Neudle.com: subarachnoid hemorrhage familial

Differential
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abdominal distention

abducens nerve paralysis

abscess, intracerebral

abscess, intracranial

abscess, perivalvular

absence

acid maltase deficiency

acid maltase deficiency, adult

acrocyanosis

acromicria

acyl CoA dehydrogenase deficiency

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adult-onset leukodystrophy, with neuroaxonal spheroids

advances in neurology

adverse drug reaction

agammaglobulinemia

agoraphobia

Aicardi-Goutieres syndrome

alcohol

Alexanders disease

Alexanders disease, adult onset

algorithm

alpha-fetoprotein

alternating hemiplegia

alternating hemiplegia of childhood

Alzheimer's disease

Alzheimer's disease, preclinical

amniocentesis

amyloid angiopathy, cerebral

amyloid beta protein

amyloidosis

amyloidosis, oculoleptomeningeal, familial

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, misdiagnosis

aneurysm

aneurysm, asymptomatic

aneurysm, berry

aneurysm, intracranial

aneurysm, intracranial, detection

aneurysm, intracranial, familial

aneurysm, intracranial, natural history

aneurysm, intracranial, screening for

aneurysm, intracranial, treatment of

aneurysm, multiple intracranial

angiitis, granulomatous of CNS

angiitis, isolated of CNS

angiography, cerebral

angioid streaks

anterior horn cell disease

antibiotic prophylaxis

anticonvulsants

anticonvulsants, discontinuation in seizure-free epileptics

anticonvulsants, selection of

anxiety

aortic valve, bicuspid

aortic valve, lesion of

aphasia

aphasia, progressive, primary

apraxia of eye movements

arterial dissection, aorta

arterial dissection, carotid

arterial dissection, cerebral

arterial dissection, intracranial

arterial dissection, multiple

arterial dissection, precipitating events

arterial dissection, recurrent

arterial dissection, renal artery

arterial dissection, ruptured

arterial dissection, spontaneous

arterial dissection, vertebral

arteriopathy

arteriovenous malformation

arteriovenous malformation, cerebral

arteriovenous malformation, multiple

ataxia telangiectasia

attention deficit disorder with hyperactivity

atypical

autonomic dysfunction

axonal spheroid

Babinski sign

bacterial endocarditis, neurologic manifestations of

bacterial infection

bacterial infection, CNS

basal ganglia, calcification of

basal ganglia, infarction

basal ganglia, lesion of

behavior, combative

behavioral disorder

benign essential tremor

benign familial nocturnal alternating hemiplegia of childhood

beta adrenergic blocker

biologic markers

biopterin deficiency

bitemporal visual field defect

blepharospasm

blindness

blood dyscrasias, neurologic findings with

bone marrow transplantation

botulinum toxin

brachial plexus

brachial plexus neuropathy

brainstem, infarction of

brainstem, lesion of

brainstem, neoplasms of

brucellosis

brucellosis, nervous system involvement with

calcification, intracranial

calcifications, intracranial, punctate

calf hypertrophy

cane

carbamazepine

carcinoembryonic antigen

carcinoma

carcinoma of pancreas

carotid artery occlusion, bilateral

carotid artery stenosis, intracranial

CAT scan

CAT scan, abnormal

CAT scan, angiography

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, serial

cataracts

cauda equina

cauda equina, lesion of

cavernous hemangioma

cavernous sinus

cavernous sinus, lesion of

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar infarction

cerebellum, neoplasms of

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral embolism

cerebral infarction

cerebral infarction, small, deep

cerebral infarction, subcortical

cerebral ischemia

cerebral palsy

cerebral venous thrombosis

cerebritis

cerebroretinal vasculopathy

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, biochemical markers of CNS disease

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, red cells in

cerebrospinal fluid, xanthochromia of

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, cardiac disease causing

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, mimics

cerebrovascular accident, multiple

cerebrovascular accident, non atherosclerotic cause of

cerebrovascular accident, nonvascular territory

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

cerebrovascular disease

ceruloplasmin, serum

Charcot-Marie-Tooth

cherry red spot-myoclonus syndrome

chilbran skin lesions

chromosomal abnormality

chronic progressive external ophthalmoplegia

cigarette smoking

cirrhosis

Clinical Pathologic Conference(C.P.C.)

