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accomodation, abnormal

advances in neurology

adverse drug reaction

anesthesia, general

anterior tibial muscle weakness

antiviral agents

arrhythmia, cardiac

arthrogryposis multiplex

atrial fibrillation

atrial paralysis

atrioventricular block

attention deficit disorder with hyperactivity

autoimmune disease

autonomic dysfunction

basal ganglia, calcification of

biopterin deficiency

blinking, reduced

bone marrow transplantation

brainstem, atrophy

Brown-Vialetto-Van Laere syndrome

burning paresthesia

calcification, intracranial

calf hypertrophy

cardiovascular disease

carpal tunnel syndrome

CAT scan, abnormal

central core disease

cerebellar atrophy, primary

cerebral cortical atrophy

cerebral embolism

cerebral embolism, carotid origin

cerebrospinal fluid, abnormal

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, oligoclonal IgG in

cerebrovascular accident

cerebrovascular accident, cardiac disease causing

cerebrovascular accident, young adult

ceruloplasmin, serum

cervical spine abnormality

Charcot-Marie-Tooth

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

clubbing of fingers

clubfoot as related to neurologic disease

Cockayne's syndrome

cogwheel rigidty

congenital infection, CNS

congenital myopathy

congenital myopathy, inflammatory

congestive heart failure

contractures, joint

contrast agents, neurotoxicity of

convergence, impaired

cornea, opacity of

corpus callosum, lesion of

cranial neuropathy

cranial neuropathy, multiple

crawl regression

C-reactive protein, elevated

creatine phosphokinase MB isoenzyme elevation

creatine phosphokinase(CPK)elevated

cytomegalovirus infection

cytomegalovirus infection, congenital

decision analysis

dermatomyositis

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes mellitus

diamond on quadriceps

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

disability rating scale, neurological

disability, neurological

dislocated hip, congenital

distal muscle atrophy

distal muscle weakness

diurnal variation

dopa responsive dystonia

drug induced neurologic disorders

dysostosis multiplex

dystonia, children

dystonia, treatment of

dystrophic calcification

electrocardiogram, abnormal

Emery-Dreifuss muscular dystrophy

encephalopathy, progressive

enzyme, muscle disease

eosinophilia-myalgia syndrome

eosinophilic fasciitis

epidemiology of neurology

epileptic encephalopathy

exome sequencing

facial appearance, abnormal

facial weakness

failure to thrive

FARS2 deficiency

feeding disorder

fetal movements, reduced

fine motor function, impaired

fracture, long bone

gait, festinating

gamma amino butyric acid

genetic counselling

genetic neurologic disorders

genetic testing

glutamic acid decarboxylase, antibody

Gowers maneuver

growth retardation

Guillain Barre syndrome

heart block, complete

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatosplenomegaly

high arched feet

histochemistry of muscle

hyperpigmentation of skin

hypoparathyroidism

hypotonia, infants

iatrogenic neurologic disorders

immunosuppressive agents

implantable cardioverter defibrillator

inclusion body myositis

infection, recurrent

influenza A virus

influenza B virus

injection neuropathy

intellectual deficit

intellectual deterioration

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

intrinsic hand muscles, wasting of

jaw contractures

joint hypermobility

Kayser-Fleischer ring

kinesia paradoxica

Krabbe's disease

kyphoscoliosis, neurologic causes of

lactic dehydrogenase(LDH)

lateral cutaneous nerve of forearm

life expectancy

limb-girdle weakness

liver function enzymes

liver transplantation

lymphadenopathy

lymphadenopathy, axillary

lymphadenopathy, paraaortic

lysosomal storage disease

malignant hyperpyrexia

marche a petits pas

median neuropathy

meningitis, CSF cell count-normal

mental retardation

mitochondrial disease

mitral valve prolapse

molecular genetics

monoclonal antibodies

movement disorder

movement disorder, extrapyramidal

MRI, complications with

MRI, contraindications

MRI, contrast enhanced

multiple system atrophy

muscle atrophy, progressive

muscle atrophy, static

muscle stiffness

muscle strength, testing

muscle tenderness

muscle weakness

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, congenital, Ullrich

muscular dystrophy, differential diagnosis of

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, limb-girdle

muscular dystrophy, pattern of muscle involvement

myasthenia gravis

myasthenia gravis, familial incidence of

myasthenic syndrome

myocardial biopsy

myopathy, hypocalcemic

myopathy, quadriceps

myositis, acute of childhood

myositis, post infectious

myotonia dystrophica

myotonic discharges

nephrogenic systemic fibrosis

nerve conduction studies

nerve enlargement

nerve hypertrophy

neurocutaneous disease

neuroendocrinology

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neuromuscular disease, electrodiagnosis of

