Neudle.com: abnormal mitochondria

Neurology Specific Literature Search

Differential
(Click to cross reference)

abdominal distention

acquired immunodeficiency syndrome

acute disseminated encephalomyelitis

adrenoleukodystrophy

advances in neurology

adverse drug reaction

agammaglobulinemia

Alexanders disease

alternating hemiplegia

Alzheimer's disease

Alzheimer's disease, pathogenesis

aminoacidopathies

amyloid angiopathy, cerebral

amyloid beta protein

aneurysm, intracranial, familial

angiitis, granulomatous of CNS

angiitis, isolated of CNS

anterior tibial muscle weakness

anticonvulsants

anticonvulsants, selection of

antiviral agents

Arnold Chiari malformation

arrhythmia, cardiac

ataxia telangiectasia

ataxia, cerebellar

ataxia, progressive

ataxia, truncal

autoimmune disease

azidodeoxythymidine

B 12 deficiency

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar artery occlusion

Bassen-Kornzweig syndrome

Behcet's syndrome

Behr's optic atrophy

beriberi, infantile

bitemporal visual field defect

blindness, sudden

blood dyscrasias, neurologic findings with

brainstem, lesion of

calcification, intracranial

Canavan's disease

carbon monoxide poisoning

CAT scan, abnormal

CAT scan, contrast enhanced

CAT scan, dense artery sign

CAT scan, disappearing lesion on

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, muscle

CAT scan, xenon-enhanced

cataracts, congenital

caudate nucleus

caudate nucleus, lesion of

caudate nucleus, lesion of, bilateral

central core disease

central nervous system, infection of

central pontine myelinolysis

cerebellar ataxia, children

cerebellar ataxia, children, differential diagnosis of

cerebellar ataxia, primary

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 embolism

cerebral embolism, cardiac origin

cerebral glucose metabolism

cerebral infarction

cerebral infarction, small, deep

cerebral venous infarction

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebro hepato renal syndrome

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

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

chemotherapy, CNS treatment and complications with

cherry red spot-myoclonus syndrome

chromosomal abnormality

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

Cockayne's syndrome

coenzyme Q10 deficiency

color vision, impaired

congenital birth defects

congenital myopathy

congestive heart failure

cornea, abnormal

corpus callosum, lesion of

cortical blindness

cortical blindness, transient

cortical infarction

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

cricopharyngeal bar

cultured skin fibroblasts

cyst, parenchymal

cytochrome c oxidase

cytochrome c oxidase, deficiency

cytomegalovirus infection

deafness, congenital

deep gray nuclei

degenerative diseases of CNS

dementia, rapidly progressive

demyelinating disease

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes mellitus

differential diagnosis

diplegia, brachial

distal muscle weakness

drug induced neurologic disorders

drug induced neurologic disorders in children

dyschromatopsia

Ekbom's Syndrome

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electron microscopy

electronystagmography

electroretinograph

encephalitis, human immunodeficiency virus type 1

encephalitis, Japanese

encephalitis, viral

encephalomyopathy

encephalopathy, metabolic

encephalopathy, neonatal

encephalopathy, progressive

epidemiology of neurology

epilepsia partialis continua

epileptic encephalopathy

evoked potentials

exercise intolerance

exome sequencing

extraocular muscle atrophy

extraocular muscle lesion

eye movement, disorders of

Fabry's disease

facial nerve palsy

facial nerve palsy, bilateral

facial nerve, lesion of

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

failure to thrive

FARS2 deficiency

fine motor function, impaired

flaccid paralysis

fontanel, bulging

foot ulcer, neuropathic

fourth ventricle, enlargement of

Friedreich's ataxia

fundus, abnormality of

funduscopic exam

gastrointestinal disease, neurologic complications

gastrointestinal motility

genetic counselling

genetic linkage

genetic neurologic disorders

genetic testing

gliomatosis cerebri

glutaric acidemia

gonadal dysgenesis

growth retardation

gyrus, abnormal

Hallervorden Spatz disease

Hallgren's syndrome

headache, recurrent

headache, sudden onset of

headache, treatment of

hearing loss, bilateral

hemianopia, alternating

hemianopia, homonymous

hemianopia, recurrent

hemianopia, transient

hemiparesis, transient

hepatic failure

hepatolenticular degeneration(Wilson's disease)

