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Differential
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abdominal muscle paralysis
abducens nerve paralysis
abducens nerve paralysis, bilateral
abortion, spontaneous
acanthocytosis
acid maltase deficiency
acid maltase deficiency, adult
acromicria
agenesis of aqueduct of Sylvius
aggression
alien hand syndrome
alpha glucosidase
amniocentesis
amyloidosis
amyotrophic chorea-acanthocytosis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, bulbar
amyotrophic lateral sclerosis, atypical
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, etiology of
amyotrophic lateral sclerosis, juvenile
amyotrophic lateral sclerosis, misdiagnosis
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, sensory symptoms in
amyotrophic lateral sclerosis, treatment of
anemia
anemia, megaloblastic
Angelman syndrome
angiography, posterior fossa
anorexia
anterior horn cell disease
aphonia
apraxia
apraxia of eye movements
aqueduct of Sylvius, stenosis
aqueductal stenosis
areflexia
arterial dissection, carotid
arthralgia
arthritis
arylsulfatase B
aspartate aminotransferase
aspiration
ataxia
ataxia, cerebellar
ataxic gait
attention span
autoimmune disease
automobile accidents
B 12 deficiency
Babinski sign
Babinski-Nageotte syndrome
basal ganglia
basal ganglia, degeneration
behavior, combative
behavioral disorder
Behcet's syndrome
blue tongue virus
bone marrow biopsy
brachial plexus
brachial plexus injury
brachial plexus, lesion of
brachycephaly
bradykinesia
brain atrophy
brain biopsy
brainstem, infarction of
brainstem, lesion of
brainstem, metastasis to
bright tongue sign
bulbar palsy
bulbar palsy, progressive
burning hands
burning paresthesia
C9orf72
CAG repeats
carcinoma
cardiomyopathy
carotid angiogram
carpal tunnel syndrome
CAT scan
CAT scan, abnormal
CAT scan, base of skull
CAT scan, emission, abnormal
CAT scan, false negative
caudate nucleus, atrophy
celiac disease, adult
celiac disease, childhood
central nervous system, infection of
cerebellar atrophy, primary
cerebellar lesion
cerebral cortical atrophy
cerebrospinal fluid, elevated protein of
cerebrovascular accident
cervical osteophyte
cervical spine
cervical spine abnormality
cervical spine disease
chewing, impaired
children
chorea
chorein
chromosomal abnormality
chromosome 15
chromosome 5
Clinical Pathologic Conference(C.P.C.)
clinodactyly
cognition
conduction block
congenital bilateral perisylvian syndrome
congenital heart disease
congestive heart failure
cornea, opacity of
corpus callosum, lesion of
cortical-basal ganglionic degeneration
cranial nerve palsies
cranial nerve palsies, unilateral
cranial nerve tumor
cranial neuropathy
cranial neuropathy, multiple
cranio-cervical junction
creatine phosphokinase(CPK)elevated
cry, abnormal
cry, weak
crying, pathologic
cultured skin fibroblasts
cyst, porencephalic
deafness
degenerative diseases of CNS
dementia
dementia, frontal lobe type
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
denervation of muscle
denervation potentials
dermatitis herpetiformis
developmental milestones, loss of
developmental retardation
dexterity, impaired
diarrhea
differential diagnosis
diplegia, brachial
diplopia
disability, neurological
dissociated sensory loss
distal muscle atrophy
distal muscle weakness
drooling
dysarthria
dyskinesia, buccal lingual facial
dysmorphic
dysphagia
dysphonia
dyspnea
dyspraxia
dystonia
