Neudle.com: enzyme serum

Differential
(Click to cross reference)

abducens nerve paralysis

acanthocytosis

acetaminophen

acetazolamide

acid maltase deficiency

acid maltase deficiency, adult

aciduria

acquired immunodeficiency syndrome

acromegaly

acute disseminated encephalomyelitis

addiction, heroin-neurologic complications with

adolescent medicine

adult polyglucosan body disease

adult T-cell leukemia-lymphoma

advances in neurology

adverse drug reaction

Africa

agranulocytosis

alcohol, neurologic complications with

altered states of consciousness

Alzheimer's disease

Alzheimer's disease, treatment of

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, treatment of

anasarca

anemia

anemia, hemolytic

anemia, megaloblastic

anesthesia, general

angiitis

angina pectoris

angiography, neurologic complications with

angiotensin-converting enzyme

angiotensin-converting enzyme, inhibitors

anterior horn cell disease

antibiotics

anticholinergic drugs

anticholinesterase

anticoagulant, complications of

anticoagulant, treatment

anticoagulant, treatment in CVD

anticonvulsants

anticonvulsants, blood level determination of

anticonvulsants, compliance

anticonvulsants, effectiveness

anticonvulsants, enzyme inducing

anticonvulsants, hypersensitivity syndrome

anticonvulsants, mechanism of action of

anticonvulsants, selection of

anticonvulsants, teratogenicity of

anticonvulsants, untoward effects of

antithyroid antibodies

aspartate aminotransferase

atherosclerosis, generalized

atrial fibrillation

atrial fibrillation, nonvalvular

atrial myxoma

atrioventricular block

bacterial infection, CNS

BAL

bartonella henselae

basal ganglia

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basophilic stippling of red blood cells

behavioral disorder

behavioral disorder, acute

blood dyscrasias, neurologic findings with

blood transfusion

bone age

bone demineralization

bone loss

bone marrow biopsy

bone marrow infarction

bone marrow necrosis

bone marrow suppression

brain biopsy, stereotaxic

brain natriuretic peptide

brucellosis, nervous system involvement with

calcification, intracranial

calcification, liver

calcification, lymph node

carbamazepine, toxicity

carbamyl phosphate synthetase-I deficiency

carcinoma

carcinoma of lung

carcinoma of pancreas

cardiac arrest

cardiac catheterization, neurologic complications

cardiac enzymes

cardiac surgery, neurologic complications with

cardiac tumor

cardiomegaly

cardiomyopathy

cardiovascular disease

carnitine deficiency myopathy

carotid artery atherosclerosis

carotid artery atherosclerosis, pathogenesis

carotid artery plaque

CAT scan, emission, abnormal

cataracts

catechol-o-methyltransferase inhibitor

cathartic

cat-scratch disease

cauda equina, lesion of

CD4 counts

celiac disease, adult

celiac disease, childhood

central nervous system, infection of

central nuclei, muscle

cerebellar hemorrhage

cerebellar infarction

cerebellar lesion

cerebral cortex

cerebral cortical atrophy

cerebral edema

cerebral edema, vasogenic

cerebral embolism

cerebral embolism, cardiac origin

cerebral infarction

cerebral infarction, hemorrhagic

cerebral palsy

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, absorption

cerebrospinal fluid, biochemical markers of CNS tumors

cerebrospinal fluid, cell count, normal

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, enzymes in

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, gold sol.curve of

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, complications with

cerebrovascular accident, multiple

cerebrovascular accident, pathophysiology

cerebrovascular accident, prevention of

cerebrovascular accident, prognosis in

cerebrovascular accident, seizure with

cerebrovascular accident, young adult

cerebrovascular disease

cerebrovascular disease, cardiovascular disease with

chemotherapy, CNS treatment and complications with

chest pain

chest x-ray, abnormal

chromosomal abnormality

Churg-Strauss syndrome

cingulate gyrus

cirrhosis

Clinical Pathologic Conference(C.P.C.)

