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Differential
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abdominal distention
aciduria
agenesis of corpus callosum
aggression
Alzheimer's disease
Alzheimer's disease, risk factors in
aminoacidopathies
aminoacidurias
amyloidosis
anemia
anemia, megaloblastic
aneurysm
aneurysm, intracranial
aneurysm, intracranial, familial
angiography, cerebral
anorexia
anticoagulant, treatment
anticoagulant, treatment in CVD
apnea
arachnodactyly
areflexia
arrhythmia, cardiac
arterial dissection
arterial dissection, carotid
arterial dissection, spontaneous
arterial dissection, vertebral
arteriopathy
ataxia
ataxic gait
atrial myxoma
B 12 deficiency
B 12 deficiency, infants
B 12 metabolism, defective
Babinski sign
bacterial infection
bedridden
behavior, combative
behavioral disorder
bradycardia
brain atrophy
brainstem, atrophy
breast feeding
calcification, intracranial
cardiomyopathy
carotid artery disease
carotid artery stenosis
CAT scan, abnormal
cavernous hemangioma
central nervous system, infection of
cerebral embolism
cerebral infarction
cerebral ischemia
cerebral vasculature, calcification
cerebral vasculature, calcification, premature
cerebral venous infarction
cerebral venous thrombosis
cerebral venous thrombosis, etiology
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, red cells in
cerebrovascular accident
cerebrovascular accident, etiology
cerebrovascular accident, familial occurrence
cerebrovascular accident, infancy and childhood
cerebrovascular accident, postpartum
cerebrovascular accident, prevention of
cerebrovascular accident, recurrent
cerebrovascular accident, silent
cerebrovascular accident, women
cerebrovascular accident, work up for
cerebrovascular accident, young adult
cerebrovascular disease
cerebrovascular disease, premature
cerebrovascular disease, risk factors in
children
cholelithiasis
Clinical Pathologic Conference(C.P.C.)
clonus
coagulopathy
cobalamin C deficiency
codfish vertebrae
cognition
collagen vascular disease
coma
comorbidities
confusion
consanguinity
controversies in neurology
cortical blindness
cortical vein thrombosis
cyanosis
cystinuria
D-dimer
delusion
dementia
developmental retardation
dexterity, impaired
diet
distal muscle weakness
drug abuse
dural sinus thrombosis
dysmorphic
ecchymoses
echocardiogram
Ehlers-Danlos syndrome
electroencephalogram, abnormalities of
emotional lability
encephalopathy
enzyme, defect
exome sequencing
Fabry's disease
facial anomalies
facial appearance, abnormal
facial hypoplasia
familial
fatigue
fibromuscular dysplasia
fingers, abnormal
folic acid
folic acid deficiency
frontal bossing
gait disorder
gait, spastic
gene mutation
genetic neurologic disorders
genetic testing
gout
gray hair
head bobbing
headache
headache, positional
heart murmur
hemoglobin abnormality, neurologic complications of
heralding manifestation
hereditary hemorrhagic telangiectasia(HHT)
homocysteine, lowering
homocysteine, serum
homocystinuria
homocystinuria, heterozygous
hydrocephalus
hyperbilirubinemia
hypercoagulable state
hyperhomocysteinemia
hyperpigmentation of skin
hyperreflexia
hypersegmented polys
hypomyelination
hypothermia
hypotonia
hypotonia, infants
imbalance
inappropriate behavior
inattention
inborn errors of metabolism
infantile hemiplegia
infantile hemiplegia, causes of
insulin resistance
intellectual deficit
intellectual deterioration
intracerebral hemorrhage
intracerebral hemorrhage, young adult
kyphoscoliosis, neurologic causes of
lactic dehydrogenase(LDH)
lateral sinus thrombosis
laughing, pathologic
lens, dislocation of
lens, ectopic
lethargy
leukoencephalopathy
Lhermitte's sign
livedo reticularis
malformation, vascular
malformation, vascular, cerebral
malformation, vascular, familial
malignant external otitis
marfanoid skeletal abnormalities
mastoiditis
melanomatosis, primary malignant
memory, defect of recent
memory, impairment of
meningitis
mental status, abnormal
metabolic disorder, primary
metabolic disorder, primary-screening tests
methylene tetrahydrofolate reductase
methylenetetrahydrofolate reductase deficiency
methylmalonic acid, serum
methylmalonic acidemia
methylmalonic aciduria
microangiopathy, brain
microcephaly
microspherophakia
migraine
migraine, hemiplegic
mimics
misdiagnosis
mitral valve prolapse
mortality
moyamoya
MRI
MRI, abnormal
MRI, diffusion weighted
MRI, spinal cord
MRI, spinal cord, increased intramedullary cord signal
MRI, venography
multiple sclerosis, differential diagnosis of
myelitis, longitudinal
myeloneuropathy
myocardial infarction
myopia
nausea and vomiting
neurocutaneous disease
neurofibromatosis 1
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic examination, focal
neurologic history
neuropathy
neuropathy, sensory
neuropathy, toxic
neurotoxic
night sweats
nitrous oxide
numbness, ascending
numbness, generalized
old age, neurology of
optic nerve, hypoplasia of
osteoporosis
otitis, neurologic complications with
pancytopenia
papilledema
paraparesis, spastic
paresthesias
paresthesias, feet
paresthesias, generalized
paresthesias, hands
pectus excavatum
pediatric neurology
pernicious anemia
phenylketonuria
pleocytosis of cerebrospinal fluid
polycythemia, primary
pons, atrophy
posterior column disease
postpartum
precipitating factors
pregnancy, neurologic complications in
prethrombotic state
prevention of neurologic disorders
prognathism
prognosis
progressive neurologic disorder
protein C deficiency
pseudoxanthoma elasticum
psychiatric problems in neurologic disorders
psychosis
psychotic behavior
pulmonary embolism
renal failure
renal stones
respiratory failure
review article
risk factors
Romberg's sign
scoliosis
scoliosis, neurologic association with
seizure
sensory level
sensory loss
sensory loss, glove-stocking
short stature
sickle cell disease
skin, lesions in neurologic disorders
speech, pressured
spinal cord
spinal cord, lesion of
splenomegaly
subarachnoid hemorrhage
superior sagittal sinus thrombosis
systemic illness
tangential
thrombocytopenia
thrombophlebitis
transient ischemic attack
trauma
treatment of neurologic disorder
tuberous sclerosis
urinary incontinence
urine test for metabolic disorders
varicella zoster virus
vasculopathy
vegetarianism
vein of Galen
venous thrombosis, non-cerebral
vibratory sensation, abnormal
violent behavior
visual tracking
vitamin deficiency
vitamin supplementation
vitamin therapy
vitamin, multiple
Von Hippel Lindau
walking, difficulty with
weakness
weakness, progressive
white matter disease
workup
Showing articles 0 to 42 of 42

