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Differential
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abdominal muscle paralysis

abductor pollicis brevis

abscess, vertebral

acid maltase deficiency

acid maltase deficiency, adult

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome, congenital

acquired immunodeficiency syndrome, infants and children

Addison's disease

advances in neurology

alcohol intoxication

alcohol, neurologic complications with

alcoholic polyneuropathy

alien hand syndrome

alternating rapid movement

alveolar hypoventilation

amyloid plaques

amyotrophic chorea-acanthocytosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, complications with

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, misdiagnosis

amyotrophic lateral sclerosis, Parkinson-dementia-complex

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

amyotrophic lateral sclerosis-like syndrome

anemia, megaloblastic

anesthesia, general

aneurysm, intracranial

Angelman syndrome

angiography, neurologic complications with

ankle reflex, absent

anterior horn cell disease

anterior interosseous neuropathy

anterior tibial muscle weakness

anti citrullinated antibody

anti mGluR1 encephalitis

anti Tr antibodies

anti Yo antibody

anticoagulant, complications of

anticoagulant, treatment

anticonvulsants, untoward effects of

antithyroid antibodies

antiviral agents

aphasia, progressive, primary

apraxia of eye movements

apraxia, constructional

arm swing, reduced

arrhythmia, cardiac

arterial dissection

arterial dissection, carotid

arthrogryposis multiplex

arylsulfatase A

arylsulfatase B

ascending paralysis

ataxia telangiectasia

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

ataxia, sensory

ataxia, truncal

atlanto axial dislocation, congenital

atrioventricular block

atrophy, muscle

attention deficit disorder with hyperactivity

autoimmune cerebellar ataxia

autoimmune disease

autonomic dysfunction

autoregulation, cerebral

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

B 12 deficiency

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basement membrane

basement membrane thickening

basophilic stippling of red blood cells

behavior, combative

behavioral disorder

Bence Jones protein

benign essential tremor

biologic markers

bitemporal visual field defect

blind spot, enlarged

blinking, reduced

bone marrow suppression

bone marrow transplantation

border zone infarct

botulinum toxin

botulinum toxin, complications of

brachial neuritis

brachial plexus

brachial plexus injury

brachial plexus neuropathy

brachial plexus neuropathy, familial

brachial plexus neuropathy, recurrent

brachial plexus, lesion of

brainstem, atrophy

brainstem, lesion of

brainstem, neoplasms of

bruit, supraclavicular

bulbar palsy, progressive

burning paresthesia

calcification, intracranial

calf hypertrophy

campylobacter infection

carcinoma of lung

carcinoma of ovary

cardiac catheterization, neurologic complications

cardiovascular disease

carotid artery atherosclerosis

carotid artery disease

carotid artery stenosis

carpal tunnel syndrome

carpo-pedal spasm

Castleman's disease

CAT scan, abdomen

CAT scan, abnormal

CAT scan, contrast enhanced

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, pelvis

cavernous sinus, syndrome

central core disease

central nervous system, infection of

cerebellar ataxia, autosomal recessive

cerebellar ataxia, hereditary

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar disease, eye movement disorder in

