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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 700 to 750 of 844 << Previous Next >>

Fatal Familial Insomnia & Dysautonomia with Selective Degeneration of Thalamic Nuclei
NEJM 315:997-1003, Lugaresi,E.,et al, 1986

The AIDS Dementia Complex:I. Clinical Features
Ann Neurol 19:517-524, Navia,B.A.,et al, 1986

HTLV/LAV Infection of the Central Nervous System in a 57-Year-Old Man with Progressive Dementia of Unknown Cause
NEJM 314:1191-1192, Mirra,S.S.,et al, 1986

The AIDS Dementia Comples:II. Neuropathology
Ann Neurol 19:525-535, Navia,B.A.,et al, 1986

Clinicopath. Conference
Amyloid Polyneuropathy, Case Record 26-1986, NEJM 315:45-55986., , 1986

The Neuroleptic Malignant Syndrome:Agent and Host Interaction
Acta Psychiatr Scand 73:337-347, Shaley,A.&Munitz,H., 1986

Parkinsonism Following Dystonia in Three Patients
Movement Disorders 1:151-157, Katchen,M.&Duvoisin,R.C., 1986

Neurologic Signs in Senescence
Arch Neurol 42:1154-1157, Jenkyn,L.R.,et al, 1985

Neurological Complications in Infants & Children with Acquired Immune Deficiency Syndrome
Ann Neurol 18:560-566, Belman,A.L.,et al, 1985

Isolation of HTLV-III from CSF & Neural Tissues of Patients with Neurologic Syndromes Related to AIDS
NEJM 313:1493-1497, 15381985., Ho,D.D.,et al, 1985

Limb Shaking-A Carotid TIA
Stroke 16:444-448, Baquis,G.D.,et al, 1985

Repetitive Involuntary Movement Associated with Episodic Cerebral Ischemia
Ann Neurol 18:244-250, Yanagihara,T.,et al, 1985

Primary Writing Tremor & Myoclonic Writer's Cramp
Neurol 35:1387-1391, Ravits,J.,et al, 1985

The Heterogeneity of Parkinson's Disease:Clinical & Prognostic Implications
Neurol 35:522-526, Zetusky,W.J.,et al, 1985

Autosomal Recessive Distal Muscular Dystrophy:A Comparative Study with Distal Myopathy with Rimmed Vacuole Formation
Ann Neurol 17:51-59, Nonaka,I.,et al, 1985

Creutzfeldt-Jakob Disease of Long Duration:Clinicopathological Characteristics
Ann Neurol 16:295-304, Brown,P.,et al, 1984

Chediak-Higashi Syndrome
Arch Neurol 41:1001-1002, Pettit,R.E.,et al, 1984

Frequent Neurologic Toxicity Associated with Amiodarone Therapy
Neurol 34:669-671, Charness,M.E.,et al, 1984

Orthostatic Tremor
Arch Neurol 41:880-881, Heilman,K.M., 1984

Vidarabine Encephalopathy
JNNP 47:1351-1354, Cullis,P.A.,et al, 1984

Cyclosporine-Associated Central-Nervous-System Toxicity after Allogeneic Bone-Marrow Transplantation
NEJM 310:527, Atkinson,K.,et al, 1984

Complex Visual Hallucinations & Cyclosponine
Arch Neurol 41:329-330, Noll,R.B.,et al, 1984

Acquired Immune Deficiency Syndrome & Multiple Tract Degeneration in a Homosexual Man
Ann Neurol 15:502-505, Horoupian,D.S.,et al, 1984

Monomelic Amyotrophy
Arch Neurol 41:388-394, Gourie-Devi,M.,et al, 1984

Clinicopathological Conference
Maroteaux-Lamy Syndrome, Case 44-1983, NEJM 309:1109-1117983., , 1983

Action Tremor as a Manifestation of Chylomicron Retention Disease
Ann Neurol 14:591, Gauther,S.,et al, 1983

Clin. Path. Conference
Multiple-System Atrophy with Parkinsonism, Case 28-13, NEJM 308:1406-1414983., , 1983

Hand Difficulties Among Musicians
JAMA 249:1869-1872, Hochberg,F.H.,et al, 1983

Ischemic Monomelic Neuropathy
Neurol 33:447-451, Wilbourn,A.J.,et al, 1983

Tetrahydrocannabinol for Tremor in Multiple Sclerosis
Ann Neurol 13:699-671, Clifford,D.B., 1983

Neurologic Symptoms Associated with Parenteral Acyclovir Treatment after Marrow Transplantation
Ann Int Med 98:921-925, Wade,J.C.,et al, 1983

Aseptic Meningitis & High School Football Players 1978 & 1980
JAMA 249:2039-2042, Moore,M.,et al, 1983

Neurological Aspect of Hyponatraemia
Postgrad Med J 58:737-740, Daggett,P.,et al, 1982

Primary Writing Tremor:A Selective Action Tremor
Neurol 32:203-206, Klawans,H.L.,et al, 1982

Primary Pontine Hemorrhage & the Dysarthria-clumsy Hand Syndrome
Neurol 32:1027-1028, Tuhrim,S.,et al, 1982

Treatment of Action Tremor in Multiple Sclerosis with Isoniazid
Neurol 32:912-913, Sabra,A.F.,et al, 1982

Tremor After Head Injury & Its Treatment by Stereotaxic Surgery
JNNP 45:815-819, Andrew,J.,et al, 1982

Writers'Cramp-A Focal Dystonia
Brain 105:461-480, Sheehy,M.P.,et al, 1982

The Clinical Relevance of CSF Viral Culture
JAMA 247:1843-1847, Chonmaitree,T.,et al, 1982

Aseptic Meningitis Among Members of a High School Football Team
JAMA 248:1724-1727, Baron,R.C.,et al, 1982

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

Showing articles 700 to 750 of 844 << Previous Next >>