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 650 to 700 of 895 << Previous Next >>

Paraneoplastic Cerebellar Degeneeration with Anti-Yo Antibody in a Man
Neurol 45:1226-1227, Felician,O.,et al, 1995

Multifocal Motor Neuropathy with Conduction Block:A Study of 24 Patients
JNNP 59:38-44, Bouche,P.,et al, 1995

Clinical Experience with Excitatory Amino Acid Antagonist Drugs
Stroke 26:503-513, Muir,K.W.&Lees,K.R., 1995

Anticardiolipin Antibodies in Normal Subjects:Neuropsychological Correlates and MRI Findings
Stroke 26:749-754, Schmidt,R.,et al, 1995

Dentatorubral-Pallidoluysian Atrophy:Clin Features Closely Related to Unstable Expansion of Trinucleotide (CAG) Repeat
Ann Neurol 37:769-775, Ikeuchi,T.,et al, 1995

Apolipoprotein E Genotype in Diverse Neurodegenerative Disorders
Ann Neurol 38:131-135, Schneider,J.A.,et al, 1995

Neuropsychiatric Lupus Erythematosus:A 10-Year Prospective Study on the Value of Diagnostic Tests
Am J med 99:153-163, West,S.G.,et al, 1995

Myositis:Immunologic Contributions to Understanding Cause, Pathogenesis, and Therapy
Ann Int Med 122:715-724, Plotz,P.H.,et al, 1995

Calcium-Channel Antibodies in the Lambert-Eaton Syndrome and Other Paraneoplastic Syndromes
NEJM 332:1467-1474, Lennon,V.A.,et al, 1995

Genotype-Phenotype Correlation in Adult-Onset Acid Maltase Deficiency
Ann Neurol 38:450-454, Wokke,J.H.J.,et al, 1995

Clinical Variability in Adult-Onset Acid Maltase Deficiency:Report of Affected Sibs and Review of Literature
Medicine 74:131-135, Felice,K.J.,et al, 1995

Machado Joseph Disease Maps to Same Region of Chromosome 14 as Spinocerebellar Ataxia Type 3 Locus
J Med Genet 32:25-31, Twist,E.C.,et al, 1995

Lambert-Eaton Myasthenic Syndrome:Clinical Diagnosis,Immune-Mediated Mechanisms,and Update on Therapies
Ann Neurol 37:S63-S73, Sanders,D.B., 1995

Magnetic Resonance Imaging of Brain Iron in Health and Disease
J Neurol Sci 134:19-26,1, Vymazal,J.,et al, 1995

Treatable Gait Disorder & Polyneuropathy Assoc with High Titer Serum IgM Binding to Atg that Copurify with MAG
Muscle & Nerve 17:1293-1300994., Pestronk,A.,et al, 1994

Ocular Myasthenia:A Protean Disorder
Survey of Ophthalmology 39:169-210, Weinberg,D.A.,et al, 1994

The Apolipoprotein E Alleles as Major Susceptibility Factors for Creutzfeldt-Jakob Disease
Lancet 344:1315-1318, 13101994., Amouyel,P.,et al, 1994

The Ischemic Penumbra, Injury Thresholds, and the Therapeutic Window for Acute Stroke
Ann Neurol 36:553-554, 5571994., Ginsberg,M.D.&Pulsinelli,W.A., 1994

Trinucleotide Repeat Expansion in Neurological Disease
Ann Neurol 36:814-822, LaSpada,A.R.,et al, 1994

Clinical and Biochemical Features of 10 Adult Patients with Muscle Phosphorylase Kinase Deficiency
Neurol 44:461-466, Wilkinson,D.A.,et al, 1994

Anti-Hu-Associated Peripheral Nerve and Muscle Microvasculitis
Neurol 44:181-183, Younger,D.S.,et al, 1994

Subependymal Heterotopia:A Distinct Neuronal Migration Disorder Associated with Epilepsy
JNNP 57:1195-1202, Raymond,A.A.,et al, 1994

Excitatory Amino Acids as a Final Common Pathway for Neurologic Disorders
NEJM 330:613-622, Lipton,S.A.&Rosenberg,P.A., 1994

The Clinical Correlates of High-Titer IgG Anti-GM1 Antibodies
Ann Neurol 35:234-237, Kornberg,A.J.,et al, 1994