cerebellar hypoplasia

cerebellar lesion

cerebellar vermis

cerebellum, disease of

cerebral cortical atrophy

cerebral embolism

cerebral embolism, artery to artery

cerebral embolism, cardiac origin

cerebral infarction

cerebral infarction, small, deep

cerebral ischemia

cerebral peduncle

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, enzymes in

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrovascular accident

cerebrovascular accident, complications with

cerebrovascular accident, incidence of

cerebrovascular accident, location of

cerebrovascular accident, mimics

cervical collar

cervical myelopathy

Charcot-Marie-Tooth

cheiralgia paresthetica

chelation therapy

chemotherapy, CNS treatment and complications with

cherry red spot

cherry red spot-myoclonus syndrome

chest x-ray, abnormal

chewing, impaired

cholesterol, HDL

choreoathetosis

choroid plexus, abnormality of

chromosomal abnormality

chronic progressive external ophthalmoplegia

claudication, extremity

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

Cockayne's syndrome

cogwheel rigidty

cold hands sign

cold temperature

collagen vascular disease

compartment syndrome

compartment syndrome, medial brachial fascial

compression neuropathy

conduction block

confusional state, acute

congenital infection, CNS

congenital myopathy

congestive heart failure

contractures, joint

conversion reaction

cornea, opacity of

corneal reflex, abnormal

corneal reflex, absent

corpus callosotomy

corpus callosum

corpus callosum, atrophy of

corpus callosum, infarction of

corpus callosum, lesion of

corpus callosum, neoplasm of

corpus callosum, thinning

cortical hand knob

cortical hand knob infarct

cortical infarction

cortical infarction, small

cortical muscular atrophy

cortical topography

cortical wrist drop

cortical-basal ganglionic degeneration

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

craniopharyngioma

creatine phosphokinase(CPK)elevated

crying, pathologic

cryptococcal meningitis

cryptococcoma, cerebral

cultured skin fibroblasts

Cushing's syndrome

cyclophosphamide

cyst, perineural

cytomegalovirus infection

cytomegalovirus infection, congenital

degenerative diseases of CNS

delay in diagnosis

delayed dentition

dementia, childhood

dementia, familial

denervation of muscle

denervation potentials

dentate nuclei, lesion of

dermatomyositis

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diabetic mononeuropathy

diagnostic criteria

diaphragmatic paralysis

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

diplegia, brachial

disability, neurological

disc space infection

disc space narrowing

disconnection syndrome

dislocated hip, congenital

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

dopa responsive dystonia

down-beat nystagmus

down-beat nystagmus, primary position of gaze

drug induced neurologic disorders

dysdiadochokinesia

dysferlinopathy

dyskinesia, buccal lingual facial

dystonia, children

dystonia, focal

dystonia, post traumatic

dystonia, treatment of

dystrophic calcification

eating disorder

electrical sensation

electrical stimulation, spinal nerves

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electromyogram, decremental response

