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Differential
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abscess, intracerebral
abscess, intracerebral, recurrent
abscess, intracranial
acanthosis nigricans
algorithm
alpha-fetoprotein
ANA
anemia
aneurysm
aneurysm, berry
aneurysm, intracranial, screening for
angiography, cerebral
antibiotic prophylaxis
antibiotics
apraxia of eye movements
arachnoiditis
areflexia
Arnold Chiari malformation
arteriovenous malformation
arteriovenous malformation, cerebral
arteriovenous malformation, multiple
arteriovenous malformation, pulmonary
arteritides
arthralgia
arthritis
aspiration
astrocytoma
asymptomatic
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, truncal
ataxic gait
athetosis
autoimmune disease
biologic markers
blood dyscrasias, neurologic findings with
brain biopsy
brain biopsy, stereotaxic
brain scan, abnormal
brainstem, vascular malformation of
bruit
cafe au lait spots
calcification, intracranial
calcification, muscle
calf hypertrophy
capillary blush
carcinoembryonic antigen
carcinoma
carcinoma of breast
carcinoma of lung
CAT scan
CAT scan, abnormal
CAT scan, abscess, cerebral
CAT scan, chest
CAT scan, ring sign
cavernous hemangioma
central nervous system, infection of
cerebellar ataxia, autosomal recessive
cerebellar ataxia, children
cerebellar ataxia, children, differential diagnosis of
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebellar degeneration
cerebellar vermis
cerebral embolism
cerebral infarction
cerebral palsy
cerebrospinal fluid, xanthochromia of
cerebrovascular accident
cerebrovascular accident, familial occurrence
chest x-ray, abnormal
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 11
chromosome 9
cirrhosis
cisterna magna
cisterna magna, enlarged
Clinical Pathologic Conference(C.P.C.)
clubbing of fingers
Coats syndrome
coin lesion on chest X-ray
collagen vascular disease
complications
confusion
congestive heart failure
contraindications
controversies in neurology
C-reactive protein, elevated
creatine phosphokinase(CPK)elevated
CREST syndrome
cyanosis
degenerative diseases of CNS
dental procedure, neurologic complications with
dermatomyositis
dermatomyositis, childhood
diabetes mellitus
diagnostic criteria
DiGeorge syndrome
dizziness
drooling
dysarthria
dysdiadochokinesia
dysmetria
dysphagia
dyspnea
dystonia
dystrophic calcification
early draining vein
echocardiogram
echocardiogram, contrast
edema, periorbital
electroencephalogram, abnormalities of
electromyogram
electronystagmography
electrophoretic pattern, serum
embolism, air
embolism, paradoxical
embolism, septic
encephalopathy
endocarditis, prophylaxis
endovascular therapy
epistaxis
epistaxis, recurrent
Epstein-Barr virus
esophageal reflux
esophageal varices
eye movement, disorders of
false positive VDRL
familial
fever
fibrinolytic agents, contraindications
fistula, arterio-venous
fistula, arterio-venous, pulmonary
fourth ventricle, enlargement of
Friedreich's ataxia
gait disorder
gastrointestinal bleeding
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
glioma
gray hair
growth retardation
head injury
headache
headache, sudden onset of
hearing loss
hearing problems in children
heliotrope rash
hemangioma, internal organs
hematuria, gross
hematuria, microscopic
hemiparesis
hemiplegia
hemoptysis
hemorrhagic diathesis
hepatic encephalopathy
hepatolenticular degeneration(Wilson's disease)
hepatomegaly
hepatosplenomegaly
heralding manifestation
hereditary hemorrhagic telangiectasia(HHT)
hypergammaglobulinemia
hyperglycemia
hypogonadism
hypotonia
hypoxia
imbalance
immunodeficiency
immunoelectrophoresis, serum
immunologic disease
immunosuppression
immunosuppressive agents
incoordination
infection
insulin resistance
intracerebral hemorrhage
intracerebral hemorrhage, familial
intracerebral hemorrhage, multiple
intracranial hemorrhage
irritability
Leigh's disease
leukemia
leukemia, neurologic findings assoc.with
leukocytosis
leukoencephalopathy
lipid storage disorder of CNS
liver disease
lymphadenopathy
lymphoma
malabsorption
malformation, vascular
malformation, vascular, cerebral
malformation, vascular, cryptic
malformation, vascular, familial
malformation, vascular, screening for
malformation, Vein of Galen
Marinesco-Sjogren syndrome
masked facies
meningismus
meningitis
mental retardation
microhemorrhage, intracerebral
migraine
misdiagnosis
mitral valve prolapse
molecular genetics
mongolism
mononeuropathy
mononeuropathy multiplex
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, angiography
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, diffusion weighted
MRI, false negative
MRI, hypointense signal foci on
MRI, negative
MRI, perfusion
MRS
multiple sclerosis
multiple system atrophy
muscle biopsy
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, facioscapulohumeral
myelomalacia
myopathy
myopathy, inflammatory
myositis
neoplasm, primary intracerebral
nerve biopsy
nerve conduction studies
neurocutaneous disease
neuroendocrinology
neurologic complications of, chronic pulmonary disease
neurologic disease, diagnoses of
neurologic disease, tempo
neurologic examination, focal
neuropathology
neuropathy
neuropathy, peripheral
neuropathy, vasculitic, systemic
nystagmus
ocular motility, disorders of
ophthalmoplegia
optokinetic nystagmus(O.K.N.)
papilledema
paraparesis
pathology
patient information and support
pericarditis
platelet inhibiting drugs
pneumonia
poliomyelitis
poliomyelitis vaccine
polycythemia, secondary
polymyositis
polyneuropathy
portal caval shunt
pregnancy, neurologic complications in
prevention of neurologic disorders
progeria
prognosis
progressive neurologic disorder
pseudohypertrophy
pulmonary disease
pulmonary hypertension
pulmonary infection
pulmonary infiltrates
pulmonary nodules
radiation hypersensitivity
radiation therapy, CNS treatment and complications with
radiation therapy, stereotactic
rash
Raynaud's phenomenon
recurrent
remote effect of cancer on the nervous system
retinal detachment
retinopathy
review article
rheumatoid arthritis factor(R.A.factor)
risk factors
saccadic eye movements
saccadic eye movements, abnormal
scannig speech
sclerodactyly
scleroderma
scleroderma, neurologic involvement with
screening
sedimentation rate, elevated
seizure
sensorineural hearing loss
skin, biopsy
skin, darkening of
skin, lesions in neurologic disorders
skull x-ray, abnormal
slurred speech
spinal cord
spinal cord, lesion of
spinal cord, vascular malformation of
spinal muscular atrophy
spinocerebellar degeneration
staggering
subarachnoid hemorrhage
tandem gait, ataxic
telangiectases
telangiectases, periungual
telangiectases, retinal
thyroiditis
tongue, red papules
transient ischemic attack
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, intention
trigeminal neuropathy
trigeminal neuropathy, sensory
ulcers, fingertip
undiagnosed
uremia
vaccination, neurologic complications with
vaccine
vasculitides
vasculopathy
Venereal Disease Research Laboratory test
vertigo
viral infection
viral infection, CNS
vision, failure of in childhood
visual loss
vitamin E deficiency
vitiligo
Von Hippel Lindau
walking, difficulty with
weight loss
wheelchair
white matter disease
workup
Showing articles 0 to 50 of 52 Next >>

