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Differential
(Click to cross reference)
abdominal distention
abdominal muscle paralysis
abducens nerve paralysis, bilateral
abiotrophy
acanthocytosis
acid maltase deficiency
adrenoleukodystrophy
adult polyglucosan body disease
advances in neurology
adverse drug reaction
agammaglobulinemia
akinesia of eyelid function
algorithm
alopecia
alveolar hypoventilation
Alzheimer's disease
amniocentesis
amyloidosis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
ANA
analgesic
anesthesia, general
anterior interosseous neuropathy
anterior tibial muscle weakness
anxiety
apnea
apraxia of eyelid opening
areflexia
arrhythmia, cardiac
arthrogryposis multiplex
aspiration
asymptomatic
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
atrial fibrillation
atrial flutter
atrial paralysis
atrioventricular block
attention deficit disorder with hyperactivity
autoimmune disease
automatic implantable cardioverter-defibrillator
axonopathy, distal
azathioprine
Babinski sign
baldness
basal ganglia, calcification of
basal ganglia, lesion, bilateral
Bassen-Kornzweig syndrome
benign congenital hypotonia
bent spine syndrome
benzodiazepine
bladder dysfunction
blepharospasm
blindness
blood dyscrasias, neurologic findings with
botulism
brachial neuritis
bradycardia
brainstem, lesion of
brainstem, tuberculoma of
bulging of biceps
bulimia
bulimia nervosa
cachexia
CAG repeats
calcification, intracranial
calcium antagonist
calf atrophy
calf hypertrophy
calpain III deficiency
camptocormia
cancer of colon
carcinoma
carcinoma of ovary
carcinoma of pancreas
carcinoma of uterus
cardiac arrest
cardiac arrest and resuscitation
cardiac surgery, neurologic complications with
cardiac transplantation
cardiomegaly
cardiomyopathy
cardiovascular disease
carnitine deficiency myopathy
case studies
CAT scan
CAT scan, abnormal
CAT scan, false negative
CAT scan, muscle
cataracts
cathartic
cause of death
celiac disease, childhood
central core disease
central nervous system, infection of
cerebellar ataxia, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebral cortical atrophy
cerebral embolism
cerebral embolism, cardiac origin
cerebral embolism, carotid origin
cerebral palsy
cerebrospinal fluid, lactic acid concentration
cerebrovascular accident
cerebrovascular accident, cardiac disease causing
cerebrovascular accident, multiple
cerebrovascular accident, young adult
cervical spine injury
Charcot-Marie-Tooth
Charcot's sign
chemosis
children
chromosomal abnormality
chromosome 1
chromosome 14
chromosome 17
chromosome 19
chromosome 3
chronic polyneuritis, children
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
Coats syndrome
Cockayne's syndrome
coenzyme Q10 deficiency
cogwheel rigidty
collagen vascular disease
coma
complications
compression fracture
compression neuropathy
concussion
conduction block
confidentiality
congenital birth defects
congenital heart disease
congenital myopathy
congestive heart failure
conjunctival injection
consanguinity
contractures, joint
controversies in neurology
conversion reaction
cornea, abnormal
corpus callosum, lesion of
cost
cost effectiveness
CPAP
creatine phosphokinase isoenzyme elevation
creatine phosphokinase MB isoenzyme elevation
creatine phosphokinase(CPK)elevated
cricopharyngeal bar
cry, weak
cyclosporine
cyst, parenchymal
cytochrome c oxidase
cytochrome c oxidase, deficiency
deafmute
deafness
deep gray nuclei
defibrillator, implanted
degenerative diseases of CNS
delay in diagnosis
dementia
dentatorubral-pallidoluysian atrophy
dermatomyositis
descending paralysis
developmental disability
developmental milestones
developmental retardation
diabetes mellitus
diagnostic criteria
diamond on quadriceps
diaphragmatic paralysis
diarrhea
dieting
differential diagnosis
difficulty climbing stairs
digitalis intoxication
diltiazem
diplopia
disability, neurological
distal muscle atrophy
distal muscle weakness
DNA probes
dropped head syndrome
drug induced neurologic disorders
dwarfism
dying
dysarthria
DYSF gene
dysferlin
dysferlinopathy
dysphagia
dyspnea
dyspraxia
dysthyroid ocularmyopathy
dystonia
dystroglycanopathies
dystrophin
dystrophin associated proteins
eating disorder
echinocyte
echocardiogram
edema, periorbital
efficacy
ejection fraction
