Neudle.com: muscle wasting diffuse

Differential
(Click to cross reference)

abdominal distention

acid maltase deficiency

acid maltase deficiency, adult

aciduria

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, heralded by neurologic invol

acrocyanosis

acute disseminated encephalomyelitis

acyclovir

addiction, heroin

addiction, heroin-neurologic complications with

Addison's disease

Adies pupil

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adult polyglucosan body disease

advances in neurology

adverse drug reaction

affect, inappropriate

agenesis of corpus callosum

Aicardi-Goutieres syndrome

akinetic mute

albendazole

Alexanders disease

Alexanders disease, adult onset

algorithm

alpha glucosidase

altered states of consciousness

alveolar hypoventilation

Alzheimer's disease

Alzheimer's disease, treatment of

AMPA receptor antibodies

amyloid angiopathy, cerebral

amyloidoma

amyloid-related imaging abnormalities

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, juvenile

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

amyotrophic lateral sclerosis-like syndrome

ANA

anemia

anesthesia, general

angiitis, granulomatous of CNS

angiitis, isolated of CNS

angiography, cerebral, false negative

angiography, cerebral, negative

animal exposure

ankylosing spondylitis

anorexia

anterior horn cell disease

anterior tibial muscle weakness

antibodies to measles

antiphospholipid antibodies

aspartate aminotransferase

ataxia telangiectasia

ataxia, cerebellar

ataxia, sensory

ataxic gait

attention deficit disorder with hyperactivity

atypical

audiogram

auditory evoked brainstem potentials

autoantibodies

autoimmune basal ganglia encephalitis

autoimmune disease

autonomic dysfunction

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basement membrane

basement membrane thickening

baylisascariasis

behavioral disorder

behavioral disorder, acute

bone marrow infarction

bone marrow necrosis

bone marrow transplantation

brain biopsy, false negative

brucellosis, nervous system involvement with

bulbar palsy

bulbar palsy, progressive

burning skin

cachexia

CAG repeats

calcification, intracranial

Canavan's disease

carbon monoxide poisoning

carbon monoxide poisoning, chronic

carboxyhemoglobin

carcinoma

cardiac arrest

cardiac arrest and resuscitation

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, spine

cataracts

cataracts, congenital

catatonia

cauda equina, enhancement

CD4 counts

central nervous system, infection of

central pontine myelinolysis

cerebellar ataxia, autosomal recessive

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellar vermis

cerebellum

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral embolism

cerebral vasculature

cerebral venous thrombosis

cerebrospinal fluid, abnormal

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, proteincytologic dissociation

cerebrovascular accident

cerebrovascular accident, infancy and childhood

cerebrovascular accident, mimics

cerebrovascular accident, recurrent

cerebrovascular accident, women

cervical spine

Charcot-Marie-Tooth

chasing the dragon

chemotherapy, CNS treatment and complications with

chilbran skin lesions

Clinical Pathologic Conference(C.P.C.)

