Neudle.com: DNA linkage

Differential
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acoustic neurinoma

acoustic neurinoma, bilateral

acquired immunodeficiency syndrome

adrenoleukodystrophy

adrenomyeloneuropathy

advances in neurology

adverse drug reaction

Alzheimer's disease, diagnosis of

Alzheimer's disease, early onset

Alzheimer's disease, familial

amniocentesis

amyloid angiopathy, cerebral

amyloid angiopathy, hereditary cystatin C

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, familial

apraxia of eye movements

arteriopathy

ataxia

ataxia telangiectasia

ataxia, cerebellar

ataxia, hereditary

ataxia, truncal

attention deficit disorder with hyperactivity

autonomic dysfunction

basal ganglia, degeneration

basal ganglia, lesion of

Bassen-Kornzweig syndrome

benign familial neonatal convulsions

brachial neuritis

brachial plexus neuropathy

brachial plexus neuropathy, familial

brain biopsy

brainstem, lesion of

brainstem, neoplasms of

bulbar palsy, progressive

cafe au lait spots

carcinoembryonic antigen

carcinoma

carcinoma of pancreas

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar degeneration

cerebellar lesion

cerebellum, neoplasms of

cerebral atherosclerosis

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy

cerebral infarction

cerebral infarction, subcortical

cerebral ischemia

cerebro hepato renal syndrome

cerebrovascular accident

cerebrovascular accident, familial occurrence

cerebrovascular accident, young adult

Charcot-Marie-Tooth

chorea

choreoathetosis

choreoathetosis, paroxysmal

chromosomal abnormality

clubfoot as related to neurologic disease

Cockayne's syndrome

coma

compression neuropathy

compression neuropathy, recurrent

cost effectiveness

creatine phosphokinase(CPK)elevated

Creutzfeldt-Jakob disease, genetic

cryptococcal meningitis

cyst, neoplastic cerebellum

cytomegalovirus infection

degenerative diseases of CNS

dementia

dementia, familial

dementia, presenile

dementia, rapidly progressive

dementia, transmissible

dentate nuclei

dentate nuclei, lesion of

developmental retardation

diabetes mellitus

DNA probes

drooling

drug induced neurologic disorders

dysarthria

dysmorphic

dystonia

dystonia musculorum deformens

electronystagmography

electroretinograph

encephalitis

encephalitis, focal

encephalitis, Rasmussen's

encephalitis, viral

enzyme, muscle disease

epidemiology of neurology

ethics in neurology

eye movement, disorders of

face, elongated

facial appearance, abnormal

familial

fasciculation

fatal familial insomnia

fragile-X syndrome

Friedreich's ataxia

fundus, abnormality of

gadolinium

gait disorder

gaze palsy

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

Gerstmann-Straussler-Scheinker disease

GFAP gene

gonadotropin-releasing hormone

growth retardation

gynecomastia

Hallervorden Spatz disease

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

Huntington's chorea, genetic counselling

Huntington's chorea, presymptomatic detection of

hyperactivity

hyperekplexia

hyperhidrosis

hyperkalemic periodic paralysis

immunoperoxidase staining

immunosuppression

in situ hybridization

inclusion bodies, intracytopasmic

insomnia

intracerebral hemorrhage

intracerebral hemorrhage, familial

intracerebral hemorrhage, young adult

Jakob-Creutzfeldt disease

joint hypermobility

Kallmann's syndrome

Kearns-Sayre syndrome

KRIT1 gene

Kugelberg-Welander syndrome

Laurence-Moon-Bardet-Biedl syndrome

malformation, vascular

malformation, vascular, cerebral

malformation, vascular, familial

malignant hyperpyrexia

manic-depressive

medulla oblongata

medulla oblongata, atrophy

medulla oblongata, lesion of

meningitis

meningitis, recurrent

meningitis, relapse

mental retardation

mental retardation, familial

mononeuropathy, recurrent

mortality

motor neuron disease

movement disorder

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, contrast enhanced

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

mucopolysaccharidoses

mucopolysacchariduria

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, familial

multiple sclerosis, misdiagnosis

multiple system atrophy

muscular dystrophy, Becker

muscular dystrophy, differential diagnosis of

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, Duchenne, neonatal screening

