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Differential
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abdominal contractions
adverse drug reaction
agenesis of corpus callosum
Alexanders disease
Alexanders disease, adult onset
alveolar hypoventilation
aminoacidurias
anesthesia, general
anisocoria
anticonvulsants
anticonvulsants, blood level determination of
anticonvulsants, selection of
anticonvulsants, teratogenicity of
anticonvulsants, untoward effects of
aphasia, children
aphonia
apraxia, speech
areflexia
arm weakness
arrhythmia, cardiac
arthrogryposis multiplex
aspiration
astrogliopathy
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, truncal
ataxic gait
attention deficit disorder with hyperactivity
autism
autoantibodies
autoimmune disease
autonomic dysfunction
baldness
Benedict's solution test
benzodiazepine
bifid uvula
bone age
botulinum toxin
botulism
brachial plexus neuropathy
brachial plexus neuropathy, familial
brainstem, dysfunction, eye movement disorders with
brainstem, infarction of
brainstem, lesion of
Brueghel's syndrome
bulbar palsy
bulbar palsy, acute
cachexia
caffeine
calcification, intracranial
carbamazepine
cardiomyopathy
CAT scan
CAT scan, abnormal
cataracts
celiac disease, adult
cerebellar atrophy, primary
cerebellar degeneration
cerebellar disease, eye movement disorder in
cerebellum, disease of
cerebral palsy
cerebral palsy, associated problems with
cerebral palsy, pure ataxic
cerebrovascular accident
chromosomal abnormality
chromosome 19
cleft lip
cleft palate
Clinical Pathologic Conference(C.P.C.)
clinodactyly
clonazepam
clubfoot as related to neurologic disease
complications
congenital birth defects
congenital deformities
congenital heart disease
congenital heart disease, CNS complications with
congenital malformation
congenital malformation, dilantin therapy causing
congenital malformation, non CNS
congenital myasthenic syndromes
congenital myopathy
consanguinity
Cornelia de Lange syndrome
cranial nerve enhancement
cranial nerve palsies
cranial nerve tumor
cranial neuropathy
cranial neuropathy, multiple
Craniosynostosis
creatine phosphokinase(CPK)elevated
cry, abnormal
cryptorchidism
deafness
deafness, unilateral
degenerative diseases of CNS
dementia
demyelinating disease
developmental retardation
digits, abnormal
dilantin
dilantin, toxicity
dinitrophenylhydrazine(D.N.P.H.)reaction
diphtheria
diplegia, atonic
diplegia, spastic cerebral
diplopia
distal muscle weakness
dizziness
dropped head syndrome
Duane syndrome
dysarthria
dysdiadochokinesia
dysmetria
dysmorphic
dysphagia
dysphonia
dysplasia of C.N.S.
dyspnea
ear, abnormal
ear, clicking of
electrocardiogram, abnormal
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
encephalopathy
epilepsia partialis continua
exome sequencing
eye movement, disorders of
eyebrows, abnormal
facial anomalies
facial appearance, abnormal
facial nerve palsy
facial weakness
facial weakness, bilateral
failure to thrive
familial
fatigue
ferric chloride test
fetal alcohol syndrome
fine motor function, impaired
frontal balding
gadolinium
gait disorder
gastroparesis
gender
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
GFAP gene
glutamic acid decarboxylase, antibody
growth retardation
head nodding
hearing loss
hearing loss, unilateral
hearing problems in children
heart block
heart sign
hemorrhagic diathesis
heterotopia
high arched palate
Hirschprung's disease
hirsutism
histiocytosis
hoarseness
Holt-Oram syndrome
hypercapnia
hyperreflexia
hypertelorism
hypogeusia
hypoglycorrhachia
hypometric saccades
hypospadias
hypotelorism
hypotonia, infants
imbalance
inferior olivary nucleus
intellectual deficit
intellectual deficit, treatable causes of
intelligence quotient
internuclear ophthalmoplegia
internuclear ophthalmoplegia, bilateral
intestinal biopsy
jugular foramen syndrome
karyotyping
klippel feil syndrome
lamotrigine
language disorders in children
lateropulsion
leukodystrophy
leukoencephalopathy, differential diagnosis
low birth weight
macrocephaly
malabsorption syndrome
malformation, CNS, congenital
malformation, vascular
maple syrup urine disease
meningeal biopsy
meningeal enhancement
meningitis
meningitis, monocytic
mental retardation
mestinon
microcephaly
micrognathia
micromelia
midbrain
midbrain, infarction of
midline defect in children
misdiagnosis
molecular genetics
mortality
movement disorder
MRI
MRI, abnormal
MRI, contrast enhanced
multiple sclerosis
multiple sclerosis, misdiagnosis
muscle atrophy, progressive
muscle biopsy
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, cardiovascular changes with
myelodysplasia
myoclonus
myoclonus, abdominal
myoclonus, segmental
myoclonus, treatment of
myopathy
myotonia
myotonia dystrophica
myotonia dystrophica, classification
nasal speech
nausea and vomiting
neck weakness
nemaline rod myopathy
neoplasm, metastatic to CNS
neoplasm, primary of CNS
neural tube defect
neurofibroma
neurologic disease
neurologic evaluation
neuroma
neuromuscular blockade
neuromuscular junction, abnormality of
neuropathy, diphtheritic
neurotoxin
nystagmus
nystagmus, gaze-evoked
nystagmus, monocular
nystagmus, pendular
nystagmus, primary position of gaze
nystagmus, upbeating on upgaze
nystagmus, vertical
obesity
ocular dysmetria
oligodactyly
olivary degeneration, hypertrophic
opened mouth
ophthalmoplegia
optic atrophy
oscillopsia
pain, abdominal
palatal myoclonus
palatal myoclonus, essential
palate, paralysis
palate, paralysis-unilateral
palatopharyngeal incompetence
paraparesis
paraparesis, spastic
paroxysmal neurologic deficits
percussion induced muscle contraction
phenobarbital
phenylketonuria
phocomelia
polydactyly
polypharmacy
posterior inferior cerebellar artery syndrome
Prader-Labhart-Willi syndrome
precocious puberty
pregnancy, anticonvulsants during
pregnancy, neurologic complications in
primary CNS histiocytic sarcoma
prognosis
progressive ataxia and palatal tremor
progressive neurologic disorder
psychological testing, neurologic problems
psychosis
psychosis, childhood
psychosocial aspects
ptosis
ptosis, bilateral
ptosis, unilateral
pupil, abnormality in neurologic disorders
pupil, ectopic-congenital
pupil, oval
Purkinje cell
pyramidal tract dysfunction
remote effect of cancer on the nervous system
respiratory failure
review article
risk factors
Rosenthal fibers
saddle nose
safety
salivation, excessive
sarcoma
schwannoma
seizure
seizure, advice to parents and teachers regarding
seizure, clicking sound with
seizure, focal
seizure, maternal
seizure, pregnancy
seizure, psychosocial aspects of
seizure, treatment of
septicemia
short stature
simian crease
skin, lesions in neurologic disorders
sleep
slit lamp examination
sodium valproate
somnolence
speech disorder
speech disorder, childhood
speech disorder, non aphasic
spina bifida
spinal accessory nerve palsy
spinal cord, injury of
spinal cord, lesion of
spinocerebellar ataxia type 1
spinopontine atrophy, dominant
sternocleidomastoid weakness
stiff man syndrome
stuttering
syndactyly
synophrys
syringomyelia
tachycardia
tandem gait, ataxic
taste
temporalis muscle wasting
temporalis muscle weakness
temporomandibular joint, dislocation
teratogenesis
teratogenic drugs
tinnitus
tinnitus, pulsatile
tongue, hemiatrophy of
tongue, impaired movements of
tongue, weakness
topiramate
trapezius weakness
treatment of neurologic disorder
triangle of Guillain and Mollaret
trimethadione
trinucleotide repeats
tumor pseudoprogression
type 1 muscle fiber
urine test for metabolic disorders
vocal cord paralysis
weakness
weakness, fatiguable
weakness, generalized
weakness, proximal
Wernekinck commissure syndrome
wheelchair
Whipple's disease
white matter disease
Wildervanck's syndrome
winging of scapula
Showing articles 0 to 50 of 17117 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