collagen vascular disease

congenital birth defects

congenital infection, CNS

congenital infection, viral

congenital malformation

congenital malformation, non CNS

congenital myopathy

congestive heart failure

copper metabolism, abnormal

cornea, abnormal

coronary artery bypass

C-reactive protein, elevated

creatine kinase

creatine phosphokinase isoenzyme elevation

creatine phosphokinase MB isoenzyme elevation

creatine phosphokinase(CPK)elevated

creatinine, elevated

critical care unit

cryoglobulinemia

cultured skin fibroblasts

cytomegalic inclusion disease

cytomegalovirus infection

cytomegalovirus infection, congenital

dementia, diagnostic evaluation of

dementia, differential diagnosis of

dementia, treatment of

deprenyl

depression

depression, psychotic

dermatitis

dermatitis herpetiformis

dermatomyositis

developmental disability

developmental milestones, loss of

developmental retardation

differential diagnosis

difficulty climbing stairs

dilantin

dilantin, factors influencing metabolism of

dilantin, hypersensitivity to

dilantin, serum level

diplopia

disability, neurological

disorientation

disseminated intravascular coagulation(DIC)

distal muscle atrophy

distal muscle weakness

drug induced neurologic disorders

dystrophic calcification

dystrophin

eating disorder

echocardiogram

echocardiogram, transesophageal

eclampsia

eclampsia, postpartum

ejection fraction, abnormal

electrical fields, alternating

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, triphasic delta waves

electromyogram

electron microscopy

electrophoretic pattern, serum

embolism

embolism, atheromatous

embolism, cholesterol

emergencies, neurologic

encephalomyelitis, postinfectious

encephalopathy

encephalopathy, Hashimoto's

encephalopathy, neonatal

endemic area

endocarditis

endocarditis, marantic

enzyme, muscle disease

enzyme, serum

eosinophilia

eosinophilia-myalgia syndrome

eosinophilic granulomatosis with polyangiitis

epidemiology of neurology

epistaxis

Epstein-Barr virus

Epstein-Barr virus, negative

extraocular muscle enlargement

extraocular muscle lesion

Fabry's disease

face, numbness of

facial anomalies

facial appearance, abnormal

facial expression abnormality

facial hypoplasia

facial nerve palsy

facial nerve palsy, bilateral

femoral artery catheterization

fine motor function, impaired

fingernails, abnormal

gammaglobulin therapy, intravenous

gastroenteritis

gastrointestinal bleeding

genetic neurologic disorders

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glucose tolerance test, abnormal

glucosephosphate isomerase

gluten sensitivity

glycogen debranching enzyme deficiency

glycogen storage disease

Gowers maneuver

granuloma, eosinophilic

granulomatous disease

gray matter

growth hormone antagonist

growth retardation

grunting

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, sensory

Guillain Barre syndrome, variant forms of

Haiti

hallucination

hallucination, visual

headache, retro-orbital

heavy metal intoxication

HELLP syndrome

hematuria, microscopic

hemiparesis

hemochromatosis

hemoglobin abnormality, neurologic complications of

hemoglobinuria

hemolytic-uremic syndrome

hemophagocytic lymphohistiocytosis

hemophagocytosis

hemophilia

hemorrhagic diathesis

hepatic encephalopathy

hepatic encephalopathy, acute

hepatic failure

hepatic failure, acute

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), late onset

hepatolenticular degeneration(Wilson's disease), presymptomatic

hepatolenticular degeneration(Wilson's disease), screening for

hepatomegaly

hepatosplenomegaly

heralding manifestation

hereditary hemorrhagic telangiectasia(HHT)

herniation syndromes, intracranial

herpes simplex encephalitis

herpes virus

herpes zoster

herpes zoster, disseminated

heterophile antibody test

hip flexor weakness

HMGcoA reductase inhibitors

homocysteine, serum

homocystinuria

homosexual

hot, red, angry babies

human granulocytic anaplasmosis

human immunodeficiency virus type 1

human immunodeficiency virus type 1, acute infection

human parechovirus

human T-lymphotropic virus type I(HTLV-I)