cocaine

cognition

cognitive delay

collapsin response mediator protein 5 IgG

coma

complications

confusion

congestive heart failure

corpus callosum, infarction of

corpus callosum, lesion of

cortical blindness

cortical blindness, transient

cortical infarction

cortical ribbon sign

cranial nerve enhancement

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

critical care unit

cry, abnormal

crying, pathologic

cultured skin fibroblasts

degenerative diseases of CNS

Dejerine-Sottas syndrome

delayed dentition

dementia

dementia, childhood

dementia, frontal lobe type

dementia, frontotemporal

dementia, rapidly progressive

demyelinating disease

denervation of muscle

denervation potentials

dentate nuclei

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

depression

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diagnostic criteria

diarrhea

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

diffuse idiopathic skeletal hyperostosis

diplopia

diplopia, transient

disability, neurological

distal muscle weakness

disulfiram

DPPX, antibodies, encephalitis

drooling

dropped head syndrome

drug abuse

drug abuse, inhalation

drug abuse, neurologic complications of

drug abuse, toxic screen In

dural sinus thrombosis

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, diffuse slowing

electroencephalogram, periodic complexes

encephalitis, autoimmune

encephalitis, etiology

encephalitis, focal

encephalitis, human immunodeficiency virus type 1

encephalitis, viral

encephalopathy

encephalopathy, acute

encephalopathy, anoxic

encephalopathy, delayed

encephalopathy, metabolic

encephalopathy, post anoxic

encephalopathy, progressive

enzyme treatment

enzyme, defect

enzyme, muscle disease

eosinophilia

epidemiology of neurology

episodic neurologic deficits

extraocular muscle lesion

eye movement, disorders of

facial appearance, abnormal

facial expression abnormality

facial nerve palsy

facial weakness

facial weakness, bilateral

faciobrachial dystonic seizure

fluorescein angiography

foot deformity

foot drop

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

Friedreich's ataxia

frontal lobe, atrophy

frontal lobe, behavior with disease of

frontal lobe, lesion of

frontal lobe, pathologic signs of

fundus, abnormality of

funduscopic exam

gait disorder

gait, spastic

gamma amino butyric acid receptor antibody

gangliosidosis GM2

gastric partitioning

gastrointestinal disease, neurologic complications

gastrointestinal motility

genetic diagnosis, prenatal

genetic neurologic disorders

genetic testing

genu of corpus callosum

globus pallidus, hemorrhage

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glycogen storage disease

GM1 ganglioside antibodies

Guillain Barre syndrome, differential diagnosis of

hair analysis

hallucination

hallucination, olfactory

hallucination, visual

hearing loss, bilateral

hearing loss, sudden, bilateral

heart block

helminthic infection of CNS

hemiparesis

hemiparesis, transient

hemiplegia

hemiplegia, progressive

hemoglobin abnormality, neurologic complications of

hepatomegaly

hepatosplenomegaly

heralding manifestation

herpes simplex encephalitis

herpes simplex virus

herpes virus

herpes virus infection

hexosaminidase-A

high arched feet

high arched palate

highly active antiretroviral therapy

hoarseness

hospice

human immunodeficiency virus type 1

Huntington's chorea

hydrocephalus

hydroxyglutaric aciduria

hyperpigmentation of skin

hyperpyrexia, CNS disorder causing

hyperreflexia

hypertension

hypertensive encephalopathy

hypotension, systemic

hypothermia

hypotonia

hypotonia, infants

hypoxic encephalopathy

iatrogenic neurologic disorders

imbalance

immunosuppressive agents

immunotherapy

inborn errors of metabolism

incidence

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

incontinence, fecal

incoordination

infection

infectious mononucleosis

infectious mononucleosis, neurologic findings with

insomnia

insular cortex

intellectual deficit

intellectual deterioration

interferon alpha

internal capsule

intestinal pseudoobstruction

intracerebral hemorrhage

intrauterine

intrinsic hand muscles, wasting of

irritability

Jakob-Creutzfeldt disease

lactic dehydrogenase(LDH)

