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acanthocytosis
acetazolamide
acid maltase deficiency
adrenoleukodystrophy
advances in neurology
adverse drug reaction
airway obstruction
alveolar hypoventilation
amniocentesis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
anesthesia, general
anterior tibial muscle weakness
antiarrhythmic drugs
antibodies to voltage-gated calcium channels
anticonvulsants
antihistamines
aqueduct of Sylvius, stenosis
aqueductal stenosis
arrhythmia, cardiac
arthrogryposis multiplex
ataxia
ataxia, cerebellar
ataxia, paroxysmal
autoimmune disease
automatic implantable cardioverter-defibrillator
baldness
Bassen-Kornzweig syndrome
benign congenital hypotonia
blindness
botulism
brainstem, lesion of
calcium antagonist
calcium channel dysfunction
carbamazepine
carcinoma
cardiac surgery, neurologic complications with
cardiac transplantation
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, muscle
cataracts
cataracts, congenital
central core disease
central nervous system, infection of
cerebellar hypoplasia
cerebral cortical atrophy
Charcot-Marie-Tooth
chewing, impaired
children
chloride channel dysfunction
chromosomal abnormality
chromosome 1
chronic polyneuritis, children
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
Coats syndrome
Cockayne's syndrome
complications
conduction block
congenital birth defects
congenital heart disease
congenital myopathy
congestive heart failure
consanguinity
contractures, joint
controversies in neurology
cornea, abnormal
cornea, opacity of
corpus callosum
corpus callosum, thinning
creatine phosphokinase(CPK)elevated
cry, weak
deafmute
deafness
degenerative diseases of CNS
developmental disability
developmental milestones
developmental retardation
differential diagnosis
dilantin
disability, neurological
distal muscle weakness
dropped head syndrome
drug induced neurologic disorders
dwarfism
dystroglycanopathies
dystrophin
dystrophin associated proteins
ejection fraction
ejection fraction, abnormal
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electromyogram
electron microscopy
Emery-Dreifuss muscular dystrophy
encephalocele
encephalopathy
encephalopathy, anoxic
encephalopathy, neonatal
epidemiology of neurology
eye closure
facial appearance, abnormal
facial expression abnormality
facial nerve palsy
facial nerve palsy, bilateral
facial nerve, lesion of
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
falling
familial
familial hemiplegic migraine
Fazio-Londe's disease
feeding disorder
fetal movements, reduced
fetus
floppy infant
foot drop
Friedreich's ataxia
frontal balding
gait disorder
gargoylism
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
glaucoma
glycosyltransferase
Gowers maneuver
Hallgren's syndrome
heart block
heavy metal intoxication
high arched feet
high arched palate
histochemistry
histochemistry of muscle
Huntington's chorea
Hurler's syndrome
hydrocephalus
hydrocephalus, congenital
hyperkalemic periodic paralysis
hypokalemia
hypokalemic periodic paralysis
hyporeflexia
hypotonia
hypotonia, causes of
hypotonia, infants
hypoxic encephalopathy
immunohistochemistry
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion body myositis
joint hypermobility
kaliuresis
Kearns-Sayre syndrome
keratoconus
Kugelberg-Welander syndrome
laminopathies
Laurence-Moon-Bardet-Biedl syndrome
leukodystrophy
lid closure, weakness of
life expectancy
lissencephaly
LMNA gene
lordosis
macrocephaly
malformation, CNS, congenital
malignant hyperpyrexia
Melkersson's syndrome
mental retardation
merosin
metabolic acidosis
mexiletine
micrognathia
micropthalmia
migraine
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
molecular genetics
motor neuron disease
MRI
MRI, abnormal
MRI, disappearing lesion on
MRI, muscle
MRI, serial
mucopolysaccharidoses
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle hypertrophy
muscle pain
muscle stiffness
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, cardiovascular changes with
muscular dystrophy, central nervous system abnormality
muscular dystrophy, classification
muscular dystrophy, congenital
muscular dystrophy, congenital, Fukuyama type
muscular dystrophy, congenital, Ullrich
muscular dystrophy, differential diagnosis of
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, LAMA2
muscular dystrophy, limb-girdle
muscular dystrophy, neurogenic hypothesis of
myasthenia gravis
myasthenia gravis, distal weakness
myasthenia gravis, limb-girdle
myoglobinuria
myopathy
myopathy, centronuclear
myopathy, distal
myopathy, drug-induced
myopathy, mitochondrial
myopia
myotonia
myotonia congenita
myotonia dystrophica
myotonia dystrophica, classification
myotonia, treatment of
neck weakness
nemaline rod myopathy
neoplasm, metastatic to CNS
neoplasm, primary of CNS
neuritis
neurofibrillary degeneration
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic evaluation
neuropathology, brain
neuropathy
newborn, evaluation of
nifedipine
obesity
ocular myopathy
oculopharyngeal muscular dystrophy
opened mouth
ophthalmoplegia
Oppenheim muscular dystrophy
orbicularis oculi muscle
pacemaker, cardiac-transvenous
paramyotonia congenita
paresthesias
paroxysmal neurologic deficits
percussion induced muscle contraction
periodic paralysis
poison, mercury
poison, neurologic problems with
polydactyly
polymerase chain reaction
polymerase chain reaction, false negative
polymerase chain reaction, false positive
polymicrogyria
polymyositis
polymyositis, infantile
postoperative neurologic complications
potassium channel antibodies
potassium channel dysfunction
pregnancy, neurologic complications in
prenatal diagnosis by amniocentesis
procainamide
progeria
prognosis
progressive muscular dystrophy
progressive neurologic disorder
pseudoretinitis pigmentosa
psychiatric disorder
psychomotor retardation
ptosis
quality of life
respirator
respiratory failure
retinal detachment
retinal dysplasia
retinitis pigmentosa
retinopathy
review article
rhabdomyolysis
rigid spine syndrome
schizophrenia
scoliosis
seizure
skin, biopsy
sloped shoulders
sodium channel dysfunction
Spielmeyer Vogt syndrome
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 6
steroid
suck, poor
sudden death
syncope
systemic illness
temporalis muscle wasting
term infant
tocainide
transverse smile
treatment of neurologic disorder
tricresylphosphate
trinucleotide repeats
tubular aggregates, muscle
ultrasonography
Usher's syndrome
viral infection, CNS
visual field defect
visual fields, constricted
vital capacity
Walker-Warburg syndrome
walking, difficulty with
weakness
weakness, congenital
weakness, generalized
weakness, progressive
weaning from respirator, failure to
Werdnig-Hoffman disease
wheelchair
whistle, inability to
white matter disease
wide based gait
winging of scapula
workup
x-linked hydrocephalus
x-linked mental retardation
Showing articles 400 to 450 of 1797 << Previous Next >>