eating disorder
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electromyogram
electromyogram, decremental response
electron microscopy
embryogenesis
emotional lability
encephalomalacia
entrapment neuropathy
enzyme treatment
enzyme, defect
epidemiology of neurology
face, inexpressive
facial appearance, abnormal
facial expression abnormality
facial weakness
facial weakness, bilateral
failure to thrive
falling
familial
fasciculation
fatigable chewing
fatigue
feeding disorder
fever
fibrillations
fish
flail arm syndrome
fluorescene in situ hybridization
foot drop
foramen magnum, lesion of
frontal lobe, atrophy
frontotemporal dementia, behavioral variant
gadolinium
gag reflex, depressed
gait disorder
gait, spastic
gait, waddling
gammaglobulin therapy, intravenous
gastrointestinal disease, neurologic complications
gaze palsy
gaze palsy, supranuclear
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic screening
genetic testing
genital ulcerations
glomus jugulare tumor
gluten ataxia
gluten sensitivity
gluten-free diet
glycogen storage disease
GM1 ganglioside antibodies
grasp reflex
growth hormone deficiency
growth retardation
Guillain Barre syndrome
gunshot wounds
gynecomastia
hallucination
hand flapping
hand weakness
head injury
headache
headache, intermittent
headache, severe
headache, unilateral
hearing loss
hemiparesis
hepatitis
hepatomegaly
herpes simplex virus
HLA
hoarseness
hydranencephally
hydrocephalus
hyperactivity
hypercalcemia
hyperparathyroidism
hyperphagia
hyperreflexia
hypersegmented polys
hypogeusia
hypoglossal nerve
hypoglossal nerve paralysis
hypogonadism
hypopigmentation of skin
hyporeflexia
hypotonia
hypotonia, infants
imbalance
immunosuppression
infectious mononucleosis, neurologic findings with
influenza A virus
insular cortex
intellectual deficit
intellectual deterioration
intrinsic hand muscles, wasting of
jaundice
jaw closure weakness
jaw jerk, abnormal
jugular foramen syndrome
lactic dehydrogenase(LDH)
language disorders in children
laughing, pathologic
leg weakness, bilateral
leg weakness, unilateral
levitation
lip, biting
lobar atrophy
locked-in syndrome
lymphoma
lymphoma involving CNS
lysosomal storage disease
lysosomes, abnoral
macrognathia
malabsorption
malformation, CNS, congenital
masseter muscle wasting
masseter muscle weakness
mastectomy, radical
medial medullary syndrome
medulla oblongata, infarction of
medulla oblongata, lesion of
medulla oblongata, neoplasm of
meningioma
mental retardation
mental status, abnormal
methylmalonic acid, serum
microcephaly
misdiagnosis
misdirection
molecular genetics
monoclonal gammopathy
mononeuropathy
mortality
motor neuron disease
movement disorder
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, skull bone changes
MRI, spinal cord
mucopolysaccharidoses
multiple sclerosis
multiple sclerosis, differential diagnosis of
mumps virus
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle stiffness
muscle twitching
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
mutism
myelopathy
myeloschisis
myoclonic jerks
myopathy
myopathy, amyloid
myopathy, vacuolar
nasal speech
nasopharyngeal carcinoma
neck pain
neck weakness
neonatal infection, viral
nerve conduction studies
nerve conduction studies, motor
neuroendocrinology
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neuroma
neuromuscular disease, electrodiagnosis of
neuronopathy
neuropathology
neuropathy
neuropathy, motor