collagen vascular disease

coloboma

coma

complications

compression neuropathy

compression neuropathy, recurrent

confusion

congenital heart disease

congenital malformation

congenital malformation, non CNS

congestive heart failure

consanguinity

controversies in neurology

copper metabolism, abnormal

corpus callosum

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cortical blindness, transient

cost effectiveness

cranial nerve enlargement

cranial nerves

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

cry, abnormal

cry, weak

crying, pathologic

cultured skin fibroblasts

degenerative diseases of CNS

Dejerine-Sottas syndrome

delay in diagnosis

delusion

dementia

dementia, age at onset

dementia, cerebrovascular disease causing

dementia, childhood

dementia, familial

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, subcortical

demyelinating disease

dental procedure, neurologic complications with

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

depression

developmental milestones, loss of

developmental retardation

diabetes mellitus

diagnostic criteria

diaphragmatic paralysis

diarrhea

diet

differential diagnosis

difficulty climbing stairs

dilated aortic root

diplopia

disinhibition-dementia-parkinsonism-amyotrophic complex

distal muscle atrophy

distal muscle weakness

diurnal variation

dizziness

dopa responsive dystonia

dopamine agonist

drooling

dropped head syndrome

drug induced neurologic disorders

dying

dysarthria

dysarthria-clumsy hand syndrome

dystonia musculorum deformens

dystonia, children

dystonia, classification

dystonia, etiology of

dystonia, evaluation of

dystonia, face

dystonia, focal

dystonia, painful

dystonia, treatment of

dystrophin

dystrophin associated proteins

DYT1 mutation

ear, pain in

ears of the Lynx MR sign

eating disorder

echocardiogram

echocardiogram, transesophageal, false negative

echocardiogram, transthoracic

echocardiogram, transthoracic, false negative

Ehlers-Danlos syndrome

Ehlers-Danlos syndrome, classification

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, video monitoring with

embolism, paradoxical

embolism, septic

embolization, therapeutic

emotional lability

encephalopathy

encephalopathy, anoxic

encephalopathy, metabolic

encephalopathy, neonatal

encephalopathy, progressive

endocarditis

endocarditis, acute bacterial

endovascular therapy

enzyme treatment

enzyme, defect

epidemiology of neurology

epileptic encephalopathy

extraocular muscle lesion

eye movement, disorders of

eye, pain in

Fabry's disease

facial appearance, abnormal

facial nerve palsy

facial weakness

facial weakness, bilateral

factor VII, deficiency

fatty acid, elevated plasma content

feeding disorder

fever

fibrillations

fibromuscular dysplasia

fine motor function, impaired

fingers, abnormal

fistula, arterio-venous

fistula, arterio-venous, carotid-cavernous

fistula, arterio-venous, dural

fistula, arterio-venous, pulmonary

Friedreich's ataxia, late onset

frontotemporal dementia, behavioral variant

fundus, abnormality of

funduscopic exam

gabapentin

gait disorder

gastrointestinal bleeding

gastrointestinal disease, neurologic complications

gastrointestinal motility

gastrointestinal perforation

gastroparesis

gaze palsy

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

GLUT1 deficiency syndrome

glycogen storage disease

Gowers maneuver

gram negative rod

granular osmiphilic material

granulomatosis with polyangiitis

growth hormone deficiency

hearing loss, bilateral

hearing problems in children

hematuria, microscopic

hemianopia

hemianopia, transient

hemiparesis

hemiparesis, transient

hemiplegia

hemoglobin abnormality, neurologic complications of

hemoptysis

hemorrhage, putamenal

hemorrhage, thalamic

hemorrhagic diathesis

hemosiderosis of CNS, superficial

hepatic encephalopathy

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatomegaly

hepatosplenomegaly

heralding manifestation

hereditary hemorrhagic telangiectasia(HHT)

herpes simplex encephalitis

herpes simplex encephalitis, differential diagnosis of

human immunodeficiency virus type 1

human T-lymphotropic virus type I(HTLV-I)

