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Differential
(Click to cross reference)
acromicria
angiokeratoma
anterior horn cell disease
areflexia
arrhythmia, cardiac
asthma
asthma, poliomyelitis-like syndrome with
ataxia
ataxia, truncal
ataxic gait
atlanto-axial subluxation
basilar impression
benign essential tremor
bladder dysfunction
bone biopsy
bone marrow transplantation
brainstem, hypoplasia
brainstem, malformation
carbamazepine
cardiomyopathy
cataracts
central core disease
cerebellar peduncle
cerebral palsy
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrovascular accident
cerebrovascular accident, young adult
Charcot-Marie-Tooth
children
chromosomal abnormality
chromosome 11
chromosome 5
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
codfish vertebrae
cold hands sign
collagen vascular disease
congenital heart disease
congenital malformation
consanguinity
constipation
contractures, joint
cornea, abnormal
cornea, opacity of
corpus callosum, atrophy of
corpus callosum, thinning
cystinuria
deafness
developmental milestones, loss of
developmental retardation
diagnostic criteria
differential diagnosis
dilantin
dimple
dislocated hip, congenital
distal muscle atrophy
distal muscle weakness
dysmorphic
dysostosis multiplex
dyspnea
dysraphism, spinal
electrocardiogram, abnormal
electromyogram
encephalopathy
enzyme, defect
eye movement, disorders of
facial anomalies
facial appearance, abnormal
facial hypoplasia
facial weakness
facial weakness, bilateral
familial
fasciculation
finger tapping
flaccid paralysis
foam cells
foot deformity
foot drop
foot ulcer, neuropathic
fourth ventricle, enlargement of
Friedreich's ataxia
frontal bossing
fucosidosis
gait disorder
gaze palsy
gaze palsy, congenital horizontal
gaze palsy, horizontal
gaze palsy, horizontal-bilateral
gender
gene mutation
genetic counselling
genetic neurologic disorders
genetic screening
genetic testing
genu valgum
glycoprotein
growth retardation
hearing loss
heart murmur
hemorrhage, intracranial, newborn
hepatomegaly
hepatosplenomegaly
heralding manifestation
HGPPS
hoarseness
homocystinuria
hyperhomocysteinemia
hyperreflexia
hypertonia
hypertrichosis
hyporeflexia
hypotonia
hypotonia, infants
incontinence, fecal
infection, recurrent
insulin resistance
intellectual deficit
intellectual deterioration
intracranial hemorrhage
intrinsic hand muscles, wasting of
Isaacs syndrome
kyphoscoliosis, neurologic causes of
kyphosis
laryngeal spasm
leg weakness, bilateral
leg weakness, unilateral
lens, dislocation of
lens, ectopic
Lhermitte's sign
lipoma of CNS
lipoma of skin
livedo reticularis
lysosomal storage disease
malformation, CNS, congenital
malignant hyperpyrexia
medulla oblongata
medulla oblongata, lesion of
medulla oblongata, malformation
melanomatosis, primary malignant
mental retardation
metabolic disorder, primary
microcephaly
microspherophakia
mitral valve prolapse
monoparesis
Morquio syndrome
mortality
motor neuron disease
MRI, abnormal
mucopolysaccharidoses
muscle atrophy, progressive
muscle atrophy, static
muscle pain
muscle weakness
muscle weakness, proximal
muscular dystrophy
myelomeningocele
myelopathy
myokymia
myokymia, facial
myopathy
myopia
neurofibromatosis 1
neurologic disease, diagnoses of
neuromyotonia
neuroophthalmology
neuropathy
neuropathy, ataxic
neuropathy, hereditary peripheral
neuropathy, hypertrophic
neuropathy, onion bulb
neuropathy, peripheral
night blindness
nusinersen
nystagmus
ocular motility, disorders of
optic atrophy
osteogenesis imperfecta
osteoporosis
otosclerosis
pain
pain, anal
pain, leg
pain, perineum
paraparesis, spastic
paraplegia
pectus carinatum
pectus excavatum
peroxisomal disease
pes cavus
phytanic acid
pleocytosis of cerebrospinal fluid
poliomyelitis
poliomyelitis-like illness
polyneuropathy
pons, hypoplasia
postural abnormality
pregnancy, neurologic complications in
prenatal diagnosis by amniocentesis
prognathism
prognosis
progressive neurologic disorder
psychiatric problems in neurologic disorders
psychosis
pyramidal tract, uncrossed
radiculopathy
Refsum's disease
respiratory failure
retinitis pigmentosa
Rett's syndrome
review article
root lesion, nerve
sclerae, blue
scoliosis
scoliosis, neurologic association with
screening
seizure
sensorineural hearing loss
sensory loss
short neck
short stature
skin, lesions in neurologic disorders
SMN1 gene
spasticity
spinal cord, compression of
spinal cord, neoplasm
spinal muscular atrophy
spinal muscular atrophy, classification
spinal stenosis
splenomegaly
steppage gait
stereotyped behavior
sudden death
syringomyelia
tethered spinal cord
tongue, fasciculations of
trauma
treatment of neurologic disorder
tremor
urinary incontinence
visual fields, constricted
vocal cord paralysis
weakness
weakness, progressive
wheelchair
x-ray, lumbar spine
Showing articles 0 to 50 of 23509 Next >>

