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Differential
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acanthocytosis
adrenoleukodystrophy
adverse drug reaction
alopecia
anisocoria
anosmia
aphasia
areflexia
Argyll Robertson pupil
arrhythmia, cardiac
ataxia
ataxia, cerebellar
ataxic gait
Babinski sign
baclofen
basal ganglia
basal ganglia, calcification of
basal ganglia, lesion of
basal ganglia, lesion, bilateral
Bassen-Kornzweig syndrome
battered child syndrome
behavioral disorder
bladder dysfunction
blepharospasm
blindness
bradykinesia
brain atrophy
brainstem, atrophy
bulbar palsy
cachexia
calcification, intracranial
cardiomyopathy
caries
CAT scan
CAT scan, abnormal
CAT scan, false negative
cataracts
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebral cortical atrophy
cerebro hepato renal syndrome
cerebrospinal fluid, elevated protein of
cerebrovascular accident
cerebrovascular accident, young adult
children
chorea
choreoathetosis
chorioretinitis
chromosomal abnormality
chromosome 20
chronic progressive external ophthalmoplegia
cisterna magna, enlarged
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
Cockayne's syndrome
conjunctival biopsy
consanguinity
contractures, joint
cornea, abnormal
cornea, opacity of
craniopharyngioma
cry, weak
cryptorchidism
cytochrome c oxidase
cytochrome c oxidase, deficiency
deafmute
deafness
deep gray nuclei
degenerative diseases of CNS
dementia
developmental milestones, loss of
developmental retardation
diabetes insipidus
diabetes mellitus
diarrhea
differential diagnosis
diplegia, spastic cerebral
DNA probes
drug induced neurologic disorders
dwarfism
dysarthria
dysmorphic
dysphagia
dystonia
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electron microscopy
electronystagmography
electroretinograph
enzyme, defect
eye injury
eyes, sunken
facial appearance, abnormal
falling
false negative
false negative VDRL
familial
fasciculation
feeding disorder
fingerprint bodies
fluorescein angiography
fluorescent treponema antibody absorption(FTA-ABS)
foot deformity
Friedreich's ataxia
fundus, abnormality of
funduscopic exam
gait disorder
gargoylism
gastrointestinal motility
gene
gene mutation
genetic linkage
genetic neurologic disorders
glaucoma
globus pallidus
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
growth retardation
Hallervorden Spatz disease
Hallervorden Spatz disease, late onset
Hallgren's syndrome
headache
hearing loss
hearing loss, bilateral
hearing loss, congenital
heart block
Hurler's syndrome
hydrocephalus
hyperpigmentation of skin
hyperreflexia
hypocholesterolemia
hypogonadism
hypoparathyroidism
hyposmia
imbalance
immunofluorescence
inclusion bodies
intellectual deficit
intellectual deterioration
intestinal pseudoobstruction
iris, atrophy of
iron, brain
Kearns-Sayre syndrome
keratoconus
kyphoscoliosis, neurologic causes of
kyphosis
lactic acidemia
Laurence-Moon-Bardet-Biedl syndrome
Leber's hereditary optic neuropathy
Leigh's disease
lens, dislocation of
lenticular nucleus, lesion of, bilateral
leukodystrophy
leukoencephalopathy
light-near dissociation, causes of
macular degeneration
malabsorption
malformation, CNS, congenital
marche a petits pas
Marcus Gunn pupil
MELAS syndrome
memory, impairment of
mental retardation
MERRF syndrome
microcephaly
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, eye of tiger sign
MRI, paramagnetic effect
MRI, serial
mucopolysaccharidoses
muscle atrophy, progressive
myelopathy
myoclonus
myopathy
myopathy, mitochondrial
myopia
nausea and vomiting
neuritis
neurocutaneous disease
neuroichthyosis
neurologic complications of, systemic cancer
neurologic disease, diagnoses of
neurologic signs
neuronal ceroid-lipofuscinosis
neuroophthalmology
neuropathology, brain
neuropathy
neuropathy, ataxic
neuropathy, hereditary peripheral
neuropathy, hypertrophic
neuropathy, onion bulb
neuropathy, peripheral
neurosyphilis
night blindness
nystagmus
nystagmus, pendular
obesity
ocular myopathy
ophthalmoplegia
ophthalmoplegia, progressive external
optic atrophy
optic glioma
optic nerve
optic nerve, neoplasm of
optic neuropathy
optical coherence tomography
palilalia
pancytopenia
PANK2 mutation
paraparesis
paraparesis, spastic
Parkinson disease
Parkinsonism syndrome
PAS positive material in the brain
peroxisomal disease
pes cavus
photosensitivity, skin
phytanic acid
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
polydactyly
polyneuropathy
postural abnormality
progeria
prognosis
progressive neurologic disorder
pseudoretinitis pigmentosa
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
ptosis
pupil
pupil, abnormality in neurologic disorders
pupil, light reflex, abnormal
putamen, lesion of
putamen, lesion of, bilateral
pyramidal tract
pyramidal tract dysfunction
ragged-red fibers
rash
refractive errors
Refsum's disease
retina, abnormal
retinal degeneration
retinal detachment
retinal lesion
retinitis pigmentosa
retinoblastoma
retinopathy
review article
rigidity
roving eye movements
schizophrenia
scotoma
scotoma, central
sea-blue histiocytes
sedimentation rate, elevated
seizure
sensorineural hearing loss
sensory loss
serologic test for syphilis
sheathing of retinal veins
short stature
Sjogren-Larsson syndrome
skin, biopsy
skin, lesions in neurologic disorders
spastic diplegia
spasticity
speech disorder
speech disorder, childhood
Spielmeyer Vogt syndrome
spinocerebellar ataxia type 1
spinocerebellar degeneration
steatorrhea
stooped posture
substantia nigra
sudden death
syphilis, diagnosis and treatment
syphilis, neurologic complications with
syphilis, ocular
tabes dorsalis
Tangier's disease
tapetoretinal degeneration
trauma
treatment of neurologic disorder
tremor
Usher's syndrome
uveitis
vision loss, sequential
vision, failure of in childhood
visual acuity
visual acuity, decreased
visual acuity, decreased, monocular
visual evoked response
visual field defect
visual field defect, altitudinal
visual fields, constricted
visual impairment
visual loss
visual loss, progressive
visual loss, slow
vitamin A
vitamin deficiency
vitamin E
vitamin E deficiency
vitamin K
vitritis
walking, difficulty with
weakness
weight loss
white matter disease
Wolfram syndrome
workup
Showing articles 750 to 800 of 824 << Previous Next >>

