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Differential
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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
asymptomatic
ataxia
ataxia, cerebellar
ataxia, paroxysmal
atlanto axial dislocation, congenital
atrial fibrillation
autoimmune disease
autonomic neuropathy
basal ganglia, lesion of
basal ganglia, lesion, bilateral
bicarbonate
bitemporal visual field defect
brachial neuritis
cachexia
calcification, intracranial
calcium channel dysfunction
carpo-pedal spasm
case studies
CAT scan
CAT scan, abdomen
CAT scan, muscle
cavernous sinus, syndrome
CD4 counts
central core disease
cerebrospinal fluid, childhood
channelopathy
chloride channel dysfunction
Chvostek sign
Clinical Pathologic Conference(C.P.C.)
coinfection
coma
congenital myopathy
conjunctival injection
craniopharyngioma
creatine phosphokinase(CPK)elevated
Cushing's syndrome
cystoisospora belli
deep tendon reflexes
Dengue fever
diabetes mellitus
diabetes mellitus, neurologic manifestations of
diarrhea
dichlorphenamide
diet
drug abuse, inhalation
drug induced neurologic disorders
dysmorphic
electrocardiogram, abnormal
electromyogram
electron microscopy
encephalitis
encephalocele
encephalopathy
enteritis
epidemiology of neurology
episodic disorders
episodic neurologic deficits
exercise
exophthalmus
facial weakness
facial weakness, bilateral
familial
familial hemiplegic migraine
fasciculation
fatigue
flaccid paralysis
flavivirus
gait disorder
gaze palsy, supranuclear
gender
gene
gene mutation
genetic linkage
genetic neurologic disorders
Gitelman's syndrome
Guillain Barre syndrome
gynecomastia
hallucination, auditory
Hand-Schuller-Christian disease
headache
hemangioma
heralding manifestation
homosexual
human immunodeficiency virus type 1
hyperadrenalism
hypercalcemia
hyperinsulinism
hyperkalemia
hyperkalemic periodic paralysis
hyperparathyroidism
hypertension
hyperthyroidism
hypocalcemia
hypocalcuria
hypokalemia
hypokalemic paralysis
hypokalemic periodic paralysis
hypomagnesemia
hypoparathyroidism
hypophosphatemia
hyporeflexia
hypothalamus
hypothalamus, disturbance of
inclusion body myositis
India
infantile tremor syndrome
infection
insomnia
intrinsic hand muscles, wasting of
islet cell tumor
leg numbness
leg weakness, bilateral
leukocytosis
liver function enzymes
malformation, CNS, congenital
malformation, vascular
malformation, vascular, cerebral
malignant hyperpyrexia
metabolic alkalosis
methyl benzene
mexiletine
migraine
migraine, hemiplegic
molecular genetics
mortality
motor neuron disease
motor neuron disease, juvenile form
MRI
MRI, abnormal
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, hypokalemic
myopathy, mitochondrial
myositis
myotonia congenita
myotonia dystrophica
myxedema coma
myxedema, neurologic manifestations of
nausea and vomiting
neoplasm, pituitary
Nepal
neuroendocrinology
neurologic disease
neurologic disease, diagnoses of
neuropathy
ophthalmoplegia
ophthalmoplegia, painful
ophthalmoplegia, total
optic neuropathy
pain, abdominal
pain, leg
papilledema
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paralysis, acute
paralysis, acute areflexic
paralysis, recurrent
paramyotonia congenita
paranoia
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paraparesis, acute
paraparesis, transient
paraplegia, recurrent
parathyroid adenoma
paresthesias
paroxysmal neurologic deficits
periodic paralysis
periodic paralysis, thyrotoxic
pheochromocytoma
polymyositis
potassium
potassium channel antibodies
potassium channel dysfunction
precipitating factors
primary aldosteronism
prognosis
protozoan infection
psychosis
quadriparesis
quadriparesis, acute
quadriplegia
quadriplegia, transient
race
rash
renal tubular acidosis
retinopathy
review article
rhabdomyolysis
risk factors
screening
seizure
sicca syndrome
Sjogren's syndrome
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
travel, foreign
treatment of neurologic disorder
tremor
Trousseau's sign
tubular aggregates, muscle
viral infection
viral infection, CNS
walking, difficulty with
weakness
weakness, acute
weakness, episodic
weakness, generalized
weakness, progressive
weakness, proximal
weight loss
yersinia enterocolitica
Showing articles 0 to 50 of 2601 Next >>

