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abdominal distention

acetylcholine receptor antibody

acid maltase deficiency

acid maltase deficiency, adult

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome, congenital

acquired immunodeficiency syndrome, infants and children

acute intermittant porphyria

adrenoleukodystrophy

adverse drug reaction

agenesis of corpus callosum

Aicardi-Goutieres syndrome

airway obstruction

alcohol, neurologic complications with

alpha glucosidase

alpha-fetoprotein

alternating hemiplegia

alternating hemiplegia of childhood

alveolar hypoventilation

amaurosis fugax, unilateral vs.bilateral

aminoacidopathies

aminoacylase 1 deficiency

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, differential diagnosis

aneurysm, aortic arch

Angelman syndrome

ankle, swelling of

anterior horn cell disease

antiviral agents

aortic arch stenosis

aortic arch study

apraxia of eye movements

aromatic amino acid decarboxylase deficiency

arrhythmia, cardiac

arterial dissection, aorta

arteritis, temporal

arthrogryposis multiplex

ascending paralysis

aspartate aminotransferase

ataxia telangiectasia

ataxia, cerebellar

ataxia, progressive

ataxia, truncal

athetosis, infant

attention deficit disorder with hyperactivity

auditory and vestibular pathways

autoimmune disease

autonomic dysfunction

axonal degeneration

B 12 deficiency

B 12 deficiency, infants

Babinski sign in new born

bacterial infection

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavior, combative

behavioral disorder

biologic markers

biopterin deficiency

biotin deficiency

biotin deficiency, acquired

biotin deficiency, juvenile form

biotinidase deficiency

bladder dysfunction

blindness, sudden

bone density, increased

bone marrow biopsy

bone marrow transplantation

botulinum toxin

botulism antitoxin

botulism immune globulin

botulism, infant

brainstem, atrophy

brainstem, lesion of

breech delivery

Brown-Vialetto-Van Laere syndrome

brucellosis, nervous system involvement with

bulbar palsy, childhood

calcification, intracranial

Canavan's disease

carcinoembryonic antigen

carcinoma of breast

cardiac surgery, hypothermia and circulatory arrest for

cardiac surgery, neurologic complications with

carnitine deficiency

carnitine deficiency myopathy

CAT scan, abnormal

CAT scan, angiography

CAT scan, chest

CAT scan, emission, abnormal

cataracts, congenital

cauda equina, enhancement

caudate nucleus, atrophy

caudate nucleus, lesion of

caudate nucleus, lesion of, bilateral

celiac disease, childhood

central core disease

central hypoventilation, congenital

central nervous system, infection of

cerebellar ataxia, autosomal recessive

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar disease, eye movement disorder in

