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Differential
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acrochordon
Addison's disease
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
adrenomyeloneuropathy
advances in neurology
adverse drug reaction
affect, inappropriate
alcoholism
anemia
anemia, megaloblastic
ankle, swelling of
anorexia
arrhythmia, cardiac
arthralgia
ascites
aspartate aminotransferase
ataxia
ataxia, cerebellar
ataxic gait
autoantibodies
autonomic dysfunction
B 12 deficiency
bladder dysfunction
blindness
bone marrow transplantation
brain natriuretic peptide
burning hands
burning paresthesia
calf hypertrophy
cardiomyopathy
cardiovascular disease
cerebellar ataxia, neuropathy and vestibular areflexia syndrome
cerebellum, disease of
cerebrovascular accident
cervical spondylosis
children
cirrhosis
Clinical Pathologic Conference(C.P.C.)
complications
contractures, joint
cortical blindness
cough
creatine phosphokinase(CPK)elevated
critical care unit
crying, pathologic
cultured skin fibroblasts
dantrolene sodium
deafness
decerebrate posture
delay in diagnosis
dementia, childhood
demyelinating disease
depression
dermal sinus tract
dermoid
developmental retardation
dexterity, impaired
diagnostic criteria
diamond on quadriceps
diastematomyelia
diet
differential diagnosis
difficulty climbing stairs
dimple
down-beat nystagmus
drug induced neurologic disorders
dysarthria
dysdiadochokinesia
dysmetria
dysphagia
dyspraxia
dysraphism, spinal
dystrophin
electroencephalogram, abnormalities of
electromyogram
epidemiology of neurology
exercise
facial weakness
falling
familial
fatigue
fatty acid, elevated plasma content
fever
fibrillations
fine motor function, impaired
foot numbness
gait disorder
gait, waddling
gender
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
glucose tolerance test, abnormal
Gowers maneuver
hand weakness
hemochromatosis
hemochromatosis, primary
hepatic encephalopathy
hepatolenticular degeneration(Wilson's disease)
HMGcoA reductase inhibitors
hung reflex
hyperpigmentation of skin
hyperreflexia
hypersegmented polys
hypertrichosis
hypogonadism
hypopigmentation of skin
hypothyroidism
iatrogenic neurologic disorders
intellectual deterioration
jaundice
lactic dehydrogenase(LDH)
learning disability
learning disability, in children
leukodystrophy
level of consciousness, decreased
limb-girdle weakness
lipoma of CNS
lipoma of skin
liver function enzymes
Lorenzo's oil
metabolic disorder, primary
methylmalonic acid, serum
misdiagnosis
mood change
mortality
movement disorder
MRI
MRI, abnormal
MRI, spine
multiple system atrophy
muscle biopsy
muscle pain
muscle stiffness
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, cardiovascular changes with
muscular dystrophy, central nervous system abnormality
muscular dystrophy, Duchenne
muscular dystrophy, limb-girdle
muscular dystrophy, pattern of muscle involvement
myelopathy
myoedema
myoglobinuria
myopathy
myopathy, drug-induced
myopathy, necrotizing, autoimmune
myxedema, neurologic manifestations of
neurocutaneous disease
neurofibromatosis 1
neuroleptic
neuroleptic malignant syndrome
neurologic disease, diagnoses of
neurologic signs
neuronopathy
neuronopathy, sensory
neuropathy
neuropathy, sensory
nutritional deficiency
nystagmus
ochronosis
osteoarthrosis
osteoporosis
pain, abdominal
paraparesis
paraparesis, spastic
paresthesias
paresthesias, hands
peripheral blood smear, abnormal
pernicious anemia
peroxisomal disease
personality change
phlebotomy
prenatal diagnosis by amniocentesis
prognosis
progressive neurologic disorder
proximal muscle atrophy
pruritus
pseudobulbar palsy
ptosis
quadriparesis
renal failure
renal stones
respiratory failure
review article
RFC1 gene
rhabdomyolysis
rigidity
Romberg's sign
sarcoglycan
sarcoglycanopathy
sclerae, hyperpigmented
seizure
sensorineural hearing loss
sensory loss, leg
serum alanine aminotransferase
sex reassignment surgery
skin, biopsy
skin, darkening of
skin, lesions in neurologic disorders
sleep apnea
speech disorder
speech disorder, childhood
speech, delayed development of
speech, slowed
spina bifida
spondylolysis
statin therapy
systemic illness
tandem gait, ataxic
testicular atrophy
tethered spinal cord
toe walking
tongue, smooth
tongue, swelling
transgender
treatment of neurologic disorder
tremor
tremor, intention
trifluoperazine
tripping
urinary incontinence
urine, dark
very long chain fatty acids
vestibular areflexia
walking, difficulty with
walking, difficulty with in dark
weakness
weakness, generalized
weakness, progressive
weakness, proximal
weight loss
white matter disease
wide based gait
winging of scapula
workup
Showing articles 1250 to 1300 of 1589 << Previous Next >>