Spinal Muscular Atrophy
UpToDate, Oct, Bodamer,O.A., 2022

A Middle-aged Woman with Severe Scoliosis and Encephalopathy
JAMA Neurol 78:251-252, Mohan, G.,et al, 2021

Clinicopathologic Conference, Homocystinuria caused by Cystathionine B-Synthase Deficiency
NEJM 375:1879-1890, Case 34-2016, 2016

Neurologic Features of Horizontal Gaze Palsy and Progressive Scoliosis with Mutations in ROBO3
Neurol 64:1196-1203, Bosley, T.M.,et al, 2005

Poliomyelitis-Like paralysis During Recovery from Acute Bronchial Asthma:Possible Etiology and Risk Fators
Pediatrics 88:276-279, Shahar,E.M.,et al, 1991

Fucosidosis Revisited:A Review of 77 Patients
Am J Med Genet 38:111-131, Willems,P.J.,et al, 1991

Refsum Disease
In Rowland's Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8thEd, p. 509, Menkes,J.H., 1989

Friedreich Ataxia
In Rowland, L. P. Merritt's Textbook of Neurology, 8th Ed, Lea & Febiger, Phila, Ch 13, p627, Rosenberg,R.N., 1989

Central Core Disease, Clinical Features in 13 Patients
Medicine 66:389-396, Shuaid,A.,et al, 1987

Tethered Cord Syndrome in Adults
J Neurosurg 57:32-47, Pang,D.&Wilberger,J.E.Jr., 1982

Isaac Syndrome with Laryngeal Involvement:An Unusual Presentation of Myokymia
Neurol 29:1612-1615, Jackson,D.L.,et al, 1979

Clinical Symposia, Scoliosis
CIBA, 30:21978., Keim,H.A., 1978

Charcot-Marie-Tooth Disease Associated With"Essential Tremor"
Neurol Sciences 28:17-40, Salisachs,P.J., 1976

Osteogenesis Imperfecta, in Heritable Disorders of Connective Tissue
(Ed) , 4th edition, The C. V. Mosby Company St. Louis, Chap. 8, pp. 390. , 1972, McKusick,V.A., 1972

Scoliosis
Neurologic Association with-Ciba Symposium, Vol 24, #1972., , 1972

Mucopolysaccaridosis IV (Morquio Syndrome) , in Heritable Disorders of Connective Tissue
(Ed) 4th Ed, The C. V. Mosby Co, St. Louis, p. 583, McKusick,V.A., 1972

Morquio's Disease, A Radiologic & Morphologic Study
Pediatrics 34:839-850, Schenk,E.A.&Haggerty,J., 1964

Congenital Zika Syndrome
NEJM 394:e2, Bacin,F. & Montenegro,M.A., 2026

Systematic Genetic Assessment in Young Patients with Cryptogenic Stroke: The ES-EASY Project
Stroke 57:148-156, Mania-Paris,L.,et al, 2026

CT Perfusion Abnormality in Hypoglycemic Focal Neurological Deficits
Stroke 57:e6-e7, Mikito,S.,et al, 2026

Reversible Leukoencephalopathy and Parkinsonism Due to CNS Involvement in Cryoglobulinemia
Neurol 106:e214622, German,A.,et al, 2026

Progressive Quadriparesis and Falls in a 66-Year-Old Man With Longstanding Human Immunodeficiency Virus
Neurol 106:e214621, Ong,B.A. & Carlson,A.K., 2026

Intravenous Thrombolysis Use in the Late Time Window Before Interhospital Transfer for Thrombectomy
JAMA Neurol 83:60-67, Seners,P.,et al, 2026

