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Differential
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abstract reasoning

abulia

accommodation

accomodation, abnormal

aciduria

acquired immunodeficiency syndrome

acrocyanosis

acute cerebellar ataxia

addiction, heroin

addiction, heroin-neurologic complications with

Addison's disease

Adies pupil

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adult polyglucosan body disease

adult-onset leukodystrophy, with neuroaxonal spheroids

advances in neurology

affect, flat

affect, inappropriate

Aicardi-Goutieres syndrome

akinetic mute

alcohol

alcohol intolerance

alcohol, neurologic complications with

alternating hemiplegia

alternating rapid movement

alternating rapid movement, impaired

aluminum

Alzheimer's disease

Alzheimer's disease, diagnosis of

Alzheimer's disease, preclinical

Alzheimer's disease, visual variant

aminoacidurias

amnesia

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

angiography, cerebral

antibiotics, neurologic complications with

anticholinergic drugs

aphasia

aphasia, children

aphasia, progressive

aphasia, progressive, primary

aphasia, transcortical

aphasia, transcortical-sensory

aphonia

apraxia

apraxia of eye movements

arthrogryposis multiplex

ataxia telangiectasia

attention deficit disorder with hyperactivity

attention span

atypical

auditory processing, impaired

autism

autoantibodies

automobile accidents

autonomic dysfunction

autonomic nervous system

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

Benedict's solution test

bone marrow transplantation

brainstem, infarction of

bulbar palsy, progressive

burning feet

burning feet, differential diagnosis of

cafe au lait spots

CAG repeats

calcification, intracranial

carbon monoxide poisoning

carcinoembryonic antigen

carotid artery occlusion, bilateral

carotid artery occlusion, intracranial

carotid artery occlusion, neck

carotid siphon

carotid-siphon occlusion

carpo-pedal spasm

CAT scan

CAT scan, abnormal

CAT scan, angiography

CAT scan, angiography, false negative

CAT scan, chest

CAT scan, emission

CAT scan, emission, abnormal

caudate nucleus, infarction

caudate nucleus, lesion of, bilateral

central hypoventilation

central nervous system, infection of

central pontine myelinolysis

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar cognitive affective syndrome

cerebellar degeneration

cerebellar disease, eye movement disorder in

cerebellar hypoplasia

cerebellum, disease of

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral dominance

cerebral infarction

cerebral infarction, small, deep

cerebral infarction, subcortical

cerebral palsy

cerebral palsy, associated problems with

cerebral palsy, pure ataxic

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, enzymes in

cerebrospinal fluid, gammaglobulin of

cerebrovascular accident

cerebrovascular accident, bilateral

cerebrovascular accident, complications with

cerebrovascular accident, familial occurrence

cerebrovascular accident, multiple

cerebrovascular accident, recurrent

cerebrovascular accident, silent

cerebrovascular disease

ceruloplasmin, serum

chasing the dragon

chelation therapy

chemotherapy, CNS treatment and complications with

chest x-ray, abnormal

chilbran skin lesions

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

comprehension, impaired

confusion

congenital bilateral perisylvian syndrome

congenital infection, CNS

congenital malformation

congenital myasthenic syndromes

controversies in neurology

convergence

convergence, impaired

copper

copper metabolism, abnormal

corpus callosum, hypoplastic

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cortical-basal ganglionic degeneration

