Neudle.com: familial stroke syndrome

Differential
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abdominal cramps

abducens nerve paralysis

abscess, intracerebral

abscess, intracranial

abscess, perivalvular

acid maltase deficiency

acid maltase deficiency, adult

acral sensory symptoms

activated protein C resistance

acute disseminated encephalomyelitis

alpha galactosidase A deficiency

amyloid angiopathy, cerebral

amyloid angiopathy, cerebral, Dutch type

amyloid angiopathy, hereditary cystatin C

amyloidosis

amyloidosis, oculoleptomeningeal, familial

anatomy of

anemia

aneurysm

aneurysm, asymptomatic

aneurysm, berry

aneurysm, intracranial

aneurysm, intracranial, familial

aneurysm, intracranial, screening for

aneurysm, intracranial, treatment of

aneurysm, multiple intracranial

aneurysm, size

aneurysm, unruptured

angina pectoris

angiography, cerebral

angiography, posterior fossa

angioid streaks

anhidrosis

antibiotic prophylaxis

anticoagulant, contraindications

anticoagulant, treatment

antiphospholipid antibodies

antithrombin III deficiency

anxiety

aortic valve, bicuspid

aortic valve, lesion of

arterial dissection, aorta

arterial dissection, carotid

arterial dissection, cerebral

arterial dissection, intracranial

arterial dissection, multiple

arterial dissection, recurrent

arterial dissection, renal artery

arterial dissection, ruptured

arterial dissection, vertebral

arteriopathy

arteriovenous malformation

arteriovenous malformation, cerebral

arteriovenous malformation, pulmonary

ataxia telangiectasia

ataxia, progressive

ataxic gait

atherosclerosis, premature

atrial appendage closure

atrial fibrillation

atrial fibrillation, surgical treatment

atrial fibrillation, treatment

atrial myxoma

atrioventricular block

attention deficit disorder with hyperactivity

autonomic dysfunction

Babinski sign

bacterial endocarditis, neurologic manifestations of

bacterial infection

bacterial infection, CNS

basal ganglia, calcification of

basal ganglia, hemorrhage

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar impression

behavioral disorder

Behcet's syndrome

benign essential tremor

Binswanger disease

bleeding disorder

blood dyscrasias, neurologic findings with

brainstem, dysfunction

brainstem, hypoplasia

brainstem, infarction of

brainstem, lesion of

brainstem, malformation

brainstem, neoplasms of

brainstem, vascular malformation of

brucellosis

brucellosis, nervous system involvement with

calcification, intracranial

calcification, muscle

calcium oxalate crystals

calf hypertrophy

Canavan's disease

capillary blush

carbon monoxide poisoning

carcinoma

carcinoma of pancreas

carotid artery disease

carotid artery occlusion, bilateral

carotid artery occlusion, intracranial

carotid artery stenosis, intracranial

CAT scan

CAT scan, abnormal

CAT scan, abscess, cerebral

CAT scan, angiography

CAT scan, chest

CAT scan, disappearing lesion on

CAT scan, emission

CAT scan, false negative

cataracts

catecholamine

cavernous hemangioma

central nervous system, infection of

cerebellar atrophy, primary

cerebellar hemorrhage

cerebellar infarction

cerebellar peduncle

cerebellum, neoplasms of

cerebral atherosclerosis

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral edema, vasogenic

cerebral embolism

cerebral embolism, cardiac origin

cerebral embolism, carotid origin

cerebral infarction

cerebral infarction, hemorrhagic

cerebral infarction, small, deep

cerebral infarction, subcortical

cerebral ischemia

cerebral palsy

cerebral palsy, risk factors

cerebral peduncle

cerebral vasculature, calcification

cerebral venous infarction

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebral venous thrombosis, etiology

cerebritis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, red cells in

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, bilateral

cerebrovascular accident, cardiac disease causing

cerebrovascular accident, cryptogenic

cerebrovascular accident, etiology

cerebrovascular accident, familial occurrence

cerebrovascular accident, genetic

cerebrovascular accident, infancy and childhood

cerebrovascular accident, intrauterine

cerebrovascular accident, location of

cerebrovascular accident, mimics

cerebrovascular accident, multiple

cerebrovascular accident, neonatal

cerebrovascular accident, non atherosclerotic cause of

cerebrovascular accident, nonvascular territory

cerebrovascular accident, prevention of

cerebrovascular accident, recurrent

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, surgical treatment of

Charcot-Marie-Tooth

chest x-ray, abnormal

chromosomal abnormality

chronic progressive external ophthalmoplegia

cigarette smoking

cirrhosis

Clinical Pathologic Conference(C.P.C.)

