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acetazolamide
Addison's disease
advances in neurology
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, Parkinson-dementia-complex
Andersen syndrome
antibodies to voltage-gated calcium channels
areflexia
arrhythmia, cardiac
Asians
ataxia
ataxia, cerebellar
ataxia, paroxysmal
atlanto axial dislocation, congenital
atrial fibrillation
autoimmune disease
bicarbonate
bitemporal visual field defect
calcification, intracranial
calcium channel dysfunction
carpo-pedal spasm
case studies
CAT scan
CAT scan, muscle
cavernous sinus, syndrome
central core disease
cerebrospinal fluid, childhood
channelopathy
chloride channel dysfunction
Chvostek sign
Clinical Pathologic Conference(C.P.C.)
coma
congenital myopathy
conjunctival injection
craniopharyngioma
creatine phosphokinase(CPK)elevated
Cushing's syndrome
deep tendon reflexes
diabetes mellitus
diabetes mellitus, neurologic manifestations of
diarrhea
dichlorphenamide
diet
drug abuse, inhalation
drug induced neurologic disorders
dysmorphic
electrocardiogram, abnormal
electromyogram
electron microscopy
encephalocele
epidemiology of neurology
episodic disorders
episodic neurologic deficits
exercise
exophthalmus
facial weakness
facial weakness, bilateral
familial
familial hemiplegic migraine
fasciculation
fatigue
flaccid paralysis
gait disorder
gaze palsy, supranuclear
gender
gene
gene mutation
genetic linkage
genetic neurologic disorders
gynecomastia
hallucination, auditory
Hand-Schuller-Christian disease
hemangioma
hyperadrenalism
hypercalcemia
hyperinsulinism
hyperkalemia
hyperkalemic periodic paralysis
hyperparathyroidism
hyperthyroidism
hypokalemia
hypokalemic paralysis
hypokalemic periodic paralysis
hypoparathyroidism
hypophosphatemia
hyporeflexia
hypothalamus
hypothalamus, disturbance of
inclusion body myositis
infantile tremor syndrome
insomnia
intrinsic hand muscles, wasting of
islet cell tumor
leg numbness
leg weakness, bilateral
malformation, CNS, congenital
malformation, vascular
malformation, vascular, cerebral
malignant hyperpyrexia
methyl benzene
mexiletine
migraine
migraine, hemiplegic
molecular genetics
motor neuron disease
motor neuron disease, juvenile form
MRI
MRI, muscle
multiple sclerosis
muscle biopsy
muscle cramp
muscle diseases, characteristics of
muscle pain
muscle weakness
muscle weakness, causes of
muscle weakness, proximal
muscle weakness, sudden onset of
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, Duchenne
myasthenia gravis
myasthenic syndrome
myoedema
myoglobinuria
myopathy
myopathy, drug-induced
myopathy, mitochondrial
myotonia congenita
myotonia dystrophica
myxedema coma
myxedema, neurologic manifestations of
neoplasm, pituitary
neuroendocrinology
neurologic disease
neurologic disease, diagnoses of
ophthalmoplegia
ophthalmoplegia, painful
ophthalmoplegia, total
pain, leg
papilledema
paralysis
paralysis, acute
paralysis, acute areflexic
paralysis, recurrent
paramyotonia congenita
paranoia
paraparesis
paraparesis, acute
paraparesis, transient
paraplegia, recurrent
parathyroid adenoma
paroxysmal neurologic deficits
periodic paralysis
periodic paralysis, thyrotoxic
pheochromocytoma
polymyositis
potassium
potassium channel antibodies
potassium channel dysfunction
precipitating factors
primary aldosteronism
prognosis
psychosis
quadriparesis
quadriparesis, acute
quadriplegia
quadriplegia, transient
race
renal tubular acidosis
review article
rhabdomyolysis
seizure
sodium channel dysfunction
spina bifida
spinocerebellar ataxia
spinocerebellar ataxia type 6
subacute myelo-opticoneuropathy(S.M.O.N.)complex
subarachnoid hemorrhage
sudden death
tetany
thiazide diuretic
thyroid function tests
thyroid gland, enlarged
thyrotoxicosis
Tolosa Hunt syndrome
transient neurologic deficit
treatment of neurologic disorder
tremor
Trousseau's sign
tubular aggregates, muscle
walking, difficulty with
weakness
weakness, acute
weakness, episodic
weakness, generalized
weakness, proximal
weight loss
Showing articles 1600 to 1650 of 3257 << Previous Next >>

