Neudle.com: muscle tone

Differential
(Click to cross reference)

abdominal distention

acetylcholine receptor antibody

acid maltase deficiency

acid maltase deficiency, adult

aciduria

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome, congenital

acquired immunodeficiency syndrome, infants and children

acrocyanosis

acromicria

acute intermittant porphyria

adrenoleukodystrophy

adverse drug reaction

agenesis of corpus callosum

agitation

Aicardi-Goutieres syndrome

airway obstruction

alcohol

alcohol, neurologic complications with

alternating hemiplegia

alternating hemiplegia of childhood

alveolar hypoventilation

amaurosis fugax, unilateral vs.bilateral

aminoacidopathies

aminoacidurias

aminoacylase 1 deficiency

amitriptyline

amniocentesis

amphiphysin antibodies

amyloidosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, differential diagnosis

ANA

anesthesia, general

aneurysm, aortic arch

anterior horn cell disease

apraxia of eye movements

areflexia

aromatic amino acid decarboxylase deficiency

arrhythmia, cardiac

arterial dissection, aorta

arteritis, temporal

arthralgia

arthrogryposis multiplex

arthropathy

ascending paralysis

ascites

aspartate aminotransferase

aspartocyclase

ataxia

ataxia telangiectasia

attention deficit disorder with hyperactivity

atypical

audiogram

auditory and vestibular pathways

autism

autoantibodies

autoimmune disease

autonomic dysfunction

axonal degeneration

B 12 deficiency

B 12 deficiency, infants

Babinski sign

Babinski sign in new born

baclofen

bacterial infection

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

biotin deficiency, acquired

biotin deficiency, juvenile form

biotinidase deficiency

bone density, increased

bone marrow biopsy

bone marrow transplantation

botulinum toxin

botulism

botulism antitoxin

botulism immune globulin

Brown-Vialetto-Van Laere syndrome

brucellosis

brucellosis, nervous system involvement with

bruit

bulbar palsy

bulbar palsy, childhood

burning feet

bursitis

CAG repeats

calcification, intracranial

carcinoembryonic antigen

carcinoma

carcinoma of breast

cardiac surgery, hypothermia and circulatory arrest for

cardiac surgery, neurologic complications with

cardiomyopathy

carnitine deficiency

carnitine deficiency myopathy

CAT scan

CAT scan, abnormal

CAT scan, angiography

CAT scan, chest

CAT scan, emission, abnormal

cataplexy

cataracts

cataracts, congenital

cauda equina, enhancement

caudate nucleus, atrophy

caudate nucleus, lesion of

caudate nucleus, lesion of, bilateral

celiac disease, childhood

central core disease

central hypoventilation, congenital

central nervous system, infection of

cerebellar ataxia, autosomal recessive

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar disease, eye movement disorder in

cerebellar hypoplasia

cerebellar vermis

cerebral cortical atrophy

cerebral embolism

cerebral infarction

cerebral palsy

cerebral palsy, associated problems with

cerebral vasculature

cerebral venous thrombosis

cerebro hepato renal syndrome

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, glycine

cerebrospinal fluid, protein of

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, red cells in

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, infancy and childhood

cerebrovascular accident, intrauterine

cerebrovascular accident, neonatal

cerebrovascular accident, postpartum

ceruloplasmin, serum

cervical spine injury

channelopathy

chelation therapy

cherry red spot

chest x-ray, abnormal

chewing, impaired

chilbran skin lesions

chorea, Sydenham's, recurrent

chorea, treatment of

choreoathetosis

choreoathetosis, paroxysmal

chorioamnionitis

chorioretinitis

chromosomal abnormality

chronic progressive external ophthalmoplegia

cirrhosis

cirrhosis, infancy

Clinical Pathologic Conference(C.P.C.)