ejection fraction, abnormal
electrocardiogram, abnormal
electrocardiogram, LVH
electroencephalogram, abnormalities of
electromyogram
electron microscopy
ELISA
embolism
emerin
Emery-Dreifuss muscular dystrophy
Emery-Dreifuss muscular dystrophy, carrier
encephalopathy
encephalopathy, anoxic
encephalopathy, neonatal
encephalopathy, progressive
entrapment neuropathy
enzyme, defect
enzyme, muscle disease
enzyme, serum
epidemiology of neurology
erythrocyte
ethics in neurology
euthanasia
evidence-based research
exercise
exercise intolerance
extraocular muscle atrophy
extraocular muscle enlargement
extraocular muscle lesion
extrapyramidal movement disorder, progressive
eye closure
eye movement, disorders of
eye, pain in
face, numbness of
facial appearance, abnormal
facial expression abnormality
facial nerve palsy
facial nerve palsy, bilateral
facial nerve, lesion of
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
falling
false negative
familial
family planning
fasciculation
fatigue
Fazio-Londe's disease
feeding disorder
femoral neuropathy
fetal movements, reduced
fetus
fever
fibrillations
fine motor function, impaired
Fisher C.M.
fistula, arterio-venous, carotid-cavernous
floppy infant
fluorescein angiography
foot drop
fracture, long bone
fragile-X syndrome
Friedreich's ataxia
frontal balding
gait disorder
gait, waddling
gargoylism
gastric dilatation, acute
gastrocnemius muscle weakness
gastrointestinal disease, neurologic complications
gastrointestinal motility
gastroparesis
gaze palsy
gaze palsy, horizontal
gaze palsy, vertical
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
glabellar sign
glaucoma
glioma
glycogen storage disease
glycosyltransferase
Gowers maneuver
Graves ophthalmopathy
Guillain Barre syndrome
Guyon's canal
Hallgren's syndrome
hammertoes
hand weakness
head injury
headache
hearing loss
hearing problems in children
heart block
heart block, complete
heart murmur
heavy metal intoxication
hemianopia, homonymous
hemophilia
hepatic failure
hepatomegaly
heralding manifestation
high arched feet
high arched palate
hip pain
hippus
Hispanics
histochemistry
histochemistry of muscle
Holter monitoring
hospice
hunger
huntingtin
Huntington's chorea
Hurler's syndrome
hydrocephalus
hypercapnia
hypersomnia
hyperthyroidism
hypoglycemia
hypoglycemic coma
hypoglycorrhachia
hypogonadism
hypokalemia
hyporeflexia
hypotonia
hypotonia, infants
hypoxic encephalopathy
idebenone
imbalance
immunohistochemistry
immunosuppressive agents
implantable cardioverter defibrillator
inability to stand on tiptoes
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion body myositis
influenza
influenza immunization
intellectual deficit
intelligence quotient
intermittent positive pressure breathing
intestinal pseudoobstruction
iris, abnormal
jaw jerk, abnormal
Jewish
joint hypermobility
Kearns-Sayre syndrome
keratoconus
klippel feil syndrome
Kugelberg-Welander syndrome
kyphosis
lactic acidemia
lactic dehydrogenase(LDH)
laminopathies
Laurence-Moon-Bardet-Biedl syndrome
L-dopa
learning disability
learning disability, in children
Leber's hereditary optic neuropathy
left ventricular dilatation
leg weakness, bilateral
Leigh's disease
leukocyte enzyme abnormality
leukodystrophy
leukoencephalopathy
leukoencephalopathy, differential diagnosis
level of consciousness, decreased
lid closure, weakness of
life expectancy
life sustaining treatment
limb-girdle weakness
liver function enzymes
LMNA gene
locked-in syndrome
lordosis
low back pain
lymphocyte capping, diminished
machine learning
macrocephaly
malformation, CNS, congenital
malignancy screen
malignant hyperpyrexia
masked facies
medial rectus palsy
median neuropathy
medical-legal aspects of neurology
medulla oblongata, lesion of
MELAS syndrome
Melkersson's syndrome
meningitis
meningitis, TB
mental retardation
merosin
MERRF syndrome
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
migraine
misdiagnosis
mitochondrial disease
mitochondrial disease, pathogenesis
mitochondrial encephalomyopathy
mitral valve prolapse
MNGIE syndrome
molecular genetics
mononeuropathy
morphine
mortality
motor neuron disease
movement disorder
MRI
MRI pattern
MRI, abnormal
MRI, contrast enhanced
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, muscle
MRI, serial
MRS