hydrocephalus

hyperammonemic encephalopathy

hyperamylasemia

hyperbilirubinemia

hypercalcemia

hypercoagulable state

hyperparathyroidism, secondary

hyperphosphatasia

hyperreflexia

hypersegmented polys

hypersensitivity reaction

hypertension

hypertensive encephalopathy

hyperthermia

hypertriglyceridemia

hypertrophic intracranial pachymeningitis

hypokalemic paralysis

hyponatremia

hypoparathyroidism

hypoparathyroidism, idiopathic

hypophosphatemia

hypopituitarism

hyporeflexia

hypothalamus, neoplasm of

iatrogenic neurologic disorders

idiosyncratic reaction

immunosuppressive agents

impotence

impulsivity

inappropriate antidiuretic(A.D.H.)hormone

inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with

inattention

inborn errors of metabolism

inclusion bodies

inclusion body myositis

incoordination

indinavir

infection

infectious mononucleosis

infectious mononucleosis, neurologic findings with

influenza A virus

infusion-associated reaction

intellectual deterioration

interferon

interferon alpha

interferon antibodies

intracerebral hemorrhage

intracranial pressure monitoring

intracranial pressure, increased

intrauterine infection

intrauterine infection, viral

iritis

iron, serum

iron, serum, elevated

irritability

ischemic exercise test

Kayser-Fleischer ring

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

lactate

lactic dehydrogenase(LDH)

laminar necrosis, cortical

lamotrigine

laquinimod

L-dopa

L-dopa, drug interactions with and side effects of

learning disability

learning disability, in children

lecithin

leg numbness

leg weakness, bilateral

Legionella pneumophilia

Legionnaires'disease

Lennox-Gastaut syndrome

leukocyte enzyme abnormality

leukocytosis

leukoencephalopathy

leukopenia

level of consciousness, decreased

liver function enzymes

liver nodules

liver scan

liver transplantation

lymphadenopathy, axillary

lymphadenopathy, cervical

lymphadenopathy, hilar

lymphadenopathy, paraaortic

lymphocytic choriomeningitis

lymphocytosis

lymphoma

lymphoma involving CNS

lymphoma, primary of CNS

lymphopenia

lysosomal storage disease

malignant hyperpyrexia

melanomatosis, primary malignant

memory, impairment of

meningeal biopsy

meningeal enhancement

meningeal gliomatosis

meningismus

meningitis

meningitis, aseptic

meningitis, bacterial

meningitis, basilar

meningitis, carcinomatous

meningitis, chronic

meningitis, leptospira

meningitis, leukemic

meningitis, lymphomatous

meningitis, plasma cell

meningitis, recurrent

mental status, abnormal

metabolic acidosis

metabolic disorder, primary

metastasis to bone

methylmalonic acid, serum

methylmalonic acidemia

microangiopathic hemolytic anemia

microcephaly

microspherophakia

migraine, seizures in

mononeuropathy multiplex

movement disorder, drug induced

movement disorder, extrapyramidal

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, FLAIR

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, starfield pattern

MRI, T1 weighted high signal foci

MRI, volumetry

multiple organ failure

multiple sclerosis

multiple sclerosis, children

multiple sclerosis, early onset

multiple sclerosis, prophylaxsis

multiple sclerosis, relapsing

multiple sclerosis, treatment of

muscle atrophy, progressive

muscle biopsy

muscle cramp

muscle pain

muscle phosphofructokinase deficiency

muscle phosphorylase deficiency

muscle spasm

muscle stiffness

muscle strength, testing

muscle tenderness

muscle wasting, diffuse

muscle weakness

muscle weakness, causes of

muscle weakness, insidious onset of

muscle weakness, intermediate onset of

muscle weakness, proximal

muscle weakness, sudden onset of

muscular dystrophy

muscular dystrophy, central nervous system abnormality

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, Duchenne, neonatal screening

