Neudle.com: myopathy distal Laing

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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 1550 to 1600 of 1838 << Previous Next >>

Childhood Dermatomyositis:Factors Predicting Functional Outcome and Development of Dystrophic Calcification
Pediatrics 103:882-888, Bowyer,L.S.,et al, 1983

Type I Fiber Atrophy & Internal Nuclei, A Form of Centronuclear Myopathy
Arch Neurol 39:520-524, Peyronnard,J-M.,et al, 1982

Nonfamilial Amyotrophy with Dementia, etc
Advances in Neurology, Human Motor Neuron Diseases, Ed. Rowland, Raven Press, NY 1982 vol 36, p 173., Tyler,H.R., 1982

Fragile X Chromosome & X-Linked Mental Retardation
CMA Journal 127:123-126, Larbrisseau,A.,et al, 1982

Ipecac-induced Myopathy Simulating Dermatomyositis
Neurol 32:91-94, Bennett,H.S.,et al, 1982

Transient Myopathy Apparently Due to Tetracycline
NEJM 307:821-822, Sinclair,D.,et al, 1982

Myopathy Due to Mercaptopropionyl Glycine
BMJ 285:939, Hales,D.S.M.,et al, 1982

Inflammatory Facioscapulohumeral Muscular Dystrophy & Coats Syndrome
Ann Neurol 12:398-401, Wulff,J.D.,et al, 1982

Enigmatic Dyspnoea:An Unusual Presentation of Motor-Neuron Disease
Lancet 1:933-935, Nightingale,S.,et al, 1982

Long-Term Management of Respiratory Failure in Amyotrophic Lateral Sclerosis
Ann Neurol 12:18-23, Sivak,E.,et al, 1982

Benign Familial Spinal Muscular Atrophy With Hypertrophy of the Calves
Arch Neurol 39:657-660, D'Alessandro,R.,et al, 1982

Amyotrophic Lateral Sclerosis & Paraproteinemia
Neurol 32:896-898, Krieger,C.,et al, 1982

External Carotid-Cavernous Sinus Fistula Simulating Unilateral Graves Ophthalmopathy
J Comput Assist Tomogr 6:1006-1009, Merlis,A.L.,et al, 1982

Clinical Use Of Nuclear Magnetic Resonance In The Investigation Of Myopathy
Lancet 1:725-730, Edwards,R.H.T.,et al, 1982

Inclusion Body Myositis Associated With Sjogren's Syndrome
Arch Neurol 39:186-188, Chad,D.,et al, 1982

Sjogren's Syndrome & Polymyositis or Dermatomyositis
Arch Neurol 39:157-163, Ringel,S.P.,et al, 1982

Global Aphasia Without Hemiparesis:A Sign of Embolic Encephalopathy
Neurol 32:403-406, VanHorn,G.,et al, 1982

Fusiform Basilar Aneurysm As A Cause of Embolic Stroke
Stroke 13:712-716, Steel,J.G.,et al, 1982

Aspergillosis of the Nervous System
Neurol 32:473-479, Beal,M.F.,et al, 1982

Classic Amyotrophic Lateral Sclerosis With Dementia
Arch Neurol 39:681-683, Wilkstrom,J.,et al, 1982

Trigeminal Neuropathy in Progressive Systemic Sclerosis
Am J Med 73:57-62, Farrell,D.A.,et al, 1982

Multifocal Interstitial Myositis Associated With Localized Lipoatrophy
Arch Neurol 39:722-724, Palliyath,S.,et al, 1982

Middle Cerebral Artery Occlusion with Migraine
Stroke 13:308-311, Castaldo,J.E.,et al, 1982

Remission From Polymyositis After Total Body Irradiation
BMJ 284:1915-1916, Hubbard,W.N.,et al, 1982

Inclusion Body Myositis
Arch Neurol 39:760-764, Danon,M.J.,et al, 1982

Necrotizing Myopathy Associated with Steroid Therapy, Report of Two Cases
Pathology 14:435-438, Ojeda,V.J., 1982

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

Chronic Focal Polymyositis in the Adult
JNNP 44:419-425, Bharucha,N.E.,et al, 1981

Plasmapheresis in Idiopathic Inflammatory Myopathy Experience With 35 Patients
Arch Neurol 38:544-552, Dau,P.C., 1981

Pharyngeal Dysphagia in Alcoholic Myopathy
Ann Int Med 95:189-191, Weber,L.D.,et al, 1981

Acute Polymyopathy During Total Parenteral Nutrition
BMJ 283:1578, Stewart,P.M.,et al, 1981

Biochemical Genetics Of Neurologic Disease
NEJM 305:1181-1193, Rosenberg,R.N., 1981

Circulating Immune Complexes in Neurologic Disease
Neurol 31:1402-1407, Noronha,A.B.C.,et al, 1981

Successful Treat. of Echovirus Meningoenceph & Myo Fasciitis With Immune Glob Therapy In X-Linked Agammaglob
NEJM 304:1278-1281, Mease,P.J.,et al, 1981

Polymyositis & Diffuse Interstitial Lung Disease
Arch Int Med 141:1005-1010, Salmeron,G.,et al, 1981

Polymyositis Beginning as a Focal Process
Arch Neurol 38:439-442, Heffner,R.R.Jr.,et al, 1981

Eosinophilic Myositis, An Unusual Cause of Pseudotumor & Eosinophilia
JAMA 246:70-71, Agrawal,B.L.,et al, 1981

Labetalol-induced Toxic Myopathy
BMJ 282:1824-1825, Teicher,A.,et al, 1981

Lipid Storage Myopathy:Successful Treatment with Propranolol
BMJ 282:1997-1999, Martyn,C.,et al, 1981

Myopathy Induced by Rifampicin
BMJ 283:105-106, Jenkins,P.,et al, 1981

Motor Neuron Disease:Decremental Responses to Repetitive Nerve Stimulation
Neurol 31:202-204, Bernstein,L.P.,et al, 1981

Scintigraphic Appearance of Anton's Syndrome
JAMA 245:1248-1249, Cusumano,J.V.,et al, 1981

Computerized Tomography & Pure Sensory Stroke
Neurol 31:217-220, Rosenberg,N.L.,et al, 1981

Cimetidine Toxic Reactions Masquerading as Delirium Tremens
JAMA 245:1058-1059, Weddington,W.W.,et al, 1981

Vitamin E Deficiency in Werdnig-Hoffmann Disease
Ann Neurol 10:266-268, Shapira,Y.,et al, 1981

Occipital Lobe Infarctions:Perimetry & Computed Tomography
Neurol 31:1098-1106, Spector,R.H.,et al, 1981

Visual Evoked Potentials in Occipital Lobe Lesions
Arch Neurol 38:80-85, Streletz,L.J.,et al, 1981

Preservation of the Phrenic Motorneurons in Werdnig-Hoffman Disease
Ann Neurol 9:506-510, Kuzuhara,S.,et al, 1981

Amyotrophic Lateral Sclerosis & its Association with Dementia, Parkinsonism & Other Neurological Disorders:A Review
Brain 104:217-247, Hudson,A.J., 1981

Ciguatera Fish Poisoning in Miami
JAMA 244:254-258, Lawrence,D.N.,et al, 1980

Showing articles 1550 to 1600 of 1838 << Previous Next >>