clonazepam

clubfoot as related to neurologic disease

cobalamin C deficiency

Coffin-Siris syndrome

collagen vascular disease

concentration, impaired

conduction block

confusion

confusional state, acute

congenital heart disease

congenital heart disease, CNS complications with

congenital infection, CNS

congenital infection, viral

congenital malformation

congenital myopathy

congenital myopathy, inflammatory

congestive heart failure

contactin associated protein like 2 antibodies

contractures, joint

controversies in neurology

conversion reaction

cornea, abnormal

cornea, opacification in infancy-causes of

cornea, opacity of

corpus callosum

corpus callosum, atrophy of

corpus callosum, hypoplastic

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cranial nerve enhancement

cranial neuropathy

cranial neuropathy, multiple

C-reactive protein

C-reactive protein, elevated

creatine phosphokinase(CPK)elevated

cultured skin fibroblasts

cytochrome c oxidase, deficiency

cytomegalic inclusion disease

cytomegalovirus infection

cytomegalovirus infection, congenital

Dandy Walker malformation

dantrolene sodium

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

delayed dentition

delayed muscle relaxation

delivery, complicated

dementia

dementia, childhood

dementia, rapidly progressive

dentate nuclei

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

developmental abnormality of brain

developmental disability

developmental evaluation

developmental milestones

developmental milestones, loss of

developmental retardation

differential diagnosis

digits, abnormal

dilantin

diphtheria-tetanus-pertussis immunization

diplopia

disability, neurological

dislocated hip, congenital

distal muscle atrophy

distal muscle weakness

dropped head syndrome

drug induced neurologic disorders

drug induced neurologic disorders in children

drug overdose

dural arteriovenous malformation

dural sinus thrombosis

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, video monitoring with

electromyogram

electron microscopy

embolism, paradoxical

emergencies, neurologic

encephalopathy, acute

encephalopathy, anoxic

encephalopathy, neonatal

enzyme treatment

enzyme, defect

epidemiology of neurology

epileptic encephalopathy

episodic disorders

evoked potentials

executive dysfunction

eye movement, disorders of

facial anomalies

facial appearance, abnormal

facial expression abnormality

facial nerve palsy, bilateral

facial weakness

facial weakness, bilateral

fasciculation, benign

fatigue

fatty acid, elevated plasma content

feeding disorder

fetal alcohol syndrome

fetal movements, reduced

fine motor function, impaired

fingernails, abnormal

fingernails, hypoplastic

fistula, arterio-venous, dural

fistula, arterio-venous, dural, spinal

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

Friedreich's ataxia

fucosidosis

fundus, abnormality of

gag reflex, depressed

gamma amino butyric acid

gamma loop mechanism

gammaglobulin therapy, intravenous

gangliosidosis GM1

gangliosidosis GM2

gastrocnemius muscle weakness

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

genital hypoplasia

globus pallidus, hemorrhage

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glucosamine

GLUT1

GLUT1 deficiency syndrome

glutamic acid decarboxylase, antibody

gluten-free diet

glycine

glycogen storage disease

glycoprotein

Gowers maneuver

growth hormone deficiency

growth retardation

guanidine

Guillain Barre syndrome

head retraction reflex

hematuria, microscopic

hemiplegia

hemorrhagic diathesis

hepatolenticular degeneration(Wilson's disease)

Hirschprung's disease

histochemistry

histochemistry of muscle

homocystinuria

honey

Horner's syndrome

Horner's syndrome, bilateral

Horner's syndrome, congenital

human genome

Hunter's syndrome

Huntington's chorea

Huntington's disease, children

hydrocephalus

hydrocephalus, communicating

hydrocephalus, congenital

hydrocephalus, exvacuo

hydroxyglutaric aciduria

hyperexcitable peripheral nerve disorder

hyperpyrexia, CNS disorder causing

hypertonia, congential

hypertrichosis

hypertrophic cardiomyopathy

hypocalcemia

hypodontia

hypogammaglobulinemia

hypopigmentation of skin

hypoxic encephalopathy

iatrogenic neurologic disorders

imbalance

immunization, neurologic complications with

immunodeficiency

immunoelectrophoresis, serum

immunomodulation

immunosuppression

immunosuppressive agents

inability to stand on tiptoes

inappropriate antidiuretic(A.D.H.)hormone

inborn errors of metabolism

inclusion bodies

inclusion bodies, intracytopasmic

incoordination

infant, evaluation of

infantile hemiplegia

infantile neuronal degeneration

intellectual deterioration

intelligence quotient

interferon alpha

intestinal biopsy

intrauterine

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

ischemic exercise test

islet cell tumor

Jakob-Creutzfeldt disease

kyphoscoliosis, neurologic causes of

lactic acidemia

lactic dehydrogenase(LDH)

