Neudle.com: whole genome sequencing

Differential
(Click to cross reference)

acanthocytosis

adult polyglucosan body disease

adult-onset leukodystrophy, with neuroaxonal spheroids

alternating hemiplegia

alternating hemiplegia of childhood

amimia

ammonia

amyloid angiopathy, cerebral

amyloid angiopathy, cerebral, Dutch type

anterior tibial muscle weakness

antiviral agents

aphasia

areflexia

arthrogryposis multiplex

ataxic-dystonia syndromes

ATP1A3 gene

attention deficit disorder with hyperactivity

atypical

autonomic dysfunction

Babinski sign

basal ganglia, lesion, bilateral

calcification, intracranial

candida albicans

cardiomyopathy

CAT scan, abnormal

CAT scan, emission, abnormal

catalepsy

cataplexy

cerebellar ataxia, children

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral palsy

cerebral palsy, etiology

cerebral palsy, work up

cerebrospinal fluid, beta-D-glucan

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, proteincytologic dissociation

cerebrovascular accident

cerebrovascular accident, cryptogenic

cerebrovascular accident, nonvascular territory

cerebrovascular accident, young adult

chest x-ray, abnormal

children

chorea

choreoathetosis

chromosomal abnormality

cingulate gyrus

Clinical Pathologic Conference(C.P.C.)

clonus

clubfoot as related to neurologic disease

Coats plus

cobalamin C deficiency

congenital myasthenic syndromes

consanguinity

corpus callosum

corpus callosum, hypoplastic

corpus callosum, lesion of

corpus callosum, thinning

cortical ribbon sign

cranial nerve enhancement

creatine phosphokinase(CPK)elevated

cyst

cyst, benign intracranial

cyst, cortical parenchyma

developmental disability

developmental retardation

diabetes mellitus

diagnostic criteria

diet

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

disease modifying agents

distal muscle atrophy

distal muscle weakness

DNA sequencing

double-cortex syndrome

encephalopathy, acute

eosinophilia

executive dysfunction

exome sequencing

Fabry's disease

facial appearance, abnormal

fatal familial insomnia

fourth ventricle, compression

fungal infection

fungal infection, CNS

gaze palsy, supranuclear

genetic neurologic disorders

genetic screening

genetic testing

globus pallidus, lesion of, bilateral

headache, awakening with

headache, positional

headache, progressive

hearing loss

helminthic infection of CNS

hemianopia, homonymous

hemiparesis, transient

hemophagocytic lymphohistiocytosis

hydrocephalus, non-communicating(obstructive)

hyperammonemic encephalopathy

hypogonadism, hypogonadotropic

inborn errors of metabolism

inclusion bodies, intranuclear

insular cortex, lesion

intellectual deficit

interstitial pulmonary fibrosis

intracerebral hemorrhage

intravenous drug abuse

intrinsic hand muscles, wasting of

Leber's hereditary optic neuropathy

leg weakness, bilateral

leukodystrophy

leukoencephalopathy

leukoencephalopathy with calcification and cysts

level of consciousness, decreased

lipid storage disorder of CNS

lung nodule

lung-brain syndromes

lysosomal storage disease

malformation, CNS, congenital

McLeod syndrome

megalencephaly

MELAS syndrome

memory, impairment of

meningeal enhancement

meningeal sarcomatosis

meningitis, neutrophilic

mental retardation

mestinon

metabolic acidosis

methylmalonic acidemia

microcephaly

microhemorrhage, intracerebral

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

mitochondrial disease

mitochondrial encephalomyopathy

MRI, contrast enhanced

MRI, diffusion weighted

MRI, mass effect on

MRI, muscle

MRI, negative

MRI, nodular enhancement

MRI, spinal cord

muscle biopsy

muscle weakness, proximal

neonatal intensive care unit

neonatal screening, genetic neurologic disorders

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neuronal intranuclear inclusion disease

