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Differential
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abdominal distention
acid maltase deficiency
acid maltase deficiency, adult
advances in neurology
adverse drug reaction
afebrile
amyloidosis
anesthesia, general
aneurysm
anterior horn cell disease
anti MAG antibodies
anticonvulsants
areflexia
arrhythmia, cardiac
asymptomatic
autism
autoimmune disease
bulging of biceps
calf hypertrophy
carbamazepine
carcinoma
cardiomegaly
cardiomyopathy
cardiovascular disease
CAT scan
CAT scan, abnormal
CAT scan, emission, abnormal
central nervous system, infection of
cerebral cortical encephaliis
chewing, impaired
children
chromosome 17
Clinical Pathologic Conference(C.P.C.)
CLOVES syndrome
clubfoot as related to neurologic disease
complications
confusion
congenital malformation
congenital myopathy
congestive heart failure
contractures, joint
corticotropin level
corticotropin-releasing factor
cortisol, elevated
cotton-wool spots
cranial nerve enhancement
cranial nerve enlargement
cranial nerve palsies
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
Cushing's syndrome
cysticercosis, cerebral
cysticercosis, disseminated
cysticercosis, intraventricular
cysticercosis, miliary
delay in diagnosis
denervation of muscle
developmental retardation
diabetes mellitus
diagnostic criteria
diamond on quadriceps
diaphragmatic paralysis
differential diagnosis
difficulty climbing stairs
dilantin
diplopia
distal muscle atrophy
distal muscle weakness
dysferlinopathy
dysplasia of C.N.S.
dyspnea
dystonia
dystonia, post traumatic
dystrophin
dystrophin associated proteins
echocardiogram, LVH
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
electron microscopy
empty sella
entrapment neuropathy
enzyme, defect
epidermal nevus syndrome
Epstein-Barr virus
exercise
exophthalmus
eye, pain in
facial hair, excessive
facial pain
facial pain, atypical
facial weakness
falling
false positive
familial
fatigue
fever
fine motor function, impaired
foot drop
gait disorder
gait, waddling
gender
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
globe, flattened posteriorly
Gowers maneuver
headache
hearing loss
heart murmur
hemiatrophy, congenital
hemidiaphragm, paralysis of
hemihypertrophy, congenital
hemihypertrophy, facial
hemimegalencephaly
hemiparesis
hepatomegaly
heralding manifestation
hereditary myopathy with early respiratory failure
heterotopia
hirsutism
histochemistry
hoarseness
hypercalcemia
hypertension
hypokalemia
hypomelanosis of Ito
hypopigmentation of skin
hypothyroidism
inability to sit up
infantile spasm
infectious mononucleosis
infectious mononucleosis, neurologic findings with
intellectual deficit
intracranial hypertension, benign
intracranial hypertension, benign, differential diagnosis
intracranial hypertension, benign, pathogenesis of
Isaacs syndrome
Kobberling-Dunnigan syndrome
Kugelberg-Welander syndrome
learning disability
learning disability, in children
leg swelling
leukocytosis
life expectancy
limb hypertrophy
limb-girdle weakness
lipodystrophy
liver function enzymes
lordosis
lymphadenopathy
lymphopenia
macrocephaly
malformation, CNS, congenital
malignant hyperpyrexia
malignant optic glioma of adulthood
mental retardation
mental status, abnormal
metabolic alkalosis
mexiletine
misdiagnosis
molecular genetics
monoclonal gammopathy
mononeuropathy
motor neuron disease
movement disorder
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, muscle
MRI, orbit
MRI, venography
multiple myeloma
muscle atrophy, focal
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle hypertrophy
muscle hypertrophy, congenital
muscle pain
muscle stiffness
muscle swelling
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, Becker, carrier
muscular dystrophy, cardiovascular changes with
muscular dystrophy, central nervous system abnormality
muscular dystrophy, classification
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, dystrophin normal
muscular dystrophy, facioscapulohumeral
muscular dystrophy, female occurrence of
muscular dystrophy, limb-girdle
muscular dystrophy, pattern of muscle involvement
myelitis
myelitis, transverse
myoedema
myoglobinuria
myokymia
myopathy
myopathy, amyloid
myopathy, focal
myopathy, hereditary
myopathy, metabolic
myopathy, monomelic
myopathy, quadriceps
myopathy, vacuolar
myostatin
myotonia
myotonia congenita
nausea and vomiting
neoplasm, hormone producing, ectopic
nerve conduction studies
nerve injury
neurocutaneous disease
neuroendocrinology
neuroinfectious diseases
neurologic disease, diagnoses of
neurologic examination
neuromyotonia
neuropathy
neuropathy, hereditary peripheral
neuropathy, peripheral
night sweats
obesity
optic chiasm, lesion of
optic disc
optic disc edema
optic glioma
optic nerve sheath enhancement
optic nerve, enhancement
optic nerve, enlarged
optic nerve, neoplasm of
optic nerve, tortuosity
optic neuritis
optic neuropathy, ischemic
optic neuropathy, ischemic, anterior
optical coherence tomography
orthopnea
pain
pain, leg
palpitations
percussion induced muscle contraction
perineuritis
phakomatoses
plasma cell dyscrasia
polyneuropathy
post polio syndrome
postural abnormality
prenatal diagnosis by amniocentesis
prognosis
progressive neurologic disorder
proximal muscle atrophy
pseudohypertrophy
pseudomyotonia
ptosis
pulmonary embolism
pupil, tonic
radiculopathy
Red flags
respiratory failure
review article
rhabdomyolysis
rippling muscle disease
root lesion, nerve
sarcoglycan
sarcoglycanopathy
sciatic neuropathy
scoliosis
scotoma, central
seizure
shoulder, elevation
skin, lesions in neurologic disorders
speech disorder, childhood
speech, delayed development of
spinal accessory nerve
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, intermediate form
splenomegaly
steppage gait
steroid
steroid therapy, CNS treatment and complications with
strokelike episodes
subarachnoid hemorrhage
subcutaneous nodules
survival motor neuron gene
syringomyelia
systemic illness
telangiectases, retinal
third nerve palsy
thirst
tinnitus
titinopathy
toe walking
tongue, enlarged
tongue, weakness
trauma
treatment of neurologic disorder
tripping
urinary frequency
urine, dark
visual acuity, decreased, monocular
visual loss
visual loss, progressive
visual loss, slow-unilateral
visual symptoms
vital capacity
weakness
weakness, progressive
weakness, proximal
web sites
weightlifting
wheelchair
winging of scapula
workup
Showing articles 300 to 350 of 1609 << Previous Next >>

