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abdominal muscle paralysis

acetylcholine receptor antibody

acid maltase deficiency

acid maltase deficiency, adult

Addison's disease

advances in neurology

alveolar hypoventilation

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, guamian type of

amyotrophic lateral sclerosis, misdiagnosis

amyotrophic lateral sclerosis, treatment of

amyotrophic lateral sclerosis-like syndrome

anesthesia, general

anterior horn cell disease

anterior interosseous neuropathy

anterior tibial muscle weakness

arrhythmia, cardiac

arthrogryposis multiplex

ascending paralysis

ataxia, cerebellar

ataxia, sensory

atrioventricular block

autoimmune disease

basal ganglia, infarction

basophilic stippling of red blood cells

benign congenital hypotonia

bitemporal visual field defect

bone marrow suppression

brachial neuritis

bulbar palsy, acute

bulging of biceps

burning paresthesia

calcification, intracranial

calf hypertrophy

cardiovascular disease

carpo-pedal spasm

central core disease

cerebrospinal fluid, elevated protein of

cerebrovascular accident

cerebrovascular accident, infancy and childhood

cerebrovascular accident, multiple

cerebrovascular accident, recurrent

Charcot-Marie-Tooth

chewing, impaired

chromosomal abnormality

chronic polyneuritis, children

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

collagen vascular disease

compression neuropathy

conduction block

congenital heart disease

congenital myopathy

congestive heart failure

contractures, joint

controversies in neurology

cortical hand knob

cost effectiveness

coxsackievirus, myopathy with

craniopharyngioma

creatine phosphokinase(CPK)elevated

critical illness

Cushing's syndrome

degenerative diseases of CNS

delay in diagnosis

dermatomyositis

developmental retardation

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diaphragmatic paralysis

differential diagnosis

difficulty climbing stairs

distal muscle atrophy

distal muscle weakness

dropped head syndrome

dysferlinopathy

dystrophic calcification

electrocardiogram, abnormal

electromyogram, decremental response

electron microscopy

encephalitis, brainstem

encephalopathy, anoxic

encephalopathy, neonatal

entrapment neuropathy

enzyme, muscle disease

epidemiology of neurology

evidence-based research

evoked potentials

facial appearance, abnormal

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

failure to thrive

fatigable chewing

Fazio-Londe's disease

fine motor function, impaired

finger flexor weakness

finger weakness

fingernails, abnormal

foot drop, bilateral

fracture, long bone

fragile-X syndrome

gag reflex, depressed

gammaglobulin therapy, intravenous

gastrocnemius muscle weakness

gastroenteritis

genetic counselling

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

glycogen debranching enzyme deficiency

glycogen storage disease

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

hallucination, auditory

Hand-Schuller-Christian disease

heart block, complete

heavy metal intoxication

hemidiaphragm, paralysis of

heralding manifestation

hereditary myopathy with early respiratory failure

high arched feet

high arched palate

histochemistry of muscle

Huntington's chorea

hyperadrenalism

hyperamylasemia

hyperinsulinism

hyperparathyroidism

hyperthyroidism

hypokalemic periodic paralysis

hypoparathyroidism

hypothalamus, disturbance of

hypotonia, infants

hypoxic encephalopathy

immunohistochemistry

immunologic disease

immunosuppressive agents

inability to sit up

inability to stand on tiptoes

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

inclusion body myositis

intermittent positive pressure breathing

intrinsic hand muscles, wasting of

islet cell tumor

klippel feil syndrome

Kugelberg-Welander syndrome

leg weakness, bilateral

leg weakness, unilateral

lenticular nucleus, lesion of, bilateral

level of consciousness, decreased

lid closure, weakness of

life expectancy

liver function enzymes

median neuropathy

mental retardation

middle cerebral artery, occlusion of

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

monoclonal gammopathy

monoclonal gammopathy of uncertain significance

mononeuritis multiplex

motor neuron disease

movement disorder

multiple myeloma

multiple sclerosis

muscle atrophy, focal

muscle atrophy, progressive

muscle atrophy, static

muscle diseases, characteristics of

muscle hypertrophy

muscle stiffness

muscle strength, testing

muscle swelling

muscle tenderness

muscle wasting, diffuse

muscle weakness

muscle weakness, causes of

muscle weakness, insidious onset of

muscle weakness, proximal

muscle, metabolic disorders of

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, Becker, carrier

muscular dystrophy, cardiovascular changes with

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, differential diagnosis of

muscular dystrophy, distal, Miyoshi

muscular dystrophy, Duchenne

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenia gravis, diagnosis

myasthenia gravis, distal weakness

myasthenia gravis, limb-girdle