electron microscopy

electrophoretic pattern, CSF

Emery-Dreifuss muscular dystrophy

emotional lability

empyema, epidural-spinal

encephalitis, autoimmune

encephalitis, episodic

encephalitis, human immunodeficiency virus type 1

encephalopathy, progressive

enterovirus infection of CNS

entrapment neuropathy

enzyme, muscle disease

epidemiology of neurology

episodic neurologic deficits

erectile dysfunction

evoked potentials

exercise intolerance

exercise-induced vascular symptoms

exome sequencing

extremity, cold

eye movement, disorders of

face, numbness of

facial appearance, abnormal

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

failure to thrive

fatigable chewing

feeding disorder

fetal movements, reduced

fine motor function, impaired

finger flexor weakness

finger nose finger test

finger swelling

finger weakness

fingernails, abnormal

fingerprint bodies

foot drop, bilateral

fornix, lesion of

fracture, long bone

fracture, long bones, nerve injury with

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

Friedreich's ataxia

Friedreich's ataxia, late onset

frontal behavioral spatial syndrome

frontal lobe, behavior with disease of

frontal lobe, infarction

frontal lobe, lesion of

fungal infection, CNS

gammaglobulin therapy, intravenous

Gantzer's muscle

gastrocnemius muscle weakness

gastroenteritis

gastrointestinal perforation

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic diagnosis, prenatal

genetic neurologic disorders

genetic testing

genital hypoplasia

Gerstmann-Straussler-Scheinker disease

giant cell arteritis

girdle sensation

globus pallidus

globus pallidus, lesion of

glycogen debranching enzyme deficiency

glycogen storage disease

GM1 ganglioside antibodies

Gowers maneuver

granular osmiphilic material

granulomatous disease

growth hormone deficiency

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, prognosis of

Hallervorden Spatz disease

hallucination, auditory

handcuff neuropathy

handlebar palsy

Hand-Schuller-Christian disease

heart block, complete

heavy metal intoxication

heel-knee-shin test

hemidiaphragm, paralysis of

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatosplenomegaly

heralding manifestation

hereditary myopathy with early respiratory failure

herniated disc, thoracic

high arched feet

high arched palate

histamine-2 receptor blockers

histochemistry of muscle

Horner's syndrome

human immunodeficiency virus type 1

hyperadrenalism

hyperamylasemia

hyperhidrosis, palmar

hyperhomocysteinemia

hyperinsulinism

hyperparathyroidism

hyperpigmentation of skin

hypersegmented polys

hyperthyroidism

hypogonadism, hypogonadotropic

hypokalemic periodic paralysis

hypomyelination

hypoparathyroidism

hypopigmentation of skin

hypotension, systemic

hypothalamus, disturbance of

hypothalamus, lesion of

hypotonia, infants

iatrogenic neurologic disorders

ideomotor apraxia

imbalance, postural

immunologic disease

immunosuppressive agents

inability to sit up

inability to stand on tiptoes

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

inclusion body myositis

infant, evaluation of

infantile tremor syndrome

injection neuropathy

intellectual deficit

intellectual deterioration

intelligence quotient

interosseous muscles

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

intrinsic hand muscles

intrinsic hand muscles, wasting of

islet cell tumor

Jakob-Creutzfeldt disease

jaw jerk, abnormal

juvenile distal and segmental muscular atrophy

Klinefelter's syndrome

Krabbe's disease

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

lactic acidemia

lactic dehydrogenase(LDH)

laminectomy, lumbar

lateral cutaneous nerve of forearm

laughing, pathologic

learning disability

learning disability, in children

leg weakness, bilateral

leg weakness, unilateral

Leigh's disease

lenticular nucleus, lesion of

lenticular nucleus, lesion of, bilateral

leukoencephalopathy

leukoencephalopathy, differential diagnosis

level of consciousness, decreased

Lhermitte's sign

lid closure, weakness of

life expectancy

life support, withdrawal of

lipid storage disorder of CNS

liver function enzymes

lumbrical muscles

lymph node biopsy

lymphadenopathy

lymphadenopathy, hilar

lymphoma involving CNS

lysosomal storage disease

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

malignant hyperpyrexia

Man-In-The-Barrel syndrome

marche a petits pas

Martin-Gruber anastamosis

mastoid opacification

mechlorethamine

median nerve, lesion of

median neuropathy

medical-legal aspects of neurology

medulla oblongata, neoplasm of

memory, defect of recent

memory, impairment of

meningeal enhancement

meningitis, aseptic

meningitis, bacterial

meningitis, carcinomatous

meningitis, children

meningitis, factors influencing mortality in

meningitis, late neurologic sequelae in

meningitis, lymphomatous

meningitis, neurologic aspects and complications of

mental retardation

mental status, abnormal

metachromatic leukodystrophy

metachromatic leukodystrophy, juvenile

methylmalonic acid, serum

methylmalonic acidemia

microangiopathy, brain

microglial nodules

midbrain, atrophy

midbrain, lesion of

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

middle cerebral artery territory infarction

middle cerebral artery, emboli to

middle cerebral artery, occlusion of

mitochondrial disease

mitral valve prolapse

molecular genetics

monoclonal gammopathy

monoclonal gammopathy of uncertain significance

monomelic amyotrophy

mononeuritis multiplex

mononeuropathy, motor

monoparesis, focal

motor dysfunction

motor neuron disease

motor neuron disease, juvenile form

motor neuron disease, spontaneous recovery

movement disorder

movement disorder, extrapyramidal

MRI, brachial plexus

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, false negative

MRI, high signal foci on

MRI, mass effect on

MRI, peripheral nerve

MRI, skull bone changes

MRI, spinal cord

MRI, T1 weighted fat suppression

mucopolysaccharidoses

multifocal acquired demyelinating sensory motor neuropathy

multiple myeloma

multiple sclerosis

multiple system atrophy

muscle atrophy, focal

muscle atrophy, progressive

muscle atrophy, static

muscle spasm, paraspinal

muscle stiffness

muscle strength, testing

muscle tenderness

muscle wasting, diffuse

muscle weakness

muscle weakness, causes of

muscle weakness, insidious onset of

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, Becker, carrier

muscular dystrophy, cardiovascular changes with

muscular dystrophy, central nervous system abnormality

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, congenital, Fukuyama type

muscular dystrophy, differential diagnosis of

muscular dystrophy, distal, Miyoshi

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenia gravis, distal weakness

