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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
anticonvulsants
anticonvulsants, untoward effects of
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
collagen vascular disease
complications
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
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
Dupuytren's contractures
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
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
Ledderhose disease
leg dragging
leg swelling
leprosy
leukocytosis
leukodystrophy
life expectancy
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
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
mysoline
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
Peyronie's disease
phenobarbital
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
riboflavin transporter deficiency
rickets
rigid spine syndrome
rigidity
rippling muscle disease
safety
Samoa
sarilumab
scoliosis
scoliosis, neurologic association with
sedimentation rate
sedimentation rate, elevated
seizure
seizure, children
seizure, neonatal
sensorineural hearing loss
serositis
short stature
shoulder, frozen
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
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
web sites
weight loss
wheelchair
white matter disease
wide based gait
winging of scapula
wrist drop
x-ray, cervical spine
Showing articles 0 to 50 of 54 Next >>

A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
JAMA Neurol 81:83-84, Hua,L.,et al, 2024

Clinicopathologic Conference, Hypocalcemic Myopathy Due to Hypoparathyroidism
NEJM 388:1513-1520, Case 12-2023, 2023

Skin Lesions, Foot Drop, and Hand Contractures
JAMA doi:10.1001/JAMA.2023.9915, Filley,A.R.,et al, 2023

Polymyalgia Rheumatica
Lancet 402:1459-1472, Espigol-Frigole,G.,et al, 2023

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

A 31-year-Old Man with Bilateral Limited Mobility of Joints
JAMA Neurol 79:1083-1084, Wang, Z.,et al, 2022

Clinicopathologic Conference, Systemic Juvenile Idiopathic Arthritis
NEJM 385:1220-1229, Case 29-2021, 2021

Pes Cavus and Neuropathy
Neurol 93:e823-e826, Alderson,J.,& Ghosh,P.S., 2019

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

Clinical Reasoning: Cardioembolic Stroke in a 23-year-old Man with Elbow Contracture
Neurol 90:e172-e176, Roy, B. & Raynor, E., 2018

Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss
Neurol 90:e625-e631, Set, K.K.,et al, 2018

Disability in adults with arthrogryposis is severe, partly invisible, and varies by genotype
Neurol 90:e1596-e1604, Dai, S.,et al, 2018

Wilson Disease
Yamada Textbook of Gastroenterology Chp 102, Metabolic Diseases of Liver, 6th Ed, Sunderam, S.S., & Sokol, R.J., 2016

Degenerative Diseases of the Nervous System, Hereditary Spastic Paraplagia
Adams & Victors Principles of Neurology, Chp 39, pg 1119, Ropper, A.H.,et al, 2014

Diagnosis and New Treatments in Muscular Dystrophies
JNNP 80:706-714, Manzur,A.Y. &Muntoni,F., 2009

A 49-Year-Old Man with Contractures, Weakness, and Cardiac Arrhythmia
Neurol 72:2036-2043, Kissel,J.T.,et al, 2009

Gadolinium-Based MR Contrast Agents and Nephrogenic Systemic Fibrosis
Radiology 242:647-649, Kuo,P.H.,et al, 2007

Congenital Muscular Dystrophy
eMedicine (Jan), Lopate,G., 2007

Dopamine-Responsive Dystonia
eMedicine (Apr), Nikhar,N.K., 2006

Hereditary Motor and Sensory Neuropathies
Peripheral Neuropathy, Dyck,P.J. & Thomas,P.K. (Ed). Elsevier Publ, Vol 2, Ch 69: 1623-1635, Shy,M.E., et al, 2005

Benign Acute Childhood Myositis, Laboratory and Clinical Features
Neurol 53:2127-2131, Mackay,M.T.,et al, 1999

Congenital Muscular Dystrophy:Clinical & Pathologic Study of 50 Pts with Classical (Occidental) Merosin-Positive Form
Neurol 46:815-818, Kobayashi,O.,et al, 1996

