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Differential
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abdominal cramps
accomodation, abnormal
Alexanders disease
Alexanders disease, adult onset
alveolar hypoventilation
aminoacidurias
anesthesia, general
anisocoria
antineutrophil cytoplasmic autoantibodies
aphasia, children
aphonia
apraxia, speech
arm weakness
arrhythmia, cardiac
arthralgia
arthrogryposis multiplex
ascending paralysis
aspiration
astrogliopathy
ataxia
ataxia, cerebellar
attention deficit disorder with hyperactivity
autism
autonomic dysfunction
baldness
Benedict's solution test
bifid uvula
botulism
brainstem, hematoma
brainstem, hemorrhage, primary
brainstem, infarction of
brainstem, vascular malformation of
bulbar palsy
bulbar palsy, acute
cachexia
calcification, intracranial
cardiomyopathy
CAT scan
CAT scan, abnormal
cataracts
cavernous hemangioma
central pontine myelinolysis
cerebellar infarction
cerebral infarction
cerebral palsy
cerebral palsy, associated problems with
cerebral palsy, pure ataxic
cerebrovascular accident
cerebrovascular accident, multiple
chromosome 19
cleft palate
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
congenital heart disease
congenital malformation
congenital myasthenic syndromes
congestive heart failure
consanguinity
corona radiata
cranial nerve enhancement
cranial nerve palsies
cranial nerve tumor
cranial neuropathy
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
deafness
deafness, unilateral
deep gray nuclei
developmental retardation
diarrhea
dinitrophenylhydrazine(D.N.P.H.)reaction
diphtheria
diplegia, atonic
diplegia, spastic cerebral
diplopia
distal muscle weakness
drooling
dropped head syndrome
Duane syndrome
dysarthria
dysphagia
dysphonia
dysplasia of C.N.S.
dyspnea
edema, laryngeal
edema, palate
electrocardiogram, abnormal
electroencephalogram
electromyogram
encephalitis
encephalopathy
exome sequencing
eye movement, disorders of
facial appearance, abnormal
facial nerve palsy
facial weakness
facial weakness, bilateral
failure to thrive
familial
fasciculation
fatigue
ferric chloride test
fever
frontal balding
gadolinium
gag reflex, depressed
gastroparesis
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
GFAP gene
granulomatosis with polyangiitis
granulomatous disease
headache
hearing loss
hearing loss, unilateral
hearing problems in children
heart block
hemiparesis
herpes simplex encephalitis
high arched palate
Hirschprung's disease
histiocytosis
hoarseness
Holt-Oram syndrome
hypercapnia
hyperreflexia
hypogeusia
hypoglossal nerve paralysis
hypoglycorrhachia
imbalance
infection
intellectual deficit
intellectual deficit, treatable causes of
intelligence quotient
jugular foramen syndrome
karyotyping
klippel feil syndrome
language disorders in children
leukodystrophy
leukoencephalopathy, differential diagnosis
macrocephaly
malformation, vascular
maple syrup urine disease
medulla oblongata
medulla oblongata, hemorrhage of
medulla oblongata, lesion of
meningeal biopsy
meningeal enhancement
meningitis
meningitis, monocytic
mental retardation
mestinon
midline defect in children
molecular genetics
mortality
MRI
MRI, abnormal
MRI, contrast enhanced
multiple sclerosis, misdiagnosis
muscle atrophy, progressive
muscle biopsy
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, cardiovascular changes with
myelodysplasia
myotonia
myotonia dystrophica
myotonia dystrophica, classification
nasal speech
nausea and vomiting
neck pain
neck weakness
neoplasm, metastatic to CNS
neoplasm, primary of CNS
neurofibroma
neurologic evaluation
neuroma
neuromuscular blockade
neuromuscular junction, abnormality of
neuropathy, diphtheritic
neurotoxin
nystagmus
opened mouth
operculum syndrome
operculum syndrome, bilateral
ophthalmoplegia
osmotic demyelination syndrome
pain, abdominal
palatal myoclonus
palate, paralysis
palate, paralysis-unilateral
palatopharyngeal incompetence
paraparesis
paraparesis, spastic
paroxysmal neurologic deficits
percussion induced muscle contraction
phenylketonuria
pleocytosis of cerebrospinal fluid
pons, infarction of
pregnancy, neurologic complications in
primary CNS histiocytic sarcoma
prognosis
progressive neurologic disorder
psychological testing, neurologic problems
psychosis
psychosis, childhood
psychosocial aspects
ptosis
ptosis, bilateral
ptosis, unilateral
pupil, abnormality in neurologic disorders
pupil, oval
regional enteritis
respiratory failure
review article
Rosenthal fibers
salivation, excessive
sarcoma
schwannoma
seizure
seizure, advice to parents and teachers regarding
seizure, psychosocial aspects of
seizure, treatment of
septicemia
slit lamp examination
small vessel disease
somnolence
speech disorder, childhood
spina bifida
spinal accessory nerve palsy
sternocleidomastoid weakness
steroid therapy, CNS treatment and complications with
stridor
stuttering
syringomyelia
tachycardia
taste
temporalis muscle wasting
temporalis muscle weakness
temporomandibular joint, dislocation
tinnitus
tinnitus, pulsatile
tongue, hemiatrophy of
tongue, impaired movements of
tongue, weakness
trapezius weakness
treatment of neurologic disorder
trinucleotide repeats
ulcerative colitis
upgaze, paralysis of
urine test for metabolic disorders
vasculitides
vasculopathy
vertigo
vision, blurred
vocal cord paralysis
weakness
weakness, fatiguable
weakness, generalized
weakness, proximal
wheelchair
white matter disease
Wildervanck's syndrome
winging of scapula
Showing articles 0 to 50 of 2651 Next >>