neuropathy, motor, multifocal
neuropathy, multifocal
neuropathy, sensory
nonverbal
nusinersen
nystagmus
obesity
occipital condyle fracture
occipital condyle syndrome
occipital pain
opened mouth
operculum syndrome
operculum syndrome, bilateral
ophthalmoplegia
optic nerve
oral ulcerations
osteomalacia
osteoporosis
pain
pain, abdominal
palate, paralysis-unilateral
papilledema
paranoia
paraparesis, spastic
paraspinal muscle
paraspinal muscle weakness
parathyroid adenoma
paresthesias
paresthesias, hands
parvovirus
peripheral blood smear, abnormal
peripheral nerve, lesion of
pernicious anemia
plasma cell dyscrasia
pleocytosis of cerebrospinal fluid
pneumoencephalogram(PEG)
polyneuropathy, chronic inflammatory demyelinating
Pompe's disease of glycogen storage
posterior inferior cerebellar artery syndrome
postural abnormality
Prader-Labhart-Willi syndrome
pregnancy, neurologic complications in
prenatal diagnosis by amniocentesis
primary lateral sclerosis
prognathism
prognosis
progressive neurologic disorder
progressive spinal muscular atrophy
proximal muscle atrophy
pseudobulbar palsy
pseudohypertrophy
pseudomyotonia
psychiatric problems in neurologic disorders
puberty
puberty, delayed
pyramidal tract
pyramidal tract dysfunction
quadriparesis
quadriplegia
radiation therapy, CNS treatment and complications with
recurrent laryngeal nerve paralysis
renal stones
repetitive nerve stimulation
respiratory failure
review article
rheumatoid arthritis
rheumatoid arthritis, neurologic complications of
rheumatoid pachymeningitis
rigidity
risk factors
Romberg's sign
rubella virus
saccadic eye movements, abnormal
scleritis
scoliosis
scoliosis, neurologic association with
screening
seizure
seizure, recurrent
sensory loss
sensory loss, cortical
sensory nerve action potentials
sensory symptoms
serologic testing
short stature
Sicard-Collet syndrome
skin, biopsy
skin, lesions in neurologic disorders
skull fracture, basal
smiling
SMN1 gene
spasticity
speech disorder
speech disorder, childhood
speech, delayed development of
speech, loss of
spinal cord, compression of
spinal muscular atrophy
spinal muscular atrophy, classification
standing difficulty
sternocleidomastoid wasting
sternocleidomastoid weakness
strabismus
suck, poor
symmetric brain lesions
systemic illness
tandem gait, ataxic
Tapia's syndrome
taste
teeth, wide-spaced
temper tantrums
temporal lobe, atrophy
temporal lobe, lesion
temporal lobe, lesion, bilateral
temporalis muscle wasting
teratogenesis
teratogenesis, viral
third nerve palsy
tinnitus
tinnitus, pulsatile
tongue deviation
tongue, atrophy
tongue, biting
tongue, enlarged
tongue, fasciculations of
tongue, hemiatrophy of
tongue, impaired movements of
tongue, protrusion of
tongue, smooth
tongue, swelling
tongue, ulcer
tongue, weakness
transient ischemic attack
trapezius weakness
trauma
treatment of neurologic disorder
tremor
tremor, postural
tremulousness
urine, dark
vagal neuropathy
vagus nerve, lesion of
vasculitides
viral infection
viral infection, CNS
visual acuity, decreased
visual field defect
vocal cord paralysis
vocalizations
Waldenstrom's macroglobulinemia
walking, difficulty with
weakness
weakness, fatiguable
weakness, generalized
weakness, progressive
weakness, proximal
weight loss
wheelchair
wide based gait
winging of scapula
word-finding difficulty
writing
X-linked bulbospinal neuronopathy
Showing articles 1350 to 1400 of 2496 << Previous Next >>