Clinicopathologic Conference, Malaria
NEJM 373:1060-1067, Case 28-2015, 2015

Non-Alzheimers Dementia 2 Lewy Body Dementias
Lancet 386:1683-1697, Walker, Z.,et al, 2015

Lafora Periodic Acid-Schiff Inclusion Bodies
Neurol 85:e130-e131, de Assis Franco, I.,et al, 2015

Coiling-Associated Delayed Cerebral Hypersensitivity: Is Nickel the Link?
Neurol 84:97-99, Lobotesis, K.,et al, 2015

A 12-Year Old Child with Fever, Headache, Shock and Coma
Lancet 385:576, Amores-Hernandez, I.,et al, 2015

Efficacy and Safety of Cholinesterase Inhibitors and Memantine in Cognitive Impairment in Parkinsons Disease, Parkinsons Disease Dementia, and Dementia with Lewy Bodies: Systematic Review with Meta-Analysis and Trial Sequential Analysis
JNNP 86:135-143, Wang, H.F.,et al, 2015

The Spectrum of Acute Encephalitis
Neurol 84:359-366, Singh, T.D.,et al, 2015

A 45 Year Old Patient with Headache, Fever, and Hyponatraemia
BMJ 350:h962, Fountas, A.,et al, 2015

Clinicopathologic Conference, Frontotemporal Lobar Degeneration with Tau-positive Inclusions (Picks Disease Subtype) Due to a Gly389Arg MAPT Mutation, Resulting in the Behavioral Variant of Frontotemporal Dementia with Parkinsonism
NEJM 372:1151-1162, Miller, B.L.,et al, 2015

Clinicopathologic Conference, Invasive Neisseria Meningitidis Infection and Primary C8 Deficiency
NEJM 372:1454-1462, Case 11-2015, 2015

A 57-Year-Old Woman Who Developed Acute Amnesia Following Fever and Upper Respiratory Symptoms
Neurol 84:e102-e106, McCray, B.A.,et al, 2015

Inflammatory Muscle Diseases
NEJM 372:1734-1747, Dalakas, M.C., 2015

Prevalence of Cerebral Amyloid Pathology in Persons without Dementia
JAMA 313-1924-1938,1913, Jansen, W.J.,et al, 2015

Prevalence of Amyloid PET Positivity in Dementia Syndromes
JAMA 313:1939-1949,1913, Ossenkoppele, R.,et al, 2015

Obesity Increases Risk of Ischemic Stroke in Young Adults
Stroke 46:1690-1692, Mitchell, A.B.,et al, 2015

A Variegated Squirrel Bornavirus Associated with Fatal Human Encephalitis
NEJM 373:154-162, Hoffmann, B.,et al, 2015

Hypometabolism of the Primary Motor Cortex in Primary Lateral Sclerosis
Neurol 84:e206, Cosgrove, J.,et al, 2015

Clinical manifestations and diagnosis of Listeria monocytogenes infection
www.UptoDate June, Gelfand, M.S., 2015

Neurological Manifestations of Scrub Typhus
JNNP 86:761-766, Misra, U.K.,et al, 2015

Paraneoplastic Neurological Syndromes and Glutamic Acid Decarboxylase Antibodies
JAMA Neurol 72:874-881,861, Arino, H.,et al, 2015

Clinicopathologic Conference, Borrelia Miyamotoi Infection and Possible Borrelia Burgdorferi Infection
NEJM 373:408-475, Case 24-2015, 2015

