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abdominal distention
acanthocytosis
acquired immunodeficiency syndrome
adrenoleukodystrophy
advances in neurology
adverse drug reaction
agammaglobulinemia
alcoholism
aminoacidopathies
anterior tibial muscle weakness
anticonvulsants
anticonvulsants, selection of
aphasia
areflexia
arrhythmia, cardiac
aspirin
asymptomatic
ataxia
ataxia, cerebellar
ataxia, progressive
ataxic gait
autoimmune disease
azidodeoxythymidine
basal ganglia, calcification of
basal ganglia, infarction
basal ganglia, lesion, bilateral
Bassen-Kornzweig syndrome
blindness
blindness, sudden
botulism
brain biopsy
brainstem, lesion of
bulbar palsy
cachexia
calcification, intracranial
carcinoma
cardiomegaly
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, disappearing lesion on
CAT scan, emission
CAT scan, emission, abnormal
CAT scan, false negative
CAT scan, muscle
CAT scan, xenon-enhanced
cataracts
cataracts, congenital
cause of death
central core disease
central nervous system, infection of
cerebellar ataxia, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebral blood flow
cerebral cortical atrophy
cerebral edema, cytotoxic
cerebral embolism
cerebral embolism, cardiac origin
cerebral glucose metabolism
cerebral infarction
cerebro hepato renal syndrome
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, lactic acid concentration
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, infancy and childhood
cerebrovascular accident, mimics
cerebrovascular accident, multiple
cerebrovascular accident, nonvascular territory
cerebrovascular accident, recurrent
cerebrovascular accident, young adult
cherry red spot-myoclonus syndrome
children
chromosomal abnormality
chronic progressive external ophthalmoplegia
Chvostek sign
Clinical Pathologic Conference(C.P.C.)
Cockayne's syndrome
coenzyme Q10
coenzyme Q10 deficiency
coma
congenital birth defects
congenital myopathy
consanguinity
cornea, abnormal
corpus callosum, lesion of
cortical blindness
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
cricopharyngeal bar
cultured skin fibroblasts
cyst, parenchymal
cytochrome c oxidase
cytochrome c oxidase, deficiency
deafmute
deafness
deep gray nuclei
degenerative diseases of CNS
dementia
dementia, rapidly progressive
dentatorubral-pallidoluysian atrophy
depression
developmental retardation
diabetes mellitus
diarrhea
differential diagnosis
diplopia
distal muscle weakness
dizziness
DNA probes
drug induced neurologic disorders
dwarfism
dyschromatopsia
dysphagia
dyspnea
dyspraxia
dystonia
Ekbom's Syndrome
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electromyogram
electron microscopy
electronystagmography
electroretinograph
encephalomyopathy
encephalopathy
encephalopathy, progressive
enzyme, defect
epilepsia partialis continua
evoked potentials
exercise
exercise intolerance
extraocular muscle atrophy
extraocular muscle lesion
eye closure
eye movement, disorders of
facial nerve palsy
facial nerve palsy, bilateral
facial nerve, lesion of
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
failure to thrive
falling
false negative
familial
fatigue
fever
fibrillations
foot drop
foot ulcer, neuropathic
Friedreich's ataxia
fundus, abnormality of
gadolinium
gait disorder
gargoylism
gastrointestinal disease, neurologic complications
gastrointestinal motility
gastroparesis
gaze palsy
gene
gene mutation
gene therapy
genetic counselling
genetic linkage
genetic neurologic disorders
genetic testing
glaucoma
gonadal dysgenesis
growth retardation
Hallervorden Spatz disease
Hallgren's syndrome
headache
headache, sudden onset of
hearing loss
heart block
hemianopia
hemianopia, homonymous
hemianopia, transient
hemiparesis
hepatic failure
hepatomegaly
heralding manifestation
herpes simplex encephalitis
herpes simplex encephalitis, differential diagnosis of
hirsutism
histochemistry of muscle
human immunodeficiency virus type 1
Huntington's chorea
Hurler's syndrome
hydrocephalus
hypocalcemia
hypomagnesemia
hypoparathyroidism
hypoparathyroidism, idiopathic
hypophonia
hypothyroidism
hypotonia
ileus, paralytic
imbalance
impulsivity
inclusion bodies
inclusion bodies, intranuclear
inclusion body myositis
intellectual deficit
intellectual deterioration
intelligence quotient
intestinal pseudoobstruction
ischemic exercise test
Kearns-Sayre syndrome
keratoconus
lactate
lactic acidemia
Lafora's disease
laminar necrosis, cortical
