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Differential
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abducens nerve paralysis, bilateral
acanthocytosis
advances in neurology
adverse drug reaction
amniocentesis
ANA
arrhythmia, cardiac
ataxia
ataxia, cerebellar
atrial fibrillation
autoimmune disease
baldness
basal ganglia, calcification of
Bassen-Kornzweig syndrome
blindness
brainstem, lesion of
brainstem, tuberculoma of
calf hypertrophy
cancer of colon
carcinoma
carcinoma of ovary
carcinoma of pancreas
carcinoma of uterus
cardiomyopathy
CAT scan, abnormal
cataracts
central nervous system, infection of
cerebral cortical atrophy
cerebral palsy
cerebrovascular accident
cerebrovascular accident, young adult
chemosis
children
chromosomal abnormality
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
Cockayne's syndrome
collagen vascular disease
complications
congenital birth defects
congenital heart disease
congestive heart failure
conjunctival injection
consanguinity
contractures, joint
cornea, abnormal
creatine phosphokinase(CPK)elevated
deafmute
deafness
degenerative diseases of CNS
delay in diagnosis
dementia
dermatomyositis
developmental disability
developmental milestones
developmental retardation
diabetes mellitus
diagnostic criteria
difficulty climbing stairs
digitalis intoxication
disability, neurological
distal muscle weakness
dropped head syndrome
dwarfism
dysphagia
dysthyroid ocularmyopathy
dystonia
dystroglycanopathies
dystrophin
edema, periorbital
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electromyogram
Emery-Dreifuss muscular dystrophy
enzyme, defect
enzyme, muscle disease
enzyme, serum
epidemiology of neurology
extraocular muscle enlargement
eye, pain in
Fabry's disease
face, numbness of
facial appearance, abnormal
facial weakness
falling
familial
fetal movements, reduced
fetus
fine motor function, impaired
Fisher C.M.
floppy infant
fragile-X syndrome
Friedreich's ataxia
frontal balding
gait disorder
gargoylism
gaze palsy, horizontal
gene
gene mutation
gene therapy
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
glaucoma
glioma
Gowers maneuver
Graves ophthalmopathy
Hallgren's syndrome
headache
hearing loss
heart block
heart murmur
hemianopia, homonymous
high arched palate
hippus
histochemistry
histochemistry of muscle
Huntington's chorea
Hurler's syndrome
hyperthyroidism
hypoglycorrhachia
hypotonia
hypotonia, infants
immunologic disease
immunosuppressive agents
inclusion bodies, intracytopasmic
inclusion bodies, intranuclear
intestinal pseudoobstruction
joint hypermobility
Kearns-Sayre syndrome
keratoconus
Laurence-Moon-Bardet-Biedl syndrome
learning disability
learning disability, in children
Leber's hereditary optic neuropathy
Leigh's disease
leukodystrophy
life expectancy
lipid storage disorder of CNS
liver function enzymes
malformation, CNS, congenital
malignancy screen
medulla oblongata, lesion of
MELAS syndrome
meningitis
meningitis, TB
mental retardation
merosin
MERRF syndrome
metachromatic leukodystrophy
methotrexate
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
mitral valve prolapse
molecular genetics
MRI
MRI, abnormal
MRI, disappearing lesion on
MRI, serial
mucopolysaccharidoses
muscle biopsy
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, cardiovascular changes with
muscular dystrophy, central nervous system abnormality
muscular dystrophy, classification
muscular dystrophy, congenital
muscular dystrophy, congenital, Fukuyama type
muscular dystrophy, congenital, Ullrich
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
muscular dystrophy, neurogenic hypothesis of
myelopathy
myocarditis
myoclonus
myoglobinuria
myopathy
myopathy, inflammatory
myopathy, mitochondrial
myopathy, steroid induced
myopia
myositis
myotonia
myotonia dystrophica
myotonia dystrophica, classification
neck weakness
neoplasm, metastatic to CNS
neoplasm, primary intracerebral
neoplasm, primary intracranial
neoplasm, primary of CNS
neuritis
neurofibromatosis 1
neurologic complications of, systemic cancer
neurologic disease
neurologic disease, diagnoses of
neuronal migration disorder
neuropathy
nystagmus
nystagmus, vertical
obesity
obicularis oculi, weakness of
occipital lobe, lesion of
ocular myopathy
one and a half syndrome
ophthalmoplegia
ophthalmoplegia, painful
ophthalmoplegia, plus syndrome
optic disc edema
optic neuritis
optic neuropathy
orbit, lesions of
ovarian tumor
pancytopenia
photophobia
photophobia, central
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
poliomyelitis
polydactyly
polymerase chain reaction
polymerase chain reaction, false negative
polymerase chain reaction, false positive
polymyositis
pons, lesion of
prenatal diagnosis by amniocentesis
prognosis
progressive neurologic disorder
proptosis
proptosis, bilateral
pseudoretinitis pigmentosa
psychiatric disorder
psychiatric problems in neurologic disorders
ptosis
ptosis, bilateral
pulmonary infiltrates
pupil, abnormality in neurologic disorders
pupil, dilated and fixed, bilateral
pupil, dilated and fixed, unilateral
quality of life
ragged-red fibers
rash
Raynaud's phenomenon
respirator
respiratory failure
retinitis pigmentosa
retinopathy
review article
risk factors
schizophrenia
scintillations
scleroderma
scleroderma, neurologic involvement with
scoliosis
scoliosis, neurologic association with
screening
sedimentation rate
seizure
sensorineural hearing loss
short stature
skin, lesions in neurologic disorders
skin, tight
speech disorder, childhood
speech, delayed development of
Spielmeyer Vogt syndrome
spinal cord, neoplasm
spinocerebellar degeneration
steroid
steroid therapy, CNS treatment and complications with
suck, poor
sudden death
syringomyelia
systemic illness
Tay-Sachs disease
tongue, fasciculations of
treatment of neurologic disorder
trinucleotide repeats
tripping
tuberculoma of CNS
tuberculosis
tuberculosis, miliary
Usher's syndrome
viral infection, CNS
visual field defect
visual fields, constricted
visual loss
Walker-Warburg syndrome
walking, difficulty with
weakness
weakness, congenital
weakness, generalized
weakness, progressive
weight loss
white matter disease
xanthopsia
X-linked bulbospinal neuronopathy
Showing articles 150 to 200 of 15699 << Previous Next >>

