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Differential
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abdominal distention
acid maltase deficiency
acid maltase deficiency, adult
advances in neurology
adverse drug reaction
afebrile
amyloidosis
anesthesia, general
aneurysm
anterior horn cell disease
anti MAG antibodies
anticonvulsants
areflexia
arrhythmia, cardiac
asymptomatic
autism
autoimmune disease
bulging of biceps
calf hypertrophy
carbamazepine
carcinoma
cardiomegaly
cardiomyopathy
cardiovascular disease
CAT scan
CAT scan, abnormal
CAT scan, emission, abnormal
central nervous system, infection of
cerebral cortical encephaliis
chewing, impaired
children
chromosome 17
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
corticotropin level
corticotropin-releasing factor
cortisol, elevated
cotton-wool spots
cranial nerve enhancement
cranial nerve enlargement
cranial nerve palsies
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
Cushing's syndrome
cysticercosis, cerebral
cysticercosis, disseminated
cysticercosis, intraventricular
cysticercosis, miliary
delay in diagnosis
denervation of muscle
developmental retardation
diabetes mellitus
diagnostic criteria
diamond on quadriceps
diaphragmatic paralysis
differential diagnosis
difficulty climbing stairs
dilantin
diplopia
distal muscle atrophy
distal muscle weakness
dysferlinopathy
dysplasia of C.N.S.
dyspnea
dystonia
dystonia, post traumatic
dystrophin
dystrophin associated proteins
echocardiogram, LVH
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
electron microscopy
empty sella
entrapment neuropathy
enzyme, defect
epidermal nevus syndrome
Epstein-Barr virus
exercise
exophthalmus
eye, pain in
facial hair, excessive
facial pain
facial pain, atypical
facial weakness
falling
false positive
familial
fatigue
fever
fine motor function, impaired
foot drop
gait disorder
gait, waddling
gender
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
globe, flattened posteriorly
Gowers maneuver
headache
hearing loss
heart murmur
hemiatrophy, congenital
hemidiaphragm, paralysis of
hemihypertrophy, congenital
hemihypertrophy, facial
hemimegalencephaly
hemiparesis
hepatomegaly
heralding manifestation
hereditary myopathy with early respiratory failure
heterotopia
hirsutism
histochemistry
hoarseness
hypercalcemia
hypertension
hypokalemia
hypomelanosis of Ito
hypopigmentation of skin
hypothyroidism
inability to sit up
infantile spasm
infectious mononucleosis
infectious mononucleosis, neurologic findings with
intellectual deficit
intracranial hypertension, benign
intracranial hypertension, benign, differential diagnosis
intracranial hypertension, benign, pathogenesis of
Isaacs syndrome
Kobberling-Dunnigan syndrome
Kugelberg-Welander syndrome
learning disability
learning disability, in children
leg swelling
leukocytosis
life expectancy
limb hypertrophy
limb-girdle weakness
lipodystrophy
liver function enzymes
lordosis
lymphadenopathy
lymphopenia
macrocephaly
malformation, CNS, congenital
malignant hyperpyrexia
malignant optic glioma of adulthood
mental retardation
mental status, abnormal
metabolic alkalosis
mexiletine
misdiagnosis
molecular genetics
monoclonal gammopathy
mononeuropathy
motor neuron disease
movement disorder
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, muscle
MRI, orbit
MRI, venography
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
myelitis
myelitis, transverse
myoedema
myoglobinuria
myokymia
myopathy
myopathy, amyloid
myopathy, focal
myopathy, hereditary
myopathy, metabolic
myopathy, monomelic
myopathy, quadriceps
myopathy, vacuolar
myostatin
myotonia
myotonia congenita
nausea and vomiting
neoplasm, hormone producing, ectopic
nerve conduction studies
nerve injury
neurocutaneous disease
neuroendocrinology
neuroinfectious diseases
neurologic disease, diagnoses of
neurologic examination
neuromyotonia
neuropathy
neuropathy, hereditary peripheral
neuropathy, peripheral
night sweats
obesity
optic chiasm, lesion of
optic disc
optic disc edema
optic glioma
optic nerve sheath enhancement
optic nerve, enhancement
optic nerve, enlarged
optic nerve, neoplasm of
optic nerve, tortuosity
optic neuritis
optic neuropathy, ischemic
optic neuropathy, ischemic, anterior
optical coherence tomography
orthopnea
pain
pain, leg
palpitations
percussion induced muscle contraction
perineuritis
phakomatoses
plasma cell dyscrasia
polyneuropathy
post polio syndrome
postural abnormality
prenatal diagnosis by amniocentesis
prognosis
progressive neurologic disorder
proximal muscle atrophy
pseudohypertrophy
pseudomyotonia
ptosis
pulmonary embolism
pupil, tonic
radiculopathy
Red flags
respiratory failure
review article
rhabdomyolysis
rippling muscle disease
root lesion, nerve
sarcoglycan
sarcoglycanopathy
sciatic neuropathy
scoliosis
scotoma, central
seizure
shoulder, elevation
skin, lesions in neurologic disorders
speech disorder, childhood
speech, delayed development of
spinal accessory nerve
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, intermediate form
splenomegaly
steppage gait
steroid
steroid therapy, CNS treatment and complications with
strokelike episodes
subarachnoid hemorrhage
subcutaneous nodules
survival motor neuron gene
syringomyelia
systemic illness
telangiectases, retinal
third nerve palsy
thirst
tinnitus
titinopathy
toe walking
tongue, enlarged
tongue, weakness
trauma
treatment of neurologic disorder
tripping
urinary frequency
urine, dark
visual acuity, decreased, monocular
visual loss
visual loss, progressive
visual loss, slow-unilateral
visual symptoms
vital capacity
weakness
weakness, progressive
weakness, proximal
web sites
weightlifting
wheelchair
winging of scapula
workup
Showing articles 1300 to 1350 of 1609 << Previous Next >>

