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 1250 to 1300 of 2319 << Previous Next >>

The Value of Brain Imaging in Children with Headaches
Pediatrics 96:413-416, Maytal,J.,et al, 1995

Mild Traumatic Brain Injury:Pathophysiology, Natural History, and Clinical Management
Neurol 45:1253-1260, 12511995., Alexander,M.P., 1995

Cerebrospinal Fluid Concentration of Neuron-specific Enolase in Diagnosis of Creutzfeldt-Jakob Disease
Lancet 345:1609-1610, Zerr,I.,et al, 1995

Dementia Associated with the Acquired Immunodeficiency Syndrome
NEJM 332:934-940, Lipton,S.A.&Gendelman,H.E., 1995

Adverse Outcomes of Bacterial meningitis in School-Age Survivors
Pediatrics 95:646-655, Grimwood,K.,et al, 1995

Deficiency of Brain Synaptic Dystrophin in Human Duchenne Muscular Dystrophy
Ann Neurol 38:446-449, Kim,T.W.,et al, 1995

Brain Abnormalities in Duchenne Muscular Dystrophy:Phosphorus-31 Magnetic Resonance Spectroscopy & Neuropsych Study
Lancet 345:1260-1264, Tracey,I.,et al, 1995

Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995

The Eosinophilia-Myalgia Syndrome:Status of 205 Patients and Results of Treatment 2 Years After Onset
Ann Int Med 122:851-855, Hertzman,P.A.,et al, 1995

Natural History in Proximal Spinal Muscular Atrophy
Arch Neurol 52:518-523, Zerres,K.&Rudnik-Schoneborn,R., 1995

Persistence of MRI Hyperintensity of the Globus Pallidus in Cirrhotic Patients:A 2-year Follow-up Study
Neurol 45:995-997, Kulisevsky,J.,et al, 1995

MR of Oculomotor Nerve Plasy
AJNR 16:1665-1672, Blake,P.Y.,et al, 1995

Folic Acid and the Prevention of NEural Tube Defects
BMJ 310:1019-1020, Wald,N.J.&Bower,C., 1995

Diagnostic Yield of the Neurologic Assessment of the Developmentally Delayed Child
J Pediatr 127:193-199, Majnemer,A.&Shevell,M.I., 1995

Perioperative Imaging Strategies for Carotid Endarterectomy:Analysis of Morbidity & Cost-Effectiveness in Symptomatic Patients
JAMA 274:888-893, Kent,K.C.,et al, 1995

Complex Partial Status Epilepticus Accompanied by Serious Morbidity and Mortality
Neurol 45:1499-1504, Krumholz,A.,et al, 1995

The Effect of Education on the Incidence of Dementia and Alzheimer's Disease in the Framingham Study
Neurol 45:1707-1712, Cobb,J.L.,et al, 1995

Research Involv Subj with Dementia & Other Cognitive Impairments:NIH, & Ethical Considerations
Neurol 45:1777-1778, Wichman,A.&Sandler,A.L., 1995

Psychosis as the Initial Manifestation of Adult-Onset Niemann-Pick Disease Type C
Neurol 45:1739-1743, Shulman,L.M.,et al, 1995

Influence of Vascular Risk Factors for Atherosclerotic Carotid Artery Plaque Progression
Stroke 26:2016-2022, Delcker,A.,et al, 1995

Familial Hemiplegic Migraine and Autosomal Dominant Arteriopathy with Leukoencephalopathy (CADASIL)
Ann Neurol 38:817-824, Hutchinson,M.,et al, 1995

Clinical Spectrum of CADASIL:A Study of 7 Families
Lancet 346:934-939, Chabriat,H.,et al, 1995

New Phenotype of the Cerebral Autosomal Dominant Arteriopathy Mapped to Chromosome 19:Migraine as the Prominent Clinical Feature
JNNP 59:579-585, Verin,M.,et al, 1995

Image Analysis of B-Amyloid Load in Alzheimer's Disease and Relation to Dementia Severity
Lancet 346:1524-1528, Cummings,B.J.&Cotman,C.W., 1995

Apolipoprotein E Allele E4, Dementia, and Cognitive Decline in a Population Sample
Lancet 346:1387-1390, Henderson,A.S.,et al, 1995

