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acid maltase deficiency
acid maltase deficiency, adult
advances in neurology
amyloidosis
anesthesia, general
aneurysm
anterior horn cell disease
areflexia
arrhythmia, cardiac
asymptomatic
bulging of biceps
calf hypertrophy
cardiomegaly
cardiomyopathy
cardiovascular disease
CAT scan
children
chromosome 17
clubfoot as related to neurologic disease
complications
congenital myopathy
congestive heart failure
contractures, joint
creatine phosphokinase(CPK)elevated
delay in diagnosis
developmental retardation
diabetes mellitus
diagnostic criteria
diamond on quadriceps
diaphragmatic paralysis
differential diagnosis
difficulty climbing stairs
dilantin
distal muscle atrophy
distal muscle weakness
dysferlinopathy
dyspnea
dystrophin
dystrophin associated proteins
electromyogram
electron microscopy
enzyme, defect
exercise
facial weakness
falling
familial
fine motor function, impaired
foot drop
gait disorder
gait, waddling
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
Gowers maneuver
hearing loss
hemidiaphragm, paralysis of
hepatomegaly
hereditary myopathy with early respiratory failure
histochemistry
hoarseness
hypercalcemia
hypothyroidism
inability to sit up
Isaacs syndrome
Kobberling-Dunnigan syndrome
Kugelberg-Welander syndrome
learning disability
learning disability, in children
life expectancy
limb-girdle weakness
lipodystrophy
liver function enzymes
lordosis
misdiagnosis
molecular genetics
monoclonal gammopathy
motor neuron disease
MRI, muscle
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
myoedema
myoglobinuria
myokymia
myopathy
myopathy, amyloid
myopathy, focal
myopathy, hereditary
myopathy, metabolic
myopathy, monomelic
myopathy, quadriceps
myopathy, vacuolar
nerve conduction studies
neurologic disease, diagnoses of
neurologic examination
neuromyotonia
orthopnea
percussion induced muscle contraction
plasma cell dyscrasia
prenatal diagnosis by amniocentesis
prognosis
progressive neurologic disorder
proximal muscle atrophy
pseudohypertrophy
pseudomyotonia
radiculopathy
respiratory failure
review article
rhabdomyolysis
rippling muscle disease
sarcoglycan
sarcoglycanopathy
sciatic neuropathy
scoliosis
speech disorder, childhood
speech, delayed development of
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, intermediate form
steppage gait
steroid therapy, CNS treatment and complications with
subarachnoid hemorrhage
survival motor neuron gene
systemic illness
telangiectases, retinal
titinopathy
toe walking
tongue, enlarged
tongue, weakness
treatment of neurologic disorder
tripping
urine, dark
vital capacity
weakness
weakness, progressive
weakness, proximal
web sites
wheelchair
winging of scapula
workup
Showing articles 100 to 135 of 135 << Previous

Gliomas of the Anterior Visual Pathway
Surv Ophthalmol 38:427-452, Dutton, J., 1994

The Nondystrophic Myotonias
In Myology, McGraw-Hill, 2nd Ed, Ch49, p1291-13024., Rudel,R.,et al, 1994

Predictive Value of Clin Hx & EKG in Pts with TIA or Minor Stroke for Sub Cardiac & Cerebral Ischemic Events
Arch Neurol 51:333-341, Pop,G.A.M.,et al, 1994

Left Ventricular Mass and Risk of Stroke in an Elderly Cohort:The Framingham Heart Study
JAMA 272:33-36, 711994., Bikkina,M.,et al, 1994

Orbital and Optic Pathway Sarcoidosis:MR Findings
AJNR 15:775-783, Carmody,R.F.,et al, 1994

Pseudotumor Cerebri:CT Findings and Correlation with Vision Loss
AJR 160:143-146, Gibby,W.A.,et al, 1993

Idiopathic, Progressive Mononeuropathy in Young People
Arch Neurol 50:20-23, Engstrom,J.W.,et al, 1993

Asymptomatic Nerve Hypertrophy in Lepromatous Leprosy:A Clin Electrophysiolog & Morphol Study
J Neurol 239:367-374, Tzourio,C.,et al, 1992

Hypomelanosis of Ito
Editorial, Lancet 339:651-6521992., , 1992

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

MR Fat Suppression Combined with Gd-DTPA Enhancement in Optic Neuritis and Perineuritis
J Comput Assist Tomogr 15:223-227, Tien,R.D.,et al, 1991

Risk Factors for Stroke in Middle Aged British Men
BMJ 302:1111-1114, Shaper,A.G.,et al, 1991

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

Optic Nerve Sheath Hemorrhage
In Walsh & Hoyt's Clinical Neuro-ophthalmology, Williams & Wilkins, Baltimore, Vol4, p. 2082-2085, 2, 52-2454, 19Miller, N. R., 1991

Magnetic Resonance Imaging of Radiation Optic Neuropathy
Am J Ophthalmol 110:389-394, Zimmerman,C.F.,et al, 1990

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

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

Surgical Treatment of Progressive Visual Loss in Traumatic Optic Neuropathy, Report of Two Cases
J Neurosurg 70:799-801, Guy,J.,et al, 1989

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

Chronic Unilateral Optic Neuropathy:A Magnetic Resonance Study
Ann Neurol 24:3-11, Eidelberg,D.,et al, 1988

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

Polyarteritis Manifesting as Calf Myositis & Fever
Am J Med 80:312-315, Ferreiro,J.E.,et al, 1986

The Value of Visual Evoked Potential as a Screening Test in Neurofibromatosis
Arch Neurol 42:1072-1074, Jabbari,B.,et al, 1985

Hypertrophic Neuropathy & Multiple Sclerosis
Neurol 33:1361-1364, Rosenberg,N.L.,et al, 1983

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

Bilateral Vocal Cord Paralysis in a Patient With Familial Hypertrophic Neuropathy
Arch Neurol 38:532, Johnson,J.A.,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

Dejerine-Sottas Disease Revisited
Arch Neurol 37:67-68, Stran,R., 1980

Bilateral Involvement of the Lateral Cutaneous Nerve of Calf in a Diabetic
Ann Neurol 4:480-481, Finelli,P.F.,et al, 1978

Cervical Myelographic Changes in Hypertrophic Interstitial Polyneuropathy
Ann Neurol 2:83, Hammerschlag,S.B.,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

Electocardiographic Left Ventricular Hypertrophy & Risk of Coronary Heart Disease
Ann Int Med 72:813, Kannel,Wm.,et al, 1970



Showing articles 100 to 135 of 135 << Previous