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Differential
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ACTH, ectopic syndrome of
acute disseminated encephalomyelitis
acyl CoA dehydrogenase deficiency
Addison's disease
aldolase
allodynia
anemia
aneurysm, intracranial
ankle clonous
ankle edema
ankle reflex, absent
ankle reflex, preserved
ankle, swelling of
anterior tibial muscle weakness
antiviral agents
areflexia
Arnold Chiari malformation
arrhythmia, cardiac
arsenic
ascending paralysis
ascites
ataxia
ataxia, cerebellar
ataxia, progressive
ataxic gait
atrial flutter
attention deficit disorder with hyperactivity
autonomic dysfunction
autosomal rcessive spastic ataxia of Charlevoix-Saguenay
B 12 deficiency
Babinski sign
BAL
basophilic stippling of red blood cells
bone biopsy
bone marrow suppression
bone scanning
brain biopsy
brain biopsy, stereotaxic
brainstem, lesion of
burning paresthesia
calculations
calf atrophy
carcinoma of lung
cardiomegaly
cardiomyopathy
CAT scan, abnormal
CAT scan, emission, abnormal
CAT scan, ring sign
cauda equina, enhancement
cauda equina, lesion of
cerebellar atrophy, primary
cerebellar degeneration
cerebrospinal fluid, cytology
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
Charcot-Marie-Tooth
children
Clinical Pathologic Conference(C.P.C.)
cognition
confusion
consanguinity
corpus callosum, lesion of
corpus callosum, thinning
cranial nerve enhancement
cranial neuropathy
cyanosis
cytokines
dental procedure, neurologic complications with
dermatitis
developmental disability
diaphragmatic paralysis
diaphragmatic paralysis, causes of
diarrhea
differential diagnosis
difficulty going down stairs
disability, neurological
distal muscle weakness
dysphagia
dyspnea
edema, pedal
electrocardiogram, abnormal
encephalopathy
eosinophilia
episodic disorders
episodic neurologic deficits
erectile dysfunction
erythrocyte
exercise
exome sequencing
falling
familial
fasciculation
fatigue
fever
finger naming
finger nose finger test
finger swelling
fingernails, abnormal
flushing, unilateral
foot deformity
foot drop
foot drop, bilateral
foot, weakness
fracture, long bone
F-wave response
gadolinium
gait disorder
gastroenteritis
gene mutation
genetic neurologic disorders
genetic testing
guanethidine
Guillain Barre syndrome
Guillain Barre syndrome, differential diagnosis of
hammertoes
hand weakness
handwriting
headache
heavy metal intoxication
hemoglobinuria
hepatitis
hepatomegaly
hepatosplenomegaly
herpes zoster
high arched feet
H-reflex testing
hyperamylasemia
hypercalcemia
hypercapnia
hyperhidrosis
hyperkeratosis
hyperreflexia
hypogammaglobulinemia
hypoglycorrhachia
hypogonadism
hypokalemia
hypokalemic alkalosis
hyponatremia
hypopigmentation of skin
hyporeflexia
imbalance
inborn errors of metabolism
incoordination
infection
interobserver agreement
jaundice
Krabbe's disease
lead poisoning
leg numbness
leg weakness, bilateral
leukodystrophy
leukoencephalopathy, differential diagnosis
leukopenia
livedo reticularis
liver disease
liver function enzymes
liver scan
long bone lesion
low back pain
Lyme disease
lymphoma involving CNS
lysosomal storage disease
Mees lines
misdiagnosis
monoclonal gammopathy
motor neuron disease
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, spinal cord
multiple myeloma
muscle atrophy, progressive
muscle biopsy
muscle pain
muscle weakness
myelitis
myeloma, osteosclerotic
myelopathy
myelopathy, carcinomatous
myocardial infarction
myopathy
myopathy, metabolic
nausea and vomiting
neoplasm, hormone producing
neoplasm, hormone producing, ectopic
nerve conduction studies
neuritis, heavy metals causing
neuroendocrinology
neurologic complications of, systemic cancer
neurologic disease, diagnoses of
neurologic examination
neuromuscular disease, electrodiagnosis of
neuropathy
neuropathy, demyelinating
neuropathy, diabetic
neuropathy, hereditary peripheral
neuropathy, peripheral
neuropathy, short-fiber
neuropathy, toxic
occupational neurologic disorders
occupational neuropathies
old age, neurology of
organomegaly
osteoporosis
pain
pain, foot
pain, leg
pancreatitis
pancytopenia
papilledema
paralysis
paralysis, use-related
paraparesis, familial spastic
paraparesis, familial spastic, classification
paraparesis, familial spastic, variants
paraparesis, spastic
paresthesias
paresthesias, feet
paresthesias, hands
past pointing
pericardial effusion
peripheral blood smear
peripheral blood smear, abnormal
pes cavus
physical activity
physical therapy
plasmacytoma
pleocytosis of cerebrospinal fluid
pleural effusion
POEMS syndrome
poliomyelitis
poliomyelitis, provocation
polymyositis
polyneuropathy
polyneuropathy, carcinomatous
pons, lesion of
position sensation, abnormal
prognosis
progressive neurologic disorder
proprioception, abnormal
proteinuria
psychosis
pulmonary infiltrates
quadriparesis
quadriparesis, progressive
quadriplegia
quadriplegia, transient
rabies, nervous system involvement with
reflex sympathetic dystrophy
reflex sympathetic dystrophy, children
remote effect of cancer on the nervous system
respirator
respiratory failure
retrograde axonal flow
retroperitoneal mass
review article
riboflavin
Romberg's sign
sclerosis, bone
sedimentation rate, elevated
sensory loss
skin, discoloration
skin, lesions in neurologic disorders
skin, temperature difference
spasticity
spinal cord, lesion of
splenomegaly
stem cell transplantation
steppage gait
sweating, abnormality of
sympathetic block
syringomyelia
systemic illness
tachycardia
tandem gait, ataxic
tetanus
thermography
thrombocytopenia
thrombocytosis
toe walking
trauma
treatment of neurologic disorder
tremor
tremor, intention
tripping
unconsciousness
uremia
urinary retention
urine test in toxic screen
vascular endothelial growth factor
vibratory sensation, abnormal
viral infection
viral infection, CNS
walking, delayed
walking, difficulty with
weakness
weakness, acute
weakness, episodic
weakness, generalized
weakness, progressive
weaning from respirator, failure to
white matter disease
wide based gait
word-finding difficulty
Showing articles 50 to 100 of 709 << Previous Next >>

