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Differential
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abdominal muscle paralysis

acetylcholine in CNS

acid maltase deficiency

acid maltase deficiency, adult

acral sensory symptoms

acyl CoA dehydrogenase deficiency

adenosine deaminase deficiency

adrenoleukodystrophy

adrenomyeloneuropathy

advances in neurology

adverse drug reaction

agalsidase alfa

agranulocytosis

alpha galactosidase A deficiency

alpha glucosidase

Alzheimer's disease

aminoacidopathies

aminoacylase 1 deficiency

anemia, hemolytic

anesthesia, general

angina pectoris

angiography, cerebral, negative

angiography, neurologic complications with

angiotensin-converting enzyme

animal exposure

anorexia nervosa

anterior horn cell disease

anticholinergic drugs

anticoagulant, complications of

anticonvulsants

anticonvulsants, hypersensitivity syndrome

anticonvulsants, untoward effects of

antiphospholipid antibodies

apraxia of eye movements

aromatic amino acid decarboxylase deficiency

arrhythmia, cardiac

arthropathy, neuropathic

arylsulfatase A

ascending paralysis

aspartate aminotransferase

ataxia, cerebellar

atherosclerosis, generalized

autonomic dysfunction

bacterial infection

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basophilic stippling of red blood cells

behavioral disorder

biotin deficiency

biotinidase deficiency

blood dyscrasias, neurologic findings with

bone marrow infarction

bone marrow necrosis

bone marrow suppression

bone marrow transplantation

brain biopsy, false negative

brainstem, infarction of

brainstem, lesion of

burning feet, differential diagnosis of

burning paresthesia

calcification, intracranial

calf hypertrophy

Canavan's disease

cancer, cerebrovascular accident complicating patients with

carbamazepine, toxicity

carbamyl phosphate synthetase-I deficiency

carbonic anhydrase II deficiency

carcinoma of lung

cardiac catheterization, neurologic complications

cardiac surgery, neurologic complications with

CAT scan, abnormal

CAT scan, chest

CAT scan, false negative

caudate nucleus, lesion of

central nervous system, infection of

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar hemorrhage

cerebellar infarction

cerebellar lesion

cerebellar vermis

cerebral cortical atrophy

cerebral embolism

cerebral embolism, cardiac origin

cerebral embolism, multiple

cerebral infarction

cerebral infarction, hemorrhagic

cerebral infarction, subcortical

cerebral ischemia

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, glycine

cerebrospinal fluid, protein of

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, xanthochromia of

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, bilateral

cerebrovascular accident, cryptogenic

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, multiple

cerebrovascular accident, non atherosclerotic cause of

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

cerebrovascular disease

cerebrovascular disease, rapidly progressive

ceruloplasmin, serum

chemotherapy, CNS treatment and complications with

cherry red spot

cherry red spot-myoclonus syndrome

chest x-ray, abnormal

choline acetyltransferase

choline chloride

choreoathetosis

chromosomal abnormality

cirrhosis, infancy

Clinical Pathologic Conference(C.P.C.)

codfish vertebrae

coenzyme Q10 deficiency

compression fracture

congestive heart failure

contractures, joint

cooling therapy

copper metabolism, abnormal

cornea, opacification in infancy-causes of

cornea, opacity of

corneal dystrophy

coronary artery bypass

corpus callosum, infarction of

cortical blindness

cranial nerve enlargement

cranial nerve palsies

crawl regression

C-reactive protein, elevated

creatine phosphokinase isoenzyme elevation

creatine phosphokinase(CPK)elevated

creatinine, elevated

cultured skin fibroblasts

cyclophosphamide

cystoisospora belli

cytochrome c oxidase

cytochrome c oxidase, deficiency

decerebrate posture

decision analysis

deep gray nuclei

deficiency of ADA2

degenerative diseases of CNS

dementia, presenile

demyelinating disease

dentate nuclei, lesion of

developmental milestones, loss of

developmental retardation

diaphragmatic paralysis

disseminated intravascular coagulation(DIC)

