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 100 to 150 of 290 << Previous Next >>

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Frequent Amyloid Deposition Without Significant Cognitive Impairment Among the Elderly
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Metabolic Patterns Associated with the Clinical Response to Galantamine Therapy
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Diagnostic Evaluation of Patients with a Brain Mass as the Presenting Manifestation of Cancer
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Showing articles 100 to 150 of 290 << Previous Next >>