cerebellar hypoplasia

cerebellar vermis

cerebral cortical atrophy

cerebral embolism

cerebral infarction

cerebral palsy, associated problems with

cerebral vasculature

cerebral venous thrombosis

cerebro hepato renal syndrome

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, glycine

cerebrospinal fluid, protein of

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, red cells in

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, infancy and childhood

cerebrovascular accident, intrauterine

cerebrovascular accident, neonatal

cerebrovascular accident, postpartum

ceruloplasmin, serum

cervical spine injury

chelation therapy

cherry red spot

chest x-ray, abnormal

chilbran skin lesions

chorea, Sydenham's

chorea, Sydenham's, recurrent

chorea, treatment of

choreoathetosis

chorioamnionitis

chorioretinitis

chromosomal abnormality

chronic progressive external ophthalmoplegia

cirrhosis, infancy

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

cobalamin C deficiency

Coffin-Siris syndrome

cognitive delay

cogwheel rigidty

cold hands sign

cold intolerance

collagen vascular disease

conduction block

congenital heart disease

congenital heart disease, CNS complications with

congenital infection, CNS

congenital infection, viral

congenital malformation

congenital myopathy

congenital myopathy, inflammatory

congestive heart failure

contactin associated protein like 2 antibodies

contractures, joint

conversion reaction

cornea, abnormal

cornea, opacification in infancy-causes of

cornea, opacity of

corpus callosum

corpus callosum, atrophy of

corpus callosum, hypoplastic

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cranial nerve enhancement

cranial neuropathy

cranial neuropathy, multiple

C-reactive protein

C-reactive protein, elevated

creatine phosphokinase(CPK)elevated

crying, pathologic

cultured skin fibroblasts

cyst, parenchymal

cytochrome c oxidase

cytochrome c oxidase, deficiency

cytomegalic inclusion disease

cytomegalovirus infection

cytomegalovirus infection, congenital

Dandy Walker malformation

dantrolene sodium

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

delayed dentition

delayed muscle relaxation

delivery, complicated

dementia, childhood

dementia, rapidly progressive

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

descending paralysis

developmental abnormality of brain

developmental disability

developmental evaluation

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes mellitus

diagnostic criteria

differential diagnosis

digits, abnormal

diphtheria-tetanus-pertussis immunization

disability, neurological

dislocated hip, congenital

distal muscle atrophy

distal muscle weakness

dropped head syndrome

dural arteriovenous malformation

dural sinus thrombosis

dysdiadochokinesia

dysferlinopathy

dysostosis multiplex

dystonia, children

eating disorder

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electron microscopy

embolism, paradoxical

emergencies, neurologic

emotional lability

encephalomyelitis

encephalopathy, acute

encephalopathy, anoxic

encephalopathy, neonatal

enzyme treatment

epidemiology of neurology

epileptic encephalopathy

evoked potentials

executive dysfunction

exome sequencing

eye movement, disorders of

facial anomalies

facial appearance, abnormal

facial expression abnormality

facial nerve palsy, bilateral

facial weakness

facial weakness, bilateral

failure to thrive

FARS2 deficiency

fatty acid, elevated plasma content

feeding disorder

fetal alcohol syndrome

fetal movements, reduced

fine motor function, impaired

fingernails, abnormal

fingernails, hypoplastic

fistula, arterio-venous, dural

fistula, arterio-venous, dural, spinal

food-borne infection

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

Friedreich's ataxia

fundus, abnormality of

gag reflex, depressed

gammaglobulin therapy, intravenous

gangliosidosis GM1

gangliosidosis GM2

gastrocnemius muscle weakness

genetic counselling

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

genital hypoplasia

globus pallidus, hemorrhage

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

GLUT1 deficiency syndrome

glutamic acid decarboxylase, antibody

gluten-free diet

glycogen storage disease

Gowers maneuver

growth hormone deficiency

growth retardation

Guillain Barre syndrome

head circumference

headache, bifrontal

headache, positional

health insurance

hemorrhagic diathesis

hepatolenticular degeneration(Wilson's disease)