Surgical Treatment of Intractable Neonatal-Onset Seizures:The Role of Positron Emission Tomography
Neurol 38:1178-1188, Chugani,H.T.,et al, 1988

Disconnection & Cerebral Metabolism, The Case of Conduction Aphasia
Arch Neurol 45:275-279, Kempler,D.,et al, 1988

Clinicopath Conf
Leukemia, Mycotic Aneurysm, Asperigillosis, Subarachnoid Hemorrhage, Fungal Intracran Aneurysm, Case, 7-198M 319:427-440,1988., 1988

Immunotherapy of Multiple Sclerosis
Ann Neurol 23:211-223, Weiner,H.L.&Hafler,D.A., 1988

Vertebral Osteomyelitis Presenting as Spinal Compression Fracture, Six Pts with Underlying Osteoporosis
Arch Int Med 148:417-423, McHenry,M.C.,et al, 1988

Infantile Gaucher's Disease:A Case with Neuronal Storage
Ann Neurol 23:300-303, Grafe,M.,et al, 1988

Treatment of Epidural Cord Compressions from Hodgkin's Disease with Chemotherapy
Am J Med 84:555-558, Burch,P.A.&Grossman,S.A., 1988

Neonatal Brain Tumors:CT & MR Findings
J Comput Assist Tomogr 12:10-20, Radkowski,M.A.,et al, 1988

Recurrent Fever of Unknown Origin, Coma, & Meningismus Due to a Leaking Craniopharyngioma
Am J Med 84:543-545, Krueger,D.W.&Larson,E.B., 1988

Cerebellar & Brainstem Hypometabolism in Olivo-pontocerebellar Atrophy Detected with Positron Emission Tomography
Ann Neurol 23:223-230, Gilman,S.,et al, 1988

Clinicopath Conf
Dermoid Cyst of Left Frontal Lobe, Case Record 17-1988, NEJM 318:316-322988., , 1988

Brain Glucose Metabolism in Thalamic Syndrome
JNNP 51:427-428, Laterre,E.C.,et al, 1988

Predictive Value of Resting Electrocardiograms for 12-Year Incidence of Stroke in the Honolulu Heart Program
Stroke 19:555-559, Knutsen,R.,et al, 1988

Cerebral Hypometabolism in Progressive Supranuclear Palsy Studied with Positron Emission Tomography
Ann Neurol 24:399-406, Foster,N.L.,et al, 1988

Dementia in Down's Syndrome:Cerebral Glucose Utilization, Neuropsychological Assessment, and Neuropathology
Neurol 38:938-942, Schapiro,M.B.,et al, 1988

Septic Thrombosis of the Cavernous Sinuses
Arch Neurol 45:567-572, DiNubile,M.J., 1988

Diffuse Lewy Body Disease and Progressive Dementia
Neurol 38:1520-1528, Burkhardt,C.R.,et al, 1988

An Adolescent with Intermittent Headache, Transient Hemiparesis, and Urinary Abnormalities
J Pediatr 113:769-776, Gruskin,A.B.&Chang,C., 1988

Lyme Disease:Acute Focal Meningoencephalitis in a Child
Pediatrics 82:931-934, Feder,H.M.,et al, 1988

Brain Metabolism in Mitochondrial Encephalomyopathy:A PET Study
J Comput Assist Tomogr 12:854-857, DeVolder,A.,et al, 1988

Dysphagia in Inclusion Body Myositis
JNNP 51:1542-1545, Wintzen,A.R.,et al, 1988

Positron Emission Tomography-A New Approach to Brain Chemistry
JAMA 260:2704-2710, Jacobson,H.G., 1988

