Neudle.com: focal myopathy

Differential
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abdominal protrusion

acetylcholine receptor antibody

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

addiction, heroin

Addison's disease

Adies pupil

adverse drug reaction

akinesia of eyelid function

algorithm

amaurosis fugax

amphiphysin antibodies

amyloid

amyloidosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, misdiagnosis

anemia

anoctaminopathy

anorexia

anterior horn cell disease

anterior interosseous neuropathy

anterior tibial muscle weakness

anticholinergic drugs

anticoagulant, treatment

anticoagulant, treatment in CVD

aphasia

apraxia of eyelid opening

aqueduct of Sylvius, obstruction

arthrogryposis multiplex

ascending paralysis

aspiration

asthma

asthma, poliomyelitis-like syndrome with

autonomic dysfunction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basophilic stippling of red blood cells

benign essential tremor

bent spine syndrome

bitemporal visual field defect

blepharophimosis

blepharospasm

bone biopsy

bone marrow suppression

brain biopsy, negative

brain biopsy, stereotaxic

calcification, intracranial

cardiovascular disease

CAT scan, disappearing lesion on

CAT scan, false negative

cerebellar ataxia, children

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellum

cerebral cortex

cerebral cortical atrophy

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrovascular accident

cerebrovascular accident, familial occurrence

cerebrovascular accident, mimics

cerebrovascular accident, multiple

cerebrovascular accident, prognosis in

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

chromosomal abnormality

chromosome 17

chronic progressive external ophthalmoplegia

Chvostek sign

cisterna magna

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

cogwheel rigidty

collagen vascular disease

collapsin response mediator protein 5 IgG

coma

complications

compression neuropathy

confusion

congenital myopathy

congestive heart failure

conjunctivitis

constipation

contactin associated protein like 2 antibodies

contractures, joint

conversion reaction

corpus callosum, atrophy of

cortical blindness

coumarin

cranial neuropathy

cranial neuropathy, multiple

craniopharyngioma

creatine phosphokinase(CPK)elevated

Creutzfeldt-Jakob disease, genetic

cryptococcal meningitis

cultured skin fibroblasts

Cushing's syndrome

cyst, cortical parenchyma

cyst, ventricular

cysticercosis

cysticercosis, cerebral

cysticercosis, intraventricular

cysticercosis, subarachnoid

cystinosis

cytomegalovirus infection

delay in diagnosis

dementia

dementia, frontotemporal

dementia, rapidly progressive

depression

dermatitis

dermatomyositis

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diabetic amyotrophy

diaphragmatic paralysis

diarrhea

differential diagnosis

difficulty climbing stairs

diplopia

disability rating scale, neurological

disability, neurological

distal muscle atrophy

distal muscle weakness

doxycycline

dropped head syndrome

dystonia, drug induced

dystonia, face

dystonia, focal

dystonia, post traumatic

dystonia, treatment of

dystrophin

ear, abnormal

edema, pedal

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electromyogram

electromyogram, decremental response

electron microscopy

ELISA

encephalitis

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, focal

encephalitis, human immunodeficiency virus type 1

encephalitis, paraneoplastic

encephalomyelitis

encephalopathy

encephalopathy, progressive

endemic area

enterovirus

entrapment neuropathy

enzyme, defect

enzyme, muscle disease

eosinophilia

epidemiology of neurology

epilepsia partialis continua

episodic neurologic deficits

extrapyramidal movement disorder, progressive

eye movement, disorders of

fetal movements, reduced

fetus

fever

fibrillations

fine motor function, impaired

finger flexor weakness

finger weakness

fingernails, abnormal

fourth ventricle, cyst

gadolinium

gait disorder

gait, waddling

gammaglobulin therapy, intravenous

gastroenteritis

gaze palsy

gaze palsy, supranuclear

genetic neurologic disorders

genetic testing

glabellar sign

glycogen debranching enzyme deficiency

glycogen storage disease

Gowers maneuver

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guyon's canal

gynecomastia

hallucination, auditory

hammertoes

hand deformity

hand weakness

Hand-Schuller-Christian disease

heavy metal intoxication

helminthic infection of CNS

hemianopia

hemianopia, homonymous

heralding manifestation

herpes simplex encephalitis

herpes simplex encephalitis, differential diagnosis of

histochemistry of muscle

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

homosexual

hot bath test

human immunodeficiency virus type 1

human immunodeficiency virus type 1, pathogenesis

hydrocephalus

hydrocephalus, non-communicating(obstructive)

