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Differential
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accommodation
accomodation, abnormal
advances in neurology
adverse drug reaction
ammonia
ANA
anasarca
anesthesia, general
angiokeratoma
ankle edema
anorexia
anterior tibial muscle weakness
antiviral agents
areflexia
arrhythmia, cardiac
arthralgia
arthritis
arthrogryposis multiplex
ascites
ataxia
ataxic gait
atrial fibrillation
atrial paralysis
atrioventricular block
attention deficit disorder with hyperactivity
autoantibodies
autoimmune disease
autonomic dysfunction
Babinski sign
basal ganglia, calcification of
biopterin deficiency
blinking
blinking, reduced
bone marrow transplantation
bradycardia
bradykinesia
brain atrophy
brainstem, atrophy
Brown-Vialetto-Van Laere syndrome
burning paresthesia
cachexia
calcification, intracranial
calf hypertrophy
carcinoma
cardiomegaly
cardiomyopathy
cardiovascular disease
caries
carpal tunnel syndrome
CAT scan, abnormal
cataracts
causalgia
central core disease
cerebellar atrophy, primary
cerebral cortical atrophy
cerebral embolism
cerebral embolism, carotid origin
cerebral palsy
cerebrospinal fluid, abnormal
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, oligoclonal IgG in
cerebrovascular accident
cerebrovascular accident, cardiac disease causing
cerebrovascular accident, young adult
ceruloplasmin, serum
cervical spine
cervical spine abnormality
Charcot-Marie-Tooth
children
cholelithiasis
chorea
chromosomal abnormality
chromosome 14
chromosome 17
Clinical Pathologic Conference(C.P.C.)
clubbing of fingers
clubfoot as related to neurologic disease
Cockayne's syndrome
cognition
cogwheel rigidty
congenital infection, CNS
congenital myopathy
congenital myopathy, inflammatory
congestive heart failure
consanguinity
contractures, joint
contrast agents, neurotoxicity of
convergence
convergence, impaired
cornea, opacity of
corpus callosum, lesion of
cough
cranial neuropathy
cranial neuropathy, multiple
crawl regression
C-reactive protein, elevated
creatine phosphokinase MB isoenzyme elevation
creatine phosphokinase(CPK)elevated
cry, weak
cryptorchidism
cytomegalovirus infection
cytomegalovirus infection, congenital
D-dimer
decision analysis
dementia
dermatomyositis
developmental disability
developmental milestones
developmental milestones, loss of
developmental retardation
diabetes mellitus
dialysis
diamond on quadriceps
differential diagnosis
difficulty climbing stairs
difficulty going down stairs
disability rating scale, neurological
disability, neurological
dislocated hip, congenital
distal muscle atrophy
distal muscle weakness
diurnal variation
dopa responsive dystonia
drooling
drug induced neurologic disorders
dysarthria
dysmorphic
dysostosis multiplex
dysphagia
dyspnea
dyspraxia
dystonia
dystonia, children
dystonia, treatment of
dystrophic calcification
dystrophin
electrocardiogram, abnormal
electromyogram
Emery-Dreifuss muscular dystrophy
encephalopathy
encephalopathy, progressive
endemic area
enzyme, defect
enzyme, muscle disease
eosinophilia
eosinophilia-myalgia syndrome
eosinophilic fasciitis
epidemiology of neurology
epileptic encephalopathy
equinovarus
exercise
exome sequencing
eyes, sunken
facial appearance, abnormal
facial weakness
failure to thrive
falling
familial
FARS2 deficiency
fasciculation
fatigue
feeding disorder
fetal movements, reduced
fetus
fever
fibrillations
fine motor function, impaired
floppy infant
foot deformity
foot drop
fracture, long bone
fucosidosis
gadolinium
gait disorder
gait, festinating
gait, spastic
gait, waddling
galactorrhea
gamma amino butyric acid
gene
gene mutation
gene therapy
genetic counselling
genetic neurologic disorders
genetic testing
glabellar sign
glutamic acid decarboxylase, antibody
glycoprotein
Gowers maneuver
grimacing
groove sign
growth retardation
Guillain Barre syndrome
hammertoes
hand deformity
hand pain
hand weakness
handwriting
headache
hearing loss
heart block
heart block, complete
heart murmur
hepatic failure
hepatitis
hepatolenticular degeneration(Wilson's disease)
hepatomegaly
hepatosplenomegaly
high arched feet
histochemistry
histochemistry of muscle
hyperpigmentation of skin
hyperreflexia
hypertonia
hypogonadism
hypoparathyroidism
hypophonia
hyporeflexia
hypotonia
hypotonia, infants
iatrogenic neurologic disorders
imbalance
immunosuppressive agents
implantable cardioverter defibrillator
inclusion body myositis
infection, recurrent
influenza A virus
influenza B virus
injection neuropathy
intellectual deficit
intellectual deterioration
intrauterine
intrauterine infection
intrauterine infection, viral
intrauterine infection, viral of CNS
intrinsic hand muscles, wasting of
