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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 1550 to 1589 of 1589 << Previous

Specific Learning Disorders in Childhood
Psych Annals 2:, 1972 May., Gomez,M.R., 1972

The Relationship of Motility Problems to Reading Problems
MCV Quart 8:298, McNeer,K., 1972

Mucopolysaccaridosis IV (Morquio Syndrome) , in Heritable Disorders of Connective Tissue
(Ed) 4th Ed, The C. V. Mosby Co, St. Louis, p. 583, McKusick,V.A., 1972

Aphasia Current Conceps
NEJM 284:654, Geschwind,N., 1971

Parkinsonism-Physiology & Pharmacology
BMJ 3:693, Calne,D.B., 1971

Associative Visual Agnosia
Arch Neurol 24:305, Rubens,A.,et al, 1971

Neurologic Complications of Malignant External Otitis
Neurol 21:1077, Schwarz,G.A.,et al, 1971

Neurologic Aspects of Malignant External Otitis:Report of Three Cases
Mayo Clin Proc 46:339, Dinapoli,R.P.,et al, 1971

Right Hemianopia with Memory & Color Deficits in Circumscribed Left Posterior Cerebral Artery Territory Infarction
Neurol 2l:1104-1113, 1971, Mohr,J.P.,et al, 1971

Respiratory Manifestations & Disorders of Alvelo-capillary Diffusion During Horton's Disease
J Fr Med Chir Thorac 25:775-783, Modal,J.,et al, 1971

Fibrous Dysplasia, In Neurology In Pediatrics
(Ed) , 1970 Year Book Med. Publishers, p. 165., Bray,P.F., 1970

Brain Stem Tumors of Childhood & Adolescence
Am J Dis Child 119:465-472, Panitch,H.S.,et al, 1970

Whipple's Disease:A Review of 19 Pnts from one Hospital & a Review of the Literature since 1950
Medicine 49:175, Maizel,H.,et al, 1970

The Neuropathy of Acute Intermittent Porphyria
Quart J Med 38:307, 1969 July., Ridley,A., 1969

Ocular Myopathy
Arch Neurol 20:1, Magora,A.,et al, 1969

The Alexias
Handbook of Clinical Neurology, Vol 4, (Chapter 7) p. 112., Benson,F.&Geschwind,N., 1969

Congenital Word Blindness of Specific Developmental Dyslexia:A Review
Med J Aust 1:783, Hagger,T.D., 1968

Clinical & Pathological Findings in a Child with a Developmental Learning Disability
J Lear Dis 1:486, Drake,V.E., 1968

The Oculopharyngeal Syndrome
JAMA 203:1003, Murphy,S.F.,et al, 1968

Cerebral Dominance & Its Disturbances
Ped Clin North Am 15:759-769, Benson,D.F.,et al, 1968

Corticodentatonigral Degeneration with Neuronal Achromasia
Arch Neurol 18:20-33, Rebeiz,J.J.,et al, 1968

Huntington's Chorea
Bruyn, G. W. In Vinken & Bruyn, Handbk of Clin Neurol, North-Holland Publ Co, Amsterdam, 6:298, , 1968

Parkinson's Disease
In Handbk of Clinical Neurology, Vinken, P. J. & Bruyn, G. W. , Ed, North-Holland Publ Co, Amsterdam, 6:173, 1968. Selby, G., 1968

Color-Naming Defects in Association With Alexia
Arch Neurol 15:137-146, Geschwind,N.,et al, 1966

Addison's Disease, In The Diagnosis of Stupor & Coma
& Posner, J. , FA Davis Co. 1966, p. 145-146., Plum,F., 1966

The Uveomeningoencephalitic Syndrome
Neurol 16, 6031966., Riehl,J.L.,et al, 1966

Bladder Dysfunction in Multiple Sclerosis
BMJ 1:1265-1269, Miller,H.,et al, 1965

Non-Aphasia Disorders of Speech
International Jour Neurol 4:207-214, Geschwind,N., 1964

Neurological Complications of Endometriosis
Proc Royal Society Medicine 56:874-875, Kohorn,E.I., 1963

Brain Stem Tumors Occuring in Adults
Neurol 13:292, While,H.H., 1963

The Anatomy of Acquired Disorders of Reading
In Money, J. (Ed. ) , Reading Disability, Baltimore:Johns Hopkins Press, 1962 P. 115-129., Geschwind,N., 1962

Acute Cerebellar Syndrome Secondary to Infectious Mononucleosis in a Fifty-Two Yealr Old Man
Ann Int Med 55:147-149, Bennett,D.R.&Peters,H.A., 1961

Neurologic Manifestations of Chronic Pulmonary Insufficiency
NEJM 257:579-590, Austen,F.K.,et al, 1957

Anomic Aphasia- (differential diagnosis & cerebral localization of lesion in twenty cases)
JAMA 151:462, Suter,C., 1956

An Unusual Variant of Acute Idiopathic Polyneuritis (Syndrome of Ophthalmoplegia, Ataxia, & Areflexia)
NEJM 255:57, Fisher,C.M., 1956

Uncommon symptoms of migraine
Trans Ophthal Soc U K 61:205, Butler,T.H., 1941

An Acute Syndrome of Ocular Oscillations & Truncal Ataxis
p. 96-99., Winkler,G.,et al, 1850

An 81-Year-Old Man with Imbalance and Memory Impairment
, Golbe,L.I.,et al,

MR Imaging of Central Nervous System Whipple Disease: A 15-Year Review
AJNR 31:1493-1497, Black,D.F.,et al,

Clinical Study of Nine Patients with ReNU Syndrome
, Okamoto,N.,et al,



Showing articles 1550 to 1589 of 1589 << Previous