coin lesion on chest X-ray

COL4A1 related disorder

collagen vascular disease

collateral circulation

coma

complications

compression neuropathy

confusion

congenital heart disease

congenital malformation

congestive heart failure

controversies in neurology

cornea, abnormal

cornea, opacity of

corneal dystrophy

coronary artery disease

corpus callosum

corpus callosum, infarction of

corpus callosum, lesion of

cortical blindness

cortical blindness, transient

cranial neuropathy, multiple

craniopharyngioma

creatine phosphokinase(CPK)elevated

Creutzfeldt-Jakob disease, genetic

cultured skin fibroblasts

deafness, bilateral progressive vs.unilateral acute

deafness, unilateral

deep gray nuclei

deficiency of ADA2

degenerative diseases of CNS

delay in diagnosis

dementia

dementia, cerebrovascular disease causing

dementia, rapidly progressive

dementia, subcortical

dementia, thalamic

demyelinating disease

dental procedure, neurologic complications with

dentate nuclei

dentate nuclei, lesion of

depression

developmental abnormality of brain

developmental retardation

developmental venous anomalies

diagnostic criteria

diaphragmatic paralysis

diarrhea

differential diagnosis

dilated aortic root

diplopia

diplopia, transient

disability rating scale, neurological

dizziness

DNA probes

dopamine

dural sinus thrombosis

dystonia musculorum deformens

ear, pain in

early draining vein

echocardiogram

echocardiogram, contrast

echocardiogram, transesophageal, false negative

echocardiogram, transthoracic

echocardiogram, transthoracic, false negative

ectatic basilar artery

edema, pedal

Ehlers-Danlos syndrome

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electroencephalogram, monitoring, continuous

