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Differential
(Click to cross reference)
airway obstruction
angiitis
ankle reflex, absent
anosmia
areflexia
arrhythmia, cardiac
arthrogryposis multiplex
aspartate aminotransferase
asthma
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, truncal
ataxic gait
autonomic dysfunction
autonomic neuropathy
autonomic neuropathy, idiopathic
autosomal rcessive spastic ataxia of Charlevoix-Saguenay
Babinski sign
benign essential tremor
bladder dysfunction
brainstem, atrophy
bulbar palsy
calf hypertrophy
carcinoma
carcinoma of thyroid
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
cataracts
cataracts, congenital
central core disease
cerebellar ataxia, children
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebral cortical atrophy
Charcot-Marie-Tooth
children
chromosomal abnormality
chromosome 17
chromosome 9
Churg-Strauss syndrome
clubfoot as related to neurologic disease
cognition
compression fracture
congenital bilateral perisylvian syndrome
congenital malformation
congenital myasthenic syndromes
consanguinity
constipation
contractures, joint
corpus callosum
corpus callosum, thinning
creatine phosphokinase(CPK)elevated
deafness
deep tendon reflexes
degenerative diseases of CNS
developmental abnormality of brain
developmental retardation
diabetes insipidus
diabetes mellitus
diabetes mellitus, ocular complications in
diabetic cranialneuropathies
differential diagnosis
dimple
dislocated hip, congenital
distal muscle atrophy
distal muscle weakness
diurnal variation
dopa responsive dystonia
drooling
dysarthria
dyskinesia, buccal lingual facial
dysmorphic
dysphagia
dysraphism, spinal
dystonia
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electromyogram
endemic area
eosinophilia
eosinophilic granulomatosis with polyangiitis
evoked potentials
exome sequencing
facial weakness
facial weakness, bilateral
falling
familial
fatigue
fine motor function, impaired
finger nose finger test
foot deformity
foot drop
foot ulcer, neuropathic
frataxin
Friedreich's ataxia
gag reflex, depressed
gait disorder
gait, waddling
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic testing
giant axonal neuropathy
granuloma, eosinophilic
hammertoes
hand deformity
hand weakness
hearing loss
high arched feet
high arched palate
hydrocephalus
hyperphosphatasia
hyperreflexia
hypertrichosis
hypogonadism
hypogonadism, hypogonadotropic
hyporeflexia
hyposmia
hypotonia
hypotonia, infants
imbalance
incontinence, fecal
incoordination
intellectual deficit
intrinsic hand muscles, wasting of
iritis
kyphoscoliosis, neurologic causes of
kyphosis
L-dopa
leg weakness, bilateral
leg weakness, unilateral
leprosy
Lhermitte's sign
light-near dissociation, causes of
lipoma of CNS
lipoma of skin
liver function enzymes
lordosis
malaise
malformation, CNS, congenital
malignant hyperpyrexia
Marinesco-Sjogren syndrome
mental retardation
mestinon
micrognathia
mitral valve prolapse
molecular genetics
MRI
MRI, abnormal
multiple endocrine neoplasia
muscle atrophy, progressive
muscle atrophy, static
muscle biopsy
muscle cramp
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker
myelomalacia
myelomeningocele
myopathy
myotonia congenita
myotonia dystrophica
nasal speech
nerve conduction studies
nerve enlargement
nerve hypertrophy
neuroendocrinology
neurologic disease, diagnoses of
neuroma
neuropathy
neuropathy, ataxic
neuropathy, hereditary peripheral
neuropathy, hypertrophic
neuropathy, onion bulb
neuropathy, painful
neuropathy, peripheral
neuropathy, sensory
neuropathy, sensory, hereditary
neuropathy, small-fiber, painful sensory
night blindness
nonverbal
nystagmus
nystagmus, rotary
nystagmus, upbeating-in primary position of gaze
nystagmus, vertical
opened mouth
operculum syndrome, bilateral
ophthalmoplegia
optic atrophy
optic disc cup
pain
pain, anal
pain, foot
pain, leg
pain, perineum
palmar erythema
paraparesis
paraparesis, familial spastic
paraparesis, spastic
paresthesias
Parkinson disease
past pointing
peroneal muscle atrophy, causes of
peroxisomal disease
pes cavus
petechiae
phytanic acid
polymerase chain reaction
polymicrogyria
polyneuropathy
polyneuropathy, familial
pons, lesion of
prognosis
progressive neurologic disorder
pseudobulbar palsy
pseudohypertrophy
ptosis
ptosis, bilateral
pupil, abnormality in neurologic disorders
pupil, light reflex, abnormal
pyramidal tract dysfunction
radiculopathy
rash
rash, hand
Red flags
Refsum's disease
respiratory failure
retinitis pigmentosa
review article
Romberg's sign
Samoa
scoliosis
scoliosis, neurologic association with
seizure
sensorineural hearing loss
sensory loss
skin, biopsy
skin, lesions in neurologic disorders
smell
spasticity
spinal stenosis
steppage gait
sudden death
synkinesis
temporalis muscle wasting
term infant
tethered spinal cord
toe walking
trauma
treatment of neurologic disorder
tremor
tremor, intention
trichopoliodystrophy
trinucleotide repeats
tripping
urinary incontinence
uveitis
vibratory sensation, abnormal
visual evoked response
visual fields, constricted
vitamin deficiency
vitamin E
vitamin E deficiency
walking
walking frame
walking, difficulty with
weakness
weakness, fatiguable
weakness, progressive
weakness, proximal
weight loss
wheelchair
white matter disease
Wolfram syndrome
x-ray, lumbar spine
Showing articles 50 to 100 of 440 << Previous Next >>

