Neudle.com: myopathy distal

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abdominal muscle paralysis

acetylcholine receptor antibody

acid maltase deficiency

acid maltase deficiency, adult

ACTH, ectopic syndrome of

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

asthma, poliomyelitis-like syndrome with

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

brainstem, lesion of

bulbar palsy, acute

bulging of biceps

burning paresthesia

calcification, intracranial

calf hypertrophy

carcinoma of lung

cardiovascular disease

carpo-pedal spasm

central core disease

cerebellar degeneration

cerebrospinal fluid

cerebrospinal fluid, abnormal

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

flaccid paralysis

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

human T-lymphotropic virus type I(HTLV-I)

Huntington's chorea

hyperadrenalism

hyperamylasemia

hyperinsulinism

hyperparathyroidism

hyperthyroidism

hypokalemic alkalosis

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

kyphoscoliosis, neurologic causes of

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

muscular dystrophy, neurogenic hypothesis of

myasthenia gravis

myasthenia gravis, diagnosis

myasthenia gravis, distal weakness

myasthenia gravis, limb-girdle

myasthenia gravis, misdiagnosis of

myasthenia gravis, treatment of

myasthenic crisis

myelopathy, carcinomatous

myelopathy, chronic progressive

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, inflammatory

myopathy, mitochondrial

myopathy, myofibrillar

myopathy, necrotizing

myopathy, neurogenic hypothesis of

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, hormone producing

neoplasm, hormone producing, ectopic

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

overlap syndrome

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

pleocytosis of cerebrospinal fluid

pleural effusion

poison, mercury

poison, neurologic problems with

poliomyelitis-like illness

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

remote effect of cancer on the nervous system

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 1450 to 1500 of 2033 << Previous Next >>

Occlusion of the Middle Cerebral Artery Due to Cysticercotic Angiitis
Stroke 20:1095-1099, Rodriguez-Carbajal,J.,et al, 1989

MR Imaging of Postpartum Cortical Blindness
J Comput Assist Tomogr 13:572-576, Coughlin,W.F.,et al, 1989

Middle Cerebral Artery Pial Territory Infarcts:A Study of the Lausanne Stroke Registry
Ann Neurol 25:555-560, Bogousslavsky,J.,et al, 1989

Comparison of Cerebral Angiography and Transcranial Doppler Sonography in Acute Stroke
Stroke 20:899-903, Zanette,E.M.,et al, 1989

Intraluminal Clot in the Vertebrobasilar Circulation:Clinical and Radiologic Features
Neurol 39:515-522, Levine,S.R., 1989

Intracranial Branch Atheromatous Disease:A Neglected, Understudied, and Underused Concept
Neurol 39:1246-1250, Caplan,L.R., 1989

MR Imaging of Intracranial Carotid Occlusion
AJR 152:1271-1276, Katz,B.H.,et al, 1989

Diagnosis of Gerstmann-Straussler Syndrome in Familial Dementia with Prion Protein Gene Analysis
Lancet 2:15-17, Collinge,J.,et al, 1989

The Effect of Radiation of Carotid Arteries, A Review Article
Arch Neurol 46:449-455, Murros,K.E.&Toole,J.F., 1989

AIDS and the Nervous System
JAMA 261:2396-2399, Dalakas,M.,et al, 1989

Zidovudine-Associated Myopathy
Am J Med 86:814-818, Gertner,E.,et al, 1989

HTLV-I Polymyositis in a Patient Also Infected with the Human Immunodeficiency Virus
NEJM 320:992-995, Wiley,C.A.,et al, 1989

Computeritis, Who's Responsible When PCs Make Employees Sick?
Infoworld 11:51-54, Flynn,L., 1989

The Chronic Fatigue Syndrome-One Entity or Many?
NEJM 319:1726-1728, Swartz,M.N., 1989

Aseptic Meningitis Complicating Adult Kawasaki Disease:Case Report and Review of the Literature
Am J Med 87:106-110, McIlroy,M.A.,et al, 1989

Flaccid Quadriparesis Associated with Yersinia Enterocolitis-Induced Hypokalemia
Arch Int Med 149:1193-1194, Orman,R.A.&Lewis,J.B., 1989

Current Concepts in the Idiopathic Inflammatory Myopathies:Polymyositis, Dermatomyositis, and Related Disorders
Ann Int Med 111:143-157, Plotz,P.H.,et al, 1989

Molecular Biology of Duchenne and Becker's Muscular Dystrophy:Clinical Applications
Ann Neurol 26:189-194, Gutmann,D.H.&Fischbeck,K.H., 1989

Improved Diagnosis of Becker Muscular Dystrophy by Dystrophin Testing
Neurol 39:1011-1017, Hoffman,E.P.,et al, 1989

