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acquired immunodeficiency syndrome
acute intermittant porphyria
addiction, heroin
addiction, heroin-neurologic complications with
Addison's disease
advances in neurology
adverse drug reaction
agitation
alcohol
alcoholism
aminoacidurias
anemia
anemia, megaloblastic
anesthesia, general
ankle, swelling of
anorexia
anticholinergic drugs
anticholinergic drugs, side effects of
areflexia
arrhythmia, cardiac
arthralgia
ascites
aspartate aminotransferase
aspergillosis
asterixis
asymptomatic
ataxia
ataxia, cerebellar
ataxic gait
autoantibodies
autonomic dysfunction
azidodeoxythymidine
B 12 deficiency
B 12 deficiency, infants
brain natriuretic peptide
breast feeding
bulbar palsy
bulimia
bulimia nervosa
burning hands
burning paresthesia
calf hypertrophy
carbon monoxide poisoning
cardiomyopathy
carnitine deficiency
carnitine deficiency myopathy
CAT scan
CAT scan, muscle
CAT scan, pelvis
catatonia
catatonia, lethal
cathartic
cerebrovascular accident
cervical spondylosis
children
chromosome 19
Clinical Pathologic Conference(C.P.C.)
clofibrate
coenzyme Q10
coenzyme Q10 deficiency
colchicine
coma
compartment syndrome
compartment syndrome, gluteal
complications
compression neuropathy
confusion
confusional state, acute
congenital myopathy
conjunctivitis
contractures, joint
contraindications
cortisol, low
C-reactive protein, elevated
creatine phosphokinase(CPK)elevated
critical care unit
cultured skin fibroblasts
dantrolene sodium
deafness
delay in diagnosis
delirium
depression
dermatomyositis
developmental retardation
dexterity, impaired
diabetes insipidus
diagnostic criteria
differential diagnosis
difficulty climbing stairs
drug abuse
drug abuse, neonatal abstinence syndrome with
drug abuse, neurologic complications of
drug addiction
drug induced neurologic disorders
drug induced neurologic disorders in children
drug interactions
drug withdrawal
dysphagia
dystonia
dystonia musculorum deformens
dystrophin
eating disorder
ecchymoses
ECHO virus
electrocardiogram, abnormal
electromyogram
emergencies, neurologic
encephalomyopathy
encephalopathy
encephalopathy, metabolic
endophthlamitis
enterovirus
enzyme, defect
enzyme, muscle disease
enzyme, serum
epsilon-aminocaproic acid(E.A.C.A.)
etonogestrel
exercise
exercise intolerance
eye, pain in
facial weakness
falling
familial
fatigue
fever
fibrillations
fine motor function, impaired
fungal infection
gait disorder
gait, waddling
gasoline sniffing
gene
gene mutation
genetic neurologic disorders
genetic screening
genetic testing
glycogen storage disease
Gowers maneuver
hand weakness
head injury
hearing loss
hematuria, microscopic
hepatolenticular degeneration(Wilson's disease)
histochemistry of muscle
HMGcoA reductase inhibitors
homocystinuria
hormone replacement
hormone therapy
human immunodeficiency virus type 1
hung reflex
hypercapnia
hypernatremia
hyperpigmentation of skin
hypersegmented polys
hyperthermia
hypokalemia
hyponatremia
hyponatremic encephalopathy
hypotension, systemic
hypothermia
hypothyroidism
hypotonia, infants
iatrogenic neurologic disorders
implant contraceptives
inappropriate antidiuretic(A.D.H.)hormone
inborn errors of metabolism
inclusion body myositis
injection neuropathy
intellectual deterioration
intravenous drug abuse
ischemic exercise test
jaundice
lactic acidemia
lactic dehydrogenase(LDH)
learning disability
learning disability, in children
leg weakness, bilateral
leg weakness, unilateral
lethargy
leukocytosis
level of consciousness, decreased
lipid lowering agent
lithium
liver function enzymes
malignant hyperpyrexia
McArdle's disease
McArdle's disease, adult onset
mental status, abnormal
metabolic acidosis
metabolic disorder, primary
methylmalonic acid, serum
mimics
misdiagnosis
mitochondrial disease
molecular genetics
mononeuropathy
mononeuropathy multiplex
mood change
mortality
movement disorder
MRI
MRI, muscle
MRI, spine
muscle atrophy, progressive
muscle atrophy, static
muscle biopsy
muscle cramp
muscle pain
muscle phosphofructokinase deficiency
muscle phosphorylase deficiency
muscle stiffness
muscle tenderness
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, central nervous system abnormality
muscular dystrophy, Duchenne
muscular dystrophy, limb-girdle
myelopathy
myoclonus
myocytolysis
myoedema
myoglobinuria
myopathy
myopathy, acute
myopathy, drug-induced
myopathy, metabolic
myopathy, mitochondrial
myopathy, necrotizing
myopathy, necrotizing, autoimmune
myopathy, proximal
myopathy, toxic
myositis
myotonia dystrophica
myxedema, neurologic manifestations of
nausea and vomiting
nephrotic syndrome
neuroleptic
neuroleptic malignant syndrome
neurologic complications of, surgery
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neuropathy
neuropathy, acute
neuropathy, painful
neuropathy, peripheral
neuropathy, sensory
ochronosis
osteoarthrosis
osteoporosis
pain
pain, abdominal
pain, buttock
pain, leg
paraparesis, spastic
paresthesias
paresthesias, hands
PAS positive
periarteritis nodosa
periodic paralysis
peripheral blood smear, abnormal
pernicious anemia
personality change
phosphorylase b kinase deficiency
polyneuropathy
polyneuropathy, chronic inflammatory demyelinating
porphyria
precipitating factors
prevention of neurologic disorders
prognosis
progressive neurologic disorder
proteinuria
proximal muscle atrophy
pruritus
psychiatric problems in neurologic disorders
psychosis
psychosis, acute
ptosis
quadriplegia
recurrent
red eye
renal failure
renal failure, acute
renal stones
respiratory failure
review article
rhabdomyolysis
rigidity
risk factors
Romberg's sign
sciatic neuropathy
sclerae, hyperpigmented
second wind phenomena
seizure
seizure, neonatal
seizure, neonatal abstenence syndrome
selective serotonin reuptake inhibitors
sensorineural hearing loss
serotonin syndrome
serum alanine aminotransferase
sex reassignment surgery
sleep apnea
somnolence
speech disorder
speech disorder, childhood
speech, delayed development of
speech, slowed
spondylolysis
statin therapy
status epilepticus
strychnine poisoning
stuporous
subdural hematoma
systemic illness
tachycardia
tachypnea
tetanus
toe walking
toilet seat neuropathy
tongue, smooth
tongue, swelling
transgender
treatment of neurologic disorder
tremor
trifluoperazine
tripping
unconsciousness
undiagnosed
urinary incontinence
urine osmolality, elevated
urine test in toxic screen
urine, dark
uveitis
vegetarianism
viral infection
viral myopathy
vision, blurred
visual acuity, decreased, monocular
visual loss
vitamin deficiency
vitritis
vomiting, recurrent
walking, difficulty with
weakness
weakness, acute
weakness, generalized
weakness, progressive
weakness, proximal
weight loss
winging of scapula
Showing articles 0 to 50 of 223 Next >>