Spinal Metastases
JAMA 323:2438, Chiu, R.G.,et al, 2020

A 40-Year-Old Woman Presenting with Distal Leg Weakness
Neurol 92:242-247, Fam, D.,et al, 2019

A Pregnant Woman with Chin Numbness
Neurol 92:e996-e999, Arnold, A.J.,et al, 2019

A 54-year-old man with Dyspnea and Muscle Weakness
Neurol 92:e1136-e1140, Chertcoff, A.,et al, 2019

Antiepileptic Drug Treatment Patterns in Women of Childbearing Age with Epilepsy
JAMA Neurol 76:783-790, Kim, H.,et al, 2019

Risk of 23 Specific Malformations Associated with Prenatal Exposure to 10 Antiepileptic Drugs
Neurol 93:e167-e180, Blotiere, P.O.,et al, 2019

A Middle Aged Man with Back Pain and Heavy Legs
BMJ 366:e2420, Chanchlani, N. & Reading, N.G., 2019

Bilateral Alopecia as Clue to Diagnosis of Gomez-Lopez-Hernandez Syndrome in a 38-Year-Old Man
Neurol 93:408-410, Kronlage,C.&Healy,D.G., 2019

Declining Malformation Rates with Changed Antiepileptic Drug Prescribing, An Observational Study
Neurol 93:e831-e840, Tomson,T.,et al, 2019

Basa Ganglia Calcifications (Fahrs Syndrome): Related Conditions and Clinical Features
Neurol Sci 40:2251-2263, Donzuso,G.,et al, 2019

Acute Paraplegia in a Healthy Child
BMJ 367:L6257, Haque, A.K.M.,et al, 2019

Surveillance for Matastatic Hemangiopericytoma-Solitary Fibrous Tumors-Systematic Literature Review on Incidence,Predictors and Diagnosis of Extra-Carnial Disease
J Neurooncol 138:447-467, Ratneswaren,T.,et al, 2018

Clinicopathologic Conference, Lyme Meningoradiculitis
NEJM 379:1862-1868, Case 34-2018, 2018

Hearing and Vision Loss in an Older Man
JAMA Neurol 75:1439-1440, Ho, V.M.,et al, 2018

Foot Drop
WebMD, Bernstein, L., 2018

Pontine Tegmental Cap Dysplasia in a Neonate
Neuol 91:e2100-e2101, Bilgin, N.,et al, 2018

Congenital Asymmetric Crying Facies Syndrome, A Case Report
Medicine 97:31(e11403), Liang,X. & He,B., 2018

Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss
Neurol 90:e625-e631, Set, K.K.,et al, 2018

Adult-Onset Vanishing White Matter Disease
Neurol 90:e1091-e1092, Villar-Quiles, R.N.,et al, 2018

Progressive Weakness and Memory Impairment in a Middle-aged Man
JAMA 320:197-198, DeFilippis, E.M.,et al, 2018

Clinicopathologic Conference, Vitamin C Deficiency (Scurvey), Vitamin B6 & Folate Deficiencies
NEJM 379:282-289, Case 22-2018, 2018