hepatosplenomegaly

hexosaminidase-A

high arched feet

Hirschprung's disease

histochemistry of muscle

Horner's syndrome

Horner's syndrome, bilateral

Horner's syndrome, congenital

Hunter's syndrome

Huntington's chorea

Huntington's disease, children

hydrocephalus, communicating

hydrocephalus, congenital

hydrocephalus, exvacuo

hydroxyglutaric aciduria

hyperbilirubinemia

hyperglycinemia

hyperhomocysteinemia

hyperpyrexia, CNS disorder causing

hypertrophic cardiomyopathy

hypogammaglobulinemia

hypoglycorrhachia

hypomelanosis of Ito

hypomyelination

hypopigmentation of skin

hypotonia, causes of

hypotonia, infants

hypoxic encephalopathy

iatrogenic neurologic disorders

immunization, neurologic complications with

immunodeficiency

immunomodulation

immunosuppression

immunosuppressive agents

inability to stand on tiptoes

inappropriate antidiuretic(A.D.H.)hormone

inborn errors of metabolism

inclusion bodies

inclusion bodies, intracytopasmic

infant, evaluation of

infantile hemiplegia

infantile neuronal degeneration

infection, recurrent

intellectual deficit

intellectual deterioration

intelligence quotient

interferon alpha

intestinal biopsy

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

Isaacs syndrome

islet cell tumor

Jakob-Creutzfeldt disease

joint hypermobility

keratoconjunctivitis

kyphoscoliosis, neurologic causes of

lactic acidemia

leg spasms, painful

leg weakness, bilateral

Leigh's disease

lens, dislocation of

leukoencephalopathy

leukoencephalopathy, differential diagnosis

lid abnormalities

lid closure, weakness of

lipid storage disorder of CNS

listeria monocytogenes

liver function enzymes

Lowe's syndrome

lumbar puncture

lymphadenopathy

lysosomal storage disease

lysosomes, abnoral

malformation, CNS, congenital

malignant hyperpyrexia

mediastinum, mass of

memory, impairment of

meningitis, carcinomatous

meningitis, CSF cell count-normal

mental retardation

metabolic acidosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

methylene tetrahydrofolate reductase

methylenetetrahydrofolate reductase deficiency

methylmalonic acidemia

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine, seizures in

mitochondrial disease

mitral valve prolapse

molecular genetics

Morvan's fibrillary chorea

motor neuron disease

movement disorder

movement disorder, extrapyramidal

movement disorder, hyperkinetic

MRI, angiography

MRI, contrast enhanced

MRI, diffusion weighted

MRI, high signal foci on

MRI, hypointense signal foci on

MRI, spinal cord

MRI, susceptibility weighted

mucopolysaccharidoses

mucopolysacchariduria

multicore myopathy

multiminicore disease

multiple sclerosis

multiple sclerosis, diet in

multiple sclerosis, treatment of

multiple system atrophy

muscle atrophy, progressive

muscle atrophy, static

muscle diseases, characteristics of

muscle stiffness

muscle tenderness

muscle twitching

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscle weakness, sudden onset of