Hereditary Hemorrhagic Telangiectasia, Clinical Presentations, and Management
Stroke 54:e512-e515, Silveira,L.,et al, 2023

Recurrent Epistaxis in an Adolescent
BMJ 367:I5393, McLaren, O. & Ronan, N., 2019

Clinicopathologic Conference, Vascular Malformations in Liver, Stomach, Esophagus, and Lungs that are Consistent with Hereditary Hemorrhagic Telangiectasia, Complicated
NEJM 376:972-980, Case 7-2017, 2017

Cerebral Abnormalities in Adults with Ataxia-Telangiectasia
AJNR 35:119-123, Lin, D.D.M.,et al, 2014

Red Papules on the Tongue of a Patient with Hemiparesis
JAMA 312:741-742, Chiu, H.Y. & Lin, S.J., 2014

Brain Arteriovenous Malformation Multiplicity Predicts the Diagnosis of Hereditary Hemorrhagic Telangiectasia Quantitive Assessment
Stroke 43:72-78, Bharatha, A.,et al, 2012

The Autosomal Recessive Cerebellar Ataxias
NEJM 366:636-646, Anheim,M.,et al, 2012

An unusual cause of stroke and hypoxia
BMJ 342:c7200, Bell, S.L. & Eveson, D.J., 2011

Hereditary Hemorrhagic Telangiectasia (Osler-Weber-Rendu Syndrome)
UpToDate, Feb, Shovlin, C., 2011

Clinicopath Conf., Brain Abscess, Pulmonary Arteriovenous Malformation Due to Hereditary Hemorrhagic Telangiectasia
NEJM 362:1326-1333, Case 10-2010, 2010

Pulmonary AVMs, including hereditary hemorrhagic telangiectasia: Diagnosis and Treatment
UpTo Date, August, Gossage, J.R., 2010

Clinical Spectrum of Ataxia-Telangiectasia in Adulthood
Neurol 73:430-437, Verhagen,M.M.M.,et al, 2009

Pulmonary Arteriovenous Malformations in Hereditary Hemorrhagic Telangiectasia: A Series of 126 Patients
Medicine 86:1-7, Cottin,V.,et al, 2007

