Neudle.com: developmental regression

Differential
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acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome, congenital

acquired immunodeficiency syndrome, infants and children

acromicria

ACTH

advances in neurology

Aicardi-Goutieres syndrome

Alexanders disease

anemia

aneurysm

aneurysm, asymptomatic

aneurysm, intracranial

anorexia

apraxia of eye movements

aqueduct of Sylvius, stenosis

B 12 deficiency, infants

Babinski sign

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

Brown-Vialetto-Van Laere syndrome

cachexia

calcification, gyral

calcification, intracranial

cerebral cortical atrophy

cerebral ischemia

cerebral palsy

cerebral vasculature

cerebral venous infarction

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, proteincytologic dissociation

cerebrovascular accident

cerebrovascular accident, mimics

cerebrovascular disease

cherry red spot

cherry red spot-myoclonus syndrome

children

chorea

choreoathetosis

chromosomal abnormality

chromosome 3

Clinical Pathologic Conference(C.P.C.)

clinodactyly

cold hands sign

complications

congenital infection, CNS

consanguinity

contractures, joint

controversies in neurology

corpus callosum, atrophy of

corpus callosum, thinning

cough

cranial nerve enhancement

cranial nerve enlargement

cranial neuropathy

cranial neuropathy, multiple

crawl regression

cry, abnormal

crying

cultured skin fibroblasts

degenerative diseases of CNS

delay in diagnosis

dementia

dementia, childhood

demyelinating disease

dentate nuclei

dentate nuclei, lesion of

developmental milestones

developmental milestones, loss of

developmental retardation

diagnostic criteria

differential diagnosis

difficulty climbing stairs

diplopia

dopa responsive dystonia

drooling

dropped head syndrome

electroencephalogram, abnormalities of

encephalitis

encephalitis, autoimmune

encephalomalacia

encephalopathy

encephalopathy, neonatal

encephalopathy, progressive

endoscopic surgery

endoscopy

enzyme, defect

epileptic encephalopathy

episodic disorders

evoked potentials

eye movement, disorders of

facial weakness

facial weakness, bilateral

fine motor function, impaired

fundus, abnormality of

gaze palsy, supranuclear

genetic neurologic disorders

glutamic acid decarboxylase, antibody

granular osmiphilic material

growth retardation

gyrus, abnormal

Hallervorden Spatz disease

human immunodeficiency virus type 1

human immunodeficiency virus type 1, infants and children

hydrocephalus

hydrocephalus, complications with

hydrocephalus, etiology

hydrocephalus, fetal

hydrocephalus, non-communicating(obstructive)

