Neudle.com: X linked myopathy

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Differential
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abdominal tenderness

abducens nerve paralysis

abducens nerve paralysis, bilateral

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

advances in neurology

adverse drug reaction

allergic angiitis

alpha-fetoprotein

amaurosis fugax

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, misdiagnosis

anesthesia, general

angiotensin-converting enzyme

anticonvulsants, hypersensitivity syndrome

anticonvulsants, untoward effects of

anti-myeloperoxidase

antineutrophil cytoplasmic autoantibodies

aortic valve, insufficiency

arcuate scotoma, differential diagnosis of

arrhythmia, cardiac

ascending paralysis

aspartate aminotransferase

ataxia telangiectasia

ataxia, cerebellar

ataxia, progressive

atrial fibrillation

atrioventricular block

attention deficit disorder with hyperactivity

autoimmune disease

autonomic dysfunction

bacterial endocarditis, neurologic manifestations of

bacterial infection

Balint's syndrome

basophilic stippling of red blood cells

Bassen-Kornzweig syndrome

bitemporal visual field defect

bone marrow suppression

bone marrow transplantation

brainstem, infarction of

brainstem, lesion of

brainstem, neoplasms of

brainstem, tuberculoma of

burning paresthesia

calcification, intracranial

calcification, muscle

calf hypertrophy

carcinoma of lung

carcinoma of pancreas

cardiovascular disease

carpo-pedal spasm

CAT scan, abnormal

CAT scan, chest

CAT scan, muscle

cauda equina, lesion of

central nervous system, infection of

central nuclei, muscle

cerebellar ataxia, children

cerebellum, disease of

cerebellum, neoplasms of

cerebral embolism

cerebral infarction

cerebro hepato renal syndrome

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, red cells in

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, multiple

cervical spine abnormality

chest x-ray, abnormal

chromosomal abnormality

Churg-Strauss syndrome

Clinical Pathologic Conference(C.P.C.)

Cockayne's syndrome

Cogan's syndrome

collagen vascular disease

congenital myopathy

congestive heart failure

conjunctival injection

contractures, joint

corpus callosum, lesion of

corpus callosum, thinning

cortical infarction

cranial nerve palsies

cranial neuropathy, multiple

craniopharyngioma

creatine phosphokinase(CPK)elevated

cultured skin fibroblasts

Cushing's syndrome

cyclophosphamide

deafness, bilateral

deafness, unilateral

degenerative diseases of CNS

dementia, childhood

demyelinating disease

dermatomyositis

dermatomyositis, childhood

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diagnostic criteria

differential diagnosis

difficulty climbing stairs

digits, abnormal

dilantin, hypersensitivity to

disseminated intravascular coagulation(DIC)

distal muscle atrophy

distal muscle weakness

diurnal variation

dopa responsive dystonia

drug induced neurologic disorders

dysarthria-clumsy hand syndrome

dystonia, etiology of

dystonia, painful

dystrophic calcification

echocardiogram, transesophageal

echocardiogram, transthoracic, false negative

edema, periorbital

ejection fraction

ejection fraction, abnormal

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electronystagmography

electroretinograph

embolism, septic

Emery-Dreifuss muscular dystrophy

encephalomyelitis

endocarditis, acute bacterial

endocarditis, infectious

endophthlamitis

eosinophilia-myalgia syndrome

eosinophilic fasciitis

epidemiology of neurology

erectile dysfunction

erythema multiforme

eye movement, disorders of

face, numbness of

facial nerve palsy

facial nerve palsy, bilateral

facial weakness

false positive VDRL

fatty acid, elevated plasma content

ferritin, elevated

fingernails, abnormal

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

Friedreich's ataxia

fundus, abnormality of

gammaglobulin therapy, intravenous

gastroenteritis

gastrointestinal bleeding

gaze palsy, horizontal

gaze palsy, supranuclear

genetic counselling

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

Gowers maneuver

granuloma, eosinophilic

granulomatosis, allergic

granulomatous disease

granulomatous hypophysitis

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Hallervorden Spatz disease

hallucination, auditory

hallucination, visual

Hand-Schuller-Christian disease

headache, bifrontal

headache, positional

headache, progressive

headache, severe

heavy metal intoxication

heliotrope rash

hemangioblastoma

hematuria, microscopic

hemianopia, homonymous

hemophilus influenza

hepatosplenomegaly

histochemistry of muscle

hormone replacement

Huntington's chorea

hydrocephalus, congenital

hydrocephalus, fetal

hydrocephalus, intrauterine

hyperadrenalism

hyperamylasemia

hypereosinophilic syndrome(HES)