Cerebro-ocular Dysgenesis (Walker-Warberg Syndrome) :Neuropathologic & Etiologic Analysis
Neurol 34:1531-1541, Williams,R.S.,et al, 1984

Computed Tomographic Patterns of Muscles in Neuromuscular Diseases
Arch Neurol 41:383-387, Hawley,R.J.,et al, 1984

Duchenne Muscular Dystrophy:Carrier Detection by Ultrasound & Computerised Tomography
Lancet 2:1199-1200, Rott,H., 1983

Families with Myotonic Dystrophy with & without Cardiac Involvement
Arch Int Med 143:2134-2136, Hawley,R.J.,et al, 1983

Oligoclonal IgG Bands in Cerebrospinal Fluid in Various Neurological Diseases
Ann Neurol 13:434-439, Chu,A.B.,et al, 1983

Myotonic Dystrophy, Mitral Valve Prolapse, and Cerebral Embolism
Stroke 13:93-94, Morris,L.K.,et al, 1982

External Carotid-Cavernous Sinus Fistula Simulating Unilateral Graves Ophthalmopathy
J Comput Assist Tomogr 6:1006-1009, Merlis,A.L.,et al, 1982

Facioscapulohumeral Dystrophy Associated with Hearing Loss & Coats Syndrome
Ann Neurol 12:395-398, Taylor,D.A.,et al, 1982

Santavuori Disease:Diagnosis by Leukocyte Ultrastructure
Neurol 32:1277-1281, Baumann,R.J.,et al, 1982

The Reflex Sympathetic Dystrophy Syndrome (RSDS)
Am J Med 70:23-30, Kozin,F.,et al, 1981

Olivopontocerebellar Atrophy in Children:A Report of Seven Cases in Two Families
Ann Neurol 10:355-363, Colan,R.V.,et al, 1981

Echocardiographic Evaluation of Cardiac Abnormalities in Duchenne's Dystrophy & Myotonic Muscular Dystrophy
Arch Neurol 37:273-277, Reeves,W.C.,et al, 1980

Retraction of the Lower Eyelid
Neurol 29:386-389, Cohen,M.M.,et al, 1979

Emery-Dreifuss Muscular Dystrophy
Ann Neurol 5:111-117, Rowland,L.P.,et al, 1979

Haemophilic Neuromyopathy
JNNP 42:600-605, Defaria,C.R.,et al, 1979

Remission of a Syndrome Indistinguishable from Motor Neuron Disease after Resection of Bronchial Carcinoma
BMJ 2:176-177, , 1979

Clinical Pathological Conference
Neuronal Veroid-lipfuscinosis, Juvenile Variant, (Batten's disease) , NEJM 299:189., , 1978

Abnormal Iris Vasculature in Myotonic Dystrophy
Arch Neurol 35:224, Stern,L.Z.,et al, 1978

