Differential (Click to cross reference) acute disseminated encephalomyelitis adrenoleukodystrophy Alexanders disease algorithm amyloid angiopathy, cerebral aneurysm, intracranial, familial angiitis, granulomatous of CNS angiitis, isolated of CNS angiography, cerebral anticoagulant, complications of anxiety aphasia arrhythmia, cardiac arteriopathy asymptomatic ataxia atrial myxoma atypical B 12 deficiency bacterial endocarditis, neurologic manifestations of basal ganglia basal ganglia, infarction basal ganglia, lesion of behavioral disorder Behcet's syndrome Binswanger disease brain atrophy brain biopsy brain volume brainstem, lesion of calcification, intracranial Canavan's disease carbon monoxide poisoning carotid artery stenosis CAT scan CAT scan, abnormal central nervous system, infection of central pontine myelinolysis cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy cerebral cortical atrophy cerebral infarction cerebral infarction, small, deep cerebral infarction, subcortical cerebral ischemia cerebral venous thrombosis cerebrospinal fluid cerebrospinal fluid, abnormal cerebrospinal fluid, elevated protein of cerebrovascular accident cerebrovascular accident, familial occurrence cerebrovascular accident, genetic cerebrovascular accident, location of cerebrovascular accident, multiple cerebrovascular accident, non atherosclerotic cause of cerebrovascular accident, recurrent cerebrovascular accident, young adult cerebrovascular disease chemotherapy, CNS treatment and complications with children chromosomal abnormality chromosome 19 cigarette smoking Clinical Pathologic Conference(C.P.C.) cocaine cognition coma complications confusion confusional state, acute corpus callosum corpus callosum, infarction of corpus callosum, lesion of cortical blindness cystic infarction cytomegalovirus infection deep gray nuclei dementia dementia, cerebrovascular disease causing dementia, rapidly progressive dementia, subcortical demyelinating disease depression differential diagnosis digital subtraction angiography disability rating scale, neurological dysarthria electrocardiogram, abnormal electroencephalogram, pediatric patients electron microscopy electroretinograph emotional lability encephalitis, human immunodeficiency virus type 1 encephalitis, viral encephalopathy encephalopathy, acute endocarditis endocarditis, infectious external capsule Fabry's disease falling false negative familial familial hemiplegic migraine fever gait disorder gaze palsy, supranuclear gene gene mutation genetic linkage genetic neurologic disorders genetic screening genetic testing gliomatosis cerebri granular osmiphilic material hallucination head injury headache hearing loss hemiparesis heralding manifestation herpes simplex encephalitis human immunodeficiency virus type 1 hypertension hypertensive encephalopathy imbalance intellectual deficit internal carotid artery intracerebral hemorrhage intracerebral hemorrhage, lobar intracerebral hemorrhage, recurrent intracerebral hemorrhage, small judgement, impaired Krabbe's disease lacunar infarction L-dopa leuko-araiosis leukodystrophy leukoencephalopathy leukoencephalopathy, differential diagnosis limbic encephalitis lymphoma lymphoma involving CNS lymphoma, primary of CNS mania manic-depressive MELAS syndrome memory, impairment of mesial temporal lobe mesial temporal sclerosis metachromatic leukodystrophy microangiopathy, brain microhemorrhage, intracerebral middle cerebral artery territory infarction middle cerebral artery, stenosis of migraine migraine with aura migraine, hemiplegic mimics misdiagnosis mitochondrial disease movement disorder moyamoya MRI MRI, abnormal MRI, angiography MRI, black holes on MRI, diffusion tensor MRI, diffusion weighted MRI, gradient-echo MRI, serial MRI, volumetry multiple sclerosis multiple sclerosis, differential diagnosis of multiple sclerosis, familial multiple sclerosis, misdiagnosis myocardial infarction myoclonus neoplasm, primary of CNS neoplastic angioendotheliosis neurologic disease, diagnoses of neuropathology neuropathy next-generation sequencing Notch3 gene Notch3 gene, false negative old age, neurology of Parkinson disease Parkinson disease, arteriosclerotic Parkinson disease, L-dopa nonresponsive Parkinsonism syndrome PAS positive PAS positive material in the brain Pelizaeus Merzbacher personality change phenylketonuria posterior leukoencephalopathy syndrome postpartum pregnancy, neurologic complications in prognosis progressive multifocal leucoencephalopathy progressive neurologic disorder pseudobulbar palsy pseudoxanthoma elasticum psychiatric disorder psychiatric problems in neurologic disorders psychological testing psychosis psychotic behavior quadriparesis radiation therapy, CNS treatment and complications with Red flags retina, abnormal retinal lesion retinopathy reversible cerebral vasoconstrictive syndromes reversible neurologic disorder review article risk factors sarcoidosis sarcoidosis, CNS schizophrenia screening seizure sickle cell disease Sjogren's syndrome Sjogren's syndrome, neurologic manifestations of skin, biopsy small vessel disease spinal cord, infarction of subarachnoid hemorrhage subcortical U fibers symmetric brain lesions syncope systemic lupus erythematosus systemic lupus erythematosus, neurologic complications with temporal lobe, lesion temporal lobe, lesion, bilateral thrombotic thrombocytopenia purpura transient ischemic attack transient ischemic attack, recurrent treatment of neurologic disorder treatment resistant unconsciousness urinary incontinence vasculitides vasculopathy vertebral artery stenosis vertigo visual evoked response walking, difficulty with wheelchair Whipple's disease white matter disease white matter disease, location white matter disease, subcortical white matter disease, unilateral workup

Showing articles 50 to 63 of 63 << Previous Quantitative MRI in CADASIL, Correlation with Disability and Cognitive Performance Neurol 52:1361-1367, Dichgans,M.,et al, 1999 Cerebrospinal Fluid Findings in CADASIL Neurol 53:233, Dichgans,M.,et al, 1999 Patterns of MRI Lesions in Cadasil Neurol 51:452-457, Chabriat,H.,et al, 1998 Acute Leukoencephalopathies:Differential Diagnosis and Investigation The Neurologist 4:148-166, Weinshenker,B.G.,et al, 1998 CADASIL in a North American Family:Clinical, Pathological, and Radiologic Findings Neurol 51:844-849, Desmond,D.W.,et al, 1998 The Phenotypic Spectrum of CADASIL:Clinical Findings in 102 Cases, Ann Neurol 44:731-739,715, Dichgans,M.,et al, 1998 Subcotical Arteriosclerotic Encephalopathy (Binswangers Disease) , Ghika,J. &Bogousslavsky, J., 1998 Unusual Clinical Features and Early Brain MRI Lesions in a Family with Cerebral Autosomal Dominant Arteriopathy Neurol 48:1200-1203, Malandrini,A.,et al, 1997 Strong Clustering and Stereotyped Nature of Notch3 Mutations, in CADASIL Patients Lancet 350:1511-1515, 14901997., Joutel,A.,et al, 1997 Autosomal Dominant Migraine with MRI White-Matter Abnormalities Mapping to the CADASIL Locus Neurol 45:1086-1091, Chabriat,H.,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 Progress in the Genetics of Cerebrovascular Disease Inherited Subcortical Arteriopathies Stroke 25:1696-1698, Bowler,J.V.&Hachinski,V., 1994 Showing articles 50 to 63 of 63 << Previous