Clinicopathologic Conference, Vitamin B12 Deficiency Due to Pernicious Anemia
NEJM 390:747-756, Case 6-2024, 2024

A Young Adult Man with Cognitive Changes, Gait Difficulty, and Renal Insufficiency
Neurol 100:206-212, Stamm,B.,et al, 2023

Clinicopathologic Conference, Functional Vitamin B12 Deficiency from Use of Nitrous Oxide
NEJM 388:1893-1900, Case 15-2023, 2023

A 13-Year-Old Boy with Subacute-Onset Spastic Gait
JAMA Neurol 78:e1-e2, Xie, N.,et al, 2021

Analysis of 70 patients with hydrocephalus due to cobalamin C deficiency
Neurol 95:e3129-e3137, He, R.,et al, 2020

A 14-Year-Old Girl with Headache, Seizures, and Confusion
Neurol 92:e161-e167, Xiao, L.,et al, 2019

Clinicopathologic Conference, Pernicious Anemia (Vitamin B12 Deficiency)
NEJM 380:665-674, Case 5-2019, 2019

Subacute Progressive Sensorimotor Symptoms
BMJ 365:doi:10.1136/bmj.l1923, Francis, A.,et al, 2019

Progressive Weakness and Memory Impairment in a Middle-aged Man
JAMA 320:197-198, DeFilippis, E.M.,et al, 2018

Clinicopathologic Conference, Homocystinuria due to genetic mutations of the gene encoding cystathionine B-synthase (CBS)
NEJM 378:941-948, Case 7-2018, 2018

Cerebral Venous Sinus Thrombosis in Homocystinuria: Dietary Intervention in Conjunction with Anticoagulation
Sage Open Med Case Reports 5:1-4, Yap, S.,et al, 2017

Clinicopathologic Conference, Homocystinuria caused by Cystathionine B-Synthase Deficiency
NEJM 375:1879-1890, Case 34-2016, 2016

Clinicopathologic Conference, Severe Methylenetetrahydrofolate Reductase Deficiency
NEJM 371:847-858, Case 27-2014, 2014

