pontine Infarction
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CAG Repeat Number Governs the Development Rate of Pathology in Huntington's Disease
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Clinicopath Conf
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Atypical MRI Features of Wilson's Disease:High Signal in Globus Pallidus on T1-Weighted Images
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Serial Neuropsychological Assess & Magnetic Resonance Imagingf Analysis in Multiple Sclerosis
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Corticobasal Degeneration:Neuropathologic and Clinical Heterogeneity
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Midline Cerebral Morphometry Distinguishes Frontotemporal Dementia and Alzheimer's Disease
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Clinical Characteristics of a Chromosome 17-Linked Rapidly Progressive Familial Frontotemporal Dementia
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Frontotemporal Dementia and Early Alzheimer Disease:Differentiation with Frontal Lobe H-1 MR Spectroscopy
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Clinical and Radiologic Findings in Progressive Facial Hemiatrophy (Parry-Romberg Syndrome)
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A 44-Month Clinical-Brain MRI Follow-Up in a Patient with B12 Deficiency
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Central Poststroke Pain & Wallenberg's Lateral Medullary Infarction:Freq, Charact & Determinants in 63 Pts
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Quadriceps Weakness and Osteoarthritis of the Knee
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Rapid Spongiform Degeneration of the Cerebrum and Cerebellum in Creutzfeldt-Jakob Encephalitis:Serial MR Findings
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Neuro-Ophthalmic Manifestations of Lyme Disease
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Clinicopath Conf
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Gene Locus for Autosomal Recessive Distal Myopathy with Rimmed Vacuoles Maps to Chromosome 9
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ALS Standard of Care Consensus
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Effect of Noninvasive Positive-Pressure Ventilation on Survival in Amyotrophic Lateral Sclerosis
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Motor Neuron Syndromes in Cancer Patients
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Familial Nature and Continuing Morbidity of the Amyotrophic Lateral Sclerosis-Parkinsonism Dementia Complex of Guam
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Spinobulbar Muscular Atrophy Can Mimic ALS:The Importance of Genetic Testing in Male Patients with Atypical ALS
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What is the Accuracy of the Clinical Diagnosis of Multiple System Atrophy
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Multiple-System Atrophy is Genet Distinct from Ident Inherited Causes of Spinocerebellar Degen
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Mononeuropathy of a Distal Branch of the Femoral Nerve in a Body Building Champion
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Complete Ophthalmoplegia After Zoster Ophthalmicus
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Showing articles 1050 to 1100 of 2428 << Previous Next >>