Neudle.com: infantile neuronal degeneration

Differential
(Click to cross reference)

abortion, spontaneous

acetylcholine receptor

acetylcholine receptor antibody

advances in neurology

adverse drug reaction

agenesis of corpus callosum

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, guamian type of

ANA

anesthesia, general

anesthesia, local

anti basal ganglia antibodies

anti MAG antibodies

antimetabolite

antistreptolysin titer

antithyroid antibodies

aphasia

areflexia

arthrogryposis multiplex

asymptomatic

ataxia

ataxia, truncal

atidarsagene autotemcel

basal ganglia, lesion of

basal ganglia, lesion, bilateral

bilateral periventricular nodular heterotopia

brain atrophy

brain biopsy

breast feeding

burst suppression pattern, electroencephalogram

CAT scan, abnormal

catatonia

central core disease

cerebellar degeneration

cerebral cortex

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cesarean section

Charcot-Marie-Tooth

cherry red spot

cherry red spot-myoclonus syndrome

children

chorioretinitis

chromosomal abnormality

chromosome 5

Clinical Pathologic Conference(C.P.C.)

coloboma

complications

confusion

confusional state, acute

congenital malformation

congenital malformation, non CNS

congenital myasthenic syndromes

corpus callosum

cortical dysplasia, focal

cyst, porencephalic

deep gray nuclei

degenerative diseases of CNS

dentate nuclei

dentate nuclei, lesion of

developmental milestones

developmental milestones, loss of

developmental retardation

differential diagnosis

drooling

dropped head syndrome

drug induced neurologic disorders

electroencephalogram, abnormalities of

emotional lability

encephalitis

encephalitis, autoimmune

encephalitis, focal

encephalitis, Rasmussen's

encephalomyelitis, postinfectious

encephalopathy

encephalopathy, Hashimoto's

enzyme, defect

epidemiology of neurology

epilepsia partialis continua

eye movement, disorders of

Fazio-Londe's disease

gammaglobulin therapy, intravenous

gangliosidosis GM2

gaze palsy

gaze palsy, supranuclear

gene

gene therapy

genetic neurologic disorders

genetic screening

hallucination

headache

heavy metal intoxication

hemihypertrophy, congenital

hexosaminidase-A and B

hypopigmentation of skin

hypotonia

hypotonia, infants

immunologic disease

immunosuppressive agents

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

infantile bilateral striatal necrosis

infantile neuronal degeneration

infantile spasm

insomnia

intellectual deficit

intellectual deterioration

iron, brain

Jewish

Kugelberg-Welander syndrome

level of consciousness, decreased

lipid storage disorder of CNS

lysosomal storage disease

macrocephaly

magnesium sulfate

malabsorption

malformation, CNS, congenital

Mary Walker phenomenon

megalencephaly

meningeal enhancement

mental retardation

mental status, abnormal

mesial temporal sclerosis

metachromatic leukodystrophy

metachromatic leukodystrophy, juvenile

metachromatic leukodystrophy, late-infantile

monoclonal antibodies

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, cortical enhancement

MRI, diffusion weighted

MRI, eye of tiger sign

MRI, gradient-echo

MRI, hypointense signal foci on

MRI, negative

MRI, paramagnetic effect

muscle biopsy

muscle spasm

muscle wasting, diffuse

muscular dystrophy, Duchenne

mutism

myasthenia gravis

myasthenia gravis, classification

myasthenia gravis, congenital

myasthenia gravis, infantile and juvenile

myasthenia gravis, neonatal

myasthenia gravis, neuromuscular junction in

myasthenia gravis, passive transfer of

myasthenia gravis, receptor site in

myasthenia gravis, seronegative

myasthenia gravis, thymectomy in

myasthenia gravis, treatment of

neoplasm, peripheral nerve

neoplasm, primary of CNS

neoplasm, primary of CNS-children

nerve conduction studies

nerve conduction studies, motor

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neurocutaneous disease

neurofibrillary degeneration

neurologic disease, diagnoses of

neurologic examination, focal

neuronal cell death

neuronal ceroid-lipofuscinosis