A Young Woman with Rapid Mental Deterioration and Leukoencephalopathy
Neurol 83:e182-e186, Biotti, D.,et al, 2014

Cerebral Vein Thrombosis Misdiagnosed and Mismanaged
Thrombosis 2012:210676, Sasidharan, P.K., 2012

Premature Intracranial Arterial Calcification in a Patient With Hyperhomocysteinemia
Neurol 75:2252, Nah,H.-W. &Kim,J.S., 2010

Cerebral Venous Thrombosis: A Descriptive Multicenter Study of Patients in Pakistan and Middle East
Stroke 39:2707-2711, Khealani,B.,et al, 2008

Efficacy of Folic Acid Supplementation in Stroke Prevention: A Meta-Analysis
Lancet 369:1876-1882,1841, Wang,X.,et al, 2007

Homocysteine and Stroke: Evidence on a Causal Link From Mendelian Randomisation
Lancet 365:224-232, 194, Casas, J.P., et al, 2005

Hyperhomocysteinemia, Low Folate and Vitamin B12 Concentrations, and Methylene Tetrahydrofolate Reductase Mutation in Cerebral Venous Thrombosis
Stroke 35:1790-1794, Cantu,C.,et al, 2004

Lowering Homocysteine in Patients with Ischemic Stroke to Prevent Recurrent Stroke, Myocardial Infarction, and Death
JAMA 291:565-575,621, Toole,J.F.,et al, 2004

Hyperhomocysteinemia in Cerebral Vein Thrombosis
Blood 102:1363-1366, Martinelli,I.,et al, 2003

Investigation of Risk Factors in Children with Arterial Ischemic Stroke
Ann Neurol 53:167-173,149, Ganesan,V.,et al, 2003

Homocysteine and Risk of Recurrent Stroke
Stroke 34;1258-1261, Boysen,G.,et al, 2003

Hyperhomocysteinemia as an Independent Risk Factor for Silent Brain Infarction
Neurol 61:1595-1599, Kim,N.K.,et al, 2003

Plasma Homocysteine as a Risk Factor for Dementia and Alzheimer's Disease
NEJM 346:476-483, 466, Seshadri,S.,et al, 2002

Hyperhomocysteinemia and Other Inherited Prothrombotic Conditions in Young Adults With a History of Ischemic Stroke
Stroke 33:51-56, Madonna,P.,et al, 2002

Homocysteine, Silent Brain Infarcts, and White Matter Lesions: The Rotterdam Scan Study
Ann Neurol 51:285-289,279, Vermeer,S.E.,et al, 2002

Spontaneous Cervical Artery Dissection
Stroke 33:657-658,664, Brandt,T. &Grond-Ginsbach,C., 2002

Homocysteine and Risk of Ischemic Heart Disease and Stroke
JAMA 288;2015-2022, The Homocysteine Studies Collaboration, 2002

Homocysteine and Neurologic Disease
Arch Neurol 57:1422-1428, Diaz-Arrastia,R., 2000

Homocysteine and Short-term Risk of Myocardial Infarction and Stroke in the Elderly
Arch Int Med 159:38-44, Bots,M.L.,et al, 1999

Homocyst(e)ine and Risk of Cerebral Infarcdtion in a Biracial Population, The Stroke Prevention in Young Women Study
Stroke 30:1554-1560, Kittner,S.J.,et al, 1999

Features, Symptoms & Neurophysiological Findings in Stroke Assoc with Hyperhomocysteinemia
Arch Neurol 54:1276-1282, Evers,S.,et al, 1997

Association Between Plasma Homocysteine Concentrations and Extracranial Carotid-Artery Stenosis
NEJM 332:286-291, 3281995., Selhub,J.,et al, 1995

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

Hereditary Defect of Cobalamin Metabolism (cblG Mutation) Presenting as a Neurologic Disorder in Adulthood
NEJM 318:1738-1741, 1752-17541988., Carmel,R.,et al, 1988

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

Heterozygosity for Homocystinuria in Premature Peripheral & Cerebral Occlusive Arterial Disease
NEJM 313:709-715, Boers,G.H.J.,et al, 1985

A Synd of Methylmal Acid, Homocystinuria, Megaloblas. Anemia & Neurol Abnor. in a Vit B-12-def Breast-fed Infant of veget
NEJM 299:317, Higginbottom,M.C., 1978

CNS Lesions in Cystinuria
Arch Neurol 34:638, Blackburn,C.R.B.,et al, 1977

Newborn Metabolic Screening:Past & Prospect
NEJM 293:824, Levy,H., 1975



Showing articles 0 to 42 of 42