hydrocephalus, transient

hypokalemic periodic paralysis

hypoparathyroidism

hyporeflexia

hypothalamus

hypothalamus, disturbance of

immunology and the nervous system

inability to stand on tiptoes

inattention

inclusion bodies

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intranuclear

inclusion body myositis

incoordination

INR values

intellectual deficit

interstitial pulmonary fibrosis

intracranial hypertension, benign

intracranial pressure, increased

intranasal medication

intrinsic hand muscles, wasting of

islet cell tumor

Jakob-Creutzfeldt disease

jaundice

jaw jerk, abnormal

Kearns-Sayre syndrome

klippel feil syndrome

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

kyphosis

lactate

lactic acidemia

laminar necrosis, cortical

leg weakness, bilateral

leg weakness, unilateral

leptospirosis

lethargy

leucine rich glioma inactivated 1 antibodies

leukocytosis

leukodystrophy

leukopenia

level of consciousness, decreased

lid closure, weakness of

life expectancy

limbic encephalitis

linear lesion

lipid storage disorder of CNS

liver disease

liver function enzymes

low back pain

lymphoma

lymphoma involving CNS

malignancy screen

malignancy, occult

Marinesco-Sjogren syndrome

memory, impairment of

meningeal enhancement

meningitis, cysticercosis

meningitis, eosinophilic

meningitis, leptospira

meningitis, neutrophilic

meningoencephalitis

mental retardation

mental status, abnormal

mitochondrial disease

mitochondrial encephalomyopathy

mixed connective tissue disease

MNGIE syndrome

molecular genetics

monoclonal gammopathy

monomelic myositis

mononeuropathy

mononeuropathy multiplex

movement disorder, drug induced

MRI

MRI, abnormal

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, muscle

MRI, perfusion

MRI, sulcal hyperintensity

MRI, susceptibility weighted

MRS

multiple myeloma

muscle atrophy, focal

muscle atrophy, progressive

muscle biopsy

muscle cramp

muscle diseases, characteristics of

muscle hypertrophy

muscle hypertrophy, congenital

muscle pain

muscle stiffness

muscle swelling

muscle swelling, focal

muscle wasting, diffuse

muscle weakness

muscle weakness, causes of

muscle weakness, proximal

muscle, metabolic disorders of

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, cardiovascular changes with

muscular dystrophy, central nervous system abnormality

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, congenital, Fukuyama type

muscular dystrophy, distal, Miyoshi

muscular dystrophy, Duchenne

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenia gravis, diagnosis

myasthenia gravis, differential diagnosis

myasthenia gravis, distal weakness

myasthenia gravis, limb-girdle

myasthenia gravis, misdiagnosis of

myasthenia gravis, paraneoplastic

myoclonus, stimulus sensitive

myopathy, carcinomatous

myopathy, distal

myopathy, distal, vacuolar

myopathy, distal, Welander's

myopathy, focal

myopathy, inclusion body

myopathy, inclusion body with Paget's disease

myopathy, inclusion body, hereditary

myopathy, inflammatory

myopathy, metabolic

myopathy, mitochondrial

myopathy, monomelic

myopathy, necrotizing

myopathy, quadriceps

myopathy, radiation-induced

myopathy, thyroid disease causing

myopathy, vacuolar

myositis

myositis, bacterial

myositis, eosinophilic

myositis, focal

myositis, fungal

myositis, granulomatous

myxedema, neurologic manifestations of

nerve conduction studies

nerve hypertrophy

neuritis, causes of

neuritis, heavy metals causing

neuroendocrinology

neurofibrillary degeneration

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic examination

neurologic examination, focal

neurologic signs

neurologic symptoms

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuromuscular junction, abnormality of

