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Differential
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acromegaly
acromicria
Addison's disease
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
adrenomyeloneuropathy
adverse drug reaction
alopecia
amenorrhea
amniocentesis
anemia
Angelman syndrome
angiography, cerebral
ankle edema
anosmia
anti Ma
anti Ta
areflexia
arrhythmia, cardiac
arthritis
ascites
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, progressive
ataxic gait
autoantibodies
autoimmune disease
azospermia
B 12 deficiency
basal ganglia, calcification of
behavior, combative
behavioral disorder
bone marrow transplantation
brain biopsy
brain scan, abnormal
bromocriptine
cabergoline
cachexia
cafe au lait spots
calcification, intracranial
carcinoma
carcinoma of lung
cardiomyopathy
caries
carotid artery occlusion, intracranial
CAT scan, abnormal
CAT scan, demyelinating disease
CAT scan, emission
CAT scan, emission, abnormal
cataracts
celiac disease, adult
celiac disease, childhood
cerebellar ataxia, primary
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrovascular accident
chiasmal syndromes
children
chromophobe adenoma
chromosomal abnormality
chromosome 15
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
Cockayne's syndrome
coenzyme Q10
coenzyme Q10 deficiency
collateral circulation
complications
contractures, joint
creatine phosphokinase(CPK)elevated
cry, abnormal
cry, weak
cryptorchidism
cultured skin fibroblasts
Cushing's syndrome
degenerative diseases of CNS
dementia
dementia, childhood
demyelinating disease
dermatitis herpetiformis
developmental retardation
diabetes insipidus
diarrhea
diet
dopamine agonist
drooling
dysarthria
dysmetria
dysmorphic
dysphagia
dysphasia
eating disorder
efficacy
electrocardiogram, abnormal
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
electron microscopy
encephalitis
encephalitis, brainstem
epidemiology of neurology
erectile dysfunction
evoked potentials
exome sequencing
eye movement, disorders of
eyes, sunken
facial appearance, abnormal
failure to thrive
familial
fatty acid, elevated plasma content
feeding disorder
fingers, abnormal
fluorescein angiography
foot drop
F-wave response
gadolinium
gait disorder
galactorrhea
gastrointestinal disease, neurologic complications
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic testing
genital hypoplasia
gluten ataxia
gluten sensitivity
gluten-free diet
gonadotropin-releasing hormone
gray hair
groin pain
growth hormone
growth hormone deficiency
growth retardation
gynecomastia
hair, loss
hand flapping
headache
hearing loss
hepatitis
hepatosplenomegaly
herniated disc
herniated disc, thoracic
hirsutism
HLA
hormone replacement
hormone therapy
hyperphagia
hyperpigmentation of skin
hypodontia
hypogonadism
hypogonadism, hypogonadotropic
hypomyelination
hypopigmentation of skin
hypopituitarism
hyposmia
hypothalamus
hypothalamus, damage to
hypothalamus, disturbance of
hypothyroidism
hypotonia
hypotonia, infants
iatrogenic neurologic disorders
imbalance
immunodeficiency
immunosuppression
impotence
inclusion bodies
inclusion bodies, intracytopasmic
incoordination
infertility
intellectual deficit
iris, abnormal
Kallmann's syndrome
Klinefelter's syndrome
learning disability
leukodystrophy
leukodystrophy, 4H
leukoencephalopathy
libido
libido, decreased
limbic encephalitis
liver disease
long bone lesion
Lorenzo's oil
low back pain
magnetic stimulation, brain
malabsorption
memory, impairment of
menses, irregular
mental retardation
misdiagnosis
molecular genetics
monoclonal gammopathy
monoparesis
mortality
moyamoya
moyamoya, adult
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, disappearing lesion on
MRI, spinal cord
multiple sclerosis, differential diagnosis of
muscle biopsy
muscular dystrophy
myeloma, osteosclerotic
myelopathy
myopia
myotonia
myotonia dystrophica
neck weakness
neoplasm, pituitary
neoplasm, pituitary, incidental
neoplasm, pituitary, treatment of
neuroendocrinology
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic signs
neuronal migration disorder
neuropathy
neuropathy, demyelinating
neuropathy, peripheral
next-generation sequencing
nystagmus
obesity
octreotide
ocular myopathy
oculopharyngeal muscular dystrophy
olfactory bulb
oligomenorrhea
oligospermia
ophthalmoplegia
optic atrophy
optic neuropathy
oral ulcerations
organomegaly
osteoporosis
ovarian dysgenesis
P300
pain
pain, abdominal
pain, back
pain, leg
papilledema
paraparesis
paraparesis, spastic
paraplegia
penis, small
perimetry
peroxisomal disease
Perrault syndrome
photosensitivity, skin
pigmentary retinopathy
pituitary
pituitary stalk
pituitary stalk, lesion of
pituitary, adenoma
pituitary, dysfunction
pituitary, hormones of
pituitary, lesion of
pituitary, microadenoma
plasmacytoma
plethora
POEMS syndrome
polyneuropathy
practice guidelines
Prader-Labhart-Willi syndrome
prenatal diagnosis by amniocentesis
progeria
prognosis
progressive neurologic disorder
prolactin
prolactin, elevated
prolactinoma
psychiatric problems in neurologic disorders
psychomotor retardation
ptosis
ptosis, familial
puberty
puberty, delayed
pulmonary infiltrates
radiation therapy, CNS treatment and complications with
rash
remote effect of cancer on the nervous system
retinopathy
review article
sarcoidosis
sarcoidosis, CNS
sclerosis, bone
seizure
sella turcica, enlargement of
sensorineural hearing loss
serologic testing
serum tumor markers
short stature
sinuses, diseases of
skin, biopsy
skin, darkening of
skin, lesions in neurologic disorders
skull x-ray, abnormal
smell
somatosensory evoked potentials
somatostatin analogue
spinal cord, compression of
splenomegaly
steroid therapy, CNS treatment and complications with
stooped posture
strabismus
suck, poor
suprasellar lesion
synkinesis
systemic illness
teeth, abnormal
temper tantrums
temporal lobe, lesion
temporal lobe, lesion, bilateral
temporalis muscle wasting
testicular atrophy
testicular biopsy
testicular germinoma
testicular teratoma
testosterone
testosterone, serum
testosterone, serum, low
third ventricle, wall
thrombocytosis
tongue, protrusion of
treatment of neurologic disorder
tremor
tremulousness
ubiquitination
urinary gonadotropin
vascular endothelial growth factor
visual acuity, decreased
visual evoked response
visual field defect
visual fields
visual loss
vitiligo
weakness, generalized
weight loss
Werner's syndrome
white matter disease
wide based gait
workup
X-linked bulbospinal neuronopathy
Showing articles 1250 to 1300 of 2365 << Previous Next >>