laminar necrosis, cortical

laughing

laughing, pathologic

leg weakness, bilateral

leg weakness, unilateral

lenticular nucleus, lesion of, bilateral

lethargy

leucine rich glioma inactivated 1 antibodies

leukocyte enzyme abnormality

leukocytosis

leukodystrophy

leukoencephalopathy

leukoencephalopathy with calcification and cysts

leukoencephalopathy, differential diagnosis

leukoencephalopathy, hereditary diffuse

leukoencephalopathy, toxic

levamisole

level of consciousness, decreased

Lewy body

Lewy body disease, diffuse

life expectancy

life support, withdrawal of

limbic encephalitis

lipid storage disorder of CNS

lobar atrophy

lymphohistiocytosis

lymphoma

lymphoma involving CNS

lymphoma, primary of CNS

lysosomal storage disease

lysosomes, abnoral

macrocephaly

malabsorption

Marinesco-Sjogren syndrome

masked facies

masseter muscle wasting

meconium staining

medulla oblongata, lesion of

megalencephaly

MELAS syndrome

memory, defect of recent

memory, impairment of

meningeal biopsy

meningeal enhancement

meningeal gliomatosis

meningismus

meningitis

meningitis, aseptic

meningitis, eosinophilic

meningitis, melanomatous

meningitis, Mollaret's

meningitis, recurrent

meningitis, treatment of

meningoencephalitis

mental retardation

mental status, abnormal

merosin

mesial temporal lobe

metabolic acidosis

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, juvenile

methylene tetrahydrofolate reductase

methylenetetrahydrofolate reductase deficiency

methylglutaconic aciduria

microaneurysm, retinal

microangiopathy, brain

microangiopathy, retina

microcephaly

microhemorrhage, intracerebral

microinfarcts

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

mitochondrial disease

mitochondrial encephalomyopathy

MNGIE syndrome

molecular genetics

monoclonal antibodies

monoclonal gammopathy

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, contrast enhanced

MRI, cortical enhancement

MRI, diffusion tensor

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, gray matter enhancement

MRI, high signal foci on

MRI, hypointense signal foci on

MRI, spinal cord, increased intramedullary cord signal

MRI, spine

MRI, susceptibility weighted

MRS

multiple organ failure

multiple sclerosis

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle atrophy, progressive

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscle weakness, sudden onset of

