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Differential
(Click to cross reference)
abdominal distention
abducens nerve paralysis
adverse drug reaction
alopecia
amenorrhea
anasarca
anemia
anorexia
arteriopathy
arteritides
arteritis, temporal
arthralgia
arthritis
ascites
aspirin
ataxia
ataxia telangiectasia
ataxic gait
autonomic dysfunction
B 12 deficiency
bacterial infection
basal ganglia, lesion of
Beau's lines
biologic markers
biotin deficiency
biotinidase deficiency
brain atrophy
brain scan, abnormal
brainstem, lesion of
breast feeding
cafe au lait spots
carcinoma
cardiomyopathy
Castleman's disease
CAT scan, emission, abnormal
cataracts
cerebral arteries
cerebral atherosclerosis
cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy
cerebral cortical atrophy
cerebral infarction
cerebral infarction, subcortical
cerebral ischemia
cerebral peduncle
cerebral vasculature
cerebral venous infarction
cerebral venous thrombosis
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, pressure increased
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, young adult
children
chorea
chromosome 8
Clinical Pathologic Conference(C.P.C.)
clubbing of fingers
coma
comorbidities
confusion
confusional state, acute
congestive heart failure
conjunctival injection
conjunctivitis
Coombs test, positive
cortical vein thrombosis
corticotropin level
corticotropin-releasing factor
cortisol, elevated
cranial nerve palsies
cranial neuropathy, multiple
Cushing's syndrome
cytoid bodies
degenerative diseases of CNS
delirium
developmental milestones, loss of
developmental retardation
diabetes insipidus
diabetes mellitus
diet
diplopia
dural sinus thrombosis
dyspnea
echocardiogram
echocardiogram, LVH
edema, pedal
ejection fraction
ejection fraction, abnormal
electrocardiogram, abnormal
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
emergencies, neurologic
encephalopathy
enzyme, defect
erythema nodosum
evoked potentials
eye movement, disorders of
facial hair, excessive
facial pain
facial weakness
failure to thrive
false positive VDRL
familial
fatigue
fever
fingernails, abnormal
fingernails, white
foot drop
fornix, lesion of
gait disorder
gammaglobulin therapy, intravenous
gene
gene mutation
genetic linkage
genetic neurologic disorders
genetic testing
glaucoma
glycosuria
gray hair
Griscelli syndrome
growth retardation
gynecomastia
hair analysis
hair, loss
hallucination
hand pain
headache
hearing loss
hemifacial atrophy
hepatomegaly
hepatosplenomegaly
herniated disc, thoracic
hirsutism
Horner's syndrome
HTRA1 gene
hypercoagulable state
hyperhidrosis
hyperhomocysteinemia
hyperpigmentation of skin
hypertension
hypertrichosis
hypocomplementemia
hypogonadism
hypokalemia
hyponatremia
hypothermia
hypotonia
immunodeficiency
immunoelectrophoresis, serum
immunosuppression
impotence
infant, evaluation of
infantile tremor syndrome
infection
internal capsule
intracranial pressure, increased
jaw pain
Kawasaki disease
leg swelling
leukemia
leuko-araiosis
leukocytosis
leukoencephalopathy
leukopenia
life expectancy
liver disease
liver function enzymes
low back pain
lymphadenopathy
lymphadenopathy, hilar
lymphohistiocytosis
lymphoma involving CNS
lymphopenia
meningitis
meningitis, aseptic
meningoencephalitis
mental status, abnormal
mesial temporal lobe
metabolic acidosis
metabolic alkalosis
microhemorrhage, intracerebral
midbrain, lesion of
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
mimics
misdiagnosis
mitoxantrone
monoclonal gammopathy
mononeuritis multiplex
mononeuropathy
mortality
MRI
MRI, abnormal
MRI, diffusion weighted
multiple myeloma
multiple sclerosis
multiple sclerosis, treatment of
muscle pain
muscle weakness, proximal
myelination of nervous system
myelitis
myeloma, osteosclerotic
myelopathy
myocardial injury
myocarditis
myoclonus
myocytolysis
myositis
nausea and vomiting
neck trauma
neonatal screening, genetic neurologic disorders
neoplasm, hormone producing, ectopic
nephritis
nerve biopsy
neuroendocrinology
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neuropathy
neuropathy, motor, multifocal
neuropathy, peripheral
neutropenia
night sweats
nystagmus
nystagmus, rotary
nystagmus, spontaneous
oculocutaneous albinism
ophthalmoplegia
optic atrophy
optic neuritis
P300
pain, back
palpitations
papilledema
paranoia
pericarditis
photophobia
pink eye
plasmacytoma
pleocytosis of cerebrospinal fluid
pleural effusion
pleurisy
POEMS syndrome
poliosis
polymyalgia rheumatica
polyneuropathy
pons, lesion of
postpartum
pregnancy, neurologic complications in
progeria
prognosis
progressive neurologic disorder
psychiatric problems in neurologic disorders
psychosis
ptosis
pulmonary embolism
purpura
quadriparesis
radiation therapy, CNS treatment and complications with
rash
Raynaud's phenomenon
retinal detachment
reversible neurologic disorder
review article
risk factors
scalp necrosis
schizophrenia
scleroderma
scleroderma, neurologic involvement with
scotoma
screening
sedimentation rate, elevated
seizure
seizure, children
seizure, drug resistance
seizure, neonatal
short stature
skin cancer
skin, lesions in neurologic disorders
skin, pale
skin, thickened
slurred speech
small vessel disease
somatosensory evoked potentials
spinal cord, lesion of
splenomegaly
spondylolysis
spondylosis
steroid psychosis
steroid therapy, CNS treatment and complications with
subcortical U fibers
subcutaneous nodules
substantia nigra
symmetric brain lesions
systemic illness
systemic lupus erythematosus
systemic lupus erythematosus, neurologic complications with
systemic lupus erythematosus, skin changes in
temporal lobe, lesion
term infant
thirst
thrombocytopenia
thrombocytosis
thrombotic thrombocytopenia purpura
tinnitus
treatment of neurologic disorder
tremor
tremor, intention
trichopoliodystrophy
tuberculosis
tuberculosis, miliary
urinary frequency
urinary tract infection
urticaria
uveitis
vasculitides
vegetarianism
Venereal Disease Research Laboratory test
vertigo
vision, blurred
visual acuity, decreased
visual loss
vitamin deficiency
vitiligo
Vogt-Koyanagi-Harada syndrome
weakness, generalized
weight loss
Werner's syndrome
white hair
white matter disease
whites
Showing articles 1250 to 1300 of 1370 << Previous Next >>