muscle-eye-brain disease

muscular dystrophy

muscular dystrophy, cardiovascular changes with

muscular dystrophy, central nervous system abnormality

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, congenital, Fukuyama type

muscular dystrophy, differential diagnosis of

muscular dystrophy, distal, Miyoshi

muscular dystrophy, LAMA2

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenia gravis, neonatal

myasthenic syndrome

myasthenic syndrome, treatment of

myoclonic jerks

myopathy, centronuclear

myopathy, mitochondrial

myopathy, necrotizing

myotonia congenita

myotonia dystrophica

nasal bridge, wide

nausea and vomiting

neonatal infection, viral

neonatal intensive care unit

neonatal screening, genetic neurologic disorders

nerve conduction studies

nerve conduction studies, motor

nerve root enhancement

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neurocutaneous disease

neuroendocrinology

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic evaluation

neurologic examination

neurologic signs

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction, abnormality of

neuromyotonia and axonal neuropathy

neuronal ceroid-lipofuscinosis

neuronal migration disorder

neuroophthalmology

neuropathology, brain

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, peripheral

neurophysiology

neurotoxicity, acute

neurotransmitter

newborn, evaluation of

next-generation sequencing

Niemann-Pick disease

Noonan Syndrome

numbness, extremity

nystagmus, monocular

nystagmus, periodic

obstetric neurologic injuries

ocular motility, disorders of

ocular myopathy

oculogyric crisis

old age, neurology of

ophthalmoplegia

ophthalmoplegia, plus syndrome

ophthalmoplegia, progressive external

optic atrophy, infants

optic nerve, hypoplasia of

optic neuropathy

optic neuropathy, ischemic

optic neuropathy, ischemic, anterior

ovarian insufficiency

palmomental response

paraparesis, familial spastic

paraparesis, spastic

paraspinal muscle weakness

parenteral alimentation

Parkinson disease

Parkinson disease, dystonia with

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

patient information and support

pectus excavatum

pediatric neurology

perineum, numbness of

periventricular leukomalacia

peroxisomal disease

personality change

pertussis immunization

phenylketonuria, variant form of

philtrum, tented

physical therapy

placenta, infection of

placenta, thrombosis of

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

poison, neurologic problems with

poliomyelitis vaccine

polycystic kidneys

polymerase chain reaction

polymyalgia rheumatica

polymyositis, infantile

polyneuropathy, chronic inflammatory demyelinating

Pompe's disease of glycogen storage

pons, lesion of

pontocerebellar atrophy

postoperative neurologic complications

postural abnormality

practice guidelines

Prader-Labhart-Willi syndrome

precipitating factors

pregnancy, neurologic complications in

premature infant

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

progressive neurologic disorder

psychiatric problems in neurologic disorders

psychomotor retardation

ptosis, bilateral

pulmonary stenosis

pupil, abnormality in neurologic disorders

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

quadriparesis, acute

radiation hypersensitivity

ragged-red fibers

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

rectal sphincter tone, decreased

Refsum's disease

remote effect of cancer on the nervous system

renal tubular acidosis

repetitive nerve stimulation

respirations in CNS disease

respiratory arrest

respiratory failure

respiratory tract infection

retinal degeneration

retinal dysplasia

Rett's syndrome

rheumatic fever

riboflavin transporter deficiency

rigid spine syndrome

rippling muscle disease

risus sardonicus

rubella vaccine

saccadic eye movements, abnormal

Schmidt syndrome

scoliosis, neurologic association with

sedimentation rate

sedimentation rate, elevated

segmental demyelination

seizure, children

seizure, injury following

seizure, neonatal

self-mutilation

semialdehyde dehydrogenase deficiency

sensorineural hearing loss

serum alanine aminotransferase

shoulder, pain in

skin, lesions in neurologic disorders

skull x-ray, abnormal

sleep pathology and physiology

small for dates infant, problems in

sodium valproate

sodium valproate, toxicity

spastic diplegia

speech disorder

speech disorder, childhood

speech, absence of

speech, delayed development of

spinal cord, enlargement

spinal cord, injury of

spinal cord, injury, New Born

spinal cord, intramedullary cyst of

spinal cord, lesion of

