Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
acyl CoA dehydrogenase deficiency
adrenoleukodystrophy
advances in neurology
alveolar hypoventilation
amniocentesis
anesthesia, general
arrhythmia, cardiac
aspiration
asymptomatic
ataxia
ataxia, hereditary
atrial fibrillation
atrial paralysis
atrioventricular block
autoimmune disease
baldness
cachexia
calf atrophy
calf hypertrophy
carcinoma
cardiomyopathy
cataracts
central nervous system, infection of
cerebral embolism
cerebral embolism, carotid origin
cerebrovascular accident
cerebrovascular accident, cardiac disease causing
cerebrovascular accident, young adult
children
chromosome 19
chromosome 3
Clinical Pathologic Conference(C.P.C.)
complications
confidentiality
congenital birth defects
congenital heart disease
contractures, joint
creatine phosphokinase(CPK)elevated
degenerative diseases of CNS
delay in diagnosis
descending paralysis
developmental retardation
diagnostic criteria
differential diagnosis
difficulty climbing stairs
distal muscle weakness
DNA probes
dropped head syndrome
dystrophin
echocardiogram
electrocardiogram, abnormal
electromyogram
Emery-Dreifuss muscular dystrophy
enzyme, defect
enzyme, muscle disease
ethics in neurology
facial appearance, abnormal
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
falling
familial
family planning
fine motor function, impaired
foot drop
fragile-X syndrome
frontal balding
gait disorder
gait, waddling
gene mutation
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
Gowers maneuver
heart block
high arched palate
Huntington's chorea
hypercapnia
implantable cardioverter defibrillator
inborn errors of metabolism
inborn errors of metabolism, screening
learning disability
learning disability, in children
lid closure, weakness of
liver function enzymes
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
mitral valve prolapse
molecular genetics
mortality
muscle atrophy, progressive
muscle biopsy
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, cardiovascular changes with
muscular dystrophy, central nervous system abnormality
muscular dystrophy, classification
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, Duchenne, neonatal screening
muscular dystrophy, Duchenne, presymptomatic detection
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myoglobinuria
myopathy
myotonia
myotonia dystrophica
myotonia dystrophica, classification
myotonia dystrophica, type 2
neck weakness
neonatal screening, genetic neurologic disorders
neoplasm, metastatic to CNS
neoplasm, primary intracranial
neoplasm, primary of CNS
nerve conduction studies
neurologic disease
neurologic disease, diagnoses of
neurologic evaluation
neuronal migration disorder
neuropathy, hereditary peripheral
pacemaker, cardiac-transvenous
percussion induced muscle contraction
polymerase chain reaction
polymerase chain reaction, false negative
polymerase chain reaction, false positive
pregnancy, neurologic complications in
prenatal diagnosis by amniocentesis
prognosis
progressive neurologic disorder
proximal muscle atrophy
proximal myotonic myopathy
ptosis
review article
rhabdomyolysis
screening
shoulder-girdle wasting
slit lamp examination
speech disorder, childhood
speech, delayed development of
spinocerebellar ataxia
spinocerebellar degeneration
systemic illness
temporalis muscle wasting
temporalis muscle weakness
temporomandibular joint, dislocation
term infant
toe walking
treatment of neurologic disorder
trinucleotide repeats
tripping
ultrasonography
urine, dark
viral infection, CNS
weakness
weakness, progressive
weakness, proximal
wheelchair
whistle, inability to
winging of scapula
X-linked bulbospinal neuronopathy
x-linked hydrocephalus
x-linked mental retardation
Showing articles 600 to 650 of 1780 << Previous Next >>

Clinical Reasoning: Encephalopathy in a 10-year-old boy
Neurol 79:e12-e18, Rodan, L. & Tein, I., 2012

Progressive Gait Deterioration in Adolescents with Dravet Syndrome
Arch Neurol 69:873-878, Rodda, J.M.,et al, 2012

Stroke Recurrence in Children with Congenital Heart Disease
Ann Neurol 72:103-111, Rodan, L.,et al, 2012

Range of Genetic Mutations Associated with Severe Non-Syndromic Sporadic Intellectual Disability: An Exome Sequencing Study
Lancet 380:1674-1682, Rauch, A.,et al, 2012

Bright Tongue Sign in ALS
Neurol 79:1520, Fox, M.D. & Cohen, A.B., 2012

Neurodegenerative causes of death among retired National Football League Players
Neurol 79:1970-1974, Lehman, E.,et al, 2012

Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability
NEJM 367:1921-1929, Ligt, J.,et al, 2012

Efficacy and Safety of Ketamine in Refractory Status Epilepticus in Children
Neurol 79:2355-2358, Rosati, A.,et al, 2012

Dopa-Responsive Dystonia Revisited
Arch Neurol 69:1558-1562, Tadic, V.,et al, 2012

Spontaneous Primary Intraventricular Hemorrhage: Clinical Features and Early Outcome
ISRN Neurology ED498303, Arboix, A.,et al, 2012

The Autosomal Recessive Cerebellar Ataxias
NEJM 366:636-646, Anheim,M.,et al, 2012

Brain Arteriovenous Malformation Multiplicity Predicts the Diagnosis of Hereditary Hemorrhagic Telangiectasia Quantitive Assessment
Stroke 43:72-78, Bharatha, A.,et al, 2012

An 8-year-old Girl with Multifocal Brain Lesions and Cerebral Edema
Neurol 78:e117-e121, Seto,E.S.,et al, 2012

Childhood Outcomes after Hypothermia for Neonatal Encephalopathy
NEJM 366:2085-2092, Shankaran, S.,et al, 2012

