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Differential
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abdominal distention
abducens nerve paralysis
acid maltase deficiency
acid maltase deficiency, adult
advances in neurology
adverse drug reaction
amyloidosis
anesthesia, general
aneurysm
anterior horn cell disease
anticonvulsants
arachnoiditis
areflexia
arrhythmia, cardiac
asymptomatic
ataxia
ataxic gait
autism
brain biopsy
bulging of biceps
calf hypertrophy
carbamazepine
carcinoma
cardiomegaly
cardiomyopathy
cardiovascular disease
caribbean
CAT scan, emission, abnormal
cataracts
cauda equina
cauda equina, enhancement
cauda equina, lesion of
cavernous sinus
cavernous sinus, lesion of
central nervous system, infection of
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
Charcot-Marie-Tooth
chewing, impaired
children
chromosomal abnormality
chromosome 17
Clinical Pathologic Conference(C.P.C.)
CLOVES syndrome
clubfoot as related to neurologic disease
confusion
congenital malformation
congenital myopathy
congestive heart failure
contractures, joint
conus medullaris, lesion of
corticotropin level
corticotropin-releasing factor
cortisol, elevated
cranial nerve enlargement
cranial nerve palsies
cranial nerves
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
Cushing's syndrome
cyst
cysticercosis
cysticercosis, cerebral
cysticercosis, disseminated
cysticercosis, intraventricular
cysticercosis, miliary
cysticercosis, spinal
cysticercosis, subarachnoid
deafness
Dejerine-Sottas syndrome
denervation of muscle
diabetes mellitus
diamond on quadriceps
diaphragmatic paralysis
differential diagnosis
dilantin
diplopia
distal muscle atrophy
distal muscle weakness
Dominican Republic
dysferlinopathy
dysphonia
dysplasia of C.N.S.
dyspnea
dystonia
dystonia, post traumatic
dystrophin
echocardiogram
echocardiogram, LVH
electrocardiogram, abnormal
electrocardiogram, LVH
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
electron microscopy
entrapment neuropathy
enzyme, defect
eosinophilia
ependymitis
epidermal nevus syndrome
exercise
exophthalmus
facial hair, excessive
facial pain
facial pain, atypical
facial weakness
facial weakness, bilateral
failed back syndrome
failed medical management
falling
familial
fatigue
fever
fine motor function, impaired
foot deformity
foot drop
fourth ventricle, cyst
gadolinium
gait disorder
gait, waddling
gammaglobulin therapy, intravenous
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
Gowers maneuver
hammertoes
hand deformity
hand weakness
headache
hearing loss
heart murmur
helminthic infection of CNS
hemiatrophy, congenital
hemidiaphragm, paralysis of
hemihypertrophy, congenital
hemihypertrophy, facial
hemimegalencephaly
hemiparesis
hepatomegaly
hereditary myopathy with early respiratory failure
herniated disc
herniated disc, lumbar
herniated disc, lumbar, recurrent
herniated disc, lumbar-laminectomy
heterotopia
high arched feet
hirsutism
hoarseness
H-reflex testing
hydrocephalus
hydrocephalus, non-communicating(obstructive)
hypercalcemia
hypertension
hypoglycorrhachia
hypokalemia
hypomelanosis of Ito
hypopigmentation of skin
hyporeflexia
hypothyroidism
IgG4-related disease
inability to sit up
incontinence, fecal
infantile spasm
intellectual deficit
intracranial pressure, increased
intrinsic hand muscles, wasting of
Isaacs syndrome
Kobberling-Dunnigan syndrome
kyphoscoliosis, neurologic causes of
left ventricular dilatation
leg atrophy
leg numbness
leg swelling
leg weakness, bilateral
leg weakness, unilateral
leukocytosis
life expectancy
limb hypertrophy