A Rare Treatable and Under Recognized Cause of Recurrent Convexity Subarachnoid Hemorrhage:Lupus anticoagulant Hypoprothombinemia Syndrome
Ann Indian Acad Neurol 24:986-989, Jain, S.,et al, 2021

A 7-Year-Old Boy with Acute-Onset Altered Mental Status
Neurol 96:e2774-e2778, Wong, G.J.,et al, 2021

Complete Evaluation of Dementia: PET and MRI Correlation and Diagnosis for the Neuroradiologist
AJNR 42:998-1007, Oldan, J.D.,et al, 2021

Congenital Cytomegalovirus Infection
BMJ 373:m1212, Pesch, M.H.,et al, 2021

A 28-Year-Old Woman with Vision Loss and an Unusual Gait
Neurol 97:e1860-e1865, Dohlman, J.C.,et al, 2021

CLOVES Syndrome
Neurol 96:e1487-e1488, Collins, M.,et al, 2021

Natural History of "Pure" Primary Lateral Sclerosis
Neurol 96:e2231-e2238, Hassan, A.,et al, 2021

Teaching Video NeuroImages: Jaw Clonus in Amyotrophic Lateral Sclerosis
Neurol 96:e2563, Goel, A.,et al, 2021

Diagnostic and Prognostic Value of Conventional Brain MRI in the Clinical Work-Up of Patients with Amyotrophic Lateral Sclerosis
J Clin Med 9:1-12, Rizzo, G.,et al, 2020

Bilateral Pseudohypopyon Causing White Eyes in a Patient with Lymphoma
Lancet 395:e74, Radhakrishnan Iyer, S.S.,et al, 2020

Ondine Curse Syndrome Cause by Dorsolateral Medullary Stroke
Neurol 94:e1557-e1558, Fiedler, E. & Gill, R., 2020

A 42-year-old Woman with Progressive Cognitive Difficulties and Gait Imbalance
Neurol 94:e1219-e1226, Slama, M.C.C.,et al, 2020

Nusinersen in Adult Patients with Spinal Muscular Atrophy
Neurol 95:e413-e416, Moshe-Lilie, O.,et al, 2020

Spinal Cord Involvement in Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia
JAMA Neurol 77:1169-1170, Li, S.,et al, 2020

Delayed Leukoencephalopathy: A Rare Complication after Coiling of Cerebral Aneurysms
AJNR 41:286-292, Ikemura, A.,et al, 2020

Hopkins Syndrome
Neurol 94:e996-e997, Sgobbi de Souza, P. V.,et al, 2020

Acute Ischemic Stroke in Adolescents
Neurol 94:e158-e169, Rambaud, R.,et al, 2020