electroencephalogram, pediatric patients

embolism, paradoxical

embolism, septic

embolism, systemic

embolization, therapeutic

emergencies, ocular

Emery-Dreifuss muscular dystrophy

emotional lability

encephalitis

encephalitis, Japanese

encephalitis, viral

encephalopathy

encephalopathy, metabolic

encephalopathy, neonatal

encephalopathy, progressive

endocarditis

endocarditis, acute bacterial

endocarditis, prophylaxis

endovascular therapy

entrapment neuropathy

enzyme, defect

epidemiology of neurology

epileptic encephalopathy

episodic neurologic deficits

eye movement, disorders of

Fabry's disease

facial anomalies

facial appearance, abnormal

facial expression abnormality

facial hypoplasia

facial nerve palsy

facial nerve palsy, bilateral

facial nevus

Factor V Leiden

factor V, deficiency

factor VII, deficiency

familial hemiplegic migraine

familial mediterranean fever

fever

fibrillations

fibrinogen

fibrinolytic agents, contraindications

fibromuscular dysplasia

fingers, abnormal

fistula, arterio-venous

fistula, arterio-venous, carotid-cavernous

fistula, arterio-venous, pulmonary

flavivirus

fluorescein angiography

foot drop

fourth ventricle, enlargement of

frontal bossing

fundus, abnormality of

gadolinium

gait disorder

galactosidase

gamma amino butyric acid

gangliosidosis GM2

gastrointestinal bleeding

gastrointestinal perforation

gaze palsy

gaze palsy, congenital horizontal

gaze palsy, horizontal

gaze palsy, horizontal-bilateral

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

genu of corpus callosum

Gilles de la Tourette syndrome

granular osmiphilic material

granulomatosis with polyangiitis

granulomatous disease

gyrus, abnormal

headache

headache, positional

headache, sudden onset of

headache, throbbing

headache, thunderclap

headache, unilateral

hearing loss

hearing loss, bilateral

heart block

heart block, complete

heart murmur

heart valve surgery

hemangioblastoma

hemangioma, brainstem

hemangioma, facial

hemangioma, internal organs

hemangioma, leptomeningeal

hemangioma, skin

hematoma, epidural-cranial

hematuria, gross

hematuria, microscopic

hemianopia

hemianopia, homonymous

hemianopia, transient

hemiparesis

hemiparesis, transient

hemiplegia

hemiplegia, congenital

hemoglobin abnormality, neurologic complications of

hemoptysis

hemorrhage, intracranial, newborn

hemorrhage, putamenal

hemorrhage, thalamic

hemorrhagic diathesis

hemorrhoids

hemosiderosis of CNS, superficial

hepatic encephalopathy

hepatic encephalopathy, treatment of

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatomegaly

hepatosplenomegaly

heralding manifestation

hereditary hemorrhagic telangiectasia(HHT)

