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 250 to 300 of 895 << Previous Next >>

A 60-year-old woman with ataxia
Neurol 90:e1627-e1630, Dandapat, S.,et al, 2018

Brain MRI Characteristics of Patients with Anti-N-Methyl-D-Aspartate Receptor Encephalitis and Their Associations with 2-Year Clinical Outcome
AJNR 39:824-829, Zhang, T.,et al, 2018

Glial Fibrillary Acidic Protein Immunoglobulin G as Biomarker of Autoimmune Astrocytopathy: Analysis of 102 Patients
Ann Neurol 81:298-309, Flanagan, E.P.,et al, 2017

Amyotrophic Lateral Sclerosis
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Dentate Update: Imaging Features of Entities that Affect the Dentate Nucleus
AJNR 38:1467-1474, Bond, K.M.,et al, 2017

A 50-year-old Woman with SLE and a Tumefactive Lesion
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Rituximab as Treatment for anti-MuSK myasthenia gravis
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Neuroimaging Changes in Menkes Disease, Part 1
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Histopathological Findings in Brain Tissue Obtained during Epilepsy Surgery
NEJM 377:1648-1656, Blumcke, I.,et al, 2017

A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
Neurol 89:e220-e223, Xiao, F. & Wang, X.F., 2017

A Patient with a History of Encephalomyelitis and Recurrent Optic Neuritis
Neurol 89:e231-e234, Gutman, J.M.,et al, 2017

An 82-year-old man with Worsening Gait
Neurol 89:e246-e252, Chew, S.,et al, 2017

Long-Term Benefit of Enzyme Replacement Therapy in Pompe Disease
Neurol 89:2365-2373, Kuperus, E.,et al, 2017

Paraneoplastic and Autoimmune Encephalitis
UptoDate July, Dalmau, J.,et al, 2017

Clinicopathologic Conference, Primary Progressive Aphasia, Semantic Variant, due to TAR DNA Binding Protein 43 associated Frontotemporal Lobar Degen
NEJM 376:158-167, Case 1-2017, 2017

Autoimmune Encephalitides: A Broadening Field of Treatable Conditions
Neurologist 22:1-13, Kalman, B., 2017

Clinical Presentation and Prognosis in MOG-antibody Disease: A UK Study
BRAIN 140:3128-3138, Jurynczyk, M.,et al, 2017

A Case of Statin-Associated Autoimmune Myopathy
Clin Med Insights: Case Reports 10:1-4, Sweidan, A.J.,et al, 2017

Characteristics in Limbic Encephalitis with Anti-Adenylate Kinase 5 Autoantibodies
Neurol 88:514-524,508, Do, L. & Chanson, E., 2017

Investigations in GABA? Receptor Antibody-Associated Encephalitis
Neurol 88:1012-1020,1010, Spatola, M.,et al, 2017

Neurological Autoantibody Prevalence in Epilepsy on Unknown Etiology
JAMA Neurol 74:397-402,384, Dubey, D.,et al, 2017

Morvan Syndrome as a Paraneoplastic Disorder of Thymoma with Anti-CASPR2 antibodies
Lancet 389:1367-1368, Vale, T.C.,et al, 2017

Clinical Manifestations of the anti-IgLON5 Disease
Neurol 88:1736-1743,1688, Gaig, C.,et al, 2017

A 45-year-old man with Weakness and Myalgia after Orthopedic Surgery
Neurol 88:e185-e189, Vazquez do Campo, R.,et al, 2017

Autoimmune Encephalitis: Pathophysiology and Imaging Review of an Overlooked Diagnosis
AJNR 38:1070-1078, Kelley, B.P.,et al, 2017

An Older Man with Memory Impairment and Convulsions
BMJ 358:J2824, Zhao, X.,et al, 2017

A Man with Rapidly Ascending Paralysis
Neurol 89:e25-e31, Rosenberg, J.,et al, 2017

Autoimmune Encephalitis: Pathophysiology and Imaging Review of an Overlooked Diagnosis
AJNR 38:1070-1078, Kelley, B.P.,et al, 2017

Autoimmune Limbic Encephalitis Associated with Type 1 Diabetes Mellitus
J Clin Res Pediatr Endocrinol 9:387-388, Akin,O.,et al, 2017

Paraneoplastic Cerebellar Degeneration with Anti-Yo Antibodies - A Review
Ann Clin Trans Neurol 3:655-663, Venkatraman,A. & Opal,P., 2016

Severe Olfactory Dysfunction in Patients with Limbic Encephalitis
Neurol 86:April, Suppl P6.133, Schmidt, F.,et al, 2016

Bright Tongue Sign in Pompe Disease
Neurol 86:401, Karam, C., 2016

Faciobrachial Dystonic Seizures
Neurol 86:e60-e61, Schmerler, D.A.,et al, 2016

Leukodystrophy and Progressive Myoclonic Epilepsy Disclosing DRPLA
Neurol 86:e58-e59, Sgobbi de Souza, P.V.,et al, 2016

Statin-Associated Autoimmune Myopathy
NEJM 374:664-669, Mammen, A.L., 2016

Acute Bulbar Palsy as a Variant of Guillain-Barre Syndrome
Neurol 86:742-747, Kim, J.K.,et al, 2016

Orthostatic Myoclonus Associated with CASPR2 Antibodies
Neurol 86:1353-1355, Govert, F.,et al, 2016

The Relevance of VGKC Positivity in the Absence of LGI1 and Caspr2 Antibodies
Neurol 86:1692-1699,1657, Sonderen, A.V.,et al, 2016

A 38-Year-Old Man with Respiratory Failure and Progressive Leg Weakness
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A Young Man with Progressive Language Difficulty and Early-Onset Dementia
JAMA Neurol 73:595-599, Botha, H.,et al, 2016

Myasthenia Gravis
NEJM 375:2570-2581, Gilhus, N.E.,et al, 2016

NMDA-Receptor Encephalitis
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Neuromyelitis Optica Spectrum Disorders
UpToDate, May, Glisson,C.C., 2016

Anti-LGI1 Encephalitis
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Human Neurexin-3a Antibodies Associate with Encephalitis and Alter Synapse Development
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Autoantibodies to Glutamic Acid Decarboxylase in Patients with Epilepsy and Their Relationship with Type 1 Diabetes: A Pilot Study
JNNP 87:676-677, Moloney T.C.,et al, 2016

Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy
JAMA Neurol 73:1297-1307, Fang, B.,et al, 2016

Autoimmune Post-Herpes Simplex Encephalitis of Adults and Teenagers
Neurol 85:1736-1743, 1730, Armangue, T.,et al, 2015

Recognizing Autoimmune-Mediated Encephalitis in the Differential Diagnosis of Limbic Disorders
AJNR 36:2196-2205, da Rocha, A.J.,et al, 2015

Multiple-System Atrophy
NEJM 372:249-263, Fanciulli, A. & Wenning, G.K., 2015

Showing articles 250 to 300 of 895 << Previous Next >>