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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 950 to 1000 of 1838 << Previous Next >>

Inclusion Body Myositis and Myopathies
Ann Neurol 38:705-713, Griggs,R.C.,et al, 1995

Myasthenic Symptoms in Patients with Mitochondrial Myopathies
Muscle & Nerve 18:1338-1340995., Forestier,N.L.,et al, 1995

Apolipoprotein E E4 in Inclusion Body Myositis
Ann Neurol 38:957-959, Garlepp,M.J.,et al, 1995

Clinicopath Conf
Multiple Myeloma with Bilateral Carpal Tunnel Syndrome Probably Due to Secondary Amyloid Deposit, Ca, e38-1995,NEJM 333:1625-1630,1995., 1995

Middle Cerebral Artery Dissection:A Clinicopathologic Study
Neurol 45:1929-1931, Sharif,A.A.,et al, 1995

Thrombolytic Therapy in Acute Occlusion of the Intracranial Internal Carotid Artery Bifurcation
AJNR 16:1977-1986, 19941995., Jansen,O.,et al, 1995

Cost-effectiveness of Emergency Intraarterial Intracerebral Thrombolysis:A Pilot Study
AJNR 16:1987-1993, 19941995., Lanzieri,C.F.,et al, 1995

Bilateral Ulnar Handcuff Neuropathies with Segmental Conduction Block
Muscle & Nerve 18:1021-1023995., Satkunam,L.&Zochodne,D., 1995

Neurological Multisystem Manifestation in Multiple Symmetric Lipomatosis:A Clinical and Electrophysiological Study
Muscle & Nerve 18:693-698995., Naumann,M.,et al, 1995

Intracranial Arteries:Prospective Blinded Comparative Study of MR Angiography and DSA in 50 patients
Radiology 195:451-456, Klaus,W.S.,et al, 1995

Anticonvulsant Hypersensitivity Syndrome
Arch Int Med 155:2285-2290, Vittorio,C.C.&Muglia,J.J., 1995

Progressive Cerebral Occlusive Disease after Radiation Therapy
Stroke 26:131-136, Bitzer,M.&Topka,H., 1995

Neurologic Aspects of Inflammatory Bowel Disease
Neurol 45:416-421, Lossos,A.,et al, 1995

Classic Neurogenic Thoracic Outlet Syndrome in a Competitive Swimmer:A True Scalenus Anticus Syndrome
Muscle & Nerve 18:229-233995., Katirji,B.&Hardy,R.W., 1995

Late-Onset Mitochondrial Myopathy
Ann Neurol 37:16-23, 31995., Johnston,W.,et al, 1995

Critical Illness Neuromuscular Disease in Children Manifested as Ventilatory Dependence
J Pediatr 126:259-261, Sheth,R.D.,et al, 1995

Gene Analysis of L1 Neural Cell Adhesion Molecule in Prenatal Diagnosis of Hydrocephalus
Lancet 345:161-162, Jouet,M.&Kenwrick,S., 1995

Acute Bacterial Myositis Due to Staphylococcus Aureus Septicemia
Neurol 45:390-391, Sato,K.,et al, 1995

Amyotrophic Lateral Sclerosis:Correlation of Clinical & MR Imaging Findings
Radiology 194:263-270, Cheung,G.,et al, 1995

Proximal Myotonic Myopathy, Clin Features of Disorder Similar to Myotonic Dystrophy
Arch Neurol 52:25-31, Ricker,K.,et al, 1995

Hemiplegia Vegetativa Alterna (Ipsilateral Horner's Synd & Contralat Hemihyperhidrosis) Post Cerebral Art Occl
Stroke 26:702-704, Bassetti,C.&Staikov,I.N., 1995

Endocarditis-Related Cerebral Aneurysms:Radiologic Changes with Treatment
AJNR 16:745-748, Corr,P.,et al, 1995

Does Arterial Recanalization Improve Outcome in Carotid Territory Stroke?
Stroke 26:581-587, vonKummer,R.,et al, 1995