hypergammaglobulinemia

hyperinsulinism

hyperparathyroidism

hypersensitivity reaction

hyperthyroidism

hypertrophic intracranial pachymeningitis

hypoglycorrhachia

hypokalemic periodic paralysis

hypokinetic left ventricle

hypoparathyroidism

hypothalamus, disturbance of

iatrogenic neurologic disorders

immunodeficiency

immunohistochemistry

immunosuppressive agents

inclusion body myositis

intellectual deficit

interferonopathy

intestinal biopsy

intracerebral hemorrhage

intracranial pressure, increased

intrinsic hand muscles, wasting of

islet cell tumor

Kawasaki disease

Kearns-Sayre syndrome

lactic dehydrogenase(LDH)

Laurence-Moon-Bardet-Biedl syndrome

leg spasms, painful

leg weakness, bilateral

Legionella pneumophilia

Legionnaires'disease

level of consciousness, decreased

life expectancy

livedo reticularis

liver function enzymes

lymphadenopathy

lymphadenopathy, hilar

lymphocyte capping, diminished

lymphoid adenohypophysitis

macular degeneration

malignant hyperpyrexia

mediastinum, mass of

medulla oblongata, lesion of

memory, impairment of

meningitis, aseptic

meningitis, basilar

meningitis, chronic

meningitis, recurrent

meningoencephalitis

meningomyelitis

mental retardation

mental retardation, familial

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

mitral valve lesion

mitral valve vegetation

molecular genetics

mononeuritis multiplex

mononeuropathy multiplex

motor neuron disease

movement disorder

movement disorder, extrapyramidal

MRI, contrast enhanced

MRI, sulcal hyperintensity

mucopolysaccharidoses

multiple sclerosis, misdiagnosis

muscle stiffness

muscle tenderness

muscle weakness

muscle weakness, causes of

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, Becker, carrier

muscular dystrophy, cardiovascular changes with

muscular dystrophy, classification

muscular dystrophy, differential diagnosis of

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

muscular dystrophy, lymphocyte capping, diminished

muscular dystrophy, systemic membrane defect

myasthenia gravis

myasthenia gravis, receptor site in

myelitis, longitudinal

myopathy, centronuclear

myopathy, distal

myopathy, drug-induced

myopathy, hereditary

myopathy, inflammatory

myopathy, mitochondrial

myopathy, quadriceps

myopathy, vacuolar

myotonia dystrophica

myotonic discharges

myxedema, neurologic manifestations of

nasal septum, perforation of

nausea and vomiting

neoplasm, pituitary

neoplasm, primary intracranial

neoplasm, primary of CNS

neoplastic angioendotheliosis

nerve conduction studies

neuritis, heavy metals causing

neuroendocrinology

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic signs

neuromuscular disease, electrodiagnosis of

neuronal ceroid-lipofuscinosis

neuronal migration disorder

neuropathology, brain

neuropathy, amyloid

neuropathy, hereditary peripheral

neuropathy, painful

neuropathy, peripheral

neuropathy, toxic

neuropathy, vasculitic, systemic

night blindness

obsessive-compulsive disorder

ocular myopathy

ophthalmoplegia

ophthalmoplegia, plus syndrome

ophthalmoplegia, total

optic neuropathy

orange peel appearance of skin

otitis, neurologic complications with

pain, abdominal

pain, testicular

paraparesis, spastic

parathyroid adenoma

paresthesias, feet

paresthesias, hands

Parkinsonism syndrome

periarteritis nodosa

pericardial effusion

periodic paralysis

peripheral blood smear

peripheral blood smear, abnormal

peripheral nerve, lesion of

peroxisomal disease

pheochromocytoma

pigmentary retinopathy

pituitary, enlargement

pituitary, lesion of

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

pleural effusion

polycystic kidneys

polymerase chain reaction

polymerase chain reaction, false negative

polymyositis, eosinophilic

pons, lesion of

position sensation, abnormal

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

primary aldosteronism