leg numbness

leg spasms

leg spasms, painful

leg weakness, bilateral

leukoencephalopathy, differential diagnosis

leukotrienes

lid

lid abnormalities

lid closure, weakness of

lid lag

lipid storage disorder of CNS

lissencephaly

listeria monocytogenes

liver biopsy

liver disease

liver function enzymes

lordosis

low back pain

low back pain, chronic

lymphoma, primary of CNS

lysosomal storage disease

malformation, CNS, congenital

malignant hyperpyrexia

memory, impairment of

meningismus

meningitis, carcinomatous

meningitis, CSF cell count-normal

mental retardation

mental status, abnormal

merosin

metabolic acidosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

methotrexate

methylene tetrahydrofolate reductase

methylenetetrahydrofolate reductase deficiency

methylmalonic acidemia

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

Middle east

migraine, seizures in

mimics

misdiagnosis

mitochondrial disease

mitral valve prolapse

mobility

mobility aids

molecular genetics

monoclonal antibodies

mood change

mortality

Morvan's fibrillary chorea

motor neuron disease

movement disorder

movement disorder, extrapyramidal

movement disorder, hyperkinetic

movement disorder, psychogenic

MRI

MRI, abnormal

MRI, angiography

MRI, contrast enhanced

MRI, diffusion weighted

MRI, fetal

MRI, high signal foci on

MRI, hypointense signal foci on

MRI, susceptibility weighted

MRS

mucopolysaccharidoses

mucopolysacchariduria

multicore myopathy

multiminicore disease

multiple sclerosis

multiple sclerosis, diet in

multiple sclerosis, treatment of

multiple system atrophy

muscle atrophy, progressive

muscle atrophy, static

muscle biopsy

muscle cramp

muscle diseases, characteristics of

muscle hypertrophy

muscle pain

muscle pain-fasciculation syndrome

muscle phosphorylase deficiency

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscle weakness, sudden onset of