neuronal degeneration

neuronal migration disorder

neuroophthalmology

neuropathology

neuropathology, brain

optic nerve, lesion of

optic neuritis

PANK2 mutation

paraparesis, familial spastic

Parkinson disease

paroxysmal neurologic disorder

patient information and support

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

poison, mercury

poison, neurologic problems with

Pompe's disease of glycogen storage

Pompe's disease, infantile

postural abnormality

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

prognosis

psychiatric problems in neurologic disorders

psychomotor retardation

psychosis, childhood

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriparesis

recurrent

respiratory depression

respiratory failure

respiratory tract infection

segmental demyelination

seizure, intractable, treatment of

seizure, neonatal

seizure, prognosis in childhood

seizure, psychomotor-temporal lobe

seizure, surgical treatment of

seizure, treatment of

serologic testing

serologic testing, false negative

seronegative

skin, biopsy

skin, lesions in neurologic disorders

speech disorder, childhood

speech, loss of

spinal cord

spinal cord degeneration

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

spinocerebellar ataxia

startle reaction

status epilepticus

steroid

steroid therapy, CNS treatment and complications with

stillbirth

storage disease of CNS

streptococcal infection

striatal encephalitis

striatonigral degeneration

striatonigral degeneration, infantile

striatum, lesion of

Sturge-Weber syndrome

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

survival motor neuron gene

symmetric brain lesions

systemic lupus erythematosus

systemic lupus erythematosus, neonatal

systemic lupus erythematosus, neurologic complications with

Tay-Sachs disease

temporal lobe, status

thalamus, lesion of

thalamus, lesion of-bilateral

thymectomy

thymus and neuromuscular function

thyroiditis

titubation

tone, muscle, increased

treatment of neurologic disorder

tremor

tremor, intention

tricresylphosphate

trinucleotide repeats

tuberous sclerosis

ventricular enlargement

visual acuity, decreased

visual fields, constricted

visual loss

weakness

weakness, generalized

Werdnig-Hoffman disease

West disease

white matter disease

wide based gait

Showing articles 1450 to 1500 of 1511 << Previous Next >>

Sparing of the Onufrowicz Nucleus in Sacral Anterior Horn Lesions
Ann Neurol 4:245-249, Iwata,M.,et al, 1978

Cerebrovascular Disease in Infants & Children:A Study of Incidence, Clinical Features, & Survival
Neurol 28:763-768, Schoenberg,B.S.,et al, 1978

Mirror Movements after Childhood Hemiparesis
Neurol 28:1152-1158, Woods,B.T.,et al, 1978

The Lissencephaly, (Agyria) Syndrome in Siblings
Arch Neurol 35:608-611, Garcia,C.A.,et al, 1978

Human Brain, (Cytoarchitectonic Left-Right Asymmetries in the Temporal Speech Region)
Arch Neurol 35:812-817, Galaburda,A.M.,et al, 1978

Clinical Syndromes of Myasthenia in Infancy & Childhood
Arch Neurol 35:97, Fenichel,G.M., 1978

Plasmapheresis & Immunosuppressive Drug Therapy in Myasthenia Gravis
NEJM 297:1134, Dau,P.C.,et al, 1977

Penicillamine-associated Myasthenia Gravis, Antiacetylcholine Receptor & Antistriational Antibodies
Am J Med 63:689, Masters,C.L.,et al, 1977

Neonatal Ophthalmoplegia with Microfibers:A Reversible Myopathy
Neurol 27:974, Hanson,P.A.,et al, 1977

Strokes in Children & Adolescents
Current Concepts of Cerebrovascular Disease, Stroke 2:291977., , 1977

Azorean Disease of the Nervous System
NEJM 296:1505, Romanul,F.C.A.,et al, 1977

Guillain-Barre Syndrome with Hydrocephalus in Early Infancy
Arch Neurol 34:567, Gilmartin,R.C.,et al, 1977

Myasthenia Gravis, Study of Humoral Immune Mechanisms by Passive Transfer to Mice
NEJM 296:125, Toyka,K.V.,et al, 1977

Effective Treatment of Infantile Myasthenia Gravis by Combined Prednisone & Thymectomy
Neurol 27:550, Sarnat,H.B.,et al, 1977

Normocalcemic Tetany
Neurol 26:825, Isgreen,W.P., 1976

Neurological Complications of Infections of the Head & Neck
Otolaryng Clin North Am 9:729, Kaplan,R.J., 1976

