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Differential
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abdominal distention
acid maltase deficiency
acid maltase deficiency, adult
acromegaly
acute intermittant porphyria
advances in neurology
adverse drug reaction
alcohol, neurologic complications with
alcoholic polyneuropathy
alcoholism
amyloid
amyloidosis
anesthesia, general
aneurysm
aneurysm, thoracic aortic
anterior horn cell disease
anticonvulsants
aortic wall, thickened
aortitis
areflexia
arrhythmia, cardiac
arterial dissection, aorta
arterial dissection, wall thickness
arteritis, temporal
asymptomatic
ataxia
ataxic gait
autism
Babinski sign
bacterial infection
blindness
botulinum toxin
brachial neuritis, acute
bruxism
bulging of biceps
calf hypertrophy
carbamazepine
carcinoma
cardiomegaly
cardiomyopathy
cardiovascular disease
CAT scan
CAT scan, abnormal
CAT scan, angiography
CAT scan, emission, abnormal
CAT scan, metrizamide
CAT scan, muscle
CAT scan, myelogram with
cataracts
cauda equina
cauda equina, enhancement
cauda equina, lesion of
cavernous sinus
cavernous sinus, lesion of
central nervous system, infection of
cerebellar lesion
cerebral ischemia
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, proteincytologic dissociation
cerebrovascular accident
cerebrovascular disease, cardiovascular disease with
cerebrovascular disease, risk factors in
Charcot-Marie-Tooth
chemosis
chewing movements
chewing, impaired
children
chromosomal abnormality
chromosome 17
claudication, intermittent of cauda equina
Clinical Pathologic Conference(C.P.C.)
CLOVES syndrome
clubfoot as related to neurologic disease
complications
confusion
congenital malformation
congenital myopathy
congestive heart failure
contractures, joint
coronary artery disease
corticotropin level
corticotropin-releasing factor
cortisol, elevated
cranial nerve enlargement
cranial nerves
cranial neuropathy
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
cry, abnormal
crying
Cushing's syndrome
cysticercosis
cysticercosis, cerebral
cysticercosis, disseminated
cysticercosis, intraventricular
cysticercosis, miliary
deafness
deep gray nuclei
Dejerine-Sottas syndrome
delay in diagnosis
denervation of muscle
dentate nuclei
dentate nuclei, lesion of
developmental milestones, loss of
developmental retardation
diabetes mellitus
diagnostic criteria
diamond on quadriceps
diaphragmatic paralysis
differential diagnosis
difficulty climbing stairs
dilantin
diplopia
distal muscle atrophy
distal muscle weakness
donut sign
dysferlinopathy
dysphonia
dysplasia of C.N.S.
dyspnea
dysthyroid ocularmyopathy
dystonia
dystonia, post traumatic
dystrophin
dystrophin associated proteins
echocardiogram
echocardiogram, LVH
edema, periorbital
electrocardiogram, abnormal
electrocardiogram, LVH
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
electron microscopy
encephalopathy
encephalopathy, progressive
entrapment neuropathy
enzyme, defect
eosinophilic fasciitis
epidermal nevus syndrome
exercise
exophthalmus
extraocular muscle enlargement
facial hair, excessive
facial pain
facial pain, atypical
facial weakness
facial weakness, bilateral
failed medical management
falling
familial
fatigue
feeding disorder
fever
fine motor function, impaired
fistula, arterio-venous, carotid-cavernous
fistula, arterio-venous, dural
foot deformity
foot drop
gadolinium
gait disorder
gait, waddling
gammaglobulin therapy, intravenous
gender
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
giant cell arteritis
globoid cells
Gowers maneuver
Graves ophthalmopathy
Guillain Barre syndrome
halo sign
hammertoes
hand deformity
hand weakness
hands, fisted
head injury
head lag
headache
headache, bilateral
headache, temporal
hearing loss
heart murmur
hemiatrophy, congenital
hemidiaphragm, paralysis of
hemihypertrophy, congenital
hemihypertrophy, facial
hemimegalencephaly
hemiparesis
hepatomegaly
hereditary myopathy with early respiratory failure
heterotopia
high arched feet
hirsutism
histochemistry
hoarseness
hypercalcemia
hyperreflexia
hypertension
hyperthyroidism
hypertonia
hypokalemia
hypomelanosis of Ito
hypopigmentation of skin
hyporeflexia
hypothyroidism
idiopathic
IgG4, serum
IgG4-related disease
inability to sit up
infantile spasm
intellectual deficit
intrinsic hand muscles, wasting of
irritability
Isaacs syndrome
Kobberling-Dunnigan syndrome
Krabbe's disease
Kugelberg-Welander syndrome
kyphoscoliosis, neurologic causes of
lacrimal gland enlargement
laminectomy, cervical
laminectomy, lumbar
learning disability
learning disability, in children
left ventricular dilatation
leg atrophy
leg numbness
leg swelling
leg weakness, unilateral
leukemia
leukocyte enzyme abnormality
leukocytosis
leukodystrophy
life expectancy
limb hypertrophy
limb-girdle weakness
lipodystrophy
liver function enzymes
lordosis
lumbosacral plexopathy
lymphoma
lymphopenia
macrocephaly
malformation, CNS, congenital
malformation, vascular
malformation, vascular, cerebral
malignant hyperpyrexia
masseter muscle hypertrophy
maxillary nerves
meconium staining
meningioma
mental retardation
mental status, abnormal
