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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 850 to 900 of 1838 << Previous Next >>

Clinicopath Conf
Acute Critical-Illness Myopathy, with Loss of Myosin Filaments, ? Induced by Steroid, Case 11-1997,, EJM 379-1088,1997., 1997

ALS & Severe Cervical Spondylotic Myelopathy in Pt with a Posterior Fossa Archnoid Cyst:Diag Dilemma
South Medical J 80:1580-1583, Lee,S.K.&Kelly,D.L., 1997

Genetic Testing for Alzheimer Disease, Practical and Ethical Issues
Arch Neurol 54:1226-1229, Roses,A.D., 1997

Fou Rire Prodromique Hearlding a Left Internal Carotid Artery Occlusion
Stroke 28:2081-2083, Carel,C.,et al, 1997

Clinicopath Conf
Rocky Mountain Spotted Fever with Meningoencephalomyelitis, Vasculitis and Focal Myocarditis, Case 3, -17,NEJM 337:1149-1156,1997., 1997

Acute Corticosteroid Myopathy in Intensive Care Patients
Muscle & Nerve 20:1371-1380997., Hanson,P.,et al, 1997

Hemiparetic Acute Myopathy of Intensive Care Progressing to Triplegia
Arch Neurol 54:1420-1422, Sun,D.Y.,et al, 1997

Arterial Injuries in Transsphenoidal Surgery for Pituitary Adenoma:The Role of Angiography and Endovascular Treatment
ANJR 18:655-665, Raymond,J.,et al, 1997

Occlusion of the Right Middle Cerebral Artery in a Man with Polycythemia vera
Rev Neurol 25:2048-2049, Guerrero,A.L. &Cacho,J., 1997

Thrombotic Thrombocytopenic Purpura:A Treatable Cause of Childhood Encephalopathy
J Pediatr 130:313-316, Lawlor,E.R.,et al, 1997

Cerebral Hemispheric Low-Flow Infarcts in Arterial Occlusive Disease:Lesion Patterns and Angiomorphological Conditions
Stroke 28:118-123, Mull,M.,et al, 1997

Few Psychological Consequences of Presymptomatic Testing for Huntington Disease
Lancet 349:4, Bundey,S., 1997

A Case of Hemichorea-Hemiballism Associated with Parietal Lobe Infarction
Eur Neurol 37:65-66, Mizushima, N.,et al, 1997

A Case of Creutzfeldt-Jakob Disease (CJD) Started with Monoparesis of the Left Arm
Rinshi Shinkeigaku 36:1245-1248, Obi, T.,et al, 1996

Motor Neuron Disease with Parkinsonism
Arch Neurol 53:987-991, Qureshi,A.I.,et al, 1996

Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996

Linomide Reduces the Rate of Active Lesions in Relapsing-Remitting Multiple Sclerosis
Neurol 47:895-900, Anderson,O.,et al, 1996

Race and Sex Differences in the Distribution of Cerebral Atherosclerosis
Stroke 27:1974-1980, Wityk,R.J.,et al, 1996

Angiotropic Large-Cell Lymphoma with Peripheral Nerve & Skeletal Muscle Involvement:Early Diagnosis & Treatment
Neurol 47:1009-1011, Levin,K.H.&Lutz,G., 1996

Good Clinical Outcome in a Pt with Large CT Scan Hypodensity Treated with Intra-Arterial Urokinase after Embolic Stroke
Neurol 47:1076-1078, Tarr,R.,et al, 1996

Adult-Onset MELAS
Stroke 27:1420-1423, Gilchrist,J.M.,et al, 1996

Prognostic Value of the Hyperdense Middle Cerebral Artery Sign and Stroke Scale Score Before Ultraearly Thrombolytic Therapy
AJNR 17:79-85, Tomsick,T.,et al, 1996

Chronic Post-Traumatic Headache Often a Myth
Neurol 46:915-916, Warner,J.S.&Fenichel,G.M., 1996