Clinicopathologic Conference, Thyrotoxic Periodic Paralysis Associated with Graves Disease
NEJM 390:1514-1522, Case 13-2024, 2024

Thyrotoxic Periodic Paralysis
UptoDate Jan, Gutmann, L. & Conwit, R., 2022

An Unusual Cause of Hypokalemic Paralysis
Neurol 87:e174-e177, Shree, R.,et al, 2016

Neurologic Complications in Dengue Virus Infection
Neurol 83:1601-1609,1590, Sahu, R.,et al, 2014

Clincopathologic Conference,Graves Disease with Thyrotoxic Periodic Paralysis
NEJM 366:553-560, Case 4-2012, 2012

Clinicopathologic Conference, Cystoisospora Belli Enteritis and HIV Infection
NEJM 365:2306-2316, Case 38-2011, 2011

Family Paralysis
Lancet 377:352, Sung,C.-C.,et al, 2011

Diagnosis and New Treatment in Muscle Channelopathies
JNNP 80:360-365, Meola,G.,et al, 2009

Woke Up Paralysed--Without Injury or Stroke
Lancet 371:870, Bawaskar,H.S. &Bawaskar,P.H., 2008

Recurrent Paralysis in a Young Man
Lancet 355:1612, Koul,P.A.&Wahid,A., 2000

Ion Channel Diseases:Episodic Disorders of the Nervous System
Semin Neurol 19:363-369, Ptacek,L.J., 1999

The Exercise Test in Andersen Syndrome
Arch Neurol 56:352-356, Katz,J.S.,et al, 1999

Ion Channels and Neurological Disease:DNA Based Diagnosis is Now Possible,and Ion Channels May be Important in Common Paroxysmal Disorders
JNNP 65:427-431, Hanna,M.G.,et al, 1998

Primary Aldosteronism
NEJM 339:1828-1834, Ganguly, A., 1998

Calcium Channels in Neurological Disease
Ann Neurol 42:275-282, Greenberg,D.A., 1997

Investigation of Muscle Disease
JNNP 60:256-274, Mastaglia,F.L.&Laing,N.G., 1996

Hyperkalemic Periodic Paralysis:Rapid Molecular Diag & Rela of Genotype to Phenotype in 12 Families
Neurol 43:668-673, Feero,W.G.,et al, 1993

Thyrotoxic Periodic Paralysis in the US, Report of 7 Cases & Review of the Literature
Medicine 71:109-120, Ober,K.P., 1992

Hyperinsulinaemia in Thyrotoxic Hypokalaemic Periodic Paralysis
Lancet 337, 1063-10641991., Lee,K.,et al, 1991

Progressive Myopathy in Hyperkalemic Periodic Paralysis
Arch Neurol 47:1013-1017, Bradkey,W.G.,et al, 1990

Flaccid Quadriparesis Associated with Yersinia Enterocolitis-Induced Hypokalemia
Arch Int Med 149:1193-1194, Orman,R.A.&Lewis,J.B., 1989

Thyrotoxic Periodic Paralysis
Am J Med 80:146-149, Ferreiro,J.E.,et al, 1986

Tubular Aggregates, Their Association with Neuromuscular Diseases, Including the Syndrome of Myalgias/Cramps
Arch Neurol 42:973-976, Rosenberg,N.L.,et al, 1985

Acute Effects of Acetazolamide in Hyperkalemic Periodic Paralysis
Neurol 31:725-729, Riggs,J.E.,et al, 1981

