Neudle.com: arm atrophy

Differential
(Click to cross reference)

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 amyotrophic diplegia

brachial neuritis

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

causalgia

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

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

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

complex regional pain syndrome

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

diagnostic criteria

diarrhea

differential diagnosis

diplegia, atonic

diplegia, brachial

diplopia

disability, neurological

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

dizziness

dorsal column stimulator

down-beat nystagmus

downward gaze

drug abuse

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

enterovirus infection of CNS

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

guanethidine

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, variant forms of

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

meningismus

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

myelitis, longitudinal

myelomalacia

myeloneuropathy

myelopathy

myelopathy, tract-specific

myocardial infarction

myoclonic jerks

myoclonus

myoclonus, cortical

myoclonus, stimulus sensitive

nausea and vomiting

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

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

pain, management of chronic

paralysis, acute areflexic

paralysis, asymmetric

parietal lobe, lesion of

parietal lobe, syndromes of

Parkinson disease, axial symptoms

Parkinson disease, tremor, absence of

Parkinsonism syndrome

patient information and support

penguin silhouette sign

peripheral blood smear

pleocytosis of cerebrospinal fluid

POEMS syndrome

poison, mercury

poliomyelitis

poliomyelitis-like illness

polyglucosan body

polyglucosan body disease

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

polyradiculoneuropathy

position sensation

positive sharp waves

post traumatic pain syndrome

posterior column disease

posterior fossa

posterior fossa, lesion of

postpartum

posttraumatic

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

quadriparesis

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

respirator

respiratory failure

respiratory tract infection

retinitis pigmentosa

retrocollis

retrovirus

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, darkening of

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

spinal cord, neoplasm

spinal cord, neoplasm, intramedullary

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 1650 to 1700 of 2530 << Previous Next >>

Neurosarcoidosis:Signs, Course and Treatment in 35 Confirmed Cases
Medicine 69:261-276, Chapelon,C.,et al, 1990

Quadriceps Myopathy:Forme Fruste of Becker Muscular Dystrophy
Ann Neurol 28:634-639, Sunohara,N.,et al, 1990

Phenotypic Heterogeneity of Spinal Muscular Atrophy Mapping to Chromosome 5q11. 2-12. 3 (SMA5q)
Neurol 40:1831-1836, Munsat,T.L.,et al, 1990

What Causes Motoneuron Disease?
Editorial, Lancet 336:1033-10351990., , 1990

Misdiagnosis in Patients with Amyotrophic Lateral Sclerosis
Arch Int Med 150:2301-2305, Belsh,J.M.&Schiffman,P.L., 1990

Non Alzheimer's Disease Forms of Cerebral Atrophy
Editorial, JNNP 53:929-9311990., Neary,D., 1990

Clioquinol (lodochlorhydrozyquin
Vioform) and Iodoquinol (Diiodohydrozyquin) :Blindness and Neuropathy, Pediatrics 86:797-7980., , 1990

Magnetic Resonance Imaging of Radiation Optic Neuropathy
Am J Ophthalmol 110:389-394, Zimmerman,C.F.,et al, 1990

Causalgia and Other Reflex Sympathetic Dystrophies
In the Management of Pain, Lea & Febiger, Phila, p. 220, Bonica,J.J., 1990

Clinical Features and Associations of 560 Cases of Motor Neuron Disease
JNNP 53:1043-1045, Li,T.,et al, 1990

Selective Involvement of the Pyramidal Tract on Magnetic Resonance Imaging in Primary Lateral Sclerosis
Neurol 40:1799-1800, Marti-Fabregas,J.&Pujol,J., 1990

X-Linked Spinal Muscular Atrophy (Kennedy's Syndrome) A Kindred with Hypobetalipoproteinemia
Arch Neurol 47:1117-1120, Warner,C.L.,et al, 1990

Anti-GM1 IgM Antibodies in Motor Neuron Disease and Neuropathy
Neurol 40:1747-1750, Nobile-Orazio,E.,et al, 1990

Serial Magnetic Resonance Imaging in Neonatal Hypoxic-Ischemic Encephalopathy
J Pediatr 117:694-700, Byrne,P.,et al, 1990

Physical Features of Prader-Willi Syndrome in Neonates
Am J Dis Child 144:1251-1254, Aughton,D.J.&Cassidy,S.B., 1990