heralding manifestation

herpes simplex encephalitis

herpes simplex encephalitis, differential diagnosis of

herpes simplex encephalitis, recurrent

histochemistry of muscle

human immunodeficiency virus type 1

Huntington's chorea

Hurler's syndrome

hydrocephalus, viral induced

hypertensive encephalopathy

hypoparathyroidism

hypoparathyroidism, idiopathic

hypotonia, infants

hypoxic encephalopathy

iatrogenic neurologic disorders

ileus, paralytic

inborn errors of metabolism

inclusion bodies

inclusion bodies, intranuclear

inclusion body myositis

infant and newborn with distress, neurologic prognosis in

infant, evaluation of

intellectual deficit

intellectual deterioration

intelligence quotient

internuclear ophthalmoplegia

internuclear ophthalmoplegia, unilateral

intestinal pseudoobstruction

intracranial hypertension, benign

intraventricular hemorrhage

ischemic exercise test

Jakob-Creutzfeldt disease

Kearns-Sayre syndrome

Krabbe's disease

lactic acidemia

Lafora's disease

laminar necrosis, cortical

Laurence-Moon-Bardet-Biedl syndrome

L-dopa, drug interactions with and side effects of

Leber's hereditary optic neuropathy

leg weakness, bilateral

Leigh's disease

Leigh's disease, adult variety

lenticular nucleus, lesion of

lenticular nucleus, lesion of, bilateral

leukocyte enzyme abnormality

leukoencephalopathy

leukoencephalopathy, differential diagnosis

lid closure, weakness of

life expectancy

limbic encephalitis

lipid storage disorder of CNS

lipomatosis, multiple symmetrical

locus ceruleus, lesion of

lymphoma involving CNS

lymphoma, primary of CNS

macular degeneration

magnetic susceptibility

malformation, CNS, congenital

manic-depressive

maple syrup urine disease

Marcus Gunn pupil

Marinesco-Sjogren syndrome

Melkersson's syndrome

memory, impairment of

meningitis, CSF cell count-normal

meningoencephalitis

mental retardation

mental status, abnormal

mesial temporal lobe

mesial temporal sclerosis

metabolic acidosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

methanol intoxication

microangiopathy, brain

microhemorrhage, intracerebral

midbrain, lesion of

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

mitochondrial disease

mitochondrial disease, pathogenesis

mitochondrial encephalomyopathy

mitochondrial recessive ataxic syndrome

molecular genetics

motor neuron disease

movement disorder

movement disorder, extrapyramidal

MRI, abnormal, seizure causing

MRI, CAT scan compared to

MRI, complications with

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, optic nerve

MRI, paramagnetic effect

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, T1 weighted high signal foci

MRI, target sign

MRS, false negative

mucopolysaccharidoses

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, familial

muscle atrophy, progressive

muscle biopsy, extraocular

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, congenital

muscular dystrophy, differential diagnosis of

muscular dystrophy, Duchenne

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenia gravis, differential diagnosis