Palatal Myoclonus, Abnormal Eye Movements, and Olivary Hypertrophy in GAD65-Related Disorder
Neurol 94:273-275, Macaron, G.,et al, 2020

Progressive Ataxia and Palatal Tremor
Neurol 94:e1445-e1447, Pradeep, S.,et al, 2020

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

Wernekink Commissure Syndrome Secondary to Bilateral Caudal Paramedian Midbrain Infarction Presenting with a Unique "Heart or V" Appearance Sign:Case Report and Review of the Literature
Front Neurol soi.10.3389/fneur.2017.00376,Aug, Zhou,C.,et al, 2017

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

Dancing Eyes and Uvula after Brain Tumour Extirpation-A Sign of Tumour Progression?
Lancet 379:1983, Kipfer, S.,et al, 2012

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

Essential Palatal Myoclonus
NEJM 362:e64, Scozzafava,J. &Yager,J., 2010

Valproic Acid Monotherapy in Pregnancy and Major Congenital Malformations
NEJM 362:2185-2193, Jentink,J., et al, 2010

Increased Frequency of Isolated Cleft Palate in Infants Exposed to Lamotrigine During Pregnancy
Neurol 70:2152-2158, Holmes,L.B.,et al, 2008

Topiramate in Pregnancy: Preliminary Experience From the UK Epilepsy and Pregnancy Register
Neurol 71:272-276, Unt,S.,et al., 2008