neuroophthalmology

neuropathy

neuropathy, demyelinating

newborn, evaluation of

next-generation sequencing

ocular motility, disorders of

opened mouth

ophthalmoplegia

organomegaly

ornithine transcarbamylase deficiency

paraparesis, familial spastic

paraparesis, spastic

parasitic infection, CNS

Parkinsonism syndrome

paroxysmal neurologic deficits

peripheral blood smear

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

polyglucosan body disease

polymicrogyria

pons, lesion of

precipitating factors

prion disease

prognosis

progressive neurologic disorder

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

respiratory tract infection

salivation, excessive

sedimentation rate, elevated

seizure

seizure, focal

seizure, laughing as manifestation

sensorineural hearing loss

short stature

shunt procedure, ventricular

shunt procedure, ventricular-complications of

sleep pathology and physiology

small vessel disease

spastic ataxia

spastic paraplegia, type 7

spasticity

speech disorder

speech, absence of

spinal cord, lesion of

spinocerebellar ataxia

spinocerebellar ataxia type 28

spinocerebellar degeneration

splenomegaly

strokelike episodes

symmetric brain lesions

systemic illness

tandem gait, ataxic

telangiectases, retinal

temporal lobe, lesion

temporal lobe, lesion, bilateral

thalamus, lesion of-bilateral

tinnitus

toe walking

treatment of neurologic disorder

tremor

tremor, intention

trinucleotide repeats

tripping

tumefactive lesion

urea-cycle enzymopathies

vision loss, sequential

vision, blurred

visual loss

visual loss, transient

visual obscurations, transient

visuospatial disturbance

walking, delayed

walking, difficulty with

weakness

weakness, fatiguable

weakness, progressive

white matter disease, unilateral

whole genome sequencing

wide based gait

workup

x-linked intellectual deficit

x-linked mental retardation

Showing articles 200 to 250 of 305 << Previous Next >>

Assessment of Fetal Tissue Transplantation in Parkinson's Disease:Does PET Play a Role
Neurol 44:1777-1780, Martin,W.R.W.&Perlmutter,J.S., 1994

Predictors of Outcome After Anterior Temporal Lobectomy:Positron Emission Tomography
Neurol 44:2331-2336, Mannon,E.M.,et al, 1994

Bilateral Spreading Cerebral Hypoperfusion During Spontaneous Migraine Headache
NEJM 331:1689-1692, 17131994., Woods,R.P.,et al, 1994

Evidence for a Dopaminergic Deficit in Sporadic Amyoptrophic Lateral Sclerosis on Positron Emission Scanning
Lancet 324:1016-1018, Takahashi,H.,et al, 1993

Total Body Irradiation for Myasthenia Gravis:A Long-Term Follow-up
Neurol 43:2215-2221, Durelli,L.,et al, 1993

Funct'l Import of Ventric Enlarge & Cortical Atrophy in Healthy Subj & Alcoholics:PET, MR, & Neuropsych Testing
Radiology 186:59-65, Wang,G.,et al, 1993

Callosal Atrophy with Reduced Cortical Oxygen Metabolism in Carotid Artery Disease
Stroke 24:88-93, Yamauchi,H.,et al, 1993

Nigral Dysfunction in Drug-Induced Parkinsonism:An F-dopa PET Study
Neurol 43:552-556, Burn,D.J.&Brooks,D.J., 1993

Presurgical Evaluation of Temporal Lobe Epilepsy Using Temporal Spikes & Positron Emission Tomography
Arch Neurol 50:45-48, Chee,M.W.L.,et al, 1993

Cerebral Glucose Metabolism as a Predictor of Recovery from Aphasia in Ischemic Stroke
Arch Neurol 50:958-964, Heiss,W.D.,et al, 1993

Positron Emission Tomographjy and Histopathology in Creutzfeldt-Jakob Disease
Neurol 43:1828-1830, Goldman,S.,et al, 1993

Comparison of Striatal 18F-dopa Uptake in Adult-Onset Dystonia-Parkinsonism, Parkinson's & Dopa-Responsive Dystonia
Neurol 43:1563-1568, Turjanski,N.,et al, 1993

PET Imaging of the Dopamine Transporter with 11C-WIN 35, 428 Reveals Marked Declines in Mild Parkinson's Disease
Ann Neurol 34:423-431, Frost,J.J.,et al, 1993

Serial Changes of Cerebral Glucose Metab & Caudate Size in Persons at Risk for Huntington's Dis
Arch Neurol 49:1161-1167, Grafton,S.T.,et al, 1992

Parkinson's Disease in Twins Studied with 18 F-Dopa and Positron Emission tomography
Neurol 42:1894-1900, Burn,D.J.,et al, 1992

Survival of Implanted Fetal Dopamine Cells & Neuro Improvement 12 to 46 Months after Transpl for Parkinson's
NEJM 327:1549-1555, 15891992., Freed,C.R.,et al, 1992

Bilateral Fetal Mesencephalic Grafting in Two Patients with Parkinsonism Induced by MPTP
NEJM 327:1556-1563, 15891992., Widner,H.,et al, 1992

Cerebral Glucose Metabolism in Parkinson's Disease with and without Dementia
Arch Neurol 49:1262-1268, Peppard,R.F.,et al, 1992

HIV Encephalopathy and Dementia
Psychiatr Clin North Am 15:455-466, Pajeau,A.K.&Roman,G.C., 1992

Striatal D2 Receptor Status in Patients with Parkinson's Disease, Striatonigral Degeneration, and PSP, (PET)
Ann Neurol 31:184-192, Brooks,D.J.,et al, 1992