myasthenia gravis, distal weakness

myasthenia gravis, limb-girdle

myasthenia gravis, misdiagnosis of

myasthenia gravis, ocular

myasthenia gravis, seronegative

myasthenic syndrome

myelitis, longitudinal

myoclonic jerks

myoclonus, epilepsy

myopathy, centronuclear

myopathy, drug-induced

myopathy, inclusion body

myopathy, inclusion body, hereditary

myopathy, mitochondrial

myopathy, proximal

myopathy, toxic

myopathy, vacuolar

myotonia dystrophica

nausea and vomiting

nemaline rod myopathy

neoplasm, primary of CNS

nephrotic syndrome

neuroendocrinology

neurofibrillary degeneration

neurofibromatosis 1

neurogenic vs.myopathic atrophy

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic examination, focal

neurologic signs

neurologic symptoms

neuromuscular blockade

neuromuscular junction, abnormality of

neuronal ceroid-lipofuscinosis

neuronopathy, sensory

neuroophthalmology

neuropathology, brain

neuropathy, ataxia, retinitis pigmentosa

neuropathy, hereditary peripheral

neuropathy, peripheral

next-generation sequencing

night blindness

nigrostriatal pathway

nutritional deficiency

nystagmus, gaze-evoked

nystagmus, rotary

occipital lobe, infarction

occipital lobe, infarction, bilateral

occipital lobe, lesion of

ocular motility, disorders of

ocular myopathy

ocular myopathy, differential diagnosis

oculopharyngeal muscular dystrophy

old age, neurology of

ophthalmoplegia

ophthalmoplegia, plus syndrome

ophthalmoplegia, progressive external

optic atrophy, bilateral

optic atrophy, hereditary

optic chiasm, enlarged

optic chiasm, lesion of

optic disc edema

optic nerve, compression of

optic nerve, enhancement

optic nerve, lesion of

optic nerve, neoplasm of

optic neuritis, bilateral

optic neuritis, treatment of

optic neuropathy

optic neuropathy, bilateral

optic neuropathy, hereditary

optic neuropathy, ischemic

optic neuropathy, nutritional

optic neuropathy, toxic

optic tract, lesion of

orbicularis oculi muscle

orbit, lesions of

osmotic demyelination syndrome

overlap syndrome

owl's eye sign of spinal cord

oxidative phosphorylation

oxidative phosphorylation defect

pain, abdominal

paraparesis, familial spastic

paraparesis, spastic

Parkinson disease

Parkinson disease, diagnosis

Parkinson disease, differential diagnosis of

Parkinson disease, etiology of

Parkinson disease, pathogenesis of

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinsonism syndrome

Pelizaeus Merzbacher

periodic paralysis

peroxisomal disease

personality change

phenylketonuria

pigmentary retinopathy

PLEDs, bilateral independent

PLEDs, etiology of

polymerase chain reaction

polymerase chain reaction, false negative

polymerase chain reaction, false positive

polymyalgia rheumatica

pons, lesion of

posterior cerebral artery territory infarction

posterior leukoencephalopathy syndrome

postictal encephalopathy

prevention of neurologic disorders

progressive infantile poliodystrophy

progressive multifocal leucoencephalopathy

progressive myoclonic epilepsy

progressive neurologic disorder

proximal muscle atrophy

pseudomyasthenia

pseudoretinitis pigmentosa

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

psychosis, acute

ptosis, bilateral

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

radiation therapy, CNS treatment and complications with

ragged-red fibers

rapidly progressing neurologic illness

red free light, fundus exam with

refractive errors

Refsum's disease

remote effect of cancer on the nervous system

renal tubular acidosis

respiratory failure

respiratory tract infection

restless leg syndrome

retina, abnormal

retinal degeneration

retinal nerve fiber layer

retinitis pigmentosa

reversible neurologic disorder

Reye's syndrome

Reye's syndrome, adult

sarcoidosis, CNS

Schilder's disease

scotoma, central

seizure, children

seizure, paradoxical

seizure, treatment of

sensorineural hearing loss

single photon emission computed tomography

small vessel disease

Southern immunoblot test

spastic diplegia

speech, loss of

Spielmeyer Vogt syndrome

spinal cord, lesion of

spinal muscular atrophy

spinocerebellar degeneration

spongy degeneration of brain

spontaneous remission

standing difficulty

status epilepticus

Stephens syndrome

steroid therapy, CNS treatment and complications with

stimulation, deep brain