progressive multifocal leucoencephalopathy

progressive neurologic disorder

proprioception, abnormal

prothrombin time, prolonged

proximal muscle atrophy

psychiatric problems in neurologic disorders

ptosis, bilateral

pulmonary edema

pulmonary infection

pulmonary infiltrates

pulmonary opacity

pyloric stenosis

quadriceps atrophy

Raynaud's phenomenon

recombinant DNA

refractive errors

Refsum's disease

renal cell carcinoma

respiratory distress syndrome, neurologic status with

respiratory failure

respiratory tract infection

reticulum cell sarcoma

retinal artery occlusion

retinal degeneration

retinal hemangioma

retinitis pigmentosa

reversible neurologic disorder

rheumatoid arthritis

rheumatoid arthritis factor(R.A.factor)

rickettsial organism

rigid spine syndrome

rippling muscle disease

Rocky Mountain spotted fever

sarcoidosis, CNS

scleroderma, neurologic involvement with

sedimentation rate

sedimentation rate, elevated

seizure, familial

sella turcica, enlargement of

sensorineural hearing loss

serologic testing

serum alanine aminotransferase

severe acute respiratory syndrome

skin, darkening of

skin, lesions in neurologic disorders

skull x-ray, abnormal

Southern immunoblot test

spinal cord, lesion of

spinal cord, neoplasm

spinal muscular atrophy

spinocerebellar degeneration

spirochete infection

splenic infarcts

splinter hemorrhages

standing difficulty

steroid therapy, CNS treatment and complications with

Stevens-Johnson syndrome

streptococcus pneumoniae

subarachnoid hemorrhage

subcutaneous edema

suprasellar lesion

sweating, abnormality of

systemic illness

systemic lupus erythematosus, drug induced

tandem gait, ataxic

tapetoretinal degeneration

telangiectases, periungual

testicular atrophy

testicular biopsy

testicular enlargement

third nerve palsy

thrombocytopenia

tongue, fasciculations of

tonsillar herniation of cerebellum

toxic encephalopathy

toxic oil syndrome

transient ischemic attack

travel, foreign

treatment of neurologic disorder

tremor, intention

tremor, postural

trigeminal neuropathy

trigeminal neuropathy, sensory

trinucleotide repeats

Trousseau's sign

tuberculoma of CNS

tuberculosis, miliary

tumor necrosis factor inhibitor

uncal herniation

urine test in toxic screen

Usher's syndrome

Venereal Disease Research Laboratory test

very long chain fatty acids

vision, blurred

visual acuity, decreased, monocular

visual field defect

visual loss, sudden-unilateral

Von Hippel Lindau

walking, difficulty with

weakness, generalized

weakness, progressive

weakness, proximal

Western immunoblot test

Whipple's disease

white matter disease

X-linked bulbospinal neuronopathy

x-linked hydrocephalus

x-linked mental retardation

X-linked myopathy

x-linked myopathy with excessive autophagy

x-ray, cervical spine

Showing articles 1250 to 1300 of 1521 << Previous Next >>

The Significance of the Incidental Finding of Basal Ganglia Calcification on Computed Tomography
JNNP 44:1168-1170, Harrington,M.G.,et al, 1981

Pituitary Metastasis:Incidence in Cancer Patients & Clinical Differentiation from Pituitary Adenoma
Neurol 31:998-1002, Max,M.B.,et al, 1981

Acute Pulmonary Disease Caused by Phenytoin
Ann Int Med 95:452-454, Michael,J.R.,et al, 1981

Skull X-rays
Lancet 2:1350, Galbraith,S.,et al, 1981

Placement Of Ventriculo-Amniotic Shunt For Hydrocephalus In A Fetus
NEJM 305:955, Clewell,W.H.,et al, 1981

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

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

Early Diagnosis of Spinal Epidural Metastases
Am J Med 70:1181-1188, Rodichok,L.D.,et al, 1981

Metastasis to the Base of the Skull:Clinical Findings in 43 Patients
Neurol 31:530-537, Greenberg,H.S.,et al, 1981

An Ultramicroscopic Study of Skin & Conjunctival Biopsies in Chronic Neuro. Disorders of Childhood
Ann Neurol 9:163-173, Arsenio-Nunes,M.L.,et al, 1981