Pott's Paraplegia Today
Lancet 346:264, Miller,J.D., 1995

Spinal Dural Arteriovenous Fistula:The Pathology of Venous Hypertensive Myelopathy
Neurol 45:1309-1313, Hurst,R.W.,et al, 1995

Transient Ictal Cortical Blindness During Middle Age:A Case Report and Review of the Literature
J Neuro-Ophthalmol 15:39-42, Joseph,J.M.&Louis,S., 1995

Ictal Amaurosis:MRI, EEG, and Clinical Features
Neurol 45:1619-1621, Gilliam,F.&Wyllie,E., 1995

The Transient Syndrome of Headache with Neurologic Deficits and CSF Lymphocytosis
Neurol 45:1648-1654, Berg,M.J.&Williams,L.S., 1995

Psychosis as the Initial Manifestation of Adult-Onset Niemann-Pick Disease Type C
Neurol 45:1739-1743, Shulman,L.M.,et al, 1995

Campylobacter Jejuni Infection and Guillain-Barre Syndrome
NEJM 333:1374-1379, 14151995., Rees,J.H.,et al, 1995

Neurologic Manifestations in Children with Lyme Disease
Pediatrics 96:1053-1056, Bingham,P.M.,et al, 1995

Myasthenic Symptoms in Patients with Mitochondrial Myopathies
Muscle & Nerve 18:1338-1340995., Forestier,N.L.,et al, 1995

Clinicopath Conf
Progressive Muscular Atrophy, Case 36-1995, NEJM 333:1406-1412995., , 1995

Neurodegeneration and Diabetes:UK Nationwide Study of Wolfram (DIDMOAD) Syndrome
Lancet 1458-1463, Barrett,T.G.,et al, 1995

Neurotoxicity in Liver Transplant Recipients with Cyclosporine Immunosuppression
Neurol 45:1962-1964, Wijdicks,E.F.M.,et al, 1995

Hereditary Hemorrhagic Telangiectasia
NEJM 333:918-924, Guttmacher,A.E.,et al, 1995

Neuromuscular Effects of Papuan Taipan Snake Venom
Ann Neurol 38:916-920, Connolly,S.,et al, 1995

Lid Nystagmus as a Sign of Intrinsic Midbrain Disease
J Neuro-Ophthalmol 15:236-240, Brodsky,M.C.&Boop,F.A., 1995

Clinical, Neuropath & Genetic Studies of Large Spinocerebellar Ataxia Type 1 (SCA1) Kindred: (CAG) n Early Premonitory Signs & Symp
Neurol 45:24-30, Genis,D.,et al, 1995

Familial Occurrence of Cluster Headache
JNNP 58:341-343, Russell,M.B.,et al, 1995

Risk of Recurrent Stroke in Patients with Sickle Cell Disease Treated with Erythrocyte Transfusions
J Pediatr 126:896-899, Pegelow,C.H.,et al, 1995

Thalamic Hemorrhage:A Prospective Study of 100 Patients
Stroke 26:964-970, Kumral,E.,et al, 1995

Vertical Gaze Palsies from Medial Thalamic Infarctions without Midbrain Involvement
Stroke 26:1467-1470, Clark,J.M.&Albers,G.W., 1995

Autosomal Dominant Migraine with MRI White-Matter Abnormalities Mapping to the CADASIL Locus
Neurol 45:1086-1091, Chabriat,H.,et al, 1995

Autosomal Dominant, Familial Spastic Paraplegia, Type I:Clinical and Genetic Analysis of a Large North American Family
Neurol 45:325-331, Fink,J.K.,et al, 1995

Critical Illness Neuromuscular Disease in Children Manifested as Ventilatory Dependence
J Pediatr 126:259-261, Sheth,R.D.,et al, 1995

Lesion Localization in Periodic Lateralized Epileptiform Discharges:Gray or White Matter
Epilepsia, 36:58-621995., Raroque,H.G.&Purdy,P., 1995