hydrocephalus, treatment of

hyperhomocysteinemia

hyperpigmentation of skin

inborn errors of metabolism

incoordination

infant, evaluation of

infantile spasm

infantile tremor syndrome

intellectual deficit

intellectual deterioration

interferon alpha

intracranial pressure, increased

laminar necrosis, cortical

L-dopa

Leigh's disease

lethargy

leukocyte enzyme abnormality

leukocytosis

leukodystrophy

leukoencephalopathy

leukoencephalopathy, differential diagnosis

life expectancy

lipid storage disorder of CNS

liver disease

liver function enzymes

lymphadenopathy

lymphadenopathy, axillary

lymphadenopathy, paraaortic

lysosomal storage disease

macrocephaly

malformation, CNS, congenital

malformation, vascular

masked facies

meconium staining

MELAS syndrome

memory, impairment of

meningeal enhancement

meningitis, CSF cell count-normal

mental retardation

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

metachromatic leukodystrophy, late-infantile

microcephaly

midbrain, lesion of

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

mongolism

monoclonal antibodies

mortality

movement disorder

movement disorder, extrapyramidal

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, gyral swelling

MRI, hypointense signal foci on

MRI, paramagnetic effect

MRI, serial

MRI, T1 weighted high signal foci

MRS

mucopolysaccharidoses

muscle biopsy

muscle spasm

myasthenia gravis

myasthenia gravis, infantile and juvenile

myelination of nervous system

myoclonus

myoclonus, epilepsy

myoclonus, multifocal

myoclonus, treatment of

nasal speech

nausea and vomiting

neck trauma

nerve conduction studies

neuroaxonal dystrophy

neurocutaneous disease

neurofibrillary degeneration

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic disease, tempo

neurologic examination

neurologic signs

neuronal ceroid-lipofuscinosis

neuroophthalmology

neuropathology

neuropathology, brain

opportunistic infection

opportunistic infection, CNS

optic atrophy

optic chiasm, enlarged

optic nerve

optic nerve, enlarged

pain

PANK2 mutation

papilledema

paraparesis, familial spastic

paraparesis, spastic

PAS positive material in the brain

pediatric neurology

pleocytosis of cerebrospinal fluid

port wine nevus

postural abnormality

prognosis

progressive myoclonic epilepsy

progressive neurologic disorder

prolactin, elevated

psychological testing

psychomotor retardation

psychosis

ptosis

pulmonary infiltrates

pyramidal tract

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

renal tubular acidosis

reversible neurologic disorder

review article

riboflavin transporter deficiency

scoliosis, neurologic association with

screening

sedimentation rate, elevated

seizure

seizure, children

seizure, crying as manifestation of

seizure, drug resistance

seizure, intractable

serositis

short stature

shunt procedure, ventricular

shunt procedure, ventricular-complications of

skin, lesions in neurologic disorders

speech disorder, childhood

speech, loss of

spinal muscular atrophy

splenomegaly

spongy degeneration of brain

spontaneous remission

striatonigral degeneration

striatonigral degeneration, infantile

strokelike episodes

Sturge-Weber syndrome

subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease

substantia nigra

suck, poor

symmetric brain lesions

systemic illness

systemic juvenile idiopathic arthritis

Tay-Sachs disease

temporal lobe, lesion, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

thrombocytosis

titubation

toe walking

tone, muscle, increased

tongue, fasciculations of

toxoplasmosis, CNS

transient neurologic deficit

treatment of neurologic disorder

tumor necrosis factor

tyrosine hydroxylase deficiency

vasculopathy

vegetarianism

ventricular enlargement

ventriculostomy

ventriculostomy, endoscopic

visual acuity, decreased

visual evoked response

visual field defect

visual fields, constricted

walking, difficulty with

weakness

weakness, generalized

weakness, progressive

Werdnig-Hoffman disease

x-linked hydrocephalus

Showing articles 950 to 1000 of 2319 << Previous Next >>

Screening for Dementia with the Memory Impairment Screen
Neurol 52:231-238,224, Buschke,H.,et al, 1999

Progressive Aphasia with Rapidly Progressive Dementia in a 49 Year Old Woman
JNNP 66:238-243, Greene,J.D.W.,et al,, 1999

Hashimoto's Encephalitis as a Differential Diagnosis of Creutzfeldt-Jakob Disease
JNNP 66:172-176, Seipelt,M.,et al, 1999

Dementia and Snoring
Lancet 353:204, Steiner,M.C.,et al, 1999

The Heidenhain Variant of Creutzfeldt-Jakob Disease
Arch Neurol 56:55-61, Kropp,S.,et al, 1999

Mild Cognitive Impairment, Clinical Characterization and Outcome
Arch Neurol 56:303-308, Petersen,R.C.,et al, 1999

High Monounsaturated Fatty Acids Intake Protects Against Age-Related Cognitive Decline
Neurol 52:1563-1569, Solfrizzi,V.,et al, 1999

Cost-Effectiveness of Donepezil in the Treatment of Mild or Moderate Alzheimer's Disease
Neurol 52:1138-1145,1115, Neumann,P,J.,et al, 1999

Rapidly Progressive Dementia
Lancet 353:1150, Bornke,C.,et al, 1999

Clinicopath Conf:Multisystem Neurodegenerative Disease with Dementia Pugilistica
NEJM 340:1269-1277, Case 12-1999, 1999

Fibromyalgia Syndrome a Decade Later
Arch Int Med 159:777-785, Goldenberg,D.L., 1999

Burden of Migraine in the United States, Disability and Economic Costs
Arch Int Med 159:813-818, Hu,X.H.,et al, 1999

Changes in Resource Use and Outcomes for Patients with Migraine Treated with Sumatriptan, A Managed Care Perspective
Arch Int Med 159:857-863, Lofland,J.H.,et al, 1999

Mortality from Dementia in Occupations at Risk of Exposure to Bovine Spongiform EncephalopathyAnalysis of Death Registrations
BMJ 318:1044-1045, Aylin,P.,et al, 1999

Prevalence and Clinical Correlates of Psychotic Symptoms in parkinson Disease
Arch Neurol 56:595-601, Aarsland,D.,et al, 1999

Efficacy, Safety, and Tolerance of the Non-Ergoline Dopamine Agonist Pramipexole in the Treatment of Advanced Parkinson's Disease:A Double Blind, Placebo Controlled, Randomised, Multicentre Study
JNNP 66:436-441, Pinter,M.M.,et al, 1999

Infantile Neuroaxonal Dystrophy,Clinical Spectrum and Diagnostic Criteria
Neurol 52:1472-1478, Nardocci,N.,et al, 1999

Brain Structure and Neurocognitive and Behavioural Function in Adolescents Who Were Born Very Preterm
Lancet 353:1653-1657, Stewart,A.L.,et al, 1999

Medial Temporal Lobe Atrophy on MRI in Dementia with Lewy Bodies
Neurol 52:1153-1158, Barber,R.,et al, 1999

Clinicopath Conf:Lymphoplasmocytic Lymphoma with Motor Neuronopathy,Waldenstrom's Macroglobulinemia
NEJM 340:1661-1669, , 1999