Central Nervous System Herpes Simplex Virus Infection in Afebrile Children with Seizures
J Child Neurol 27:445-450, Majumdar,L.,et al, 2012

An unusual cause of stroke and hypoxia
BMJ 342:c7200, Bell, S.L. & Eveson, D.J., 2011

Intraventricular Fibrinolysis Versus External Ventricular Drainage Alone in Intraventricular Hemorrhage
Stroke 42:2776-2781, Gaberel, T.,et al, 2011

Low-Dose Recombinant Tissue-Type Plasminogen Activator Enhances Clot Resolution in Brain Hemorrhage
Stroke 42:3009-3016,2999, Naff, N.,et al, 2011

Oral Acyclovir Suppression and Neurodevelopment after Neonatal Herpes
NEJM 365:1284-1292,1338, Kimberlin, D.W.,et al, 2011

Warfarin-Related Intraventricular Hemorrhage
Neurol 77:1840-1846, Biffi, A.,et al, 2011

Intraventricular Hemorrhage
UpToDate, Sept, Cucchiara B.L. and Pacelli, J.P., 2011

Hemorrhagic Transformation of Childhood Arterial Ischemic Stroke
Stroke 42:941-946, Beslow,L.A.,et al, 2011

Presentation, Diagnosis, Pathophysiology, and Treatment of the Neurological Features of Sturge-Weber Syndrome
The Neurologist 17:179-184, Comi, A.M., 2011

Predicting motor outcome and death in term hypoxic-ischemic encephalopathy
Neurol 76:2055-2061, Martinez-Biarge, M.,et al, 2011

Lumbar Puncture in Paediatric Stroke
Lancet 378:848, Neuteboom, R.F.,et al, 2011

Acute Ischemic Stroke in Children versus Young Adults
Ann Neurol 70:245-254, Bigi, S.,et al, 2011

Spinal Muscular Atrophy A Timely Review
Arch Neurol 68:979-984, Kolb, S.J.,et al, 2011

"Im fine; Im just waiting for my disease" The New and Growing Class of Presymptomatic Patients
Neurol 77:522-523, Kwon, J.M.et al, 2011

Chronic Granulomatous Herpes Encephalitis: A Rare Entity Posing a Diagnostic Challenge
J Neurosurg Pediatrics 8:402-406, Adamo, M.A.,et al, 2011

Cervical Carotid Artery Disease in Sickle Cell Anemia: Clinical and Radiological Features
Blood 118:6192-6199, Telfer, P.T.,et al, 2011

Athletics, Minor Trauma, and Pediatric Arterial Ischemic Stroke
Eur J Pediatr 169:557-562, Sepelyak, K.,et al, 2010

Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
Brain 133:655-670, Leen,W.G., et al, 2010

Long-Term Mortality in Childhood-Onset Epilepsy
NEJM 363:2522-2529, Sillanp��,M. &Shinnar,S., 2010

Personalized Approaches to Clopidogrel Therapy: Are We There Yet?
Stroke 41:2997-3002, Anderson,C.D.,et al, 2010

Clinicopath Conf, Infantile Krabbe Disease
NEJM 362:346-356, Case 3-2010, 2010

Clinical Reasoning: Seizures in a Child With Sensorineural Deafness and Agitation
Neurol 74:e61-e63, Auvin,S., et al, 2010

Clinicopath Conf., Brain Abscess, Pulmonary Arteriovenous Malformation Due to Hereditary Hemorrhagic Telangiectasia
NEJM 362:1326-1333, Case 10-2010, 2010

Intracerebral Hemorrhage in Cocaine Users
Stroke 41:680-684, Martin-Schild,S., et al, 2010

Frequency and Prognosis of Convulsive Status Epilepticus of Different Causes: A Systematic Review
Arch Neurol 67:931-940, Neligan,A., et al, 2010

Childhood Posterior Circulation Arterial Ischemic Stroke
Stroke 41:2201-2209, Mackay,M.T.,et al, 2010

Clinical and Neuroimaging Findings of Cree Leukodystrophy: A Retrospective Case Series
AJNR 31: 1418-1423, Harder,S.,et al, 2010

Guidelines for the Management of Spontaneous Intracerebral Hemorrhage
Stroke 41:2108-2129, Morgenstern,L.B.,et al, 2010

Pediatric Moyamoya Disease: An Analysis of 410 Consecutive Cases
Ann Neurol 68:92-101, Kim,S.-K., et al, 2010

Neonatal Cerebral Sinovenous Thrombosis From Symptom to Outcome
Stroke 41:1382-1388, Berfelo,F.J., et al, 2010

Recent Advances in Neuroblastoma
NEJM 362:2202-2011, Maris,J.M., et al, 2010

Clinical Reasoning: A 9-year-old Girl With Seizures and Encephalopathy
Neurol 74:e97-e100, Nguyen,T.P. &El-Hakam,L.M., 2010

Huntingtons Disease
BMJ 341:34-40, Novak,M.J. &Tabrizi,S.J., 2010

Comparison of Clinical, Familial, and MRI Features of CADASIL and NOTCH3-Negative Patients
Neurol 74:57-63, Pantoni,L.,et al, 2010

New-Onset Aferbrile Seizures in Infants: Role of Neuroimaging
Neurol 74:150-158, Hsieh,D.,et al, 2010

Ethosuximide, Valproic Acid, and Lamotrigine in Childhood Absence Epilepsy
NEJM 362:790-799, Glauser,T.A.,et al, 2010



Showing articles 600 to 650 of 1780 << Previous Next >>