muscular dystrophy, Duchenne, presymptomatic detection

muscular dystrophy, female occurrence of

muscular dystrophy, limb-girdle

myelin basic protein gene

myoclonus

myopathy

myopathy, mitochondrial

neonatal screening, genetic neurologic disorders

neoplasm, metastatic to CNS

neoplasm, posterior fossa

neoplasm, primary intracranial

neoplasm, primary of CNS

neurocutaneous disease

neurofibromatosis 2, presymptomatic

neurologic disease

neurologic disease, diagnoses of

neuronal ceroid-lipofuscinosis

neuronal migration disorder

neuropathology

neuropathology, brain

neuropathy

neuropathy, amyloid

neuropathy, hereditary peripheral

neuropathy, peripheral

night blindness

Notch3 gene

ocular motility, disorders of

oculopharyngeal muscular dystrophy

paraparesis, familial spastic

paraparesis, spastic

paroxysmal dystonic choreoathetosis

paroxysmal neurologic deficits

pathology

patient information and support

periodic paralysis

peroxisomal disease

pheochromocytoma

pigmentary retinopathy

polycystic kidneys

polymerase chain reaction

polyneuropathy, familial

posterior fossa, lesion of

practice guidelines

prenatal diagnosis by amniocentesis

prion disease

progeria

prognosis

progressive multifocal leucoencephalopathy

progressive spinal muscular atrophy

proximal myotonic myopathy

radiation hypersensitivity

seizure, intractable, treatment of

seizure, neonatal

sensorineural hearing loss

simian crease

skin, lesions in neurologic disorders

skull x-ray, abnormal

sleep pathology and physiology

small vessel disease

Southern immunoblot test

spasticity

spinal cord

spinal cord, lesion of

spinal cord, neoplasm

spinal muscular atrophy

spine, metastasis to

spinocerebellar ataxia

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar degeneration

spondylosis

spongy degeneration of brain

startle reaction

stuporous

subarachnoid hemorrhage

synkinesis

tapetoretinal degeneration

telangiectases

testicular enlargement

thalamus, lesion of

tinnitus

tomaculous neuropathy

trauma

treatment of neurologic disorder

trinucleotide repeats

Usher's syndrome

ventricular garlands

vibratory sensation, abnormal

Von Hippel Lindau, carrier

Von Hippel Lindau, screening protocol for

walking, difficulty with

Werdnig-Hoffman disease

Western immunoblot test

wheelchair

white matter disease

X-linked bulbospinal neuronopathy

x-linked mental retardation

X-linked neuropathy

Showing articles 150 to 175 of 175 << Previous

Progressive Multifocal Leukoencephalopathy:Failure of Cytarabine Therapy
Neurol 32:200-203, Smith,C.R.,et al, 1982

Duration of Vidarabine Therapy in Biopsy-Negative Herpes Simplex Encephalitis
JAMA 247:332-334, Landry,M.L.,et al, 1982

Repeated Suppression Of Creutzfeldt-Jakob Disease With Vidarabine
Jr. , et al, Lancet 2:564-56582., Furlow,T.W., 1982

Acyclovir
BMJ 285:1223-1224, Timbury,M.C., 1982

Herpes-zoster Myelitis Treated Successfully with Vidarabine
BMJ 283:698-699, Corston,R.N.,et al, 1981

Herpes Simplex Encephalitis
NEJM 304:313-318, Whitley,R.J.,et al, 1981

Fatal Vidarabine Toxicity in a Patient With Normal Renal Function
JAMA 246:1703-1705, VanEtta,L.,et al, 1981

Antiviral Agents, (First of Two Parts, )
NEJM 302:903-907, Hirsch,M.S.,et al, 1980

Progressive Multifocal Leukoencephalopathy
Arch Neurol 37:497-501, Boudewijn,A.C.,et al, 1980

The Decision to Biopsy, Treat, or Wait in Suspected Herpes Encephalitis
Ann Int Med 92:641-649, Barza,M.,et al, 1980

Brain Biopsy in Herpes Simplex Encephalitis
NEJM 303:700-701, Caplan,L.R., 1980

Herpes Simplex Encephalitis:Need for Accurate Diagnosis
JAMA 244:371-372, Whitley,R.J.,et al, 1980

The Clinical Management of Suspected Herpes Virus Encephalitis
Am J Med 69:895-902, Braun,P., 1980

Post-Infectious Encephalomyelitis After Successful Treatment of Herpes Simplex Encephalitis with Adenine Arabinoside
NEJM 300:1089-1093, Koenig,H.,et al, 1979

Clinical Pathological Conference
Herpes Simplex Encephalitis, Case Record 44-1979, NEJM 301:987-994979., , 1979

Deoxyribonucleic Acid Determination in Human Cerebrospinal Fluid
Ann Neurol 2:357, Weisz,R.,et al, 1977

Adenine Arabinoside Therapy of Biopsy-proved Herpes Simplex Encephalitis
NEJM 297:289, Whitley,R.J.,et al, 1977

Herpes Simplex Encephalitis Treated with Vidarbine (Adenine Arabinoside)
Arch Neurol 34:608, Taber,L.H.,et al, 1977

Central Nervous System Involvement in SLE
Arth & Rheum 20:869977., Small,P.,et al, 1977

Herpes Simplex & the Human Nervous System
Milit Med 140:765, Finelli,P.F., 1975

Neuropathy Due to Cytosine Arabinoside
BMJ 2:652-653, Russell,J.A.,et al, 1974

IUDR:Given Intraventricularly in the Treatment of PML
Cancer Chemoter Repts 57:73, Tarsy,D.,et al, 1973

Chemotherapy of Viral Infections
NEJM 289:725, Weinstein,J., 1973

Idoxuridine in Herpes Simplex Virus (Type 1) Encephalitis
Ann Int Med 78:243-246, Nolan,D.C.,et al, 1973

Cytosine Arabinoside Versus Virus or Man
NEJM 289:912, Karchmer,A.W., 1973

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

Showing articles 150 to 175 of 175 << Previous