Huntington's chorea

Huntington's chorea, late onset

Huntington's chorea, misdiagnosis of

Huntington's chorea, sporadic form

hyperactivity

hyperhomocysteinemia

hyperphagia

hyperpigmentation of skin

hyperpyrexia, CNS disorder causing

hypopigmentation of skin

hypoxic encephalopathy

iatrogenic neurologic disorders

inborn errors of metabolism

incoordination

infection

inflexibility, mental

intellectual deficit

intellectual deterioration

interferon alpha

interobserver agreement

intestinal pseudoobstruction

intracerebral hemorrhage

intracerebral hemorrhage, familial

intracerebral hemorrhage, young adult

intracranial hemorrhage

intrauterine

intrinsic hand muscles, wasting of

iron, brain

iron, serum

irritability

ischemic exercise test

islet cell tumor

jaw closure weakness

Jervell Lange-Neilson syndrome

joint hypermobility

juvenile myoclonus epilepsy

Kayser-Fleischer ring

Kearns-Sayre syndrome

learning disability, in children

Leber's congenital amaurosis

Leber's hereditary optic neuropathy

leukoencephalopathy, adult onset, sporadic

leukoencephalopathy, differential diagnosis

Lewy body

Lewy body disease, diffuse

lifestyle modification

lipid storage disorder of CNS

liver disease

liver function enzymes

malformation, vascular

malformation, vascular, cerebral

malformation, vascular, familial

malformation, vascular, screening for

masseter muscle weakness

McArdle's disease

MELAS syndrome

memory, impairment of

meningeal enhancement

meningitis, brucellosis

meningitis, CSF cell count-normal

mental retardation

mental status, abnormal

MERRF syndrome

metabolic disorder, primary

metoprolol

microangiopathy, brain

microcephaly

microhemorrhage, intracerebral

middle cerebral artery, stenosis of

mitochondrial disease

mitochondrial encephalomyopathy

mitral valve prolapse

MNGIE syndrome

molecular genetics

molybdenum cofactor deficiency

monomelic amyotrophy

mononeuropathy

mononeuropathy multiplex

mortality

motor neuron disease

movement disorder

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, treatment of

MRI, contrast enhanced

MRI, cranial nerves

MRI, diffusion weighted

MRI, disappearing lesion on

multiple sclerosis, differential diagnosis of

multiple sclerosis, familial

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle atrophy, progressive

muscle phosphorylase deficiency

muscle stiffness

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, cardiovascular changes with