distal muscle atrophy

distal muscle weakness

dopa responsive dystonia

dropped head syndrome

dysdiadochokinesia

dysostosis multiplex

dystonia, children

dystonic reaction, acute

edema, periorbital

ejection fraction

ejection fraction, abnormal

electrocardiogram, abnormal

electron microscopy

embolism, atheromatous

embolism, cholesterol

embolism, retinal

emergencies, medical

emergencies, neurologic

encephalomyelitis

encephalopathy, acute

encephalopathy, neonatal

encephalopathy, progressive

endocarditis, marantic

enzyme treatment

enzyme, muscle disease

epidemiology of neurology

Epstein-Barr virus

Epstein-Barr virus, negative

esophageal varices

exercise intolerance

eye movement, disorders of

Fabry's disease

facial anomalies

facial appearance, abnormal

facial expression abnormality

facial hypoplasia

facial weakness

failure to thrive

Farber's disease

fatty acid, elevated plasma content

feeding disorder

femoral artery catheterization

ferritin, elevated

fibrin split products

fingernails, abnormal

flow study, carotid artery

flu-like illness

fornix, lesion of

fracture, pathologic

frontal bossing

frontal lobe, behavior with disease of

frontal lobe, lesion of

fundus, abnormality of

galactocerebrosidase

gangliosidosis GM1

gangliosidosis GM2

gangliosidosis GM2-AB variant

gastroenteritis

Gaucher's disease

genetic counselling

genetic diagnosis, prenatal

genetic neurologic disorders

genetic screening

genetic testing

Gilles de la Tourette syndrome

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glucocerebrosidase

glutamate dehydrogenase deficiency

glutaric acidemia

glutaric aciduria

glycogen debranching enzyme deficiency

glycogen storage disease

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

hallucination, auditory

headache, progressive

headache, severe

headache, thunderclap

heavy metal intoxication

hematopoietic tissue, extramedullary

hematuria, microscopic

hemianopia, homonymous

hemoglobin abnormality, neurologic complications of

hemolytic-uremic syndrome

hepatic encephalopathy

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

hepatolenticular degeneration(Wilson's disease), screening for

hepatosplenomegaly

heralding manifestation

herniated disc, thoracic

heterophile antibody test

hexosaminidase-A

hexosaminidase-A and B

histochemistry of muscle

human granulocytic anaplasmosis

human immunodeficiency virus type 1

human immunodeficiency virus type 1, acute infection

Hurler's syndrome

hydrocephalus, normal pressure

hydroxytryptophan L-5(L-5 HTP)

hyperammonemic encephalopathy

hyperamylasemia

hyperbilirubinemia

hyperglycinemia

hyperhomocysteinemia

hypersensitivity reaction

hypoalbuminemia

hypogammaglobulinemia

hypoglycorrhachia

hypokalemic paralysis

hypomyelination

hypotonia, infants

iatrogenic neurologic disorders

ileus, paralytic

immunosuppression

immunosuppressive agents

inborn errors of metabolism

inborn errors of metabolism, screening

inclusion bodies, intracytopasmic

infection, recurrent

infectious mononucleosis

insulin resistance

intellectual deficit

intellectual deterioration

intelligence quotient

interferon antibodies

interferon beta 1-a

interferon beta 1-b

internal capsule

internuclear ophthalmoplegia

internuclear ophthalmoplegia, unilateral

intracerebral hemorrhage

ischemic exercise test

Kayser-Fleischer ring

Kearns-Sayre syndrome

Korsakoff's psychosis

Krabbe's disease

kyphoscoliosis, neurologic causes of

lactic dehydrogenase(LDH)