jaw contractures
joint hypermobility
Kayser-Fleischer ring
kinesia paradoxica
Krabbe's disease
kyphoscoliosis, neurologic causes of
lactic dehydrogenase(LDH)
lateral cutaneous nerve of forearm
L-dopa
leg dragging
leg swelling
leprosy
leukocytosis
leukodystrophy
life expectancy
limb-girdle weakness
liver disease
liver function enzymes
liver transplantation
lordosis
L-tryptophan
lymphadenopathy
lymphadenopathy, axillary
lymphadenopathy, paraaortic
lysosomal storage disease
malignant hyperpyrexia
marche a petits pas
masked facies
median neuropathy
meningitis, CSF cell count-normal
mental retardation
merosin
microcephaly
micrographia
misdiagnosis
mitochondrial disease
mitral valve prolapse
molecular genetics
monoclonal antibodies
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, complications with
MRI, contraindications
MRI, contrast enhanced
multiple system atrophy
muscle atrophy, progressive
muscle atrophy, static
muscle biopsy
muscle cramp
muscle pain
muscle spasm
muscle stiffness
muscle strength, testing
muscle tenderness
muscle weakness
muscle weakness, proximal
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, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, limb-girdle
muscular dystrophy, pattern of muscle involvement
myasthenia gravis
myasthenia gravis, familial incidence of
myasthenic syndrome
myocardial biopsy
myocarditis
myoglobinuria
myopathy
myopathy, hypocalcemic
myopathy, quadriceps
myositis
myositis, acute of childhood
myositis, post infectious
myotonia dystrophica
myotonic discharges
neck extension
neck weakness
nephrogenic systemic fibrosis
nerve conduction studies
nerve enlargement
nerve hypertrophy
nerve injury
neurocutaneous disease
neuroendocrinology
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neuromuscular disease, electrodiagnosis of
neuropathology
neuropathy
neuropathy, demyelinating
neuropathy, hereditary peripheral
neuropathy, hypertrophic
neuropathy, iatrogenic
neuropathy, peripheral
neurotoxic
nystagmus
optic atrophy
optic neuropathy
orange peel appearance of skin
overlap syndrome
pacemaker, cardiac-transvenous
pain
pain, calf
pain, leg
paraparesis, familial spastic
paraparesis, familial spastic, classification
paraparesis, familial spastic, variants
paraparesis, spastic
paresthesias
paresthesias, feet
paresthesias, hands
Parkinson disease
Parkinson disease, diagnosis
Parkinson disease, differential diagnosis of
Parkinson disease, juvenile
Parkinsonism syndrome
periventricular leukomalacia
personality change
pes cavus
phlebotomy
photosensitivity, skin
pigmentary retinopathy
pneumonia
polymerase chain reaction
polymyalgia rheumatica
polymyositis
pons, atrophy
positive sharp waves
practice guidelines
prayer sign
premature infant
prenatal diagnosis by amniocentesis
prognosis
progressive neurologic disorder
prolactin, elevated
proximal muscle atrophy
pruritus
pseudohypertrophy
psychiatric problems in neurologic disorders
psychomotor retardation
pulmonary infiltrates
pyramidal tract dysfunction
rash
Red flags
reflex sympathetic dystrophy
renal failure
renal tubular acidosis
repetitive nerve stimulation
respiratory failure
retinopathy
retropulsion
review article
rhabdomyolysis
riboflavin transporter deficiency
rickets
rigid spine syndrome
rigidity
rippling muscle disease
safety
Samoa
sarcoglycan
sarcoglycanopathy
sarilumab
scoliosis
scoliosis, neurologic association with
sedimentation rate
sedimentation rate, elevated
seizure
seizure, children
seizure, neonatal
sensorineural hearing loss
serositis
short stature
shoulder, pain in
sinemet
skin, biopsy
skin, lesions in neurologic disorders
skin, thickened
spastic diplegia
spasticity
speech disorder
speech disorder, childhood
splenomegaly
stare
steppage gait
steroid
steroid therapy, CNS treatment and complications with
stiff joints
stiff man syndrome
stillbirth
stooped posture
suck, poor
sudden death
systemic illness
systemic juvenile idiopathic arthritis
tandem gait, ataxic
tenderness
thrombocytosis
tocilizumab
toe walking
toxic oil syndrome
treatment of neurologic disorder
tremor
tremor, intention
tremor, postural
tremor, resting
tripping
type 1 muscle fiber
type 2 muscle fiber
tyrosine hydroxylase deficiency
urea-cycle enzymopathies
uremia
urine test for metabolic disorders
urine, dark
viral infection
viral myopathy
vital capacity
voice, abnormality of
Walker-Warburg syndrome
walking
walking frame
walking, delayed
walking, difficulty with
weakness
weakness, congenital
weakness, generalized
weakness, progressive
weakness, proximal
web sites
weight loss
wheelchair
white matter disease
wide based gait
winging of scapula
workup
wrist drop
x-ray, cervical spine
Showing articles 50 to 100 of 844 << Previous Next >>