spinal cord, transection

spinal cord, vascular malformation of

spinal muscular atrophy

spinal muscular atrophy, classification

spinocerebellar ataxia

splenium of corpus callosum

spongy degeneration of brain

standing difficulty

startle reaction

status epilepticus

stereotyped behavior

steroid therapy, CNS treatment and complications with

stiff limb syndrome

stiff man syndrome

streptococcal infection

subdural effusion

sulfite oxidase deficiency

superior sagittal sinus thrombosis

sweating, abnormality of

symmetric brain lesions

syphilis, neurologic complications with

tandem gait, ataxic

Tay-Sachs disease

teeth, abnormal

teeth, number of in infants

temper tantrums

temporal artery, biopsy

temporal artery, tender

temporalis muscle wasting

testicular enlargement

tetrahydrobiopterin

thalamus, lesion of

thalamus, lesion of-bilateral

thiamine deficiency

thrombocytopenia

tone, muscle, increased

tongue, enlarged

tongue, fasciculations of

tongue, protrusion of

tongue, weakness

toxic encephalopathy

toxins, nervous system

toxoplasmosis, CNS

transient loss of muscle tone

transient neurologic deficit

transilumination of skull

treatment of neurologic disorder

tremor, cerebellar

tremor, intention

trichopoliodystrophy

trinucleotide repeats

ultrasonography

ultrasonography, head

ultrasonography, head, fetus-neonate

urinalysis, abnormal

urinary incontinence

urine test for metabolic disorders

vaccination, neurologic complications with

vertigo, cervical

vertigo, treatment of

viral infection, CNS

vision, failure of in childhood

visual evoked response

visual impairment

visual tracking

vitamin deficiency

vitamin E deficiency

vomiting, recurrent

Walker-Warburg syndrome

walking, difficulty with

weakness, acute

weakness, congenital

weakness, generalized

weakness, infant

weakness, progressive

weakness, proximal

Werdnig-Hoffman disease

Wernicke's encephalopathy

white matter disease

whole genome sequencing

wide based gait

x-linked intellectual deficit

x-linked mental retardation

Showing articles 700 to 750 of 6579 << Previous Next >>

Clinicopathological Conference
Angiitis of Central Nervous System, Case 35-1985, NEJM 313:566-575985., , 1985

Vascular Compression, Hemifacial Spasm, & Multiple Cranial Neuropathy
Neurol 35:712-716, Eidelman,B.H.,et al, 1985

Takayasu's Arteritis & Its Therapy
Ann Int Med 103:121-126, Shelhamer,J.H.,et al, 1985

Sarcoidosis & Its Neurological Manifestations
Arch Neurol 42:909-917, Stern,B.J.,et al, 1985

Mitochondrial Myopathies
Ann Neurol 17:521-538, DiMauro,S.,et al, 1985

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

Cysticercosis-Review of 230 Patients
Bull Clin Neurosci 50:76-101, McCormick.G.F., 1985

Alexander's Disease, A Disease of Astrocytes
Brain 108:367-385, Borrett,D.&Becker,L.E., 1985

Hearing Loss as an Initial Symptom of the Opsoclonus-Myoclonus Syndrome
Arch Neurol 41:998-999, Rosenberg,N.L., 1984

Graves'Disease Presenting with Bilateral Acute Painful Proptosis, Ptosis, Ophthalmoplegia, & Visual Loss
Lancet 2:431-433, Leonard,T.J.K.,et al, 1984

Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, & Strokelike Episodes:A Distinctive Clinical Syndrome
Ann Neurol 16:481-488, Pavlakis,S.G.,et al, 1984

Myasthenia Gravis & Myasthenic Syndromes
Ann Neurol 16:519-534, Engel,A.G., 1984

Transient Neurologic Dysfunction Following Moderate-Dose Methotrexate for Undifferentiated Lymphoma
Cancer 54:2003-2005, Martino,R.L.,et al, 1984

The Neurotoxicity of Antibacterial Agents
Ann Int Med 101:92-104, Snavely,S.R.,et al, 1984

Human Cytomegalovirus Infection & Disorders of the Nervous System
Jr. , Arch Neurol 41:310-320984., Bale,J.F., 1984

Clinicopathological Conference
Case 2-1984, Fabry's Disease, NEJM 310:106-114984., , 1984

Clinicopathological Conference
Maroteaux-Lamy Syndrome, Case 44-1983, NEJM 309:1109-1117983., , 1983

Chronic Progressive External Ophthalmoplegia (CPEO) :Clinical, Morphologic, & Biochemical Studies
Neurol 33:452-461, Mitsumoto,H.,et al, 1983

Neurodegenerative Disease of Infancy & Childhood
Ann Neurol 13:351-364, Dyken,P.,et al, 1983

Hyperekplexia
Arch Neurol 40:246-248, Kurczysnki,T.W., 1983

Adult Polyglucosan Body Disease:Clinical & Nerve Biopsy Findings in Two Cases
Ann Neurol 13:440-444, Vos,A.L.M.,et al, 1983

Thoracic Root Pain in Diabetes:The Spectrum of Clinical & Electromyographic Findings
Ann Neurol 11:80-85, Kikta,D.G.,et al, 1982

The Neuroleptic Malignant Syndrome
Arch Int Med 142:1183-1185, Smego,R.A.,et al, 1982

Cardiomyopathy Associated with the Syndrome of Amyotrophic Chorea & Acanthocytosis
Ann Int Med 96:616-617, Faillace,R.T.,et al, 1982