mucopolysaccharidoses
multiple sclerosis
muscle atrophy, focal
muscle atrophy, progressive
muscle biopsy
muscle biopsy, extraocular
muscle cramp
muscle diseases, characteristics of
muscle hypertrophy
muscle pain
muscle relaxant
muscle stiffness
muscle swelling
muscle wasting, diffuse
muscle weakness
muscle weakness, causes of
muscle weakness, insidious onset of
muscle weakness, intermediate onset of
muscle weakness, proximal
muscle weakness, sudden onset of
muscle, metabolic disorders of
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, Becker, carrier
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, differential diagnosis of
muscular dystrophy, distal, Miyoshi
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, Duchenne, neonatal screening
muscular dystrophy, Duchenne, presymptomatic detection
muscular dystrophy, dystrophin normal
muscular dystrophy, facioscapulohumeral
muscular dystrophy, female occurrence of
muscular dystrophy, LAMA2
muscular dystrophy, limb-girdle
muscular dystrophy, lymphocyte capping, diminished
muscular dystrophy, neurogenic hypothesis of
muscular dystrophy, pattern of muscle involvement
muscular dystrophy, systemic membrane defect
myasthenia gravis
myasthenia gravis, differential diagnosis
myasthenia gravis, distal weakness
myasthenia gravis, drug induced
myasthenia gravis, limb-girdle
myasthenia gravis, misdiagnosis of
myasthenia gravis, ocular
myasthenia gravis, seronegative
myasthenic crisis
myasthenic syndrome
myelomalacia
myeloneuropathy
myelopathy
myoblast transfer
myocardial biopsy
myocarditis
myoclonus
myoglobinuria
myopathy
myopathy, carcinomatous
myopathy, centronuclear
myopathy, distal
myopathy, distal, vacuolar
myopathy, drug-induced
myopathy, metabolic
myopathy, mitochondrial
myopathy, myofibrillar
myopathy, necrotizing
myopathy, neurogenic hypothesis of
myopathy, quadriceps
myopathy, steroid induced
myopathy, thyroid disease causing
myopathy, vacuolar
myopia
myositis
myositis, ocular
myotonia
myotonia congenita
myotonia dystrophica
myotonia dystrophica, classification
myotonia dystrophica, type 2
myotonic discharges
nausea and vomiting
neck weakness
negative
nemaline rod myopathy
neonatal screening, genetic neurologic disorders
neoplasm, metastatic to CNS
neoplasm, primary intracerebral
neoplasm, primary intracranial
neoplasm, primary of CNS
nerve biopsy
nerve conduction studies
neuritis
neuritis, causes of
neurocardiology
neuroendocrinology
neurofibrillary degeneration
neurofibromatosis 1
neurofibromatosis 2
neurogenic bladder
neurogenic vs.myopathic atrophy
neurologic complications of, surgery
neurologic complications of, systemic cancer
neurologic complications of, systemic disease
neurologic consultation
neurologic disease
neurologic disease, diagnoses of
neurologic evaluation
neurologic examination
neurologic signs
neurologic symptoms
neuromuscular blockade
neuromuscular disease, electrodiagnosis of
neuromuscular junction, abnormality of
neuronal migration disorder
neuroophthalmology
neuropathy
neuropathy, amyloid
neuropathy, ataxia, retinitis pigmentosa
neuropathy, diabetic
neuropathy, hereditary peripheral
neuropathy, motor, multifocal
neuropathy, peripheral
neuropathy, sensory
newborn, evaluation of
next-generation sequencing
normal
nystagmus
nystagmus, vertical
obesity
obicularis oculi, weakness of
occipital lobe, lesion of
ocular motility, disorders of
ocular myopathy
ocular myopathy, differential diagnosis
oculopharyngeal muscular dystrophy
old age, neurology of
one and a half syndrome
opened mouth
ophthalmoplegia
ophthalmoplegia, painful
ophthalmoplegia, plus syndrome
ophthalmoplegia, progressive external
Oppenheim muscular dystrophy
optic atrophy
optic disc edema
optic neuritis
optic neuropathy
orbicularis oculi muscle
orbit
orbit, lesions of
ovarian tumor
oxygen therapy
pacemaker, cardiac-transvenous
pain
pain, abdominal
pain, foot
pain, leg
palliative care
pancytopenia
paraparesis
paraparesis, spastic
paraspinal muscle
paraspinal muscle weakness
Parkinson disease
Parkinsonism syndrome
pathology
pediatric neurology
pediatric neurology, transition to adult care
percussion induced muscle contraction
periodic paralysis
phosphorylase b kinase deficiency
photophobia
photophobia, central
phrenic nerve pacemaker
physical therapy
