Neudle.com: "Hurler's syndrome"

Differential
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acanthocytosis

acquired immunodeficiency syndrome

activated protein C resistance

addiction, heroin

adrenoleukodystrophy

adverse drug reaction

anticardiolipin antibodies

anticoagulant, treatment

antiphospholipid antibodies

antithrombin III deficiency

arylsulfatase B

aspirin

ataxia, cerebellar

atlanto-axial subluxation

Bassen-Kornzweig syndrome

Behcet's syndrome

birth injury

blindness

blood dyscrasias, neurologic findings with

bone biopsy

bone marrow transplantation

carbenoxolone

cardiac arrest

cardiac arrest and resuscitation

cardiomyopathy

CAT scan

CAT scan, abnormal

CAT scan, delta sign, empty

CAT scan, venography

cataracts

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

children

chloroquine

cholesterol

chromosomal abnormality

cisterna magna, enlarged

Clinical Pathologic Conference(C.P.C.)

compression neuropathy

cornea, opacification in infancy-causes of

cornea, opacity of

corneal dystrophy

corpus callosum

corpus callosum, lesion of

cost effectiveness

craniectomy, decompressive

degenerative diseases of CNS

dementia

developmental milestones, loss of

developmental retardation

dipyridamole

disseminated intravascular coagulation(DIC)