cranial nerve palsies

cranial nerve palsies, bilateral

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

Creutzfeldt-Jakob disease, genetic

crying

crying, pathologic

cryptococcal antigen

cryptococcal meningitis

cultured skin fibroblasts

cyanosis

cytomegalic inclusion disease

cytomegalovirus infection

degenerative diseases of CNS

dementia, age at onset

dementia, childhood

dementia, differential diagnosis of

dementia, familial

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, subcortical

dementia, thalamic

dementia, transmissible

demyelinating disease

denervation of muscle

denervation potentials

dentate nuclei

dentate nuclei, lesion of

depression

dermatitis

developmental abnormality of brain

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

differential diagnosis

difficulty climbing stairs

dinitrophenylhydrazine(D.N.P.H.)reaction

diplegia, atonic

diplegia, spastic cerebral

diplopia

disability rating scale, neurological

disability, neurological

disease modifying agents

disorientation

distal muscle weakness

drug abuse, inhalation

drug abuse, neurologic complications of

drug induced neurologic disorders

dural arteriovenous malformation

dying

dysarthria

dysdiadochokinesia

dysequilibrium syndrome

dyskinesia, buccal lingual facial

ears of the Lynx MR sign

echolalia

edema, pedal

electroencephalogram

electroencephalogram, abnormalities of

electromyogram

electron microscopy

electrophoretic pattern, CSF

emotional lability

encephalitis

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, viral

encephalomalacia

encephalomyelitis, postinfectious

encephalopathy

encephalopathy, delayed

encephalopathy, metabolic

enzyme, defect

epilepsia partialis continua

executive dysfunction

exome sequencing

eye movement, disorders of

face, inexpressive

face, numbness of

facial appearance, abnormal

facial expression abnormality

facial weakness

facial weakness, bilateral

fetal alcohol syndrome

fetus

fever

fine motor function, impaired

finger nose finger test

fingerprint bodies

fish

Fisher C.M.

fistula, arterio-venous, dural

fluency

fluorescene in situ hybridization

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

frataxin

Friedreich's ataxia

frontal lobe, atrophy

frontal lobe, behavior with disease of

frontal lobe, pathologic signs of

frontotemporal dementia, behavioral variant

fucosidosis

fungal infection

fungal infection, CNS

gag reflex, depressed

gammaglobulin therapy, intravenous

gastroenteritis

gaze palsy

gaze palsy, horizontal

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

Gerstmann-Straussler-Scheinker disease

glabellar sign

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glossitis

glycogen storage disease

GM1 ganglioside antibodies

Gowers maneuver

grandiosity

granular osmiphilic material

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

hallucination

hallucination, visual

headache, intermittent

headache, intractable

headache, severe

headache, sudden onset of

headache, vascular

hearing loss

hearing problems in children

heel-knee-shin test

hemianopia, homonymous

hemiballismus

hemifacial spasm

hemiparesis

hemiparesis, transient

hemorrhage, thalamic

hepatic encephalopathy

hepatic failure

hepatitis

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

hepatolenticular degeneration(Wilson's disease), screening for

hepatomegaly

hepatosplenomegaly

heralding manifestation

human immunodeficiency virus type 1

Huntington's chorea

hydrocephalus

hydroxyglutaric aciduria

hyperactivity

hyperkalemia

hyperlipoproteinemia

hyperpigmentation of skin

hyperpyrexia, CNS disorder causing

hypopigmentation of skin

hyposmia

hypotension, systemic

hypothyroidism

hypothyroidism, congenital

inborn errors of metabolism

incarceration

inclusion bodies

inclusion bodies, intracytopasmic

incontinence, fecal

incoordination

infection, recurrent

infectious mononucleosis

infectious mononucleosis, neurologic findings with

infertility

inflexibility, mental

intellectual deficit, treatable causes of

intellectual deterioration

intelligence quotient

interferon alpha

internal capsule

internuclear ophthalmoplegia

intracranial pressure, increased

intrauterine

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, variant

Kayser-Fleischer ring

kinesia paradoxica

klippel feil syndrome

language development, neurologic basis of

language disorder in adults

language disorders in children

learning disability, in children

left-right orientation

leg dragging

leg weakness, bilateral

leg weakness, unilateral

Leigh's disease

lenticular nucleus, lesion of, bilateral

leukemia

leukocyte alkaline phosphotase

leukocytosis

leukodystrophy

leukoencephalopathy

leukoencephalopathy, toxic

lipid storage disorder of CNS

Lisch nodules

listeria monocytogenes

listeriosis, CNS

lithium

liver disease

liver function enzymes

liver transplantation

lumbar puncture, complications of

lymphoma

lymphoma involving CNS

lymphoma, primary of CNS

lysosomal storage disease

macrocephaly

macrognathia

magnetic source image

magnetoencephalography

malformation, CNS, congenital

mania

maple syrup urine disease

marche a petits pas

masked facies

masseter muscle wasting

mediastinum, mass of

megalencephaly

megalencephaly, idiopathic

memory, defect of recent

memory, impairment of

meningeal enhancement

meningeal enhancement, nodular

meningismus

meningitis

meningitis, fungal

meningitis, neutrophilic

meningitis, neutrophilic, persistent

mental retardation

mental status, abnormal

mesial temporal lobe

mestinon

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, juvenile

microangiopathy, brain

microangiopathy, retina

microcephaly

micrographia

microhemorrhage, intracerebral

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

midline defect in children

mitochondrial disease

molecular genetics

monoclonal gammopathy

monoparesis

Montreal cognitive assessment

movement disorder, extrapyramidal

MRI, angiography, false negative

MRI, contrast enhanced

MRI, diffusion weighted

MRI, eye of tiger sign

MRI, nodular enhancement

MRI, paramagnetic effect

MRI, punctate pattern

multiple sclerosis, differential diagnosis of

multiple sclerosis, familial

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle atrophy, progressive

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, central nervous system abnormality