muscle-eye-brain disease

muscular dystrophy

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, LAMA2

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenia gravis, neonatal

myasthenic syndrome

myasthenic syndrome, treatment of

myopathy, centronuclear

myopathy, hypocalcemic

myopathy, mitochondrial

myopathy, necrotizing

myopathy, thyroid disease causing

neonatal infection, viral

neonatal intensive care unit

neonatal screening, genetic neurologic disorders

nerve conduction studies

nerve conduction studies, motor

nerve root enhancement

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neurocutaneous disease

neuroendocrinology

neuroleptic

neuroleptic malignant syndrome

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic evaluation

neurologic examination

neurologic signs

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction, abnormality of

neuromyotonia

neuromyotonia and axonal neuropathy

neuronal ceroid-lipofuscinosis

neuronal migration disorder

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, peripheral

newborn, evaluation of

next-generation sequencing

obstetric neurologic injuries

ocular motility, disorders of

ocular myopathy

oculogyric crisis

odynophagia

old age, neurology of

opened mouth

ophthalmoplegia

ophthalmoplegia, plus syndrome

ophthalmoplegia, progressive external

ophthalmoplegic migraine

optic atrophy

optic atrophy, infants

optic nerve

optic nerve, hypoplasia of

optic neuropathy

optic neuropathy, ischemic

optic neuropathy, ischemic, anterior

osteoarthritis, lumbar spine

osteopetrosis

ovarian insufficiency

paramyotonia congenita

paraparesis

paraparesis, familial spastic

paraparesis, spastic

paraplegia, acute

paraspinal muscle

paraspinal muscle weakness

parenteral alimentation

Parkinson disease, dystonia with

Parkinsonism syndrome

paroxysmal dystonic choreoathetosis

paroxysmal hemiplegia

paroxysmal neurologic deficits

paroxysmal neurologic disorder

PAS positive

pathology

patient information and support

pectus excavatum

pediatric neurology

percussion induced muscle contraction

perineum, numbness of

periodic paralysis, thyrotoxic

periventricular leukomalacia

peroxisomal disease

peroxisomes

personality change

pertussis immunization

petechiae

phenothiazine

phenylketonuria, variant form of

philtrum, tented

phosphorylase b kinase deficiency

placenta, infection of

placenta, thrombosis of

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

poison, neurologic problems with

poliomyelitis

poliomyelitis vaccine

POLR3B

polycystic kidneys

polyhydramnios

polymerase chain reaction

polymicrogyria

polymyalgia rheumatica

polymyositis

polymyositis, infantile

polyneuropathy, chronic inflammatory demyelinating

polysomnogram

Pompe's disease of glycogen storage

pons, atrophy

pons, lesion of

pontocerebellar atrophy

postoperative neurologic complications

postpartum

postural abnormality

potassium channel antibodies

practice guidelines

Prader-Labhart-Willi syndrome

precipitating factors

pregnancy, neurologic complications in

premature infant

prenatal

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

progeria

prognosis

progressive neurologic disorder

proximal muscle atrophy

pruritus

psychiatric problems in neurologic disorders

psychomotor retardation

pupil, abnormality in neurologic disorders

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

quadriparesis

quadriparesis, acute

quadriplegia

quadriplegia, transient

radiation hypersensitivity

radiculitis

ragged-red fibers

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

rash

rectal sphincter tone, decreased

recurrent

reflex, stretch

reflex, tonic stretch

Refsum's disease

remote effect of cancer on the nervous system

renal failure

renal tubular acidosis

ReNU syndrome

repetitive nerve stimulation

respirations in CNS disease

respirator

respiratory arrest

respiratory failure

respiratory tract infection

riboflavin transporter deficiency

rickets

rigid spine syndrome

rigidity

rippling muscle disease

risus sardonicus

Romberg's sign

rubella vaccine

saccadic eye movements, abnormal

salivation, excessive

sarilumab

Schmidt syndrome

Schwartz-Jampel syndrome

scoliosis

scoliosis, neurologic association with

scooters

screaming

screening

second wind phenomena

sedimentation rate

sedimentation rate, elevated

segmental demyelination

seizure

seizure, children

seizure, differential diagnosis of

seizure, duration

seizure, focal

seizure, injury following

seizure, neonatal

seizure, nonepileptic

self-mutilation

semialdehyde dehydrogenase deficiency

sensorineural hearing loss

sensory loss

septicemia

serum alanine aminotransferase

skin, lesions in neurologic disorders

skull x-ray, abnormal

sleep

sleep pathology and physiology

small for dates infant, problems in

SMN1 gene

sodium channel dysfunction

sodium valproate

sodium valproate, toxicity

spastic diplegia

spasticity

spasticity, treatment of

speech disorder

speech disorder, childhood

speech, absence of

speech, delayed development of

speech, slowed

spinal cord, enlargement

spinal cord, injury of

spinal cord, injury, New Born

spinal cord, intramedullary cyst of

spinal cord, lesion of

spinal cord, transection

spinal cord, vascular malformation of

spinal muscular atrophy

spinal muscular atrophy, classification

spinocerebellar ataxia

splenium of corpus callosum

splenomegaly

spongy degeneration of brain

steroid therapy, CNS treatment and complications with

streptococcal infection

sulfite oxidase deficiency

superior sagittal sinus thrombosis

sweating

sweating, abnormality of

symmetric brain lesions

syphilis, neurologic complications with

teeth, number of in infants

telangiectases

temper tantrums

temporal artery, biopsy

temporal artery, tender

temporalis muscle wasting

testicular enlargement

tetany

tetrahydrobiopterin

thalamus, lesion of

thalamus, lesion of-bilateral

tone, muscle, increased

tongue, enlarged

tongue, fasciculations of

tongue, protrusion of

tongue, weakness

tonic spasms

toxic encephalopathy

toxins, nervous system

toxoplasmosis, CNS

tracheostomy

transient loss of muscle tone

transient neurologic deficit

transilumination of skull

treatment of neurologic disorder

tricyclic antidepressant

trinucleotide repeats

tuberculosis

ultrasonography

ultrasonography, head

ultrasonography, head, fetus-neonate

uric acid, low

urinalysis, abnormal

urinary incontinence

urine test for metabolic disorders

urine test in toxic screen

urine, dark

vaccination, neurologic complications with

vertigo, treatment of

viral infection, CNS

vision, blurred

vision, failure of in childhood

visual evoked response

Walker-Warburg syndrome

walking frame

walking, difficulty with

Wartenberg Pendulum Test

weakness, generalized

weakness, infant

weakness, progressive

weakness, proximal

weight loss

Werdnig-Hoffman disease

Wernicke's encephalopathy

wheelchair

white matter disease

whole genome sequencing

wide based gait

workup

wrist drop

x-linked intellectual deficit

x-linked mental retardation

Showing articles 1800 to 1850 of 3169 << Previous Next >>

Amyotrophic Lateral Sclerosis:T2 Shortening in Motor Cortex at MR Imaging
Radiology 189:843-846, Oba,H.,et al, 1993

