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Differential
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advances in neurology
algorithm
ammonia
anesthesia, general
anterior tibial muscle weakness
antiviral agents
areflexia
ataxia
ataxic gait
atrial fibrillation
atrial paralysis
atrioventricular block
attention deficit disorder with hyperactivity
Babinski sign
biopterin deficiency
bradycardia
bradykinesia
calf hypertrophy
cardiomegaly
cardiomyopathy
cerebral embolism
cerebral embolism, carotid origin
cerebral palsy
cerebrovascular accident
cerebrovascular accident, cardiac disease causing
cerebrovascular accident, young adult
Charcot-Marie-Tooth
children
chromosomal abnormality
chromosome 14
Clinical Pathologic Conference(C.P.C.)
cognition
cogwheel rigidty
consanguinity
contractures, joint
corpus callosum, lesion of
cough
creatine phosphokinase(CPK)elevated
developmental disability
developmental milestones, loss of
differential diagnosis
difficulty climbing stairs
difficulty going down stairs
distal muscle atrophy
distal muscle weakness
diurnal variation
dopa responsive dystonia
dysarthria
DYSF gene
dysferlin
dysferlinopathy
dyspraxia
dystonia
dystonia, treatment of
dystrophin
electrocardiogram, abnormal
electromyogram
Emery-Dreifuss muscular dystrophy
encephalopathy
epileptic encephalopathy
exome sequencing
failure to thrive
falling
familial
FARS2 deficiency
fasciculation
fever
fibrillations
fine motor function, impaired
foot deformity
foot drop
foot drop, bilateral
gait disorder
gait, spastic
gastrocnemius muscle weakness
gene
gene mutation
gene therapy
genetic neurologic disorders
genetic testing
Gowers maneuver
growth retardation
hand weakness
heart block
heart block, complete
heart murmur
high arched feet
hyperreflexia
hyporeflexia
hypotonia
imbalance
implantable cardioverter defibrillator
inability to stand on tiptoes
inclusion bodies, intranuclear
influenza A virus
influenza B virus
Krabbe's disease
L-dopa
leg weakness, bilateral
leukodystrophy
life expectancy
liver disease
lysosomal storage disease
malignant hyperpyrexia
meningitis, CSF cell count-normal
mental retardation
microcephaly
misdiagnosis
mitochondrial disease
molecular genetics
movement disorder
MRI, abnormal
muscle atrophy, progressive
muscle biopsy
muscle pain
muscle stiffness
muscle tenderness
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, Becker, carrier
muscular dystrophy, cardiovascular changes with
muscular dystrophy, classification
muscular dystrophy, differential diagnosis of
muscular dystrophy, distal, Miyoshi
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, limb-girdle
myoglobinuria
myopathy
myopathy, distal
myopathy, distal, vacuolar
myopathy, inclusion body
myopathy, inclusion body, hereditary
myopathy, quadriceps
myopathy, vacuolar
myositis
myositis, acute of childhood
myositis, post infectious
neck weakness
neurologic disease, diagnoses of
neuropathy
neuropathy, demyelinating
neuropathy, hereditary peripheral
old age, neurology of
pacemaker, cardiac-transvenous
pain, calf
paraparesis, familial spastic
paraparesis, familial spastic, classification
paraparesis, familial spastic, variants
paraparesis, spastic
Parkinson disease, differential diagnosis of
Parkinson disease, juvenile
Parkinsonism syndrome
pes cavus
positive sharp waves
prognosis
progressive neurologic disorder
proximal muscle atrophy
pyramidal tract dysfunction
Red flags
review article
rippling muscle disease
scoliosis
seizure
seizure, children
short stature
sinemet
spastic diplegia
spasticity
standing difficulty
steppage gait
steroid therapy, CNS treatment and complications with
sudden death
tandem gait, ataxic
tenderness
toe walking
treatment of neurologic disorder
tremor
tremor, intention
tremor, postural
tripping
urea-cycle enzymopathies
viral infection
viral myopathy
walking
walking frame
walking, delayed
walking, difficulty with
weakness
weakness, progressive
web sites
wheelchair
white matter disease
wide based gait
winging of scapula
Showing articles 0 to 15 of 15

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

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

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

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

New Aspects on Patients Affected by Dysferlin Deficient Muscular Dystrophy
JNNP 81:946-953, Klinge,L.,et al, 2010

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

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

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

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

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

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



Showing articles 0 to 15 of 15