myasthenia gravis, misdiagnosis of

myasthenia gravis, treatment of

myasthenic crisis

myopathy, amyloid

myopathy, autoimmune

myopathy, carcinomatous

myopathy, centronuclear

myopathy, desmin

myopathy, distal

myopathy, distal Laing

myopathy, distal, vacuolar

myopathy, distal, Welander's

myopathy, hereditary

myopathy, inclusion body

myopathy, inclusion body, hereditary

myopathy, mitochondrial

myopathy, myofibrillar

myopathy, necrotizing

myopathy, proximal

myopathy, quadriceps

myopathy, steroid induced

myopathy, thyroid disease causing

myopathy, vacuolar

myotonia congenita

myotonia dystrophica

myxedema, neurologic manifestations of

nausea and vomiting

nemaline rod myopathy

nemaline rod myopathy, adult onset

neoplasm, pituitary

neoplasm, primary intracranial

neoplasm, primary of CNS

nerve conduction studies

nerve hypertrophy

neuritis, causes of

neuritis, heavy metals causing

neuroendocrinology

neurofibrillary degeneration

neurologic complications of, systemic cancer

neurologic consultation

neurologic disease

neurologic disease, diagnoses of

neurologic evaluation

neurologic examination

neurologic signs

neurologic symptoms

neuromuscular disease, electrodiagnosis of

neuromuscular junction, abnormality of

neuronal migration disorder

neuropathy, diabetic

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, motor, multifocal

neuropathy, painful

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, toxic

newborn, evaluation of

next-generation sequencing

occipital lobe, infarction

occipital lobe, lesion of

oculopharyngeal muscular dystrophy

old age, neurology of

ophthalmoplegia

ophthalmoplegia, total

Oppenheim muscular dystrophy

paraspinal muscle

paraspinal muscle weakness

parathyroid adenoma

paresthesias, feet

paresthesias, hands

percussion induced muscle contraction

pericardial effusion

peripheral blood smear

peripheral blood smear, abnormal

pheochromocytoma

phosphorylase b kinase deficiency

phrenic nerve pacemaker

pleural effusion

poison, mercury

poison, neurologic problems with

polymerase chain reaction

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, chronic inflammatory demyelinating, variant form

polyneuropathy, chronic inflammatory demyelinating-pure motor syn

polyneuropathy, chronic inflammatory demyelinating-sens atax var

polyneuropathy, chronic inflammatory demyelinating-variant forms

polyneuropathy, familial

position sensation, abnormal

positive sharp waves

post polio syndrome

posterior interosseous neuropathy

pregnancy, neurologic complications in

primary aldosteronism

progressive muscular dystrophy

progressive neurologic disorder

progressive spinal muscular atrophy

proprioception, abnormal

proximal muscle atrophy

pseudohypertrophy

quadriceps atrophy

quadriceps weakness

quality of life

repetitive nerve stimulation

respiratory depression

respiratory failure

rheumatoid arthritis

scoliosis, neurologic association with

seizure, children

seizure, treatment of

serologic testing

severe acute respiratory syndrome

skin, lesions in neurologic disorders

slit lamp examination

spinal cord, injury of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

spinocerebellar degeneration

standing difficulty

steroid therapy, CNS treatment and complications with

stiff man syndrome

survival motor neuron gene

sweating, abnormality of

tandem gait, ataxic

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

thoracic outlet syndromes

thrombocytopenia

tongue, enlarged

tongue, fasciculations of

tongue, weakness

treatment of neurologic disorder

tremor, postural

tricresylphosphate

trinucleotide repeats

Trousseau's sign

ulnar neuropathy

urine test in toxic screen

viral infection

viral infection, CNS

visual evoked response

walking, difficulty with

weakness, fatiguable

weakness, generalized

weakness, progressive

weakness, proximal

Werdnig-Hoffman disease

whistle, inability to

winging of scapula

X-linked bulbospinal neuronopathy

Showing articles 1750 to 1800 of 1838 << Previous Next >>

Pathology of Malignant Hyperpyrexia
BMJ Editorial 249, 1973, Feb., , 1973

Neurologic Manifestations of Progressive Systemic Sclerosis, 1972
Nebraska Med J 58:106, Aita,J.A., 1973

Diphenylhydantoin for Myotonia Congenita-Correspondence
NEJM 286:893, , 1972

Case Record of MGH
NEJM Amyloidosis & Multiple Myeloma, 86:53472., , 1972

Lead Encephalopathy in Adults
Am J Med 52:289, Whitfield,C.L.,et al, 1972

Thromboangiitis Obliterans Cerebri
Edited by, Vinken, E. , Handbook Clinical Neurol 12:3842., Bernsmeier,A.&Held,K., 1972

Congenital Dystrophia Myotonica
Neurol 22:443, Dyken,P.D., 1972

Injuries to the Major Branches of Peripheral Nerves of the Forearm
W. B. Saunders Pub. Co72., Spinner,M., 1972

Muscular Syndrome after Clofibrate
NEJM 286:1110, Katsilambros,N., 1972

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

The Association of Parkinsonism & Motor Neuron Disease
Neurol 22:443, Brait,K., 1972

The Geography of Neurology
BMJ 2:506, Spillane,J.D., 1972

Occlusion of Large Cerebral Vessels in Sickle-Cell Anemia
NEJM 287:845, Stockman,J.A.,et al, 1972

