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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 150 to 180 of 180 << Previous

Distal Vacuolar Myopathy in Nephropathic Cystinosis
Ann Neurol 35:181-188, Charnas,L.R.,et al, 1994

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

Gerstmann's Syndrome
Arch Neurol 49:445-447, Benton,A.L., 1992

Clinicopath Conf
Acute & Chronic BActerial Osteomyelitis & Diskitis with Epidural Abscess, Case 16-1992, NEJM 326:107, -1076,, 1992

"Numb, Clumsy Hands" and Tactile Agnosia Sescondary to High Cervical Spondylotic Myelopathy: A Clinical and Electrophysiological Correlation
Acta Neurol Scand 86:622-625, Chang,M.,et al, 1992

Scleroderma and Central Nervous System Vasculitis
Stroke 22:410-413, Pathak,R.&Gabor,A.J., 1991

Barbiturate-Related Connective Tissue Disorder
Arch Int Med 149:911-914, Mattson,R.H.,et al, 1989

Peripheral Nerve Disorders in Instrumentalists
Ann Neurol 26:640-646, Lederman,R.J., 1989

Rett Syndrome:Natural History and Management
Pediatrics 82:1-10, Moeschler,J.B.,et al, 1988

Myelopathy Hand
Editorial, Lancet 2:721-7221987., , 1987

Clinical Spectrum of Hereditary Hemorrhagic Telangiectasia (Osler-Wever-Rendu Disease)
Am J Med 82:989-997, Perry,W.H., 1987

Progressive Multifocal Leukoencephalopathy Associated with Human Immunodeficiency Virus Infection
Ann Int Med 107:78-87, Berger,J.R., 1987

Acute Arsenic Intoxication Presenting as Guillain-Barre-Like Syndrome:Donofrio
P. D. , et al, Muscle & Nerve 10:114-120, , 1987

Vertigo and Dizziness
In Diseases of the Nervous System, Asbury, A. K. , et al, W B Saunders, p. 561, Brandt,T., 1986

Clinicopath. Conference
Acquired Immunodeficiency Syndrome, Rhabdomyosarcoma, with Extensive Metastases, Case 9-1986, NEJM 3, 4:620,1986., 1986

Central Nervous System Infections Associated with Hereditary Hemorrhagic Telangiectasia
Am J Med 77:86-92, Press,O.L.W.,et al, 1984

Sclerosteosis:Neurogenetic & Pathophysiologic Analysis of an American Kinship
Neurol 33:267-277, Stein,S.A.,et al, 1983

Fibrodysplasia Ossificans Progressiva, The Clinical Features & Natural Hx of 34 Pts
J Bone Joint Surg 64B:76-83, Connor,J.M.&Evans,D.A.P., 1982

Confrontation Visual Field Techniques in the Detection of Anterior Visual Pathway Lesions
Ann Neurol 10:28-34, Trobe,J.D.,et al, 1981

Finger Wrinkling after Immersion in Water
BMJ 281:586-587, Alvarez,G.,et al, 1980

Skin Wrinkling on Immersion of Hands
Arch Neurol 36:113-114, Braham,J.,et al, 1979

Polyneuropathy, Skin Hyperpigmentation, Edema, & Hypertrichosis in Localized Osteosclerotic Myeloma
Neurol 27:675, Iwashita,H.,et al, 1977

Neurologic Aspects of Hereditary Hemorrhagic Telangiectasia
Arch Neurol 34:101, Adams,H.P.,et al, 1977

Neuro Complica of Coeliac Disease & Trop Sprue, Neurology of GI Disease
1974, Major Problems in Neurology V-3, W. B. Saunders Co, Ltd., Pallis,C.A.&Lewis,P.D., 1974

Neurologic Manifest. of Infective Endocarditis:A Review
Stroke 4:958, Greenlee,J.E.,et al, 1973

Genetic Counseling in Retinitis Pigmentosa
MCV Quart 8:283, Noah,V., 1972

Syndromes of Central Motor Disorder
in Vinken, P. J. , Bruyn, G. W. , ed. , Handbook of Clinical Neurology, Vol. 1, North-Holland Publ C, , Amsterdam, 19Rondot, P., 1969

Surgical Anatomy of the Hand
Clinical Symposia,Ciba 21:66-109, Lampe,E.W., 1969

Neurological Disorders Associated with Adult Celiac Disease
Brain 89:683, Cooke,W.T.,et al, 1966

The Cornelia de Lange Syndrome
J Pediatr 63:1000-1020, Ptacek,L.J., 1963

Electric Shocks and Weakness of the Right Hand in a Young Man:Hirayama Disease
, Witiw,C.D.&OToole,J.E.,

Showing articles 150 to 180 of 180 << Previous