muscular dystrophy, Duchenne

mutism

myasthenia gravis

myasthenia gravis, congenital

myasthenia gravis, familial incidence of

myoclonus, stimulus sensitive

myoglobinuria

myxedema, neurologic manifestations of

nasal speech

nausea and vomiting

neck weakness

neoplasm, primary of CNS

neoplasm, primary of CNS-treatment of

neoplastic angioendotheliosis

nerve biopsy

nerve conduction studies

neurocutaneous disease

neuroendocrinology

neurofibrillary degeneration

neurofibroma

neurofibromatosis 1

neurogenic bladder

neurologic complications

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic examination, focal

neurologic examination, non-focal

neurologic signs

neurologic symptoms

neurologic testing

neuromuscular junction

neuronal ceroid-lipofuscinosis

neuronopathy

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuroprotective agents

neurosyphilis

neurotoxic

neurotoxin

next-generation sequencing

ocular motility, disorders of

old age, neurology of

opened mouth

operculum syndrome

operculum syndrome, bilateral

ophthalmoplegia

opsoclonus

optic atrophy

optokinetic nystagmus, abnormal

oral ulcerations

otitis, neurologic complications with

ovarian insufficiency

pain, increased response

palatal myoclonus

palatopharyngeal incompetence

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

paraphasias

paraplegia

paraplegia, in flexion

parasomnia

paresthesias

Parkinson disease

Parkinson disease, diagnosis

Parkinson disease, freezing phenomena in

Parkinson disease, pathogenesis of

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinsonism syndrome

PAS positive

PAS positive material in the brain

peripheral blood smear

peripheral blood smear, abnormal

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

pneumoencephalogram(PEG)

polycythemia, primary

polyglucosan body

polyglucosan body disease

polymicrogyria

polyneuropathy

polyneuropathy, uremic

pons, infarction of

post infectious cerebellar ataxia

posterior cortical atrophy

postinfectious

postural abnormality

preclinical

pregnancy, neurologic complications in

prenatal

prevention of neurologic disorders

primary lateral sclerosis

progressive multifocal leucoencephalopathy

progressive myoclonic epilepsy

progressive neurologic disorder

progressive supranuclear palsy

protein 14-3-3, cerebrospinal fluid

pruritus

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychological testing, neurologic problems