Moderate Alcohol Consumption and Loss of Cerebellar Purkinje Cells
BMJ 308:1663-1667, Karhunen,P.J.,et al, 1994

Friedreich's Ataxia:MR Findings Involving the Cervical Portion of the Spinal Cord
AJR 163:187-191, Mascalchi,M.,et al, 1994

Bilateral Distal Upper Limb Amyotrophy and Watershed Infarcts from Vertebral Dissection
Stroke 25:1870-1872, Pullicino,P., 1994

Ataxia-Telangiectasia:MR and CT Findings
J Comput Assist Tomogr 18:724-727, Farina,L.,et al, 1994

Initial and Follow-up Brain MRI Findings and Correlation with the Clinical Course in Wilson's Disease
Neurol 44:1064-1068, Roh,J.K.,et al, 1994

Phenotype of Chromosome 14-Linked Familial Alzheimer's Disease in a Large Kindred
Ann Neurol 36:368-378, Lampe,T.H.,et al, 1994

Peripheral Nerve Injury and Causalgia Secondary to Routine Venipuncture
Neurol 44:962-964, Horowitz,S.H., 1994

Visual Loss from Idiopathic Intracranial Pachymeningitis
Neurol 44:694-698, Lam,B.L.,et al, 1994

Mitochondrial Neurogastrointestinal Encephalomyopathy (MMGIE) :Clin Biochem & Genetic Features of Auto Recess Mitochond Disorder
Neurol 44:721-727, Hirano,M.,et al, 1994

Gadolinium Enhancement of the Leptomeninges Caused by Hydrocephalus:A Potential Mimic of Leptomeningeal Metastasis
AJNR 15:639-641, Schumacher,D.J.,et al, 1994

MR of Sarcoidosis in the Head and Spine:Spectrum of Manifestations and Radiographic Response to Steroid Therapy
AJNR 15:973-982, Lexa,F.J.&Grossman,R.I., 1994

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

Intestinal Pseudo-Obstruction in Adult Spinal Muscular Atrophy
Muscle & Nerve 17:946-948994., Ionasescu,V.,et al, 1994

Location of the Corticospinal Tract in the Internal Capsule at MR Imaging
Radiology 191:455-460, Yagishita,A.,et al, 1994

Motor Neuron Disease
JNNP 57:886-896, Leigh,P.N.&Ray-Chaudhuri,K., 1994

Recent Developments in the Drug Treatment of Motor Neurone Disease
BMJ 309:140-141, , 1994

Sequences Specific for Enterovirus Detected in Spinal Cord from Patients with Motor Neurone Disease
BMJ 308:1541-1543, Woodall,C.J.,et al, 1994

Methylmercury Poisoning:Long-Term Clinical, Radiological, Toxicological, and Pathological Studies of an Affected Family
Ann Neurol 35:680-688, Davis,L.E.,et al, 1994

MR Findings in Seven Patients with Organic Mercury Poisoning (Minamata Disease)
AJNR 15:1575-1578, Korogi,Y.,et al, 1994

Focal Tectal Tumors:Management and Prognosis
Neurol 44:953-956, Squires,L.A.,et al, 1994

MRI Pallidal Hyperintensity & Brain Atrophy in Cirrhotic Pts:2 Different MRI Patterns of Clin Deterior?
Neurol 43:2570-2573, Kulisevsky,J.,et al, 1993

Brain Imaging in Late-Onset CM2 Gangliosidosis
Neurol 43:2055-2058, Streifler,J.Y.,et al, 1993

The Motor Disorder of Multiple System Atrophy
JNNP 56:1239-1242, Quinn,N.P.&Marsden,C.D., 1993

Inherited Primary Peripheral Neuropathies
JAMA 270:2326, 23301993., Lupski,J.R.,et al, 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

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

Frequency and Characteristics of Visual Field Deficits after Surgery for Mesial Temporal Sclerosis
Neurol 43:1235-1238, Tecoma,E.S.,et al, 1993

Collosal Disconnection in Multiple Sclerosis
Neurol 43:1243-1245, Schnider,A.,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

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



Showing articles 1250 to 1300 of 2365 << Previous Next >>