herpes simplex encephalitis

herpes simplex encephalitis, differential diagnosis of

hypercoagulable state

hyperglycemia

hyperhomocysteinemia

hyperlipidemia

hyperpigmentation of skin

hypersomnia

hypertension

hypertension, cerebrovascular disease with

hypertrophic cardiomyopathy

hypogammaglobulinemia

hypoxic encephalopathy

hypoxic-ischemic leukoencephalopathy

iatrogenic neurologic disorders

ileus, paralytic

imbalance

impulsivity

inborn errors of metabolism

intellectual deterioration

internuclear ophthalmoplegia

interobserver agreement

intracerebral hemorrhage

intracerebral hemorrhage, familial

intracerebral hemorrhage, lobar

intracerebral hemorrhage, recurrent

intracerebral hemorrhage, small

intracerebral hemorrhage, work up

intracerebral hemorrhage, young adult

intracranial hemorrhage

intrauterine

intraventricular hemorrhage

iris, abnormal

iron, brain

Jakob-Creutzfeldt disease

joint hypermobility

klippel feil syndrome

Krabbe's disease

KRIT1 gene

kyphoscoliosis, neurologic causes of

lactate

lactic acidemia

lacunar infarction

laminar necrosis, cortical

L-dopa

left atrial appendage, percutaneous closure

level of consciousness, decreased

lifestyle modification

linear lesion

lipid storage disorder of CNS

lymphoma involving CNS

lymphomatoid granulomatosis

lysosomal storage disease

macrocephaly

magnetic susceptibility

malaise

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

malformation, vascular, familial

malformation, vascular, screening for

malformation, Vein of Galen

manganese intoxication

mania

manic-depressive

maple syrup urine disease

Marfan syndrome

marihuana

medulla oblongata

medulla oblongata, lesion of

medulla oblongata, malformation

melanoma, malignant

melanomatosis, primary malignant

MELAS syndrome

memory, impairment of

meningeal enhancement

meningitis, brucellosis

mental retardation

mental status, abnormal

metabolic disorder, primary

methemoglobin

methylene tetrahydrofolate reductase

metronidazole

Mexican

microangiopathy, brain

microhemorrhage, intracerebral

microspherophakia

midbrain, lesion of

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

middle cerebral artery territory infarction

middle cerebral artery, occlusion of

middle cerebral artery, stenosis of

mitochondrial disease

mitochondrial disease, pathogenesis

mitochondrial encephalomyopathy

mitral valve lesion

mitral valve prolapse

molecular genetics

monoamines

mononeuropathy multiplex

MRI, CAT scan compared to

MRI, complications with

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, false negative

MRI, gradient-echo

MRI, incidental finding

MRI, paramagnetic effect

MRI, repeat

MRI, serial

MRI, spinal cord

MRI, susceptibility weighted

MRI, T1 weighted high signal foci

MRS

multiple endocrine neoplasia

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, familial

multiple sclerosis, misdiagnosis

muscle atrophy, progressive

muscle biopsy

muscle hypertrophy

muscle weakness

muscle weakness, proximal

muscular dystrophy

myasthenia gravis, differential diagnosis

myasthenia gravis, misdiagnosis of

myelinolysis, extrapontine

myelopathy

myocardial abscess

myocardial infarction

myoclonic jerks

myoclonus

myoclonus, cortical

myoclonus, stimulus sensitive

myopathy

myopathy, metabolic

myopathy, mitochondrial

neonatal epilepsy syndromes

neonatal epileptic encephalopathy

neoplasm, primary of CNS

nephrocalcinosis

nerve conduction studies

nerve root enhancement

neurocutaneous disease

neuroendocrinology

neurofibroma

neurofibromatosis 1

neurologic complications of, chronic pulmonary disease

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic examination, focal

neurologic signs

neurologic symptoms

neurologic testing

neuromuscular disease, electrodiagnosis of

neuropathy, hereditary peripheral

neuropathy, peripheral

neuropathy, vasculitic, systemic

neurosis

neurotoxin

neurotransmitter

next-generation sequencing

nystagmus, dissociated

nystagmus, vertical

obesity

occipital lobe

occipital lobe, infarction

occipital lobe, lesion of

ocular motility, disorders of

operculum syndrome

operculum syndrome, bilateral

ophthalmic artery occlusion

ophthalmoplegia

ophthalmoplegia, progressive external

optic atrophy

optic nerve, lesion of

organ rupture

ornithine transcarbamylase deficiency

orthopnea

osmotic demyelination syndrome

osteogenesis imperfecta

osteoporosis

otosclerosis

oxalosis, primary

pacemaker, cardiac-transvenous

Parkinson disease, arteriosclerotic

Parkinsonism syndrome

paroxysmal neurologic deficits

PAS positive

PAS positive material in the brain

patent foramen ovale

patient information and support

platelet inhibiting drugs

pleocytosis of cerebrospinal fluid

pneumothorax

POLG1 gene

polycystic kidneys

polycythemia, primary

polycythemia, secondary

polymerase chain reaction

posterior cerebral artery territory infarction

posterior leukoencephalopathy syndrome

pregnancy, neurologic complications in

premature infant

prenatal diagnosis by amniocentesis

prethrombotic state

prevention of neurologic disorders

prion disease

prognathism

prognosis

progressive neurologic disorder

protein C deficiency

protein S deficiency

proteinuria

proximal muscle atrophy