psychomotor retardation

pursuit eye movements, abnormal

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

quadriparesis

quadriplegia

radiation hypersensitivity

radiculopathy

rapidly progressing neurologic illness

real-time quaking-induced conversion

Red flags

rehabilitation for neurologic disorders

release phenomena

remote effect of cancer on the nervous system

renal failure

renal stones

renal transplantation

ReNU syndrome

repetition, impaired

respirations in CNS disease

respirator

respiratory failure

restless leg syndrome

reticulum cell sarcoma

retina, abnormal

retinal branch artery occlusion

rubella encephalitis, progressive

rubella syndrome

rubella virus

saccadic eye movements, abnormal

salivation, excessive

seizure, advice to parents and teachers regarding

seizure, focus

seizure, laughing as manifestation

seizure, psychosocial aspects of

seizure, recurrent

seizure, surgical treatment of

seizure, treatment of

seizure, workup of

semantic dementia

sensorineural hearing loss

serologic testing

serologic testing of cerebrospinal fluid

short stature

sign language

sinemet

single photon emission computed tomography

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skew deviation

skin, biopsy

skin, lesions in neurologic disorders

sleep

sleep apnea, obstructive

sleep pathology and physiology

slit lamp examination

slow virus infection of CNS

spastic paraplegia, type 11

spasticity

speech disorder

speech disorder, childhood

speech disorder, non aphasic

speech lateralization

speech therapy

speech, absence of

speech, delayed development of

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 7

spinopontine atrophy, dominant

splenium of corpus callosum

splenomegaly

spongy degeneration of brain

stem cell transplantation

stereotyped behavior

stooped posture

striopallidodentate calcifications, familial idiopathic

stuporous

stuttering

stuttering following CVA

symmetric brain lesions

syphilis, diagnosis and treatment

syphilis, neurologic complications with

temporal lobe, atrophy

temporal lobe, lesion

temporal lobe, lesion, bilateral

term infant

testicular enlargement

tetany

thalamus, lesion of

thalamus, lesion of-bilateral

third nerve palsy

third nerve palsy, bilateral

tongue, fasciculations of

tongue, impaired movements of

tongue, protrusion of

tongue, ulcer

tonic spasms

toxoplasmosis, acquired

toxoplasmosis, CNS

treatment of neurologic disorder

trientine dihydrochloride

trinucleotide repeats

uremic encephalopathy

uremic twitching

urinary incontinence

urine test for metabolic disorders

urine, dark

vasculopathy

vegetarianism

Venereal Disease Research Laboratory test

venous hypertension

venous ischemia

very long chain fatty acids

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visual impairment

visual loss

visual loss, progressive

visual loss, slow

visuospatial disturbance

vitamin deficiency

vitamin supplementation

vocal cord paralysis

voice, abnormality of

Waldenstrom's macroglobulinemia

walking frame

walking, difficulty with

weakness

weakness, fatiguable

weakness, generalized

weakness, progressive

weakness, proximal

weight loss

Wernicke's aphasia

Wernicke's encephalopathy

wheelchair

Whipple's disease

white matter disease

whole genome sequencing

wide based gait

Wolfram syndrome

word-finding difficulty

work loss

workup

writing

x-linked intellectual deficit

x-linked mental retardation

zinc

Showing articles 1950 to 2000 of 3235 << Previous Next >>

Advances in Molecular Analysis of Fragile X Syndrome
552, Warren,W.T.&Nelson,D.L.JAMA 271:536-553, 1994

Acute Pseudobulbar Mutism with Good Functional Recovery
Neurol 44:176-177, Chesser,M.Z.,et al, 1994

Assessment:Melodic Intonation Therapy
Report Therap/Tech Assess Sub AAN, Neurol 44:566-5681994., , 1994

Cerebrotendinous Xanthomatosis:Molecular Diagnosis Enables Presymptomatic Detection of a Treatable Disease
Neurol 44:288-290, Meiner,V.,et al, 1994

Familial Sneddon's Syndrome:Clinical, Hematologic, and Radiographic Findings in Two Brothers
Neurol 44:399-405, Pettee,A.D.,et al, 1994

The Value of Diagnostic Information to Patients with Suspected Multiple Sclerosis
Arch Neurol 51:67-72, Mushlin,A.I.,et al, 1994

Effect of Diagnostic Testing for Multiple Sclerosis on Patient Health Perceptions
Arch Neurol 51:46-51, O'Connor,P.,et al, 1994

Diagnostic Value of SPECT with Tc 99m HMPAO in Alzheimer's Disease:A Population-Based Study
Neurol 44:454-461, Claus,J.J.,et al, 1994

Are Multiple Cerebral Infarcts Synergistic?
Arch Neurol 51:211-215, Wolfe,N.,et al, 1994

Cross-National Interrater Agreement on the Clinical Diagnostic Criteria for Dementia
Neurol 44:239-242, Baldereschi,M.,et al, 1994

Prevalence of Dementia in Old Age:Clinical Diagnosis in Subjects Aged 95 Years and Older
Neurol 44:250-253, Wernicke,T.F.&Reischies,F.M., 1994

Effects of Diets High in Sucrose or Aspartame on the Behavior and Cognitive Performance of Children
NEJM 330:301-307, 3551994., Wolraich,M.L.,et al, 1994

Serial Neurologic Examinations After Near Drowning and Outcome
Arch Pediatr Adolesc Med 148:167-170, Bratton,S.L.,et al, 1994

Clinical Genetics in Neurological Disease
JNNP 57:7-15, MacMillan,J.C.&Harper,P.S., 1994

Posttraumatic Headache
Semin Neurol 14:40-45, Packard,R.C., 1994

Mild Head Injury
(Ed) , Semin Neurol 14:1-9294., Packard,R.C., 1994

Longitudinal MRI in Multiple Sclerosis:Correlation Between Disability and Lesion Burden
Neurol 44:2120-2124, Khoury,S.J.,et al, 1994

Brain Single-Photon Emission Computed Tomography
Neurol 44:1970-1977, Masdeu,J.C.,et al, 1994

Electroencephalography
JNNP 57:1308-1319, Binnie,C.D.&Prior,P.F., 1994

Neurological Differences Between 9-Year-Old Children Fed Breast-Milk or Formula-Milk as Babies
Lancet 344:1319-1322, Lanting,C.I.,et al, 1994

Myotonic Dystrophy
In Myology, Engel & Franzini-Armstrong, McGraw-Hill, Inc, New York V2, Ch 43, P1192, Harper,P.S.&Rudel,R., 1994

Clinical Features of Myasthenia Gravis
Neurol Clin N Am 12:243-261, Hopkins,L.C., 1994

