Neudle.com: whole exome sequencing

Differential
(Click to cross reference)

abscess, intracranial

acanthocytosis

achilles tendon, enlarged

aciduria

acute disseminated encephalomyelitis

adult polyglucosan body disease

adult-onset leukodystrophy, with neuroaxonal spheroids

adverse drug reaction

akathisia

algorithm

alternating hemiplegia

alternating hemiplegia of childhood

amimia

ammonia

amyloid angiopathy, cerebral

amyloid angiopathy, cerebral, Dutch type

aneurysm

anterior tibial muscle weakness

antiviral agents

aphasia

areflexia

arthrogryposis multiplex

ataxia

ataxia, cerebellar

ataxia, progressive

ataxic-dystonia syndromes

ATP1A3 gene

attention deficit disorder with hyperactivity

autoantibodies

autoimmune basal ganglia encephalitis

autoimmune disease

autoimmune meningitis

autonomic dysfunction

axonal degeneration

axonal spheroid

Babinski sign

basal ganglia, lesion, bilateral

brain biopsy, false negative

brain biopsy, indication

calcification, intracranial

CAT scan, disappearing lesion on

CAT scan, emission, abnormal

central nervous system, infection of

cerebellar ataxia, children

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral infarction, subcortical

cerebral palsy

cerebral palsy, etiology

cerebral palsy, work up

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, beta-D-glucan

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, proteincytologic dissociation

cerebrovascular accident

cerebrovascular accident, cryptogenic

cerebrovascular accident, mimics

cerebrovascular accident, nonvascular territory

cerebrovascular accident, young adult

chemical meningitis

chest x-ray, abnormal

chromosomal abnormality

cingulate gyrus

Clinical Pathologic Conference(C.P.C.)

clonus

clubfoot as related to neurologic disease

Coats plus

cobalamin C deficiency

cognition

coinfection

cold intolerance

collagen vascular disease

congenital myasthenic syndromes

consanguinity

corpus callosum

corpus callosum, hypoplastic

corpus callosum, lesion of

corpus callosum, thinning

cranial nerve enhancement

cranial neuropathy

creatine phosphokinase(CPK)elevated

crying, pathologic

cryptococcal meningitis

cyst

cyst, benign intracranial

cyst, cortical parenchyma

cyst, parenchymal

cystatin C mutation

deafness

degenerative diseases of CNS

delay in diagnosis

delayed muscle relaxation

dementia

dementia, presenile

dementia, rapidly progressive

dental infection

developmental disability

developmental retardation

diabetes mellitus

diagnostic criteria

diet

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

diplopia

distal muscle atrophy

distal muscle weakness

DNA sequencing

dopa responsive dystonia

double-cortex syndrome

drug induced neurologic disorders

Ehlers-Danlos syndrome

Ehlers-Danlos syndrome, classification

encephalitis, autoimmune

encephalitis, diagnosis of

encephalitis, etiology

encephalitis, Japanese

encephalitis, viral-causes of

encephalopathy

encephalopathy, acute

eosinophilia

Erdheim-Chester disease

exome sequencing

Fabry's disease

facial appearance, abnormal

fatal familial insomnia

fine motor function, impaired

fish

floppy infant

foam cells

fourth ventricle, compression

fungal infection

fungal infection, CNS

genetic neurologic disorders

genetic screening

genetic testing

geographic location

globus pallidus, lesion of, bilateral

GLUT1 deficiency syndrome

glycogen storage disease

headache, awakening with

headache, positional

headache, progressive

hearing loss

heel swelling

helminthic infection of CNS

hemianopia, homonymous

hemiparesis, transient

hemophagocytic lymphohistiocytosis

heralding manifestation

herpes simplex encephalitis

hydrocephalus, non-communicating(obstructive)

