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

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 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 disease

cherry red spot

cherry red spot-myoclonus syndrome

children

chorea

choreoathetosis

chromosomal abnormality

chromosome 3

Clinical Pathologic Conference(C.P.C.)

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

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

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 tremor syndrome

intellectual deficit

intellectual deterioration

interferon alpha

intracranial pressure, increased

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, vascular

masked facies

meconium staining

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

monoclonal antibodies

mortality

movement disorder

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, angiography

MRI, contrast enhanced

MRI, diffusion weighted

MRI, hypointense signal foci on

MRI, paramagnetic effect

MRS

mucopolysaccharidoses

muscle biopsy

muscle spasm

myasthenia gravis

myasthenia gravis, infantile and juvenile

myelination of nervous system

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, 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

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

thalamus, lesion of

thalamus, lesion of-bilateral

thrombocytosis

titubation

toe walking

tone, muscle, increased

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 2050 to 2100 of 2279 << Previous Next >>

Sarcoidosis Presenting as Senile Dementia
Neurol 31:1148-1151, Cordingley,G.,et al, 1981

Whipple's Disease Sonfined to the Nervous System
JNNP 44:1104-1109, Pollock,S.,et al, 1981

Subcortical Arteriosclerotic Encephalopathy:A Clinical & Radiological Investigation
JNNP 44:294-304, Loizou,L.A.,et al, 1981

Lipomembranous Polycystic Osteodysplasia with Progressive Dementia
J Comput Assist Tomogr 5:580-582, Laasonen,E.M.,et al, 1981

Encephalopathy Complicating Whipple's Disease
Ann Int Med 94:51-52, Schmitt,B.P.,et al, 1981

Effects of Prophyl. Treat. of CNS on Intellect. Funct. of Children with Acute lymph. Leuk
Am J Med 71:47-52, Moss,H.A., 1981

Depression, Intellectual Impairment & Parkinson Disease
Neurol 31:645-650, Mayeux,R.,et al, 1981

Ataxia with Aniridia of Gillespie:A Case Report
Neurol 31:95-97, Lechtenberg,R.,et al, 1981

Von Recklinghausen Neurofibromatosis
NEJM 305:1617-1627, Riccardi,V.M., 1981

Neurologic Complications of Hyperthyroidism
Arch Neurol 38:669-670, Bulens,C., 1981

Septo-optic Dysplasia in an Infant of a Diabetic Mother
Arch Neurol 38:590-591, Donat,J.F.G., 1981

Encephalopathy in Infants & Children With Chronic Renal Disease
Arch Neurol 38:656-658, Foley,C.M.,et al, 1981

Progressive Infantile Poliodystrophy, Assoc. With Disturbed Pyruvate Oxidation in Muscle & Liver
Arch Neurol 38:767-772, Prick,M.J.J.,et al, 1981

Biotin-Responsive Carboxylase Deficiency Associated With Subnormal Plasma & Urinary Biotin
NEJM 304:817-820, Thoene,J.,et al, 1981

Cerebral Disorder In Alcoholism, Syndromes Of Impairment
Brain 104:1-20, Lishman,W.A., 1981

Amyotrophic Lateral Sclerosis & its Association with Dementia, Parkinsonism & Other Neurological Disorders:A Review
Brain 104:217-247, Hudson,A.J., 1981

Temporal Arteritis Presenting as Ataxia and Dementia
Post Grad Med 69:246-249, Shenberger,K.N.,et al, 1981

Handedness, Clumsiness & Cognitive Ability
Develop Med Child Neurol 22:569-579, Bishop,D.V.M., 1980

Leukoencephalopathy & Elevated Levels Of Myelin Basic Protein In The CSF Of Patients With Acute Lymphoblastic Leukemia
NEJM 303:19-21, Gangji,D.,et al, 1980

Acquired Aphasia with Convulsive Disorder:Course & Prognosis
Neurol 30:524-529, Mantovani,J.F.,et al, 1980

Human Cerebellar Hypoplasia, A Syndrome of Diverse Causes
Arch Neurol 37:300-305, Sarnatt,H.B.,et al, 1980

Idiopathic Hyperammonemia Associated with Cerebral arteriovenous Malformation
Arch Neurol 37:111-112, Michaelson,P.S., 1980