muscular dystrophy, Duchenne, presymptomatic detection

mycoplasma

mycoplasma pneumoniae

myelin basic protein

myelitis, longitudinal

myelomalacia

myeloneuropathy

myelopathy

myocardial infarction

myocardial infarction, acute

myopathy, centronuclear

myopathy, critically ill

myopathy, distal, vacuolar

myopathy, drug-induced

myopathy, hypokalemic

myopathy, inflammatory

myopathy, metabolic

myopathy, necrotizing

myopathy, necrotizing, autoimmune

neonatal infection, viral

neonatal screening, genetic neurologic disorders

neoplasm, metastatic to CNS

neoplasm, pituitary

neoplasm, pituitary, treatment of

neoplastic angioendotheliosis

nephritis

nephrotic syndrome

nerve biopsy

nerve conduction studies

neuritis, heavy metals causing

neuroendocrinology

neurogenic bladder

neuroleptic

neuroleptic malignant syndrome

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic evaluation

neurologic signs

neurologic symptoms

neuromuscular disease, electrodiagnosis of

neuroophthalmology

neuropathology

neuropathy

neuropathy, cryoglobulinemic

neuropathy, painful

neuropathy, peripheral

neuropathy, sensory

neuropathy, small-fiber, painful sensory

neuropathy, toxic

neuropathy, vasculitic, nonsystemic

nonsteroidal anti-inflammatory drug

normal

nutritional deficiency

obesity

obstetric neurologic injuries

occupational neurologic disorders

oculopharyngeal muscular dystrophy

odynophagia

old age, neurology of

opened mouth

opisthotonus

opportunistic infection

organ transplantation

ornithine transcarbamylase deficiency

osteomalacia

osteomyelitis

osteomyelitis, spinal

parasitic infection, CNS

parathormone

parechovirus encephalitis

Parkinson disease, treatment of

Parkinsonism syndrome

parvovirus

pathology

patient information and support

peripheral blood smear

peripheral blood smear, abnormal

phosphorylase b kinase deficiency

pituitary stalk

pituitary, adenoma

platelet inhibiting drugs

pleocytosis of cerebrospinal fluid

polyglucosan body disease

polymerase chain reaction

polymerase chain reaction, false negative

polymyalgia rheumatica

polymyositis

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

polypharmacy

polyuria

Pompe's disease of glycogen storage

position sensation, abnormal

postpartum

postpartum coma

postpartum cortical blindness

postural abnormality

practice guidelines

precipitating factors

preclinical

pre-eclampsia

pregnancy, anticonvulsants during

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

pressure sores

prevention of neurologic disorders

prisoner

prognathism

prognosis

progressive neurologic disorder

prolactin, elevated

proprioception, abnormal

protease inhibitor, HIV-1

proteinuria

prothrombin time, prolonged

protozoan infection

pruritus

psychiatric disorder

psychiatric problems in neurologic disorders

pulmonary function tests

pulmonary infiltrates

range-of-motion, neck

renal transplantation

respiratory distress syndrome, neurologic status with

respiratory failure

respiratory tract infection

reticulum cell sarcoma

retro-orbital pain

retrovirus

reversible neurologic disorder

review article

Reye's syndrome

Reye's syndrome, adult

risk-benefit assessment

Sabin-Feldman dye test

safety

salivary gland biopsy

salivation, excessive

scoliosis, neurologic association with

screaming

season

sedimentation rate

sedimentation rate, elevated

seizure

seizure, children

seizure, drop

seizure, drug-induced

seizure, elderly

seizure, neonatal

seizure, pregnancy

seizure, treatment of

seizure, treatment of, monotherapy

seizure, women

selective serotonin reuptake inhibitors

sensorineural hearing loss

sensory loss

septicemia

serologic testing

serologic testing, false negative

seronegative

serositis

serum alanine aminotransferase

serum gamma glutamyl transferase

serum glutamic oxaloacetic transaminase

serum glutamic pyruvic transaminase

serum lipase, elevated

serum sickness

severe acute respiratory syndrome