Mitochondrial Myopathies, Mechanisms Now Better Understood
BMJ 298:1127-1128, Schapira,A.H.V., 1989

Mitochondrial DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre Syndrome
NEJM 320:1293-1299, Moraes,C.T.,et al, 1989

Mitochondrial Encephalomyopathy with Associated Aminoacidopathy in a Male Sibship
J Pediatr 115:81-88, Sooth,F.A.,et al, 1989

The Effects of Alcoholism on Skeletal and Cardiac Muscle
NEJM 320:409-415, 458-4601989., Urbano-Marquez,A.,et al, 1989

Stroke in Patients with Fusiform Vertebrobasilar Aneurysms
Neurol 39:16-21, Pessin,M.S.,et al, 1989

Molecular Genetics of Amyloid Neuropathy in Europe
Lancet 1:524-526, Holt,I.J.,et al, 1989

Von Hippel-Lindau Disease Affecting 43 Members of a Single Kindred
Medicine 68:1-29, Lamiell,J.M.,et al, 1989

Occipital Infarction with Hemianopsia from Carotid Occlusive Disease
Stroke 20:409-411, Pessin,M.S.,et al, 1989

Predictive Testing for Huntington's Disease, Progress and Problems
BMJ 298:404-405, 1989, Harper,P.S.&Morris,M.J., 1989

Motoneuron Disease:A Disorder Secondary to Solvent Exposure?
Lancet 1:73-76, 82-831989., Hawkes,C.H.,et al, 1989

Polymyositis and HTLV-I Antibodies
Ann Neurol 25:311, Francis,D.A.&Hughes,R.A.C., 1989

Distinction of Becker from Limb-Girdle Muscular Dystrophy by Means of Dystrophin cDNA Probes
Lancet 1:466-468, Norman,A.,et al, 1989

Respiratory Complications and Their Management in Motor Neuron Disease
Brain 112:1155-1170, Howard,R.S.,et al, 1989

Internuclear Ophthalmoplegia in Tuberculous Meningitis
Tubercle 70:61-64, Teoh,R.,et al, 1989

Mitochondrial Myopathies:Clinical & Biochem Features of 30 Patients with Major Deletions of Muscle Mitochondrial DNA
Ann Neurol 26:699-708, Hold,I.J.,et al, 1989

Familial X-linked Myalgia and Cramps:A Nonprogressive Myopathy Associated with a Deletion in the Dystrophin Gene
Neurol 39:1277-1280, Gospe,S.M.,et al, 1989

Eosinophilia-Myalgia Syndrome-New Mexico
JAMA 262:3116, Belvins,W.L.,et al, 1989

Neuromuscular Involvement in Mild, Asymptomatic Primary Hyperparathyroidism
Am J Med 87:553-557, Turken,S.A., 1989

The Remote Effects of Cancer on the Nervous System
in Neurol Manif of Systemic Dis, W. B. Saunders, Co, Phila, Neurologic Clinics 7:579-603, Dropcho,E.J., 1989

Life-Threatening Cranial Dystonia Following Trihexyphenidyl Withdrawal
Movement Disorders 4:349-353, Gimenez-Roldan,S.,et al, 1989

Hypothyroidism
In Neurologic Clinics, W. B. Saunders Co, Phila, 7:492-493., Kaminski,H.J.&Ruff,R.L., 1989

Antecollis in Parkinsonism
Lancet 1:1320-1321, Jorens,P.G.,et al, 1989

Human Leptospirosis-A Review of 50 Cases
Infection 17:10-14, Lecour,H.,et al, 1989

Rigid Spine Syndrome and Rigid Spine Sign in Myopathies
J Child Neurol 4:273-282, Merlini,L.,et al, 1989

Chronic Progressive Spinobulbar Spasticity, A Rare Form of Primary Lateral Sclerosis
Arch Neurol 45:509-513, Gastaut,J.L.,et al, 1988

Trauma-Triggered Migraine:An Explanation for Common Neurological Attacks after Mild Head Injury
J Neurosurg 68:181-188, Haas,D.C.&Lourie,H., 1988

The Lambert-Eaton Myasthenic Syndrome, A Review of 50 Cases
Brain 111, 577-5961988., O'Neill,J.H.,et al, 1988

Amyotrophic Lateral Sclerosis Presenting with Sleep Hypopnea Syndrome
Chest 93:1309-1312, Carre,P.C.,et al, 1988

Neuro-Ophthalmologic Complications of Cardiac Catheterization
Neurol 38:483-485, Kosmorsky,G.,et al, 1988

Retinitis Pigmentosa
Surv Ophthalmol 33:137-177, Pagon,R.A., 1988

Dysphagia in Inclusion Body Myositis
JNNP 51:1542-1545, Wintzen,A.R.,et al, 1988

Showing articles 1450 to 1500 of 2033 << Previous Next >>