hyperammonemic encephalopathy

hypogonadism, hypogonadotropic

immunosuppressive agents

immunotherapy

inattention

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

lysosomal storage disease

malformation, CNS, congenital

memory, defect of recent

memory, impairment of

meningeal enhancement

meningeal sarcomatosis

meningitis

meningitis, aseptic

meningitis, bacterial

meningitis, basilar

meningitis, candida

meningitis, carcinomatous

meningitis, chronic

meningitis, diagnosis

meningitis, fungal

meningitis, helminthic

meningitis, neutrophilic

meningitis, noninfectious

meningitis, parameningeal

meningitis, parasitic

meningitis, TB

meningitis, treatment of

meningitis, treatment of, empirical

meningitis, viral

meningitis, viral etiology in

meningitis-encephalitis PCR panel

mental retardation

mental status, abnormal

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, nodular enhancement

MRI, spinal cord

muscle atrophy, progressive

muscle biopsy

muscle stiffness

muscle twitching

muscle wasting, diffuse

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, limb-girdle

mutism

myasthenia gravis

myasthenia gravis, congenital

myasthenia gravis, misdiagnosis of

myasthenia gravis, seronegative

myasthenia gravis, treatment of

neonatal intensive care unit

neonatal screening, genetic neurologic disorders

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic examination, focal

neuromyotonia

neuromyotonia and axonal neuropathy

neuronal intranuclear inclusion disease

neuronopathy, sensory

neuroophthalmology

neuropathy

neuropathy, demyelinating

neurotomy

newborn, evaluation of

next-generation sequencing

nystagmus, gaze-evoked

occipital lobe

ocular motility, disorders of

opened mouth

ophthalmoplegia

opportunistic infection

opportunistic infection, CNS

ornithine transcarbamylase deficiency

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

parasitic infection, CNS

Parkinsonism syndrome

paroxysmal neurologic deficits

pathologic reflex

peripheral blood smear

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

POLG1 gene

polyglucosan body disease

polymerase chain reaction

polymicrogyria

Pompe's disease of glycogen storage

pons, lesion of

precipitating factors

prion disease

prognosis

progressive neurologic disorder

proximal muscle atrophy

pseudobulbar palsy

pseudoxanthoma elasticum

psychiatric problems in neurologic disorders

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

respiratory tract infection

salivation, excessive

sedimentation rate, elevated

seizure

seizure, focal

sensorineural hearing loss

seronegative

short stature

shunt procedure, ventricular

shunt procedure, ventricular-complications of

skin, biopsy

skin, hyperextensible

skin, lesions in neurologic disorders

skin, thin

skin, translucent

sleep pathology and physiology

small vessel disease

small vessel disease, cerebral

spastic ataxia

spastic paraplegia, type 7

spasticity

speech disorder

speech, absence of

spinal cord, lesion of

spinocerebellar ataxia

spinocerebellar ataxia type 28

spinocerebellar degeneration

standing difficulty

status epilepticus

striatal encephalitis

strokelike episodes

subarachnoid hemorrhage

symmetric brain lesions

systemic illness

tandem gait, ataxic

telangiectases, retinal

temporal lobe, lesion

temporal lobe, lesion, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

tinnitus

toe walking

tone, muscle, increased

tongue, enlarged

treatment of neurologic disorder

treatment, empirical

tremor

tremor, intention

trinucleotide repeats

tripping

tumefactive lesion

urea-cycle enzymopathies

vision loss, sequential

vision, blurred

visual field defect

visual loss

visual loss, progressive

visual loss, transient

visual obscurations, transient

walking, delayed

walking, difficulty with

weakness

weakness, fatiguable

weakness, generalized

weakness, progressive

white matter disease, subcortical

white matter disease, unilateral

whole genome sequencing

x-linked intellectual deficit

x-linked mental retardation

Showing articles 250 to 290 of 290 << Previous

Cerebral Glucose Metabolism in Wernicke's Broca's, and Conduction Aphasia
Arch Neurol 46:27-34, Metter,E.J.,et al, 1989

Cerebral Glucose Metabolism in the Course of Subacute Sclerosing Panencephalitis
Arch Neurol 46:97-100, Huber,M.,et al, 1989

Cyanide-Induced Parkinsonism:Clinical, MRI, and 6-Fluorodopa PET Studies
Neurol 39:142-144, Rosenberg,N.L.,et al, 1989

Normal-Pressure Hydrocephalus and the Saga of the Treatable Dementias
JAMA 262:2577-2581, 2592-25931989., Friedland,R.P., 1989

Positron Emission Tomography-A New Approach to Brain Chemistry
JAMA 260:2704-2710, Jacobson,H.G., 1988

Disconnection & Cerebral Metabolism, The Case of Conduction Aphasia
Arch Neurol 45:275-279, Kempler,D.,et al, 1988

Immunotherapy of Multiple Sclerosis
Ann Neurol 23:211-223, Weiner,H.L.&Hafler,D.A., 1988

Positron Emission Tomography in a Patient with Progressive Multifocal Leukoencephalopathy
Neurol 38:1864-1867, Kiyosawa,M.,et al, 1988

Brain Metabolism in Mitochondrial Encephalomyopathy:A PET Study
J Comput Assist Tomogr 12:854-857, DeVolder,A.,et al, 1988

Diagnosis & Treatment of Aphasia, Part I & Part II
JAMA 259:1043-1047, 1205-12101988., Albert,M.L.&Helm-Estabrooks,N., 1988

Cerebellar & Brainstem Hypometabolism in Olivo-pontocerebellar Atrophy Detected with Positron Emission Tomography
Ann Neurol 23:223-230, Gilman,S.,et al, 1988