muscular dystrophy, central nervous system abnormality

muscular dystrophy, Duchenne

muscular dystrophy, dystrophin normal

muscular dystrophy, limb-girdle

mutism

myasthenia gravis

myasthenia gravis, congenital

myasthenia gravis, differential diagnosis

myasthenia gravis, misdiagnosis of

myasthenia gravis, seronegative

myasthenia gravis, treatment of

myelitis, longitudinal

myelomalacia

myelopathy

myelopathy, chronic progressive

myopathy, mitochondrial

neoplasm, primary of CNS

neoplasm, primary of CNS-familial occurrence

nerve conduction studies

nerve hypertrophy

nerve root enhancement

nerve root hypertrophy

neuroaxonal leukodystrophy

neurocutaneous disease

neuroendocrinology

neurofibromatosis 1

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic examination, focal

neurologic history

neurologic signs

neurologic symptoms

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction, abnormality of

neuronal ceroid-lipofuscinosis

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, vasculitic, systemic

next-generation sequencing

obsessive-compulsive disorder

occipital lobe, infarction

occipital lobe, lesion of

ocular motility, disorders of

old age, neurology of

ophthalmoplegia

ophthalmoplegia, progressive external

opiate

optic atrophy

optic nerve, lesion of

optic neuropathy

optic neuropathy, bilateral

optic neuropathy, hereditary

optokinetic nystagmus, abnormal

organ rupture

orthopnea

osteogenesis imperfecta

pain, increased response

palatal myoclonus

palliative care

pallido-ponto-nigral degeneration

panic attacks

papilledema

paraparesis

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

paraparesis, spastic, tropical

Parkinson disease, arteriosclerotic

Parkinson disease, diagnosis

Parkinson disease, differential diagnosis of

Parkinson disease, drug induced

Parkinson disease, juvenile

Parkinson disease, misdiagnosis

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

paroxysmal extreme pain disorder

paroxysmal neurologic deficits

PAS positive

PAS positive material in the brain

pathology

patient information and support

phenylketonuria, adult onset

pheochromocytoma

phosphorylase b kinase deficiency

pleocytosis of cerebrospinal fluid

pneumonia

pneumothorax

polycystic kidneys

polycythemia, primary

polymerase chain reaction

polyneuropathy, chronic inflammatory demyelinating

Pompe's disease of glycogen storage

portal caval shunt

posterior cerebral artery territory infarction

postural abnormality

Prader-Labhart-Willi syndrome

pramipexole

precipitating factors

preclinical

pregnancy, neurologic complications in

prenatal

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

primary lateral sclerosis

progeria

prognosis

progressive myoclonic epilepsy

progressive neurologic disorder

progressive subcortical gliosis

progressive supranuclear palsy

proprioception, abnormal

pseudoxanthoma elasticum

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

pyramidal tract dysfunction

quadriparesis

quadriplegia

radiation hypersensitivity

radiation therapy, stereotactic

ragged-red fibers

rapidly progressing neurologic illness

restless leg syndrome

reversible neurologic disorder

risk factors, modification

risk-benefit assessment

second wind phenomena

seizure

seizure, cardiac arrhythmia causing

seizure, children

seizure, diagnosis of

seizure, differential diagnosis of

seizure, familial

seizure, intractable

seizure, neonatal

seizure, nonepileptic

seizure, paradoxical

seizure, prognosis in adults

seizure, psychomotor-temporal lobe

seizure, stimulus sensitive

seizure, treatment of

sensorineural hearing loss

sensory loss

sensory polyneuropathy

single photon emission computed tomography

skin, biopsy

skin, darkening of

skin, hyperextensible

skin, lesions in neurologic disorders

skin, thin

skin, translucent

skull x-ray, abnormal

small vessel disease

small vessel disease, cerebral

sodium channel dysfunction

sodium valproate

spastic ataxia

spastic diplegia

spastic paraplegia, type 11

spasticity

speech disorder

speech disorder, childhood

speech, delayed development of

speech, loss of

spinal cord

spinal cord, compression of

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, vascular malformation of

spinal muscular atrophy

splenomegaly

spontaneous remission

staphylococcus aureus

steroid therapy, CNS treatment and complications with

stimulation, deep brain

strabismus

streptococcal infection

streptococcus viridans

stridor

strokelike episodes

subarachnoid hemorrhage

subarachnoid hemorrhage, familial

subarachnoid hemorrhage, prognosis

subarachnoid hemorrhage, recurrent

subdural hematoma

suck, poor

sudden death

superior sagittal sinus thrombosis

symmetric brain lesions

telangiectases, retinal

temper tantrums

temporal artery, biopsy

temporal lobe, lesion

temporal lobe, lesion, bilateral

tomaculous neuropathy

tongue, enlarged

tongue, fasciculations of

tongue, impaired movements of

tongue, protrusion of

tongue, weakness

torsades de points

torticollis

transient ischemic attack

transient ischemic attack, recurrent

transient neurologic deficit

trauma

treatment of neurologic disorder

trigeminal nerve, hypertrophy

trinucleotide repeats

Unverricht-Lundborg disease

ventricular tachycardia

very long chain fatty acids

vibratory sensation, abnormal

vision, failure of in childhood

visual acuity, decreased

visual field defect

visual loss

visual loss, congenital

visual loss, slow

vital capacity

Von Hippel Lindau

walking, difficulty with

weakness

weakness, fatiguable

weakness, generalized

weakness, progressive

weaning from respirator, failure to

weight loss

wheelchair

white matter disease

white matter disease, subcortical

wide based gait

word-finding difficulty

workup

wound healing, poor

X-linked bulbospinal neuronopathy

Showing articles 100 to 150 of 5904 << Previous Next >>

Hereditary Adult-Onset Alexander's Disease with Palatal Myoclonus, Spastic Paraparesis and Cerebellar Ataxia
Neurol 45:2266-2271, Schwankhaus,J.D.,et al, 1995

Panic Attacks and Panic Disorder:The Great Neurologic Imposters
Semin Neurol 15:126-132, Stahl,S.M.&Soefje,S., 1995

Psychosis as the Initial Manifestation of Adult-Onset Niemann-Pick Disease Type C
Neurol 45:1739-1743, Shulman,L.M.,et al, 1995

Familial Aorto-Cervicocephalic Arterial Dissections and Congenitally Bicuspid Aortic Valve
Stroke 26:1935-1940, Schievink,W.I.&Mokri,B., 1995

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

Predictors of Neonatal Encephalopathy in Full Term Infants
BMJ 331:598-602, Adamson,S.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

Parkinsonism-Recognition and Differential Diagnosis
BMJ 310:447-452, Quinn,N., 1995

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

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

Benign Familial Nocturnal Alternating Hemiplegia of Childhood
Neurol 44:1812-1814, Andermann,E.,et al, 1994

Monomelic Amyotrophy
Muscle & Nerve 17:1129-1134994., Donofrio,P.D., 1994

On the Inheritance of Intracranial Aneurysms
Stroke 25:2028-2037, Schievnink,W.I.,et al, 1994

Clin & Path Features of an Autosomal Dominant, Adult-Onset Leukodystrophy Simul Chronic Progressive MS
Arch Neurol 51:757-766, Schwankhaus,J.D.,et al, 1994