Do We Have Drugs for Dementia? No
Arch Neurol 56:735-737, Pryse-Phillips,W., 1999

Do We Have a Treatment for Alzheimer Disease? Yes
Arch Neurol 56:738-739,735, Gauthier,S., 1999

Low-Density Lipoprotein Cholesterol and the Risk of Dementia with Stroke
JAMA 282:254-260, Moroney,J.T.,et al, 1999

Risk of Transmission of Bovine Spongiform Encephalopathy to Humans in the United States, Report of the Council on Scientific Affairs
JAMA 281:2330-2339, Tan,L.,et al, 1999

Benign Multiple Sclerosis? Clinical Course, Long Term Follow Up, and Assessment of Prognostic Factors
JNNP 67:148-152,138, Hawkins,S.A.&McDonnell,G.V., 1999

Recent Advances, Neurology
BMJ 319:362-366, Larner,A.J.&Farmer,S.F., 1999

Maternal Thyroid Deficiency During Pregnancy and Subsequent Neuropsychological Development of the Child
NEJM 341:549-555,601, Haddow,J.E.,et al, 1999

Optic Nerve Enlargement in Krabbe's Disease
AJNR 20:1228-1231, Jones,B.V.,et al, 1999

Folic Acid for the Prevention of Neural Tube Defects
Pediartrics 104:325-327, Committee on Genetics, 1999

Highly Active Antiretroviral Therapy Reverses Brain Metabolite Abnormalities in Mild HIV Dementia
Neurol 53:782-789, Chang,L.,et al, 1999

Rehabilitation of Persons With Traumatic Brain Injury
JAMA 282:974-983,989, NIH Consensus Development Panel on Rehab with TBI, 1999

Multiple Sclerosis That is Progressive From the Time of Onset, Clinical Characteristics and Progression of Disability
Arch Neurol 56:1138-1142, Andersson,P.B.,et al, 1999

A Randomized Trial of Risperidone,Placebo,and Haloperidol for Behavioral Symptoms of Dementia
Neurol 53:946-955,899, DeDeyn,P.P.,et al, 1999

Clinicopath Conf, Creutzfeldt-Jakob Disease,Case 28-1999
NEJM 341:901-908, , 1999

Optimality Score for the Neurologic Examination of the Infant at 12 and 18 Months of Age
J Pediatr 135:153-161,140, Haataja,L.,et al, 1999

A Case of Sporadic Pick Disease With Onset at 27 Years
Arch Neurol 56:1289-1291, Jacob,J.,et al, 1999

New Developments in the Neurobiology of the Tuberous Sclerosis Complex
Neurol 53:1384-1390, Crino,P.B.&Henske,E.P., 1999

Altered Brain Activation in Cognitively Intact Individuals at High Risk for Alzheimer's Disease
Neurol 53:1391-1396, Smith,C.D.,et al, 1999

Diagnosing Dementia with Lewy Bodies
Lancet 354:1227-1228, McKeith,I.G.,et al, 1999

Tube Feeding in Patients with Advanced Dementia,A Review of the Evidence
JAMA 282:1365-1370, Finucane,T.E.,et al, 1999

Creutzfeldt-Jakob Disease and Related Transmissible Spongiform Encephalopathies
NEJM 339:1994-2004, Johnson,R.T. & Gibbs,Jr.,C.J., 1998

Clinical Approach to Inherited Peroxisomal Disorders: A Series of 27 Patients
Ann Neurol 44:720-730,713, Baumgartner,M.R.,et al, 1998

Randomised Double-Blind Placebo-Controlled Study of Interferon B-1a in Relapsing/Remitting Multiple Sclerosis
Lancet 352:1498-1504,1486, PRISMS, 1998

A 29-Year-Old Man with Multiple Sclerosis
JAMA 280:1432-1439, Rudick,R.A., 1998

The Phenotypic Spectrum of CADASIL:Clinical Findings in 102 Cases,
Ann Neurol 44:731-739,715, Dichgans,M.,et al, 1998

The HCFA New Exam Document Criteria:Mini Auditing Stnds for Neurol Exam to be Used by Payors
Neurol 50:497-500, 3261998., Newer,M.R.&Sigsbee,B., 1998

Long-Term Postoperative Cognitive Dysfunction in the Elderly:ISPOCD1 Study
Lancet 351:857-861, Moller,J.T.,et al, 1998

Cognitive Function in Nondemented Older Women who Took Estrogen after Menopause
Neurol 50:368-373, Jacobs,D.M.,et al, 1998

Estrogen Therapy in Postmenopausal Women, Effects on Cognitive Function and Dementia
JAMA 279:688-695, Yaffe,K.,et al, 1998

The APOE-e4 Allele and the Risk of Alzheimer Disease Among AFrican Americans, Whites and Hispanics
JAMA 279:751-755, 7881998., Tang,M.,et al, 1998

Showing articles 950 to 1000 of 2319 << Previous Next >>