Neudle.com: "Batten's disease"

Differential
(Click to cross reference)

acquired immunodeficiency syndrome

activated protein C resistance

addiction, heroin

adrenoleukodystrophy

adverse drug reaction

alcohol

algorithm

alternating rapid movement

amniocentesis

amphotericin B

amyotrophic lateral sclerosis, guamian type of

anticardiolipin antibodies

anticoagulant, treatment

anticonvulsants

anticonvulsants, selection of

antiphospholipid antibodies

antithrombin III deficiency

basal ganglia, lesion of

basal ganglia, lesion, bilateral

Bassen-Kornzweig syndrome

behavioral disorder

Behcet's syndrome

blindness

blood dyscrasias, neurologic findings with

cardiac arrest and resuscitation

cardiomyopathy

CAT scan

CAT scan, abnormal

CAT scan, delta sign, empty

CAT scan, venography

cataracts

cerebellar atrophy, primary

cerebellar degeneration

cerebral cortical atrophy

cerebral infarction

cerebral ischemia

cerebral venous infarction

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebral venous thrombosis, etiology

cerebral venous thrombosis, recurrent

cerebro hepato renal syndrome

cerebrovascular accident

cerebrovascular accident, acute management of

cerebrovascular accident, cost of

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, prevention of

cerebrovascular accident, recurrent

cerebrovascular accident, thrombolytic agents in treatment

cerebrovascular accident, women

cerebrovascular accident, work up for

cerebrovascular accident, young adult

cerebrovascular disease, risk factors in

cerebrovascular disease, treatment of

cherry red spot

cherry red spot-myoclonus syndrome

children

chloroquine

cholesterol

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

craniectomy, decompressive

D-dimer

deep gray nuclei

degenerative diseases of CNS

dementia

dentatorubral-pallidoluysian atrophy

developmental milestones, loss of

developmental retardation

diagnostic criteria

dipyridamole

disseminated intravascular coagulation(DIC)

diuretic

DNA probes

drug induced neurologic disorders

dural sinus thrombosis

dysarthria

dysmetria

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electron microscopy

electronystagmography

enzyme, muscle disease

epidemiology of neurology

epsilon-aminocaproic acid(E.A.C.A.)