lacunar infarction

Leber's hereditary optic neuropathy

leg weakness, bilateral

Legionella pneumophilia

Legionnaires'disease

Leigh's disease

Leigh's disease, adult variety

lens, dislocation of

Lesch-Nyhan syndrome

leukemia, neurologic findings assoc.with

leukocyte enzyme abnormality

life expectancy

lipid storage disorder of CNS

livedo reticularis

liver function enzymes

liver transplantation

lymph node biopsy

lymphadenopathy

lymphadenopathy, axillary

lymphadenopathy, cervical

lymphadenopathy, paraaortic

lymphocytic choriomeningitis

lymphoma involving CNS

lysosomal storage disease

lysosomes, abnoral

malignant hyperpyrexia

McArdle's disease

meconium staining

melanomatosis, primary malignant

memory, defect of recent

meningitis, aseptic

meningitis, plasma cell

menses, irregular

mental retardation

mental status, abnormal

mesial temporal lobe

metabolic acidosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

microangiopathic hemolytic anemia

microhemorrhage, intracerebral

microspherophakia

mitochondrial disease

mitochondrial encephalomyopathy

mitral valve vegetation

molecular genetics

motor neuron disease

movement disorder

movement disorder, drug induced

movement disorder, extrapyramidal

MRI, CAT scan compared to

MRI, demyelinating disease

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, eye of tiger sign

MRI, false negative

MRI, gradient-echo

MRI, hypointense signal foci on

MRI, paramagnetic effect

MRI, susceptibility weighted

MRI, vessel wall

MRI, vessel wall enhancement

mucopolysaccharidoses

multiple sclerosis

multiple sclerosis, children

multiple sclerosis, differential diagnosis of

multiple sclerosis, early onset

multiple sclerosis, relapsing

multiple sclerosis, treatment of

multiple system atrophy

muscle atrophy, progressive

muscle hypertrophy

muscle phosphofructokinase deficiency

muscle phosphorylase deficiency

muscle stiffness

muscle wasting, diffuse

muscle weakness

muscle weakness, insidious onset of

muscle weakness, proximal

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, neonatal screening

mycoplasma pneumoniae

myocardial injury

myoclonic jerks

myopathy, distal, vacuolar

myopathy, metabolic

myopathy, mitochondrial

myopathy, necrotizing

myopathy, vacuolar

nausea and vomiting

neonatal screening, genetic neurologic disorders

neoplastic angioendotheliosis

nerve conduction studies

neuraminidase deficiency

neuritis, heavy metals causing

neuroleptic malignant syndrome

neurologic complications

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic examination

neurologic signs

neuromuscular disease, electrodiagnosis of

neuropathy, ataxia, retinitis pigmentosa

neuropathy, painful

neuropathy, peripheral

neuropathy, toxic

neurotransmitter

nonsteroidal anti-inflammatory drug

oculogyric crisis

ophthalmoplegia

ophthalmoplegia, progressive external

opportunistic infection

optic chiasm, enlarged

optic nerve, enlarged

organ transplantation

ornithine transcarbamylase deficiency

pain, abdominal

paraparesis, spastic

paraspinal muscle

paraspinal muscle weakness

paresthesias, feet

paresthesias, hands

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

PAS positive material in the brain

patient information and support

pectus excavatum

pediatric neurology

periarteritis nodosa

pericardial effusion

peripheral blood smear

peripheral blood smear, abnormal

peroxisomal disease

personality change

phenylketonuria

phosphorylase b kinase deficiency

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

pleural effusion

polymerase chain reaction

Pompe's disease of glycogen storage

position sensation, abnormal

postpartum coma

postural abnormality

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

progressive neurologic disorder

prolactin, elevated

proprioception, abnormal

protozoan infection

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychomotor retardation

pulmonary function tests

pulmonary infiltrates

putamen, lesion of

pyramidal tract

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

pyruvate-kinase deficiency anemia

renal failure, acute

renal transplantation

renal tubular acidosis

respiratory failure

respiratory tract infection

retinal degeneration

retinal hemorrhages

reversible cerebral vasoconstrictive syndromes

reversible neurologic disorder

Reye's syndrome

rickettsial organism

salivation, excessive

