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NeurologicDX: The Diagnostic Checklist
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Differential Diagnosis
acquired immunodeficiency syndrome
addiction,heroin-neurologic complications with
adverse drug reaction
anticholinergic drugs,side effects of
arrhythmia,cardiac
aspergillosis
B 12 deficiency
bulbar palsy
bulimia
carnitine deficiency
catatonia
coma
compartment syndrome
compression neuropathy
congenital myopathy
dermatomyositis
drug abuse
drug abuse,neurologic complications of
drug addiction
drug induced neurologic disorders
drug withdrawal
dystonia
dystonia musculorum deformens
eating disorder
encephalopathy
gasoline sniffing
genetic neurologic disorders
glycogen storage disease
homocystinuria
human immunodeficiency virus type 1
hypothyroidism
iatrogenic neurologic disorders
inborn errors of metabolism
inclusion body myositis
injection neuropathy
intravenous drug abuse
lactic acidemia
lithium
malignant hyperpyrexia
McArdle's disease
mitochondrial disease
mononeuropathy
mononeuropathy multiplex
muscle phosphofructokinase deficiency
muscle phosphorylase deficiency
muscular dystrophy
muscular dystrophy,Becker
muscular dystrophy,Duchenne
muscular dystrophy,limb-girdle
myopathy
myositis
myotonia dystrophica
myxedema,neurologic manifestations of
neuroleptic malignant syndrome
neuropathy
neuropathy,painful
neuropathy,peripheral
neuropathy,sensory
periarteritis nodosa
periodic paralysis
pernicious anemia
phosphorylase b kinase deficiency
polyneuropathy
polyneuropathy,chronic inflammatory demyelinating
psychosis
rhabdomyolysis
sciatic neuropathy
seizure
sensorineural hearing loss
serotonin syndrome
sleep apnea
status epilepticus
strychnine poisoning
tetanus
toilet seat neuropathy
uveitis
vegetarianism
viral infection
viral myopathy
vitamin deficiency
vitritis

Related Terms
addiction,heroin
advances in neurology
agitation
alcohol
alcoholism
aminoacidurias
anemia
anemia,megaloblastic
anesthesia,general
anorexia
anticholinergic drugs
areflexia
arthralgia
asymptomatic
ataxia
ataxia,cerebellar
ataxic gait
autonomic dysfunction
azidodeoxythymidine
B 12 deficiency,infants
breast feeding
bulimia nervosa
burning hands
burning paresthesia
cardiomyopathy
carnitine deficiency myopathy
CAT scan
CAT scan,muscle
CAT scan,pelvis
catatonia,lethal
cathartic
children
chromosome 19
Clinical Pathologic Conference(C.P.C.)
clofibrate
coenzyme Q10
coenzyme Q10 deficiency
colchicine
compartment syndrome,gluteal
confusion
confusional state,acute
conjunctivitis
contractures,joint
contraindications
C-reactive protein,elevated
creatine phosphokinase(CPK)elevated
critical care unit
cultured skin fibroblasts
dantrolene sodium
deafness
dexterity,impaired
drug abuse,neonatal abstinence syndrome with
drug induced neurologic disorders in children
drug interactions
dystrophin
ecchymoses
ECHO virus
electrocardiogram,abnormal
electromyogram
emergencies,neurologic
encephalomyopathy
endophthlamitis
enterovirus
enzyme,defect
enzyme,muscle disease
epsilon-aminocaproic acid(E.A.C.A.)