Juvenile Amaurotic Idiocy (Neuronal Ceroid Lipofuscinosis) & Lymphocyte Fingerprint Profiles
Ann Neurol 4:531-536, Baumann,R.J.,et al, 1978

Neurological Complications of Infections of the Head & Neck
Otolaryng Clin North Am 9:729, Kaplan,R.J., 1976

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

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

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

Neurological Problems in Endocrine Diseases
Med Clin North Am 56:1029, Dale,A., 1972

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

Parietal Lobe Syndromes
In Handbk of Clinical Neurology, Vinken & Bruyn, Ed, North-Holland Publ Co, Amsterdam, V2, Ch21, p., 84wesbury,E.C.O., 1969

Rubella, Clinical Manifestations & Management
Am J Dis Child 118:18-29, Cooper,L.Z.,et al, 1969

The Remote Effects of Cancer on the Nervous System
Proc Roy Soc Med 60:683, Wilkinson,M., 1967

Clinical Cases-Dx:Functional Approach to Neuroanatomy pp 477-490 Earl Lawrence House
McGraw Hill 1967., , 1967

Diseases of Muscles-Clinical Manifestations & Differential Diagnosis
The New Physic 263, 1967, Oct., Boshes,L., 1967

Neuro CPC of MGH
Cervical Spondylosis with Protruded Disk, NEJM 261:715-7201959., , 1959

Localization of Lesions Causing Horner's Syndrome
Arch Ophthamol 44:710, Jaffe,N., 1950

Five Types of Dystrophy
Together with Other Conditions Producing Insidious Muscle Weakness-Table 1-Hospital Med p. 60., , 1850

Congenital Zika Syndrome
NEJM 394:e2, Bacin,F. & Montenegro,M.A., 2026

A 41-Year-Old Man with Steroid-Responsive Hemiparesis
Neurol 106:e214088, Obaidi,Z.A.,et al, 2026

Reversible Leukoencephalopathy and Parkinsonism Due to CNS Involvement in Cryoglobulinemia
Neurol 106:e214622, German,A.,et al, 2026

Progressive Quadriparesis and Falls in a 66-Year-Old Man With Longstanding Human Immunodeficiency Virus
Neurol 106:e214621, Ong,B.A. & Carlson,A.K., 2026

Clinicopathologic Conference, Disseminated Infection with Hypervirulent Klebsiella Pneumoniae
NEJM 394:282-294, Case 202026, 2026

Clinicopathologic Conference, Lyme Neuroborreliosis and Coinfection with Babesia Microti
NEJM 394:383-391, Case 3-2026, 2026

Mucormycosis
NEJM 394:684-698, Kontoyiannia,D.P. & Walsh, T.J., 2026

Treatment for Brain Metastases with Stereotactic Radiation vs Hippocampal-Avoidance Whole Brain Radiation, A Randomzid Clinical Trial
JAMA doi.10.1001/JAMA.2026.0076;2026, Aizer,A.A.,et al, 2026

Unilateral Primary Angiitis of the Central Nervous System: A Rare and Under-Recognized Entity
AJNR 47:589-595, Rai,P.,et al, 2026

Brain CT for Diagnosis of Intracranial Disease in Ambulatory Patients with Cancer:Assessment of the Diagnostic Value of Scanning without Contrast Prior to With Contrast
AJNR 47:694-698, Wang,E.,et al, 2026

A 49-Year-Old Man with Meningoencephalitis and Persistent Altered Mental Status
Neurol 106:e214777, Hariswar,P.T.,et al, 2026

Iatrogenic Cerebral Amyloid Angiopathy after Cardiac Surgery, Two Case Reports
Neurol 106:e214819, Brunet de Courssou,J-B.,et al, 2026

Clinical Manifestations of Primary CNS T-Cell Lymphoma, Retrospective Study of Histopathologic, Molecular, and Neuroimaging Fetures
Neurol 106:e24744, Muller,K.J.,et al, 2026

Patterns and Factors Associated with Cerebral Infarction on MRi in Tuberculous Meningitis: Secondary Anlysis of the ACT-TBM Trial
Stroke 57:856-864, Chandu,M.,et al, 2026

Syphilis as an Important Modern-Day Risk Factor for Intracranial Vasculopathy and Ischemic Stroke:A Teaching Case
Stroke 57:e108-e111, Higham-Kessler,C.,et al, 2026

Cerebral Amyloid Angiopathy
NEJM 394:1836-1845, Greenberg,S.M., 2026

A 28-Year-Old Man with Seizures and Thalamic Lesions
Neurol 106:e218065, Santos-Rojo,A.B.,et al, 2026



Showing articles 150 to 200 of 15699 << Previous Next >>