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Differential
(Click to cross reference)
ankle reflex, absent
areflexia
arrhythmia, cardiac
ataxia
ataxia, cerebellar
ataxia, progressive
ataxic gait
autosomal rcessive spastic ataxia of Charlevoix-Saguenay
Babinski sign
benign essential tremor
Brown-Vialetto-Van Laere syndrome
calf hypertrophy
cardiomyopathy
central core disease
cerebellar atrophy, primary
Charcot-Marie-Tooth
children
chromosomal abnormality
chromosome 17
clubfoot as related to neurologic disease
cognition
consanguinity
contractures, joint
corpus callosum, thinning
cranial neuropathy
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
developmental milestones, loss of
differential diagnosis
dislocated hip, congenital
distal muscle atrophy
distal muscle weakness
diurnal variation
dopa responsive dystonia
dysarthria
dystonia
endemic area
evoked potentials
facial weakness
failure to thrive
falling
familial
fine motor function, impaired
finger nose finger test
foot deformity
foot drop
gait disorder
gait, waddling
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
hammertoes
hand deformity
hand weakness
hearing loss
high arched feet
hyperreflexia
hyporeflexia
hypotonia
hypotonia, infants
imbalance
incoordination
intrinsic hand muscles, wasting of
kyphoscoliosis, neurologic causes of
L-dopa
leg weakness, bilateral
leprosy
lordosis
malignant hyperpyrexia
microcephaly
mitral valve prolapse
molecular genetics
MRI, abnormal
muscle atrophy, static
muscle biopsy
muscle cramp
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker
myopathy
nerve conduction studies
nerve enlargement
nerve hypertrophy
neuropathy
neuropathy, hereditary peripheral
neuropathy, hypertrophic
neuropathy, peripheral
nystagmus
pain, foot
Parkinson disease
past pointing
pes cavus
polymerase chain reaction
polyneuropathy
polyneuropathy, familial
pons, lesion of
prognosis
progressive neurologic disorder
pseudohypertrophy
pyramidal tract dysfunction
rash
Red flags
renal tubular acidosis
review article
riboflavin transporter deficiency
Romberg's sign
Samoa
scoliosis
scoliosis, neurologic association with
sensory loss
skin, biopsy
skin, lesions in neurologic disorders
steppage gait
toe walking
treatment of neurologic disorder
tremor
tremor, intention
tripping
visual evoked response
walking
walking frame
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
wheelchair
wide based gait
wrist drop
Showing articles 750 to 800 of 872 << Previous Next >>

Aseptic Meningitis & High School Football Players 1978 & 1980
JAMA 249:2039-2042, Moore,M.,et al, 1983

Clinicopathological Conference
Maroteaux-Lamy Syndrome, Case 44-1983, NEJM 309:1109-1117983., , 1983

Clinical Epidemology of Toxic-Oil Syndrome
NEJM 309:1408-1414, Kilbourne,E.M.,et al, 1983

Neurological Aspect of Hyponatraemia
Postgrad Med J 58:737-740, Daggett,P.,et al, 1982

Primary Writing Tremor:A Selective Action Tremor
Neurol 32:203-206, Klawans,H.L.,et al, 1982

Primary Pontine Hemorrhage & the Dysarthria-clumsy Hand Syndrome
Neurol 32:1027-1028, Tuhrim,S.,et al, 1982

Treatment of Action Tremor in Multiple Sclerosis with Isoniazid
Neurol 32:912-913, Sabra,A.F.,et al, 1982

Tremor After Head Injury & Its Treatment by Stereotaxic Surgery
JNNP 45:815-819, Andrew,J.,et al, 1982

Writers'Cramp-A Focal Dystonia
Brain 105:461-480, Sheehy,M.P.,et al, 1982

The Clinical Relevance of CSF Viral Culture
JAMA 247:1843-1847, Chonmaitree,T.,et al, 1982

Aseptic Meningitis Among Members of a High School Football Team
JAMA 248:1724-1727, Baron,R.C.,et al, 1982

Distal Myopathy, Histochemical & Ultrastructural Studies
Arch Neurol 39:367-371, Kumamoto,T.,et al, 1982

Immediate & Delayed Neurotoxicity After Mechlorethamine Preparation for Bone Marrow Transplantation
Ann Int Med 97:182-189, Sullivan,K.M.,et al, 1982

Dysaesthesias & Dysautonomia:A Self-limited Syndrome of Painful Dysaesthesias & Autonomic Dysfunction in Childhood
JNNP 45:162-165, Nass,R.,et al, 1982

Tethered Cord Syndrome in Adults
J Neurosurg 57:32-47, Pang,D.&Wilberger,J.E.Jr., 1982

Neurologic Signs In Uncomplicated Aging (Senscence)
Seminars In Neurology, Thieme-Stratton Inc. , New York, N. Y. pp. 21-30, Jenkyn,L.R.&Reeves,A.G., 1981