sex reassignment surgery

short stature

shunt procedure, ventricular

sickle cell crisis

sickle cell disease

skin, biopsy

skin, lesions in neurologic disorders

slit lamp examination

slurred speech

small for dates infant, problems in

small vessel disease

sodium valproate

sodium valproate, toxicity

soluble interlukin 2 receptor

speech disorder, childhood

speech, delayed development of

speech, pressured

spinal cord

spinal cord, compression of

spinal cord, lesion of

spinal muscular atrophy

spinal muscular atrophy, adult onset

stem cell transplantation

steroid

steroid therapy, CNS treatment and complications with

superior cerebellar artery infarction

suprasellar lesion

sweating

sweating, abnormality of

symmetric brain lesions

syncope

systemic illness

systemic juvenile idiopathic arthritis

tachycardia

tangential

Tanzania

temporal artery, biopsy

temporal artery, tender

tenderness

teratogenic drugs

term infant

testosterone, serum, low

tetrahydroaminoacridine

tetrathiomolybdate

Texas

thalamus, lesion of

thalamus, lesion of-bilateral

thrombotic microangiopathy

thyroid function tests

toxoplasma complement fixation test

toxoplasma gondii

toxoplasmosis, acquired

toxoplasmosis, CNS

toxoplasmosis, muscle

tranquilizers, neurologic complications with

transgender

transluminal angioplasty, coronary artery

travel history

travel, foreign

treatment of neurologic disorder

tremor

tremor, intention

tremor, wing beating

trientine dihydrochloride

triglycerides

tripping

Trousseau's syndrome

tumor necrosis factor inhibitor

type 2 muscle fiber

typhus, murine

ultrasonography

ultrasonography, head

ultrasonography, head, fetus-neonate

uncal herniation

unconsciousness

urea

urea-cycle enzymopathies

uremia

urinary casts

urinary incontinence

urinary tract infection

urine test for metabolic disorders

urine test in toxic screen

vascular headache, food causing

vision, blurred, monocular

visual acuity, decreased, monocular

visual impairment

visual loss

visual loss, sudden-unilateral

visual loss, transient

vitamin supplementation

vitamin, multiple

walking, difficulty with

weakness

weakness, generalized

weakness, progressive

Showing articles 950 to 1000 of 1009 << Previous Next >>

Chronic Hexosaminidase A & B Deficiency
et al. , Ann Neurol 2:156977., Goldie,W.D., 1977

Neuropathology of Sanfilippo Syndrome
Ann Neurol 2:161, Ghatak,N.R.,et al, 1977

Phenytoin Intoxication During Concurrent Diazepam Therapy
JNNP 40:890, Rogers,H.J.,et al, 1977

Phenytoin-related Cerebellar Degeneration Without Seizures
II, et al, Ann Neurol 2:437977., Rapport,R.L., 1977

Possible Pathophysiology of Neurologic Abnormalities assoc. with Nonketotic hyperglycinemia
NEJM 294:1295, Ramson,B.R., 1976

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

Normocalcemic Tetany
Neurol 26:825, Isgreen,W.P., 1976

Phenytoin-induced Ophthalmoplegia
Neurol 26:1031, Spector,R.H.,et al, 1976

Drug Therapy of Parkinsonism
NEJM 295:814, Bianchine,J.R., 1976

Diabetic Polyneuropathy:The Import. of Insulin Deficiency, Hyperglycemia & Myoinositol Metabol. in Pathogen
NEJM 295:1416, Winegrad,A.I.,et al, 1976

Rifampin Induced Methadone Withdrawal
NEJM 294:1104, Kreek,M.J.,et al, 1976

Acute Meningoencephalitis Assoc. with Isoiazid Admin
JAMA 235:1141, Garagusi,V.F.,et al, 1976

Treatment of Hydrazine-Induced Coma with Pyridoxine
NEJM 294:938, Kirklin,J.K.,et al, 1976

Phenytoin & Methadone Tolerance
NEJM 294:227, Finelli,P.F., 1976

Interaction of Quinidine with Anticonvulsant Drugs
NEJM 294:699, Data,J.L.,et al, 1976

Use of Phenytoin Serum Levels in a Case of Status Epilepticus
Neurol 26:879, Fincham,R.W.,et al, 1976

MGH-CPC-Ataxic Telangiectasia & Left Frontal Lobe Glioma
NEJM 292:1231, , 1975

Case Records of the MassGeneral Hospital, Case 41-1975, Acute Intermittent Porphyria
NEJM 293:817, Woods,B., 1975

Microsomal Enzume Induction by Methadone & its Implications on Toler. to Methad. Tox
Nature 253:200, Masten,L.W.,et al, 1975