pruritus

pseudobulbar palsy

pseudoxanthoma elasticum

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

pulmonary infiltrates

pyramidal tract dysfunction

pyramidal tract, uncrossed

quadriparesis

quadriplegia, transient

radiation therapy, CNS treatment and complications with

radiation therapy, stereotactic

ragged-red fibers

rapidly progressing neurologic illness

rash

real-time quaking-induced conversion

retinal artery tortuosity

retinal microvascular disease

retinal tumor

retinal vasculitis

retinal vasculopathy

retinal vasculopathy with cerebral leukodystrophy

retinopathy

reversible neurologic disorder

review article

Riley-Day syndrome

risk factors

risk factors, modification

risk-benefit assessment

scoliosis, neurologic association with

screening

seizure

seizure, children

seizure, complications following

seizure, diagnosis of

seizure, treatment of

seizure, workup of

sensorineural hearing loss

skin, hyperextensible

skin, lesions in neurologic disorders

skin, thin

skull x-ray, abnormal

slit lamp examination

small vessel disease

small vessel disease, cerebral

Sneddon's syndrome

speech disorder

spinal cord

spinal cord, compression of

spinal cord, infarction of

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, vascular malformation of

splenium of corpus callosum

splenomegaly

spondylolysis

spondylosis

spontaneous remission

staphylococcus aureus

stare

stereotaxic surgery

steroid therapy, CNS treatment and complications with

straight sinus

streptococcal infection

streptococcus viridans

striatonigral degeneration

strokelike episodes

Sturge-Weber syndrome

subarachnoid hemorrhage

subarachnoid hemorrhage, familial

subarachnoid hemorrhage, prognosis

subarachnoid hemorrhage, recurrent

subcortical U fibers

subdural hematoma

sudden death

superior sagittal sinus thrombosis

sweating

sweating, abnormality of

symmetric brain lesions

telangiectases, retinal

temporal lobe, lesion

temporal lobe, lesion, bilateral

term infant

thalamic tumors

thalamic tumors, bilateral

thalamus

thalamus, infarction of

thalamus, infarction, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

thiamine deficiency

thromboangiitis obliterans cerebri

thrombocytopenia

thrombophlebitis

thrombotic thrombocytopenia purpura

tic

tinnitus

tissue plasminogen activator, intravenous

toe walking

tongue, enlarged

tongue, weakness

top of the basilar syndrome

torticollis

transient global amnesia

transient ischemic attack

transient ischemic attack, recurrent

transient neurologic deficit

trauma

treatment of neurologic disorder

urea-cycle enzymopathies

uremia

urinary catecholamines

vertebral-basilar insufficiency

vertigo

Virchow-Robin spaces, dilated

visual acuity, decreased

visual field defect

visual loss

visual loss, progressive

visual loss, slow

visual loss, transient

vital capacity

vitreous opacities

Von Hippel Lindau

walking, difficulty with

weakness, progressive

web sites

weight loss

Wernicke's encephalopathy

white matter disease

white matter disease, location

white matter disease, subcortical

Showing articles 100 to 150 of 9025 << Previous Next >>

Adult-Onset MELAS
Stroke 27:1420-1423, Gilchrist,J.M.,et al, 1996

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

Stroke in Williams Syndrome
Stroke 27:143-146, Wollack,J.B.,et al, 1996

Intracranial Aneurysms:MR Angiographic Screening in 400 Asymptomatic Individuals with Increased Familial Risk
Radiology 195:35-40, Ronkainen,A.,et al, 1995

Outcome in Familial Subarachnoid Hemorrhage
Stroke 26:961-963, Bromberg,J.E.C.,et al, 1995

Autosomal Dominant Migraine with MRI White-Matter Abnormalities Mapping to the CADASIL Locus
Neurol 45:1086-1091, Chabriat,H.,et al, 1995

Ischemic Stroke in Young Pts with Activated Protein C Resistance:Rpt of Three Cases Belonging to Three Different Kindreds
Stroke 26:885-890, Simioni,P.,et al, 1995

Familial Subarachnoid Hemorrhage:Distinctive Features and Patterns of Inheritance
Ann Neurol 38:929-934, Bromberg,J.E.C.,et al, 1995

Familial Hemiplegic Migraine and Autosomal Dominant Arteriopathy with Leukoencephalopathy (CADASIL)
Ann Neurol 38:817-824, Hutchinson,M.,et al, 1995

Clinical Spectrum of CADASIL:A Study of 7 Families
Lancet 346:934-939, Chabriat,H.,et al, 1995

New Phenotype of the Cerebral Autosomal Dominant Arteriopathy Mapped to Chromosome 19:Migraine as the Prominent Clinical Feature
JNNP 59:579-585, Verin,M.,et al, 1995

Hereditary Hemorrhagic Telangiectasia
NEJM 333:918-924, Guttmacher,A.E.,et al, 1995

Cerebrovascular Complications in Ehlers-Danlos Syndrome Type IV
Ann Neurol 38:960-964, North,K.N.,et al, 1995

Familial Cerebral Cavernous Angiomas:Clinical and Radiologic Studies
Neurol 45:492-497, Kattapong,V.J.,et al, 1995

Subarachnoid Hemorrhage and Family History:A Population-Based Case-Control Study
Arch Neurol 52:202-204, Wang,P.S.,et al, 1995

The Importance of Family History in Cerebrovascular Disease
Stroke 25:1599-1604, Graffagnini,C.,et al, 1994

Progress in the Genetics of Cerebrovascular Disease Inherited Subcortical Arteriopathies
Stroke 25:1696-1698, Bowler,J.V.&Hachinski,V., 1994

Familial Sneddon's Syndrome:Clinical, Hematologic, and Radiographic Findings in Two Brothers
Neurol 44:399-405, Pettee,A.D.,et al, 1994