metabolic alkalosis
mexiletine
misdiagnosis
molecular genetics
monoclonal gammopathy
mononeuritis multiplex
mononeuropathy
mononeuropathy chronic inflammatory demyelinating
mortality
motor neuron disease
movement disorder
MRI
MRI, abnormal
MRI, angiography
MRI, contrast enhanced
MRI, cranial nerves
MRI, hypointense signal foci on
MRI, lumbosacral plexus
MRI, muscle
MRI, optic nerve
MRI, orbit
MRI, peripheral nerve
MRI, spinal cord
MRI, spine
MRI, vessel wall
MRI, vessel wall enhancement
MRS
mucormycosis
multimodal neuroimaging
multiple myeloma
muscle atrophy, focal
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle hypertrophy
muscle hypertrophy, congenital
muscle pain
muscle stiffness
muscle swelling
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, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, dystrophin normal
muscular dystrophy, facioscapulohumeral
muscular dystrophy, female occurrence of
muscular dystrophy, limb-girdle
muscular dystrophy, pattern of muscle involvement
myelogram
myelopathy
myeloradiculopathy
myocardial infarction
myoedema
myoglobinuria
myokymia
myopathy
myopathy, amyloid
myopathy, focal
myopathy, hereditary
myopathy, metabolic
myopathy, monomelic
myopathy, quadriceps
myopathy, vacuolar
myositis, ocular
myostatin
myotonia
myotonia congenita
nausea and vomiting
neoplasm, hormone producing, ectopic
neoplasm, metastatic to muscle
neoplasm, metastatic to orbit
neoplasm, peripheral nerve
nerve biopsy
nerve conduction studies
nerve enlargement
nerve hypertrophy
nerve injury
nerve root enhancement
nerve root hypertrophy
neuritis
neuritis, causes of
neuritis, heavy metals causing
neurocutaneous disease
neuroendocrinology
neurofibroma
neurofibromatosis 1
neurofibromin
neurologic disease, diagnoses of
neurologic examination
neurologic history
neurologic signs
neuromyotonia
neuroophthalmology
neuropathology
neuropathy
neuropathy, amyloid
neuropathy, ataxic
neuropathy, demyelinating
neuropathy, hereditary peripheral
neuropathy, hypertrophic
neuropathy, medication induced
neuropathy, onion bulb
neuropathy, peripheral
night blindness
night sweats
ophthalmic artery
opisthotonus
optic atrophy
optic chiasm, enlarged
optic nerve
optic nerve sheath enhancement
optic nerve, compression of
optic nerve, enlarged
optic nerve, lesion of
optic neuropathy
optic neuropathy, bilateral
orbit, cellulitis of
orbit, inflammation in
orbit, lesions of
orbit, mass
orbit, meningioma of
orbit, neoplasms of
orbit, pseudotumor of
orthopnea
pain, leg
palpitations
paraparesis
paresthesias
paresthesias, feet
paresthesias, lower extremity
PAS positive material in the brain
pathology
percussion induced muscle contraction
perineuritis
perineuritis, optic
peripheral nerve, lesion of
peroxisomal disease
pes cavus
phakomatoses
phytanic acid
plasma cell dyscrasia
polyneuropathy
polyneuropathy, chronic idiopathic
polyneuropathy, chronic inflammatory demyelinating
polyneuropathy, chronic relapsing
polyneuropathy, familial
post polio syndrome
postural abnormality
prenatal diagnosis by amniocentesis
prognosis
progressive neurologic disorder
proptosis
proximal muscle atrophy
pseudohypertrophy
pseudomyotonia
ptosis
pulmonary embolism
pupil, tonic
pyramidal tract
radiculopathy
Refsum's disease
respiratory failure
retinitis pigmentosa
review article
rhabdomyolysis
rhabdomyosarcoma
rhabdomyosarcoma of orbit
rigidity
rippling muscle disease
risk factors
root lesion, nerve
sarcoglycan
sarcoglycanopathy
sarcoidosis
scalp tenderness
sciatic neuropathy
scoliosis
seizure
sensorineural hearing loss
sensory loss
shoulder, elevation
sinuses, diseases of
sinusitis
skin, lesions in neurologic disorders
somnolence
spasticity
speech disorder, childhood
speech, delayed development of
spinal accessory nerve
spinal cord, compression of
spinal cord, neoplasm
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, intermediate form
spinal stenosis
spinal stenosis, familial
startle reaction
steppage gait
steroid
steroid therapy, CNS treatment and complications with
subarachnoid hemorrhage
subcutaneous nodules
sudden death
superior ophthalmic vein
survival motor neuron gene
symmetric brain lesions
syncope
syringomyelia
systemic illness
telangiectases, retinal
temporal artery
temporalis muscle enhancement
temporalis muscle hypertrophy
temporalis muscle swelling
thalamus, lesion of-bilateral
thirst
thyrotoxicosis
tinnitus
titinopathy
toe walking
tongue, enlarged
tongue, weakness
tonic spasms
tram-track sign
transient ischemic attack
trauma
treatment of neurologic disorder
trigeminal nerve
trigeminal nerve, abnormality of
trigeminal nerve, hypertrophy
trigeminal nerve, lesion of
trigeminal neuralgia
tripping
ultrasonography, nerve
urinary frequency
urine, dark
vasculitis, large vessel
vertebral artery wall thickness
vision, blurred
visual acuity, decreased
visual fields, constricted
visual loss
vital capacity
weakness
weakness, generalized
weakness, progressive
weakness, proximal
web sites
weightlifting
wheelchair
white matter disease
winging of scapula
workup
x-ray, spine
Showing articles 50 to 100 of 2814 << Previous Next >>

