Neudle.com: "Krabbe's disease"

Differential
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acquired immunodeficiency syndrome

activated protein C resistance

acute disseminated encephalomyelitis

addiction, heroin

adrenoleukodystrophy

advances in neurology

anterior tibial muscle weakness

anticardiolipin antibodies

anticoagulant, treatment

antiphospholipid antibodies

antithrombin III deficiency

antiviral agents

aspirin

asymptomatic

attention deficit disorder with hyperactivity

Babinski sign

Behcet's syndrome

blindness

blood dyscrasias, neurologic findings with

bone marrow transplantation

Canavan's disease

carbenoxolone

cardiac arrest

cardiac arrest and resuscitation

cardiomyopathy

CAT scan

CAT scan, abnormal

CAT scan, contrast enhanced

CAT scan, delta sign, empty

CAT scan, false negative

CAT scan, venography

cerebellar lesion

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral infarction

cerebral ischemia

cerebral venous infarction

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebral venous thrombosis, etiology

cerebral venous thrombosis, recurrent

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, protein of

cerebrospinal fluid, proteincytologic dissociation

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

children

chloroquine

cholesterol

chronic graft versus host disease

Clinical Pathologic Conference(C.P.C.)

corpus callosum, lesion of

cost effectiveness

cranial nerve enlargement

craniectomy, decompressive

cry, abnormal

crying

cultured skin fibroblasts

D-dimer

deep gray nuclei

degenerative diseases of CNS

dementia

dementia, thalamic

demyelinating disease

dentate nuclei

dentate nuclei, lesion of

developmental disability

developmental milestones, loss of

developmental retardation

differential diagnosis

difficulty going down stairs

dipyridamole

disseminated intravascular coagulation(DIC)