dissociated sensory loss

diuretic

DNA probes

drug induced neurologic disorders

dural sinus thrombosis

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electron microscopy

electronystagmography

enzyme, muscle disease

epidemiology of neurology

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

evidence-based research

fibrinolytic agents, intra-venous local infusion

foam cells

Friedreich's ataxia

fundus, abnormality of

gadolinium

gangliosidosis GM1

gangliosidosis, generalized

gargoylism

gene mutation

gene therapy

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic testing

genu valgum

glaucoma

glycogen storage disease

growth retardation

Hallervorden Spatz disease

Hallgren's syndrome

head injury

head injury, pediatric

hemoglobin abnormality, neurologic complications of

hepatosplenomegaly

human immunodeficiency virus type 1

hypoxic encephalopathy

inborn errors of metabolism

incidence

infantile hemiplegia

intelligence quotient

interobserver agreement

intracranial hypertension, benign

intracranial pressure, increased

ipecac

Kearns-Sayre syndrome

keratoconus

Krabbe's disease

kyphoscoliosis, neurologic causes of

Laurence-Moon-Bardet-Biedl syndrome

leukemia

leukemia, neurologic findings assoc.with

leukodystrophy

level of consciousness, decreased

life expectancy

lipid lowering agent

lipid storage disorder of CNS

lipid storage myopathy

lipids

liquorice

lupus anticoagulant

lysosomal storage disease

lysosomes, abnoral

macrocephaly

macular degeneration

malformation, CNS, congenital

meningitis

mental retardation

metabolic disorder, primary

metachromatic leukodystrophy

middle cerebral artery territory infarction

middle cerebral artery, occlusion of

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, disappearing lesion on

MRI, false negative

MRI, high signal foci on

MRI, negative

MRI, venography

MRS

mucopolysaccharidoses

mucopolysacchariduria

muscle weakness, causes of

myelopathy

myeloproliferative disorder

myopathy, drug-induced

myopathy, hypokalemic

myopathy, mitochondrial

myopathy, proximal

myopathy, steroid induced

myopia

nausea and vomiting

neuritis

neuroaxonal dystrophy

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic examination, focal

neuron specific enolase

neuronal ceroid-lipofuscinosis

neuropathology

neuropathy

neuropathy, hereditary peripheral

Niemann-Pick disease

night blindness

nonsteroidal anti-inflammatory drug

obesity

ocular myopathy

ophthalmoplegia, plus syndrome

oral contraceptives, cerbrovascular disease and

oral contraceptives, neurologic complications with

osteoporosis

papilledema

paraparesis, spastic

paroxysmal nocturnal hemoglobinuria

pectus carinatum

perhexiline maleate

peroxisomal disease

pigmentary retinopathy

pitfalls

plasminogen deficiency

platelet inhibiting drugs

polycythemia, primary

polydactyly

practice guidelines

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

prethrombotic state

primary thrombocythemia

prognosis

protein C deficiency

protein S deficiency

pseudoretinitis pigmentosa

psychiatric disorder

psychological testing

psychological testing, children

sensorineural hearing loss

Spielmeyer Vogt syndrome

spinal cord, compression of

spinocerebellar degeneration

stem cell transplantation

steroid

straight sinus

sulfinpyrazone

superior sagittal sinus thrombosis

tapetoretinal degeneration

thrombocytopenia

thrombophlebitis

tissue plasminogen activator, intravenous

tongue, enlarged

transient ischemic attack

transient ischemic attack, treatment of

treatment of neurologic disorder

triglycerides

Usher's syndrome

vincristine neurotoxicity

visual acuity, decreased

visual field defect

visual fields, constricted

visual loss

white matter disease

workup

Showing articles 0 to 50 of 50

Hematopoietic Stem - and Progenitor-Cell Gene Therapy for Hurler Syndrome
NEJM 385:1929-1940, Gentner, B.,et al, 2021

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

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

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

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

Brain Magnetic Resonance Imaging in 23 Patients with Mucopolysaccharidoses and the Effect of Bone Marrow Transplantation
Ann Neurol 50:79-92, Seto,T.,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

Follow-up of Nine Patients with Hurler Syndrome After Bone Marrow Transplantation
J Pediatr 133:119-125, 71998., Guffon,N.,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

Mucopolysaccharidosis III (Sanfilippo Syndrome) Type B:Cranial Imaging in Two Cases
J Comput Assist Tomogr 21:897-899, Petitti,N.,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

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

Hunter Disease (Mucopolysaccharidosis Type II) in a Karyotypically Normal Girl
Clin genet 37:355-362, Clarke,J.T.,et al, 1990

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

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

Bone-Marrow Transplantation for Neurovisceral Storage Disorders
Editorial, Lancet 2:788-7891986., , 1986

Clinicopathological Conference
Maroteaux-Lamy Syndrome, Case 44-1983, NEJM 309:1109-1117983., , 1983

Mucopolysaccaridosis IV (Morquio Syndrome) , in The Metabolic Basis of Inherited Disease
(Ed) 5th Ed. , McGraw-Hill, New York, p. 766, Stanbury,J.B., 1983

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

Biochemical Genetics Of Neurologic Disease
NEJM 305:1181-1193, Rosenberg,R.N., 1981

Myelopathy in Mucopolysacchariodsis Type II (Hunter Syndrome)
Ann Neurol 7:382-385, Ballenger,C.E.,et al, 1980

Compressive Myelopathy in Maroteaux-Lamy Syndrome:Clinical & Pathological Findings
Ann Neurol 8:336-340, Young,R.,et al, 1980

Deficiency of Arylsulfatase B in 2 Brothers Aged 40 & 38 Years (Maroteaux-Lamy Syndrome, Type B)
Ann Neurol 6:315-325, Pilz,H.,et al, 1979

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

Neuropathology of Sanfilippo Syndrome
Ann Neurol 2:161, Ghatak,N.R.,et al, 1977

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

Infantile Metachromatic Leukodystrophy
NEJM 288:1365, 14051973., Leroy,J.,et al, 1973

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

Genetic Counseling in Retinitis Pigmentosa
MCV Quart 8:283, Noah,V., 1972

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

Corneal Opacification in Infancy
MCV Quart 8:230, Ching,F., 1972

Mucopolysaccaridosis IV (Morquio Syndrome) , in Heritable Disorders of Connective Tissue
(Ed) 4th Ed, The C. V. Mosby Co, St. Louis, p. 583, McKusick,V.A., 1972

The Mucopolysaccharidoses
(Ed) , 4th Edition, the C. V. Mosby Co, 1971, Chp. 11, p. p. 521-686., McKusick,V.A., 1971

Hunter's Syndrome, In Recognizable Patterns Of Human Malformation, Genetic, Embryologic, & Clinical Aspects, by Smith
W. B. , Saunders Co. , 1970, 248-249., David,W., 1970

Prenatal Genetic Diagnosis
NEJM 283:1370, Milunsky,A.,et al, 1970

Showing articles 0 to 50 of 50