Neudle.com: neuronal storage disease

Differential
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abdominal cramps

acid maltase deficiency

acid maltase deficiency, adult

acral sensory symptoms

adrenoleukodystrophy

adrenomyeloneuropathy

adult polyglucosan body disease

adverse drug reaction

agalsidase alfa

agitation

alpha glucosidase

alternating rapid movement

aminoacidopathies

aminoacidurias

amniocentesis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, guamian type of

angina pectoris

angiokeratoma

anhidrosis

anterior horn cell disease

anterior tibial muscle weakness

anti GQ1b IgG antibody

anticonvulsants

anticonvulsants, selection of

Arnold Chiari malformation

arthropathy

arthropathy, neuropathic

arylsulfatase A

aspartate aminotransferase

aspiration

asymptomatic

ataxia

ataxia telangiectasia

atidarsagene autotemcel

attention

attention deficit disorder with hyperactivity

attention span

atypical

autoantibodies

autonomic dysfunction

axonal degeneration

axonal spheroid

Babinski sign

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar impression

Bassen-Kornzweig syndrome

behavioral disorder

bladder dysfunction

blindness

blood dyscrasias, neurologic findings with

bone marrow biopsy

bone marrow transplantation

bradykinesia

brain atrophy

brain biopsy

brain biopsy, complications of

brain biopsy, false negative

brain biopsy, indication

brainstem, infarction of

bulbar palsy

burning feet

burning feet, differential diagnosis of

CAT scan, false negative

catalepsy

cataplexy

cataracts

cerebellar ataxia, children

cerebellar ataxia, children, differential diagnosis of

cerebellar atrophy, primary

cerebellar degeneration

cerebellar infarction

cerebral cortical atrophy

cerebral ischemia

cerebro hepato renal syndrome

cerebrospinal fluid, gammaglobulin of

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, cryptogenic

cerebrovascular accident, familial occurrence

cerebrovascular accident, non atherosclerotic cause of

cerebrovascular accident, young adult

cerebrovascular disease

cerebrovascular disease, cardiovascular disease with

cherry red spot

cherry red spot-myoclonus syndrome

children

chorea

choreoathetosis

chromosomal abnormality

chronic graft versus host disease

Clinical Pathologic Conference(C.P.C.)

congestive heart failure

cornea, opacification in infancy-causes of

cornea, opacity of

corneal dystrophy

corpus callosum

corpus callosum, hypoplastic

corpus callosum, lesion of

creatine phosphokinase(CPK)elevated

creatinine, elevated

cry, abnormal

cultured skin fibroblasts

cystinosis

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia

dementia, childhood

dementia, diagnostic evaluation of

dementia, presenile

dentatorubral-pallidoluysian atrophy

depression

developmental disability

developmental milestones, loss of

developmental retardation

diagnostic criteria

diarrhea

differential diagnosis

difficulty going down stairs

diplopia

disease modifying agents

distal muscle weakness

DNA probes

drooling

dropped head syndrome

drug induced neurologic disorders

electroencephalogram, abnormalities of

electromyogram

electron microscopy

electronystagmography

electroretinograph

encephalitis, brainstem

episodic neurologic deficits

executive dysfunction

exercise intolerance

exome sequencing

eye movement, disorders of

Fabry's disease

facial appearance, abnormal

fine motor function, impaired

fundus, abnormality of

gangliosidosis, generalized

gargoylism

Gaucher's disease

gaze palsy

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

glucocerebrosidase

glycogen storage disease

glycoprotein

GM1 ganglioside

GM1 ganglioside antibodies

granular osmiphilic material

growth retardation

Guillain Barre syndrome, ophthalmoplegia in

Hallervorden Spatz disease

hallucination

hallucination, visual

hemorrhagic diathesis

hepatic failure

hepatitis

hepatolenticular degeneration(Wilson's disease)