myasthenia gravis, limb-girdle

myeloneuropathy

myelopathy, chronic progressive

myocardial biopsy

myocardial infarction

myoclonic jerks

myoclonus, epilepsy

myopathy, amyloid

myopathy, autoimmune

myopathy, centronuclear

myopathy, desmin

myopathy, distal

myopathy, distal, vacuolar

myopathy, distal, Welander's

myopathy, hereditary

myopathy, inclusion body

myopathy, inclusion body, hereditary

myopathy, mitochondrial

myopathy, myofibrillar

myopathy, proximal

myopathy, quadriceps

myopathy, steroid induced

myopathy, vacuolar

myotonia dystrophica

myxedema, neurologic manifestations of

nausea and vomiting

nemaline rod myopathy

nemaline rod myopathy, adult onset

neoplasm, pituitary

neoplasm, primary of CNS

neoplasm, primary of CNS-children

nerve conduction studies

nerve conduction studies, motor

nerve conduction studies, sensory

nerve hypertrophy

nerve repair, end to end

neuritis, heavy metals causing

neuroendocrinology

neurofibrillary degeneration

neurofibromatosis 1

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic disease, tempo

neurologic evaluation

neurologic examination, focal

neurologic signs

neurologic symptoms

neurolymphomatosis

neuromuscular disease, electrodiagnosis of

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuronopathy, sensory and motor

neuroophthalmology

neuropathology, brain

neuropathy, bicycle

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, iatrogenic

neuropathy, medication induced

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, multifocal

neuropathy, painful

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, sensory

neuropathy, toxic

neuroprotective agents

next-generation sequencing

Niemann-Pick disease

nitrogen mustard

numbness, ascending

numbness, extremity

numbness, generalized

nystagmus, rotary

occupational neurologic disorders

occupational neuropathies

ocular motility, disorders of

old age, neurology of

ophthalmoplegia

ophthalmoplegia, painful

ophthalmoplegia, progressive external

ophthalmoplegia, total

opportunistic infection

opportunistic infection, CNS

optic neuritis, bilateral

optic neuropathy

optic neuropathy, bilateral

orthostatic hypotension

osteomyelitis, spinal

ovarian dysgenesis

pacemaker, cardiac-transvenous

pain, abdominal

pain, interscapular

palliative care

paracentral lobule

paralysis, asymmetric

paraparesis, spastic

paraspinal muscle

paraspinal muscle weakness

parathyroid adenoma

paresthesias, feet

paresthesias, hands

parietal lobe, lesion of

Parkinson disease

Parkinson disease, axial symptoms

Parkinson disease, L-dopa nonresponsive

Parkinson disease, tremor, absence of

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

PAS positive material in the brain

penguin silhouette sign

percussion induced muscle contraction

pericardial effusion

periodic paralysis

periodic paralysis, thyrotoxic

peripheral blood smear

peripheral blood smear, abnormal

periventricular leukomalacia

pernicious anemia

Perrault syndrome

personality change

pheochromocytoma

photosensitivity, skin

physical therapy

pigmentary retinopathy

pituitary stalk

pituitary, lesion of

pleocytosis of cerebrospinal fluid

pleural effusion

pneumoencephalogram(PEG)

polyclonal gammopathy

polymerase chain reaction

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, chronic inflammatory demyelinating, variant form

polyneuropathy, chronic inflammatory demyelinating-pure motor syn

polyneuropathy, chronic inflammatory demyelinating-sens atax var

polyneuropathy, chronic inflammatory demyelinating-variant forms

polyneuropathy, familial

pons, lesion of

position sensation, abnormal

positional head-hanging test

positive sharp waves

posterior column disease

posterior fossa

posterior fossa, lesion of

posterior interosseous neuropathy

postoperative neurologic complications

postural abnormality

Prader-Labhart-Willi syndrome

precentral gyrus

pregnancy, neurologic complications in

premature infant

prenatal diagnosis by amniocentesis

primary aldosteronism

prisoners of war, neurologic complications in

progressive multifocal leucoencephalopathy

progressive myoclonic epilepsy

progressive neurologic disorder

progressive spinal muscular atrophy

progressive supranuclear palsy

prolactin, elevated

pronator syndrome

proprioception, abnormal

proximal muscle atrophy

pseudobulbar palsy

pseudohypertrophy

pseudomedian nerve palsy

pseudoperipheral palsy

pseudoradial nerve palsy

pseudoulnar palsy

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychological testing, neurologic problems