Mosaic Express of Dystrophin in Carriers of Becker's Muscular Dyst & X-Linked Synd of Myalgia & Cramps
NEJM 327:1100, Minetti,C.&Bonilla,E., 1992

Isolated Muscle Hypertrophy as a Sign of Radicular or Peripheral Nerve Injury
JNNP 54:325-329, Mattle,H.P.,et al, 1991

Epidermal Nevus Synd:A Neurologic Variant with Hemimegalencephaly, Gyral Malf, Mental Retard, Seizures & Facial Hemihyper
Neurol 41:266-271, Pavone,L.,et al, 1991

Congenital Monomelic Hypertrophy with Progressive Myopathy
Arch Neurol 48:107-110, Shukla,A.,et al, 1991

Refsum Disease
In Rowland's Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8thEd, p. 509, Menkes,J.H., 1989

Compression Syndromes Due to Hypertrophic Nerve Roots in Hereditary Motor Sensory Neuropathy Type I
Neurol 39:1173-1177, Rosen,S.A.,et al, 1989

Computed Tomographic Features of Nonthyroid Extraocular Muscle Enlargement
Ophthalmol 96:1038-1047, Patrinely,J.R.,et al, 1989

Hypertrophy of the Calf with S-1 Radiculopathy
Arch Neurol 45:660-664, Ricker,K.,et al, 1988

Proximal Weakness of the Extremities as Main Feature of Amyloid Myopathy
JNNP 50:1353-1358, Jennekens,F.G.I.&Wokke,J.H.J., 1987

Acid Maltase Deficiency
Engel, A. G. in Engel and Banker, Myology, McGraw-Hill Co, New York, Ch 55, p. 1629-1651, , 1986

Muscular Hypertrophy after Chronic Radiculopathy
Arch Neurol 41:397-398, Montagna,P.,et al, 1984

Isaacs'Syndrome with Muscle Hypertrophy Reversed by Phenytoin Therapy
Arch Neurol 40:241-242, Zisfein,J.,et al, 1983

Unilateral Calf Enlargement Following S1 Radiculopathy
Muscle & Nerve 5:434-438982., Mielke,U.,et al, 1982

The Female Carrier of Duchenne Muscular Dystrophy
BMJ 284:1423-1424, Dubowitz,V., 1982

Benign Familial Spinal Muscular Atrophy With Hypertrophy of the Calves
Arch Neurol 39:657-660, D'Alessandro,R.,et al, 1982

Neurological Aspects of Thyroid Dysfunction
Mayo Clin Proc 56:504-512, Swanson,J.W.,et al, 1981