neuronal cell surface antigen

neuronopathy, sensory

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, motor, multifocal

neuropathy, painful

neuropathy, paraneoplastic

neuropathy, peripheral

neuropathy, short-fiber

ocular myopathy, differential diagnosis

old age, neurology of

onconeural antibodies

ophthalmoplegia

ophthalmoplegia, progressive external

ophthalmoplegia, total

opsoclonus-myoclonus syndrome

paralysis, acute areflexic

paralysis, asymmetric

paraneoplastic cerebellar degeneration

paranoia

paraplegia

paraproteinemia

parasitic infection, CNS

paraspinal muscle

paraspinal muscle weakness

peripheral blood smear

peripheral blood smear, abnormal

peripheral nerve, lesion of

PLEDs, bilateral independent

PLEDs, etiology of

pleocytosis of cerebrospinal fluid

pleural effusion

POEMS syndrome

poliomyelitis

poliomyelitis vaccine

poliomyelitis-like illness

polymerase chain reaction

polymerase chain reaction, false negative

polymyositis

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, familial

polyradiculoneuropathy

polyuria

pons, lesion of

porphyria

position sensation, abnormal

positive sharp waves

posterior interosseous neuropathy

postural abnormality

prevention of neurologic disorders

primary aldosteronism

prion disease

prognosis

progressive multifocal leucoencephalopathy

progressive neurologic disorder

progressive supranuclear palsy

proprioception, abnormal

proteinuria

proximal muscle atrophy

pseudobulbar palsy

pseudohypertrophy

psychiatric problems in neurologic disorders

psychological testing

pupil, abnormality in neurologic disorders

radiation therapy, CNS treatment and complications with

radiculopathy

ragged-red fibers

rapidly progressing neurologic illness

real-time quaking-induced conversion

Red flags

remote effect of cancer on the nervous system

renal failure

repetitive nerve stimulation

respiratory failure

respiratory tract infection

Schwartz-Jampel syndrome

sedimentation rate, elevated

seizure

seizure, focal

sensorineural hearing loss

serologic testing

short stature

shunt procedure, ventricular

sicca syndrome

single-fiber electromyography

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, lesions in neurologic disorders

spinal cord, lesion of

steroid therapy, CNS treatment and complications with

sweating, abnormality of

symmetric brain lesions

syphilis, neurologic complications with

systemic illness

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

tandem gait, ataxic

temporal lobe, lesion

temporal lobe, lesion, bilateral

temporalis muscle wasting

tensilon test, false positive

tetany

thalamus, infarction, bilateral

thalamus, lesion of

thirst

thoracic outlet syndromes

thrombocytopenia

thymoma

thyrotoxicosis

tongue, fasciculations of

tongue, weakness

torticollis

torticollis, post traumatic

toxoplasmosis, CNS

transient ischemic attack

trauma

travel, foreign

treatment of neurologic disorder

urine test in toxic screen

visual evoked response

visual field defect

visual loss

walking, difficulty with

weakness, generalized

weakness, progressive

weakness, proximal

weight loss

Werdnig-Hoffman disease

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Status Epilepticus Associated with Cefepime
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The DYT1 Phenotype and Guidelines for Diagnostic Testing
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Clinicopath Conf., Pick's Disease, Case 11-2000
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Early Diffusion-Weighted MR Imaging Abnormalities in Sustained Seizure Activity
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Clinical Features of Nipah Virus Encephalitis Among Pig Farmers in Malaysia
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Motor Strokes Sparing the Leg
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Managing Status Epilepticus
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Clinicopath Conf, Neurocysticercosis, Left Temporal Lobe, End-Stage with Calicification, Epilepsy
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Life-Threatening Tinnitus
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Levetiracetam for Partial Seizures: Results of A Double-Blind, Randomized Clinical Trial
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Disease Progression in Sporadic Inclusion Body Myositis: Observations in 78 Patients
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C1/C2 Rotary Subluxation Due to Spasmodic Torticollis
JNNP 69:135-136, Dalvie,S. et al, 2000

