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Differential
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aneurysm, intracranial, familial
aphasia
arginine
arteriopathy
asymptomatic
ataxia
ataxia, progressive
ataxic gait
basal ganglia
basal ganglia, calcification of
basal ganglia, infarction
basal ganglia, lesion of
basal ganglia, lesion, bilateral
blindness, sudden
brain atrophy
brain biopsy
brainstem, lesion of
calcification, intracranial
carbon monoxide poisoning
carcinoma
cardiomegaly
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, disappearing lesion on
CAT scan, false negative
CAT scan, xenon-enhanced
cataracts
caudate nucleus, lesion of
cause of death
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar lesion
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral blood flow
cerebral cortex
cerebral cortical atrophy
cerebral edema, cytotoxic
cerebral infarction
cerebral infarction, small, deep
cerebral venous thrombosis, deep
cerebrospinal fluid, lactic acid concentration
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, infancy and childhood
cerebrovascular accident, location of
cerebrovascular accident, mimics
cerebrovascular accident, multiple
cerebrovascular accident, non atherosclerotic cause of
cerebrovascular accident, nonvascular territory
cerebrovascular accident, prevention of
cerebrovascular accident, recurrent
cerebrovascular accident, young adult
children
chromosomal abnormality
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
coenzyme Q10 deficiency
coma
corpus callosum, lesion of
cortical blindness
cortical blindness, transient
cyanide poison
cyst, parenchymal
deafness
deep gray nuclei
dementia
dementia, rapidly progressive
depression
developmental retardation
diabetes mellitus
differential diagnosis
diplopia
dysphagia
dystonia
echocardiogram
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electron microscopy
encephalopathy
encephalopathy, metabolic
encephalopathy, progressive
epilepsia partialis continua
exercise intolerance
eye movement, disorders of
failure to thrive
false negative
familial
fatigue
fever
fourth ventricle, enlargement of
gadolinium
gene mutation
gene therapy
genetic counselling
genetic neurologic disorders
genetic testing
gray matter
growth retardation
gyrus, abnormal
Hallervorden Spatz disease
headache
headache, recurrent
headache, sudden onset of
headache, treatment of
hearing loss
hearing loss, bilateral
heart block
hemianopia
hemianopia, alternating
hemianopia, homonymous
hemianopia, recurrent
hemianopia, transient
hemiparesis
hemiparesis, transient
hemiplegia
heralding manifestation
herpes simplex encephalitis
herpes simplex encephalitis, differential diagnosis of
herpes simplex encephalitis, recurrent
hirsutism
human immunodeficiency virus type 1
hydrocephalus
ileus, paralytic
imbalance
impulsivity
intellectual deficit
intellectual deterioration
intestinal pseudoobstruction
Kearns-Sayre syndrome
lactate
lactic acidemia
laminar necrosis, cortical
Leber's hereditary optic neuropathy
Leigh's disease
lenticular nucleus, lesion of, bilateral
leukocyte enzyme abnormality
leukodystrophy
leukoencephalopathy
manic-depressive
MELAS syndrome
mental retardation
mental status, abnormal
MERRF syndrome
metabolic disorder, primary
methanol intoxication
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
migraine
mimics
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
mortality
MRI
MRI pattern
MRI, abnormal
MRI, ADC maps
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, serial
MRI, spinal cord
MRI, spinal cord, increased intramedullary cord signal
MRI, target sign
MRS
multiple sclerosis, differential diagnosis of
muscle biopsy
muscle weakness
muscle weakness, proximal
myasthenia gravis, differential diagnosis
myasthenia gravis, misdiagnosis of
myelitis
myelitis, longitudinal
myelopathy
myoclonus
myoclonus, epilepsy
myopathy
myopathy, mitochondrial
nausea and vomiting
negative
neuroendocrinology
neurofibromatosis 1
neurologic complications of, systemic cancer
neurologic disease, diagnoses of
neurologic examination, focal
neurons
neuroophthalmology
neuropathology
neuropathy
neuropathy, ataxia, retinitis pigmentosa
neuroradiology
neurotoxin
next-generation sequencing
normal
occipital lobe
occipital lobe, infarction
occipital lobe, infarction, bilateral
occipital lobe, lesion of
ophthalmoplegia
ophthalmoplegia, progressive external
optic atrophy
optic neuropathy
overlap syndrome
owl's eye sign of spinal cord
pancytopenia
personality change
pigmentary retinopathy
PLEDs
PLEDs, bilateral independent
PLEDs, etiology of
polymerase chain reaction
posterior cerebral artery territory infarction
prevention of neurologic disorders
prognosis
progressive neurologic disorder
proteinuria
psychiatric problems in neurologic disorders
psychosis
psychosis, acute
ptosis
putamen, lesion of, bilateral
radiation therapy, CNS treatment and complications with
ragged-red fibers
rapidly progressing neurologic illness
recurrent
renal failure
respiratory tract infection
retinopathy
reversible neurologic disorder
review article
Schilder's disease
schizophrenia
seizure
seizure, children
seizure, focal
sensorineural hearing loss
short stature
single photon emission computed tomography
small vessel disease
spinal cord, lesion of
spontaneous remission
steroid therapy, CNS treatment and complications with
striatal encephalitis
striatum, lesion of, bilateral
strokelike episodes
subependymal nodules
substantia nigra
succinate dehydrogenase deficiency
sumatriptan
symmetric brain lesions
temporal lobe, lesion
thalamus, lesion of
thalamus, lesion of-bilateral
transient neurologic deficit
treatment of neurologic disorder
triptans
tuberous sclerosis
upgaze, paralysis of
uremic encephalopathy
vasculopathy
visual acuity, decreased
visual field defect
visual loss
visual loss, progressive
walking, difficulty with
weakness
weight loss
white matter disease
white matter disease, pattern
workup
Showing articles 0 to 50 of 50