Late Onset of Wilson's Disease
Arch Neurol 38:729-730, Czlonkowska,A.,et al, 1981

Encephalopathy in Infants & Children With Chronic Renal Disease
Arch Neurol 38:656-658, Foley,C.M.,et al, 1981

Asperger's Syndrome:A Clinical Account
Psychological Medicine 11:115-129, Wing,L., 1981

Handedness, Clumsiness & Cognitive Ability
Develop Med Child Neurol 22:569-579, Bishop,D.V.M., 1980

Interaction of Lithium & Phenytoin
BMJ 1:610-611, MacCallu,W.A., 1980

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

A pedigree of Amyotrophic Chorea With Acantho-cytosis
Arch Neurol 37:514-517, Kito,S.,et al, 1980

Diagnosis & Treatment, Physiologic & Pathologic Tremors
Ann Int Med 93:460-465, Jankovic,J.,et al, 1980

Motor Neuropathy Associated with Cimetidine
BMJ 281:974-975, Walls,T.J.,et al, 1980

An Autosomal Dominant Syndrome of Hemiplegic Migraine, Nystagmus, & Tremor
Ann Neurol 8:329-332, Zifkin,B.,et al, 1980

Myositis, Myoglobinemia, & Myoglobinuria Associated With Enterovirus Echo 9 Infection
Arch Neurol 37:457-458, Jehn,U.W.,et al, 1980

Congenital Myotonic Dystrophy
Arch Neurol 37:693-696, Argov,Z.,et al, 1980

Successful Treatment of Inorganic Mercury Neurotoxicity with N-acetyl-penicillamine Despite an Adverse Reaction
Neurol 30:1000-1001, Markowitz,L.,et al, 1980

Metrizamide Encephalopathy
Ann Neurol 7:494, Vincent,F.M.,et al, 1980

Human Cerebellar Hypoplasia, A Syndrome of Diverse Causes
Arch Neurol 37:300-305, Sarnatt,H.B.,et al, 1980

Juvenile Metachromatic Leukodystrophy
Arch Neurol 37:42-46, Haltia,T.,et al, 1980

Amyloid Neuropathy & Tremor in Waldenstrom's Macroglobulinemia
Arch Neurol 37:240-242, Bajada,S.,et al, 1980

Juvenile Muscular Atrophy Localized to Arms
Arch Neurol 37:297-299, Singh,N.,et al, 1980

Cerebellar Involvement in Multifocal Eosinophilic Granuloma:Demonstration by CT Scan
Ann Neurol 7:125-129, Adornato,B.T.,et al, 1980

Multiple Endocrine Neoplasia, Type 2b:Phenotype Recognition; Neurological Features & Their Pathological Basis
Ann Neurol 6:302-314, Dyck,P.J.,et al, 1979

Acute Generalized Polyneuropathy Accompanying Lithium Poisoning
Ann Neurol 6:360-362, Brust,J.C.M.,et al, 1979

Hereditary Myoclonus & Progressive Distal Muscular Atrophy
Ann Neurol 6:227-231, Jankovic,J.,et al, 1979

Valproic Acid, Review of a New Antiepileptic Drug
Arch Neurol 36:393-398, Bruni,J.,et al, 1979

Tremor Due to Sodium Valproate
Neurol 29:1177-1180, Hyman,N.M.,et al, 1979

Clinical Pathological Conference, Peripheral Neuropathy in Leprosy
NEJM 300:546-553, Dawson,D., 1979

Emery-Dreifuss Muscular Dystrophy
Ann Neurol 5:111-117, Rowland,L.P.,et al, 1979

Congenital Ocular Motor Apraxia
Arch Neurol 36:29-31, Orrison,W.W.,et al, 1979

Giant Axonal Neuropathy
Arch Neurol 36:107-108, Mizuno,Y.,et al, 1979

Upper Trunk Brachial Plexopathy in Football Players
JAMA 241:1480-1482, Robertson,W.C.,et al, 1979

Dysarthria-Clumsy Hand Syndrome Produced by Capsular Infarct
Ann Neurol 6:263-265, Spertell,R.B.,et al, 1979

Familial Periodic Ataxia
Arch Neurol 36:568-569, Donat,J.R.,et al, 1979

Isolated Trigeminal Sensory Neuropathy:Early Manifestation of Mixed Connective Tissue Disease
Neurol 28:1286-1289, Searles,R.P.,et al, 1978

Adult Onset Nemaline Myopathy
Neurol 28:1306-1309, Brownell,A.K.W.,et al, 1978

Distal Chronic Spinal Muscular Atrophy Involving the Hands
JNNP 41:653-658, O'Sullivan,D.J.,et al, 1978



Showing articles 750 to 800 of 872 << Previous Next >>