physician assisted suicide
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
poison, mercury
poison, neurologic problems with
POLG1 gene
poliomyelitis
polydactyly
polyglucosan body
polyglucosan body disease
polymerase chain reaction
polymerase chain reaction, false negative
polymerase chain reaction, false positive
polymicrogyria
polymyositis
polymyositis, infantile
polyneuropathy
pons, lesion of
porphyria
positive sharp waves
posterior interosseous neuropathy
postoperative neurologic complications
postural abnormality
practice guidelines
pregnancy, neurologic complications in
prenatal diagnosis by amniocentesis
prevention of neurologic disorders
progeria
prognosis
progressive infantile poliodystrophy
progressive muscular dystrophy
progressive neurologic disorder
progressive spinal muscular atrophy
progressive supranuclear palsy
proptosis
proptosis, bilateral
proptosis, unilateral
prostigmine
proteinuria
proximal muscle atrophy
proximal myotonic myopathy
pseudobulbar palsy
pseudohypertrophy
pseudomyasthenia
pseudoretinitis pigmentosa
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychological testing, children
psychosis
ptosis
ptosis, bilateral
ptosis, familial
pulmonary embolism
pulmonary function tests
pulmonary infiltrates
pupil, abnormality in neurologic disorders
pupil, dilated and fixed, bilateral
pupil, dilated and fixed, unilateral
quadriceps atrophy
quadriceps weakness
quality of life
ragged-red fibers
Raynaud's phenomenon
recombinant DNA
recurrent
respirator
respiratory depression
respiratory failure
respiratory tract infection
retina, abnormal
retinal degeneration
retinal detachment
retinal lesion
retinitis pigmentosa
retinopathy
retropulsion
review article
RFLPs
rhabdomyolysis
right to die
rigid spine syndrome
rigidity
rippling muscle disease
risk factors
safety
sarcoglycan
sarcoglycanopathy
sarcoidosis
schizophrenia
scintillations
scleroderma
scleroderma, neurologic involvement with
scoliosis
scoliosis, neurologic association with
screening
sedation
sedimentation rate
seizure
sensorineural hearing loss
sensory loss
seronegative
serum glutamic oxaloacetic transaminase
serum glutamic pyruvic transaminase
short stature
shoulder, pain in
shoulder-girdle wasting
skin, biopsy
skin, tight
sleep apnea
slit lamp examination
sloped shoulders
somnolence
Southern immunoblot test
spasticity
speech disorder, childhood
speech, delayed development of
Spielmeyer Vogt syndrome
spinal cord, injury of
spinal cord, neoplasm
spinal fusion
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar degeneration
standing difficulty
Stephens syndrome
steroid
steroid therapy, CNS treatment and complications with
stiff man syndrome
stooped posture
strokelike episodes
succinate dehydrogenase deficiency
suck, poor
sudden death
symmetric brain lesions
symptomatic
syncope
syringomyelia
systemic illness
Tay-Sachs disease
telangiectases
telangiectases, retinal
teleconsulting
telemedicine
teleneurology
telestroke
temporalis muscle wasting
temporalis muscle weakness
temporomandibular joint, dislocation
term infant
testicular atrophy
thalamus, lesion of-bilateral
thoracic outlet syndromes
thrombus, mural
toe walking
tongue, fasciculations of
torticollis
tracheostomy
transient ischemic attack
transverse smile
treatment of neurologic disorder
tricresylphosphate
trinucleotide repeats
tripping
tuberculoma of CNS
tuberculosis
tuberculosis, miliary
type 2 muscle fiber
ulnar neuropathy
ultrasonography
upgaze, paralysis of
urinary incontinence
urine, dark
Usher's syndrome
vaccine
valium
ventricular tachycardia
vertebral fracture
viral infection, CNS
vision, failure of in childhood
visual field defect
visual fields, constricted
visual loss
vital capacity
Walker-Warburg syndrome
walking frame
walking, difficulty with
weakness
weakness, congenital
weakness, fatiguable
weakness, generalized
weakness, progressive
weakness, proximal
weaning from respirator, failure to
web sites
weight loss
Werdnig-Hoffman disease
Western immunoblot test
wheelchair
whistle, inability to
white matter disease
white matter disease, pattern
wide based gait
winging of scapula
workup
xanthopsia
X-linked bulbospinal neuronopathy
x-linked hydrocephalus
x-linked mental retardation
Showing articles 750 to 800 of 2310 << Previous Next >>