psychomotor retardation

ptosis, unilateral

puberty, delayed

pure motor stroke

purple glove syndrome

pursuit eye movements, abnormal

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriceps atrophy

quadriceps weakness

quality of life

radial nerve, palsy of

radial pulse, unilateral decrease of

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

Raynaud's phenomenon

reading disorder, acquired

recruitment, reduced

reflex sympathetic dystrophy

reflex sympathetic dystrophy, children

release phenomena

remote effect of cancer on the nervous system

repetitive nerve stimulation

respiratory failure

respiratory tract infection

retinal degeneration

retinitis pigmentosa

retrobulbar neuritis

Rett's syndrome

reverse split hand sign

reversible neurologic disorder

rheumatoid arthritis

rheumatoid arthritis, neurologic complications of

rigid spine syndrome

rigidity, axial

rippling muscle disease

Rolandic artery

root lesion, nerve

rubella encephalitis

rubella encephalitis, progressive

saccadic eye movements, abnormal

salivation, excessive

sarcoidosis, CNS

scalenus anticus syndrome

scleroderma, neurologic involvement with

scoliosis, neurologic association with

sea-blue histiocytes

sedimentation rate

sedimentation rate, elevated

seizure, children

seizure, neonatal

sensorimotor stroke

sensorineural hearing loss

sensory loss, cortical

sensory loss, glove-stocking

sensory loss, patchy

sensory loss, pseudoradicular

sensory loss, truncal

sensory symptoms

sensory testing, quantitative

sequencing difficulty

serologic testing

serologic testing of cerebrospinal fluid

shoulder, numbness

shoulder, pain in

shoulder, swelling of

shoulder-hand syndrome

single photon emission computed tomography

sinuses, diseases of

skin, discoloration

skin, lesions in neurologic disorders

skin, temperature difference

skull bone, erosion

sleep pathology and physiology

slit lamp examination

small vessel disease

speech disorder

speech disorder, childhood

speech disorder, non aphasic

speech, delayed development of

speech, loss of

spinal cord, cervical

spinal cord, compression of

spinal cord, compression, epidural abscess causing

spinal cord, ischemic lesion of

spinal cord, lesion of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinocerebellar ataxia