Sandhoff's disease

Sanfilippo syndrome

scalp tenderness

scoliosis, neurologic association with

second wind phenomena

sedimentation rate

sedimentation rate, elevated

seizure, children

seizure, drug-induced

seizure, elderly

seizure, neonatal

seizure, psychomotor-temporal lobe

self-mutilation

semialdehyde dehydrogenase deficiency

serologic testing

serum alanine aminotransferase

serum glutamic oxaloacetic transaminase

sickle cell disease

skin, lesions in neurologic disorders

slit lamp examination

small vessel disease

sodium valproate

sodium valproate, toxicity

speech disorder

speech disorder, childhood

sphingolipodoses

spinal cord, compression of

spinal cord, lesion of

spinocerebellar ataxia type 1

spinocerebellar degeneration

splinter hemorrhages

spongy degeneration of brain

startle reaction

stem cell transplantation

steroid therapy, CNS treatment and complications with

striatum, lesion of

subarachnoid hemorrhage

subarachnoid hemorrhage, cerebral convexity

subcutaneous nodules

substantia nigra

superior cerebellar artery infarction

sweating, abnormality of

symmetric brain lesions

systemic illness

systemic juvenile idiopathic arthritis

Tay-Sachs disease

temporal lobe, lesion

tetrahydrobiopterin

thalamus, lesion of

thalamus, lesion of-bilateral

thrombocytopenia

tone, muscle, increased

tongue, enlarged

tongue, weakness

tranquilizers, neurologic complications with

transluminal angioplasty, coronary artery

treatment of neurologic disorder

trientine dihydrochloride

tyrosine hydroxylase deficiency

umbilical-cord blood transplantation

unconsciousness

urea-cycle enzymopathies

urinary incontinence

urinary tract infection

urine test for metabolic disorders

urine test in toxic screen

vertebral infarction

vertebral-basilar insufficiency

vertigo, episodic

viral infection

viral infection, CNS

vision, blurred

visual acuity, decreased

vitamin deficiency

walking, difficulty with

weakness, generalized

weakness, progressive

weakness, proximal

Wernicke's encephalopathy

white matter disease

winging of scapula

Showing articles 250 to 300 of 6302 << Previous Next >>

Bacterial Meningitis in Elderly Patients:Clinical Picture and Course
Age & Ageing 21:216-220, Rasmussen,H.H.,et al, 1992

Clinicopath Conf
Thrombotic Thrombocytopenic Purpura, Case 30-1991, NEJM 325:265-273991., , 1991

Cyclosporine-Assoc Seizures in Bone Marrow Transplant Given Busulfan & Cyclophosphamide Prep
Transplantation 52:310-315, Ghany,A.M.,et al, 1991

Sarcoidosis of the Nervous System, A Clinical Approach
Arch Int Med 151:1317-1321, Sharma,Om.P.&Sharma,A.D., 1991

Staphylococcal Pyomyositis in Patients Infected by the Human Immunodeficiency Virus
Am J Med 90:595-600, Schwartzman,W.A.,et al, 1991

Carbamazepine-Induced Antinuclear Antibodies & Systemic Lupus Erythematosus-Like Syndrome
Epilepsia 32:128-129, DeGiorgio,C.M.,et al, 1991

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

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

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

Progressive Multifocal Leukoencephalopathy-Remission with Cytarabine
J Infection 20:51-54, O'Riordan,T.,et al, 1990

Hypersensitivity to Carbamazepine Presenting with a Leukemoid Reaction, Eosinophilia, Erythroderma, and Renal Failure
Neurol 39:436-438, Ray-Chaudhuri,K.,et al, 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

Cholesterol Embolism:Experience with 22 Histologically Proven Cases
Surgery 105:737-746, Dahlberg,P.J.,et al, 1989

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

Neurologic Complications of Bone marrow Transplantation
In Neurol Complic of Transplants, Neurologic Clinics, 6:377-378988., Davis,D.G.&Patchell,R.A., 1988

Pyomyositis in a Patient with the Acquired Immunodeficiency Syndrome
Arch Int Med 148:1608-1610, Gaut,P.,et al, 1988

Clinicopath Conf
Progressive Multifocal Leukoencephalopathy, Chronic Lymphocytic Leukemia, Case Record 45-1988, NEJM, 19:8-1280,1988., 1988

Positron Emission Tomography in a Patient with Progressive Multifocal Leukoencephalopathy
Neurol 38:1864-1867, Kiyosawa,M.,et al, 1988

Neuroleptic Malignant Syndrome:Review and Analysis of 115 Cases
Biol Psychiatry 22:1004-1020, Addonizio,G.,et al, 1987

Neurologic Manifestations of AIDS
Medicine 66:407-437, McArthur,J.C., 1987

Cogan's Syndrome:18 Cases & a Review of the Literature
Mayo Clin Proc 61:344-361, Vollertsen,R.S.,et al, 1986