limb-girdle weakness
lipodystrophy
lordosis
lumbosacral plexopathy
lymphoma
lymphoma, primary of CNS
lymphopenia
macrocephaly
malformation, CNS, congenital
malignant hyperpyrexia
meningitis, aseptic
meningitis, cysticercosis
meningitis, eosinophilic
mental retardation
mental status, abnormal
metabolic alkalosis
mexiletine
misdiagnosis
molecular genetics
monoclonal gammopathy
mononeuropathy
mononeuropathy chronic inflammatory demyelinating
motor neuron disease
movement disorder
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, contrast enhanced, postoperative
MRI, cranial nerves
MRI, lumbosacral plexus
MRI, muscle
MRI, peripheral nerve
MRI, spinal cord
MRI, spine
MRI, spine, postoperative
multiple myeloma
muscle atrophy, focal
muscle atrophy, progressive
muscle biopsy
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, classification
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, dystrophin normal
muscular dystrophy, female occurrence of
muscular dystrophy, limb-girdle
muscular dystrophy, pattern of muscle involvement
myelopathy
myeloradiculopathy
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
neoplasm, peripheral nerve
nerve biopsy
nerve conduction studies
nerve enlargement
nerve hypertrophy
nerve injury
nerve root biopsy
nerve root enhancement
nerve root hypertrophy
neurocutaneous disease
neuroendocrinology
neurofibroma
neurofibromatosis 1
neurofibromin
neurologic disease, diagnoses of
neurologic examination
neurolymphomatosis
neuromyotonia
neuropathology
neuropathy
neuropathy, ataxic
neuropathy, hereditary peripheral
neuropathy, hypertrophic
neuropathy, onion bulb
neuropathy, peripheral
night blindness
night sweats
optic nerve, enlarged
orthopnea
pain
pain, leg
palpitations
papilledema
paraparesis
parasitic infection, CNS
percussion induced muscle contraction
peripheral nerve, lesion of
peroxisomal disease
pes cavus
phakomatoses
phytanic acid
plasma cell dyscrasia
pleocytosis of cerebrospinal fluid
polyneuropathy
polyneuropathy, chronic inflammatory demyelinating
post polio syndrome
postoperative lumbar spine
postural abnormality
prenatal diagnosis by amniocentesis
prognosis
progressive neurologic disorder
proptosis
proximal muscle atrophy
pseudohypertrophy
pseudomyotonia
ptosis
pulmonary embolism
pupil, tonic
quadriplegia
radicular pain
radiculopathy
recurrent
Refsum's disease
respiratory failure
retinitis pigmentosa
review article
rhabdomyolysis
rippling muscle disease
root lesion, nerve
saddle anesthesia
sarcoglycan
sarcoglycanopathy
sciatic neuropathy
sciatica
scoliosis
sedimentation rate, elevated
seizure
sensorineural hearing loss
sensory loss
serologic testing
shoulder, elevation
skin, lesions in neurologic disorders
spinal accessory nerve
spinal cord, compression of
spinal cord, extramedullary cyst of
spinal cord, neoplasm
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, intermediate form
standing difficulty
stem cell transplantation
steppage gait
steroid
steroid therapy, CNS treatment and complications with
subarachnoid hemorrhage
subcutaneous nodules
sudden death
survival motor neuron gene
syringomyelia
thirst
tinnitus
titinopathy
toe walking
tongue, enlarged
tongue, weakness
trauma
treatment of neurologic disorder
trigeminal nerve
trigeminal nerve, hypertrophy
urinary frequency
urinary incontinence
urine, dark
ventriculitis
visual acuity, decreased
visual fields, constricted
vital capacity
weakness
weakness, generalized
weakness, progressive
weakness, proximal
web sites
weightlifting
wheelchair
winging of scapula
workup
Showing articles 50 to 100 of 1496 << Previous Next >>