Laurence-Moon-Bardet-Biedl syndrome
Leber's hereditary optic neuropathy
leg numbness
leg weakness, bilateral
Leigh's disease
lenticular nucleus, lesion of, bilateral
leukocyte enzyme abnormality
leukodystrophy
leukoencephalopathy
lid closure, weakness of
life expectancy
lipoma of skin
lipomatosis
lipomatosis, multiple symmetrical
lordosis
macular degeneration
malaise
malformation, CNS, congenital
MELAS syndrome
Melkersson's syndrome
memory, impairment of
mental retardation
MERRF syndrome
microangiopathy, brain
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
migraine
mimics
misdiagnosis
mitochondrial disease
mitochondrial disease, pathogenesis
mitochondrial encephalomyopathy
mitochondrial recessive ataxic syndrome
MNGIE syndrome
molecular genetics
mortality
motor neuron disease
movement disorder
MRI
MRI pattern
MRI, abnormal
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, muscle
MRI, serial
MRS
mucopolysaccharidoses
muscle atrophy, progressive
muscle biopsy
muscle biopsy, extraocular
muscle cramp
muscle pain
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
myelopathy
myoclonic jerks
myoclonus
myoclonus, epilepsy
myoglobinuria
myopathy
myopathy, centronuclear
myopathy, drug-induced
myopathy, inclusion body
myopathy, inclusion body, hereditary
myopathy, mitochondrial
myopathy, proximal
myopathy, toxic
myopathy, vacuolar
myopia
myotonia
myotonia dystrophica
nausea and vomiting
neck weakness
negative
nemaline rod myopathy
neoplasm, primary of CNS
nephrotic syndrome
neuritis
neuroendocrinology
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
neurons
neuroophthalmology
neuropathology
neuropathy
neuropathy, ataxia, retinitis pigmentosa
neuropathy, hereditary peripheral
neuropathy, peripheral
next-generation sequencing
night blindness
normal
nystagmus
obesity
occipital lobe, infarction
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
optic atrophy, hereditary
optic disc edema
optic nerve
optic nerve, compression of
optic neuropathy
optic neuropathy, bilateral
optic neuropathy, hereditary
orbicularis oculi muscle
orbit, lesions of
pain
pain, abdominal
pancytopenia
paraparesis
paraparesis, spastic
Parkinsonism syndrome
periodic paralysis
peroxisomal disease
personality change
pes cavus
pigmentary retinopathy
PLEDs
PLEDs, bilateral independent
PLEDs, etiology of
POLG1 gene
polydactyly
polymerase chain reaction
polymerase chain reaction, false negative
polymerase chain reaction, false positive
polymyalgia rheumatica
polymyositis
polyneuropathy
prognosis
progressive infantile poliodystrophy
progressive myoclonic epilepsy
progressive neurologic disorder
prostigmine
proteinuria
proximal muscle atrophy
pseudomyasthenia
pseudoretinitis pigmentosa
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychosis
psychosis, acute
ptosis
ptosis, bilateral
ragged-red fibers
rapidly progressing neurologic illness
refractive errors
Refsum's disease
renal failure
research
respiratory tract infection
retina, abnormal
retinal degeneration
retinal lesion
retinitis pigmentosa
retinopathy
review article
Reye's syndrome
Reye's syndrome, adult
RFLPs
rhabdomyolysis
Romberg's sign
schizophrenia
screening
seizure
seizure, focal
seizure, paradoxical
seizure, treatment of
sensorineural hearing loss
sensory loss
seronegative
short stature
single photon emission computed tomography
sore throat
Southern immunoblot test
spasticity
Spielmeyer Vogt syndrome
spinal muscular atrophy
spinocerebellar degeneration
spongy degeneration of brain
standing difficulty
Stephens syndrome
strokelike episodes
succinate dehydrogenase deficiency
symmetric brain lesions
systemic illness
tapetoretinal degeneration
temporal lobe, lesion
thalamus, lesion of-bilateral
transverse smile
treatment of neurologic disorder
trinucleotide repeats
undiagnosed
Unverricht-Lundborg disease
upgaze, paralysis of
Usher's syndrome
viral infection, CNS
visceral neuropathy
vision, failure of in childhood
visual acuity, decreased
visual field defect
visual fields, constricted
visual loss
visual loss, progressive
walking, difficulty with
weakness
weakness, fatiguable
weakness, generalized
weakness, progressive
weakness, proximal
weakness, rapidly progressive
weaning from respirator, failure to
web sites
weight loss
wheelchair
whistle, inability to
white matter disease
white matter disease, pattern
wide based gait
winging of scapula
workup
Showing articles 150 to 200 of 1110 << Previous Next >>