Sustained Myoglobinuria:The Presenting Manifestation of Dermatomyositis
Neurol 47:119-123, Rose,M.R.,et al, 1996

Multiple Mitochondrial DNA Deletions in Sporadic Inclusion Body Myositis:A Study of 56 Patients
Ann Neurol 39:789-795, Santorelli,F.M.,et al, 1996

Acute Type II Myofiber Atrophy in Critical Illness
Neurol 46:819-821, 6001996., Gutman,L.,et al, 1996

Muscle is Electrically Inexcitable in Acute Quadriplegic Myopathy
Neurol 46:731-736, 6001996., Rich,M.M.,et al, 1996

Neurogenic Muscle Hypertrophy
Muscle & Nerve 19:811-818996., Gutmann,L., 1996

Diagnosis of McArdle's Disease by Molecular Genetic Analysis of Blood
Neurol 47:579-580, El-Schahawi,M.,et al, 1996

Congenital Muscular Dystrophy:Clinical & Pathologic Study of 50 Pts with Classical (Occidental) Merosin-Positive Form
Neurol 46:815-818, Kobayashi,O.,et al, 1996

Congenital Muscular Dystrophy Syndromes Distinguished by Alkaline and Acid Phosphatase, Merosin, & Dystrophin Staining
Neurol 46:810-814, Connolly,A.M.,et al, 1996

Mushroom Myopathy
Muscle & Nerve 19:790-792996., Gonzalez,J.,et al, 1996

Isolated Neck Extensor Myopathy:A Common Cause of Dropped Head Syndrome
Neurol 46:917-921, Katz,J.S.,et al, 1996

Investigation of Muscle Disease
JNNP 60:256-274, Mastaglia,F.L.&Laing,N.G., 1996

Brain and Spinal Cord MRI in Motor Neuron Disease
JNNP 61:314-317, Thorpe,J.W.,et al, 1996

Amyotrophic Lateral Sclerosis and Occupational History
Arch Neurol 53:730-733, Strickland,D.,et al, 1996

Avoiding False Positive Diagnoses of Motor Neuron Disease:Lessons from the Scottish Motor Neuron Disease Register
JNNP 60:147-151, Davenport,R.J.,et al, 1996

Diagnosing Motor Neurone Disease
BMJ 312:650-651, Chancellor,A.M., 1996

Motor Neuron Disease
BMJ 313:244, Shneerson,J.M., 1996

Motor Neuron Disease Presenting as Acute Respiratory Failure:A Clinical and Pathological Study
JNNP 60:455-458, Chen,R.,et al, 1996

Dose-Ranging Study of Riluzole in Amyotrophic Lateral Sclerosis
Lancet 347:1425-1431, Lacomblez,L.,et al, 1996

Skin Involvement in Amyotrophic Lateral Sclerosis
lancet 347:1226-1227, Kolde,G.,et al, 1996

AAEM Case Report#13:Diabetic Amyotrophy
Muscle & Nerve 19:939-945996., Chokroverty,S.&Sander,H.W., 1996

Ethylene Oxide Neurotoxicity:A Cluster of 12 Nurses with Peripheral and Central Nervous System Toxicity
Neurol 46:992-998, Brashear,A.,et al, 1996

Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
Ann Neurol 39:343-351, Rahman,S.,et al, 1996

Niemann-Pick Disease Type C from Bench to Bedside
JAMA 276:561-564, Schiffmann,R., 1996

Development of General Weakness in a Patient with Amyotrophic Lateral Sclerosis after Focal Botulinum Toxin Injection
Neurol 46:845-846, Mezaki,T.,et al, 1996

Yelling Attacks and Wasted Hands
Lancet 348:238, Bosboom,W.M.J.,et al, 1996

Critical Illness Myopathy and Neuropathy
Lancet 347:1579-1582, Latronico,N.,et al, 1996

Clinicopath Conf
Tangier Disease, Case 16-1996, NEJM 334:1389-1394996., , 1996

Showing articles 850 to 900 of 1838 << Previous Next >>