A 60-Year-Old Man with Weakness and Gait Dysfunction
JAMA Neurol 82:305-306, Jones,F.J.S.,et al, 2025

Congenital Titinopathy:Comprehensive Characterization of the Most Severe End of the Disease Spectrum
Ann Neurol 97:611-628, Coppens,S.,et al, 2025

A Toddler with Acute-Onset Hypotonia, Areflexia, and Ataxia
Neurol 104:e213593, Pence, K.L. &Clark, R.A., 2025

Postprocedural Brachial Neuritis:Clinical, Electrodiagnostic, and Neuroimaging Features
AJNR 46:1050-1055, Ambati,V.S.,et al, 2025

Intracranial Hypertension Associated with Poly-Cranio-Radicular-Neuropathies A Case Report and Review of the Literature
Neurologist 29:166-169, Eaton,J.E.,et al, 2024

A 60-Year-Old Woman with Rapidly Progressive Muscle Weakness and Ophthalmoparesis
Neurol 103:e209708, Wannarong,T.,et al, 2024

A 26-Year-Old Woman with Chronic Progressive Gait Dysfunction
Neurol 103:e2098-e2030, Jones,F.J.S. & Orthmann-Murphy,J., 2024

Isolated Primary Central Nervous System Lymphoma of the Optic Nerve, A Case Report and Review of the Literature
Neurologist 29:351-355, Keertana,J.,et al, 2024

A 65-Year-Old Woman with Isolated Macroglossia as the Initial Presentation of a Rare Disease
Neurol 103:e210070, Lara,C.,et al, 2024

Sarcoidosis of the Pituitary Gland and Stalk in a Man Presenting Asthenia, Impotence, Loss of Libido, Polyuria, and Polydipsia
Lancet 404:2460-2461, Clement,J., et al, 2024

A 32-Year-Old Man with Painless Bilateral Shoulder Girdle Weakness and Atrophy
Neurol 103:e209915, Gutti,N.B.,et al, 2024

A 22-Year-Old Woman with Episodic Weakness and Jaundice
Neurol 103:e210018, Rathinasbapathi,M.,et al, 2024

Clinicopathologic Conference, Myasthenia Gravis
NEJM 391:1441-1450, Case 32-2024, 2024

A 19-Month Old Girl with Infantile-Onset Myopathy and White Matter Changes
Neurol 102:e209258, Lail,G.,et al, 2024

Clinicopatholigic Conference, Rheumatoid Arthritis with Vasculitis Causing A Confluent Mononeuritis Multiplex
NEJM 390:1312-1322, Case 11-2024, 2024

Clinicopathologic Conference, Thyrotoxic Periodic Paralysis Associated with Graves Disease
NEJM 390:1514-1522, Case 13-2024, 2024

Clinical and Imaging Features of Cobb Syndrome
Neurol 102:e208118, Yang,X.,et al, 2024

Clinicopathologic Conference, Infant Botulism, Case 3-2024
NEJM 390:358-366, Case 3-2024, 2024

IgG4-Related Orbital Inflammation
https://EyeWiki.org, Oct, Chelnis,J. & Gervasio,K.A., 2023

Clinical Features and Diagnosis of Intramedullary Spinal Cord Abscess in Adults, A Systematic Review
Neurol 101:e836-e844, Harrold,G.K.,et al, 2023

A Woman With Multifocal Ischemic Strokes and Progressive Cognitive Impairment Due to Intravascular Lymphoma
Stroke 54:e488-e451, Stamm,B., et al, 2023

A Young Woman with Rapidly Progressive Weakness and Paresthesia
Neurol 101:676-681, Alwakeel,S.S.,et al, 2023

Clinicopathologic Conference,Limb-Shaking Transient Ischemia Attacks
NEJM 389:1416-1423, Case 31-2023, 2023

MR Imaging Patterns and Prognosis in Powassan Virus Encephalitis
Neurologist doi.10.1097/NRI.0000000000000533, Finelli,P.F., 2023