Congenital Muscular Dystrophy Syndromes Distinguished by Alkaline and Acid Phosphatase, Merosin, & Dystrophin Staining
Neurol 46:810-814, Connolly,A.M.,et al, 1996

Charcot-Marie-Tooth Disease and Related Inherited Neuropathies
Medicine 75:233-250, Murakami,T.,et al, 1996

The Synd of Autosomal Recessive Pontocerbellar Hypoplasia, Microcephaly, & Extrapyr Dyskinesia (Pontocereb Hypopl Type 2)
Neurol 45:311-317, Barth,P.G.,et al, 1995

Peripheral Nerve Injury and Causalgia Secondary to Routine Venipuncture
Neurol 44:962-964, Horowitz,S.H., 1994

Arginase Deficiency Presenting as Cerebral Palsy
Pediatrics 91:995-996, Scheuerle,A.E.,et al, 1993

Cockayne Syndrome: Review of 140 Cases
Am J Med Genet 42:68-84, Nance,M.A. &Berry,S.A., 1992

Clinicopath Conf
Emery-Dreifus Muscular Dystrophy, NEJM 327:548-5571992., , 1992

Lethal Cytomegalovirus Infection in Preterm Infants:Clinical, Radiological, and Neuropathological Findings
Ann Neurol 31:64-68, Perlman,J.M.&Argyle,C., 1992

Polymyositis, Dermatomyositis, and Inclusion-Body Myositis
NEJM 325:1487-1498, Dalakas,M.C., 1991

Fucosidosis Revisited:A Review of 77 Patients
Am J Med Genet 38:111-131, Willems,P.J.,et al, 1991

Congenital Inflammatory Myopathy
Neurol 40:1111-1114, Shevell,M.,et al, 1990

Clinicopath Conf
Eosinophilic Fasciitis, Case Study 4-1990, NEJM 322:252-261, 93190., , 1990

Development of Diffuse Fasciitis with Eosinophilia During L-Tryptophan Treatment:Elevated Type I Collagen Gene
Ann Int Med 112:344-351, Varga,J.,et al, 1990

Eosinophilia-Myalgia Syndrome-New Mexico
JAMA 262:3116, Belvins,W.L.,et al, 1989

Improved Diagnosis of Becker Muscular Dystrophy by Dystrophin Testing
Neurol 39:1011-1017, Hoffman,E.P.,et al, 1989

Congenital Muscular Dystrophy
J Pediatr 115:214-221, Leyten,Q.H.,et al, 1989

Dopa Responsive Dystonia:A Treatable Condition Misdiagnosed as Cerebral Palsy
BMJ 298:1019-1020, Boyd,K.&Patterson,V., 1989

Rigid Spine Syndrome and Rigid Spine Sign in Myopathies
J Child Neurol 4:273-282, Merlini,L.,et al, 1989

Barbiturate-Related Connective Tissue Disorder
Arch Int Med 149:911-914, Mattson,R.H.,et al, 1989

Emery-Dreifuss Muscular Dystrophy:Disease Spectrum and Differential Diagnosis
Neuropediatrics 19:62-71, Voit,T.,et al, 1988

Autoantibodies to Glutamic Acid Decarboxylase in Pt with Stiff-Man Syndr, Epilepsy & Type I Diabetes Mellitus
NEJM 318:1012-1020, Solimena,M.,et al, 1988

Early-Onset Benign Autosomal Dominant Limb-Girdle with Contractures (Bethlem Myopathy)
Neurol 38:573-580, Mohire,M.D.,et al, 1988

Hand Contractures in Parkinson's Disease
JNNP 51:1221-1223, Kyriakides,T.&Hewer,R.L., 1988

Central Core Disease, Clinical Features in 13 Patients
Medicine 66:389-396, Shuaid,A.,et al, 1987

Clinical Epidemology of Toxic-Oil Syndrome
NEJM 309:1408-1414, Kilbourne,E.M.,et al, 1983

Congenital Myotonic Dystrophy
Arch Neurol 37:693-696, Argov,Z.,et al, 1980



Showing articles 0 to 50 of 54 Next >>