Cerebrovascular Manifestations in 321 Cases of Hereditary Hemorrhagic Telangiectasia
Stroke 32:877-882, Maher,C.O.,et al, 2001

Dermatomyositis
Lancet 355:53-57, Callen,J.P., 2000

Angiographic and Clinical Characteristics of Patients with Cerebral Arteriovenous Malformations Associated with Hereditary Hemorrhagic Telangiectasia
AJNR 21:1016-1020, Matsubara,S.,et al, 2000

Abnormal White Matter Signal in Ataxia Telangiectasia
AJNR 21:1483-1485, Ciemins,J.J. & Horowitz,A.L., 2000

Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
Pediatrics 102:98-100, Cabana,M.D.,et al, 1998

A Case-Control and Nerve Biopsy Study of CREST Mutliple Mononeuropathy
Neurol 49:1641-1645, Dyck,P.J.B.,et al, 1997

Exceptional Multiplicity of Cerebral AVMs Assoc with Hereditary Hemorrhagic Telangiectasia (Osler-Weber-Rendu Syndrome)
AJNR 17:1733-1742, Putman,C.M.,et al, 1996

Cranial MRI in Ataxia-Telangiectasia
Neuroradiology 37:77-82, Sardanelli,F.,et al, 1995

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

Facioscapulohumeral Muscular Dystrophy in Early Childhood
Arch Neurol 51:387-394, Brouwer,O.F.,et al, 1994

Ataxia-Telangiectasia:MR and CT Findings
J Comput Assist Tomogr 18:724-727, Farina,L.,et al, 1994

Radiation-Induced Telangiectasia in the Brain Simulates Cryptic Vascular Malformations at MR Imaging
Radiology 193:629-636, Gaensler,E.H.L.,et al, 1994

Cardiac Anomalies in Ataxia-Telangiectasia
Am J Dis Child 147:20-21, Bastianon,V.,et al, 1993

Ataxia-Telangiectasia in a Child with Vaccine-Associated Paralytic Poliomyelitis
J Pediatr 121:405-407, Pohl,K.R.E.,et al, 1992

Scleroderma and Central Nervous System Vasculitis
Stroke 22:410-413, Pathak,R.&Gabor,A.J., 1991

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

Relative Increase of T Cells Expressing Gamma/Delta Rather than Alpha/Beta Receptor in Ataxia-Telangietasia
NEJM 322:73-76, 1241990., Carbonari,M.,et al, 1990

Breast & Other Cancers in Families with Ataxia-Telangiectasia
NEJM 316:1289-1294, Swift,M.,et al, 1987

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

Central Nervous System Infections Associated with Hereditary Hemorrhagic Telangiectasia
Am J Med 77:86-92, Press,O.L.W.,et al, 1984

Ataxia-Telangiectasia:A Multisystem Hereditary Disease with Immunodeficiency
Ann Int Med 99:367-379, Waldmann,T.A.,et al, 1983

Facioscapulohumeral Dystrophy Associated with Hearing Loss & Coats Syndrome
Ann Neurol 12:395-398, Taylor,D.A.,et al, 1982

Epstein-Barr-virus-carrying Lymphoma in a Patient with Ataxia-telangiectasia
BMJ 282:425-427, Saemundsen,A.K.,et al, 1981

Computed Tomography in Ataxia-Telangiectasia
J Comput Assist Tomogr 5:660-661, Assencio-Ferreira,V.J.,et al, 1981

Helper & Suppressor T-Lymphocyte Leukemia In Ataxia Telangiectasia
NEJM 300:700-704, Saxon,A.,et al, 1979

Extreme Insulin Resistance in Ataxia Telangiectasia
NEJM 298:1164, Bar,R.S.,et al, 1978

Familial Cavernous Angiomas
Arch Neurol 35:746-749, Bicknell,J.M.,et al, 1978

Ataxia Telangiectasia
Arch Neurol 35:553-554, Teplitz,R.L., 1978

Eye Movements in Ataxia-telangiectasia
Neurol 28:1099-1104, Baloh,R.W.,et al, 1978

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

Clinical Pathological Conference
Dermatomyositis, Case Record, 33-1977, NEJM 297:37877., , 1977

DiGeorge Syndrome Associated with Glioma & Two Kinds of Viral Infection
NEJM 296"1235, Asamoto,H., 1977

Neurologic Aspects of Hereditary Hemorrhagic Telangiectasia
Arch Neurol 34:101, Adams,H.P.,et al, 1977

MGH-CPC-Ataxic Telangiectasia & Left Frontal Lobe Glioma
NEJM 292:1231, , 1975

Ataxia-Telangiectasia-Clonal Growth of Translocation Lymphocytes
NEJM 289:286, Hecht,F.,et al, 1973

Neurologic Manifestations of Progressive Systemic Sclerosis, 1972
Nebraska Med J 58:106, Aita,J.A., 1973



Showing articles 0 to 50 of 52 Next >>