Transplantation of Fetal Dopamine Neurons in Parkinson's Disease:PET Studies in 2 Pts with Putaminal Implants
Ann Neurol 31:166-173, Sawle,G.V.,et al, 1992

FDG-PET in Pediatric Posterior Fossa Brain Tumors
J Comput Assist Tomogr 16:62-68, Hoffman,J.M.,et al, 1992

Infantile Spasms:II. Lenticular Nuclei and Brain Stem Activation on Positron Emission Tomography
Ann NEurol 31:212-219, Chugani,H.T.,et al, 1992

Crossed Cerebellar Diaschisis and Crossed Cerebellar Atrophy:MR Findings & Clin Symptoms in 26 Pts
AJR 158:1155-1159, Tien,R.D.&Ashdown,B.C., 1992

Hypertensive Encephalopathy:Findings on CT, MR Imaging, and SPECT Imaging in 14 Cases
AJR 159:379-383, Schwartz,R.B.,et al, 1992

New Anatomical and Functional Imaging Methods
Ann Neurol 32:395-400, Prichard,J.W.&Brass,L.M., 1992

Advances in Neurology
NEJM 326:1608-1616, 1671-16761992., Gilman,S., 1992

Rasmussen's Encephgalitis:Neuroimaging Findings in Four Patints
AJR 158:1329-1332, Tien,R.D.,et al, 1992

Cerebral Brain Metabolism in Adult Dyslexic Subj Assessed with PET Scan During Auditory Task
ARch Neurol 49:734-739, Hagman,J.O.,et al, 1992

The Biology of Developmental Dyslexia
JAMA 268:912-915, Rumsey,J.M., 1992

Blinded Clinical Evaluation of Positron Emission Tomography for Diagnosis of Probable Alzheimer's Disease
Neurol 42:765-770, Powers,W.J.,et al, 1992

Assessment:Positron Emission Tomography
Report of Therapeutics & Technology Assessment Subcommittee of the AAN, Neurol 41:163-16791., , 1991

PET:Its Clinical Role in Neurology
JNNP 54:1-5, Brooks,D.J., 1991

Widespread Functional Effects of Discrete Thalamic Infarction
Arch Neurol 48:178-182, Szelies,B.,et al, 1991

Identification of Early Recurrence of Primary Central Nervous System Tumors by (18F) Fluorodeoxyglucose PET
Ann Neurol 29:347-355, 3451991., Glantz,M.J.,et al, 1991

Posterior Cortical Dementia with Alexia:Neurobehavioural, MRI, and PET Findings
JNNP 54:443-448, Freedman,L.,et al, 1991

Positron Emission Tomography in Progressive Supranuclear Palsy
Arch Neurol 48:389-391, Bhatt,M.H.,et al, 1991

Dopa-responsive Dystonia:[18F]Dopa Positron Emission Tomography
Ann Neurol 30:24-30, Sawle,G.V.,et al, 1991

Preclinical Detection of Parkinson's Disease
Neurology Suppl 2, 41:5-921991., Koller,W.C.&Langston,J.W., 1991

Technology Assessment Revisited:Does Positron Emission Tomography Have Proven Clinical Efficacy?
Neurol 41:1339-1340, Powers,W.J.,et al, 1991

Visual Loss in Tuberous Sclerosis
Neurol 41:1915-1917, Dotan,S.A.,et al, 1991

Positron Emission Tomography in Neuropsychiatric Lupus Erythematosus
Neurol 40:304-308, Stoppe,G.,et al, 1990

Preliminary Report:Activation of the Cerebellum in Essential Tremor
Lancet 336:1028-1030, Colebatch,J.G.,et al, 1990

Cerebral Glucose Hypermetabolism in Friedreich's Ataxia Detected with Positron Emission Tomography
Ann Neurol 28:750-757, Gilman,S.,et al, 1990

Clinical & PET Studies in the'Extrapyramidal Syndrome'of Dementia of the Alzheimer Type
Arch Neurol 47:1318-1323, Tyrrell,P.J.,et al, 1990

Plasticity in the Aging Brain
Arch Neurol 47:1336-1341, Kaye,J.A.,et al, 1990

The Nigrostriatal Dopaminergic System Assessed in Vivo by PET Volunteers & Pts with Parkinson's Disease
Arch Neurol 47:1290-1298, Leenders,K.L.,et al, 1990

Cerebral Glucose Metabolism in Adults with Hyperactivity of Childhood Onset
NEJM 323:1361-1366, 1413-14151990., Zametkin,A.J.,et al, 1990

The Marinesco-Sjogren Syndrome Examined by CT, MR, and 18F-2-Fluoro-2-Deoxy-D-Glucose & PET
Arch Neurol 47:1239-1242, Bromberg,M.B.,et al, 1990

A Brain Transplant that Works
Lancet 335:445-446, , 1990

Showing articles 200 to 250 of 305 << Previous Next >>