Fibrodysplasia Ossificans Progressiva, The Clinical Features & Natural Hx of 34 Pts
J Bone Joint Surg 64B:76-83, Connor,J.M.&Evans,D.A.P., 1982

Biotin-Responsive Carboxylase Deficiency Associated With Subnormal Plasma & Urinary Biotin
NEJM 304:817-820, Thoene,J.,et al, 1981

Biotin Deficiency:An Unusual Complication Of Parenteral Alimentation
NEJM 304:820-823, Mock,D.M.,et al, 1981

Ethamsylate Reduces The Incidence Of Periventricular Haemorrhage in Very Low Birth-Weight Babies
Lancet 2:830-831, Morgan,M.E.I.,et al, 1981

Computed Tomography of Cerebral Syphilis
J Comput Assist Tomogr 5:345-347, Ganti,S.R.,et al, 1981

Acute Thallium Poisoning, Toxicological & Morphological Studies of the Nervous System
Ann Neurol 10:38-44, Davis,L.E.,et al, 1981

Abrupt Neurological Deterioration in Children With Kearns-Sayre Syndrome
Arch Neurol 38:247-250, Coulter,D.L.,et al, 1981

Ophthalmoplegia-Plus
Arch Neurol 38:423-426, Okamoto,T.,et al, 1981

The Adrenoleukomyeloneuropathy Complex:Expression in Four Generations
Neurol 31:151-156, O'Neill,B.P.,et al, 1981

Subcortical Arteriosclerotic Encephalopathy:A Clinical & Radiological Investigation
JNNP 44:294-304, Loizou,L.A.,et al, 1981

Neonatal Intraventricular Hemorrhage
NEJM 304:886-891, Volpe,J.J., 1981

Biochemical Evidence Of Dysfunction Of Brain Neurotransmitters In The Lesch-Nyhan Syndrome
NEJM 305:1106-1111, Lloyd,K.G.,et al, 1981

Leukoencephalopathy & Elevated Levels Of Myelin Basic Protein In The CSF Of Patients With Acute Lymphoblastic Leukemia
NEJM 303:19-21, Gangji,D.,et al, 1980

Clin. Path. Conference
Lymphoplasmacytic Intersitial Pneumonitis, Progressive Multifocal Leukoencephalopathy. Case Record 1, -10,NEJM 302:795,1980., 1980

Periventricular Leukomalacia, A one-Year Autopsy Study
Arch Neurol 37:231-235, Shuman,R.M.,et al, 1980

Valproic Acid
NEJM 302:661-666, Brown,T.R., 1980

Plasma Cell Dyscrasia with Polyneuropathy, Organomegaly, Endocrinopathy, M Protein, & Skin Changes:The POEMS Syndrome
Medicine 59:311-322, Bardwick,P.A., 1980

Adrenoleukodystrophy:Elevated C26 Fatty Acid in Cultured Skin Fibroblasts
Ann Neurol 7:542-549, Moser,H.W.,et al, 1980

Adrenoleukodystrophy. Report of Two Cases With Relapsing & Remitting Courses
Arch Neurol 37:448-450, Walsh,R., 1980