Brain Glucose Metabolism in Thalamic Syndrome
JNNP 51:427-428, Laterre,E.C.,et al, 1988

Cerebral Hypometabolism in Progressive Supranuclear Palsy Studied with Positron Emission Tomography
Ann Neurol 24:399-406, Foster,N.L.,et al, 1988

Dementia in Down's Syndrome:Cerebral Glucose Utilization, Neuropsychological Assessment, and Neuropathology
Neurol 38:938-942, Schapiro,M.B.,et al, 1988

Surgical Treatment of Intractable Neonatal-Onset Seizures:The Role of Positron Emission Tomography
Neurol 38:1178-1188, Chugani,H.T.,et al, 1988

The Metabolic Pathology of the AIDS Dementia Complex
Ann Neurol 22:700-706, Rottenberg,D.A.,et al, 1987

Normal Caudate Glucose Metabolism in Persons at Risk for Huntington's Disease
Arch Neurol 44:254-257, Young,A.B.,et al, 1987

The Lennox-Gastaut Syndrome:Metabolic Subtypes Determined by FDG Positron Emission Tomography
Ann Neurol 21:4-13, Chugani,H.T.,et al, 1987

Cerebral Glucose Metabolism in the Lennox-Gastaut Syndrome
Ann Neurol 21:14-21, Theodore,W.H.,et al, 1987

Primary Progressive Aphasia-Differentiation from Alzheimer's Disease
Ann Neurol 22:533-534, Mesulam,M.M., 1987

The Combined Use of Positron Emission Tomography & DNA Polymorphisms for Preclinical Detection of Huntington's Disease
Neurol 37:1441-1447, Hayden,M.R.,et al, 1987

Wilson's Disease Studies with FDG & Positron Emission Tomography
Neurol 37:1707-1711, Hawkins,R.A.,et al, 1987

Total Lymphoid Irradiation in Multiple Sclerosis:Blood Lymphocytes & Clinical Course
Ann Neurol 22:634-638, Cook,S.D.,et al, 1987

Metabolic & Clinical Correlates of Acute Ischemic Infarction
Neurol 37:1103-1110, Kushner,M.,et al, 1987

Positron Emission Tomography Studies of Cerebral Glucose Metabolism in Chronic Partial Epilepsy
Ann Neurol 22:480-486, Abou-Khalil,B.W.,et al, 1987

Borderzone Ischemia
Ann Neurol 22:707-713, Leblanc,R.,et al, 1987

Differences in Cerebral Blood Flow & Glucose Utilization in Vegetative Versus Locked-in Patients
Ann Neurol 22:673-682, Levy,D.E.,et al, 1987

Effect of Total Lymphoid Irradiation in Chronic Progressive Multiple Sclerosis
Lancet 1:1405-1409, Cook,S.D.,et al, 1986

Alzheimer's Disease
NEJM 314:964-973, Katzman,R., 1986

Comparison of PET, MRI, & CT with Pathology in a Proven Case of Alzheimer's Disease
Neurol 36:1569-1574, McGeer,P.L.,et al, 1986

PET, CT, & MR Imaging in Cerebrovascular Disease
J Comput Assist Tomogr 10:903-911, Heiss,W.D.,et al, 1986

Alzheimer's Disease & Down's Syndrome:New Insights
Ann Int Med 103:566-578, Cutler,N.R.,et al, 1985

Positron Emission Tomography & its Application to the Study of Cerebrovascular Disease in Man
Stroke 16:361-376, Powers,W.J.,et al, 1985

Pure Hemidystonia with Basal Ganglion Abnormalities on Positron Emission Tomography
Ann Neurol 15:228-233, Perlmutter,J.S.,et al, 1984

Parkinson's Disease, 1984
Lancet 1:829-830, Williams,D.,et al, 1984

The Fluorodeoxyglucose 18F Scan in Alzheimer's Disease & Multi-infarct Dementia
Arch Neurol 40:711-714, Benson,D.F.,et al, 1983

Positron Computed Tomography for Studies of Myocardial & Cerebral Function
Ann Int Med 98:339-359, Phelps,M.E.,et al, 1983

Alzheimer's Disease:Focal Cortical Changes Shown by Positron Emission Tomography
Neurol 33:961-965, Foster,N.L.,et al, 1983

Regional Cerebral Metab. Alter. in Dementia of the Alzheimer Type:Positron Emission Tomogr
J Comput Assist Tomogr 4:590-598, Friedland,R.P.,et al, 1983

Remission From Polymyositis After Total Body Irradiation
BMJ 284:1915-1916, Hubbard,W.N.,et al, 1982

Emission & Transmission Brain Tomography
BMJ 1:438-440, Ell,P.J.,et al, 1980

Showing articles 250 to 290 of 290 << Previous