distal muscle weakness

diuretic

drug induced neurologic disorders

dural sinus thrombosis

dysmorphic

electrocardiogram, abnormal

encephalopathy, progressive

enzyme, muscle disease

epidemiology of neurology

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

evidence-based research

exome sequencing

facial appearance, abnormal

fibrinolytic agents, intra-venous local infusion

flow study, carotid artery

genetic diagnosis, prenatal

genetic neurologic disorders

head injury, pediatric

hemoglobin abnormality, neurologic complications of

hepatosplenomegaly

high arched feet

human immunodeficiency virus type 1

hypoxic encephalopathy

incidence

infantile hemiplegia

interobserver agreement

intracranial hypertension, benign

intracranial pressure, increased

leukemia, neurologic findings assoc.with

leukocyte enzyme abnormality

leukodystrophy

leukoencephalopathy

leukoencephalopathy, differential diagnosis

level of consciousness, decreased

lipid lowering agent

lipid storage disorder of CNS

lipids

liquorice

lupus anticoagulant

lysosomal storage disease

lysosomes, abnoral

meconium staining

meningitis

metachromatic leukodystrophy

middle cerebral artery territory infarction

middle cerebral artery, occlusion of

misdiagnosis

mitochondrial disease

mortality

MRI

MRI, abnormal

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, false negative

MRI, hypointense signal foci on

MRI, negative

MRI, venography

MRS

mucopolysaccharidoses

multiple sclerosis

multiple sclerosis, familial

muscle weakness, causes of

myelinolysis, extrapontine

myeloproliferative disorder

myopathy, drug-induced

myopathy, hypokalemic

myopathy, proximal

myopathy, steroid induced

nausea and vomiting

nerve biopsy

nerve conduction studies

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic examination

neurologic examination, focal

neurologic signs

neuron specific enolase

neuropathology

neuropathy

neuropathy, demyelinating

neuropathy, peripheral

Niemann-Pick disease

nonsteroidal anti-inflammatory drug

opisthotonus

optic atrophy

optic chiasm, enlarged

optic nerve

optic nerve, enlarged

optic nerve, lesion of

oral contraceptives

oral contraceptives, cerbrovascular disease and

oral contraceptives, neurologic complications with

paraparesis, spastic

paroxysmal nocturnal hemoglobinuria

PAS positive material in the brain

plasminogen deficiency

platelet inhibiting drugs

polycythemia, primary

pons, lesion of

practice guidelines

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

prethrombotic state

primary thrombocythemia

prognosis

protein C deficiency

protein S deficiency

psychological testing

psychological testing, children

stem cell transplantation

steroid

straight sinus

sulfinpyrazone

superior sagittal sinus thrombosis

symmetric brain lesions

tandem gait, ataxic

Tay-Sachs disease

thalamic tumors

thalamic tumors, bilateral

thalamus

thalamus, infarction of

thalamus, infarction, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

thiamine deficiency

thrombocytopenia

thrombophlebitis

tissue plasminogen activator, intravenous

toe walking

tonic spasms

top of the basilar syndrome

transient ischemic attack

transient ischemic attack, treatment of

treatment of neurologic disorder

umbilical-cord blood transplantation

vincristine neurotoxicity

visual loss

walking, delayed

walking, difficulty with

Wernicke's encephalopathy

white matter disease

white matter disease, unilateral

wide based gait

workup

Showing articles 0 to 49 of 49

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

Pes Cavus and Neuropathy
Neurol 93:e823-e826, Alderson,J.,& Ghosh,P.S., 2019

Inherited Metabolic Diseases of the Nervous System, Globoid Cell Leukodystrophy (Krabbe Disease, Galactocerebrosidase)
Adams & Victors Principles of Neurology, Chp 37, pg 959, Ropper, A.H.,et al, 2014

Intracranial Optic Nerve Enlargement in Infantile Krabbe Disease
Neurol 78: e126, Shah, S.,et al, 2012

Unilateral White Matter Involvement in Krabbe Disease
Arch Neurol 68:130-131, Lemmens,R.,et al, 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

Patient with Unilateral White Matter Involvement Does Not Have Krabbe Disease
Arch Neurol 68:1345, Van der Knaap, M.S. and Wenger, D.A., 2011

Clinicopath Conf, Infantile Krabbe Disease
NEJM 362:346-356, Case 3-2010, 2010

Differential Diagnosis of Bilateral Thalamic Lesions
Clin Neuroradiol 17:3-22, Linn,J.,et al, 2007

Peripheral Neuropathy in Krabbe Disease. Effect of Hematopoietic Stem Cell Transplantation
Neurol 67:268-272, Siddiqi, Z.A.,et al, 2006

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

Familial Multiple Sclerosis and Other Inherited Disorders of the White Matter
The Neurologist 10:201-215, Kalman,B. &Leist,T.P., 2004

Insights Into the Diagnosis and Treatment of Lysosomal Storage Diseases
Arch Neurol 60:322-328, Wegner,D.A.,et al, 2003

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

MR Imaging and Proton MR Spectorscopy in Adult Krabbe Disease
AJNR 21:1478-1482, Farina,L. et al, 2000

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

Optic Nerve Enlargement in Krabbe's Disease
AJNR 20:1228-1231, Jones,B.V.,et al, 1999

Hematopoietic Stem-Cell Transplantation in Globoid-Cell Leukodystrophy
NEJM 338:1119-1126, Krivit,W.,et al, 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

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

Adult-Onset Krabbe Disease with Mutation in the Galactocerebrosidase Gene, MRI of Corticospinal Tract Demyelin
Neurol 49:1392-1399, Satoh,J.-I.,et al, 1997

Adult-Onset Krabbe's Disease in Siblings with Novel Mutations in the Galactocerebrosidase Gene
Ann Neurol 41:111-114, Bernardini,G.L.,et al, 1997

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

Globoid Cell Leukodystrophy:A Family with Both Late-Infantile and Adult Type
Neurol 41:1382-1384, Verdru,P.,et al, 1991

The Diagnosis of Childhood Neurodegenerative Disorders Presenting as Dementia in Adults
Neurol 41:794-798, Coker,S.B., 1991

Late Onset Globoid Cell Leukodystrophy
JNNP 54:1011-1012, Grewal,R.P.,et al, 1991

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

MR Findings in Globoid Cell Leucodystrophy
Neuroradiology 32:520-522, Demaerel,Ph.,et al, 1990

Childhood Stroke Associated with Protein C or S Deficiency
J Pediatr 111:562-564, Israels,S.J.&Seshia,S.S., 1987

Krabbe Disease:Specific MRI & CT Findings
Neurol 36:111-115, Baram,T.Z.,et al, 1986

Computed Tomography in White Matter Diseases
Ann Neurol 17:314-315, Ferriero,D.,et al, 1985

Computed Tomography in Krabbe's Disease:Comparison with Neuropathology
Neuroradiology 25:323-327, Ieshima,A.,et al, 1983

Perinatal Neuropathy as an Early Manifestation of Krabbe's Disease
Arch Neurol 37:446-447, Lieberman,J.S.,et al, 1980

Drug-Induced Myopathies In Man
Lancet 2:562-566, Lane,R.J.M.,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 49 of 49