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

A 47-Year-Old Man With an Upper Respiratory Infection, Acute Confusion, Dysarthria, and Ataxia
Neurol 100:978-983, Kubicki,K.,et al, 2023

Focusing on the Eye Signs of Alport Syndrome in a 40-Year-Old Man Who Previously Had a Kidney Transplant and Hearing Loss
Lancet 401:e2, Kovalchuk,B. & Khoramnia,R., 2023

Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
JAMA Neurol 80:107-108, Bernaola,M.T.,et al, 2023

A 67-Year-Old Woman with Progressive Tingling Sensations and Imlalance
Neurol 100:151-157, Horta,L.F.B.,et al, 2023

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

A Young Man With Subacute Onset of Spastic Paraparesis
Neurol 100:199-205, Rossi,S.,et al, 2023

New Onset Focal Tremor in Patient with Human Immunodeficienccy Virus
Clin Infect Dis 75:1861-1863, Finelli,P.F., 2022

Re-Emergency of Poliovirus in the United States:Considerations and Implications
Ann Neurol 92:725-728, Russo,G.B.,et al, 2022

A 23-Year-Old Woman Presenting with Cognitive Impairment and Gait Disturbance
Neurol 99:997-1003, Chaity,D.K.,et al, 2022

A 36-Year-Old Man With Asymmetric Muscle Weakness
Neurol 99"1057-1061, Harada,Y.,et al, 2022

An 80-Year-Old Woman with a Homonymous Hemianopsia
Neurol 99:713-717, Tajfirouz, D.,et al, 2022

Miller Fisher Syndrome and Acute Motor and Sensory Axonal Neuropathy (AMSAN) Variant Guillain-Barre Overlap Syndrome (MFS/AMSAN-GBS) After Upper Respiratory Tract Infection (URTI)
Acta Sci Clin Case Reports 3:19-24, Chau,T.C. & Muhamad,N.A.N., 2022

A 56-Year-Old Man with Unusual Presentation of Subacute Encephalopathy and Seizure
Neurol 98:e95-e102, Wang, T.,et al, 2022

Clinicopathologic Conference, Anti-IgLON5 IgG-Associated Neurologic Disorder
NEJM 386:173-180, Case 1-2022, 2022

Spectrum of Neuroradiologic Findings Associated with Monogenic Interferonopathies
AJNR 43:2-10, Benjamin, P.,et al, 2022

A 31-Year-Old Man with Sequential Vision Loss
Neurol 98:163-169, Fortes, B.,et al, 2022

A 64-Year-Old Man with History of Meningitis Presenting with Proximal Weakness of the Arms
Neurol 98:208-213, Karschnia, P.,et al, 2022

A 57-Year-Old Man with Stepwise Progressive Paraparesis, Sensory Loss, Urinary Retention, and Constipation
Neurol 98:e555-e560, Alkabie, S.,et al, 2022

A 67-Year-Old Woman with Progressive Diplopia, Vertigo, and Ataxia
Neurol 98:e669-e674, Sakoda, M.,et al, 2022

Clinicopathologic Conference, Neurosyphilis
NEJM 386:583-590, Case 4-2022, 2022

Thyrotoxic Periodic Paralysis
UptoDate Jan, Gutmann, L. & Conwit, R., 2022

A 6-Year-Old Girl with Progressive Toe Walking
Neurol 98:e769-e773, Libdeh, A.A. & Ibrahim, A., 2022

Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
NEJM 386;674-687, Case 5-2022, 2022

Clinicopathologic Conference, Diffuse Large B-Cell Lymphoma
NEJM 386:977-986, Case 7-2022, 2022

Longitudinally Extensive Spinal Cord Lesions in a Middle-Aged Man
Neurol 98:419-424, Xi, N. & Zhou, Y., 2022

A Dizzy Architect
Neurol 98:543-549, Scutelnic, A.,et al, 2022

A 72-Year-Old Woman with Rapidly Progressive Bilateral Hearing Loss
Neurol 98:632-637, Alsalem, A.,et al, 2022

A 48-Year-Old Woman Presenting with Vertigo, Ptosis, and Red Eyes
Neurol 98:678-683, Kim, K.T.,et al, 2022

A 37-Year-Old Man with Involuntary Movements, Gait Disturbance, and Hyperasthesia
Neurol 98:851-853, Meng, D.,et al, 2022

A 77-Year-Old Man with Involuntary Movements, Sleep Changes, Falls, Bulbar Symptoms, and Cognitive Complaints
Neurol 99:26-30, Cao, T.Q.,et al, 2022

Bilateral Complete Ophthalmoplegia in a 50-Year-Old Man
JAMA Neurol 79:724-725, Arora, N.,et al, 2022

Diagnosis and Subtyping of Listeria Ventriculitis in an Immunocompetent Host
Neurol 99:123-126, Zhao, C.W.,et al, 2022

A 67-Year-Old Woman with Abdominal Pain, Constipation, and Urinary Retention
Neurol 99:117-122, Hanna, S.S.,et al, 2022

A 48-Year-Old Woman with 6 Months of Vivid Visual Hallucinations
Neurol 99:166-171, Kizza, J.,et al, 2022

Bilateral Hearing Loss and Constricted Visual Fields
BMJ 378:e070672, Sachdeva, G. & Shafquat, S., 2022

More Than a Little Unsteady
NEJM 387:e9, Kraft, A.W.,et al, 2022

Epidemiology, Survival, and Clinical Characteristics of Inclusion Body Myositis
Ann Neurol 92:201-212, Lindgren, U.,et al, 2022

Clinicopathological Conference, Chronic Candida Albicans Meningitis
NEJM 387:641-650, Case 25-2022, 2022

What All Physicians Need to Know About the Polio Resurgence in New York State
JAMA online e1-e3, Larkin, H., 2022

Clinicopathologic Conference, Granulomatosis with Polyangiitis
NEJM 387:1022-1032, Case 28-2022, 2022

Fragile X-Associated Tremor or Ataxia Syndrome in a Patient with Difficulty Walking, Falls, a Tremor, and Erectile Dysfunction
Lancet 400:1144, Sabino de Oliveira, D.,et al, 2022

Sturge-Weber Syndrome
www.UptoDate.com,Dec, Patterson,M.C., 2022

Spontaneous Escherichia Coli Meningitis and Brain Abscess in an Immunocompetent Adult
Cureus doi.10.7759/CUREUS.208728, Jeter,K.et al, 2022

Severe High Cervical Cord Compression Due to Large Bilateral Neurofibromas in a Patient with Neurofibromatosis Type 1: A Case Report and Review of Literature
CUREUS doi:10.7759/CUREUS.27211, Sadeh,M. & Farhat, H., 2022

The Phenotypic Continuum of ATP1A3-Related Disorders
Neurol 99:e1511-e1526, Vezyroglou,A., et al, 2022

A Middle-Aged Man with Progressive Gait Abnormalities
Neurol 97:e2423-e2428, Lin, J.,et al, 2021

A 65-Year-Old Woman with Tremor
Neurol 97:e1257-e1261, Ye, J.,et al, 2021

Fluorosis
Neurol 97:e1973-e1974, Saluja, A.,et al, 2021

A Middle-Aged Man with a History of Muscle Pain Presenting with Progressive Leukoencephalopathy and Subsequent Coma
Neurol 97:910-915, Jakobsson, A.S.,et al, 2021



Showing articles 750 to 800 of 2310 << Previous Next >>