A 67-Year-Old Woman with Progressive Tingling Sensations and Imlalance
Neurol 100:151-157, Horta,L.F.B.,et al, 2023

A Young Man With Subacute Onset of Spastic Paraparesis
Neurol 100:199-205, Rossi,S.,et al, 2023

Cerebral Alveolar Echinococcosis
NEJM 388:453, Ju,H. & Liu,C., 2023

Cashew Nut Sign:A Concave Parenchymal Hemorrhage Caused by Cerebral Venous Thrombosis
Stroke 54:e38-e39, Schlechter,M.,et al, 2023

Progressive Camptocormia with Head Drop and Dysphagia
JAMA Neurol 80:209-210, El-Wahsh,S., et al, 2023

A 60-Year Old Man with Asymmetric Weakness and Persistent Fever
Neurol 100:530-536, Zheng,Y.,et al, 2023

A 26-Year-Old Woman with Recurrent Pain, Weakness, and Atrophy in Bilateral Upper Limbs During Pregnancy and Puerperium
Neurol 100:631-637, Zeng,T.f.,et al, 2023

A 23-Year-Olf Man With Progressibe Asymmetric Weakness and Numbness
Neurol 100:674-682, Kaplan,E.H.,et al, 2023

Clinicopathologic Conference, Hypocalcemic Myopathy Due to Hypoparathyroidism
NEJM 388:1513-1520, Case 12-2023, 2023

Early Surgery for Sciatics, Does New Evidence Challenge a Stepped Care Approach for all Patients?
BMJ 381:791, Schmid,A.B.,et al, 2023

Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease (MOGAD): Clinical Features and Diagnosis
UptoDate.com, March, Flanagan,E.P. & Tillema,J-M, 2023

Severe Hippocampal Atrophy in a Patient with Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy
JAMA Neurol 80:642-643, Bartels,F.,et al, 2023

Clinicopathologic Conference, Facioscapulohumeral Muscular Dystrophy
NEJM 388:2379-2387, Case 19-2023, 2023

A 40-Year-Old Woman Presenting with Encepatholopathy and Paraparesis
Neurol 101:e94-e98, AlSabah,A.,et al, 2023

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

Cases with IgG4-related Ophthalmic Disease with Mass Lesions Surrounding the Optic Nerve
Am J Ophthalmol 25:101324, Hamaoka, S.,t al, 2022

Severe Vitamin B12 Deficiency Presenting as Pancytpenia, Hemolytic Anemia, and Parasthesia:Could Your B12 Be Any Lower?
Cureus doi:10.7759/cureus 29225, Pelling,M.M., et al, 2022

Spontaneous Escherichia Coli Meningitis and Brain Abscess in an Immunocompetent Adult
Cureus doi.10.7759/CUREUS.208728, Jeter,K.et al, 2022

Saturday Night Myelopathy Flexion Myelopathy Related to Drug Intoxication
Neurologist 27:27-29, Martin, A.J.&Garcia,M.C., 2022

Acute Myelopathy in a Man with Cutaneous Papules
JAMA Neurol 79:84-85, Neo, S.,et al, 2022

A 64-Year-Old Man with History of Meningitis Presenting with Proximal Weakness of the Arms
Neurol 98:208-213, Karschnia, P.,et al, 2022

A 57-Year-Old Man with Stepwise Progressive Paraparesis, Sensory Loss, Urinary Retention, and Constipation
Neurol 98:e555-e560, Alkabie, S.,et al, 2022

Thyrotoxic Periodic Paralysis
UptoDate Jan, Gutmann, L. & Conwit, R., 2022

Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
NEJM 386;674-687, Case 5-2022, 2022

Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis
UptoDate 2022 Jan, Darras, B.T., 2022

Clinicopathologic Conference, Diffuse Large B-Cell Lymphoma
NEJM 386:977-986, Case 7-2022, 2022



Showing articles 50 to 100 of 1496 << Previous Next >>