exercise
exercise intolerance
eye,pain in
familial
fatigue
fever
fungal infection
gait disorder
gene mutation
genetic screening
hand weakness
hearing loss
hematuria,microscopic
histochemistry of muscle
HMGcoA reductase inhibitors
hung reflex
hypercapnia
hyperpigmentation of skin
hypersegmented polys
hyperthermia
hypokalemia
hypothermia
hypotonia,infants
ischemic exercise test
jaundice
lactic dehydrogenase(LDH)
leg weakness,unilateral
leukocytosis
level of consciousness,decreased
lipid lowering agent
McArdle's disease,adult onset
mental status,abnormal
metabolic acidosis
methylmalonic acid,serum
misdiagnosis
molecular genetics
mortality
MRI
MRI,muscle
muscle atrophy,progressive
muscle atrophy,static
muscle biopsy
muscle cramp
muscle pain
muscle stiffness
muscle tenderness
muscle weakness
muscle weakness,proximal
myocytolysis
myoedema
myoglobinuria
myopathy,acute
myopathy,drug-induced
myopathy,metabolic
myopathy,mitochondrial
myopathy,necrotizing
myopathy,proximal
myopathy,toxic
nephrotic syndrome
neuroleptic
neurologic complications of,systemic disease
neurologic disease,diagnoses of
pain
pain,abdominal
paresthesias
paresthesias,hands
PAS positive
peripheral blood smear,abnormal
personality change
prevention of neurologic disorders
prognosis
proximal muscle atrophy
psychosis,acute
ptosis
quadriplegia
red eye
renal failure
renal failure,acute
respiratory failure
review article
rigidity
risk factors
Romberg's sign
second wind phenomena
seizure,neonatal
seizure,neonatal abstenence syndrome
selective serotonin reuptake inhibitors
statin therapy
tachycardia
tachypnea
toe walking
tongue,smooth
tongue,swelling
treatment of neurologic disorder
trifluoperazine
undiagnosed
urine test in toxic screen
urine,dark
vision,blurred
visual acuity,decreased,monocular
visual loss
weakness
weakness,generalized
weakness,progressive
weight loss
Remote Results

Citations
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Expand Heterogeneity of Coenzyme Q10 DeficiencyHeterogeneity of Coenzyme Q10 Deficiency
Expand Clinicalpathologic Conference, Vitamin B12 Deficiency due to Pernicious AnemiaClinicalpathologic Conference, Vitamin B12 Deficiency due to Pernicious Anemia
Expand Myoglobinuria and Muscle Pain are Common in Patients With Limb-Girdle Muscular Dystrophy 21Myoglobinuria and Muscle Pain are Common in Patients With Limb-Girdle Muscular Dystrophy 21
Expand Clincopath Conference, Endogenous Endophthalmitis Due to Aspergillus NigerClincopath Conference, Endogenous Endophthalmitis Due to Aspergillus Niger
Expand Toxic and Drug-Induced MyopathiesToxic and Drug-Induced Myopathies
Expand Polyarteritis Nodosa Presenting as RhabdomyolysisPolyarteritis Nodosa Presenting as Rhabdomyolysis
Expand Malignant Hyperthermia, Update on Susceptibility TestingMalignant Hyperthermia, Update on Susceptibility Testing
Expand Rhabdomyolysis: An Evaluation of 475 Hospitalized PatientsRhabdomyolysis: An Evaluation of 475 Hospitalized Patients
Expand AAC/AHA/NHLBI Clinical Advisory on the Use and Safety of StatinsAAC/AHA/NHLBI Clinical Advisory on the Use and Safety of Statins
Expand Clinicopath Conf, Strychnine Poisoning, Case 12-2001Clinicopath Conf, Strychnine Poisoning, Case 12-2001
Expand "Toilet Seat" Sciatic Neuropathy"Toilet Seat" Sciatic Neuropathy
Expand Muscle Pain after ExerciseMuscle Pain after Exercise
Expand Exercise Intolerance Due to Mutations in the Cytochrome b Gene of Mitochondrial DNAExercise Intolerance Due to Mutations in the Cytochrome b Gene of Mitochondrial DNA