Azathioprine Toxicity in Neuromuscular Disease
Neurol 36:35-39, Kissel,J.T.,et al, 1986

Cerebral Venous Thrombosis-A Review of 38 Cases
Stroke 16:199-213, Bousser,M.,et al, 1985

Takayasu Arteritis, A Study of 32 North American Patients
Medicine 64:89-99, Hall,S.,et al, 1985

CT Abnormalities & Altered Methotrexate Clearance in Children with CNS Leukemia
Neurol 34:229-233, Duffner,P.K.,et al, 1984

Neurological Complications of Acquired Immune Deficiency Syndrome:Analysis of 50 Patients
Ann Neurol 14:403-418, Snider,W.D.,et al, 1983

Sphenoid Sinusitis
NEJM 309:1149-1154, Lew,D.,et al, 1983

Brain Biopsy in the Diagnosis of Cerebral Mycosis Fungoides
JNNP 45:175-178, Tremblay,G.F.,et al, 1982

Carbamazepine & Hematological Monitoring
Ann Neurol 11:309-312, Hart,R.G.,et al, 1982

Leukoencephalopathy & Elevated Levels Of Myelin Basic Protein In The CSF Of Patients With Acute Lymphoblastic Leukemia
NEJM 303:19-21, Gangji,D.,et al, 1980

Status Epilepticus
Am J Med 69:657-665, Aminoff,M.J.,et al, 1980

Long-term Neurological Implications of Somnolence Syndrome in Children with Acute Lymphocyte Leukemia
Ann Neurol 8:273-277, Ch'ien,L.T.,et al, 1980

Leukaemia:Neurological Involvement
in Handbk of Clinical Neurology, Vinkin PJ & Bruyn GW, Ed, North-Holland Publ Co, Amsterdam 39:1, Yuill,G.M., 1980

Haemophilic Neuromyopathy
JNNP 42:600-605, Defaria,C.R.,et al, 1979

Phenytoin Hypersensitivity:38 Cases
Neurol 29:1480-1485, Harunda,F., 1979

Neurologic Manifestations of Cogan Syndrome
Neurol 28:278, Bicknell,J.M.,et al, 1978

Leukoencephalopathy in Childhood Leukemia
et al. , Neurol 27:609977., Devivo,D.C., 1977

Eosinophilic Polymyositis
Ann Neurol 1:65, Layzer,R.B.,et al, 1977

Spinal Cord Compression Due to Pseudomonas in a Heroin Addict
Neurol 27:1034, Jabbari,B.,et al, 1977

Cardiac Myxoma:A Diagnostic Challenge for the Neurologist
Neurol 26:1060, Yufe,R.,et al, 1976

Bilateral Scalp Necrosis in Temporal Arteritis
Am J Med 61:541, Soderstrom,C.W.,et al, 1976

Case Records of the MGH
Giant cell Angiitis, intracranial NEJM 295:9441976., , 1976

Neurologic Complications After Treatment for Whipple's Disease:A Report of Four Patients
Medicine 55:467, Knox,D.L.,et al, 1976

Case Record of MGH-Crytococcal Meningitis in Hodgkins Disease
NEJM 295:34, , 1976

Neuropsychiatric Manifest. of SLE:Diagnosis, Clinical Spectrum, & Relationship to Other Features of the Disease
Medicine 55:323, Feinglass,E.J.,et al, 1976

Case Record, PVAH, (Case A-77-75) Toxoplasmosis
December 10, Finelli,P.F.,et al, 1975

Recurrent Aseptic Meningitis in an Elderly Male, Unusual Prodromal Manifestation of SLE
JAMA 235:1142, Finelli,P.F.,et al, 1975

Case Records of MGH-Polycythemia
Carotid Occlusion & Cerebral Infarcts, NEJM 291:96674., , 1974

Central Nervous System Infections in Patients with Cancer
Medicine 52:563, Chernik,N.L.,et al, 1973

Case Records of MGH-NEJM 286:1047
1972 Progressive Multifocal Leukoencephalopathy., , 1972

Showing articles 250 to 300 of 6302 << Previous Next >>