Clinicopathologic Conference, Lebers Hereditary Optic Neuropathy
NEJM 381:164-172, Case 21-2019, 2019

Clinicopathologic Conference, Statin-Associated Autoimmune Myopathy
NEJM 381:275-283, Case 22-2019, 2019

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

Progressive Proximal Weakness in a 56-year-old Man with Bone Pain
Neurol 93:939-944, Torabi,T.,et al, 2019

Subacute Paresis in a 28-year-old man with HIV
Neurol 90:432-435, Harada, Y.,et al, 2018

Dysphagia and a rash
BMJ 361:k1590, McFarlane, M. & Disney, B., 2018

Clinicopathologic Conference, Cushings syndrome due to a well-differentiated, low-grade thymic neuroendocrine tumor with corticotropin
NEJM 378:2322-2332, Case 18-2018, 2018

A Curable Myopathy Manifesting as Exercixe Intolerance and Respirtory Failure
Neurol 91:187-190, Silva,A.M.S.,et al, 2018

A Headache of a Diagnosis
NEJM 379:475-479, Stern,R.M.,et al, 2018

A Child with Arthrogryposis
Neurol 91:e995-e998, Irumudomom, O. & Ghosh, P.S., 2018

Immune Checkpoint Inhibitor-Related Myositis and Myocarditis in Patients with Cancer
Neurol 91:e985-e994, Touat, M.,et al, 2018

Making Sense of the Clinical Spectrum of Limb Girdle Muscular Dystrophies
Pract Neurol 18:201-210, Khadilkar,S.V.,et al, 2018

Pyruvate Dehydrogenase Deficiency (PDCD)
eMedicine.medscape,com, Aug, Frye,R.E.,et al, 2018

A 42-year-old man with unilateral leg weakness
Neurol 90:e1085-e1090, Schneider, R.,et al, 2018

Clinicopathologic Conference, Granulomatosis with Polyangiitis
NEJM 379:2452-2461, Case 39-2018, 2018

FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance
Mol Genet Metab 125:281-291, Almannai, M.,et al, 2018

Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
Front Neurol doi:10.3389/fneur.2017.00472, Velazquez-Perez, L.C.,et al, 2017

A 45-year-old man with Weakness and Myalgia after Orthopedic Surgery
Neurol 88:e185-e189, Vazquez do Campo, R.,et al, 2017

A Case of Statin-Associated Autoimmune Myopathy
Clin Med Insights: Case Reports 10:1-4, Sweidan, A.J.,et al, 2017

Use of MRI in the Diagnosis of Fetal Brain Abnormalities in Utero (MERIDIAN): A Multicentre, Prospective Cohort Study
Lancet: 389:538-546,483, Griffiths, P.D.,et al, 2017

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

A Woman in Her 60s with Chronic Meningitis from Aspergillus
JAMA Neurol 74:348-352, Pichler, M.R.,et al, 2017