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

A 42-Year-Old Woman with Mysterious Monocytic Meningitis
Neurol 97:449-454, Nothem, M.E., et al, 2021

A 40-Year-Old Woman With Scapular Winging and Dysphonia
Neurol 97:503-507, Aladawi, M.,et al, 2021

A Child with Arthrogryposis
Neurol 91:e995-e998, Irumudomom, O. & Ghosh, P.S., 2018

Clinicopathologic Conference, Botulism
NEJM 372:364-372, Case 3-2015, 2015

Clinicopathologic Conference, Cerebral Granulomatosis with Polyangiitis
NEJM 371:162-173, Case 21-2014, 2014

Disorders of the Nervous System Caused by Drugs, Toxins, and Chemical Agents, Diptheria
Adams & Victors Principles of Neurology Chp 43, pg 1217, Ropper, A.H.,et al, 2014

GFAP Mutations, Age at Onset, and Clinical Subtypes in Alexander Disease
Neurol 77:1287-1294, Prust, M.,et al, 2011

Anterior Opercular Syndrome, Caused by Herpes Simplex Encephalitis
Neurol 49:494-497, McGrath,M.N.,et al, 1997

Hereditary Adult-Onset Alexander's Disease with Palatal Myoclonus, Spastic Paraparesis and Cerebellar Ataxia
Neurol 45:2266-2271, Schwankhaus,J.D.,et al, 1995

Primary Medullary Hemorrhage:Report of Four Cases and Review of the Literature
Stroke 25:1684-1687, Barinagarrementeria,F.&Cantu,C., 1994

Myotonic Dystrophy
In Myology, Engel & Franzini-Armstrong, McGraw-Hill, Inc, New York V2, Ch 43, P1192, Harper,P.S.&Rudel,R., 1994

Jugular Foramen Neuromas:A Review of 14 Cases
Surg Neurol 34:205-211, Tan,L.C.,et al, 1990

Unilateral Palatal Paralysis Caused by Lesion in the Corticobulbar Tract
Arch Neurol 41:782-784, Iwata,M., 1984

Granulomatous Inflammation of Mouth & Larynx, Consistent with Crohn's Disease, Case 35-1978
NEJM 299:538-544, Scully,R.E.,et al, 1978

Neuromuscular Diseases that Affect the Eye
International Ophthal Clx 18:103, Black,J., 1978

Duane Syndrome & Congential Upper-Limb Anomalies:A Familial Occurrence
Arch Neurol 34:174, Okihiro,M.M.,et al, 1977

Pediatric Neurology
Psych Annals 2:1, , 1972

A 62-Year-Old Woman with Progressive Spasticity, Weakness,and Gait Instability
Neurol 104:e210290, Voloshyna-Farber, E.Y.,et al, 2025

Black Turbinate Sign as an Early Clue of Rhino-Orbital-Cerebral Mucormycosis
Neurol 104:e210202, Xie,J.S.,et al, 2025

Clinical Presentation, Investigation Findings, and Outcomes of IgG4-Related Pachymeningitis,A Systematic Review
JAMA Neurol 82:193-199, Terrim,S.,et al, 2025

Orbital Apex Syndrome Associated with Herpes Zoster Ophthalmicus
Neurol 104:e213387, Imamura,D.,et al, 2025

A 19-Year-Old Woman with Progressive Weakness and Numbness in Her Arms and Legs
Neurol 104:e213495, Alsabah,A-A.,et al, 2025

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

A 56-Year-Old Woman with New-Onset Hoarsement and Dysphagia
Neurol 104:e213363, McAree,M. & Frontera, J.A., 2025

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

Vertebrobasilart Dolichoectasia Presenting with Multiple Cranial Nerve Involvement
Neurol 104:213541, Freiherr von Seckendorff,A.,et al, 2025

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

A 72-Year-Old Man With Meningoencephalitis
Neurol 104:e213658, Isaza-Pierotti,D.F.,et al, 2025

Progressive Headache and Diplopia in an 89-Year-Old Man
Neurol 104:e213660, Riand,M.,et al, 2025

A 59-Year-Old Man with Progressive Dysarthria and Gait Instability
Neurol 104:e213729, Shen,D.,et al, 2025

Rapidly Progressive Frontotemporal Dementia with Amytrophic Lateral Sclerosis in an Elderly Female
Cureus doi:10.7759/CUREUS.32182, Sweedan,Y.G.,et al, 2025

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 50-Year-Old Man with Ataxia, Dystonia, and Abnormal Ocular Movements
Neurol 103:e210046, Panigrahi,B.,et al, 2024

Occipital Condyle Syndrome
Neurol 103:e210067, Mirian,A.,et al, 2024

A 63-Year-Old Man With Progressive Multicranial Neuropathy and Leptomeningeal Enhancement
Neurol 103:e210100, Taga,A.,et al, 2024

Clinicopathologic Conference, Infective Endocarditis Due to Haemophilus Parainfluenza
NEJM 391:2148-2157, Case 38-2024, 2024

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

Expanding Clinical Spectrum an Anti-GQ1b Antibody Syndrome, A Review
JAMA Neurol 81:762-770, Lee,S-U.,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

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

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

Ischemic Retinopathy from Prolonged Orbital Compression
NEJM 390::e14, Chen,Y-K and Chen C-L, 2024

Clinicopathologic Conference, Myeloperoxidase antineutrophil cytoplasmic antibody-associated vasculitis
NEJM 390:843-851, Case 7-2024, 2024

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



Showing articles 0 to 50 of 2651 Next >>