Imaging Patterns Characterizing Mitochondrial Leukodystrophies
AJNR 42:1334-1340, Roosendaal, S.D.,et al, 2021

"Disappearing Infarct" Is Late-Onset MELAS
Ann Neurol 90:1001-1002, Landis,T.M.,et al, 2021

Pediatric Leigh Syndrome
Ann Neurol 88:218-232, Alves, C.A.P.F.,et al, 2020

Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
NEJM 376:1668-1678, CASE 13-2017, 2017

Longitudinally Extensive Transverse Myelitis in MELAS
Neurol 86:e37, Sgobbi de Souza, P.V.,et al, 2016

Recommendations for the Management of Strokelike Episodes in Patients with Mitochondrial Encephalomyopathy, Lactic Acidosis, and Strokelike Episodes
JAMA 73:591-594, Koenig, M.K.,et al, 2016

A Young Man with Progressive Vision and Hearing Loss
JAMA Neurol 73:880-883, Kung, N.H.,et al, 2016

Clinical Reasoning: Encephalopathy in a 10-year-old boy
Neurol 79:e12-e18, Rodan, L. & Tein, I., 2012

MELAS
MedLink.com, August, Klopstock, T., 2012

The Use of Neuroimaging in the Diagnosis of Mitochondrial Disease
Dev Disabil Res Rev 16:129-135, Friedman, S.D.,et al, 2010

Diagnosis and Therapy in Neuromuscular Disorders: Diagnosis and New Treatments in Mitochondrial Diseases
JNNP 80:943-953, Rahman,S. &Hanna,M.G., 2009

Serial Diffusion Imaging in a Case of Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes
Stroke 40:e15-e17, Tzoulis,C. &Bindoff,L.A., 2009

Multiple Simultaneous Cerebral Infarctions in Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
Cerebrovasc Dis 22:445-446, Gobron,C.,et al, 2006

Metabolic Disease and Stroke: MELAS
emedicine.com, Mandava,P.,et al, 2006

Clinicopath Conf., MELAS Syndrome
NEJM 353:2271-2280, Case 36-2005, 2005

Alternate-Sided Homonymous Hemianopia as the Solitary Presentation of Mitochondrial Encephalomyopathy, Lactic Acidosis, Stroke-Like Episodes Syndrome
Chang Gung Med J 26:199-203, Su,WY.,et al, 2003

Response to Sumatriptan in Headache of MELAS Syndrome
Neurol 61:577-578, Iizuka,T.,et al, 2003

Diagnostic Approach in Patients with Symmetric Imaging Lesions of the Deep Gray Nuclei
The Neurologist 9:250-261, Finelli,P.F.&DiMario,Jr,F.J., 2003

A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
The Neurologist 8:302-312, Thambisetty,M.,et al, 2002

Mitochondrial Disease and Stroke
Stroke 32:2507-2510, Martinez-Fernandez,E.,et al, 2001

