Neudle.com: myopathy focal

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

Showing articles 1350 to 1400 of 2801 << Previous Next >>

Adult-Onset MELAS
Stroke 27:1420-1423, Gilchrist,J.M.,et al, 1996

Acute Type II Myofiber Atrophy in Critical Illness
Neurol 46:819-821, 6001996., Gutman,L.,et al, 1996

Muscle is Electrically Inexcitable in Acute Quadriplegic Myopathy
Neurol 46:731-736, 6001996., Rich,M.M.,et al, 1996

Diagnosis of McArdle's Disease by Molecular Genetic Analysis of Blood
Neurol 47:579-580, El-Schahawi,M.,et al, 1996

Blepharospasm:Report of a Workshop
Neurol 46:1213-1218, Hallett,M.&Daroff,R.B., 1996

Yelling Attacks and Wasted Hands
Lancet 348:238, Bosboom,W.M.J.,et al, 1996

Acute Focal Neuropathy in Male Weight Lifters
Muscle & Nerve 19:897-899996., Bird,S.J.&Brown,M.J., 1996

Critical Illness Myopathy and Neuropathy
Lancet 347:1579-1582, Latronico,N.,et al, 1996

Clinicopath Conf
Tangier Disease, Case 16-1996, NEJM 334:1389-1394996., , 1996

Motor Neuropathy Due to Docetaxel and Paclitaxel
Neurol 47:115-118, Freilich,R.J.,et al, 1996

Hereditary Spastic Paraplegia:Advances in Genetic Research
Neurol 46:1507-1514, Fink,J.K.,et al, 1996

Subcortical Heterotopia:A Distinct Clinicoradiologic Entity
AJNR 17:1315-1322, Barkovich,A.J., 1996

Temporal Lobectomy for Refractory Epilepsy
JAMA 276:470-475, Sperling,M.R.,et al, 1996

A Prospective, Population-Based Epidemiologic Study of Status Epilepticus in Richmond, Virginia
Neurol 46:1029-1035, DeLorenzo,R.J.,et al, 1996

Simple Partial Status Epilepticus:Causes, Treatment and Outcome in 47 Patients
JNNP 61:90-92, Scholtes,F.B.,et al, 1996

Non-Convulsive Status Epilepticus:Causes, Treatment, and Outcome in 65 Patients
JNNP 61:93-95, Scholtes,F.B.,et al, 1996

Psychogenic Seizures
Neurol 46:1499-1507, Lesser,R.P., 1996

Efficacy of Gabapentin Therapy in Children with Refractory Partial Seizures
J Pediatr 128:829-833, Khurana,D.S.,et al, 1996

The Use of Parenteral Antiepileptic Drugs & The Role of Fosphenytoin
(Suppl Editor) , Neurol 46:S1-S2896., Wilder,B.J., 1996

Familial Temporal Lobe Epilepsy:A Common Disorder Identified in Twins
Ann Neurol 40:227-235, Berkovic,S.F.,et al, 1996

Amnesia in Acute Herpetic and Nonherpetic Encephalitis
Arch Neurol 53:972-978, Hokkanen,L.,et al, 1996

Nonconvulsive Status Epilepticus in Thrombotic Thrombocytopenic Purpura
Neurol 47:1079-1081, Blum,A.S.&Drislane,F.W., 1996

MRI Findings in Subacute Sclerosing Panencephalitis
Neurol 47:1278-1283, Anlar,B.,et al, 1996

Cerebral Syphilitic Gumma in an HIV-Negative Patient Presenting as Prolonged Focal Motor Status Epilepticus
NEJM 335:1159-1160, Suzrez,J.I.,et al, 1996

Hypomanic Symptoms Caused by Herpes Simplex Encephalitis
Neurol 47:1374-1378, Fisher,C.M., 1996

The Role of Lab Investig in the Dx & Management of Pts with Suspected Herpes Simplex Encephalitis:A Consensus Rpt
JNNP 61:339-345, Clinque,P.,et al, 1996