Evidence for a Dopaminergic Deficit in Sporadic Amyoptrophic Lateral Sclerosis on Positron Emission Scanning
Lancet 324:1016-1018, Takahashi,H.,et al, 1993

Differential Diagnosis of Guillain-Barre Synd, In Guillain-Barre Synd
Thieme Med Publ, Ch 3, p 42993., Parry,G.J., 1993

Guillain-Barre Syndrome after Exogenous Gangliosides in Italy
BMJ 307:1463-1464, Landi,G.,et al, 1993

Ifosfamide-Induced Nonconvulsive Status Epilepticus
Arch Neurol 50:1104-1105, Wengs,W.J.,et al, 1993

Signs and Symptoms of Reflex Sympathetic Dystrophy:Prospective Study of 829 Patients
Lancet 342:1012-1016, Veldman,P.H.J.M.,et al, 1993

Acute Myopathy and Neuropathy in Status Asthmaticus:Case Report and Literature Review
Muscle & Nerve 16:84-90993., Lacomis,D.,et al, 1993

Molecular Genetics in Neurology
Ann Neurol 34:757-773, Martin,J.B., 1993

Cardiomyopathy May Be the Only Clinical Manifestation in Female Carriers of Duchenne Muscular Dystrophy
Neurol 43:2342-2345, Mirabella,M.,et al, 1993

Ocular Myasthenia Gravis
J Natl Med Assoc 85:681-684, March,G.A.&Johnson,J.N., 1993

Discrete Cortical Infarction with Prominent Impairment of Thumb Flexion
Stroke 24:2118-2120, Terao,Y.,et al, 1993

Serum anti-GQ1b IgG antibody is Associated with Ophthalmoplegia in Miller Fisher Syndrome and Guillain-Barre Syndrome: Clinical and Immunohistochemical Studies
Neurol 43:1911-1917, Chiba, A.,et al, 1993

Suprascapular Nerve Entrapment:Evaluation with MR Imaging
Radiology 182:437-444, Fritz,R.C.,et al, 1992

Myopathy in Severe Asthma
Am Rev Respir Dis 146:517-519, Douglass,J.A.,et al, 1992

McArdle's Disease with Late-Onset Symptoms:Case Report & Review of the Literature
JNNP 55:407-408, Felice,K.J.,et al, 1992

Treatment of Hemifacial Spasm with Botulinum Toxin
Muscle & Nerve 15:1045-1049992., Yoshimura,D.M.,et al, 1992

A Comparison of Two-Dimen Echocard vs Carotid Duplex Scanning in Older Pts with Cerebral Ischemia
Arch Int Med 152:2089-2093, Voyce,S.J.,et al, 1992

Stroke Complic Acute MI, A Meta-Analysis of Risk Modific by Antigoac & Thrombolytic Therapy
Arch Int Med 152:2020-2024, Viatkus,P.T.,et al, 1992

MRI of Intracranial Neurovascular Compression
J Comput Assist Tomogr 16:503-505, Furuya,Y.,et al, 1992

Missed Neuroleptic Malignant Syndrome
BMJ 304:831-832, Renwick,D.S.,et al, 1992

Endovascular Treatment of Vertebral Arteriovenous Fistula
Radiology 183:361-367, Beaujeux,R.L.,et al, 1992

Juvenile Myoclonic Epilepsy, Underdiagnosed and Treatment May Have to be Life Long
BMJ 305:4-5, Timmings,P.L.&Richens,A., 1992

Coma Assoc with Bursts of Abnor Movements & Cognitive Disturb:Acute Encephalopathy of Obscure Origin
J Pediatr 121:845-851, Sebire,G.,et al, 1992

Subacute Idiopathic Demyelinating Polyradiculoneuropathy
Arch Neurol 49:612-616, Hughes,R.,et al, 1992

Repeated Coronary Artery Spasm in a Young Woman with the Eosinophilia-Myalgia Syndrome
JAMA 267:2932-2934, Hertzman,P.A.,et al, 1992

Treatment of Nocturnal Leg Cramps, A Crossover Trial of Quinine vs Vitamin E
Arch Int Med 152:1877-1880, Connolly,P.S.,et al, 1992