muscular dystrophy

muscular dystrophy, cardiovascular changes with

muscular dystrophy, central nervous system abnormality

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, congenital, Fukuyama type

muscular dystrophy, congenital, Ullrich

muscular dystrophy, LAMA2

muscular dystrophy, limb-girdle

mutism

myelination of nervous system

myelitis, transverse, recurrent

myelomalacia

myeloneuropathy

myelopathy

myelopathy, chronic progressive

myopathy, critically ill

myopathy, drug-induced

myopathy, steroid induced

neoplasm, primary of CNS

neoplastic angioendotheliosis

nerve biopsy

nerve conduction studies

nerve root enhancement

neurexin-3 alpha antibodies

neuroaxonal leukodystrophy

neurogenic bladder

neurologic complications of, surgery

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic disease, tempo

neurologic evaluation

neurologic examination

neurologic examination, focal

neurologic signs

neurologic symptoms

neuromuscular disease, electrodiagnosis of

neuronal cell surface antigen

neuronal degeneration

neuronopathy

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, peripheral

neuropathy, sensory

neuroprotective agents

neurotoxic

neurotoxicity, acute

neurotoxin

next-generation sequencing

NMDA antagonists

nutritional deficiency

nystagmus

obesity

occipital lobe, lesion of

old age, neurology of

optic chiasm, enlarged

optic nerve, enlarged

optic nerve, hypoplasia of

optic neuropathy

optic neuropathy, nutritional

orthostatic hypotension

paraparesis, familial spastic

paraparesis, spastic

paresthesias

Parkinson disease

Parkinson disease, differential diagnosis of

Parkinson disease, L-dopa nonresponsive

Parkinson disease, misdiagnosis

Parkinson disease, tremor, absence of

Parkinsonism syndrome

PAS positive material in the brain

pathology

patient information and support

pediatric neurology

percussion induced muscle contraction

peroxisomal disease

persistent vegetative state

personality change

pes cavus

phenylketonuria

pleocytosis of cerebrospinal fluid

POLR3B

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polymyositis

polyneuropathy

polyneuropathy, critically ill

polyneuropathy, critically ill, children

polyradiculoneuropathy

Pompe's disease of glycogen storage

pons, atrophy

pons, lesion of

posterior column disease

posterior leukoencephalopathy syndrome

posterior longitudinal ligament, ossification of

precipitating factors

pregnancy, neurologic complications in

prenatal

prenatal diagnosis by amniocentesis

primary lateral sclerosis

prognosis

progressive multifocal leucoencephalopathy

progressive myoclonic epilepsy

progressive neurologic disorder

proximal muscle atrophy

proximal myotonic myopathy

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

psychosis

psychotic behavior

ptosis

pupil, abnormality in neurologic disorders

pupil, dilated, bilateral

pupil, dilated, episodic

pupil, tonic

pyramidal

pyramidal tract

pyramidal tract dysfunction

quadriparesis

quadriplegia

quadriplegia, transient

raccoon

radiation therapy, CNS treatment and complications with

radiculopathy

ragged-red fibers

rapidly progressing neurologic illness

rash

reading disorder, acquired

respiratory tract infection

retina, abnormal

retinal artery occlusion

retinal branch artery occlusion

retinal infarction

retinal lesion

retinal microvascular disease

retinopathy

retrovirus

reversible neurologic disorder

saccadic eye movements, abnormal

sarcoidosis

sarcoidosis, CNS

Schilder's disease

sedimentation rate, elevated

seizure

seizure, children

seizure, drug resistance

sensorineural hearing loss

sensory loss

septicemia

serologic testing

serologic testing, false negative

sicca syndrome

sickle cell disease

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skew deviation

skin, lesions in neurologic disorders

sleep

sleep pathology and physiology

slit lamp examination

slow virus infection of CNS

small vessel disease

small-bowel resection

SMN1 gene

somatosensory evoked potentials

somnolence

spasticity

speech disorder, childhood

spinal cord

spinal cord degeneration

spinal cord, cervical

spinal cord, compression of

spinal cord, lesion of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

spinal stenosis

spinal stenosis, cervical canal

splenium of corpus callosum

spondylosis

spongy degeneration of brain

spontaneous remission

steroid therapy, CNS treatment and complications with

stimulant drugs

striatal encephalitis

striatum, lesion of

striatum, lesion of, bilateral

strokelike episodes

subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease

subarachnoid hemorrhage

subdural hematoma

suicide

superior sagittal sinus thrombosis

sural nerve

survival motor neuron gene

Susac's syndrome

sweating

symmetric brain lesions

teeth, number of in infants

temporal lobe, atrophy

temporal lobe, lesion

temporal lobe, lesion, bilateral

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

teratoma

teratoma, ovarian

thalamus, lesion of

thalamus, lesion of-bilateral

tone, muscle, increased

tongue, atrophy

tongue, biting

tongue, enlarged

tongue, fasciculations of

tongue, weakness

tonic cerebellar fits

toxic encephalopathy

transient neurologic deficit

trauma

treatment of neurologic disorder

trinucleotide repeats

tripping

unconsciousness

unconsciousness, transient

urinary incontinence

urine test for metabolic disorders

urine test in toxic screen

very long chain fatty acids

vibratory sensation, abnormal

visual acuity, decreased

visual loss

visual tracking

visuospatial disturbance

vitamin D

vitamin deficiency

vitamin E deficiency

Waldenstrom's macroglobulinemia

Walker-Warburg syndrome

walking, delayed

walking, difficulty with

weakness

weakness, acute

weakness, generalized

weakness, progressive

weakness, proximal

weaning from respirator, failure to

white matter disease, periventricular

white matter disease, subcortical

wide based gait

winging of scapula

word-finding difficulty

Showing articles 350 to 400 of 3492 << Previous Next >>

Treatment Approaches for MOG-Ab-Associated Demyelination in Children
Curr Treat Options Neurol 21:2, Hacohen, Y. & Banweil, B., 2019

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

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

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

Clinicopathologic Conference, Creutzfeldt-Jakob Disease
NEJM 381:1569-1578, Case 32-2019, 2019

A 26-Year Old Man with Right Hand and Arm Weakness
Neurol 93:e927-e933, Elliott,E.J.&Smith,J.D., 2019

Muscular Dystrophies
Lancet 394:2025-2038, Mercuri, E.,et al, 2019

A Rare Case of Metachromatic Leukodystrophy with Multiple Bilateral Cranial Nerve Enhancement
Neurol 93:e1742-e1743, Sonowal, P.,et al, 2019

A 65-year-old man with Asymmetric Weakness and Parethesias
Neurol 93:856-861, Harada, Y.,et al, 2019

Sydenham Chorea
www.UptoDate.com, Oct, Gilbert, D.L., 2019

Amphiphysin-IgG Autoimmune Neuropathy
Neurol 93:e1873-e1880, Dubey, D.,et al, 2019

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

When MRI is a Clue in Episodic Ataxia
Neurol 93:e2074-e2075, Dhawan, S.R.,et al, 2019

