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Differential
(Click to cross reference)
airway obstruction
ankle reflex, absent
anosmia
areflexia
arrhythmia, cardiac
arthrogryposis multiplex
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
clubfoot as related to neurologic disease
cognition
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
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
hammertoes
hand deformity
hand weakness
hearing loss
high arched feet
high arched palate
hydrocephalus
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
lordosis
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, peripheral
neuropathy, sensory
neuropathy, sensory, hereditary
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
paraparesis
paraparesis, familial spastic
paraparesis, spastic
Parkinson disease
past pointing
peroneal muscle atrophy, causes of
peroxisomal disease
pes cavus
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
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
wheelchair
white matter disease
Wolfram syndrome
x-ray, lumbar spine
Showing articles 50 to 100 of 218 << Previous Next >>

Foot Drop
WebMD, Bernstein, L., 2018

A 74-year-old Woman with Bilateral Foot Pain and a Palmar Rash
Neurol 88:e44-e50, Wynn, D.P.,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

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

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

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

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

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

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

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

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

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Acute Anterior Poliomyelitis
Adams & Victors Principles of Neurology, Chp 33, pg 763, Ropper, A.H.,et al, 2014

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Nonpoliovirus Poliomyelitis
Adams & Victors Principles of Neurology, Chp 33, pg 765, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Dystonia Musculorum Deformans
Adams & Victors Principles of Neurology, Chp 39, pg 1099, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Amyotrophic Lateral Sclerosis
Adams & Victors Principles of Neurology, Chp 39, pg 1109, Ropper, A.H.,et al, 2014

Enterovirus Vaccines for an Emerging Cause of Brain-Stem Encephalitis
NEJM 370:792-794, McMinn, P.C., 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

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

Erythromelalgia? A Clinical Study of People Who Experience Red, Hot, Painful Feet in the Community
Int J Vasc Med ID=864961, Friberg, D.,et al, 2013

Clinical Reasoning: A 12-year-old Boy with Ascending Weakness
Neurol 80:e110-ee114, French, K.F.,et al, 2013

Parkin Disease
JAMA Neurol 70:571-579, Doherty, K.,et al, 2013

Bilateral Peroneal Palsy after Weightlifting
Clin J Sport Med 23:400-402, Kyavar, L. & Heckmann, J.G., 2013

Bilateral Foot Drop in Polyarteritis Nodosa
NEJM 367:e9, Souza Neves, F. & Lin, K., 2012

Clinicopath Conf, The POEMS Syndrome, with Demyelinating Neuropathy and Solitary Pharmacytoma of Bone
NEJM 362:929-940, Case 7-2010, 2010

Copper Deficiency as a Treatable Cause of Poor Balance
BMJ 340:864-866, Khaleeli,Z., et al, 2010

Isolated Ischaemic Lesions in the Foot Motor Area Mimic Peripheral Lower-Limb Palsy
JNNP 81:822-823, Alonso,A., et al, 2010

Small Fiber Neuropathy: A Burning Problem
Cleve Clin J Med 76:297-305, Tavee, J. & Zhou, L., 2009

A 63-Year-Old Woman with Urinary Incontinence and Progressive Gait Disorder
Neurol 72:1607-1613, Lossos,A.,et al, 2009

A 52-Year-Old Woman With Disabling Peripheral Neuropathy: Review of Diabetic Polyneuropathy
JAMA 302:1451-1458, Rutkove,S., 2009

Viral Meningitis
BMJ 336:36-40, Logan,S.A. &MacMahon,E., 2008

Diagnosis and Management of Motor Neurone Disease
BMJ 336:658-662, McDermott,C.J. &Shaw,P.J., 2008

Neurodevelopment and Cognition in Children After Enterovirus 71 Infection
NEJM 356:1226-1234, Chang,L.-Y.,et al, 2007

A 16-Year-Old Girl With Progressive Weakness of the Left Leg
Neurol 69:84-90, Hahn,A.F.,et al, 2007

Amyotrophic Lateral Sclerosis
Lancet 369:2031-2041, Mitchell,J.D. & Borasio,G.D., 2007

Multifocal Motor Neuropathy: The Diagnostic Spectrum and Response to Treatment
Neurol 69:1680-1687, Slee,M.,et al, 2007

Charcot Neuroarthropathy in the Era of HAART
Lancet 367:274, Oh-Park,M.,et al, 2006

Clinicopath Conf, Charcot-Marie-Tooth Disease Type 2, with Aides Pupil and a Mutation in MPZ Gene
NEJM 354:2584-2592, Case 18-2006, 2006

Value of the Oral Glucose Tolerance Test in the Evaluation of Chronic Idiopathic Axonal Polyneuropathy
Arch Neurol 63:1075-1079, Hoffman-Snyder,C.,et al, 2006

MRI Detection of Cysts of the Knee Causing Common Peroneal Neuropathy
Neurol 65:1829-1831, Iverson,D.J., 2005



Showing articles 50 to 100 of 218 << Previous Next >>