Cavernous Sinus Thrombosis in Children
Stroke 46:2657-2660, Press, C.A.,et al, 2015

Demyelinating Encephalopathy in Adult Onset Stills Disease: Case Report and Review of the Literatures
Clin Neurol Neurosurg 115:2213-2216, Jie, W., et al, 2015

Seizing the Clinical Presentation in Adult Onset Stills Disease
Autoimmun Rev 14:472-477, Narula, N.,et al, 2015

Diagnostic Criteria for IgG4-Related Ophthalmic Disease
Jpn J Ophthalmol 59:1-7, Goto,JH.,et al, 2015

Primary CNS T-Cell Lymphomas: A Clinical, Morphologic, Immonophenotypic and Molecular Analysis
Am J Surg Pathol 39:1719-1729, Menon, M.P.,et al, 2015

Cerebral Microhaemorrhages Secondary to Fat Embolus Syndrome in Sickle Cell Disease
Postgrad Med Jour 91:55-56, Alobeidi, F.,et al, 2015

Rotavirus-Associated Mild Encephalopathy with a Reversible Splenial Lesion (MERS)
BMC Infect Dis 15:446, Karampatsas, K.,et al, 2015

Hepatitis Associated with Mycoplasma Pneumoniae Infection in Korean Children:A Prospective Study
Korean J Pediatr 58:211-217, Kim,K.W.,et al, 2015

Varicella Zoster Virus Meningoencephalitis Presenting with Elsberg Syndrome without a Rash in an Immunocompetent Patient
Intern Med 54:2065-2067, Abe, M.,et al, 2015

Herpes Simplex Virus Encephalitis:Clinical Manifestations,Diagnosis and Outcome in 106 Adult Patients
J Clin Virol 60:112-118, Sili,U.,et al, 2014

Extensive VZV Encephalomyelitis without Rash in an Elderly Man
Case Reports Neurol Med 2014:ID694750, Lynch, K.,et al, 2014

Paraneoplastic Neurological Syndromes
Clin Exp Immunol 175:336-348, Leypoldt, F. & Wandinger, K.-P., 2014

Bone Marrow Necrosis and Fat Embolism Syndrome in Sickle Cell Disease: Increased Susceptibility of Patients with Non-SS genotypes and a Possible Association with Human Parvovirus B19 Infection
Blood Rev 28:23-30, Tsitsikas, D.A.,et al, 2014

Stroke and Cancer - A Complicated Relationship
J Neurol Transl Neurosci 2:1039-1051, Dearborn, J.L.,et al, 2014

Co-Occurrence of Multiple Cerebral Infarctions Due to Hypercoagulability Associated with Malignancy and Meningeal Carcinomatosis as the Initial Manifestation of Gastric Cancer
BMC Neurol 14:160, Kawasaki,A.,et al, 2014

Fat Embolism Syndrome: Case Report of a Clinical Conundrum
J Anaesthesiol Clin Pharmacol 30:412-414, Nandi, R.,et al, 2014

An Unusual Case of Adult-Onset Stills Disease with Hemophagocytic Syndrome, Necrotic Leukoencephalopathy and Disseminated Intravascular Coagulation
Case Reports Rheum Article ID 128623, Namas, R.,et al, 2014

Clinicopathologic Conference, Cerebral Granulomatosis with Polyangiitis
NEJM 371:162-173, Case 21-2014, 2014

Small Strokes Causing Severe Vertigo
Neurol 83:169-173, Tehrani, A.S.S.,et al, 2014

Red Papules on the Tongue of a Patient with Hemiparesis
JAMA 312:741-742, Chiu, H.Y. & Lin, S.J., 2014

Clinicopathologic Conference, Streptococcus Bovis Associated Meningitis and the Strongyloides Stercoralis Hypertension Syndrome
NEJM 371:1051-1060, Case 28-2014, 2014

Cavernous Sinus Thrombosis: Linking a Swollen Red Eye and Headache
Lancet 384:928, Sakaida, H.,et al, 2014

Disseminated Varicella Zoster Virus Encephalitis
Lancet 384:1698, Chai, W. & Gong-Ruey Ho, M., 2014

Clinical Manifestations, Pathologic Features, and Diagnosis of Langerhans Cell Histiocytosis
UptoDate Oct. 2014, McClain, K.L., 2014

Clinicopathologic Conference, Lemierres Syndrome
NEJM 371:2018-2027, Case Record 36-2014, 2014

Apnea and Dysphagia as the Sole Features of an a-Synucleinopathy
Neurol 83:1988-1989, Gilhuis, H.J.,et al, 2014

A 75-year-old man with 3 years of Visual Difficulties
Neurol 83:e160-e165, Berkowitz, A.L.,et al, 2014

Enhancing Brain Lesions after Endovascular Treatment of Aneurysms
AJNR 35:1954-1958, Cruz, J.P.,et al, 2014

Clinicopathologic Conference, Severe Hypothyroidism
NEJM 371:2321-2327, Case 38-2014, 2014



Showing articles 300 to 350 of 1609 << Previous Next >>