Does Lamotrigine Use in Pregnancy Increase Orofacial Cleft Risk Relative to Other Malformations?
Neurol 71:714-722, Dolk,H.,et al., 2008

Glutamic Acid Decarboxylase Autoantibodies and Neurological Disorders
Neurol Sci 23:145-151, Vianello,M.,et al, 2002

Craniofacial and Cutaneous Findings Expand the Phenotype of Hereditary Neuralgic Amyotrophy
Neurol 57:1963-1968, Jeannet,P.,et al, 2001

Antiepileptic Drug Regimens and Major Congenital Abnormalities in the Offspring
Ann Neurol 46:739-746, Samren,E.B.,et al, 1999

The Diagnosis of'Essential Palatal Tremor'
Neurol 49:248-249, Vieregge,P.,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

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

Epileptic Palatal Myoclonus
Neurol 41:1305-1306, Tatum,W.O.,et al, 1991

Ear Click in Palatal Tremor:Its Origin and Treatment with Botulinum Toxin
Neurol 41:1677-1679, Deuschl,G.,et al, 1991

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

Segmental Myoclonus Clinical and Pharmacologic Study
Arch Neurol 43:1025-1031, Jankovic,J.&Pardo,R., 1986

Syndrome of Palatal Myoclonus & Progressive Ataxia:Two Cases with Magnetic Resonance Imaging
Neurol 35:1212-1214, Sperling,M.R.&Herrman,C., 1985

Adult Celiac Disease Presenting as Cerebellar Syndrome
Neurol 30:245-249 1980., Finelli,P.F.,et al, 1980

The Pregnant Epileptic, A Review & Recommendations
Arch Neurol 36:601-603, Montouris,G.D.,et al, 1979

Agenesis of the Corpus Callosum:A Study of the Frequency of Associated Malformations
Ann Neurol 6:349-354, Parrish,M.L.,et al, 1979

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

Nemaline (Rod) Myopathy:The Need for Histochemical Evaluation of Affected Families
Ann Neurol 4:37, Bender,A.N.,et al, 1978

Dominant Spinopontine Atrophy
Arch Neurol 35:156, Pogacar,S.,et al, 1978

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

Prader-Willi-Syndrome, In Endocrine & Genetic Diseases of Childhood & Adolescence
(Ed) , 1975. W. B. Saunders Co, p, Gardner,L.I., 1975

Acquired Pendular Nystagmus with Oscillopsia in Multiple Sclerosis:A Sign of Cerebellar Nuclei Disease
JNNP 37:570, Aschoff,J.C.,et al, 1974

Maternal Epilepsy & Abnormalities of the Fetus & Newborn
Lancet 839, Oct1972., Speidel,B.,et al, 1972

Pediatric Neurology
Psych Annals 2:1, , 1972

The Cornelia de Lange Syndrome
J Pediatr 63:1000-1020, Ptacek,L.J., 1963

Addressing Systemic Complications of Acute Stroke: A Scientific Statement From the American Heart Association
Stroke 56:e15-e29, Kumar,S.,et al, 2025

Rocky Mountain Spotted Fever Encephalitis and "Starry Sky" Pattern on MRI, A Case Report
Neurologist 30:34-38, Mikhaiel,J.P.,et al, 2025

Spectrum of Intracranial Hemorrhages in Cerebral Venous Thrombosis, A Pictorial Case Series and Review of Pathophysiology and Management
Neurologist 30:45-51, Jha,S.,et al, 2025

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

Automated Detection of Normal Pressure Hydrocephalus Using CT Imaging for Calculating the Ventricle-to-Subarachnoid Volume Ratio
AJNR 46:141-146, Knittel,J.J.,et al, 2025

Automated Idiopathic Normal Pressure Hydrocephalus Diagnosis via Artificial Intelligence-Based 3D T1 MRI Volumetric Analysis
AJNR 46:33-40, Lee,J.,et al, 2025

Amyloid-Related Imaging Abnormalities (ARIA) in Clinical Trials of Gantenerumab in Early Alzheimer Disease
JAMA Neurol 92:19-29, Salloway,S.,et al, 2025

Stroke-Like Migraine Attacks After Radiation Therapy Syndrome
Neurol 104:e210203, Lubotzky,A.,t al, 2025

Clinicopathologic Conference, Posterior Reversible Encephalopathy Syndrome Due to Sickle Cell Disease
NEJM 392:268-276, Case 2-2025, 2025

Efficacy and Safety of Sodium Oxybate in Isolated Focal Laryngeal Dystonia:A Phase IIb Double-Blind Placebo-Controlled Cross-Over Randomized Clinical Trial
Ann Neurol 97:329-343, Simonyan,K.,et al, 2025

Spontaneous Spinal Cord Infarction in a Young Patient: An Overview of Clinical Features and Management
Stroke 56:58-61, Chornay,C.,et al, 2025



Showing articles 0 to 50 of 17117 Next >>