spinocerebellar ataxia type 12

spinocerebellar ataxia type 3/Machado Joseph disease

splenium of corpus callosum

spontaneous muscle activity

sports medicine, neurology of

standing difficulty

status epilepticus

stem cell transplantation

stereotyped behavior

steroid therapy, CNS treatment and complications with

stooped posture

storage disease of CNS

striatonigral degeneration

striatonigral degeneration, infantile

strokelike episodes

subacute myelo-opticoneuropathy(S.M.O.N.)complex

subarachnoid hemorrhage

subclavian artery stenosis

substantia nigra

swallow evaluation

sweating, abnormality of

symmetric brain lesions

sympathetic block

syphilis, neurologic complications with

syphilis, ocular

systemic illness

tandem gait, ataxic

Tangier's disease

teeth, abnormal

teeth, number of in infants

temper tantrums

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

thalamus, lesion of

thalamus, lesion of-bilateral

thallium poisoning

thoracic outlet syndromes

thrombocytopenia

Tolosa Hunt syndrome

tongue, enlarged

tongue, fasciculations of

tongue, protrusion of

tongue, swelling

tongue, weakness

tonic foot response

torticollis, post traumatic

toxoplasmosis, CNS

transient neurologic deficit

treatment of neurologic disorder

tremor, cerebellar

tremor, intention

tremor, post traumatic

tremor, postural

tremor, resting

tremor, treatment of

tremor, writing

trigeminal nerve, abnormality of

trinucleotide repeats

Trousseau's sign

tuberculoma of CNS

tyrosine hydroxylase deficiency

ulcers, fingertip

ulnar nerve, compression of

ulnar nerve, deep palmar branch of

ulnar neuropathy

ultrasonography

upgaze, paralysis of

urine test in toxic screen

vascular endothelial growth factor

ventricular enlargement

vertebral erosion

vertigo, positional

vibratory sensation, abnormal

violent behavior

viral infection

viral infection, CNS

Virchow-Robin spaces, dilated

vision, blurred

visual acuity, decreased

visual evoked response

visual field defect

visual fields, constricted

visual symptoms

visuospatial disturbance

vitamin deficiency

vitamin E deficiency

voice, abnormality of

Volkmann's ischemia

walking, delayed

walking, difficulty with

weakness, congenital

weakness, fatiguable

weakness, generalized

weakness, progressive

weakness, proximal

Werdnig-Hoffman disease

white matter disease

wide based gait

winging of scapula

word-finding difficulty

X-linked bulbospinal neuronopathy

Showing articles 50 to 100 of 2830 << Previous Next >>

Peripheral Neuropathy - Lead Astray?
LANCET 381:1156, Pickrell, W.,et al, 2013

The Autosomal Recessive Cerebellar Ataxias
NEJM 366:636-646, Anheim,M.,et al, 2012

Clinicalpathologic Conference, Vitamin B12 Deficiency due to Pernicious Anemia
NEJM 366:1626-1633, Case 13-2012, 2012

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

Rapidly Progressive Corticobasal Degeneration Syndrome
Case Rep Neurol 3:185-190, Herrero Valverde, A.,et al, 2011

An Unusual Cause of Pseudomedian Nerve Palsy
Case Reports Neurol Med doi:10.1155/2011/474271, Manjaly, Z.M.,et al, 2011

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

Isolated Ischaemic Lesions in the Foot Motor Area Mimic Peripheral Lower-Limb Palsy
JNNP 81:822-823, Alonso,A., et al, 2010

Clinicopath Conf, Rapid-Onset-Dystonia-Parkinsonism Due to a Mutation in the ATP1A3 Gene
NEJM 362:2213-2219, Case 17-2010, 2010

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

A 75-Year-Old Woman with Progressive Right-Hand Tremor and Inability to Use Her Right Side
Neurol 73:1399-1405, Kertesz,A.,et al, 2009

Diagnosis and New Treatments in Muscular Dystrophies
JNNP 80:706-714, Manzur,A.Y. &Muntoni,F., 2009

Ischemic Stroke of the Cortical "Hand Knob" Area: Stroke Mechanisms and Prognosis
J Neurol 256:1146-1151, Peters, N.,et al, 2009

Diagnosis and Management of Motor Neurone Disease
BMJ 336:658-662, McDermott,C.J. &Shaw,P.J., 2008

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

Multifocal Motor Neuropathy: The Diagnostic Spectrum and Response to Treatment
Neurol 69:1680-1687, Slee,M.,et al, 2007

Clinicopath Conf., Multifocal Motor Neuropathy With Conduction Block
NEJM 357: 2707-2715, Case 40-2007, 2007

Clinicopath Conf., Severe Microangiopathy of Diabetic Vasculopathy with Multiple Cerebral Infarcts
NEJM 357:164-173, Case Study 21-2007, 2007

Compression of the Deep Motor Branch of the Ulnar Nerve
Arch Neurol 62:826-827, Jacob,A.,et al, 2005

Acute Painful Neuropathy in Thallium Poisoning
Neurol 65:302-304, Kuo,H.-C.,et al, 2005

Hereditary Motor and Sensory Neuropathies
Peripheral Neuropathy, Dyck,P.J. & Thomas,P.K. (Ed). Elsevier Publ, Vol 2, Ch 69: 1623-1635, Shy,M.E., et al, 2005