A Diagnostic Index of Active Demyelination:Myelin Basic Protein in Cerebrospinal Fluid
Ann Neurol 8:25-31, Cohen,S.R.,et al, 1980

Progressive Multifocal Leukoencephalopathy
Arch Neurol 37:497-501, Boudewijn,A.C.,et al, 1980

Osteopetrosis, Renal Tubular Acidosis & Basal Ganglia Calcification in Three Sisters
Am J Med 69:64-74, Whythe,M.P.,et al, 1980

Increased Hair Loss As A Side Effect of Bromocriptine Treatment
NEJM 303:1418, Blum,I.,et al, 1980

Long-term Neurological Implications of Somnolence Syndrome in Children with Acute Lymphocyte Leukemia
Ann Neurol 8:273-277, Ch'ien,L.T.,et al, 1980

Amelioration Of Neurologic Abnormalities After"Enzyme Replacement"In Adenosine Deaminase Deficiency
NEJM 303:377-380, Hirschhorn,R.,et al, 1980

Perinatal Neuropathy as an Early Manifestation of Krabbe's Disease
Arch Neurol 37:446-447, Lieberman,J.S.,et al, 1980

Status Epilepticus
Am J Med 69:657-665, Aminoff,M.J.,et al, 1980

Peripheral Neuropathy in the Cherry-Red Spot-Myoclonus Syndrome (Sialidosis Type I)
Ann Neurol 7:450-456, Steinman,L.,et al, 1980

Leukaemia:Neurological Involvement
in Handbk of Clinical Neurology, Vinkin PJ & Bruyn GW, Ed, North-Holland Publ Co, Amsterdam 39:1, Yuill,G.M., 1980

Myotonic Dystrophy
In Harrison's Principles of Internal Medicine, 9th Ed, McGraw-Hill Book Co, NY 206180., Adams,R.D.,et al, 1980

Polyneuropathy, Alopecia Areata, & Chronic Lymphocytic Thyroiditis
Neurol 29:106-108, Hart,Z.H.,et al, 1979

Intracranial Hemorrhage in the Newborn:Current Understanding & Dilemmas
Neurol 29:632-635, Volpe,J.J., 1979

Prenatal Genetic Diagnosis in 3000 Amniocenteses
NEJM 300:157-163, Golbus,M.S.,et al, 1979

Clinical & Biochemical Aspects of Trichopoliodystrophy
Ann Neurol 5:65-71, Grover,W.D.,et al, 1979

CT Scans in Menkes Disease
Neurol 29:304-312, Seay,A.R.,et al, 1979

Reduction of Angiotensin-Converting Enzyme in Substantia Nigra in Early-Onset Schizophrenia
NEJM 300:502-503, Arregui,A.,et al, 1979

Subcortical Arteriosclerotic Encephalopathy (Binswanger) :Computerized Tomography
Neurol 29:1102-1106, Rosenberg,G.A.,et al, 1979

Brainstem Auditory Evoked Responses in Leukodystrophies
Neurol 29:1089-1093, Ochs,R.,et al, 1979

Phenytoin Hypersensitivity:38 Cases
Neurol 29:1480-1485, Harunda,F., 1979

Adult Type Neuronal Storage Disease with Neuraminidase Deficiency
Ann Neurol 6:232-244, Miyatake,T.,et al, 1979

Multiple Molecular Forms of Arylsulfatase in Different Forms of Metachromatic Leukodystrophy (MLD)
Neurol 29:16-20, Farrell,D.F.,et al, 1979

Spinal Cord Compression by Extramedullary Hemopoietic Tissue in Pyruvate-Kinase-Deficiency-Caused Hemolytic Anemia
Neurol 29:510-513, Rutgers,M.J.,et al, 1979

Spinocerebellar Degeneration:Hexosaminidase A & B Deficiency in Two Adult Sisters
Neurol 29:380-384, Oonk,J.G.W.,et al, 1979

Neurological Manifestations of Fabry Disease in Female Carriers
Ann Neurol 4:537-540, Bird,T.D.,et al, 1978

Adult-onset GM2 Gangliosidosis
Neurol 28:1117-1123, O'Neill,B.,et al, 1978

Leukoencephalopathy in Oculocraniosomatic Neuromuscular Disease With Ragged-Red Fibers
Arch Neurol 35:643-647, Bertorini,T.,et al, 1978

Fatal Infantile Form of Muscle Phosphorylase Deficiency
Neurol 28:1124-1129, DiMauro,S.,et al, 1978

Late Adult-onset Metachromatic Leukodystrophy
Arch Neurol 35:475, Bosch,E.P., 1978

Possible Biochemical Basis of Memory Disorder in Alzheimer Disease
Ann Neurol 3:471, Smith,C.M.,et al, 1978

A Syndrome of Progressive Muscle Spasm, Alopecia, & Diarrhea
Neurol 28:458, Satoyoshi,E., 1978



Showing articles 1250 to 1300 of 1370 << Previous Next >>