Atypical Leber's Hereditary Optic Neuropathy with Molecular Confiramtion
Arch Neurol 50:470-473, Weiner,N.C.,et al, 1993

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

Human T Lymphotropic Virus Type I-Assoc Myelopathy, A Rpt of 10 Pts Born in US
Arch Neurol 49:1113-1118, Sheremata,W.A.,et al, 1992

Delayed Diagnosis of Juvenile Myoclonic Epilepsy
JNNP 55:497-499, Grunewald,R.A.,et al, 1992

Intracranial Aneurysms in Autosom Dominant Polycystic Kidney Disease
NEJM 327:916-920, 9531992., Chapman,A.B.,et al, 1992

Juvenile Myoclonic Epilepsy, Underdiagnosed and Treatment May Have to be Life Long
BMJ 305:4-5, Timmings,P.L.&Richens,A., 1992

Recurrent Encephalopathy and Seizures in a US Native with HTLV-I-Associated Myelopathy/Tropical Spastic Paraparesis
Neurol 42:658-661, Smith,C.R.,et al, 1992

Familial Intracranial Aneurysms, A Review
Stroke 23:1024-1030, terBerg,H.W.M.,et al, 1992

Myelopathy Associated with Human T Cell Lymphotropic Virus Type 1 in a White European Native to England
BMJ 305:453, Ali,A.&Rudge,P., 1992

Familial Association of Intracranial Aneurysms and Cervical Artery Dissections
Stroke 22:1426-1430, Schievink,W.I.,et al, 1991

Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
Medicine 70:99-117, Gatti,R.A.,et al, 1991

Clinical and Electrodignostic Features of X-Linked Recessive Bulbospinal Neuronopathy
Neurol 41:823-828, Olney,R.K.,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

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

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

Dopa Responsive Dystonia:A Treatable Condition Misdiagnosed as Cerebral Palsy
BMJ 298:1019-1020, Boyd,K.&Patterson,V., 1989

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

Follow-up and Diagnostic Reappraisal of 75 Patients with Leber's Congenital Amaurosis
Am J Ophthalmol 107:624-631, Lambert,S.R.,et al, 1989

Chronic Progressive Spinobulbar Spasticity, A Rare Form of Primary Lateral Sclerosis
Arch Neurol 45:509-513, Gastaut,J.L.,et al, 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

Clinical Assessment of 31 Patients with Wilson's Disease, Correlations with Struct. Changes on MRI
Arch Neurol 44:365-370, Starosta-Rubinstein,S.,et al, 1987

Adult Polycystic Kidney Disease & Intracranial Aneurysms
BMJ 295:526, Saifuddin,A.&Dathan,J.R.E., 1987

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

Clinical Spectrum of Hereditary Hemorrhagic Telangiectasia (Osler-Wever-Rendu Disease)
Am J Med 82:989-997, Perry,W.H., 1987

Familial Association of Intracranial Aneurysms & Multiple Congenital Anomalies
Arch Neurol 43:30-33, Berg,H.W.M.,et al, 1986

Phosphorylase Deficiency
In Englel & Banker, Myology, McGraw-Hill Book Co, Ch 52, 1585-1601, DiMauro,S.&Bresolin,N., 1986

Acid Maltase Deficiency
Engel, A. G. in Engel and Banker, Myology, McGraw-Hill Co, New York, Ch 55, p. 1629-1651, , 1986

Dominant Inheritance of Intracranial Berry Aneurysm
BMJ 283:824-825, Evans,T.W.,et al, 1981

Pseudoxanthoma Elasticum:A Review of Neurological Complications
Ann Neurol 4:18, Iqbal,A.,et al, 1978

Familial Incidence of Ruptured Intracranial Aneurysms
Arch Neurol 35:675-677, Acosta-Rua,G.J., 1978

Neurological Manifestations of Hereditary Hemorrhagic Telangiectasia (Rendu-Osler-Weber Disease)
Ann Neurol 4:130-144, Roman,G.,et al, 1978

Intracranial Aneurysms:Characteristics of Aneurysms in Siblings
NEJM 297:115, 1977. (Letter), Andrews,R.J., 1977

An unusual Cause of Apparent Epilepsy:ECG & EEG Findings in a Case of Jervell Lange-Neilson Syndrome
JNNP 40:1102, Selby,P.J.,et al, 1977

Showing articles 100 to 150 of 5904 << Previous Next >>