Cervical Spondylotic Myelopathy Secondary to Ochronotic Vertebral Arthropathy
Neurol 96:627-628, Pinto, W.,et al, 2021

Pain in Right Buttock after Carbon Monoxide Poisoning
BMJ 373:n1233, Hu, H. & Sun, Q., 2021

Duchenne Muscular Dystrophy
BMJ 368:L7012, Fox, H.,et al, 2020

Clinicopathologic Conference, Statin-Associated Autoimmune Myopathy
NEJM 381:275-283, Case 22-2019, 2019

Wilson Disease
NIDDK Oct2018, , 2018

Clinicopathologic Conference, Primary Adrenal Insufficiency (Addisons Disease)
NEJM 376:1159-1167, Case 9-2017, 2017

A 45-year-old man with Weakness and Myalgia after Orthopedic Surgery
Neurol 88:e185-e189, Vazquez do Campo, R.,et al, 2017

The Acquired Metabolic Disorders of the Nervous System, Hypernatremia
Adams & Victors Principles of Neurology Chp 40, pg 1148, Ropper, A.H.,et al, 2014

A 20-year-old Woman with Rapidly Progressive Weakness
Neurol 82:e200-e204, Paganoni, S.,et al, 2014

The Limbic-Girdle Muscular Dystrophies
Neuro Clin 32:729-749, Wicklund, M.P. and Kissel, J.T., 2014

Clinicalpathologic Conference, Vitamin B12 Deficiency due to Pernicious Anemia
NEJM 366:1626-1633, Case 13-2012, 2012

Heterogeneity of Coenzyme Q10 Deficiency
Arch Neurol 69:978-983, Emmanuele, V.,et al, 2012

Myoglobinuria and Muscle Pain are Common in Patients With Limb-Girdle Muscular Dystrophy 21
Neurol 76:194-195, Mathews,K.D.,et al, 2011

Clincopath Conference, Endogenous Endophthalmitis Due to Aspergillus Niger
NEJM 363:1749-1758, Case 33-2010, 2010

Toxic and Drug-Induced Myopathies
JNNP 80:832-838, Dalakas,M.C., 2009

Polyarteritis Nodosa Presenting as Rhabdomyolysis
J Korean Rheum Assoc Mar13(1):76-81, Bae,Y.D.,et al, 2006