Neurologic Manifestations of SLE 1972
Nebraska State Journ Med, Oct 1972, pp 395., Aita,J., 1972

Acute & Chronic Alcoholic Myopathy
Neurol, April 1972. Vol. 22., Martinez,A.J.,et al, 1972

Language Disturbances Following Anterior, Cerebral Artery Occlusion
Neurol 22:430, Rubens,A.B., 1972

Amyotrophic Lateral Sclerosis
Richard Kisonak, Associated Press, Boston Globe Apr 30972., , 1972

Reversible Forms of Motor Neuron-Disease:Lead"Neuropathy"
Neurol 22:446, Boothby,J., 1972

SLE in the Elderly
Arch Int Med 130:743, Foad,B.S.,et al, 1972

Trichinosis with Central Nervous System Involvement
Neurol 22:485-491, Kramer,M.D.,et al, 1972

Right Hemianopia with Memory & Color Deficits in Circumscribed Left Posterior Cerebral Artery Territory Infarction
Neurol 2l:1104-1113, 1971, Mohr,J.P.,et al, 1971

Electrodiagnosis Studies in Neuromuscular Disease
NEJM 285:1244, Samaha,F., 1971

Electrodiagnosis of Neuromuscular Disease
Bull Univ Maryland School Med 56:33, Kemble,F., 1971

Trigeminal Neuropathy in Connective Tissue Disease
Neurol 21:609, Ashworth,B.,et al, 1971

Infantile Spinal Muscular Atrophy
Arch Neurol 25:276, Wilkins,R.,et al, 1971

"Sick"Motoneurones A Unifying Concept of Muscle Disease
Lancet 321, 1971 Feb., McComas,A.J.,et al, 1971

Hemiplegic Syndrome of the Posterior Cerebral Artery
Stroke 2:559, Benson,D.F.,et al, 1971

Comprehensive Mangagement of Duchenne Muscular Distrophy
Arch Phys Med & Rehab Mar 1971, pp110., Johnson,E.,et al, 1971

Diphosphonate Therapy in a Patient with Myosotis Ossificans Progressiva
Ann Int Med 74:933-936, Weiss,I.W.,et al, 1971

Newer Concepts of Cerebral Vascular Disease
Med Clin North Am 54:1970., Meyer,J., 1970

The Anterior Interosseous-Nerve Syndrome (with special attention to its variations)
J Bone & Joint Surg 52-A:84970., Spinner,M.J., 1970

Cerebral Vascular Disease & Behavior
Arch Neurol 22:408, Segarra,J.M., 1970

Epidemiology & Geographic Pathology of Atherosclerotic Cerebrovascular Disease
Current Concepts of CVD 5:March 1970., Resch,J., 1970

Neurologic Manifestation in Progressive Systemic Sclerosis
Arch Neurol 22:l26, Gordon,R.M.,et al, 1970

The Incidence of the Non-Metastatic Neurological Syndromes of Obscure Origin in the Reticuloses
Brain 93:629, Currie,S.,et al, 1970

Nature of Occlusions of the Middle Cerebral Artery
Neurol 20:82, Lhermitte,F.,et al, 1970

Examination of the Brain & Spinal Cord
Neuropathology, Little, Brown & Co. (Tedeschi) 1970., Romanul,F., 1970

The Neuromyopathy of Vincristine in Man, Clinical, Electrophysiol & Pathological Studies
J Neurol Sci 10:107-131, Bradley,W.G.,et al, 1970

Balint's Syndrome, Handbook of Clinical Neurology
2:667, Vinken,P.J.,et al, 1969

Rocky Mountain Spotted Fever in the Eastern US
NEJM 280:57, Hazard,G.,et al, 1969

Neurogenic Muscular Atrophy of Infancy with Prolonged Survival
Brain 92:9, Munsat,T.,et al, 1969

Chronic Progressive External Ophthalmoplegia
Arch Ophthalmol 82:845, Daroff,R., 1969

Chronic Spinal Muscular Atrophy in Adults
J Neurol Sci 9:551, Meadows,J.C.,et al, 1969

Atheromatous Disease of the Carotid Arterial System & Embolism from Heart in Cerebral Infarct:A Morbid Anatomical Study
Brain 92:897, Blackwood,W.,et al, 1969

Ocular Myopathy
Arch Neurol 20:1, Magora,A.,et al, 1969

Neurogenic Muscular Atrophy Simulating Facioscapulohumeral Muscular Dystrophy
J Neurol Sci 9:389, Furukawa,T.,et al, 1969

Occlusion of the Middle Cerebral Artery & Its Branches:Angiographic & Clinical Correlates
Brain 92:607, Sinderman,F.,et al, 1969

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

Parietal Lobe Syndromes
In Handbk of Clinical Neurology, Vinken & Bruyn, Ed, North-Holland Publ Co, Amsterdam, V2, Ch21, p., 84wesbury,E.C.O., 1969

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

Showing articles 1750 to 1800 of 1838 << Previous Next >>