Brachial Plexus Injuries
NEJM 291:1059, 1974 & 292, 4285., Leffert,R., 1975

Polymyositis & Dermatomyositis
NEJM 292:344, 1975, 292:403975., Bohan,A.,et al, 1975

Cardiac Features of Unusual X-linked Humeroperoneal Neuromuscular Disease
et al NEJM 293:1017, Waters,D.D., 1975

Progressive Supranuclear Palsy-Case Study
NEJM 293:346, Richardson,E.P., 1975

Limitations & Complications of Myelography, in Myelography
3rd Year Book Med Publ Inc, Chicago, 1975, p. 455-462., Shapiro,R., 1975

Quadriceps Myopathy-Entity or Syndrome
Arch Neurol 31:60, Boddie,H.,et al, 1974

Transient Benign Unilateral Pupillary Dilation in Young Adults
Arch Neurol 31:12-14, Edelson,R.N.,et al, 1974

Wyburn-Mason Syndrome, Report of Two Cases Without Retinal Involvement
Arch Neurol 28:67-68, Brown,D.G.,et al, 1973

Placoid Pigment Epitheliopathy With Swelling of the Optic Disks
Arch Neurol 29:204-205, Jenkins,R.B.,et al, 1973

Case Records of MGH-NEJM 289:366
1973 Tuberculoma of Cerebral hemisphere & Brain Stem., , 1973

Epidemiology of Motor-Neuron Diseases
NEJM 288:1047, Bobwick,A.R.,et al, 1973

Visual Symptoms in the Migraine Syndrome
Neurol 23:570, Hachinski,V.,et al, 1973

Pathology of Malignant Hyperpyrexia
BMJ Editorial 249, 1973, Feb., , 1973

Possible Neurogenic Factor in Muscular Dystrophy:Its Similarity to Denervation Atrophy
JNNP 36:399-410, Dastur,D.K.,et al, 1973

Neurologic Manifestations of Rheumatic Fever
Postgrad Med 54:82, Aita,J.A., 1973

Air Embolism Complicating Percutaneous Needle Biopsy of the Lung
Chest 63:108-110, Westcott,J.L., 1973

The Facioscapulohumeral Synd, in Clinical Studies in Myology, Amsterdam, Excerpta Medica
p498-501, VanWijngaarden,G.K.&Bethlem,J., 1973