Familial Neuromuscular Disease with Type 1 Fiber Hypoplasia, Tubular Aggregates, Cardiomyopathy, & Myasthenic Features
Neurol 28:1135-1140, Dobkin,B.H.,et al, 1978

The Spectrum of Mild X-Linked Recessive Muscular Dystrophy
Arch Neurol 34:408, Ringer,S.P.,et al, 1977

Rigid Spine Syndrome:A Type I Fiber Myopathy
Arch Neurol 34:119, Seay,A.R.,et al, 1977

Parkinson's Disease
In Handbk of Clinical Neurology, Vinken, P. J. & Bruyn, G. W. , Ed, North-Holland Publ Co, Amsterdam, 6:173, 1968. Selby, G., 1968

A 62-Year-Old Woman with Progressive Spasticity, Weakness,and Gait Instability
Neurol 104:e210290, Voloshyna-Farber, E.Y.,et al, 2025

Juvenile-Onset Dopa-Responsive Dystonia-Until It Isnt
Neurol 104:e213436, Paredes,N.C.,et al, 2025

A 19-Year-Old Woman with Progressive Weakness and Numbness in Her Arms and Legs
Neurol 104:e213495, Alsabah,A-A.,et al, 2025

A 60-Year-Old Man with Weakness and Gait Dysfunction
JAMA Neurol 82:305-306, Jones,F.J.S.,et al, 2025

Rabbit Syndrome
Neurol102:e209275, Huynh,T.U., & Beckley, E.H., 2024

Clinicopatholigic Conference, Rheumatoid Arthritis with Vasculitis Causing A Confluent Mononeuritis Multiplex
NEJM 390:1312-1322, Case 11-2024, 2024

Clinicopathologic Conference, Thyrotoxic Periodic Paralysis Associated with Graves Disease
NEJM 390:1514-1522, Case 13-2024, 2024

A 55-Year -Old Woman with Painless Hand Weakness and Atrophy
Neurol 103:e209561, Ticku,H. & Katirji,B.,, 2024

Parkinsons Disease
NEJM 391:442-452, Tanner,C.M. & Ostrem,J.L., 2024

Neuroleptic Malignant Syndrome
NEJM 391:1130-1138, Wijdicks,E.F.M. & Ropper,A.H., 2024

Clinical Features, Diagnosis and Management of Klinefelter Syndrome
www.UptoDaate.com, Matsumoto,A.M. & Anawals,B.D., 2024

A 50-Year-Old Man with Ataxia, Dystonia, and Abnormal Ocular Movements
Neurol 103:e210046, Panigrahi,B.,et al, 2024

Reversible Cerebral Atrophy and Substantia Nigra Changes after Vitamin B12 Treatment in Infantile Tremor Syndrome
Neurol 103:e210076, Singh,R.,et al, 2024

