Neudle.com: "Cockayne's syndrome"

Differential
(Click to cross reference)

acanthocytosis

acquired immunodeficiency syndrome

activated protein C resistance

addiction, heroin

adrenoleukodystrophy

adverse drug reaction

anticardiolipin antibodies

anticoagulant, treatment

antiphospholipid antibodies

antithrombin III deficiency

aspirin

ataxia, cerebellar

basal ganglia, calcification of

basal ganglia, lesion, bilateral

Bassen-Kornzweig syndrome

Behcet's syndrome

blindness

blood dyscrasias, neurologic findings with

calcification, intracranial

carbenoxolone

cardiac arrest

cardiac arrest and resuscitation

CAT scan, delta sign, empty

CAT scan, venography

cataracts

cerebellar atrophy, secondary

cerebellar degeneration

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

cisternogram, radionuclide

craniectomy, decompressive

dentate nuclei, lesion of

dermatitis

developmental retardation

dipyridamole

disseminated intravascular coagulation(DIC)

diuretic

DNA probes

drug induced neurologic disorders

dural sinus thrombosis

dwarfism

dysmorphic

ear, abnormal

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electron microscopy

electronystagmography

enzyme, muscle disease

epidemiology of neurology

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

evidence-based research

eyes, sunken

facial appearance, abnormal

fibrinolytic agents, intra-venous local infusion

Friedreich's ataxia

fundus, abnormality of

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic testing

glaucoma

growth retardation

Hallervorden Spatz disease

Hallgren's syndrome

head injury

head injury, pediatric

hemoglobin abnormality, neurologic complications of

human immunodeficiency virus type 1

Hurler's syndrome

hydrocephalus

hydrocephalus, normal pressure

hydrocephalus, normal pressure in children

hypercholesterolemia

hyperpigmentation of skin

hypogonadism

hypokalemia

hypomyelination

hypoxic encephalopathy

incidence

infantile hemiplegia

interobserver agreement

intracranial hypertension, benign

intracranial pressure, increased

ipecac

Kearns-Sayre syndrome

keratoconus

Laurence-Moon-Bardet-Biedl syndrome

leukemia

leukemia, neurologic findings assoc.with

leukodystrophy

leukoencephalopathy

level of consciousness, decreased

malformation, CNS, congenital

meningitis

mental retardation

microcephaly

middle cerebral artery territory infarction

middle cerebral artery, occlusion of

misdiagnosis

mortality

movement disorder

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

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic examination, focal

neuron specific enolase

neuronal ceroid-lipofuscinosis

neuropathology, brain

neuropathy

neuropathy, hereditary peripheral

neuropathy, peripheral

night blindness

nonsteroidal anti-inflammatory drug

oral contraceptives, cerbrovascular disease and

oral contraceptives, neurologic complications with

paroxysmal nocturnal hemoglobinuria

perhexiline maleate

peroxisomal disease

photosensitivity, skin

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

pseudoretinitis pigmentosa

psychiatric disorder

psychomotor retardation

pulmonary embolism

pupil, abnormality in neurologic disorders

putamen, lesion of

putamen, lesion of, bilateral

sensorineural hearing loss

short stature

sickle cell disease

skin, lesions in neurologic disorders

skull x-ray, bony defect on

Spielmeyer Vogt syndrome

spinocerebellar degeneration

superior sagittal sinus thrombosis

tapetoretinal degeneration

thrombocytopenia

thrombophlebitis

tissue plasminogen activator, intravenous

transient ischemic attack

transient ischemic attack, treatment of

treatment of neurologic disorder

triglycerides

Usher's syndrome

vincristine neurotoxicity

visual field defect

visual fields, constricted

visual loss

white matter disease

workup

Showing articles 0 to 37 of 37

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

The Syndrome of Cutaneous Photosensitivity, Growth Failure, and Basal Ganglia Calcification
Neurol 87:e56-e57, Saini, A.G.,et al, 2016

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

Neuroimaging in Cockayne Syndrome
AJNR 31:1623-1630, Koob,M.,et al, 2010

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

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

Cockayne Syndrome: Review of 140 Cases
Am J Med Genet 42:68-84, Nance,M.A. &Berry,S.A., 1992

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

MRI in Cockayne Syndrome Type 1
Neuroradiology 31:276-277, Boltshauser,E.,et al, 1989

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

Prenatal Diagnosis of Cockayne's Syndrome
Lancet 1:486-488, Lehmann,A.R.,et al, 1985

Ultrastructure & Electrodiagnosis of Peripheral Neuropathy in Cockayne's Syndrome
Neurol 33:1606-1609, Grunnet,M.L.,et al, 1983

Cockayne Syndrome
J Comput Assist Tomogr 6:1172-1174, Levinson,E.D.,et al, 1982

Cockayne Syndrome:Unusual Neuropathological Findings & Review of the Literature
Ann Neurol 6:340-348, 1979, Soffer,D.,et al, 1979

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

Normal Pressure Hydrocephalus, Recog & Relation to Neuro Abnormalities in Cockayne's Sydrome
Arch Neurol 35:337, Brumback,R.A.,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

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

Showing articles 0 to 37 of 37