Congential Deficienty of Factor VII in Subarachnoid Hemorrhage
Stroke 25:508-510, Papa,M.L.,et al, 1994

Neurovascular Manifestations of Heritable Connective Tissue Disorders:A Review
Stroke 25:889-903, Schievink,W.I.,et al, 1994

Neurological Involvement in Wegener's Granulomatosis:An Analysis of 324 Consecutive Pts at the Mayo Clin
Neurol 33:4-9, Nishino,H.,et al, 1993

Ornithine Transcarbamylase Deficiency Presenting with Strokelike Episodes
J Pediatrics 122:423-425, Christodoulou,J.,et al, 1993

Familial Aggregation of Stroke
Stroke 24:1366-1371, Kiely,D.K.,et al, 1993

A Study of Twins and Stroke
Stroke 23:221-223, Brass,L.M.,et al, 1992

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

A Familial Disorder with Subcortical Ischemic Strokes, Dementia, and Leukoencephalopathy
Neurol 42:1015-1019, Mas,J.L.,et al, 1992

Familial Intracranial Haemorrhage Due to Factor V Deficiency
JNNP 55:227-228, Wadia,R.S.,et al, 1992

Clinicopath Conf
Emery-Dreifus Muscular Dystrophy, NEJM 327:548-5571992., , 1992

Prenatal Origin of Hemiparetic Cerebral Palsy:How Often and Why?
Pediatrics 88:1059-1062, Nelson,K.B., 1991

Genetice of Cerebrovascular Disease
Stroke 22:276-280, Alberts,M.J., 1991

Homocystinuria Due to 5, 10-Methylenetetrahydrofolate Reductase Deficiency Revealed by Stroke in Adult Siblings
Neurol 41:1313-1315, Visy,J.M.,et al, 1991

Cerebral Haemorrhage and Berry Aneurysm:Evidence from a Family for a Pattern of Autosomal Dominant Inheritance
JNNP 54:838-840, Shinton,R.,et al, 1991

Intracranial Hemorrhage in Patients with Polycystic Kidney Disease
Stroke 21:291-294, Ryu,S.J., 1990

Premature Stroke in a Family with Lupus Anticoagulant and Antiphospholipid Antibodies
Stroke 21:66-71, Ford,P.M.,et al, 1990

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

Cerebrovascular Disease in Ehlers-Danlos Syndrome Type IV
Stroke 21:626-632, Schievink,W.I.,et al, 1990

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

Cardioembolic Stroke in Primary Oxalosis with Cardiac Involvement
DiPasquale. G. , et al, Stroke 20:1403-14069., , 1989

Von Hippel-Lindau Disease Affecting 43 Members of a Single Kindred
Medicine 68:1-29, Lamiell,J.M.,et al, 1989

Bilateral Opercular Polymicrogyria
Ann Neurol 25:90-92, Becker,P.S.,et al, 1989

Essential Tremor Cured by Infarction Adjacent to the Thalamus
JNNP 51:591-592, Duncan,R.,et al, 1988

Livedo Reticularis, Porcelain-White Scars, and Cerebral Thromboses
Lancet 1:1263-1265, Burton,J.L., 1988

Risk of Brain Infarction in Familial Hypercholesterolemia
Stroke 19:1097-1100, Kaste,M.&Koivisto,P., 1988

Mutation in Cystatin C Gene Causes Hereditary Brain Hemorrhage
Lancet 2:603-604, Palsdottir,A.,et al, 1988

Familial Oculoleptomeningeal Amyloidosis, Report of a New Family with Unusual Features
Arch Neurol 45:1118-1122, Uitti,R.J.,et al, 1988

Cerebral Cavernous Malformations:Incidence and Familial Occurrence
NEJM 319:343-347, Rigamonti,D.,et al, 1988

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

Familial Occurrence of Spontaneous Dissection of the Internal Carotid Artery
Stroke 18:246-251, Mokri,B.,et al, 1987

Cerebral Amyloid Angiopathy, A Critical Review
Stroke 18:311-324, Vinters,H.V., 1987

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

Showing articles 100 to 150 of 9025 << Previous Next >>