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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 950 to 1000 of 1521 << Previous Next >>

Myopathy and Rhabdomyolysis Associated with Lovastatin-Gemfibrozil Combination Therapy
JAMA 264:71-75, Pierce,L.R.,et al, 1990

Peripheral Neuropathy in the Eosinophilia-Myalgia Syndrome Associated with L-Tryptophan Ingestion
Neurol 40 1035-1040, Smith,B.E.&Dyck,P.J., 1990

Cranial Lymphangiomatosis Causing CSF Otorrhea and Recurrent Meningitis:CT Features
J Comput Assist Tomogr 14:121-123, Nazarian,G.K.,et al, 1990

Clinical Uses of Intravenous Immunoglobulins
Ann Int Med 112:278-292, Berkman,S.A.,et al, 1990

Hyperostosis Cranialis Interna
NEJM 322:450-463, Manni,J.J.,et al, 1990

Clinicopath Conf
Eosinophilic Fasciitis, Case Study 4-1990, NEJM 322:252-261, 93190., , 1990

Development of Diffuse Fasciitis with Eosinophilia During L-Tryptophan Treatment:Elevated Type I Collagen Gene
Ann Int Med 112:344-351, Varga,J.,et al, 1990

Clinicopath Conf
Familial Visceral Myopathy (Oculogastrointestinal Muscular Dystrophy) , Case 12-1990, NEJM 322:829-8, 1, 19, 1990

Night-Time Nasal Ventilation in Neuromuscular Disease
Lancet 335:579-582, Heckmatt,J.Z.,et al, 1990

Clinicopath Conf
Acute Renal Failure, Anemia, & Seizures in a 67-year-old Man, Am J Med 88:60-68., , 1990

Dopa-Responsive Dystonia:The Spectrum of Clinical Manifestations in a Large North American Family
Neurol 40:66-69, Nygaard,T.G.,et al, 1990

Clinicopath Conf
Hodgkin's Disease and Acute Paraneoplastic Sensory Ganglionitis, NEJM 322:531-5431990., , 1990

Late Complication of Undetected Odontoid Fracture in Children
BMJ 300:319-320, Alp,M.S.&Crockard,H.A., 1990

Risks of Acute Traumatic Intracranial Haematoma in Children and Adults
BMJ 300:363-367, Teasdale,G.M.,et al, 1990

Scleroderma, fasciitis, and Eosinophilia Associated with the Ingestion of Tryptophan
NEJM 322:874-881, 9261990., Silver,R.M.,et al, 1990

Association of the Eosinophilia-Myalgia Syndrome with the Ingestion of Tryptophan
NEJM 322:869-873, 9261990., Hertzman,P.A.,et al, 1990

Neurofibromatosis Type I in Children
J Pediatr 116:845-853, Listernick,R.&Charrow,J., 1990

Linkage of DNA Markers at Xq28 to Adrenoleukodystrophy & Adrenomyeloneuropathy Present in the Same Family
Arch Neurol 47:665-669, Willems,P.J.,et al, 1990

Reversal of Early Neurologic and Neuroradiologic Manifestations of X-Linked Adrenoleukodystrophy by Bone Marrow Transplant
NEJM 322:1860-1866, Aubourg,P.,et al, 1990

Clinicopath Conf
Malignant Angioendotheliomatosis, Am J Med 88:522-5281990., , 1990

Posttraumatic Cerebral Infarction Diagnosed by CT:Prevalence, Origin, and Outcome
AJR 154:1293-1298, Mirvis,S.E.,et al, 1990

Genetic Testing for Huntington's Disease
BMJ 300:1089-1090, Harper,P.,et al, 1990

Pulmonary Arteriovenous Malformation Presenting with Brain Abscess
Am J Dis Child 144:1045-1047, Dove,A.M.,et al, 1990

Mitochondrial Myopathy Caused by Long-Term Ziduvudine Therapy
NEJM 322:1098-1105, Dalakas,M.C.,et al, 1990

Clinicopath Conf
Acute Febrile Neutrophilic Dermatosis (Sweet's Syndrome) , Case 30-1990, NEJM 323:254-2630., , 1990

Polyneuropathy, Ophthalmoplegia, Leukoencephalopathy, and Intestinal Pseudo-Obstruction:POLIP Syndrome
Ann Neurol 28:349-360, Simon,L.T.,et al, 1990

Adult Phosphorylase b Kinase Deficiency
Ann Neurol 28:529-538, Clemens,P.R.,et al, 1990

Skeletal Muscle Pathology in AIDS:An Autopsy Study
Muscle & Nerve, 13:508-51590., Wrzolek,M.A.,et al, 1990

A Disorder of Azonal Development, Necrotizing Myopathy, Cardiomyopathy, and Cataracts:A New Familial Disease
Ann Neurol 27:193-199, Lyon,G.,et al, 1990

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

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

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

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

Encephalotrigeminal Angiomatosis
In Rowland's Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8thEd, p. 582, Gold,A.P., 1989

Adult-Onset Adrenoleukodystrophy Manifesting as Dementia
Am J Med 87:481-483, Panegyres,P.K.,et al, 1989

Dietary Erucic Acid Therapy for X-Linked Adrenoleukodystrophy
Neurol 39:1415-1422, Rizzo,W.B.,et al, 1989

MRI Detects Cerebral Involvement in Neurologically Asymptomatic Patients with Adrenoleukodystrophy
Neurol 39:1619-1621, Aubourg,P.,et al, 1989

Clinicopath Conf
Diffuse Idiopathic Skeletal Hyperostosis, Case Record 43-1989, NEJM 321:1178-1187989., , 1989

Pleural and Retroperitoneal Fibrosis from Dihydroergotamine
NEJM 321:1760, Malaquin,F.,et al, 1989

HTLV-1 and Polymyositis in Jamaica
Lancet 2:1184-1187, Morgan,O.S.,et al, 1989

HTLV-1 Associated Myelopathy and Polymyositis in a US Native
Neurol 39:1572-1575, Evans,B.K.,et al, 1989

Thyrotoxic Periodic Paralysis
Arch Int Med 149:2597-2600, Kelley,D.E.,et al, 1989

Cerebral Erdheim-Chester Disease:Persistent Enhancement with Gd-DTPA on Mr Images
Radiology 172:791-792, Tien,R.D.,et al, 1989

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

Clinicopath Conf
Chronic Osteomyelitis of Spine, with Intervertebral Diskitis (T3-T4) & Epidural Abscess (Staph Aureu, ) , Cas9,NEJM 320:1610-1618,1989., 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

Duchenne Muscular Dystrophy:Patterns of Clinical Progression and Effects of Supportive Therapy
Neurol 39:475-481, Brooke,M.H.,et al, 1989

Genetic Abnormalities in Duchenne and Becker Dystrophies:Clinical Correlations
Neurol 39:461-465, 584-5851989., Medori,R.,et al, 1989

Molecular and Clinical Correlations of Deletions Leading to Duchenne and Becker Muscular Dystrophies
Neurol 39:465-474, 584-5851989., Baumbach,L.L.,et al, 1989

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

Showing articles 950 to 1000 of 1521 << Previous Next >>