hepatomegaly

hepatosplenomegaly

heralding manifestation

herpes virus infection

hexosaminidase-A

hexosaminidase-A and B

hypotension, systemic

inborn errors of metabolism

inborn errors of metabolism, screening

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, intracytopasmic

incoordination

infection, recurrent

intellectual deficit

intellectual deterioration

intelligence quotient

internuclear ophthalmoplegia

internuclear ophthalmoplegia, bilateral

intrathecal medication

intrinsic hand muscles, wasting of

introverted

iridoplegia

Jakob-Creutzfeldt disease

jaundice

Jewish

Kearns-Sayre syndrome

klippel feil syndrome

Krabbe's disease

kyphoscoliosis, neurologic causes of

Laurence-Moon-Bardet-Biedl syndrome

lead poisoning

learning disability, in children

Leigh's disease

leukocyte enzyme abnormality

leukocyte peroxidase

leukodystrophy

leukoencephalopathy

leukoencephalopathy, hereditary diffuse

Lewy body disease, diffuse

life expectancy

limb-girdle weakness

lipid storage disorder of CNS

liver disease

lymphadenopathy

lymphocyte fingerprint profiles

lysosomal storage disease

Marinesco-Sjogren syndrome

megalencephaly

memory, defect of recent

memory, impairment of

meningitis, chronic

mental retardation

MERRF syndrome

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

metachromatic leukodystrophy, juvenile

metachromatic leukodystrophy, late-infantile

microcephaly

miglustat

mimics

Mini Mental Status Examination

misdiagnosis

mitral valve prolapse

molecular genetics

mongolism

monoclonal antibodies

mortality

motor neuron disease

movement disorder

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, hypointense signal foci on

MRI, negative

MRI, serial

MRS

mucopolysaccharidoses

multiple sclerosis

multiple sclerosis, differential diagnosis of

muscle biopsy

muscle spasm

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscular dystrophy, Duchenne

myelomalacia

myeloneuropathy

myelopathy

myocardial infarction

myopathy, mitochondrial

myopathy, vacuolar

myopia

N-acetyl-L-aspartic acid

N-acetyl-L-leucine

negative

neonatal screening, genetic neurologic disorders

neoplasm, primary of CNS

neuraminidase deficiency

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neuroaxonal leukodystrophy

neurofibrillary degeneration

neurogenic bladder

neuroichthyosis

neurolipidosis IV

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic testing

neuronal ceroid-lipofuscinosis

neuroophthalmology

neuropathic pain scale

neuropathology

neuropathy

neuropathy, ataxic

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, painful

neuropathy, small-fiber

neuropathy, small-fiber, painful sensory

neurosis

next-generation sequencing

Niemann-Pick disease

night blindness

nystagmus

nystagmus, dissociated

one and a half syndrome

ophthalmoplegia

ophthalmoplegia, acute

ophthalmoplegia, bilateral, acute

ophthalmoplegia, plus syndrome

ophthalmoplegia, progressive external

ophthalmoplegia, total

optic atrophy

optic nerve

optic neuropathy

optokinetic nystagmus, abnormal

paraparesis, familial spastic

Parkinson disease, postencephalitic

Parkinsonism syndrome

paroxysmal neurologic deficits

PAS positive

PAS positive material in the brain

pigmentary retinopathy

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polyneuropathy

Pompe's disease of glycogen storage

Pompe's disease, infantile

precipitating factors

preclinical

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

prognosis

progressive myoclonic epilepsy

progressive neurologic disorder

proteinuria

pseudobulbar palsy

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychomotor retardation

psychosis

pupil, abnormality in neurologic disorders

putamen, lesion of

putamen, lesion of, bilateral

remote effect of cancer on the nervous system

renal failure

respiratory failure

respiratory tract infection

salivation, excessive

Salla disease

Sandhoff's disease

schizophrenia

scoliosis, neurologic association with

seizure, laughing as manifestation

seizure, paradoxical

seizure, treatment of

sensorineural hearing loss

skin, lesions in neurologic disorders

skull x-ray, abnormal

slit lamp examination

slurred speech

small vessel disease

spasticity

speech, delayed development of

sphingomyelin

spinal cord, compression of

spinocerebellar degeneration

splenomegaly

startle reaction

stem cell transplantation

storage disease of CNS

strabismus

stuttering

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

subdural hematoma

systemic illness

tandem gait, ataxic

tapetoretinal degeneration

Tay-Sachs disease

thalamus, lesion of

thalamus, lesion of-bilateral

thrombocytopenia

toe walking

tone, muscle, increased

tongue, enlarged

treatment of neurologic disorder

Unverricht-Lundborg disease

urea-cycle enzymopathies

urinary incontinence

urinary sulfatidase excretion

urine test for metabolic disorders

Usher's syndrome

vasculopathy

ventricular enlargement

vertebral-basilar insufficiency

vertigo

vestibulopathy

viral infection, CNS

vision, failure of in childhood

visual acuity, decreased

visual field defect

visual fields, constricted

visual loss

visual loss, progressive

visual loss, slow

visual loss, transient

visuospatial disturbance

Von Hippel Lindau

walking, delayed

walking, difficulty with

weakness

weakness, progressive

weakness, proximal

Werdnig-Hoffman disease

West disease

wheelchair

white matter disease

whole genome sequencing

wide based gait

writing

Showing articles 850 to 895 of 895 << Previous

Olivopontocerebellar Atrophy in Children:A Report of Seven Cases in Two Families
Ann Neurol 10:355-363, Colan,R.V.,et al, 1981

Biochemical Genetics Of Neurologic Disease
NEJM 305:1181-1193, Rosenberg,R.N., 1981