Compliance in Anticonvulsant Drug Therapy
Epilepsia 16:203, Eisler,J.,et al, 1975

Elevation of Serum Angiotension-Converting-Enzyme (ACE) Level in Sarcoidosis
Am J Med 59:365-372, Lieberman,J., 1975

Clinical Pathological Conference-The Man Without a History-CA of Lung with Marantic Endocarditis & Cerebral Emboli
JAMA 227:1052, Locke,S.,et al, 1974

Hepatic Encephalopathy:Current Status
Gastroenter 66:121:1974., Schenker,S.,et al, 1974

Lupus Meningitis
Ann Int Med 80:58, Keefe,E.,et al, 1974

Neuromuscular Disease in Primary Hyperparathyroidism
Ann Int Med 80:182, Patten,B.M.,et al, 1974

Specificity of the Urine Inhibitor Test for Leigh's Disease
Neurol 24:885, Pincus,J.H.,et al, 1974

Neuro Complica of Coeliac Disease & Trop Sprue, Neurology of GI Disease
1974, Major Problems in Neurology V-3, W. B. Saunders Co, Ltd., Pallis,C.A.&Lewis,P.D., 1974

Case Records of MGH-NEJM 287:1291
1972, 289:1039, 1973 Arterio-Venous Malformation of Cerebellum., , 1973

Dilantin
NEJM 289:808, Parlatore,A.A., 1973

Case Records of MGH-NEJM 289:628
1973 Necrotizing Giant Cell Arteritis., , 1973

Neonatal Seizures
NEJM 289:413, Volpe,J., 1973

Leigh's Syndrome:The Adult Form of Subacute Necrotizing Encephalomyelopathy with Predilection for the Brainstem
Neurol 23:1030, Sipe,J.C., 1973

Hypoparathyroidism
Hospital Physician p. 62 July 1973., , 1973

Organic Disease Presenting as a Psychiatric Syndrome
Postgrad Med 54:78, , 1973

Neonatal Hypoglycemia
NEJM 289:790, Senior,B., 1973

Narcolepsy
NEJM 288:1156, Zarcone,V., 1973

Cerebral & Pontine Myelinolysis
J Neurol Sci 18:399, Finlayson,M.H.,et al, 1973

Checking Compliance of Epileptic Patients
NEJM 287:934, Livingston,S., 1972

Neurological Problems in Endocrine Diseases
Med Clin North Am 56:1029, Dale,A., 1972

Progressive Neurological Deficits in Primary Polycythaemia
BMJ 216, 1972 Jan., Kremer,M.,et al, 1972

Acute Quadriparesis with Muscle Spasms Related to Electrolyte Disturbances in Steatorrhea
Am J Med 52:849-856, Coers,C.,et al, 1972

Glutamic Oxalacetic Transaminase, Lactic Dehydrogenase, & Creatine Phosphokinase Content in CSF
Clevel Clinic Quarterly 38:113, Culebras,F.A., 1971

Pancreatic Encephalopathy
JNNP 34:357-361, Sharf,B.,et al, 1971

Early Recognition of Heterozygotes for the Gene for Dystrophia Myotonica
JNNP 33:279, Bundey,S.,et al, 1970

Monoamine Oxidase Inhibitor & L-Dopa
BMJ 3:388, Hunter,H.R.,et al, 1970

Neuralgic Amyotrophy
Handbook of Clinical Neurology 8:77, 1970 Ed by Vinken & Bruyn Chp 4., Gathier,J.,et al, 1970

Creatine Phosphokinase Content in Cerebrospinal Fluid (Findings in M. S. )
Cleveland Clin Quart 36:47, Culebras,A., 1969

Case Records of MGH
NEJM 280:1009, 1969 Systemic Lupus Erythematosus with Necrotizing Angiitis., , 1969

Subacute Necrotizing Encephalopathy in Late Adolescence
Arch Neurol 18:478, Hardman,J.M.,et al, 1968

Ataxia In Childhood
Dev Med Child Neurol 10:388-389, Wilson,J., 1968

Showing articles 950 to 1000 of 1009 << Previous Next >>