"Phacing" a New Cause of Carotid Artery Dissection
Neurologist 22:54-56, Kulyk, C.,et al, 2017

Morvan Syndrome as a Paraneoplastic Disorder of Thymoma with Anti-CASPR2 antibodies
Lancet 389:1367-1368, Vale, T.C.,et al, 2017

Acute Spinal Cord Compression
NEJM 376:1358-1369, Ropper, A.E. & Ropper, A.H., 2017

Pregabalin Use Early in Pregnancy and the Risk of Major Congenital Malformations
Neurol 88:2020-2025, Patorno, E.,et al, 2017

Outcomes of Colorado Children with Acute Flaccid Myelitis at 1 Year
Neurol 89:129-137, Martin, J.A.,et al, 2017

Amyotrophic Lateral Sclerosis
NEJM 377:162-172, Brown, R.H.,et al, 2017

A Demure Teenager and Her Dystonic Foot
Neurol 89:e71-e75, Cullinane, P.W.,et al, 2017

Approach to the Differential Diagnosis of Leg Ulcers
UptoDate Aug, Petersen, M.J., 2017

Maternal Use of antiepileptic Agents During Pregnancy and Major Congenital Malformations in Children
JAMA 318:1700-1701, Bromley, R.L.,et al, 2017

Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3
NEJM 377:2376-2385, Case 38-2017, 2017

Acute Bilateral Isolated Foot Drop: Changing the Paradigm in Management of Degenerative Spine Surgery with Percutaneous Endoscopy
World Neurosurg 110:319-322, Adsul, N.,et al, 2017

A Rare Case of Bilateral Optic Neuritis and Guillain-Barre Syndrome Post Mycoplasma Pneumoniae Infection
Neuro Opth 41:41-47, Baheerathan, A.,et al, 2017

Small Fiber Neuropathy in Fabry Disease:A Review of Pathophysiology and Treatment
JIEMS 4:1-5, Politeri,J.M.,et al, 2016

Diabetic Sensory and Motor Neuropathy
NEJM 374:1455-1464, Vinik, A.I.,et al, 2016

Diagnostic Value of Prenatal MR Imaging in the Detection of Brain Malformations in Fetuses before the 26th Week of Gestational Age
AJNR 37:946-951, Conte, G.,et al, 2016

Metastatic Spinal Cord Compression: Diagnosis and Management
BMJ 353:e2539, Al-Qurainy, R.,et al, 2016

Acute Flaccid Myelitis; A Clinical Review of US Cases 2012-2015
Ann Neurol 80:326-338, Messacar, K.,et al, 2016

A 2-year-old Child with Acute Flaccid Paralysis
Neurol 87:e149-e154, Al-Ghamdi, F. & Ghosh, P.S., 2016

Use of MRI in the Diagnosis of Fetal Brain Abnormalities in Utero (MERIDIAN): A Multicentre, Prospective Cohort Study
, Griffiths, P.D.,et al, 2016

MRI Findings in Children with Acute Flaccid Paralysis and Cranial Nerve Dysfunction Occurring during the 2014 Enterovirus D68 Outbreak
AJNR 36:245-250, Maloney, J.A.,et al, 2015

Clinical Reasoning: A 51-Year-Old Woman with Acute Foot Drop
Neurol 84:e48-e52, Rallis, D.,et al, 2015

Foot Drop
BMJ 350:h1736, Stevens, F.,et al, 2015

Burning Hands and Feet
Neurol 84:e146-e152, Chan, A.C. & Wilder-Smith, E., 2015

Acute Flaccid Myelitis of Unknown Etiology in California 2012-2015
JAMA 314:2663-2671, Van Haren, K.,et al, 2015

A 48-year-old Man with Walking Difficulty
Neurol 85:e165-e169, Kalladka, D.,et al, 2015

Motor Neurone Disease
BMJ 349:g4052, Nageshwaran, S.,et al, 2014

Paroxysmal Burning Pain Caused by Erythromelalgia
Lancet 383:1692, Kondo, T.,et al, 2014

Copper Deficiency
BMJ 348:g3691, Chhetri, S.K.,et al, 2014

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Acute Aseptic Meningitis
Adams & Victors Principles of Neurology, Chp 33, pg 744, Ropper, A.H.,et al, 2014



Showing articles 50 to 100 of 440 << Previous Next >>