Neudle.com: "Fabry's disease"

Differential
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abdominal cramps

acquired immunodeficiency syndrome

acral sensory symptoms

activated protein C resistance

alpha galactosidase A deficiency

aneurysm, intracranial

aneurysm, intracranial, familial

angina pectoris

angiography, cerebral

angiography, posterior fossa

angiokeratoma

anhidrosis

anticardiolipin antibodies

anticoagulant, treatment

antiphospholipid antibodies

antithrombin III deficiency

aortic arch ulcerated plaques

autonomic dysfunction

basal ganglia, calcification of

basilar artery occlusion

Behcet's syndrome

blood dyscrasias, neurologic findings with

brainstem, infarction of

burning feet

burning feet, differential diagnosis of

burning hands

burning paresthesia

calcification, intracranial

cancer, cerebrovascular accident complicating patients with

carbenoxolone

cardiac arrest

cardiac arrest and resuscitation

cardiomyopathy

CAT scan

CAT scan, abnormal

CAT scan, delta sign, empty

CAT scan, venography

cataracts

cavernous hemangioma

central nervous system, infection of

central pontine myelinolysis

cerebellar infarction

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy

cerebral embolism

cerebral infarction

cerebral infarction, subcortical

cerebral ischemia

cerebral venous infarction

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebral venous thrombosis, etiology

cerebral venous thrombosis, recurrent

cerebrospinal fluid, gammaglobulin of

cerebrovascular accident

cerebrovascular accident, acute management of

cerebrovascular accident, cost of

cerebrovascular accident, cryptogenic

cerebrovascular accident, etiology

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, non atherosclerotic cause of

cerebrovascular accident, prevention of

cerebrovascular accident, recurrent

cerebrovascular accident, thrombolytic agents in treatment

cerebrovascular accident, without occluded vessel

cerebrovascular accident, women

cerebrovascular accident, work up for

cerebrovascular accident, young adult

cerebrovascular disease

cerebrovascular disease, cardiovascular disease with

cerebrovascular disease, risk factors in

cerebrovascular disease, treatment of

children

chloroquine

cholesterol

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

congestive heart failure

cornea, abnormal

cornea, opacity of

corneal dystrophy

corpus callosum, lesion of

cost effectiveness

craniectomy, decompressive

dementia, rapidly progressive

diarrhea

differential diagnosis

diplopia

dipyridamole

disseminated intravascular coagulation(DIC)

diuretic

drug induced neurologic disorders

dural sinus thrombosis

dysarthria

echocardiogram

ectatic basilar artery

edema, pedal

efficacy

Ehlers-Danlos syndrome

electrocardiogram, abnormal

electron microscopy

embolic stroke of unknown source

enzyme, muscle disease

epidemiology of neurology

episodic disorders

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

evidence-based research

fibrinolytic agents, intra-venous local infusion

fibromuscular dysplasia

genetic neurologic disorders

genetic screening

genetic testing

glioma

globus pallidus, lesion of, bilateral

hand pain

head injury

head injury, pediatric

headache

headache, persistent

headache, severe

headache, thunderclap

hearing loss

heat intolerance

hemianopia, homonymous

hemiparesis

hemoglobin abnormality, neurologic complications of

hemorrhoids

hepatolenticular degeneration(Wilson's disease)

hereditary hemorrhagic telangiectasia(HHT)