Brain Abnormalities in Infants with Fotter Syndrome (oligohydramnios tetrad)
Neurol 31:1571-1574, Grunnet,M.L.,et al, 1981

Progressive Pontobulbar Palsy With Deafness
Arch Neurol 38:186-190, Brucher,J.M.,et al, 1981

Lipid Storage Myopathy:Successful Treatment with Propranolol
BMJ 282:1997-1999, Martyn,C.,et al, 1981

No Direct Correl. of Serum Ach Receptor Antib. Levels & Clin. State of Individual Patients with Myasthenia Gravis
Neurol 31:220-224, Roses,A.D.,et al, 1981

Acute Thallium Poisoning, Toxicological & Morphological Studies of the Nervous System
Ann Neurol 10:38-44, Davis,L.E.,et al, 1981

A Progressive Neurologic Syndrome In Children With Chronic Liver Disease
NEJM 304:503-508, Rosenblum,J.L.,et al, 1981

Brain Peptides
(part I & II) NEJM 304:876-885, 944-951., Krieger,D.T.&Martin,J.G., 1981

Infantile Neuronal Degeneration Masquerading as Werdnig-Hoffmann Disease
Ann Neurol 8:317-324, Steiman,G.S.,et al, 1980

Humoral Immunity in Myasthenia Gravis:Effect of Steroids & Thymectomy
Neurol 30:554-557, Tindall,R.S.A., 1980

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

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

Agenesis of the Corpus Callosum:A Study of the Frequency of Associated Malformations
Ann Neurol 6:349-354, Parrish,M.L.,et al, 1979

The Aicardi Syndrome:Report of 4 Cases & Review of the Literature
Ann Neurol 5:475-482, Bertoni,J.M.,et al, 1979

Cytoarchitectonic Abnormalities in Developmental Dyslexia:A Case Study
Ann Neurol 6:94-100, Galaburda,A.M.,et al, 1979

Neonatal Myasthenia Gravis in the Infant of a Myasthenic Mother in Remission
Ann Neurol 6:72-75, Elias,S.B.,et al, 1979

Familial Subacute Necrotizing Encephalomyelopathy of the Adult Form (Adult Leigh Syndrome)
Ann Neurol 6:200-206, Kalimo,H.,et al, 1979

Penicillamine-induced Myasthenia Gravis Associated with Antibodies to Acetylcholine Receptor
Neurol 28:847-849, Russell,A.S.,et al, 1978

Weakness in Malignancy:Evidence for a Remote Effect of Tumor on Distal Axons
Ann Neurol 4:268-274, Barron,S.A.,et al, 1978

Fatal Infantile Form of Muscle Phosphorylase Deficiency
Neurol 28:1124-1129, DiMauro,S.,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

Serum Antibodies to Cytomegalovirus in Myasthenia Gravis:Effects of Thymectomy & Steroids
Neurol 28:273, Tindall,R.S.A.,et al, 1978

Function of Circulating Antibody to Acetylcholine Receptor in Myasthenia Gravis:Investigation by Plasma Exchange
Neurol 28:266, Newsom-Davis,J.,et al, 1978

Juvenile Neuroaxonal Dystrophy:Clinical, Electrophysiological, & Neuropathological Features
Ann Neurol 3:419, Dorfman,L.J.,et al, 1978

Content of Acetylch Receptor & Antib Bound to Receptor in Myasth Gravis, Experi Autoimm Myasth Gravis, & Syndrome
Neurol 28:130, Lindstrom,J.M., 1978

Myasthenia Gravis
NEJM 298:136, Drachman,D.B., 1978

Carnitine Deficiency Acute Postpartum Crisis
Ann Neurol 4:558-561, Angelini,C.,et al, 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

The Ultrastructure of the Sural Nerve in Pompe's Disease
Ann Neurol 2:111, Goebel,H.H.,et al, 1977

EEG Recognition of Aicardi's Syndrome
Arch Neurol 34:563, Fariello,R.G.,et al, 1977

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

Anti-Acetylcholine Receptor Antibody in Neonatal Myasthenia Gravis
NEJM 296:55, Keesey,J.,et al, 1977

Anti-Acetylcholine Receptor IgG in Neonatal Masthenia Gravis
NEJM 297:169, Nakao,K., 1977

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

The Adult Form of Acid Maltase (a-1, 4-Glucosidase) Deficiency
Ann Neurol 1:276, Karpati,G.,et al, 1977

Epidemiology of Motor-Neuron Diseases
NEJM 288:1047, Bobwick,A.R.,et al, 1973

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

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

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

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

Hysterical Hemiplegia and Hemianesthesia
Postgrad Med 31:339-345, Magee,K.R., 1962

Diseases of the Basal Ganglia-Their Relation to Disorders of Movement
Lancet 1099, 1960, Nov., Denny-Brown,D., 1960

Showing articles 850 to 895 of 895 << Previous