Improved Molecular-Genetic Diagnosis of Leber's Hereditary Optic Neuropathy
NEJM 323:1488-1489, Johns,D.R., 1990

Graves Orbitopathy:Correlation of CT and Clinical Findings
Radiology 177:675-682, Nugent,R.A.,et al, 1990

Internuclear Ophthalmoplegia in the Chiari Type II Malformation
Neurol 40:1850-1854, Arnold,A.C.,et al, 1990

Magnetic Resonance Imaging of the Brain in Infants and Children Before and After Cardiac Surgery
Am J Dis Child 144:374-378, McConnell,J.R.,et al, 1990

The Spectrum of Neurologic Disease Associated with Anti-GM1 Antibodies
Neurol 40:1067-1072, Sadiq,S.A.,et al, 1990

Progressive Rubella Panencephalitis
In Handbk of Clin Neurol, Vinken & Bruyn, Ed, N Holland Publ Co, 56:405-416, Wolinsky,J.S., 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

Genetic Linkage of Hereditary Motor & SensoryNeuro Type I (Charcot-Marie-Tooth Disease) to Chrom 1 & 17
Neurol 40:1450-1453, Defesche,J.C.,et al, 1990

A Survey of Epileptic Disorders in Southwest France:Seizures in Elderly Patients
Ann Neurol 27:232-237, Loiseau,J.,et al, 1990

Encephalitis Caused by HIV:CT & MR Imaging Manifestations with Clinical and Path Correlation
Radiology 175:185-191, Chrysikopoulos,H.S.,et al, 1990

Abnormal Respiration and Sudden Death During Sleep in Multiple System Atrophy with Autonomic Failure
Neurol 40:677-679, Munschauer,F.E.,et al, 1990

Idiopathic Cerebellar Ataxia of Late Onset:Natural History and MRI Morphology
JNNP 53:297-305, Klockgether,T.,et al, 1990

Symptomatic Cerebrospinal Fluid Dissemination of Cerebral Glioblastoma
Neuroradiology 32:146-150, Onda,K.,et al, 1990

Clinical Study of 227 Patients with Lacunar Infarcts
Stroke 21:842-847, Arboix,A.,et al, 1990

Thalamic Hemorrhage with Intraventricular Hemorrhage in the Full-Term Newborn
Pediatrics 85:737-742, Rowland,E.H.,et al, 1990

Neuropsychological Changes in Olivopontocerebellar Atrophy
Arch Neurol 47:997-1001, Berent,S.,et al, 1990

A Clinical Triad to Diagnose Paraneoplastic Retinopathy
Ann Neurol 28:162-167, Jacobson,D.M.,et al, 1990

Selective Expression of Purkinje-Cell Antigens in Tumor From Pts, with Paraneoplastic Cerbellar Degeneration
NEJM 322:1844-1851, Furneaux,H.M.,et al, 1990

Autoantibody Synthesis in the Central Nervous System of Patients with Paraneoplastic Syndromes
Neurol 40:1085-1091, Furneaux,H.F.,et al, 1990

MR Imaging of Pineal Tumors
AJR 155:143-151, Tien,R.D.,et al, 1990

Congenital Brain Tumors:A Review of 45 Cases
AJR 155:587-593, Buetow,P.C.,et al, 1990

Colloid Cysts of the Third Ventricle:MR Findings
J Comput Assist Tomogr 14:527-531, Wilms,G.,et al, 1990

The Pretectal Syndrome:206 Patients
Neurol 40:684-690, Keane,J.R., 1990

Periventricular-Intraventricular Hemorrhage Sonographic Localization in Low Birth Weight Infants
Pediatrics 85:1027-1032, Krishamoorthy,K.,et al, 1990

Cerebral Cortex and Brainstem Involvement in Marinesco-Sjogren Syndrome
Ann Neurol 27:448-449, Katafuchi,Y.,et al, 1990

A Quantitative Evaluation of Pontine Volume by Computed Tomography in Patients with Cerebral Degeneration
Neurol 40:1241-1245, Chida,K.,et al, 1990

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

Syringomyelia and Arachnoiditis
JNNP 53:106-113, Caplan,L.R.,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

Acute Intermittent Porphyria
JAMA 264:1290-1293, 1315-13161990., Sack,G.H., 1990

Showing articles 1650 to 1700 of 2530 << Previous Next >>