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, iatrogenic

neuropathy, peripheral

optic neuropathy

orange peel appearance of skin

overlap syndrome

pacemaker, cardiac-transvenous

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, familial spastic, variants

paraparesis, spastic

paresthesias, feet

paresthesias, hands

Parkinson disease

Parkinson disease, diagnosis

Parkinson disease, differential diagnosis of

Parkinson disease, juvenile

Parkinsonism syndrome

periventricular leukomalacia

personality change

photosensitivity, skin

pigmentary retinopathy

polymerase chain reaction

polymyalgia rheumatica

positive sharp waves

practice guidelines

premature infant

prenatal diagnosis by amniocentesis

progressive neurologic disorder

prolactin, elevated

proximal muscle atrophy

pseudohypertrophy

psychiatric problems in neurologic disorders

psychomotor retardation

pulmonary infiltrates

pyramidal tract dysfunction

reflex sympathetic dystrophy

renal tubular acidosis

repetitive nerve stimulation

respiratory failure

riboflavin transporter deficiency

rigid spine syndrome

rippling muscle disease

sarcoglycanopathy

scoliosis, neurologic association with

sedimentation rate

sedimentation rate, elevated

seizure, children

seizure, neonatal

sensorineural hearing loss

shoulder, pain in

skin, lesions in neurologic disorders

skin, thickened

spastic diplegia

speech disorder

speech disorder, childhood

steroid therapy, CNS treatment and complications with

stiff man syndrome

stooped posture

systemic illness

systemic juvenile idiopathic arthritis

tandem gait, ataxic

toxic oil syndrome

treatment of neurologic disorder

tremor, intention

tremor, postural

tremor, resting

type 1 muscle fiber

type 2 muscle fiber

tyrosine hydroxylase deficiency

urea-cycle enzymopathies

urine test for metabolic disorders

viral infection

voice, abnormality of

Walker-Warburg syndrome

walking, delayed

walking, difficulty with

weakness, congenital

weakness, generalized

weakness, progressive

weakness, proximal

white matter disease

wide based gait

winging of scapula

x-ray, cervical spine

Showing articles 750 to 800 of 854 << Previous Next >>

Distal Myopathy, Histochemical & Ultrastructural Studies
Arch Neurol 39:367-371, Kumamoto,T.,et al, 1982

Immediate & Delayed Neurotoxicity After Mechlorethamine Preparation for Bone Marrow Transplantation
Ann Int Med 97:182-189, Sullivan,K.M.,et al, 1982

Dysaesthesias & Dysautonomia:A Self-limited Syndrome of Painful Dysaesthesias & Autonomic Dysfunction in Childhood
JNNP 45:162-165, Nass,R.,et al, 1982

Neurologic Signs In Uncomplicated Aging (Senscence)
Seminars In Neurology, Thieme-Stratton Inc. , New York, N. Y. pp. 21-30, Jenkyn,L.R.&Reeves,A.G., 1981

Late Onset of Wilson's Disease
Arch Neurol 38:729-730, Czlonkowska,A.,et al, 1981

Encephalopathy in Infants & Children With Chronic Renal Disease
Arch Neurol 38:656-658, Foley,C.M.,et al, 1981

Asperger's Syndrome:A Clinical Account
Psychological Medicine 11:115-129, Wing,L., 1981

Successful Treatment of Inorganic Mercury Neurotoxicity with N-acetyl-penicillamine Despite an Adverse Reaction
Neurol 30:1000-1001, Markowitz,L.,et al, 1980

Metrizamide Encephalopathy
Ann Neurol 7:494, Vincent,F.M.,et al, 1980

Handedness, Clumsiness & Cognitive Ability
Develop Med Child Neurol 22:569-579, Bishop,D.V.M., 1980

Human Cerebellar Hypoplasia, A Syndrome of Diverse Causes
Arch Neurol 37:300-305, Sarnatt,H.B.,et al, 1980

Juvenile Metachromatic Leukodystrophy
Arch Neurol 37:42-46, Haltia,T.,et al, 1980

Amyloid Neuropathy & Tremor in Waldenstrom's Macroglobulinemia
Arch Neurol 37:240-242, Bajada,S.,et al, 1980

Juvenile Muscular Atrophy Localized to Arms
Arch Neurol 37:297-299, Singh,N.,et al, 1980

Cerebellar Involvement in Multifocal Eosinophilic Granuloma:Demonstration by CT Scan
Ann Neurol 7:125-129, Adornato,B.T.,et al, 1980