Clozapine-Induced Myotoxicity in Patients with Chronic Psychotic Disorders
Neurol 47:1518-1523, Scelsa,S.N.,et al, 1996

Unusual Clinical Presentations of Cortical-Basal Ganglionic Degeneration
Ann Neurol 40:893-900, Bergeron,C.,et al, 1996

Genetic Factors in Alzheimer's Disease:A Review of Recent Advances
Ann Neurol 40:829-840, Levy-Lahad,E.&Bird,T.D., 1996

Practice Parameter:Genetic Testing Alert
Pract Comm Genet Testing Task Force AAN, Neurol 47:1343-13441996., , 1996

Treatment of Rasmussen's Syndrome with Ganciclovir
Neurol 47:925-928, McLachlan,R.S.,et al, 1996

Acute Myopathy of Intensive Care:Clinical, Electromyographic, and Pathological Aspects
Ann Neurol 40:645-654, Lacomis,D.,et al, 1996

Congenital Muscular Dystrophy with Primary Laminin a2 (Merosin) Deficiency Presenting as Inflammatory Myopathy
Ann Neurol 40:782-791, Pegoraro,E.,et al, 1996

Erroneous Diagnosis Corrected After 28 Years
Arch Neurol 53:1194-1196, Gordon,P.H.,et al, 1996

Confirmation of Linkage of Oculopharyngeal Muscular Dystrophy to Chromosome 14q11. 2-q13
Ann Neurol 40:801-804, Stajich,J.M.,et al, 1996

Atrophy of Bilateral Extraocular Muscles
J Neuro-Ophthalmol 16:286-288, Okamoto,K.,et al, 1996

Presymptomatic Diagnosis of Neurofibromatosis 2 Using Linked Genetic Markers, Neuroimging, and Ocular Examinations
Neurol 47:1269-1277, Baser,M.E., 1996

Status Epilepticus in Children with Epilepsy:The Role of Antiepileptic Drug Levels in Prevention
Pediatrics 98:1119-1121, Maytal,J.,et al, 1996

Acute Phenytoin Toxicity Followed by Seizure Breakthrough From a Ticlopidine-Phenytoin Interaction
Arch Neurol 53:1191-1192, Privitera,M.&Welty,T.E., 1996

Generalized Anxiety Disorder in Stroke Patients
Stroke 27:270-275, Astrom,M., 1996

Management of Patients Receiving Interferon Beta-1b for MS:Report of a Consensus Conf
Neurol 46:12-18, Lublin,F.D.,et al, 1996

Delayed-Onset Progressive Movement Disorders after Static Brain Lesions
Neurol 46:68-74, Scott,B.L.,et al, 1996

Plasmapheresis in Rasmussen's Encephalitis
Neurol 46:242-246, Andrews,P.I.,et al, 1996

Chronic Post-Traumatic Headache Often a Myth
Neurol 46:915-916, Warner,J.S.&Fenichel,G.M., 1996

Sustained Myoglobinuria:The Presenting Manifestation of Dermatomyositis
Neurol 47:119-123, Rose,M.R.,et al, 1996

Multiple Mitochondrial DNA Deletions in Sporadic Inclusion Body Myositis:A Study of 56 Patients
Ann Neurol 39:789-795, Santorelli,F.M.,et al, 1996

Is Chronic Respiratory Failure in Neuromuscular Diseases Worth Treating
JNNP 61:1-3, Shneerson,J.M., 1996

Proton Magnetic Resonance Spectroscopy in Children with Temporal Lobe Epilepsy
Ann Neurol 39:107-113, Cross,J.H.,et al, 1996

Herpes Encephalitis is a Disease of Middle Aged & Elderly People:PCR for Detection of HSV in CSF of 516 Pts with Encephalitis
JNNP 60:174-178, Koskiniemi,M.,et al, 1996

Acute Rectus Muscle Palsy in Children as a Result of Orbital Myositis
J Pediatr 128:230-233, Pollard,F.,et al, 1996

Showing articles 1350 to 1400 of 2801 << Previous Next >>