evidence-based research

eye movement, disorders of

fibrinolytic agents, intra-venous local infusion

fine motor function, impaired

fingerprint bodies

fundus, abnormality of

gadolinium

gait disorder

gangliosidosis GM1

gangliosidosis, generalized

gaze palsy

gaze palsy, supranuclear

genetic neurologic disorders

genetic testing

granular osmiphilic material

Hallervorden Spatz disease

head injury

head injury, pediatric

hemoglobin abnormality, neurologic complications of

herpes virus infection

human immunodeficiency virus type 1

hypoxic encephalopathy

inclusion bodies, eosinophilic cytoplasmic

infantile hemiplegia

intellectual deficit

intellectual deterioration

interobserver agreement

intracranial hypertension, benign

intracranial pressure, increased

introverted

ipecac

Jakob-Creutzfeldt disease

Kearns-Sayre syndrome

lactic acidemia

Lafora's disease

Laurence-Moon-Bardet-Biedl syndrome

lead poisoning

leukemia

leukemia, neurologic findings assoc.with

leukocyte peroxidase

level of consciousness, decreased

lymphocyte fingerprint profiles

lysosomal storage disease

macular degeneration

marche a petits pas

memory, impairment of

meningitis

mental retardation

MERRF syndrome

metachromatic leukodystrophy

microcephaly

middle cerebral artery territory infarction

middle cerebral artery, occlusion of

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, CAT scan compared to

MRI, contrast enhanced

mucopolysaccharidoses

muscle weakness, causes of

myeloproliferative disorder

myopathy, drug-induced

myopathy, hypokalemic

myopathy, mitochondrial

myopathy, proximal

myopathy, steroid induced

myopia

nausea and vomiting

negative

neuroaxonal dystrophy

neurofibrillary degeneration

neuroichthyosis

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic examination, focal

neuron specific enolase

neuronal ceroid-lipofuscinosis

neuroophthalmology

neuropathology

neuropathy

neuropathy, hereditary peripheral

Niemann-Pick disease

night blindness

nonsteroidal anti-inflammatory drug

ophthalmoplegia, plus syndrome

oral contraceptives, cerbrovascular disease and

oral contraceptives, neurologic complications with

paraparesis, familial spastic

Parkinson disease, postencephalitic

Parkinsonism syndrome

paroxysmal nocturnal hemoglobinuria

PAS positive

PAS positive material in the brain

perhexiline maleate

peroxisomal disease

pigmentary retinopathy

pitfalls

plasminogen deficiency

platelet inhibiting drugs

polycythemia, primary

practice guidelines

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

prethrombotic state

primary thrombocythemia

prognosis

progressive myoclonic epilepsy

progressive neurologic disorder

protein C deficiency

protein S deficiency

psychiatric problems in neurologic disorders

psychosis

pulmonary embolism

putamen, lesion of

putamen, lesion of, bilateral

seizure, treatment of

sensorineural hearing loss

sickle cell disease

skin, biopsy

skull x-ray, abnormal

slurred speech

spinocerebellar degeneration

steroid

storage disease of CNS

straight sinus

stuttering

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

sulfinpyrazone

superior sagittal sinus thrombosis

tapetoretinal degeneration

thrombocytopenia

thrombophlebitis

tissue plasminogen activator, intravenous

transient ischemic attack

transient ischemic attack, treatment of

treatment of neurologic disorder

Unverricht-Lundborg disease

Usher's syndrome

ventricular enlargement

vincristine neurotoxicity

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

Showing articles 0 to 46 of 46

A Teenager with Persistent Headache
Neurol 92:e1526-e1531, Hu, Y.,et al, 2019

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

Diagnosis and Management of Cerebral Venous Thrombosis: A Statement for Healthcare Professionals From the American Heart Association/American Stroke Association
Stroke 42:1158-1192, Saposnik,G.,et al, 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

Protein S Deficiency in HIV Associated Ischaemic Stroke:An Epiphenomenon of HIV Infection
JNNP 76:1455-1456,1331, Mochan,A.,et al, 2005

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

Use of Specialized Coagulation Testing in the Evaluation of Patients with Acute Ischemic Stroke
Neurol 56:624-627, Bushnell,C.,et al, 2001

Prethrombotic Disorders in Children with Arterial Ischemic Stroke and Sinovenous Thrombosis
Arch Neurol 56:967-971, Bonduel,M.,et al, 1999

Risk of Cerebral Sinus Thrombosis in Oral Contraceptive Users Who Are Carriers of Hered Prothrombotic Cond
BMJ 316:589-592, deBruijn,S.F.T.M.,et al, 1998

Neurology and the Blood:Haematological Abnormalities in Ischaemic Stroke
JNNP 64:150-159, Markus,H.S.&Hambley,H., 1998

Serum S-100 and Neuron-Specific Enolase for Prediction of Regaining Consciousness After Global Cerebral Ischemia
Stroke 29:2363-2366, Martens,P.,et al, 1998

Inherited Prothrombotic States and Ischaemic Stroke in Childhood
JNNP 65:508-511, Ganesan,V.,et al, 1998

Human Immunodeficiency Virus Infection and Stroke in Young Patients
Arch Neurol 54:1150-1153, Qureshi,A.I.,et al, 1997

Cerebral Venous Thrombosis in Adults:A Study of 40 Cases From Saudi Arabia
Stroke 26:1193-1195, Daif,A.,et al, 1995

Prothrombotic States in Young People with Idiopathic Stroke:Prospective Study
Stroke 25:287-290, Baringarrementeria,F., 1994

Ischemic Stroke Due to Deficiency of Coagulation Inhibitors, Report of 10 Young Adults
Stroke 24:19-25, Martinez,H.R.,et al, 1993

Free Protein S Deficiency in Acute Ischemic Stroke, A Case-Control Study
Stroke 24:224-227, Mayer,S.A.,et al, 1993

An Unusual Cause of Cerebral Venous Thrombosis in a Four-Year-Old Child
Stroke 24:603-605, Rich,C.,et al, 1993

Protein S Deficiency in Middle-Aged Women with Stroke
Neurol 42:1029-1033, Green,D.,et al, 1992

Superior Sagittal Sinus Thrombosis in a Child with Protein S Deficiency
Neurol 42:2303-2305, Prats,J.M.,et al, 1992

Superior Sagittal Sinus Thrombosis in a Patient with Protein S Deficiency
Stroke 21:633-636, Cros,D.,et al, 1990

Hematologic Disorders and Ischemic Stroke
Stroke 21:1111-1121, Hart,R.G.&Kanter,M.C., 1990

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

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

Childhood Stroke Associated with Protein C or S Deficiency
J Pediatr 111:562-564, Israels,S.J.&Seshia,S.S., 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

Drug-Induced Myopathies In Man
Lancet 2:562-566, Lane,R.J.M.,et al, 1978

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

Clofibrate-Induced Muscle Damage with Myoglobinuria & Cardiomyopathy
NEJM 296:942, Smals,A.G.H., 1977

Platelet-Inhibiting Drugs in the Prevention of Clinical Thrombotic Disease
NEJM 293:174, Genton,E.,et al, 1975

The Treatment of Cerebrovascular Disease with Clofibrate
VA Cooperative Study Group, Stroke 4:6841973., , 1973

Muscular Syndrome after Clofibrate
NEJM 286:1110, Katsilambros,N., 1972

Clofibrate for the Treatment of Occlusive CVD-Correspondence
NEJM 287:671, Hirsch,S.,et al, 1972

Showing articles 0 to 46 of 46