Interaction of Lithium & Phenytoin
BMJ 1:610-611, MacCallu,W.A., 1980

Valproic Acid
NEJM 302:661-666, Brown,T.R., 1980

A pedigree of Amyotrophic Chorea With Acantho-cytosis
Arch Neurol 37:514-517, Kito,S.,et al, 1980

Diagnosis & Treatment, Physiologic & Pathologic Tremors
Ann Int Med 93:460-465, Jankovic,J.,et al, 1980

Motor Neuropathy Associated with Cimetidine
BMJ 281:974-975, Walls,T.J.,et al, 1980

An Autosomal Dominant Syndrome of Hemiplegic Migraine, Nystagmus, & Tremor
Ann Neurol 8:329-332, Zifkin,B.,et al, 1980

Myositis, Myoglobinemia, & Myoglobinuria Associated With Enterovirus Echo 9 Infection
Arch Neurol 37:457-458, Jehn,U.W.,et al, 1980

Congenital Ocular Motor Apraxia
Arch Neurol 36:29-31, Orrison,W.W.,et al, 1979

Giant Axonal Neuropathy
Arch Neurol 36:107-108, Mizuno,Y.,et al, 1979

Upper Trunk Brachial Plexopathy in Football Players
JAMA 241:1480-1482, Robertson,W.C.,et al, 1979

Dysarthria-Clumsy Hand Syndrome Produced by Capsular Infarct
Ann Neurol 6:263-265, Spertell,R.B.,et al, 1979

Familial Periodic Ataxia
Arch Neurol 36:568-569, Donat,J.R.,et al, 1979

Acute Generalized Polyneuropathy Accompanying Lithium Poisoning
Ann Neurol 6:360-362, Brust,J.C.M.,et al, 1979

Hereditary Myoclonus & Progressive Distal Muscular Atrophy
Ann Neurol 6:227-231, Jankovic,J.,et al, 1979

Valproic Acid, Review of a New Antiepileptic Drug
Arch Neurol 36:393-398, Bruni,J.,et al, 1979

Tremor Due to Sodium Valproate
Neurol 29:1177-1180, Hyman,N.M.,et al, 1979

Clinical Pathological Conference, Peripheral Neuropathy in Leprosy
NEJM 300:546-553, Dawson,D., 1979

Isolated Trigeminal Sensory Neuropathy:Early Manifestation of Mixed Connective Tissue Disease
Neurol 28:1286-1289, Searles,R.P.,et al, 1978

Adult Onset Nemaline Myopathy
Neurol 28:1306-1309, Brownell,A.K.W.,et al, 1978

Diagnosis of Treatable Wilson's Disease
NEJM 298:1347, Cartwright,G.E., 1978

Propranolol for Severe Post-head Injury Action Tremor
Neurol 28:197, Ellison,P.H., 1978

Autosomal Dominant System Degeneration in Portugese Families of the Azores Islands
Neurol 28:703, Coutinho,P.,et al, 1978

Clinical Aspects of Spasmodic Dysphonia
JNNP 41:361, Aminoff,M.J.,et al, 1978

Juvenile Type of Distal & Segmental Muscular Atrophy of Upper Extremities
Ann Neurol 3:429, Sobue,I.,et al, 1978

Chlordecone Intoxication in Man
Neurol 28:626, Taylor,J.R.,et al, 1978

Distal Chronic Spinal Muscular Atrophy Involving the Hands
JNNP 41:653-658, O'Sullivan,D.J.,et al, 1978

Acute & Chronic Progressive Encephalopathy Due to Gasoline Sniffing
Neurol 28:507-510, Valpey,R.,et al, 1978

Peripheral Nerve Conduction in Patients with a Cervical Rib & Band
Ann Neurol 4:124-129, Gilliatt,R.W.,et al, 1978

Tricyclic Antidepressants
NEJM 299:1106-1109, 1168-11721978., Hollister,L., 1978

Reversible Cerebellocerebral Disorder in Primary Hemochromatosis
Arch Neurol 34:123, Singh,N.,et al, 1977

Familial Idiopathic Cerebral Calcifications
et al. , JNNP 40:280977., Boller,F., 1977

The Serological Diagnosis of St. Louis Encephalitis in Patient with Syndr. of Opsoclonia, Body Tremulousness, & Benign Encephalitis
Ann Neurol 1:596, Estrin,W., 1977

Hangman's Fracture Subsequent to Shaking in an Infant
Ann Neurol 2:82, McGrory,B.E., 1977

Radicular Compression in Multifocal Eosinophilic Granuloma
Arch Neurol 34:786, Eil,C.,et al, 1977

Pellagra
In Brain's Diseases of the Nervous System, 8th Ed. 1977, p 849-851, Oxford University Press., , 1977

Showing articles 750 to 800 of 854 << Previous Next >>