Acute Bilateral Cerebellar Infarction in the Territory of the Medial Branches of Posterior Inferior Cerebellar Arteries
Stroke 25:686-688, Yoshimasa,T.,et al, 1994

Neuro-Ophthalmological Presentation of Non-Invasive Aspergillus Sinus Disease in the Non-Immunocompromised Host
JNNP 57:234-237, Brown,P.,et al, 1994

Neurocysticercosis in Houston, Texas:A Report of 112 Cases
Medicine 73:37-52, Shandera,W.X.,et al, 1994

Cerebral Involvement in McLeod Syndrome
Neurol 44:117-120, Danek,A.,et al, 1994

The Clinical Correlates of High-Titer IgG Anti-GM1 Antibodies
Ann Neurol 35:234-237, Kornberg,A.J.,et al, 1994

Clinical Genetics in Neurological Disease
JNNP 57:7-15, MacMillan,J.C.&Harper,P.S., 1994

A Controlled Trial of Riluzole in Amyotrophic Lateral Sclerosis
NEJM 330:585-591, Bensimon,G.,et al, 1994

Conjugal Amyotrophic Lateral Sclerosis:A Report on Two Couples from Southern France
Neurol 44:547-548, Camu,W.,et al, 1994

Conjugal Amyotrophic Lateral Sclerosis:Report of a Young Married Couple
Neurol 43:2378-2380, Cornblath,D.R.,et al, 1993

Molecular Genetics in Neurology
Ann Neurol 34:757-773, Martin,J.B., 1993

Differential Diagnosis of Guillain-Barre Synd, In Guillain-Barre Synd
Thieme Med Publ, Ch 3, p 42993., Parry,G.J., 1993

Amyotrophic Lateral Sclerosis:T2 Shortening in Motor Cortex at MR Imaging
Radiology 189:843-846, Oba,H.,et al, 1993

Evidence for a Dopaminergic Deficit in Sporadic Amyoptrophic Lateral Sclerosis on Positron Emission Scanning
Lancet 324:1016-1018, Takahashi,H.,et al, 1993

Clinicopath Conf
progressive Supranuclear Palsy, Case 46-1993, NEJM 329:1560-1567993., , 1993

Spinal Cord MRI Using Multi-Array Coils and Fast Spin Echo, II. Findings in Multiple Sclerosis
Neurol 43:2632-2637, Kidd,D.,et al, 1993

Signs and Symptoms of Reflex Sympathetic Dystrophy:Prospective Study of 829 Patients
Lancet 342:1012-1016, Veldman,P.H.J.M.,et al, 1993

Communicating Hydrocephalus, Basilar Invagination, and Other Neurologic Features in Osteogenesis Imperfecta
Neurol 43:2603-2608, Charnas,L.R.&Marini,J.C., 1993

Cranial Nerve Palsies in Spontaneous Carotid Artery Dissection
JNNP 56:1191-1199, Sturzenegger,M.&Huber,P., 1993

Choroid Plexus Infection in Cerebral Toxoplasmosis in AIDS Patients
Neurol 43:2035-2040, Falangola,M.F.&Petito,C.K., 1993

Neurosurgical Management of the Acquired Immunodeficiency Syndrome
West J Med 158:249-253, Andrews,B.T.&Kenefick,T.P., 1993

MRI in Acute Transverse Myelopathy
Neuroradiology 35:221-226, Holtas,S.,et al, 1993

Facial Asymmetry, Hippocampal Pathology, & Remote Symptomatic Seizures:A Temporal Lobe Epileptic Syndrome
Neurol 43:725-727, Cascino,G.D.,et al, 1993

Update on Surgical Treatment of the Epilepsies, Second Intern Palm Desert Conf on Surgical Trtm of Epilepsies (1992)
Neurol 43:1612-1617, Engel,J.Jr., 1993

Early Childhood Prolonged Febrile Convulsions, Atrophy & Sclerosis of Mesial Struc & Temporal Lobe Epilepsy:An MRI Study
Neurol 43:1083-1087, Cendes,F.,et al, 1993

Magnetic Resonance Imaging in Childhood Intractable Partial Epilepsies:Pathologic Correlations
Neurol 43:681-687, Kuzniecky,R.,et al, 1993

Detection of Hippocampal Pathology in Intractable Partial Epilepsy
Neurol 43:1793-1799, Jackson,G.D.,et al, 1993

Measurement of Whole Temporal Lobe and Hippocampus for MR Volumetry:Normative Data
Neurol 43:2006-2010, Bhatia,S.,et al, 1993