A Child with Delayed Motor Milestones and Ptosis
Neurol 88:e158-e163, Ghosh, P.S., 2017

Clinicopathologic Conference, Probable Acute Leptospirosis
NEJM 377:268-278, Case 22-2017, 2017

Dentate Update: Imaging Features of Entities that Affect the Dentate Nucleus
AJNR 38:1467-1474, Bond, K.M.,et al, 2017

A Case of Fulminant Encephalopathy in a 69-year-old Woman
Neurol 89:e109-e114, Lamotte, G. and Williams, C, 2017

Clinicopathologic Conference, Eosinophilic Granulomatosis with Polyangiitis
NEJM 377:1569-1578, Case 32-2017, 2017

Clinical Pathologic Conference, West Nile Virus Encephalitis
NEJM 377:1878-1886, Case 34-2017, 2017

Long-Term Benefit of Enzyme Replacement Therapy in Pompe Disease
Neurol 89:2365-2373, Kuperus, E.,et al, 2017

Neurological Management of Von Hippel-Lindau Disease
Neurologist 21:73-78, Hodgson, T.S.,et al, 2016

A 30-year-old Man with Progressive Weakness and Atrophy
Neurol 87:e227-e230, Quinn, C.,et al, 2016

Mechanisms, Causes, and Effects of Hypercapnia
UptoDate Dec, Feller-Kopman, D.J. & Schwartzstein, R.M., 2016

Hepatitis C Virus Infection in Inclusion Body Myositis
Neurol 86:211-217, Uruha, A.,et al, 2016

A 64-year-old Man with Progressive Paraspinal Muscle Weakness
Neurol 86:e4-e9, Schneider, R.,et al, 2016

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

Zika Virus Associated with Microcephaly
NEJM 374: DOI:10.1056/NEJMoa1600651, Mlakar, J.,et al, 2016

Statin-Associated Autoimmune Myopathy
NEJM 374:664-669, Mammen, A.L., 2016

A Neonate with Micrognathia and Hypotonia
Neurol 86:e80-e84, Vawter-Lee, M.M.,et al, 2016

A 38-Year-Old Man with Respiratory Failure and Progressive Leg Weakness
Neurol 86:e190-e194, McIntosh, P. & Karam, C., 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

Clinical, Genetic, and Radiological Features of Extrapyramidal Movement Disorders in Mitochondrial Disease
JAMA Neurol 73:668-674, Martikainen, M.H.,et al, 2016

Neurological, Respiratory, Musculoskeletal, Cardiac and Ocular Side-Effects of Anti-PD-1 Therapy
Eur J Cancer 60:210-225, Zimmer, L.,et al, 2016

Mouse Infestation Likely Source of Lymphocytic Choriomeningitis in Teen
MMWR 65:248-249, Rostad, C.A. & Pickering, L.K., 2016

Epilepsy in Adults with Mitochondrial Disease: A Cohort Study
Ann Neurol 78:949-957, Whittaker, R.G.,et al, 2015

Differential Diagnosis of Finger Drop
Neurologist 19:128-131, Varatharaj, A.,et al, 2015

Neurological Manifestations of Scrub Typhus
JNNP 86:761-766, Misra, U.K.,et al, 2015

A 51-year-old Woman with Weakness and Stiff Neck
Neurol 85:e32-e36, Kassardjian, C.D. & Milone, M., 2015

Clinical Laboratory and Findings of 21 Patients with Radiation-Induced Myopathy
JNNP 86:152-158, Ghosh, P.S. & Milone M., 2015

Clinicopathologic Conference, Invasive Neisseria Meningitidis Infection and Primary C8 Deficiency
NEJM 372:1454-1462, Case 11-2015, 2015

A 57-Year-Old Woman Who Developed Acute Amnesia Following Fever and Upper Respiratory Symptoms
Neurol 84:e102-e106, McCray, B.A.,et al, 2015



Showing articles 150 to 200 of 1110 << Previous Next >>