Miller Fisher Syndrome and Acute Motor and Sensory Axonal Neuropathy (AMSAN) Variant Guillain-Barre Overlap Syndrome (MFS/AMSAN-GBS) After Upper Respiratory Tract Infection (URTI)
Acta Sci Clin Case Reports 3:19-24, Chau,T.C. & Muhamad,N.A.N., 2022

The Phenotypic Continuum of ATP1A3-Related Disorders
Neurol 99:e1511-e1526, Vezyroglou,A., et al, 2022

Facial Numbness, Dysarthria, Muscle Atrophy, and Weakness in a Young Patient
JAMA Neurol 78:1273-1274, Liu, Y.,et al, 2021

A 63-Year-Old Woman Presenting with Bilateral Leg Pain
Neurol 96:343-348, Budhu, J.,et al, 2021

A 48-Year-Old Man Presenting With Diplopia
Neurol 96:399-405, Pehere,N.K.,& Gofer,K., 2021

A Teenager with Shortness of Breath and Difficulty Walking
Neurol 96:e2346-e2350, Liu, S.C.,et al, 2021

Clinicopathologic Conference, Delayed Postthypoxic Leukoencephalopathy
NEJM 384:2438-2445, Case 19-2021, 2021

A 13-Year-Old Boy with Subacute-Onset Spastic Gait
JAMA Neurol 78:e1-e2, Xie, N.,et al, 2021

Clinicopathologic Conference, Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome
NEJM 385:165-175, Case 20-2021, 2021

A 68-Year-Old Man with Proximal Weakness and Seizures
Neurol 97:e423-e428, Chen, T., 2021

Clinical and Genetic Features in Patients with Reflex Bathing Epilepsy
Neurol 97:e577-e586, Accogli, A.,et al, 2021

A 49-Year-OLD Woman with Progressive Numbness and Gait Instability
Neurol 97:342-347, Zahid, A.,et al, 2021

A 57-Year-Old Woman with Progressive Ataxia and Falls
Neurol 95:650-656, Badahdah, A., 2020

Sensory Ganglionopathy
NEJM 383:1657-1662, Amato, A.A. & Ropper, A.H., 2020

Clinicopathologic Conference,Aceruloplasminemia, Hereditary
NEJM 383:1974-1983, Case 35-2020, 2020