Cholesterol Crystal Embolization:A Review of 221 Cases in the English Literature
Angiology 38:769-784, Fine,M.J.,et al, 1987

Bilateral Retrobulbar Optic Nerve Infarctions After Blood Loss & Hypotension, A Clinicopath Case Study
Ophthalmol 94:1577-1584, Johnson,M.W.,et al, 1987

Computed Tomography and Magnetic Resonance Imaging in the Diagnosis of Inflammatory Disease of the Optic Nerve
Surv Ophthalmol 31:352-355, McCrary,J.A.,et al, 1987

Intramedullary Spinal Cord Metastasis, Diagnostic & Therapeutic Considerations
Arch Neurol 44:526-531, Winkelman,M.D.,et al, 1987

Normal Caudate Glucose Metabolism in Persons at Risk for Huntington's Disease
Arch Neurol 44:254-257, Young,A.B.,et al, 1987

Mamillary Body Atrophy in Wernicke's Encephalopathy:Antemortem Identification Using MRI
Ann Neurol 22:595-600, Charness,M.E.&DeLaPaz,R.L., 1987

Primary Progressive Aphasia-Differentiation from Alzheimer's Disease
Ann Neurol 22:533-534, Mesulam,M.M., 1987

Assessment of Therapy for Toxoplasma Encephalitis
The TE Study Group, Am J Med 82:907-9141987., , 1987

Aortic Dissection
NEJM 317:1060-1067, DeSanctis,R.W.,et al, 1987

Analysis of Risk Factors for Stroke in a Cohort of Men Born in 1913
NEJM 317:521-526, Welin,L.,et al, 1987

The Combined Use of Positron Emission Tomography & DNA Polymorphisms for Preclinical Detection of Huntington's Disease
Neurol 37:1441-1447, Hayden,M.R.,et al, 1987

Wilson's Disease Studies with FDG & Positron Emission Tomography
Neurol 37:1707-1711, Hawkins,R.A.,et al, 1987

Total Lymphoid Irradiation in Multiple Sclerosis:Blood Lymphocytes & Clinical Course
Ann Neurol 22:634-638, Cook,S.D.,et al, 1987

Back Pain & Spinal Deformity in Cystic Fibrosis
Am J Dis Child 141:1313-1316, Rose,J.,et al, 1987

Neurologic Manifestations of AIDS
Medicine 66:407-437, McArthur,J.C., 1987

The Spectrum of Neurol Dis Assoc with Antiphospholipid Antibd, Lupus Anticoag & Anticardiolipin Antibd
Arch Neurol 44:876-883, Levin,S.R.&Welch,K.M.A., 1987

Neurologic Abnormalities & Recovery of Human Immunodeficiency Virus from Cerebrospinal Fluid
Ann Int Med 106:692-695, Hollander,H.&Levy,J.A., 1987

Human Immunodeficiency Virus-Associated Meningitis, Clinical Course & Correlations
Am J Med 83:813-816, Hollander,H.&Stringari,S., 1987

Practical Problems in the Respiratory Care of Patients with Muscular Dystrophy
NEJM 316:1197-1205, Smith,P.E.M.,et al, 1987

Spectrum of Inclusion Body Myositis
Arch Neurol 44:1154-1157, Ringel,S.P.,et al, 1987

Neuropathologic & Clinical Features of Parkinson's Disease in Alzheimer's Disease Patients
Neurol 37:754-760, Ditter,S.M.&Mirra,S.S., 1987

Parkinson's Disease & Megacolon:Concentric Hyaline Inclusions (Lewy Bodies) in Enteric Ganglion Cells
Neurol 37:1253-1255, Kupsky,W.J.,et al, 1987

Convulsions in Childhood Shigellosis, Clinical & Laboratory Features in 153 Children
Am J Dis Child 141:208-210, Ashkenazi,S.,et al, 1987

Metabolic & Clinical Correlates of Acute Ischemic Infarction
Neurol 37:1103-1110, Kushner,M.,et al, 1987

Cervical Epidural Abscess
Neurol 37:1747-1753, Lasker,B.R.&Harter,D.H., 1987

Positron Emission Tomography Studies of Cerebral Glucose Metabolism in Chronic Partial Epilepsy
Ann Neurol 22:480-486, Abou-Khalil,B.W.,et al, 1987

Natural History of Fever Following Seizures
Arch Int Med 147:1153-1155, Wachtel,T.J.,et al, 1987

Complex Partial Status Epilepticus Presenting as Fever of Unknown Origin
Arch Int Med 147:1571-1572, Semel,J.D., 1987



Showing articles 1300 to 1350 of 1609 << Previous Next >>