Hypokalemic Periodic Paralysis in Chronic Toluene Exposure
Arch Neurol 37:673, Bennett,R.H.,et al, 1980

Progressive Supranuclear Palsy & Hyperkalemic Periodic Paralysis
Arch Neurol 37:461-462, Foster,N.L.,et al, 1980

Neurological Problems in Endocrine Diseases
Med Clin North Am 56:1029, Dale,A., 1972

Periodic Paralysis:Functions of Sarcoplasmic Reticulum & Metabolism of Glycogen
Neurol 22:426, Tkagi,A.,et al, 1972

The Geography of Neurology
BMJ 2:506, Spillane,J.D., 1972

Hypokalemic Periodic Paralysis withArrhythmia
NEJM 286:253, Levitt,L.,et al, 1972

Wall-Eyed Bilateral Internuclear Ophthalmoplegia Variant Syndrome Caused by Isolated Left Thalamic Infarction
Neurol 102:e209475, Wu,B.P.,et al, 2024

Clinicopathologic Conference, Myeloperoxidase antineutrophil cytoplasmic antibody-associated vasculitis
NEJM 390:843-851, Case 7-2024, 2024

A 19-Month Old Girl with Infantile-Onset Myopathy and White Matter Changes
Neurol 102:e209258, Lail,G.,et al, 2024

Intracranial Hypertension Associated with Poly-Cranio-Radicular-Neuropathies A Case Report and Review of the Literature
Neurologist 29:166-169, Eaton,J.E.,et al, 2024

Expanding Clinical Spectrum an Anti-GQ1b Antibody Syndrome, A Review
JAMA Neurol 81:762-770, Lee,S-U.,et al, 2024

A 60-Year-Old Woman with Rapidly Progressive Muscle Weakness and Ophthalmoparesis
Neurol 103:e209708, Wannarong,T.,et al, 2024

Clinical and Imaging Features of Cobb Syndrome
Neurol 102:e208118, Yang,X.,et al, 2024

Clinicopathologic Conference, Infant Botulism, Case 3-2024
NEJM 390:358-366, Case 3-2024, 2024

Ischemic Retinopathy from Prolonged Orbital Compression
NEJM 390::e14, Chen,Y-K and Chen C-L, 2024

A 26-Year-Old Woman with Chronic Progressive Gait Dysfunction
Neurol 103:e2098-e2030, Jones,F.J.S. & Orthmann-Murphy,J., 2024

A 32-Year-Old Man with Painless Bilateral Shoulder Girdle Weakness and Atrophy
Neurol 103:e209915, Gutti,N.B.,et al, 2024

A 22-Year-Old Woman with Episodic Weakness and Jaundice
Neurol 103:e210018, Rathinasbapathi,M.,et al, 2024

Clinicopathologic Conference, Myasthenia Gravis
NEJM 391:1441-1450, Case 32-2024, 2024

A 50-Year-Old Man with Ataxia, Dystonia, and Abnormal Ocular Movements
Neurol 103:e210046, Panigrahi,B.,et al, 2024

Occipital Condyle Syndrome
Neurol 103:e210067, Mirian,A.,et al, 2024

A 63-Year-Old Man With Progressive Multicranial Neuropathy and Leptomeningeal Enhancement
Neurol 103:e210100, Taga,A.,et al, 2024

Clinicopathologic Conference, Infective Endocarditis Due to Haemophilus Parainfluenza
NEJM 391:2148-2157, Case 38-2024, 2024

Clinicopatholigic Conference, Rheumatoid Arthritis with Vasculitis Causing A Confluent Mononeuritis Multiplex
NEJM 390:1312-1322, Case 11-2024, 2024

Sarcoidosis of the Pituitary Gland and Stalk in a Man Presenting Asthenia, Impotence, Loss of Libido, Polyuria, and Polydipsia
Lancet 404:2460-2461, Clement,J., et al, 2024



Showing articles 0 to 50 of 2601 Next >>