A Family with Hereditary Ataxia:HLA Typing
Neurol 30:12-20, Nino,H.E.,et al, 1980

Creutzfeldt-Jakob Disease in a 20-year-old Woman
Neurol 30:492-496, Packer,R.J.,et al, 1980

Fetal Methylmercury Poisoning:Clinical & Toxicological Data on 29 Cases
Ann Neurol 7:348-353, Marsh,D.O.,et al, 1980

Parkinson Disease, Dementia, & Alzheimer Disease:Clinicopathological Correlations
Ann Neurol 7:329-335, Boller,F.,et al, 1980

Diagnosis of Infatile Neuroaxonal Dystrophy by Skin Biopsy
Ann Neurol 7:377-379, Wisniewski,K.,et al, 1980

Maternal & Fetal Sequelae of Anticoagulation During Pregnancy
Am J Med 68:122-140, Hall,J.G.,et al, 1980

Hazards of Oral Anticoagulants During Pregnancy
JAMA 243:1549-1551, Stevenson,R.E.,et al, 1980

Cognitive Function in Patients With Multiple Sclerosis
Arch Neurol 37:577-579, Peyser,J.M.,et al, 1980

Lafora Disease:Diagnosis by Liver Biopsy
Ann Neurol 8:409-415, Nishimura,R.N.,et al, 1980

Evidence For & Against the Transmissibility of Alzheimer Disease
Neurol 30:945-950, Goudsmit,J.,et al, 1980

Amygdaloid Changes in Aging & Dementia
Arch Neurol 37:625-629, Herzog,A.G.,et al, 1980

Demonstration of CSF Gamma-globulin Banding in Presenile Dementia
Neurol 30:882-884, Williams,A.,et al, 1980

Decreased Computerized Tomography Numbers in Patients With Presenile Dementia
Arch Neurol 37:401-409, Naeser,M.A.,et al, 1980

Presenile Alzheimer Disease:Amyloid Plaques in the Cerebellum
Neurol 30:820-825, Pro,J.D.,et al, 1980

Dementia From Aluminum Pots
NEJM 303:164, Levick,S.E., 1980

Pathological Verification of Ischemic Score in Differentiation of Dementias
Ann Neurol 7:486-488, Rosen,W.G.,et al, 1980

Reversible Dementia, Illustrative Cases, Definition, & Review
JAMA 243:2434-2439, Cummings,J.,et al, 1980

Alzheimer's Disease
Editorial, BMJ 281:1374-13751980., , 1980

Progressive White Matter Destruction Following Irradiation of an Extracranial Neoplasm
Ann Neurol 8:76-78, Rottenberg,D.A.,et al, 1980

Clin. Path. Conference
Creutzfeldt-Jakob Disease, Ataxic Type, with Kuru Plaques, Case Record 45-1980, NEJM 303:1162-11710., , 1980

Osteopetrosis, Renal Tubular Acidosis & Basal Ganglia Calcification in Three Sisters
Am J Med 69:64-74, Whythe,M.P.,et al, 1980

Amelioration Of Neurologic Abnormalities After"Enzyme Replacement"In Adenosine Deaminase Deficiency
NEJM 303:377-380, Hirschhorn,R.,et al, 1980

Ventriculitis in an Adult Delineated by Radio Nuc. Brain Scan, Asso. with Misleading Findings on CT
Arch Neurol 37:381-383, Singh,R.S.,et al, 1980

Alternating Hemiplegia in Infants:Report of Five Cases
Dev Med Child Neurol 22:784-791, Krageloh,I.&Aicardi,J., 1980

Adult Polysaccharidosis
Arch Neurol 36:840-845, Peress,N.S.,et al, 1979

Clinical Recovery from Schilder Disease
Neurol 29:244-251, Ellison,P.H.,et al, 1979

Congenital Ocular Motor Apraxia
Arch Neurol 36:29-31, Orrison,W.W.,et al, 1979

Primary Glioblastoma of the Pineal Gland
Arch Neurol 36:717-718, Kalyanaraman,U.P., 1979

Showing articles 2050 to 2100 of 2279 << Previous Next >>