Medical Management and Revascularization for Asymptomatic Carotid Stenosis
NEJM 394:219-231 296, Hrott,T.G.,et al, 2026

Clinicopathologic Conference, Disseminated Infection with Hypervirulent Klebsiella Pneumoniae
NEJM 394:282-294, Case 202026, 2026

Uncommon Faces of Disk Herniation: Atypical Imaging Presentations and Mimics
AJNR 47:244-251, Galante,M-J.,et al, 2026

Treating Hearing Loss with Hearing Aids for the Prevention of Cognitive Decline and Dementia
Neurol 106:e214572, Cribb,L.,et al, 2026

Peripheral Neuropathy, A Review
JAMA 335:255-266, Mauermann,M.L. & Staff,N.P., 2026

Clinicopathologic Conference, Lyme Neuroborreliosis and Coinfection with Babesia Microti
NEJM 394:383-391, Case 3-2026, 2026

Melas Syndrome
Stat PearlsPubl Jan 25, Pia,S. & Lui,F., 2025

Stroke Associated with Patent Foramen Ovale(PFO): Evaluation
www.UptodDate.com, Dec 2025, Messe,S.R., 2025

MELAS Presenting as Bilateral Symmetric Occipital and Temporal Cortices Lesions, A Case Report and Literature Review
Neurologist 30:75-79, Liu,Q.,et al, 2025

Trident Sign in GFAP-Associated Meningoencephalomyelitis
Neurol 106:e214566, Mallett,N.S.,et al, 2025

Large Language Models in Neurological Practice: Real-World Study
J Med Internet Res 27:e73212, Maiorana,N.V.,et al, 2025

Validation of the Boston Criteria Version 2.0 for Cerebral Amyloid Angiopathy in Patients Presenting with Intracerebral Hemorrhage
Neurol 104:e213460, Downes,M.H.,et al, 2025

Myelin Oligodendrocyte Glycoprotein Antibody - Associated Cerebral Cortical Encephalitis: A Case Report Highlighting Diagnostic Challenges and Therapeutic Implications
Front Immunol 16:1619807, Liu,M. & Li, D., 2025

From Stroke Workup to Mitochondrial Disease: A Case Report of MELAS
Radiol Case Reports 20:6248-6252, Sevencan,Y.,et al, 2025

AI: Need for Comparative Studies in Complex Neurologic Diagnosis
Ann Neurol doi:10.1002/ana.78068, Finelli,P.F., 2025

Acromegaly
NEJM 393:1926-1939, Giustina,A. & Colao,A.,, 2025

Clinicopathologic Conference, Subacute Painless Thyroiditis
NEJM 393:2036-2045, Quijije,N.V.,et al, 2025

Intravenous Thrombolysis Use Before Inter-Facility Transfer for Thrombectomy:Association with Efficacy and Safety Outcomes
Ann Neurol 98:871-880, Seners,P.,et al, 2025

An 83-Year-Old Female Patient with a Pupil Involving Oculomotor Nerve Palsy
Neurol 105:e214383, Riegel,D.C.,et al, 2025

Effectiveness and Safety of IV Thrombolysis Before Hospital Transfer for Thrombectomy in Patients With Basilar Artery Occlusion
Neurol 105:e214355, Liebart,S.,et al, 2025

Anticoagulant Usage and Risk of Thromboembolic Events After Ischemic Stroke in Adults with Cancer
Neurol 105:e214325, Balali,P.,et al, 2025

A 16-Year-Old Adolescent Boy with Ophthalmoplegia and Unilateral Ptosis
Neurol 105:e214430, Lu,Y.,, 2025

A 30-Year-Old Female Patient with Multiple Sclerosis Presenting with Rapidly Progressive Cranial Neuropathies, Weakness, and Ataxia
Neurol 105:e214429, Trentadue,T.,et al, 2025

A Randomized Trial of Shunting for Idiopathic Normal-Pressure Hydrocephalus
NEJM 393:2198-2209, 2264, Luciano,M.G.,et al, 2025

Idiopathic Normal-Pressure Hydrocephalus
NEJM 393:2243-2253, 2264, Johnson,M.D.,& Williams, M.A., 2025

Ribbon-Like Cortical Calcifications in Hereditary Cerebral Hemorrhage With Amyloidosis-Dutch Type
Neurol 106:e214464, Chen,Y.,et al, 2025



Showing articles 0 to 50 of 23509 Next >>