Glycogen Storage Disease Type III (Glucogen Debranching Enzyme Def) :Biochem Defects & Myopathy & Cardiomyopathy
Ann Int Med 116:896-900, Coleman,R.A.,et al, 1992

Electrodiagnosis Reliability in the Diagnosis of Infant Botulism
J Pediatr 120:747-749, Graf,W.D.,et al, 1992

Nerve Agents:A Review
Neurol 42:946-950, Gunderson,C.H.,et al, 1992

Anti-Hu-Associated Pareneoplastic Encephalomyelitis/Sensory Neuronopathy
Medicine 71:59-72, Dalmau,J.,et al, 1992

CNS Mycosis Fungoides:CT and MR Findings
J Comput Assist Tomogr 16:529-533, Tein,R.D.,et al, 1992

Unilateral Diaphragmatic Paralysis:An Electrophysiological Study
JNNP 55:316-318, Lagueny,A.,et al, 1992

Neurolymphomatosis:A Clinicopathologic Syndrome Re-emerges
Neurol 42:1136-1141, Diaz-Arrastia,R.,et al, 1992

Upper Arm Radial Nerve Palsy after Muscular Effort:Report of Three Cases
Neurol 42:1632-1634, Streib,E.,et al, 1992

The Dropped Head Syndrome
Neurol 42:1625-1627, Suarez,G.A.&Kelly,J.J., 1992

Decreased Glutamate Transport by the Brain and Spinal Cord in Amyotrophic Lateral Sclerosis
NEJM 326:1464-1468, 14931992., Rothstein,J.D.,et al, 1992

Intrafamilial Heterogeneity in Hereditary Motor Neuron Disease
Neurol 42:1488-1492, Applebaum,J.S.,et al, 1992

Duplication of Part of Chromosome 17 is Commonly Associated with HMSN Type I (Charcot-Marie-Tooth Disease Type 1)
Ann Neurol 31:570-572, Hallam,P.J.,et al, 1992

De-Novo Mutation in Hereditary Motor and Sensory Neuropathy Type I
Lancet 339:1081-1082, Hoogendijk,J.E.,et al, 1992

Amyotrophic Lateral Sclerosis and Lymphoma:Bone Marroe Examination and Other Diagnostic Tests
Neurol 42:1101-1102, Rowland,L.P.,et al, 1992

Werdnig-Hoffman Disease & Chronic Distal Spinal Muscular Atrophy with Apparent Autosomal Dom Inherit
Ann Neurol 32:404-407, Boylan,K.B.&Cornblath,D.R., 1992

Chronic Limb-Girdle Myasthenia Gravis
Neurol 42:1153-1156, Oh,S.J.&Kuruoglu,R., 1992

Clinical and Electrophysiologic Improvement in Lambert-Eaton Syndrome with Intravenous Immunoglobulin Therapy
Neurol 42:1422-1423, Bird,S.J., 1992

Serum Antibodies to L-Type Calcium Channels in Patients with Amyotrophic Lateral Sclerosis
NEJM 327:1721-1728, 17521992., Smith,R.G.,et al, 1992

Clinicopath Conf
Motor Neuron Disease, Progressive-Muscular-Atrophy Type, Case 43-1992, NEJM 327:1298-130592., , 1992

Familial Adult-Onset Muscular Dystrophy with Leukoencephalopathy
Ann Neurol 32:577-580, vanEngelen,B.G.M.,et al, 1992

MRI and SPECT in Amyotrophic Lateral Sclerosis, Demonstr of Upper Motor Neurone Invol by Neuroimaging
Neuroradiology 34:389-393, Udaka,F.,et al, 1992

Mosaic Express of Dystrophin in Carriers of Becker's Muscular Dyst & X-Linked Synd of Myalgia & Cramps
NEJM 327:1100, Minetti,C.&Bonilla,E., 1992

Needle Muscle Biopsy with the Automatic Biopsy Instrument
Neurol 42:2212-2213, Cote,A.M.,et al, 1992

Acute Quadriplegic Myopathy:A Complic of Treat with Steroids, Nondepolarizing Blocking Agents, or Both
Neurol 42:2082-2087, Hirano,M.,et al, 1992

Showing articles 1800 to 1850 of 3169 << Previous Next >>