Acute Convexity Subarachnoid Hemorrhage
Neurol 93:e524-e525, Theodorou, A.,et al, 2019

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

A 17-year-old Baseball Player with Right Hand Weakness
Neurol 92:e76-e80, Vachon, C. & Libdeh, A.A., 2019

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

A Pain in the Neck: Calcific Tendinitis of the Longus Colli Muscle
Lancet doi:10:1016/50140-6736(10), Bannai, T.,et al, 2019

Leptomeningeal Metastases in Glioma
Neurol 92:e2483-e2491, Andersen, B.M.,et al, 2019

Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement
AJNR 40:903-907, Hartin, I.,et al, 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

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

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

Clinicopathologic Conference, Powassan Virus Encephalitis
NEJM 380:380-387, Case 3-2019, 2019

A 40-Year-Old Woman Presenting with Distal Leg Weakness
Neurol 92:242-247, Fam, D.,et al, 2019

Leg Weakness and Stiffness at the Emergency Room
Neurol 92:e622-e625, af Edholm, K.,et al, 2019

A 54-year-old man with Dyspnea and Muscle Weakness
Neurol 92:e1136-e1140, Chertcoff, A.,et al, 2019

Acute Toxic Leukoencephalopathy: Etiologies, Imaging Findings, and Outcomes in 101 Patients
AJNR 40:267-275, Ozutemiz, C.,et al, 2019

Bismuth Neurotoxicity from Use of Topical Bismuth Dressing for Burns
Neurol 92:680-681, Saini, V.,et al, 2019

Neuromuscular Adverse Events Associated with Anti-PD-1 Monoclonal Antibodies
Neurol 92:663-674, Johansen, A.,et al, 2019

Clinicopathologic Conference, Amyotrophic Lateral Sclerosis
NEJM 380:1566-1574, Case 12-2019, 2019

Human Parechovirus Meningoencephalitis: Neuroimaging in the Era of Polymerase Chain Reaction-Based Testing
AJNR 40:1418-1421, Sarma, A.,et al, 2019

Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019

GGC Repeat Expansion of NOTCH2NLC in Adult Patients with Leukoencephalopathy
Ann Neurol 86:962-968,809, Okubo, M.,et al, 2019

Lyme Disease: What the Neuroradiologist Needs to Know
AJNR 40:1998-2000, Valand, H.A.,et al, 2019

Orofacial Dyskinesia in a Young Man
JAMA Neurol 76:1517-1518, Tian, X.,et al, 2019

Metabolic Lipid Muscle Disorders: Biomarkers and Treatment
Ther Adv Neurol Disord 12:1-15, Angelini, C.,et al, 2019

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

Wilson Disease
NIDDK Oct2018, , 2018

Neuromyelitis Optica Spectrum Disorder (NMOSD) in a Male with Hiccups and Quadriparesis
IJCMR 5:K28-K30, Tuteja,H.S.,et al, 2018

Human Parechovirus: An Increasingly Recognized Cause of Sepsis-Like Illness in Young Infants
Clin Microbiol Reviews 31:1-17, Olijve, L.,et al, 2018

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

Misdiagnosis of Multiple Sclerosis
Neurol 92:15-16, Brownlee, W.J., 2018

A 58-year-old Woman with Systemic Scleroderma and Progressive Cervical Cord Compression
Neurol 91:e1262-e1264, Karschnia, P.,et al, 2018

Distinctive Imaging in a Paucisymptomatic Child with Leukodystrophy
Neruol 91:e1368-e1369, Sharawat, I.K.,et al, 2018

Selenium Toxicity Associated with Reversible Leukoencephalopathy and Cortical Blindness
JAMA Neurol 75:1282-1283, Rae, W.,et al, 2018

Facial Myokymia and Myorhythmia in Anti-IgLON5 Disease
Neurol 91:e1659, Vetter, E.,et al, 2018

Spinal Brucellosis
NEJM 379:e28, Sacks, C.A., 2018

White Matter Lesion Related to Decompression Sickness Following Extreme Breath-Hold Diving
Neurol 91:847-848, Guerreiro, C.,et al, 2018

Showing articles 350 to 400 of 3492 << Previous Next >>