striatal encephalitis

striatonigral degeneration

striatonigral degeneration, infantile

striatum, lesion of

striatum, lesion of, bilateral

strokelike episodes

subependymal nodules

substantia nigra

subthalamic nucleus

subthalamic nucleus deep brain stimulation

succinate dehydrogenase deficiency

symmetric brain lesions

systemic illness

tapetoretinal degeneration

temporal lobe, lesion

temporal lobe, lesion, bilateral

thalamic tumors

thalamic tumors, bilateral

thalamus, infarction of

thalamus, infarction, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

thiamine deficiency

transient neurologic deficit

transverse smile

treatment of neurologic disorder

tremor, intention

tremor, thalamic stimulation for suppression of

trinucleotide repeats

tuberous sclerosis

Unverricht-Lundborg disease

upgaze, paralysis of

uremic encephalopathy

urine test for metabolic disorders

Usher's syndrome

viral infection, CNS

visceral neuropathy

vision loss, sequential

vision, blurred

vision, failure of in childhood

visual acuity, decreased

visual acuity, decreased, monocular

visual evoked response

visual field defect

visual fields, constricted

visual loss, progressive

visual loss, slow

visual loss, sudden

vitamin deficiency

Von Hippel Lindau

walking, difficulty with

weakness, fatiguable

weakness, generalized

weakness, progressive

weakness, proximal

weakness, rapidly progressive

weaning from respirator, failure to

Wernicke's encephalopathy

Whipple's disease

whistle, inability to

white matter disease

white matter disease, pattern

white matter disease, periventricular

wide based gait

winging of scapula

Showing articles 950 to 1000 of 13058 << Previous Next >>

Neurologic IgG4-Related Disease
Neurohospitalist 9:118-119, Topiwala, K.,et al, 2019

Pterygoid Myositis Mimicking Giant Cell Arteritis
Neurol 92:e2297, Na, S.,et al, 2019

Toxic Diffuse Isolated Cerebellar Edema from Over-the-Counter Health Supplements
Neurol 92:965-966, Kim, D.D.,et al, 2019

Strokelike Episodes in a Patient with Chronic Gait Abnormalities
JAMA Neurol 76:621-622, Santoro, J.D. & Chitnis, T., 2019

Pathophysiology and Management of Hyperammonemia in Organ Transplant Patients
Am J Kidney Dis PMID:31040091, Seethapathy, H. & Fenves, A.Z., 2019

A 47-year-old Man with Diffuse White Matter Disease and Rapidly Progressive Dementia
Neurol 92:e2832-e2837, Di Luca, D.G.,et al, 2019

Recurrent Involuntary Contractions of the Face, Arm, and Leg in an Elderly Man
JAMA Neurol 76:728-729, Kim, D.D.,et al, 2019

Clinical Metagenomic Sequencing for Diagnosis of Meningitis and Encephalitis
NEJM 380:2327-2340, Wilson, M.R.,et al, 2019

Antiepileptic Drug Treatment Patterns in Women of Childbearing Age with Epilepsy
JAMA Neurol 76:783-790, Kim, H.,et al, 2019

Risk of 23 Specific Malformations Associated with Prenatal Exposure to 10 Antiepileptic Drugs
Neurol 93:e167-e180, Blotiere, P.O.,et al, 2019

Kelch-Like Protein 11 Antibodies in Seminoma-Associated Paraneoplastic Encephalitis
NEJM 381:47-54, Mandel-Brehm, C.,et al, 2019

Cerebellar Microbleed Distribution Patterns and Cerebral Amyloid Angiopathy
Stroke 50:1727-1733, Pasi, M.,et al, 2019

Accidental Air Embolism
Stroke 50:e183-e186, Chuang, D.Y.,et al, 2019

Histological Features of Intracranial Thrombi in Stroke Patients with Cancer
Ann Neurol 86:143-149, Park, H.,et al, 2019

Relapsing-Remitting Severe Bickerstaffs Brainstem Encephalitis
BMJ 394:684, Tyrakowska, Z.,et al, 2019

A 68-year-old Man with Rapid Cognitive Decline
Neurol 93:315-318, Berth, S.H.,et al, 2019

Cytotoxic Lesions of the Corpus Callosum Caused by Thermogenic Dietary Supplements
AJNR 40:1304-1308, Galnares-Olalde, J.A.,et al, 2019

The Interpeduncular Angle:A Practical and Objective Marker for the Detection and Diagnosis of Intracranial Hypotension on Brain MRI
AJNR 40:1299-1303, Wang,D.J.,et al, 2019

Pes Cavus and Neuropathy
Neurol 93:e823-e826, Alderson,J.,& Ghosh,P.S., 2019

Bilateral Alopecia as Clue to Diagnosis of Gomez-Lopez-Hernandez Syndrome in a 38-Year-Old Man
Neurol 93:408-410, Kronlage,C.&Healy,D.G., 2019

Isolated and Persistent Hiccup by Tiny Ischemia at Dorsolateral Medulla
Neurol 93:e934, Seo,J.H., 2019

Declining Malformation Rates with Changed Antiepileptic Drug Prescribing, An Observational Study
Neurol 93:e831-e840, Tomson,T.,et al, 2019