Clinicopathologic conference, Frontotemporal Lobar Degeneration with tau-positive inclusions consistent with Picks disease
NEJM 383:2666-2675, Case 41-2020, 2020

Neurologic Features in Severe SARS-CoV-2 Infection
NEJM 382:2268-2270, e110, , 2020

Spasms and Myoclonus in a Young Woman with Hashimoto Thyroiditis
JAMA Neurol 77:650-651, Shen, D.,et al, 2020

Ears of the Lynx Magnetic Resonance Imaging Sign
Ann Neurol 88:16-17, Baghbanian, S.M.,et al, 2020

Rapidly Progressive Gait Disorder and Cranial Nerves Involvement in a 9-year-old boy
Neurol 94:e330-e334, Lipp, A.,et al, 2020

A 70-year-old Man with Rapid Stepwise Paraparesis and Sensory Loss
Neurol 94:e651-e655, Krause, M.A.,et al, 2020

A 59-year-old Woman with Multiple Myeloma and Lower Extremity Weakness and Numbness
Neurol 94:794-800, Gadot, R.,et al, 2020

COVID-19 Presenting with Ophthalmoparesis from Cranial Nerve Palsy
Neurol 95:221-223, Dinkin, M.,et al, 2020

A 68-year-old Man with Rapid Cognitive Decline
Neurol 93:315-318, Berth, S.H.,et al, 2019

Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019

Orofacial Dyskinesia in a Young Man
JAMA Neurol 76:1517-1518, Tian, X.,et al, 2019

GGC Repeat Expansion of NOTCH2NLC in Adult Patients with Leukoencephalopathy
Ann Neurol 86:962-968,809, Okubo, M.,et al, 2019

Testing the Reflexes
BMJ 366:l4830, Lees, A.J. & Hurwitz, B., 2019

Neurolymphomatosis
Neurol 93:e1229-e1230, DeBoer, S.R.,et al, 2019

A 14-Year-Old Girl with Headache, Seizures, and Confusion
Neurol 92:e161-e167, Xiao, L.,et al, 2019

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

A 15-year-old Boy with Bilateral Wrist Pain in the Setting of Weight Loss
Neurol 92:486-492, Lau, K.H.V.,et al, 2019

FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance
Mol Genet Metab 125:281-291, Almannai, M.,et al, 2018

Wilson Disease
NIDDK Oct2018, , 2018

Making Sense of the Clinical Spectrum of Limb Girdle Muscular Dystrophies
Pract Neurol 18:201-210, Khadilkar,S.V.,et al, 2018

Clinical Reasoning: Cardioembolic Stroke in a 23-year-old Man with Elbow Contracture
Neurol 90:e172-e176, Roy, B. & Raynor, E., 2018

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

Persistent Postural-Perceptual Dizziness (PPPD): A Common, Characteristic and Treatable Cause of Chronic Dizziness
Pract Neurol 18:5-13, Popkirov, S.,et al, 2018

Subacute Paresis in a 28-year-old man with HIV
Neurol 90:432-435, Harada, Y.,et al, 2018

A 52-year-old woman with a 3 weeks of progressive gait ataxia and dysarthria
Neurol 90:e985-e989, Ly, C.,et al, 2018

A 42-year-old man with unilateral leg weakness
Neurol 90:e1085-e1090, Schneider, R.,et al, 2018

A young woman with symmetric weakness and behavioral disturbance
Neurol 90:e1442-e1447, Rosenberg, J.,et al, 2018

Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy
Neurol 90:e1827-e1831, Xiao, F.,et al, 2018

Acute Onset of Diplopia in Pregnancy
Neurol 91:e180-e184, Munro, Z. & Fernandez, D., 2018

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

A Patient With Multiple Cranial Nerve Palsies and Areflexic Paraparesis
Neurol 91:e392-e395, Garg,R.K.,et al, 2018

A Man with Rapidly Progressive Weakness and Respiratory Failure
Neurol 91:e686-e691, Xu,D.,et al, 2018

Proptosis and Double Vision in a Child
JAMA Neurol 75:1142-1143, Lu, A.J.,et al, 2018

A 35-year-old Woman with Diplopia, Ataxia, and Altered Mental Status
Neurol 91:e1942-e1946, Bauer, Z.,et al, 2018

Progressive Gait Difficulty and Incontinence in a 40-year-old Man with HIV
Neurol 91:1065-1070, Silverman, A.,et al, 2018



Showing articles 50 to 100 of 709 << Previous Next >>