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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 177 << 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 19-Year-Old Woman with Progressive Weakness and Numbness in Her Arms and Legs
Neurol 104:e213495, Alsabah,A-A.,et al, 2025

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

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

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

A 65-Year-Old Woman with Cancer History and Wrist Drop
Neurol 99:570-576, Merrill, R.,et al, 2022

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

"Cortical" Wrist Drop due to a Cerebral Peduncle Infarct
Case Rep Neurol 12:207-211, Venketasubramanian, N.,et al, 2020

Pyogenic Brain Abscesses in a Patient with Digital Clubbing
JAMA Neurol 77:129-130, Paliwal, V.K.,et al, 2020

A 22-Year-Old Man with Progressive Bilateral Visual Loss
Neurol 94:625-630, Yang, S.L.,et al, 2020

Complex Ataxia
Neurol 95:136-141, Abkur, T.,et al, 2020

Clinicopathologic Conference, HIV Type 2 Infection & Cerebral Toxoplasmosis
NEJM 383:859-866, Case 27-2020, 2020

A 72-year-old Man with a Progressive Cognitive and Cerebellar Syndrome
Neurol 95:e2707-e2710, Lad, M. & Griffiths, T.D., 2020

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

Dupuytren, Ledderhose, and Peyronie Diseases after Primidone Use for Essential Tremor
Neurologist 24:150-151, Felipe, L.,et al, 2019

Clinicopathologic Conference, Creutzfeldt-Jakob Disease
NEJM 381:1569-1578, Case 32-2019, 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 17-year-old Baseball Player with Right Hand Weakness
Neurol 92:e76-e80, Vachon, C. & Libdeh, A.A., 2019

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

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

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

Clinicopathologic Conference, Homocystinuria due to genetic mutations of the gene encoding cystathionine B-synthase (CBS)
NEJM 378:941-948, Case 7-2018, 2018

A 52-year-old woman with a 3 weeks of progressive gait ataxia and dysarthria
Neurol 90:e985-e989, Ly, C.,et al, 2018

A 60-year-old man with arm weakness and numbness
Neurol 90:190-196, Foster, L.A.,et al, 2018

Finger Clonus
Neurol 86:e118-e119, Moccia,M.,et al, 2016

Pseudoradial Nerve Palsy Caused by Acute Ischemic Stroke
J Invest Med Case Report doi:10.1177/2324709616658310, Tahir, H.,et al, 2016

Differential Diagnosis
Thoracic Key, Southerland,A.W.,et al, 2016

A 40-year old Woman with Difficulty Going Down Stairs in High-Heeled Shoes
Ann Neurol 77:1-7, Scripko, P.,et al, 2015

Short Stature, Imperforate Anus, and Polydactyly
Neurol 84:e117, Dumitrascu, O.,et al, 2015

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

Degenerative Diseases of the Nervous System, Amyotrophic Lateral Sclerosis
Adams & Victors Principles of Neurology, Chp 39, pg 1109, Ropper, A.H.,et al, 2014

Chronic and Slowly Progressive Weakness of the Legs and Hands
BMJ 348:g459, Nightingale, H.,et al, 2014

Neurological Acro-Osteolysis
BMJ 348:g473, Mitchell, L.,et al, 2014

A 27-year-old Man with Hand Numbness
Neurol 82:e80-e84, Vijayan, J.,et al, 2014

A 75-year-old man with 3 years of Visual Difficulties
Neurol 83:e160-e165, Berkowitz, A.L.,et al, 2014

Peripheral Neuropathy - Lead Astray?
LANCET 381:1156, Pickrell, W.,et al, 2013

Clinicalpathologic Conference, Vitamin B12 Deficiency due to Pernicious Anemia
NEJM 366:1626-1633, Case 13-2012, 2012

Clinicopathologic Conference, Sjogrens syndrome with dorsal-root ganglionitis
NEJM 364:1856-1865, Case 14-2011, 2011

An unusual cause of stroke and hypoxia
BMJ 342:c7200, Bell, S.L. & Eveson, D.J., 2011

Hereditary Hemorrhagic Telangiectasia (Osler-Weber-Rendu Syndrome)
UpToDate, Feb, Shovlin, C., 2011

An Unusual Cause of Pseudomedian Nerve Palsy
Case Reports Neurol Med doi:10.1155/2011/474271, Manjaly, Z.M.,et al, 2011

A Hereditary Moyamoya Syndrome With Multisystemic Manifestations
Neurol 75:259-264, Herv�,D., et al, 2010

Critical Vasospasm During Fingolimod (FTY720) Treatment in a Patient With Multiple Sclerosis
Neurol 74:2022-2024, Schwarz,A., et al, 2010

Clinicopath Conf, Rapid-Onset-Dystonia-Parkinsonism Due to a Mutation in the ATP1A3 Gene
NEJM 362:2213-2219, Case 17-2010, 2010

Valproic Acid Monotherapy in Pregnancy and Major Congenital Malformations
NEJM 362:2185-2193, Jentink,J., et al, 2010



Showing articles 50 to 100 of 177 << Previous Next >>