The Cerebellum Contributes to Linguistic Production: A Case of Agrammatic Speech Following a Right Cerebellar Lesion
Neurol 44:2047-2050, Silveri,M.C.,et al, 1994

Molecular Genetics in Neurology
Ann Neurol 34:757-773, Martin,J.B., 1993

Dementia in AIDS Patients:Incidence and Risk Factors
Neurol 43:2245-2252, McArthur,J.C.,et al, 1993

Neurophychological Effects of Stroke in Children with Sickle Cell Anemia
J Pediatr 123:712-717, Craft,S.,et al, 1993

The Neurologic Syndrome of Vitamin E Deficiency:A Significant Cause of Ataxia
Neurol 43:2167-2169, Kayden,H.J., 1993

A 10-Year Experience with Postpump Chorea
Ann Neurol 34:820-826, Medlock,M.D.,et al, 1993

Driving and Alzheimer's Disease:The Risk of Crashes
Neurol 43:2448-2456, Drachman,D.A.,et al, 1993

End-State Alzheimer's Disease:Glasgow Coma Scale and the Neurologic Examination
Arch Neurol 50:1309-1315, Benesch,C.G.,et al, 1993

Clinicopath Conf
progressive Supranuclear Palsy, Case 46-1993, NEJM 329:1560-1567993., , 1993

Spinal Cord MRI Using Multi-Array Coils and Fast Spin Echo, II. Findings in Multiple Sclerosis
Neurol 43:2632-2637, Kidd,D.,et al, 1993

Alzheimer's Disease
BMJ 307:779-782, Rossor,M., 1993

Apathy Following Cerebrovascular Lesions
Stroke 24:1625-1630, Starkstein,S.E.,et al, 1993

Cranial Nerve Palsies in Spontaneous Carotid Artery Dissection
JNNP 56:1191-1199, Sturzenegger,M.&Huber,P., 1993

The Clinical Spectrum of Cerebral Amyloid Angiopathy:Presentations Without Lobar Hemorrhage
Neurol 43:2073-2079, Greengerg,S.M.,et al, 1993

Molecular Genetic Advances in Fragile X Syndrome
J Pediatr 122:169-185, Tarleton,J.C.&Saul,R.A., 1993

Alternating Hemiplegia of Childhood:A Study of 10 Pts & Results of Flunarizine Treatment
Neurol 43:36-41, Silver,K.&Andermann,F., 1993

Aseptic Meningitis in Infants Younger Than 2 Years of Age:Acute Illness and Neurologic Complciations
Pediatrics 92:206-211, Rorabaugh,M.L.,et al, 1993

Cerebral Abnormalities in Myotonic Dystrophy
Arch Neurol 50:917-923, Chang,L.,et al, 1993

Mitochondrial Encephalomyopathy, Lactic Acidosis, Stroke-Like Episodes (MELAS) :Clinical, Radiological, Pathol & Genetic Observ
Ann Neurol 34:25-31, Koo,B.,et al, 1993

Neurocognitive Dysfunction in the Eosinophilia-Myalgia Syndrome
Neurol 43:931-936, Krupp,L.B.,et al, 1993

Single-Photon Emission Computed Tomographic Investigation of Patients with Motor Neuron Disease
Neurol 43:1569-1573, Abe,K.,et al, 1993

Niemann-Pick Disease Type C:Diagnosis and Outcome in Children, with Particular Reference to Liver disease
J Pediatr 123:242-247, Kelly,D.A.,et al, 1993

Rapid Fragile X Carrier Screening and Prenatal Diagnosis Using a Nonradioactive PCR Test
JAMA 270:1569-1575, Brown,W.,et al, 1993

X-Chromosome Effects on Female Brain:A Magnetic Resonance Imaging Study of Turner's Syndrome
Lancet 342:1197-1200, Murphy,D.G.M.,et al, 1993

Choroido-Cerebral Calcification Syndrome with Retardation
Neurol 43:2387-2389, Singh,B.,et al, 1993

Lissencephaly:A Human Brain Malformation Associated with Deletion of the LIS1 Gene Located at Chromosome 17p13
JAMA 270:2838-2842, Dobyns,W.B.,et al, 1993

Miller-Dieker Syndrome:Detection of a Cryptic Chromosome Translocation Using in Situ Hybridization in a Family
Am J Dis Child 147:1291-1294, Alvarado,M.,et al, 1993

Risk Factors for Nursing Home Placement in Advanced Parkinson's Disease
Neurol 43:2227-2229, Goetz,C.G.&Stebbins,G.T., 1993

Showing articles 1950 to 2000 of 3235 << Previous Next >>