Case 27-2019:A 16-Year-Old Girl with Head Trauma During a Sailboat Race
CPC,Concussion,Benign Paroxysmal Positional Vertigo, Case 27-2019, NEJM 381:863-871, Iaccarino,M.A.,et al, 2019

Childhood Primary Angiitis of the Central Nervous System
www.UptoDate.com, Dec, Twilt, M. & Benseler, S., 2019

Characteristic Head Jerks in Congenital Oculomotor Apraxia due to Joubert Syndrome
Neurol 93:e1125-e1126, Borngraber, F.,et al, 2019

A 58-year-old Man with Hand Tremor and Episodes of Neck Pain
Neurol 93:557-561, Urso, D.,et al, 2019

Neurolymphomatosis
Neurol 93:e1229-e1230, DeBoer, S.R.,et al, 2019

Rapidly Progressive Vision Loss in a Patient with Breast Cancer
JAMA 322:1098-1099, Izzo, M.C.,et al, 2019

Circulating DNAs, a Marker of Neutrophil Extracellular Traposis and Cancer-Related Stroke
Stroke 50:2944-2947, Bang, O.Y.,et al, 2019

Predicting Developmental Outcomes in Preterm Infants
Neurol 93:e1231-e1240, Cayam-Rand, D.,et al, 2019

Bilateral Claude Syndrome
Neurol 93:599-600, Witsch, J.,et al, 2019

Ehlers-Danlos Syndromes
BMJ 366:I4966, Ghali, N.,et al, 2019

Standards for Detecting, Interpreting, and Reporting Noncontrast Computed Tomographic Markers of Intracerebral Hemorrhage Expansion
Ann Neurol 86:480-492, Morotti, A.,et al, 2019

Neurosyphilis
NEJM 381:1358-1363, Ropper, A.H.,et al, 2019

A 55-Year-Old Woman Presenting with Ataxia and Numbness 1 Year After Ileum Resection
Neurol 93:675-679, Cassano, V.,et al, 2019

Failing to See Blood on Susceptibility-Weighted Imaging
Neurol 93:e1495-e1496, Graham, E.,et al, 2019

High-Resolution Diffusion-Weighted Imaging Identifies Ischemic Lesions in a Majority of Transient Ischemic Attack Patients
Ann Neurol 86:452-457, Hotter, B.,et al, 2019

A Case of Muscle Twitching with Psoriasis
JAMA Neurol 76:1119-1120, Qian, M.,et al, 2019

Diagnostic Value of Cerebrospinal Fluid Neurofilament Light Protein in Neurology
JAMA Neurol 76:1035-1048, Bridel, C.,et al, 2019

Diagnostic Impact of Intracranial Vessel Wall MRI in 205 Patients with Ischemic Stroke
AJNR 40:1701-1706,1707, Schaafsma, J.D.,et al, 2019

Reversible Cerebral Vasoconstriciton Syndrome
www.UptoDate.com, June, Singhal, A., 2019

Clinicopathologic Conference, Adenovirus Meningoencephalitis
NEJM 381:1459-1470, Case 31-2019, 2019

Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
Neurol 92:101-103, Kang, M.J.,et al, 2019

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

Early Magnetic Resonance Imaging Decreases Hospital Length of Stay in Patients with Ischemic Stroke
J Stroke Cerebrovasc Dis 28:425-429, Manwani, B.,et al, 2019

MR Imaging of the Brain in Neurologic Wilson Disease
AJNR 40:178-183, Yu, X.-E.,et al, 2019

"Ears of the Lynx" MRI Sign is Associated with SPG11 and SPG15 Hereditary Spastic Paraplegia
AJNR 40:199-203, Pascual, B.,et al, 2019

The Dangers of PRES
Neurol 92:e282-e285, Chaterine, C.,et al, 2019

CRAO and Silent Brain Infarcts caused by Cardiac Myxomas in Carney Complex
Neurol 92:e286-e287, Huang, L-T.,et al, 2019

A Middle-Aged Man with New Onset Seizures and Myoclonic Jerks
Neurol 92:e274-e281, Chen, Z. & Neo, S., 2019

Showing articles 950 to 1000 of 13058 << Previous Next >>