Right-Sided Brain Lesions in Infants Following Extracorporeal Membrane Oxygenation
Pediatrics 82:155-161, Schumacher,R.E.,et al, 1988

Spontaneous Internal Carotid Artery Dissection Presenting as Hypoglossal Nerve Palsy
Stroke 19:1151-1155, Lieschke,G.J.,et al, 1988

Progressive Language Impairment without Dementia:A Case with Isolated Category Specific Semantic Defect
JNNP 51:1201-1207, Basso,A.,et al, 1988

Clinicopath Conf
Progressive Multifocal Leukoencephalopathy, Chronic Lymphocytic Leukemia, Case Record 45-1988, NEJM, 19:8-1280,1988., 1988

Lower Cranial Nerve Palsies Due to Internal Carotid Dissection
Stroke 19:1561-1564, Waespe,W.,et al, 1988

Diabetic Neuropathy Simulating Conus Medullaris Syndrome
Arch Int Med 148:459-460, Scherokman,B.&Vukelja,S., 1988

Pelagic Paralysis
Lancet 1:161-164, Mills,A.R.&Passmore,R., 1988

Clinicopath Conf
Infiltrating Carcinoma of Breast (Paraneoplastic Opsoclonus Syndrome & SIADH) Case 9-1988, NEJM 318:, 63-578., 1988

Zinc Deficiency in Children with Dyslexia:Concentrations of Zinc & Other Minerals in Sweat & Hair
BMJ 296:607-609, Grant,E.C.G.,et al, 1988

Brain Malformations in Linear Nevus Sebaceous Syndrome:An MR Study
J Comput Assist Tomogr 12:338-340, Sarwar,M.&Schafer,M.E., 1988

Clinicopath Conf
Lymphoma, Large-Cell (B type) of CNS, (Temporal & Frontal Lobes, Br Stem, Sp Cord, Meninges, & Nr Ro, t) , Case RecM 319:426-436,1988., 1988

Neuropsychiatric Disorders Caused by Cobalamin Deficiency in the Absence of Anemia or Macrocytosis
NEJM 318:1720-1728, 1752-17541988., Lindenbaum,J.,et al, 1988

Hereditary Defect of Cobalamin Metabolism (cblG Mutation) Presenting as a Neurologic Disorder in Adulthood
NEJM 318:1738-1741, 1752-17541988., Carmel,R.,et al, 1988

Transient CNS Deficits:A Common, Benign Syndrome in Young Adults
Neurol 38:831-836, Levy,D.E., 1988

Thalamic Astasia:Inability to Stand After Unilateral Thalamic Lesions
Ann Neurol 23:596-603, Masdeu,J.C.&Gorelick,P.B., 1988

A Prospective Study of Acute Idiopathic Neuropathy, I, Clinical Features & Their Prognostic Value
JNNP 51:605-612, Winer,J.B.,et al, 1988

Fatal Adult Respiratory Distress Syndrome in a Patient with Lyme Disease
JAMA 259:2737-2739, Kirsch,M.,et al, 1988

Respiratory Muscle Dysfunction in Hereditary Motor Sensory Neuropathy, Type I
Arch Int Med 148:1739-1740, Eichacker,P.Q.,et al, 1988

Neurologic Basis of Voiding Disorders in Patients with Cerbrovascular Accident
Semin Neurol 8:156-158, Khan,Z.,et al, 1988

The Lambert-Eaton Myasthenic Syndrome, A Review of 50 Cases
Brain 111, 577-5961988., O'Neill,J.H.,et al, 1988

Posterior Cortical Atrophy
Arch Neurol 45:789-793, Benson,D.F.,et al, 1988

Diaphragm Pacing for Ventilatory Insufficiency
J Inten Care Med 2:345-353, Marcy,T.W.&Loke,J.S., 1987