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

Cerebral Compression by Myeloma
JNNP 44:833-836, Stark,R.J.,et al, 1981

Adrenoleukodystrophy:Increased Plasma Content of Saturated Very Long Chain Fatty Acids
Neurol 31:1241-1249, Moser,H.W.,et al, 1981

The Adrenoleukomyeloneuropathy Complex:Expression in Four Generations
Neurol 31:151-156, O'Neill,B.P.,et al, 1981

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

Legionnaires Disease Associated With Acute Encephalomyelitis
Arch Neurol 38:462-463, Harris,L.F., 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

Meningitis, In Clinical Neurology
Harper & Row Publishers, 1981, p. 1-55., Sahs,A.L.,et al, 1981

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

Prediction of BCNU Pulmonary Toxicity In Patients With Malignant Gliomas, An Assessment of Risk Factors
NEJM 303:183-188, Aronin,P.A.,et al, 1980

Clin. Path. Conference
Lymphoplasmacytic Intersitial Pneumonitis, Progressive Multifocal Leukoencephalopathy. Case Record 1, -10,NEJM 302:795,1980., 1980

Cerebellar Involvement in Multifocal Eosinophilic Granuloma:Demonstration by CT Scan
Ann Neurol 7:125-129, Adornato,B.T.,et al, 1980

Focal Neurologic symptoms in hypercalcemia
Neurol 30:200-201, Longo,D.L.,et al, 1980

Arteriovenous Malformations of the Brain, I:Current Concepts & Treatment
Arch Neurol 37:1-5, Stein,B.M.,et al, 1980

Rhabdomyolysis During Treatment With Epsilon-Aminocaproic Acid
Arch Neurol 37:187-188, Britt,C.W.,et al, 1980

Immunosppressive Agents in Corticosteroid-Refractory Childhood Dermatomyositis
Neurol 30:286-291, Niakan,E.,et al, 1980

Acute Myopathy Associated with Influenza A/Texas/l/77 Infection
JAMA 243:461-462, Kessler,H.A.,et al, 1980

Neuropathy & Mitochondrial Myopathy
Ann Neurol 7:262-268, Peyronnard,M.J.,et al, 1980

Peripheral Source of MB Band of Creatine Kinase in Alcoholic Rhabdomyolysis
JAMA 244:580-582, Siegel,A.J., 1980

Plasma Cell Dyscrasia with Polyneuropathy, Organomegaly, Endocrinopathy, M Protein, & Skin Changes:The POEMS Syndrome
Medicine 59:311-322, Bardwick,P.A., 1980

Skin & Conjunctival Nerve Biopsies in Adreno-leukodystrophy & Its Variants
Ann Neurol 8:291-295, Martin,J.J.,et al, 1980

Adrenoleukodystrophy:Elevated C26 Fatty Acid in Cultured Skin Fibroblasts
Ann Neurol 7:542-549, Moser,H.W.,et al, 1980

Adrenoleukodystrophy. Report of Two Cases With Relapsing & Remitting Courses
Arch Neurol 37:448-450, Walsh,R., 1980

Kluver-Bucy Syndrome Caused by Adreno-leuko-dystrophy
Neurol 30:1131-1132, Powers,J.M.,et al, 1980

Legionnaires'Disease With Profound Cerebellar Involvement
Arch Neurol 37:379-380, Shetty,K.R.,et al, 1980

Influenzal Acute Myositis in the Elderly
Neurol 30:877-878, Congy,F.,et al, 1980

Myositis, Myoglobinemia, & Myoglobinuria Associated With Enterovirus Echo 9 Infection
Arch Neurol 37:457-458, Jehn,U.W.,et al, 1980

Proximal Myopathy after Prolonged Total Therapeutic Starvation
BMJ 280:1212-1213, Scobie,I.N.,et al, 1980

Acute Hydrocortisone Myopathy
BMJ 281:271-272, Marle,W.V., 1980

Cramps, Muscle Pain, & Tubular Aggregates
Arch Neurol 37:715-717, Lazaro,R.P.,et al, 1980

Acne Fulminans with Inflammatory Myopathy
Neurol 8:67-69, Noseworthy,J.H.,et al, 1980

Osteopetrosis, Renal Tubular Acidosis & Basal Ganglia Calcification in Three Sisters
Am J Med 69:64-74, Whythe,M.P.,et al, 1980

Showing articles 1250 to 1300 of 1521 << Previous Next >>