Dementia of Adult Polyglucosan Body Disease, Evidence of Cortical and Subcortical Dysfunction
Arch Neurol 51:90-94, Rifai,Z.,et al, 1994

Serum Factor in Miller-Fisher Variant of Guillain-Barre Syndrome and Neurotransmitter Release
Lancet 343:454-455, Roberts,M.,et al, 1994

A Controlled Trial of Riluzole in Amyotrophic Lateral Sclerosis
NEJM 330:585-591, Bensimon,G.,et al, 1994

Amyotrophic Lateral Sclerosis Patient Antibodies Label CA2+Channel a1 Subunit
Ann Neurol 35:164-171, 1311994., Fumiharu,K.,et al, 1994

Intravenous Immunoglobulin Trtm in Pts with Motor Neuron Syndromes Assoc with Anti-GM Antibodies:A Contrld Study
Neurol 44:429-432, Azulay,J-P.,et al, 1994

Speculations on Antineuronal Antibody-Mediated Neuropsychiatric Disorders of Childhood
Pediatrics 93:323-325, Swedo,S.,et al, 1994

Periventricular Heterotopia and Epilepsy
Neurol 44:51-55, Huttenlocher,P.R.,et al, 1994

Neuronal Migration Disorders:Positron Emission Tomography Correlations
Ann Neurol 35:290-297, Lee,N.,et al, 1994

Prophylactic Neuroprotection for Cerebral Ischemia
Stroke 25:1075-1080, Fisher,M.,et al, 1994

Differences in the Pattern of Hippocampal Neuronal Loss in Normal Ageing and Alzheimer's Disease
Lancet 344:769-772, West,M.J.,et al, 1994

Medical Aspects of the Persistent Vegetative State
NEJM 330:1499-1508, 1572-15791994., Annas,G.J.,et al, 1994

Mononeuritis Multiplex and Vasculitis:Association with Anti-Neutrophil Cytoplasmic Autoantibody
Arch Neurol 51:565-568, Kafka,S.P.,et al, 1994

Anti-Ro (SS-A) Autoantibodies in CNS Disease Assoc with Sjogren's Synd (CNS-SS) :Clin, Neuroimaging & Angiographic Correl
Neurol 44:899-908, Alexander,E.L.,et al, 1994

Oxidative Damage in Neurodegenerative Disease
Lancet 344:796-798, Jenner,P., 1994

Antineuronal Antibodies in Acute Cerebellar Ataxia Following Epstein-Barr Virus Infection
Neurol 44:1506-1507, Ito,H.,et al, 1994

Myasthenia Gravis
NEJM 330:1797-1810, Drachman,D.B., 1994

Clinicopath Conf
Small Cell CA (of lung) with Lambert-Eaton Myasthenic Syndr, Case 32-1994, NEJM 331:528-5354., , 1994

Anti-Ri Antibodies Associated with Opsoclonus and Progressive Encephalomyelitis with Rigidity
Neurol 44:1521-1522, Casado,J.L.,et al, 1994

Paraneoplastic Opsoclonus-Myoclonus Associated with Anti-Hu Antibody
Neurol 44:1754-1755, Hersh,B.,et al, 1994

Paraneoplastic Temporal Lobe Epilepsy with Testicular Neoplasm and Atypical Amnesia
neurol 44:1270-1274, Ahern,G.L.,et al, 1994

Reversal of Subacute Paraneoplastic Cerebellar Syndrome with Intravenous Immunoglobulin
Neurol 44:1184-1185, Counsell,C.E.,et al, 1994

Total Body Irradiation for Myasthenia Gravis:A Long-Term Follow-up
Neurol 43:2215-2221, Durelli,L.,et al, 1993

Myositis-Specific Autoantibodies, Touchstones for Understanding the Inflammatory Myopathies
JAMA 270:1846-1849, Miller,F.W., 1993

Regression of Small-Cell Lung Carcinoma in Patients with paraneoplastic Neuronal Antibodies
Lancet 341:21-22, Darnell,R.B.&DeAngelis,L.M., 1993

The Polymerase Chain Reaction:Application to Nervous System Disease
Ann Neurol 34:513-523, Darnell,R.B., 1993

Gene Therapy for Neurologic Disease
Arch Neurol 50:1252-1268, Suhr,S.T.&Gage,F.H., 1993

Showing articles 650 to 700 of 895 << Previous Next >>