Clinical Manifestations and Diagnostic Challenges in a 16-Year-Old With Early-Onset Ataxia
Neurol 104:e210253, Chadha,D.,et al, 2024

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

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

Rapidly Progressive Dementia in a Man With HIV Infection and Undetectable Plasma Viral Load
Neurol 100:344-348, Chishimba,L.C.,et al, 2023

Severe Cervicodynia in a Patient With Pustules on the Palms
JAMA Neurol 80:323-324, Zia,C. & Lv,Y., 2023

A 23-Year-Olf Man With Progressibe Asymmetric Weakness and Numbness
Neurol 100:674-682, Kaplan,E.H.,et al, 2023

A 48-Year-Old Man With Spasticity and Progressive Ataxia
Neurol 101:e1747-e1752, Vizcarra,J.A.,et al, 2023

Trial of Botulinum Toxin for Isolated or Essential Head Tremor
NEJM 389:1753-1765, Marques,A.,et al, 2023

Multidisciplinary End-of-Life Care for a Patient with Amyotrophic Lateral Sclerosis Requesting Euthanasia
Lancet 402:484, Kruithof,W.J.,et al, 2023

Wernekinck Commissure Syndrome
Radiopaedia doi.org/10.53347/rlD-85274, Aug, Deng,F.,et al, 2023

Current and Emerging Issues in Wilsons Disease
NEJM 389:922-938, Roberts,E.A. & Schilsky, M.L., 2023

Neurologic Complications of Babesiosis, United States, 2011-2021
Emerg Inf Dis 29:1127-1135, Locke,S.,et al, 2023

Clinicopathologic Conference,Limb-Shaking Transient Ischemia Attacks
NEJM 389:1416-1423, Case 31-2023, 2023

Severe Vitamin B12 Deficiency Presenting as Pancytpenia, Hemolytic Anemia, and Parasthesia:Could Your B12 Be Any Lower?
Cureus doi:10.7759/cureus 29225, Pelling,M.M., et al, 2022

Clinical and Structural Findings in Patients with Lesion-Induced Dystonia
Neurol 99:e1957-e1967, Corp, D.T.,et al, 2022

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

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

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

A 68-Year-Old Man with Palmar Rash, Leg Pain, and Inability to Walk
Neurol 99:347-353, YoungHun, J.,et al, 2022

A 65-Year-Old Woman with Cancer History and Wrist Drop
Neurol 99:570-576, Merrill, R.,et al, 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

Clinicopathologic Conference, Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome
NEJM 385:165-175, Case 20-2021, 2021

Clenched Fists as an Unusual Presentation of Focal Neuromyotonia
Neurol 97:e429-e430, Dhanapalaratnam, R.,et al, 2021

A 59-Year-Old Woman Presenting with Diplopia, Dysarthria, Right-sided Weakness, and Encephalopathy
Neurol 97:e859-e864, Manzano, G.S.,et al, 2021

A 49-Year-OLD Woman with Progressive Numbness and Gait Instability
Neurol 97:342-347, Zahid, A.,et al, 2021

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

Frequency and Characterization of Movement Disorders in Anti-IgLON5 Disease
Neurol 97:e1367-e1381, Gaig, C.,et al, 2021

Facial Numbness, Dysarthria, Muscle Atrophy, and Weakness in a Young Patient
JAMA Neurol 78:1273-1274, Liu, Y.,et al, 2021

Hypotonia and Delayed Teeth Eruption in a 2-Year-Old Girl
Neurol 97:875-878, Dinov, D.,et al, 2021

Choreoathetosis and Focal Dystonia in Vitamin B12 Deficiency
Neurol 97:e1545, Ng, C.F.,et al, 2021

A Middle-aged Woman with Severe Scoliosis and Encephalopathy
JAMA Neurol 78:251-252, Mohan, G.,et al, 2021

A Triad of Tremor, Ataxia, and Cognitive Impairment
Neurol 96:e1802-e1803, Au, L.W.C.,et al, 2021

A 6-Year-Old Boy with Muscle Twitching
Neurol 96:e301-e304, Lewis, H.S.,et al, 2021



Showing articles 50 to 100 of 844 << Previous Next >>