homocystinuria

human immunodeficiency virus type 1

hydrocephalus

hydronephrosis

hypercholesterolemia

hypercoagulable state

hypertension

hypohidrosis

hypokalemia

hypoxic encephalopathy

inborn errors of metabolism

incidence

infantile hemiplegia

intellectual deficit

interobserver agreement

intracerebral hemorrhage

intracerebral hemorrhage, young adult

intracranial hypertension, benign

intracranial pressure, increased

ipecac

Jakob-Creutzfeldt disease

lacunar infarction

Leigh's disease

leukemia

leukemia, neurologic findings assoc.with

leukocyte enzyme abnormality

leukodystrophy

level of consciousness, decreased

lipid lowering agent

lipid storage disorder of CNS

lysosomal storage disease

malformation, vascular

malformation, vascular, cerebral

malformation, vascular, familial

marihuana

memory, impairment of

meningitis

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

microhemorrhage, intracerebral

middle cerebral artery territory infarction

middle cerebral artery, occlusion of

migraine

migraine, hemiplegic

misdiagnosis

mitral valve prolapse

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, false negative

MRI, gradient-echo

MRI, high signal foci on

MRI, negative

MRI, T1 weighted high signal foci

MRI, venography

multiple sclerosis, differential diagnosis of

muscle weakness, causes of

muscular dystrophy, Duchenne

myeloproliferative disorder

myocardial infarction

myopathy, drug-induced

myopathy, hypokalemic

myopathy, proximal

myopathy, steroid induced

nausea and vomiting

neoplasm, primary of CNS

nerve conduction studies

neurocutaneous disease

neurofibromatosis 1

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic examination, focal

neuron specific enolase

neuropathic pain scale

neuropathology

neuropathy

neuropathy, painful

neuropathy, peripheral, treatment

neuropathy, small-fiber

neuropathy, small-fiber, painful sensory

neurosis

next-generation sequencing

nonsteroidal anti-inflammatory drug

nystagmus

oral contraceptives

oral contraceptives, cerbrovascular disease and

oral contraceptives, neurologic complications with

osmotic demyelination syndrome

pain

pain, head

pain, neuropathic

Parkinsonism syndrome

paroxysmal nocturnal hemoglobinuria

patent foramen ovale

perhexiline maleate

pitfalls

plasminogen deficiency

platelet inhibiting drugs

polycythemia, primary

pons, lesion of

practice guidelines

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

prethrombotic state

primary thrombocythemia

pseudoxanthoma elasticum

psychiatric problems in neurologic disorders

respiratory tract infection

sensorineural hearing loss

sick sinus syndrome

sickle cell disease

skin, biopsy

skin, lesions in neurologic disorders

slit lamp examination

subarachnoid hemorrhage

sulfinpyrazone

superior sagittal sinus thrombosis

sweating, abnormality of

symmetric brain lesions

systemic illness

Tay-Sachs disease

thalamic tumors

thalamic tumors, bilateral

thalamus

thalamus, infarction of

thalamus, infarction, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

thrombocytopenia

thrombophlebitis

tinnitus

tissue plasminogen activator, intravenous

transient ischemic attack

transient ischemic attack, treatment of

treatment of neurologic disorder

vertebral-basilar insufficiency

vertigo

vertigo, episodic

vincristine neurotoxicity

visual loss

visual loss, transient

Von Hippel Lindau

Wernicke's encephalopathy

white matter disease

white matter disease, subcortical

workup

Showing articles 0 to 50 of 52 Next >>

Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
Neurol 100:766-783, Manini,A.,&Pantoni,L., 2023

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

Redefining the Pulvinar Sign in Fabry Disease
AJNR 38:2264-2269, Cocozza, S.,et al, 2017

Small Fiber Neuropathy in Fabry Disease:A Review of Pathophysiology and Treatment
JIEMS 4:1-5, Politeri,J.M.,et al, 2016

Embolic Strokes of Unknown Source and Cryptogenic Stroke: Implications in Clinical Practice
Front Neurol 7:1-16, Nouh, A.,et al, 2016

Mystery Case: A 21-Year-Old Man with Visual Loss Following Marijuana Use
Neurol 84:e165-e169, Whitlock, J.B.,et al, 2015

Inherited Metabolic Diseases of the Nervous System, Fabry Disease
Adams & Victors Principles of Neurology, Chp 37, pg 991, Ropper, A.H.,et al, 2014

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

Enzyme Replacement Therapy With Agalsidase Alfa in Patients With Fabrys Disease: An Analysis of Registry Data
Lancet 374:1986-1996, 1950, Mehta,A.,et al, 2009

Bilateral Thalamic Lesions
AJR 192:W53-W62, Smith,A.B.,et al, 2009

Prevalence of Fabry Disease in Patients with Cryptogenic Stroke: A Prospective Study
Lancet 366:1794-1796,1754, Rolfs,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

Enzyme Replacement Therapy Improves Function of C-, Adelta-, and Abeta- Nerve Fibers in Fabry Neuropathy
Neurol 62:1066-1072, Hilz,M.J.,et al, 2004

Recurrent Acroparaesthesia During Febrile Infections
Lancet 363:1698, Bodamer,O.A.,et al, 2004

T1 Hyperintensity in the Pulvinar: Key Imaging Feature for Diagnosis of Fabry Disease
AJNR 24:916-921, Takanashi,J.,et al, 2003

Increased Signal Intensity in the Pulvinar on T1-Weighted Images: A Pathognomonic MR Imaging Sign of Fabry Disease
AJNR 24:1096-1101, Moore,D.F.,et al, 2003

Neurological Presentation of Fabry's Disease in a 52 Year Old Man
JNNP 73:340-342, Mohanraj,R.,et al, 2002

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

Enzyme Replacement Therapy in Fabry Disease
JAMA 285:2743-2749, Schiffmann,R.,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

Cerebrovascular Complications of Fabry's Disease
Ann Neurol 40:8-17, Mitsias,P.&Levine,S.R., 1996

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

Anderson-Fabry Disease
Editorial, Lancet 336:24-251990., , 1990

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

Screening for Inherited Metabolic Diseases in Adults with Neurological Disease
Lancet 1:1101, Wierzbicki,A.S.,et al, 1988

Nervous System Involvement in Fabry's Disease:Clinicopath & Biochemical Correlation
Ann Neurol 23:505-509, Kaye,E.M.,et al, 1988

Anderson-Fabray Disease, A Commonly Missed Diagnosis
BMJ 297:872-873, Morgan,S.H.&Crawfurd,M., 1988

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

Mendelian Etiologies of Stroke
Ann Neurol 22:175-192, Natowicz,M.&Kelley,R.I., 1987

Clinicopathological Conference
Case 2-1984, Fabry's Disease, NEJM 310:106-114984., , 1984

Prenatal Genetic Diagnosis in 3000 Amniocenteses
NEJM 300:157-163, Golbus,M.S.,et al, 1979

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

Neurological Manifestations of Fabry Disease in Female Carriers
Ann Neurol 4:537-540, Bird,T.D.,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

Diagnosis of Fabry's Disease by Tear-Galactosidase A-Correspondence NEJM 290:57
1974., , 1974

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

Showing articles 0 to 50 of 52 Next >>