Diffusion-weighted MR Imaging in a Case of Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Strokelike Episodes
AJNR 22:269-272, Yonemura,K.,et al, 2001

Advances in the Genetics of Cerebrovascular Disease and Stroke
Neurol 56:997-1008, Hademenos,G.J.,et al, 2001

Mitochondrial Dysfunction in Bipolar Disorder
Bipolar Disord 2:180-190, Kato,T., 2000

Adult-Onset MELAS Presenting as Herpes Encephalitis
Arch Neurol 56:241-243, Sharfstein,S.R.,et al, 1999

Age and Cause of Death in Mitochondrial Diseases
Neurol 53:855-857, Klopstock,T.,et al, 1999

Clinicopath Conf,Syndrome of Mitochondrial Encephalopathy,Lactic Acidosis,and Stroke-Like Episodes (MELAS),Case 39-1998
NEJM 339:1914-1923, , 1998

Neuroradiological Features of Six Kindreds with MELAS tRNA(Leu) A3243G Point Mutation: Implications for Pathogenesis
JNNP 65:233-240, Sue,C.M.,et al, 1998

Recurrent Strokes in a 34-Year-Old Man
Lancet 350:560, Chinnery,P.F.,et al, 1997

MELAS Presenting as Migraine Complicated by Stroke:Case Report
Neuroradiology 39:781-784, Ohnok,IK.,et al, 1997

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

Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995

The Syndrome of MELAS Presenting without Stroke
Arch Neurol 50:275-278, Mosewich,R.K.,et al, 1993

Cerebral Blood Flow in Mitochondrial Myopathy, Encephalopathy, lactic Acidosis, & Strokelike episodes
Stroke 24:304-309, Ooiwa,Y.,et al, 1993

Mitochondrial Encephalomyopathy, Lactic Acidosis, Stroke-Like Episodes (MELAS) :Clinical, Radiological, Pathol & Genetic Observ
Ann Neurol 34:25-31, Koo,B.,et al, 1993

Ophthalmologic Manifestations in MELAS Syndrome
Arch Neurol 50:977-980, Fang,W.,et al, 1993

MELAS Syndrome Masquerading as Herpes Simplex Encephalitis
Neurol 43:2471-2473, Johns,D.R.,et al, 1993

Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS) :Clin Features & DNA Mutation
Neurol 42:545-550, Goto,Y.,et al, 1992

N-Isopropyl-p- (123I) Iodoamphetamine SPECT in MELAS Syndrome:Comparison with CT & MR Imaging
J Comput Assist Tomogr 15:77-82, Satoh,M.,et al, 1991

Magnetic Resonance Imaging Shows Specific Abnormalities in the MELAS Syndrome
Neurol 41:1043-1046, Matthews,P.M., 1991

Mitochondril Encephalopathies:Molecular Genetic Diagnosis from Blood Samples
Lancet 337:1311-1313, Hammans,S.R.,et al, 1991

Fluctuating MR Images with Mitochondrial Encephalopathy, Lactic Acidosis, Stroke-Like Syndrome (MELAS)
Neuroradiology 32:77, Abe,K.,et al, 1990

Mitochondrial Encephalomyopathy (MELAS) with Mental Disorder, CT, MRI and SPECT Findings
Neuroradiology 32:74-76, Suzuki,T.,et al, 1990

Magnetic Resonance Imaging in MELAS Syndrome
Neuroradiology 32:168-171, Rosen,L.,et al, 1990

MELAS Syndrome:Characteristic Migrainous & Epileptic Features and Maternal Transmission
Neurol 38:751-754, Montagne,P.,et al, 1988

Diagnosis & Follow-up of Mitochondrial Encephalomyopathy:CT and MR Studies
J Comput Assist Tomogr 12:696-697, Taverni,N.,et al, 1988

Significance of Basal Ganglia Calcification on Computed Tomography in Children
Pediatr Neurosci 14:64-70, Zimmerman,L.A.,et al, 1988

MELAS Syndrome Involving a Mother & Two Children
Arch Neurol 44:971-973, Driscoll,P.F.,et al, 1987

Mitochondrial Myopathies
Ann Neurol 17:521-538, DiMauro,S.,et al, 1985

Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, & Strokelike Episodes:A Distinctive Clinical Syndrome
Ann Neurol 16:481-488, Pavlakis,S.G.,et al, 1984



Showing articles 0 to 50 of 50