Poliomyelitis:Hyperintensity of the Anterior Horn Cells on MRI Images of the Spinal Cord
AJR 161:863-865, Malzberg,M.S.,et al, 1993

Hereditary Motor-Sensory Neuropathy (Charcot-Marie-Tooth Disease) with Nerve Deafness:A New Variant
J Pediatr 123:431-434, Hamiel,O.P.,et al, 1993

Charcot-Marie-Tooth Disease Type 1A:Association with a Spontaneous Point Mutation in the PMP22 Gene
NEJM 329:96-101, Roa,B.B.,et al, 1993

Magnetic Resonance Imaging of Brain and the Neuromotor Disorder in Endemic Cretinism
Ann Neurol 34:91-94, Ma,T.,et al, 1993

Leber's Hereditary Optic Neuropathy as a Cause of Severe Visual Loss in Childhood
Pediatrics 91:988-989, Moorman,C.M.&Elston,J.S., 1993

Atypical Leber's Hereditary Optic Neuropathy with Molecular Confiramtion
Arch Neurol 50:470-473, Weiner,N.C.,et al, 1993

Leber's Hereditary Optic Neuropathy, New Genetic Considerations
Arch Neurol 50:540-548, Newman,N.J., 1993

Neuropathic Findings in Oculopharyngeal Muscular Dystrophy, Seven Cases & Review of Literature
Arch Neurol 50:481-488, Hardiman,O.,et al, 1993

Multiple System Atrophy & Prog Supranuc Palsy, Dimin Striatal D2 Dopamine Receptor Act by SPECT
Arch Neurol 50:513-516, vanRoyen,E.,et al, 1993

TORCH Infections in the Newborn
Semin Neurol 13:106-115, Donley,D.K., 1993

Embolic Cerebral Infarction:MR Findings in the First 3 Hours AFter Onset
AJR 160:1077-1082, Shimosegawa,E.,et al, 1993

Transient Neurologic and Ocular Manifestations in Primary Thrombocythemia
Neurol 43:1107-1110, Michiels,J.J.,et al, 1993

Idiopathic Granulomatous Angiitis of the Central Nervous System
Arch Neurol 50:925-930, Vollmer,T.L.,et al, 1993

MRI in Lightning Encephalopathy
Neurol 43:1437-1438, Cherington,M.,et al, 1993

Cytomegalovirus Ventriculoencephalitis in AIDS, A Syndrome with Distinct Clin & Path FEatures
Medicine 72:67-77, Kalayjian,R.C.,et al, 1993

Asymptomatic and Neurologically Symptomatic HIV-Seropositive Subjects:Results of Long-Term MR Imaging and Clinical Follow-up
AJR 188:727-733, Post,M.J.D.,et al, 1993

Diffuse Microgliosis Associated with Cerebral Atrophy in the Acquired Immunodeficiency Syndrome
Ann Neurol 34:65-70, Gelman,B.B., 1993

What Cuases Brain Atrophy in Human Immunodeficiency Virus Infection?
Ann Neurol 34:128-129, Petito,C.K., 1993

White Matter Lesions and Cerebral Atrophy on MR Images in Patients with and without AIDS Dementia Complex
AJR 161:177-181, Broderick,D.F.,et al, 1993

The Prevalence of CT Abnor of the Cerebrum in 100 Consecutive Children Symptomatic with the HIV
Ann Neurol 34:198-205, DeCarli,C.,et al, 1993

Polyglucosan Body Disease Simulating Amyotrophic Lateral Sclerosis
Neurol 43:785-790, McDonald,T.D.,et al, 1993

Images in Clinical Medicine
NEJM 328:552, Eagle,K., 1993

Clinicopath Conf
Spongiform Encephalopathy (Creutzfeldt-Jakob Disease) , with Amyloid (KURU) Plaques, Case 17-1993, N, JM 328:66,1993., 1993



Showing articles 1350 to 1400 of 2496 << Previous Next >>