Neudle.com: "ceroid-lipofuscinosis"

Differential
(Click to cross reference)

adrenoleukodystrophy

adverse drug reaction

alternating rapid movement

amniocentesis

amyotrophic lateral sclerosis, guamian type of

anticonvulsants

anticonvulsants, selection of

arm swing, reduced

ataxia

Babinski sign

basal ganglia, lesion of

basal ganglia, lesion, bilateral

Bassen-Kornzweig syndrome

cerebellar atrophy, primary

cerebellar degeneration

cerebral cortical atrophy

cerebro hepato renal syndrome

cherry red spot

cherry red spot-myoclonus syndrome

children

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

degenerative diseases of CNS

dementia

dentatorubral-pallidoluysian atrophy

developmental milestones, loss of

developmental retardation

diagnostic criteria

DNA probes

drug induced neurologic disorders

dysarthria

dysmetria

electroencephalogram, abnormalities of

electron microscopy

electronystagmography

electroretinograph

encephalopathy

eye movement, disorders of

falling

familial

fine motor function, impaired

fingerprint bodies

fundus, abnormality of

gait disorder

gangliosidosis GM1

gangliosidosis, generalized

gaze palsy

gaze palsy, supranuclear

genetic neurologic disorders

genetic testing

granular osmiphilic material

Hallervorden Spatz disease

herpes virus infection

inclusion bodies, eosinophilic cytoplasmic

intellectual deficit

intellectual deterioration

introverted

Jakob-Creutzfeldt disease

Kearns-Sayre syndrome

lactic acidemia

Lafora's disease

Laurence-Moon-Bardet-Biedl syndrome

lead poisoning

leukocyte peroxidase

lymphocyte fingerprint profiles

lysosomal storage disease

macular degeneration

marche a petits pas

memory, impairment of

mental retardation

MERRF syndrome

metachromatic leukodystrophy

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, serial

mucopolysaccharidoses

myopathy, mitochondrial

myopia

negative

neuroaxonal dystrophy

neurofibrillary degeneration

neuroichthyosis

neurologic disease, diagnoses of

neuronal ceroid-lipofuscinosis

neuroophthalmology

neuropathology

neuropathy

neuropathy, hereditary peripheral

Niemann-Pick disease

night blindness

ophthalmoplegia, plus syndrome

optic atrophy

optic nerve

optic neuropathy

paraparesis, familial spastic

Parkinson disease, postencephalitic

Parkinsonism syndrome

PAS positive

PAS positive material in the brain

peroxisomal disease

pigmentary retinopathy

prenatal diagnosis by amniocentesis

prognosis

progressive myoclonic epilepsy

progressive neurologic disorder

psychiatric problems in neurologic disorders

psychosis

putamen, lesion of

putamen, lesion of, bilateral

seizure, treatment of

sensorineural hearing loss

skin, biopsy

skull x-ray, abnormal

slurred speech

spinocerebellar degeneration

storage disease of CNS

stuttering

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

tapetoretinal degeneration

treatment of neurologic disorder

tremor

tremor, intention

tuberous sclerosis

Unverricht-Lundborg disease

Usher's syndrome

ventricular enlargement

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

walking, difficulty with

Werdnig-Hoffman disease

West disease

wheelchair

wide based gait

Showing articles 0 to 20 of 20

Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy
Neurol 90:e1827-e1831, Xiao, F.,et al, 2018

Diagnosis and Misdiagnosis of Adult Neuronal Ceroid Lipofuscinosis
Neurol 87:579-584, Berkovic, S.F.,et al, 2016

Inherited Metabolic Diseases of the Nervous System, Neuronal Ceroid Lipofuscinosis (Batten Disease)
Adams & Victors Principles of Neurology, Chp 37, pg 973, Ropper, A.H.,et al, 2014

Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis
NEJM 364:1062-1074, Case 8-2011, 2011

A 23-Year-Old Man With Seizures and Visual Deficit
Neurol 70:73-78, Boustany,R.-M.,et al, 2008

Progressive Myoclonic Epilepsies: A Review of Genetic and Therapeutic Aspects
Lancet Neurol 4:239-248, Shahwan, A., et al, 2005

Clinicopath Conf, Neuronal Ceroid Lipofuscinosis, Late-Onset Infantile Subtype
NEJM 347:672-680, Case 27-2002, 2002

Retinitis Pigmentosa
Surv Ophthalmol 33:137-177, Pagon,R.A., 1988

CT in Ceroid Lipofuscinosis
Neurol 37:1025-1026, Dunn,D.W., 1987

Progressive Myoclonus Epilepsies:Specific Causes & Diagnosis
NEJM 315:296-305, Berkovic,S.F.,et al, 1986

Prenatal Diagnosis of Neuronal Ceroid Lipofuscinosis
NEJM 310:595, MacLeod,P.M.,et al, 1984

Familial Occurrences of Adult-Type Neuronal Ceroid Lipofuscinosis
Arch Neurol 41:1091-1094, Tobo,M.,et al, 1984

Neurodegenerative Disease of Infancy & Childhood
Ann Neurol 13:351-364, Dyken,P.,et al, 1983

Santavuori Disease:Diagnosis by Leukocyte Ultrastructure
Neurol 32:1277-1281, Baumann,R.J.,et al, 1982

An Ultramicroscopic Study of Skin & Conjunctival Biopsies in Chronic Neuro. Disorders of Childhood
Ann Neurol 9:163-173, Arsenio-Nunes,M.L.,et al, 1981

Alzheimer Neurofibrillary Tangles in Diseases Other Than Senile & Presenile Dementia
Ann Neurol 5:288-294, Wisniewski,K.,et al, 1979

Clinical Pathological Conference
Neuronal Veroid-lipfuscinosis, Juvenile Variant, (Batten's disease) , NEJM 299:189., , 1978

Clinical & Extraneural Histologic Diagnosis of Neuronal Ceroidlipofuscinosis
Neurol 28:1008-1012, Miley,C.E.III.,et al, 1978

Diagnostic Significance of Myeloperoxidase Assay in Neuronal Ceroidlipofuscinoses (Batten-Vogt Syndrome)
Neurol 28:924-927, Pilz,H.,et al, 1978

Juvenile Amaurotic Idiocy (Neuronal Ceroid Lipofuscinosis) & Lymphocyte Fingerprint Profiles
Ann Neurol 4:531-536, Baumann,R.J.,et al, 1978

Showing articles 0 to 20 of 20