Feasibility, Safety, and Outcome of Endovascular Recanalization in Childhood Stroke
JAMA Neurol 77:25-34, Sporns, P.B.,et al, 2020

Vessel Wall MR Imaging for the Detection of Intracranial Inflammatory Vasculopathies
Cardiovasc Diagn Ther 10:1108-1119, Edjlali,M.,et al, 2020

"Motor Band Sign" in Susceptibility-Weighted Imaging in Motor Neuron Disease
Ann India Acad Neurol 23:821-822, Prabhu,A.N., 2020

A 26-Year Old Man with Right Hand and Arm Weakness
Neurol 93:e927-e933, Elliott,E.J.&Smith,J.D., 2019

Bilateral Alopecia as Clue to Diagnosis of Gomez-Lopez-Hernandez Syndrome in a 38-Year-Old Man
Neurol 93:408-410, Kronlage,C.&Healy,D.G., 2019

Declining Malformation Rates with Changed Antiepileptic Drug Prescribing, An Observational Study
Neurol 93:e831-e840, Tomson,T.,et al, 2019

Characteristic Head Jerks in Congenital Oculomotor Apraxia due to Joubert Syndrome
Neurol 93:e1125-e1126, Borngraber, F.,et al, 2019

A 17-year-old Baseball Player with Right Hand Weakness
Neurol 92:e76-e80, Vachon, C. & Libdeh, A.A., 2019

Fibromuscular Dysplasia and Its Neurologic Manifestations
JAMA Neurol 76:217-226, Touze, E.,et al, 2019

Management of Stroke in Neonates and Children
Stroke 50:e51-e96, Ferriero, D.M.,et al, 2019

Clinicopathologic Conference, Amyotrophic Lateral Sclerosis
NEJM 380:1566-1574, Case 12-2019, 2019

Antiepileptic Drug Treatment Patterns in Women of Childbearing Age with Epilepsy
JAMA Neurol 76:783-790, Kim, H.,et al, 2019

Risk of 23 Specific Malformations Associated with Prenatal Exposure to 10 Antiepileptic Drugs
Neurol 93:e167-e180, Blotiere, P.O.,et al, 2019

Pediatric HIV Infection: Classification, Clinical Manifestations, and Outcome
www.UptoDate.com, June, Gillespie, S.L., 2018

Bilateral Cavernous Carotid Aneurysms: Atypical Presentation of a Rare Cause of Mass Effect
Front Neurol doi:10.3389/fneur.2018.0069, Gagliardi, D.,et al, 2018

Pantothenate Kinase - Associated Neurodegeneration (PKAN)
Emedicine.Medscape Sept, Hanna, P.A. & Benbadis, S.R., 2018

Congenital Myasthenic Syndromes in Adult Neurology Clinic
Neurol 91:e1770-e1777, Kao, J.C.,et al, 2018

Pontine Tegmental Cap Dysplasia in a Neonate
Neuol 91:e2100-e2101, Bilgin, N.,et al, 2018

A 54-year-old woman with Confusion and Visual Disturbances
Neurol 91:363-367, Rossi, K.C.,et al, 2018

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

Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia: An MRI Study of 16 French Cases
AJNR 39:1657-1661, Codjia, P.,et al, 2018

Young Adult with Dysphagia and Severe Weight Loss
Neurol 91:e1083-e1086, Irumudomon, O. & Ghosh, P.S., 2018

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

Palatal tremor as a presenting symptom of amyotrophic lateral sclerosis
Neurol 90:801-802, Maghzi, A.,et al, 2018

Long-Term Risk of Hemorrhagic Stroke In Young Patients with Congenital Heart Disease
Stroke 49:1155-1162, Giang, K.W.,et al, 2018

Dyke-Davidoff-Masson syndrome
Neurol 90:e2097-e2098, Durcan, R.,et al, 2018

Nusinersen Versus Sham Control in Later-Onset Spinal Muscular Atrophy
NEJM 378:625-635, Mercuri, E.,et al, 2018

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

Congenital Asymmetric Crying Facies Syndrome, A Case Report
Medicine 97:31(e11403), Liang,X. & He,B., 2018

Single-Dose Gene-Replacement Therapy for Spinal Muscular Atrophy
NEJM 377:1713-1722,1786, Mendell, J.R.,et al, 2017

Nusinersen Versus Sham Control in Infantile-Onset Spinal Muscular Atrophy
NEJM 377:1723-1732,1786, Finkel, R.S.,et al, 2017

Maternal Use of antiepileptic Agents During Pregnancy and Major Congenital Malformations in Children
JAMA 318:1700-1701, Bromley, R.L.,et al, 2017

Population-based Study of Ischemic Stroke Risk after Trauma in Children and Young Adults
Neurol 89:2310-2316, Fox, C.K.,et al, 2017



Showing articles 400 to 450 of 1797 << Previous Next >>