Fibrodysplasia Ossificans Progressiva, The Clinical Features & Natural Hx of 34 Pts
J Bone Joint Surg 64B:76-83, Connor,J.M.&Evans,D.A.P., 1982

Neurological Aspects of Thyroid Dysfunction
Mayo Clin Proc 56:504-512, Swanson,J.W.,et al, 1981

Progressive Infantile Poliodystrophy, Assoc. With Disturbed Pyruvate Oxidation in Muscle & Liver
Arch Neurol 38:767-772, Prick,M.J.J.,et al, 1981

Sural Nerve Biopsy in Systemic Necrotizing Vasculitis
Am J Med 71:525-532, Wees,S.J.,et al, 1981

Neuroleptic Malignant Syndrome:A Pathogenetic Role for Dopamine Receptor Blockage
Neurol 31:132-137, Henderson,V.W.,et al, 1981

Progressive Pontobulbar Palsy With Deafness
Arch Neurol 38:186-190, Brucher,J.M.,et al, 1981

Diabetic Thoracoabdominal Neuropathy:Clinical & Electrodiagnostic Features
Ann Neurol 9:75-79, Sun,S.F.,et al, 1981

Acute Carbamazepine Toxicity Resulting from Overdose
Neurol 31:621-624, Sullivan,J.B.,et al, 1981

Correlation of CT Scanning and Pathologic Features of Ophthalmic Graves'Disease
Ophthalmol 88:553-564, Trokel,S.L.&Jakobiec,F.A., 1981

Myotonic Dystrophy
In Harrison's Principles of Internal Medicine, 9th Ed, McGraw-Hill Book Co, NY 206180., Adams,R.D.,et al, 1980

Neurologic Manifestations in Macroglobulinemia
In Vinken PJ, Bruyn GW, Eds, Handbook of Clin Neurol, Vol 39, North-Holland Publ Co, p. 189, Abramsky,O., 1980

Neuroleptic Malignant Syndrome
Arch Neurol 37:462-463, Morris,H.H.,et al, 1980

Progressive Bulbar Paralysis Associated With Neurgl Deafness, A Nosological Entity
Arch Neurol 37:214-216, Alberica,R.,et al, 1980

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

Valproic Acid
NEJM 302:661-666, Brown,T.R., 1980

Motor Neuropathy Associated with Cimetidine
BMJ 281:974-975, Walls,T.J.,et al, 1980

Phencyclidine Abuse Mimicking Head Injury
JAMA 243:2323-2324, Corales,R.L.,et al, 1980

Cylindrical Spirals in a Familial Neuromuscular Disorder
Ann Neurol 7:550-556, Bove,K.E.,et al, 1980

Adult Polysaccharidosis
Arch Neurol 36:840-845, Peress,N.S.,et al, 1979

Lactic Acidemia, Mitochondrial Myopathy, & Basal Ganglia Calcification
Neurol 29:1057-1061, Markesbery,Wm.R., 1979

Cranial Neuropathy, Myeloradiculopathy, & Myositis, Complications of Mycoplasma Pneumoniae Infection
Arch Neurol 36:476-477, Rothstein,T.L.,et al, 1979

Benign Acute Childhood Myositis
Neurol 29:1068-1071, Henly,J.,et al, 1979

Primary Hyperparathyroidism Presenting as Fever of Unknown Origin with Unremitting Headache
Ann Int Med 91:575-576, Blair,D.C.,et al, 1979

Gyrate Atrophy of the Choroid & Retina with Hyperornithinemia:Tubular Aggreg. & Type 2 Fiber Atrophy
Neurol 29:966, Sipila,I.,et al, 1979

Clinical Pathological Conference
Foramen Magnum Meningioma, Case Record 29-1979, NEJM 301:147-154979., , 1979

Adult Type Neuronal Storage Disease with Neuraminidase Deficiency
Ann Neurol 6:232-244, Miyatake,T.,et al, 1979

Showing articles 700 to 750 of 6579 << Previous Next >>