Congenital Hemihypertrophy:Oncogenic Potential of the Hypertrophic Side
Ann Neurol 10:199-201, Furukawa,T.,et al, 1981

Correlation of CT Scanning and Pathologic Features of Ophthalmic Graves'Disease
Ophthalmol 88:553-564, Trokel,S.L.&Jakobiec,F.A., 1981

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

Congenital Hemihypertrophy with Aortic, Skeletal, & Ocular Abnormalities
BMJ 87, 1973 Jan., Henry,M.,et al, 1973

Polyneuritis
Med Clin North Am 56:1299, Sibley,W., 1972

Rapidly Progressive Frontotemporal Dementia with Amytrophic Lateral Sclerosis in an Elderly Female
Cureus doi:10.7759/CUREUS.32182, Sweedan,Y.G.,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

Severe Myotonic Crisis Resembling Malignant Hyperthermia
Neurol 104:e213497, Wadhwani,A.R.,et al, 2025

Congenital Titinopathy:Comprehensive Characterization of the Most Severe End of the Disease Spectrum
Ann Neurol 97:611-628, Coppens,S.,et al, 2025

A Toddler with Acute-Onset Hypotonia, Areflexia, and Ataxia
Neurol 104:e213593, Pence, K.L. &Clark, R.A., 2025

Postprocedural Brachial Neuritis:Clinical, Electrodiagnostic, and Neuroimaging Features
AJNR 46:1050-1055, Ambati,V.S.,et al, 2025

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

Efficacy and Safety of IV Thrombolysis for Acute Ischemic Stroke Patients with Moyamoya Disease
Neurol 104:e210243, Chen,H.,et al, 2025

Efficacy and Safety of Sodium Oxybate in Isolated Focal Laryngeal Dystonia:A Phase IIb Double-Blind Placebo-Controlled Cross-Over Randomized Clinical Trial
Ann Neurol 97:329-343, Simonyan,K.,et al, 2025

A 68-YEar-Old Man with Progressive Numbness, Vertigo, and Cognitive Decline
Neurol 104:e213437, Regan,S.M. & Davalos,L.F., 2025

Isolated Primary Central Nervous System Lymphoma of the Optic Nerve, A Case Report and Review of the Literature
Neurologist 29:351-355, Keertana,J.,et al, 2024

Cancer Frequency in MuSK Myasthenia Gravis and Histological Evidence of Paraneoplastic Etiology
Ann Neurol 96:1020-1025, Falso,S.,et al, 2024

A 65-Year-Old Woman with Isolated Macroglossia as the Initial Presentation of a Rare Disease
Neurol 103:e210070, Lara,C.,et al, 2024

Clinicopathologic Conference, Infective Endocarditis Due to Haemophilus Parainfluenza
NEJM 391:2148-2157, Case 38-2024, 2024

Genome Sequencing in the NICU and PICU is Here to Stay
Neurol 104:e210267, Hoffman,E.P. and Kesari,A., 2024

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

A 22-Year-Old Woman with Episodic Weakness and Jaundice
Neurol 103:e210018, Rathinasbapathi,M.,et al, 2024

Clinicopathologic Conference, Myasthenia Gravis
NEJM 391:1441-1450, Case 32-2024, 2024

Diagnosis and Management of ANCA-Associated Vasculitis
Lancet 403:683-698, Kronbichler, A., et al, 2024

Risk of Stroke and Myocardial Infarction Among Initiators of Triptans
JAMA Neurol 81:248-254, Petersen,C.L.,et al, 2024

A 19-Month Old Girl with Infantile-Onset Myopathy and White Matter Changes
Neurol 102:e209258, Lail,G.,et al, 2024

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

Posttransplant Anti-GABAA Receptor Antibody-Associated Autoimmune Encephalitis
Neurol 102:e209245, Togni,C.L.,et al, 2024

Bilateral Hemifacial Spasm and Left Glossopharyngeal Neuralgia Caused by Bilateral Vertebral Artery Displacement
Neurol 102:e209422, Han,Z.,et al, 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

Clinicopathological Conference, Glutamic Acid Decarborylase 65 Autoantibody-Associated Stiff-Person Syndrome
NEJM 390:1712-1719, Case 14-2024, 2024

Intracranial Hypertension Associated with Poly-Cranio-Radicular-Neuropathies A Case Report and Review of the Literature
Neurologist 29:166-169, Eaton,J.E.,et al, 2024

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



Showing articles 50 to 100 of 2814 << Previous Next >>