Medical Complications During Stroke Rehabilitation
Stroke 26:990-994, Kalra,L.,et al, 1995

Prolonged Paralysis After Neuromuscular Blockage
Muscle & Nerve, 18:937-94295., Gooch,J., 1995

The Prevention of Neurogenetic Disease
Arch Neurol 52:356-362, 3451995., Rosenberg,R.N.&Iannaccone,S.T., 1995

Mild Traumatic Brain Injury:Pathophysiology, Natural History, and Clinical Management
Neurol 45:1253-1260, 12511995., Alexander,M.P., 1995

Lyme Neuroborreliosis
Ann Neurol 37:691-702, Garcia-Monco,J.C.&Benach,J.L., 1995

Myositis:Immunologic Contributions to Understanding Cause, Pathogenesis, and Therapy
Ann Int Med 122:715-724, Plotz,P.H.,et al, 1995

Proximal Myotonic Myopathy Syndrome in the Absence of Trinucleotide Repeat Expansions
Muscle & Nerve 18:782-783995., Stoll,G.,et al, 1995

Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995

Primary Adhalin Deficiency as a Cause of Muscular Dystrophy in Patients with Normal Dystrophin
Ann Neurol 38:367-372, 3531995., Ljunggren,A.,et al, 1995

Inclusion Body Myositis Presenting with Isolated Erector Spinae Paresis
Neurol 45:993-994, Hund,E.,et al, 1995

Common Variable Immunodeficiency and Inclusion Body Myositis:A Distinct Myopathy Mediated by Natural Killer Cells
Ann Neurol 37:806-810, Dalakas,M.C.&Illa,I., 1995

Amyloidosis Causing A Progressive Myopathy
Muscle & Nerve 18:1016-1018995., Nadkarni,N.,et al, 1995

Hypoglycaemia in Spinal Muscular Atrophy
Lancet 346:609-610, Bruce,A.K.,et al, 1995

Natural History in Proximal Spinal Muscular Atrophy
Arch Neurol 52:518-523, Zerres,K.&Rudnik-Schoneborn,R., 1995

Genotype-Phenotype Correlation in Adult-Onset Acid Maltase Deficiency
Ann Neurol 38:450-454, Wokke,J.H.J.,et al, 1995

Detection of Cortical Neuron Loss in Motor Neuron Disease by Proton Magnetic Resonance Spectroscopic Imaging in Vivo
Neurol 44:1933-1938, Pioro,E.P.,et al, 1994

Superoxide Dismutase and ALS
Lancet 344:1651-1652, Orrell,R.W.&deBelleroche,J.S., 1994

Monomelic Amyotrophy
Muscle & Nerve 17:1129-1134994., Donofrio,P.D., 1994

Becker Muscular Dystrophy with Onset after 60 Years
Neurol 44:2388-2390, Heald,A.,et al, 1994

Amyotrophic Lateral Sclerosis Patient Antibodies Label CA2+Channel a1 Subunit
Ann Neurol 35:164-171, 1311994., Fumiharu,K.,et al, 1994

Intracranial Vascular Stenosis & Occlusion:Diag Accuracy of Three-Dimensional, Time-of-Flight MR Angiography
Radiology 193:187-193, Korogi,Y.,et al, 1994

Posttraumatic Headache
Semin Neurol 14:40-45, Packard,R.C., 1994

Mild Head Injury
(Ed) , Semin Neurol 14:1-9294., Packard,R.C., 1994

Growth Factors:Potential Therapeutic Applications in Neurology
JNNP 54:1445-1450, Drago,J.,et al, 1994

Trinucleotide Repeat Expansion in Neurological Disease
Ann Neurol 36:814-822, LaSpada,A.R.,et al, 1994

Neurologic Manifestations of HIV Infection
Ann Int Med 121:769-785, Simpson,D.M.&Tagliati,M., 1994

One-and-a-Half Syndrome, Type II
Arch Neurol 51:87-89, Carter,J.E.&Rauch,R.A., 1994

Showing articles 950 to 1000 of 1838 << Previous Next >>