Neuromuscular Findings in Thyroid Dysfunction: A Prospective Clinical and Electrodiagnostic Study
JNNP 68:750-755, Duyff,R.F. et al, 2000

Intrathecal Baclofen for the Treatment of Dystonia in Patients with Reflex Sympathetic Dystrophy
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Incidence and Prevalence of Neurological Disorders Associated with HIV Since the Introduction of Highly Active Antiretroviral Therapy (HAART)
JNNP 69:376-380, Maschke,M. et al, 2000

Intravenous Valproate is Well Tolerated in Unstable Patients with Status Epilepticus
Neurol 55:722-724, Sinha,S. & Naritoku,D.K., 2000

Treatable Dropped Head Syndrome in Hypothyroidism
Neurol 55:896-897, Askmark,H. et al, 2000

Alien Hand Sign in Creutzfeldt-Jakob Disease
JNNP 68:103-104, Inzelberg,R.,et al, 2000

Microscopic Polyangiitis: Clinical and Laboratory Findings in Eighty-five Patients
Arthritis Rheum 42:421--430, Guillevin, L.,et al, 1999

Oxcarbazepine: Double-blind, Randomized, Placebo-control, Monotherapy Trial for Partial Seizures
Neurol 52:732-737, Schachter,S.C. et al, 1999

Seizures and Creutzfeldt-Jakob Disease
NCMJ 60:108-109, Cokgor,I.,et al, 1999

Creutzfeldt-Jakob Disease Presenting as Complex Partial Status Epilepticus: A Report of Two Cases
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Benign Acute Childhood Myositis, Laboratory and Clinical Features
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Distal Myopathies:Clinical and Molecular Diagnosis and Classification
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Primary and Transitional Progressive MS,A Clinical and MRI Cross-Sectional Study
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Treatment of Absence Status with Intravenous Valproate
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Possible Usefulness of Lamotrigine in the Treatment of SUNCT Syndrome
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Exercise Intolerance Due to Mutations in the Cytochrome b Gene of Mitochondrial DNA
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Weak at the Knees
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Autosomal Dominant Myofibrillar Myopathy with Arrhythmogenic Right Ventricular Cardiomyopathy Linked to Chromosome 10q
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Cervical Root Stimulation in a Case of Classic Neurogenic Thoracic Outlet Syndrome
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Nuclear Medicine in Neurology and Psychiatry
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Dementia as the Most Common Presentation of Cortical-Basal Ganglionic Degeneration
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Intravenous Immunoglobulin in the Treatment of Autoimmune Neuromuscular Diseases:Present Status and Practical Therapeutic Guidelines
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A Longitudinal Study of Brain Atrophy in Relapsing Multiple Sclerosis
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Ptosis, Blepharospasm, and Apraxia of Eyelid Opening Secondary to Putaminal Hemorrhage
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Intravenous Immunoglobulin Treatment in Neurologic Disorders
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Is the Routine Use of Intravenous Immunoglobulin Treatment in Neurologic Disorders Justified?
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Herpes Simplex Encephalitis After Brain Surgery:Case Report and Review of the Literature
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Amyloid Myopathy:An Underdiagnosed Entity
Ann Neurol 43:719-728, Spuler,S.,et al, 1999

Adult-Onset Nemaline Myopathy:Another Cause of Dropped Head
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Pathologic Heterogeneity in Clinically Diagnosed Corticobasal Degeneration
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Age and Cause of Death in Mitochondrial Diseases
Neurol 53:855-857, Klopstock,T.,et al, 1999

Brachial Amyotrophic Diplegia, A Slowly Progressive Motor Neuron Disorder
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Neurologic Manifestations of Compressive Radiculopathy of the First Thoracic Root
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A Case of Sporadic Pick Disease With Onset at 27 Years
Arch Neurol 56:1289-1291, Jacob,J.,et al, 1999

A Sartorial Challenge
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Critical Illness Neuropathy and Myopathy
Arch Neurol 56:527-528, Gutmann,L.&Gutmann,L., 1999

Neuralgic Amyotrophy with Phrenic Nerve Involvement
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Showing articles 1100 to 1150 of 2801 << Previous Next >>