Pathophysiology & Clinical Assessment of Motor Symptoms in Parkinson's Disease
In Handbk of Parkinson's Disease, Marcel Dekker, Inc, New York, p997., Jankovic,J., 1987

Alternating Hemiplegia of Childhood
Int Pediatr 2:115-119, Aicardi,J., 1987

Life Spans of Duchenne Muscular Dystrophy Patients in the Hospital Care Program in Japan
J Neurol Sci 81:155-158, Mukoyama,M.,et al, 1987

Urinary & Gait Disturbances as Markers for Early Multi-Infarct Dementia
Stroke 18:138-141, Kotsoris,H.,et al, 1987

Functional Abilities after Stroke:Measurement, Natural History & Prognosis
JNNP 50:177-182, Wade,D.T.&Hewer,R.L., 1987

Benign Transient Urinary Retention
JNNP 50:354-355, Herbaut,A.G.,et al, 1987

Endemic Tropical Spastic Paraparesis Associated with HTLV-I:A Clinical & Seroepidem Study of 25 Cases
Ann Neurol 21:123-130, Vernant,J.C.,et al, 1987

Clinical Assessment of 31 Patients with Wilson's Disease, Correlations with Struct. Changes on MRI
Arch Neurol 44:365-370, Starosta-Rubinstein,S.,et al, 1987

Neurotoxic Effects of Organophosphorus Insecticides:An Intermediate Syndrome
NEJM 316:761-763, 807-8081987., Senanayake,N.&Karalliedde,L., 1987

Idiopathic Hypoparathyroidism with Extensive Brain Calcification & Persistent Neurologic Dysfunction
Neurol 37:307-309, Friedman,J.H.,et al, 1987

Clinicopath Conf
Castleman's Disease, Synd of Polyneuropathy, Organomegally, Endocrinopathy, Monoclonal Gammopathy, &, Skin CPOEM Synd),NEJM 316:606-618,1987., 1987

Progressive Aphasia without Dementia:Two Cases with Focal Spongiform Degeneration
Ann Neurol 22:527-532, Kirshner,H.S.,et al, 1987

Primary Progressive Aphasia-Differentiation from Alzheimer's Disease
Ann Neurol 22:533-534, Mesulam,M.M., 1987

Dyslexic Doctors
NEJM 317:171, Guyer,B.P., 1987

Basilar Artery Stenosis:Middle & Distal Segments
Neurol 37:1742-1746, Pessin,M.S.,et al, 1987

Dysphagia in Acute Stroke
BMJ 295:411-414, Gordon,C.,et al, 1987

The Neurologic Examination in Patients with Probable Alzheimer's Disease
Arch Neurol 44:929-932, Huff,F.J.,et al, 1987

Adult-Onset Spinocerebellar Syndrome with Idiopathic Vitamin E Deficiency
Ann Neurol 22:84-87, Yokota,T.,et al, 1987

Tropical Spastic Paraparesis in the Seychelles Islands:A Clinical & Case-Control Neuroepidemiologic Study
Neurol 37:1323-1328, Roman,G.C.,et al, 1987

Progressive Multifocal Leukoencephalopathy Associated with Human Immunodeficiency Virus Infection
Ann Int Med 107:78-87, Berger,J.R., 1987

Clinicopath. Conf
Cryptococcal Meningitis & Septicemia, AIDS After Platelet Tranfusion, Case 41-1987, NEJM 317:946-953, , 1987

Practical Problems in the Respiratory Care of Patients with Muscular Dystrophy
NEJM 316:1197-1205, Smith,P.E.M.,et al, 1987

Cytochrome c Oxidase Deficiency in Leigh Syndrome
Ann Neurol 22:498-506, DiMauro,S.,et al, 1987

Plasma R Binder Deficiency & Neurologic Disease
NEJM 317:1330-1332, Sigal,S.H.,et al, 1987

Long Term Exposure to Hydrogen Sulphide Producing Subacute Encephalopathy in a Child
BMJ 294:614, Gaitonde,U.B.&Sellar,R.J., 1987

Update on Parkinson Disease
NY State J Med, 87:147-1531987., Lieberman,A.N., 1987

Incontinentia Pigmenti:Association with Anterior Horn Cell Degeneration
Neurol 37:446-450, Larsen,R.,et al, 1987

Peripheral Vision in Persons with Dyslexia
NEJM 316:1238-1243, 1268-12701987., Geiger,G.&Lettvin,J.Y., 1987



Showing articles 1250 to 1300 of 1589 << Previous Next >>