Neurologic Manifestations of Periarteritis Nodosa (1972)
Nebraska Med J 57:326, Aita,J.A., 1972

Congenital Dystrophia Myotonica
Neurol 22:443, Dyken,P.D., 1972

Preclinical Detection of Dystrophia Myotonica
BMJ 124, 1972 April., , 1972

Corneal Opacification in Infancy
MCV Quart 8:230, Ching,F., 1972

Mollaret's Meningitis & Differential Diagnosis of Recurrent Meningitis
Am J Med 52:128, Hermans,P.,et al, 1972

Isolated Ophthalmic Migraine:Its Frequency, Mechanism & Diff. Diagnosis
Neuro-Ophthalmol 1972-Bascom Palmer Instit Symp, Ed, J. S. Smith., Hedges,T., 1972

Diphenylhydantoin for Myotonia Congenita-Correspondence
NEJM 286:893, , 1972

Retinal Ischemic Symptoms in Cardiovascular Diagnosis
Postgrad Med 85, Oct 1972., Hoyt,W., 1972

Optic Disc Vasculitis
Br J Ophthalmol 56:652, Hayreh,S., 1972

Thalmic Neuronal Inclusion Disease
Neurol 22, 3961972., Segarra,J., 1972

Peripheral NR. Injuries & their Repairs
Surg Clin North Am Oct 1972., , 1972

Mucopolysaccaridosis IV (Morquio Syndrome) , in Heritable Disorders of Connective Tissue
(Ed) 4th Ed, The C. V. Mosby Co, St. Louis, p. 583, McKusick,V.A., 1972

Ophthalmoplegia In Myotonic Dystrophy
Am J Ophthalmol 71:1231-1235, Lessell,S.,et al, 1971

Electrodiagnosis of Neuromuscular Disease
Bull Univ Maryland School Med 56:33, Kemble,F., 1971

"Sick"Motoneurones A Unifying Concept of Muscle Disease
Lancet 321, 1971 Feb., McComas,A.J.,et al, 1971

Neurological Involvement in SLE
Singapore Med J 12:18, Tay,C.H.,et al, 1971

Comprehensive Mangagement of Duchenne Muscular Distrophy
Arch Phys Med & Rehab Mar 1971, pp110., Johnson,E.,et al, 1971

Acute Chorioretinal Infarction in Sickle Cell Trait
Arch Ophthalmol 84:485, Stein,M.,et al, 1970

The Nervous System in Sickle Cell Disease
Afr J Med Sci 1:33, Adelove,A.,et al, 1970

Retinal Lesions in Subacute Sclerosing Panencephalitis
Arch Ophthalmol 84:6l3, Nelson,D.,et al, 1970

Complains of Muscle Weakness
Patient Care Clinical Concepts, 21, 1970 Jan., , 1970

Early Recognition of Heterozygotes for the Gene for Dystrophia Myotonica
JNNP 33:279, Bundey,S.,et al, 1970

Chronic Progressive External Ophthalmoplegia
Arch Ophthalmol 82:845, Daroff,R., 1969

Chronic Spinal Muscular Atrophy in Adults
J Neurol Sci 9:527, Meadows,J.C.,et al, 1969

Ocular Myopathy
Arch Neurol 20:1, Magora,A.,et al, 1969

Whipple's Disease & Papilledema
Arch Int Med 123:74, Switz,D.M.,et al, 1969

Ophthalmic Complications in General MedicalDisorders
Trans Opthal Soc of United Kingdom 89:167, Russell,R., 1969

Biochemical Abnormalities of the Sarcoplasmic Reticulum in Muscular Dystrophy
NEJM 290:184, Samaha,F.,et al, 1969

The Use of Serum Lactate Dehydrogenase Isoenzymens in the Diagnosis of Muscle Disease
Neurol 19:26, Hooshmard,H.,et al, 1969

Neurogenic Muscular Atrophy Simulating Facioscapulohumeral Muscular Dystrophy
J Neurol Sci 9:389, Furukawa,T.,et al, 1969

Nine Neuropathies
Med Ann of the Dist of Columbia 37:89, Stevens,H., 1968

Whipple's Disease Presenting with Ocular Inflammation & Minimal Intestinal Symptoms
John's Hopkin's Med Jour 123:175, Knox,D.L.,et al, 1968

Progressive Ophthalmoplegia
Arch Neurol 19:362, Rosenberg,R.,et al, 1968



Showing articles 750 to 800 of 824 << Previous Next >>