Late-Onset Mitochondrial Myopathy
Ann Neurol 37:16-23, 31995., Johnston,W.,et al, 1995

Intramuscular Inject W/in 30 D of Immun with Oral Poliovirus Vaccine-Risk Factor for Vaccine-Assoc Paral Polio
NEJM 332:500-506, 5291995., Strebel,P.M.,et al, 1995

A Gene for Hereditary Paroxysmal Cerebellar Ataxia Maps to Chromosome 19p
Ann Neurol 37:289-293, 2851995., Vahedi,K.,et al, 1995

Gene Analysis of L1 Neural Cell Adhesion Molecule in Prenatal Diagnosis of Hydrocephalus
Lancet 345:161-162, Jouet,M.&Kenwrick,S., 1995

Anterior Communicating Artery Aneurysm Paraparesis Syndrome:Clinical Manifestations and Pathologic Correlates
Neurol 45:45-50, Greene,K.A.,et al, 1995

Diagnosis of Whipple's Disease
NEJM 332:390-392, Dobbins,W.O., 1995

Medial Medullary Syndrome:Report of 18 New Patients and a Review of the Literature
Stroke 26:1548-1552, Kim,J.S.,et al, 1995

Prolonged Paralysis After Neuromuscular Blockage
Muscle & Nerve, 18:937-94295., Gooch,J., 1995

The Narcolpetic Syndrome
JNNP 59:221-224, Parkes,J.D.,et al, 1995

The Management of Thrombosis in the Antiphospholipid-Antibody Syndrome
NEJM 332:993-997, 10251995., Khamashta,M.A.,et al, 1995

Cephalosporin-Induced Recurrent Aseptic Meningitis
Ann Neurol 37:815-817, Creel,G.B.&Hurtt,M., 1995

Cranial Nerve Enhancement in the Guillain-Barre Syndrome
AJNR 16:923-925, Fulbright,R.K.,et al, 1995

Clinical Relevance and Frequency of Transient Stenoses of the Middle and Anterior Cerebral Arteries in Bacterial Meningitis
Stroke 26:1399-1403, Muller,M.,et al, 1995

Lyme Neuroborreliosis
Ann Neurol 37:691-702, Garcia-Monco,J.C.&Benach,J.L., 1995

Neuro-Ophthalmologic Manifestations of Lyme Disease
Ophthalmology 97:699-706, Lesser,R.L.,et al, 1995

Myositis:Immunologic Contributions to Understanding Cause, Pathogenesis, and Therapy
Ann Int Med 122:715-724, Plotz,P.H.,et al, 1995

Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995

Amyloidosis Causing A Progressive Myopathy
Muscle & Nerve 18:1016-1018995., Nadkarni,N.,et al, 1995

Natural History in Proximal Spinal Muscular Atrophy
Arch Neurol 52:518-523, Zerres,K.&Rudnik-Schoneborn,R., 1995

Lambert-Eaton Myasthenic Syndrome (LEMS) in Association with Lymphoproliferative Disorders
Muscle & Nerve 18:715-719995., Argov,Z.,et al, 1995

Pamidronate Treatment of the Neurologic Sequelae of Pagetic Spinal Stenosis
Arch Int Med 155:1813-1815, Wallace,E.,et al, 1995

Genotype-Phenotype Correlation in Adult-Onset Acid Maltase Deficiency
Ann Neurol 38:450-454, Wokke,J.H.J.,et al, 1995

Clinical Variability in Adult-Onset Acid Maltase Deficiency:Report of Affected Sibs and Review of Literature
Medicine 74:131-135, Felice,K.J.,et al, 1995

The Crossed Paralyses
Arch Neurol 52:635-638, Silverman,I.E.,et al, 1995

Oculomotor Nerve Invasion by Lymphoma Demonstrated by MRI
J Comput Assist Tomogr 19:503-504, Kajiya,Y.,et al, 1995

Acute Bilateral Ophthalmoplegia Secondary to Metastatic Prostatic Carcinoma:Demonstr of Magnetic Resonance Imaging
J Neuro-Ophthalmol 15:45-47, Agarwal,P.,et al, 1995



Showing articles 1600 to 1650 of 3257 << Previous Next >>