Neurologic Disorders in Renal Failure (1st of Two Parts)
NEJM 294:143, Raskin,N.H.,et al, 1976

Congenital Rubella & Autistic Behavior
NEJM 293:198, Swisher,C.N.,et al, 1975

Diagnosis of Fabry's Disease by Tear-Galactosidase A-Correspondence NEJM 290:57
1974., , 1974

Narcotic Abuse:Neurologic Complications in Pedi & Adolescent Pts
JAMA 66:426, French,J.H.,et al, 1974

Niemann-Pick Disease
Correspondence NEJM 289:590, Dacremont,G.,et al, 1973

Neonatal Seizures
NEJM 289:413, Volpe,J., 1973

Juvenile Cerebral Arteriosclerosis & other Cerebral Arteriopathies of Childhood (Six Autopsied cases)
Acta Neurol Scand 48:479, Harvey,F.H.,et al, 1972

Section on Child Neurology-Neonatal Seizures
Neurol 22:419, Knauss,T.A., 1972

The Geography of Neurology
BMJ 2:506, Spillane,J.D., 1972

Pediatric Neurology
Psych Annals 2:1, , 1972

Prognosis in Childhood Epilepsy
NEJM 286:169, Olowach,J.,et al, 1972

Infantile Spinal Muscular Atrophy
Arch Neurol 25:276, Wilkins,R.,et al, 1971

Progressive Paresis of Vertical Gaze in Lipid Storage Disease
Neurol 21:896, Grover,W., 1971

Natural History of Acute Hemiplegia of Childhood
Brain 93:107, Soloman,G.E.,et al, 1970

Olivopontocerebellar Atrophies:A Review
Medicine 49:227, Konigsmark,B., 1970

Dopamine & Disease
C M A Journ 103:824, Barbeau,A., 1970

Electrophoretic Morphology of Gamma Globulins in Cerebrospinal Fluid of MS & other Diseases of the CNS
Neurol 20:982, Laterre,E.C.,et al, 1970

Prenatal Genetic Diagnosis
NEJM 283:1370, Milunsky,A.,et al, 1970

Neonatal Seizure States
Pediatrics 45:404, Rose,A.,et al, 1970

Abnormal Head Size, In Neurology In Pediatrics
(Ed) , 1970 Year Book Med. Publishers, p. 61., Bray,P.F., 1970

Chronic Spinal Muscular Atrophy in Adults
J Neurol Sci 9:551, Meadows,J.C.,et al, 1969

Progressive Supranuclear Palsy Clinico-Pathological Study of Four Cases
Brain 92:663, Behrman,S.,et al, 1969

Neurogenic Muscular Atrophy of Infancy with Prolonged Survival
Brain 92:9, Munsat,T.,et al, 1969

Chronic Spinal Muscular Atrophy in Adults
J Neurol Sci 9:527, Meadows,J.C.,et al, 1969

Diagnosis of Infantile Autism
Devel Med Child Neurol 11:432, Clancy,H.,et al, 1969

Acute Hemiplegia in Infancy & Childhood
Develop Med Child Neurol 2:162, Aicardi,J.,et al, 1969

Corticodentatonigral Degeneration with Neuronal Achromasia
Arch Neurol 18:20-33, Rebeiz,J.J.,et al, 1968

Infantile Spasms Favorable Response to Steroid Therapy
JAMA 201:116, Snyder,C.H., 1967

Long-Term Follow-up of Patients with Petit Mal
Arch Neurol 16:595, Charlton,M.H.,et al, 1967

Diseases of Muscles-Clinical Manifestations & Differential Diagnosis
The New Physic 263, 1967, Oct., Boshes,L., 1967

Tuberous Sclerosis:Reappraisal of a Clinical Entity
Mayo Clin Proc 42:26, Lagos,J.,et al, 1967

Breatholding Spells (Cyanotic & Pallid Infantile Syncope)
Pediatrics 39:563-581, Lombroso,C.T.,et al, 1967

Epilepsy in Children
Current Therapy, 1966, p. 574., Scholl,M.L., 1966

Current Concepts in Therapy Treatment of Seizure Disorders
NEJM 269:1304, 1963; 269:1421963., Scholl,M.L., 1963

Showing articles 1450 to 1500 of 1511 << Previous Next >>