Apolipoprotein E, Dementia, and Cortical Deposition of B-Amyloid Protein
NEJM 333:1242-1247, 12831995., Polvikoski,T.,et al, 1995

Apoliprprotein E E4 Allele & the Lifetime Risk of Alzheimer's Disease:What Physicians Know, & What They Should Know
Arch Neurol 52:1074-1079, Seshadri,S.,et al, 1995

Apolipoprotein E Genotype in Patients with Alzheimer's Disease:Implications for Risk of Dementia Among Relatives
Ann Neurol 38:797-808, Farrer,L.A.,et al, 1995

Anterior Communicating Artery Aneurysm Paraparesis Syndrome:Clinical Manifestations and Pathologic Correlates
Neurol 45:45-50, Greene,K.A.,et al, 1995

Prediction of Long-Term Outcome in the Early Hours Following Acute Ischemic Stroke
Arch Neurol 52:250-255, Fiorelli,M.,et al, 1995

Sneddon's Syndrome is a Thrombotic Vasculopathy:Neuropathologic and Neuroradiologic Evidence
Neurol 45:557-560, Geschwind,D.H.,et al, 1995

New Treatments for Multiple Sclerosis
BMJ 310:345-346, McDonald,W.I., 1995

Diagnosis and Evaluation of Dementia
Neurol 45:211-218, Corey-Bloom,J.,et al, 1995

Synergistic Effects of Traumatic Head Injury and Apolipoprotein-E4 In Patients with Alzheimer's Disease
Neurol 45:555-557, Mayeux,R.,et al, 1995

Management of the Behavioral Manifestations of Dementia
Arch Int Med 155:250-260, Yeager,B.F.,et al, 1995

Devel & Neurologic Status of Children after Heart Surgery with Hypothermic Circ Arrest or Low-Flow Cardiopul Bypass
NEJM 332:549-555, Bellinger,D.C.,et al, 1995

Plasma Cobalamin Levels Affect Information Processing Speed in a Longitudinal Study of HIV-1 Disease
Arch Neurol 52:195-198, Shor-Posner,G.,et al, 1995

Acute Viral Encephalitis in Childhood
BMJ 310:139-140, Kennedy,C., 1995

Dexamethasone Therapy for Children with Bacterial Meningitis
Pediatrics 95:21-28, 291995., Wald,E.R.,et al, 1995

Correlation Between CAT Scan Abnormalities & Neuropsychological Function in Children with Symptomatic HIV Disease
Arch Neurol 52:39-44, Brouwers,P.,et al, 1995

Hereditary Leukoencephalopathy and Palmoplantar Keratoderma:A New Disorder with Increased Skin Collagen Content
Neurol 45:331-337, Lossos,A.,et al, 1995

Parkinsonism-Recognition and Differential Diagnosis
BMJ 310:447-452, Quinn,N., 1995

Campylobacter Jejuni Infection and Guillain-Barre Syndrome
NEJM 333:1374-1379, 14151995., Rees,J.H.,et al, 1995

Non-Progressive Familial Idiopathic Intracranial Calcification:A Family Report
JNNP 59:432-434, Callender,J.S., 1995

Decreased SPECT[123I]B-CIT Striatal Uptake Correlates with Symptom Severity in Parkinson's Disease
Ann Neurol 38:589-598, Seibyl,J.P.,et al, 1995

Folate Levels and Neural Tube Defects:Implications for Prevention
JAMA 274:1698-1702, 17171995., Daly,L.E.,et al, 1995

Canavan Disease:From Spongy Degeneration to Molecular Analysis
J Pediatr 127:511-517, Matalon,R.,et al, 1995

In Utero Exposure to Phenobarbital and Intelligence Deficits in Adult Men
JAMA 274:1518-1525, Reinisch,J.M.,et al, 1995

Reversible Dementia and Apparent Brain Atrophy During Valproate Therapy
Ann Neurol 38:687-691, Papazian,O.,et al, 1995

A Low, "Normal"Score on the Mini-Mental State Exam Predicts Development of Dementia after Three Years
JAGS 43:656-661, Braekhus,A.,et al, 1995

Showing articles 1250 to 1300 of 2319 << Previous Next >>