Expand Acute, Drug-Induced, Life-Threatening Neurological SyndromesAcute, Drug-Induced, Life-Threatening Neurological Syndromes
Expand Sustained Myoglobinuria:The Presenting Manifestation of DermatomyositisSustained Myoglobinuria:The Presenting Manifestation of Dermatomyositis
Expand Investigation of Muscle DiseaseInvestigation of Muscle Disease
Expand Polyarteritis Nodosa-Induced QuadriplegiaPolyarteritis Nodosa-Induced Quadriplegia
Expand Clinical and Biochemical Features of 10 Adult Patients with Muscle Phosphorylase Kinase DeficiencyClinical and Biochemical Features of 10 Adult Patients with Muscle Phosphorylase Kinase Deficiency
Expand McArdle's Disease with Late-Onset Symptoms:Case Report & Review of the LiteratureMcArdle's Disease with Late-Onset Symptoms:Case Report & Review of the Literature
Expand Missed Neuroleptic Malignant SyndromeMissed Neuroleptic Malignant Syndrome
Expand Glucose-Induced Exertional Fatigue in Muscle Phosphofructokinase DeficiencyGlucose-Induced Exertional Fatigue in Muscle Phosphofructokinase Deficiency
Expand Progressive Neuropathy & Recurrent Myoglobinuria in a Child with Long-chain 3-Hydroxyacylcoenzyme A Dehydrogenase DeficProgressive Neuropathy & Recurrent Myoglobinuria in a Child with Long-chain 3-Hydroxyacylcoenzyme A Dehydrogenase Defic
Expand HypothyroidismHypothyroidism
Expand Improved Diagnosis of Becker Muscular Dystrophy by Dystrophin TestingImproved Diagnosis of Becker Muscular Dystrophy by Dystrophin Testing
Expand The Neuromuscular Manifestations of Human Immunodeficiency Virus InfectionsThe Neuromuscular Manifestations of Human Immunodeficiency Virus Infections
Expand McArdle's Disease:Biochemical and Molecular Genetic StudiesMcArdle's Disease:Biochemical and Molecular Genetic Studies
Expand Phosphorylase DeficiencyPhosphorylase Deficiency
Expand McArdle's Disease in the 1980sMcArdle's Disease in the 1980s
Expand Acute Ventilatory Failure & MyoglobinuriaAcute Ventilatory Failure & Myoglobinuria
Expand Nearly Fatal Muscle Carnitine Deficiency with Full Recovery after Replacement TherapyNearly Fatal Muscle Carnitine Deficiency with Full Recovery after Replacement Therapy
Expand Idiopathic Recurrent Myoglobinuria & Persistent WeaknessIdiopathic Recurrent Myoglobinuria & Persistent Weakness
Expand Acute Myopathy Associated with Gasoline SniffingAcute Myopathy Associated with Gasoline Sniffing
Expand Severe Dystonia & MyoglobinuriaSevere Dystonia & Myoglobinuria
Expand Myositis, Myoglobinemia, & Myoglobinuria Associated With Enterovirus Echo 9 InfectionMyositis, Myoglobinemia, & Myoglobinuria Associated With Enterovirus Echo 9 Infection
Expand Acute Rhabdomyolysis Associated With An Echovirus 9 InfectionAcute Rhabdomyolysis Associated With An Echovirus 9 Infection
Expand Rhabdomyolysis During Treatment With Epsilon-Aminocaproic AcidRhabdomyolysis During Treatment With Epsilon-Aminocaproic Acid
Expand Myoglobinuria & Renal Failure after Status EpilepticusMyoglobinuria & Renal Failure after Status Epilepticus
Expand A Synd of Methylmal Acid, Homocystinuria, Megaloblas. Anemia & Neurol Abnor. in a Vit B-12-def Breast-fed Infant of vegetA Synd of Methylmal Acid, Homocystinuria, Megaloblas. Anemia & Neurol Abnor. in a Vit B-12-def Breast-fed Infant of veget
Expand Clofibrate-Induced Muscle Damage with Myoglobinuria & CardiomyopathyClofibrate-Induced Muscle Damage with Myoglobinuria & Cardiomyopathy
Expand Narcotic Abuse:Neurologic Complications in Pedi & Adolescent PtsNarcotic Abuse:Neurologic Complications in Pedi & Adolescent Pts

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