A Paralysed Thumb
Lancet 363:1364, Sudo,K.,et al, 2004

Amyloid Myopathy Presenting with Distal Atrophic Weakness
Muscle Nerve 29:605-609, Smestad, C.,et al, 2004

MR Imaging Presentation of Intracranial Disease Associated with Langerhans Cell Histiocytosis
AJNR 25:880-891, Prayer, D.,et al, 2004

The Medial Brachial Fascial Compartment Syndrome Following Axillary Arteriography
Neurol 61:1037-1041, Tsao,B.E. &Wilbourn,A.J., 2003

CMT with Pyramidal Features
Neurol 60:696-699, Vucic,S.,et al, 2003

Multiple Sclerosis Presenting as Lower Motor Neuron Wasting and Weakness of the Distal Upper Extremity
Neurol 61:1303-1304, Chong,P.S.T.,et al, 2003

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

Isolated Hand Palsy Due to Cortical Infarction: Localization of the Motor Hand Area
Neurol 58:1412-1414, Takahashi,N.,et al, 2002

Clinicopath Conf, Neuronal Ceroid Lipofuscinosis, Late-Onset Infantile Subtype
NEJM 347:672-680, Case 27-2002, 2002

A Diffusion-Weighted MRI Study of Acute Ischemic Distal Arm Paresis
Neurol 57:1589-1594, Gass,A.,et al, 2001

Botulinum Toxin Type A in Primary Palmar Hyperhidrosis
Neurol 57:2095-2099, Saadia,D.,et al, 2001

Predominant Involvement of a Particular Group of Fingers Due to Small, Cortical Infarction
Neurol 56:1677-1682, Kim,J.S., 2001

Inclusiong Body Myositis Mimicking Motor Neuron Disease
Arch Neurol 58:1253-1256, Dabby,R.,et al, 2001

Clinical and Genetic Aspects of Distal Myopathies
Muscle Nerve 24:1440-1450, Saperstein,D.S.,et al, 2001

SCA-12: Tremor with Cerebellar and Cortical Atrophy is Associated with a CAG Repeat Expansion
Neruol 56:299-303,287, O'Hearn,E.,et al, 2001

Alcohol Related Neuropathy
Diagnosis and Management of Peripheral Nerve Disorders :332, Mendell,J.R.,et al, 2001

Ataxia Associated with Hashimotos Disease: Progressive Non-Familial Adult Onset Cerebellar Degeneration with Autoimmune Thyroiditis
JNNP 71:81-87, Selim, M. and Drachman, D.A., 2001

Pseudoulnar Palsy From a Small Infarct of the Precentral Knob
Neurol 54:2185, Phan,T.G.,et al, 2000

The Split Hand in ALS has a Cortical Basis
J Neurol Sci 180:66-70, Weber,M.,et al, 2000

Neurologic Manifestations of Compressive Radiculopathy of the First Thoracic Root
Neurol 53:1149-1151, Levin,K.H., 1999

Distal Myasthenic Gravis
Neurol 52:632-634, Nations,S.P.,et al, 1999

Cervical Root Stimulation in a Case of Classic Neurogenic Thoracic Outlet Syndrome
Muscle & Nerve 22:1287-1292, Felice,K.J.,et al, 1999

Isolated Weakness of the Fingers in Cortical Infarction
Neurol 50:823-824, Lee,P.,et al, 1998

Distal Hereditary Upper Limb Muscular Atrophy
JNNP 64:217-220, Gross,D.W.,et al, 1998

Clinical Presentation and Pharmacological Therapy in Corticobasal Degeneration
Arch Neurol 55:957-961, Kompoliti,K.,et al, 1998

Prader-Willi and Angelman Syndromes
Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998

Myasthenic Hand
Neurol 51:913-914, Janssen,J.C.,et al, 1998

The Wide Spectrum of Myofibrillar Myopathy Suggests a Multifactorial Etiology and Pathogenesis
Neurol 51:1646-1655, Amato,A.A.,et al, 1998

CIDP:Clinical Features & Responses to Trtm in 67 Consecutive Pts with/without a Monoclonal Gammopathy
Neurol 48:321-328, Gorson,K.G.,et al, 1997

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