Malignant Hyperthermia, Update on Susceptibility Testing
JAMA 293:2918-2924,2958, Litman,R.S.&Rosenberg,H., 2005

Rhabdomyolysis: An Evaluation of 475 Hospitalized Patients
Medicine 84:377-385, Melli,G.,et al, 2005

AAC/AHA/NHLBI Clinical Advisory on the Use and Safety of Statins
Stroke 33:2337-2341, Pasternak,R.C.,et al, 2002

Clinicopath Conf, Strychnine Poisoning, Case 12-2001
NEJM 344:1232-1239, , 2001

"Toilet Seat" Sciatic Neuropathy
Arch Neurol 56:116, Holland,N.R.,et al, 1999

Muscle Pain after Exercise
Lancet 353:1062, Nielen,C.&Mazzone,P., 1999

Exercise Intolerance Due to Mutations in the Cytochrome b Gene of Mitochondrial DNA
NEJM 341:1037-1044, 1077, Andreu,A.L.,et al, 1999

Acute, Drug-Induced, Life-Threatening Neurological Syndromes
The Neurologist 4:196-210, Richard,I.H., 1998

Sustained Myoglobinuria:The Presenting Manifestation of Dermatomyositis
Neurol 47:119-123, Rose,M.R.,et al, 1996

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

Polyarteritis Nodosa-Induced Quadriplegia
Ann Int MEd 122:731-732, Smith,D.L.,et al, 1995

Clinical and Biochemical Features of 10 Adult Patients with Muscle Phosphorylase Kinase Deficiency
Neurol 44:461-466, Wilkinson,D.A.,et al, 1994

McArdle's Disease with Late-Onset Symptoms:Case Report & Review of the Literature
JNNP 55:407-408, Felice,K.J.,et al, 1992

Missed Neuroleptic Malignant Syndrome
BMJ 304:831-832, Renwick,D.S.,et al, 1992

Progressive Neuropathy & Recurrent Myoglobinuria in a Child with Long-chain 3-Hydroxyacylcoenzyme A Dehydrogenase Defic
J Pediatr 118:744-746, Dionisi,C.,et al, 1991

Glucose-Induced Exertional Fatigue in Muscle Phosphofructokinase Deficiency
NEJM 324:364-369, 4111991., Haller,R.G.&Lewis,S.F., 1991

Improved Diagnosis of Becker Muscular Dystrophy by Dystrophin Testing
Neurol 39:1011-1017, Hoffman,E.P.,et al, 1989

Hypothyroidism
In Neurologic Clinics, W. B. Saunders Co, Phila, 7:492-493., Kaminski,H.J.&Ruff,R.L., 1989

The Neuromuscular Manifestations of Human Immunodeficiency Virus Infections
Arch Neurol 45:1084-1088, Lange,D.J.,et al, 1988

McArdle's Disease:Biochemical and Molecular Genetic Studies
Ann Neurol 24:774-781, Servidei,S.,et al, 1988

Phosphorylase Deficiency
In Englel & Banker, Myology, McGraw-Hill Book Co, Ch 52, 1585-1601, DiMauro,S.&Bresolin,N., 1986

McArdle's Disease in the 1980s
NEJM 312:370-371, Layzer,R.B., 1985

Acute Ventilatory Failure & Myoglobinuria
Neurol 34:369-371, Taverner,D.,et al, 1984

Nearly Fatal Muscle Carnitine Deficiency with Full Recovery after Replacement Therapy
Neurol 33:1629-1631, Prockop,L.D.,et al, 1983

Idiopathic Recurrent Myoglobinuria & Persistent Weakness
Neurol 33:1613-1615, Bermils,C.,et al, 1983

Acute Myopathy Associated with Gasoline Sniffing
Neurol 33:629-631, Kovanen,J.,et al, 1983

Severe Dystonia & Myoglobinuria
Neurol 32:1195-1197, Jankovic,J.,et al, 1982

Acute Rhabdomyolysis Associated With An Echovirus 9 Infection
Arch Int Med 140:1671-1672, Josselson,J.,et al, 1980

Rhabdomyolysis During Treatment With Epsilon-Aminocaproic Acid
Arch Neurol 37:187-188, Britt,C.W.,et al, 1980

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

Myoglobinuria & Renal Failure after Status Epilepticus
Neurol 28:200, Singhal,P.C.,et al, 1978

A Synd of Methylmal Acid, Homocystinuria, Megaloblas. Anemia & Neurol Abnor. in a Vit B-12-def Breast-fed Infant of veget
NEJM 299:317, Higginbottom,M.C., 1978

Clofibrate-Induced Muscle Damage with Myoglobinuria & Cardiomyopathy
NEJM 296:942, Smals,A.G.H., 1977



Showing articles 0 to 50 of 223 Next >>