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acetylcholinesterase
acetylcholinesterase deficiency
antibiotics
antibiotics, neurologic complications with
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apnea
autoimmune disease
autonomic dysfunction
botulinum toxin
botulism
botulism antitoxin
botulism immune globulin
botulism, infant
botulism, relapse
bulbar palsy
bulbar palsy, acute
bulbar palsy, childhood
canned food
children
Clinical Pathologic Conference(C.P.C.)
collagen vascular disease
congenital myasthenic syndromes
constipation
cry, abnormal
cry, weak
crying
descending paralysis
diarrhea
drooling
dysphagia
dysphonia
dyspnea
efficacy
electromyogram
epidemiology of neurology
facial weakness
facial weakness, bilateral
fatigue
feeding disorder
floppy infant
food poisoning
food-borne infection
gag reflex, depressed
gammaglobulin therapy, intravenous
genetic neurologic disorders
head bobbing
honey
hypertension
hyporeflexia
hypotonia
hypotonia, infants
ileus, paralytic
inappropriate antidiuretic(A.D.H.)hormone
infant, evaluation of
intubation
irritability
irritable baby
leg weakness, bilateral
lethargy
lid closure, weakness of
misdiagnosis
muscle weakness
muscle weakness, proximal
muscle weakness, sudden onset of
myasthenia gravis
myasthenia gravis, congenital
myasthenia gravis, distal weakness
myasthenia gravis, familial incidence of
myasthenia gravis, infantile and juvenile
myasthenia gravis, limb-girdle
myasthenia gravis, neonatal
myasthenia gravis, treatment of
myasthenic syndrome
nausea and vomiting
neck weakness
neurologic disease, diagnoses of
neurologic signs
neurological intensive care
neuromuscular blockade
neuromuscular disease, electrodiagnosis of
neuromuscular junction
neuromuscular junction, abnormality of
neurophysiology
neurotoxin
nystagmus
ophthalmoplegia
polymerase chain reaction
prognosis
ptosis
ptosis, bilateral
pupil, abnormality in neurologic disorders
pupil, light reflex, abnormal
quadriparesis, acute
repetitive nerve stimulation
respirator
respiratory arrest
respiratory failure
review article
rheumatoid arthritis
rheumatoid arthritis, neurologic complications of
standing difficulty
suck, poor
systemic lupus erythematosus
systemic lupus erythematosus, neurologic complications with
tachycardia
tongue, weakness
toxins, nervous system
tracheostomy
treatment of neurologic disorder
walking, difficulty with
weakness
weakness, acute
weakness, generalized
weakness, infant
Showing articles 0 to 50 of 1516 Next >>

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

A Teenager with Shortness of Breath and Difficulty Walking
Neurol 96:e2346-e2350, Liu, S.C.,et al, 2021

Human Botulism Immune Globulin for the Treatment of Infant Botulism
NEJM 354:462-471, Arnon,S.S.,et al, 2006

Adult-Onset "Infant" Botulism:An Unusual Cause of Weakness in the Intensive Care Unit
Neurol 53:891, Li,L.Y.J.,et al, 1999

Early Severe Infantile Botulism
J Pediatr 122:909-911, Hurst,D.L.&Marsh,W.W., 1993

Electrodiagnosis Reliability in the Diagnosis of Infant Botulism
J Pediatr 120:747-749, Graf,W.D.,et al, 1992

Infant Botulism:A Review of 12 Years'Experience at the Children; s Hosp of Phila
Pediatrics 87:159-165, Schreiner,M.S.,et al, 1991

Relapse of Infant Botulism
Ann Neurol 28:187-189, Glauser,T.A.,et al, 1990

Clinical Syndromes of Myasthenia in Infancy & Childhood
Arch Neurol 35:97, Fenichel,G.M., 1978

Diagnosis and Management of Cerebral Venous Thrombosis:A Scientific Statement From the American Heart Association
Stroke 55:e77-e90, Saposnik,G.,et al, 2024

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

Anti-NMDA Receptor Encephalitis Presenting with Cerebellitis in a Pediatric Patient
Neurol 102:e209259, Moehlman,M. & Kornbluh,A.B., 2024

A 24-Year-Old Man with Gait Impairment, Hearing Loss, and Recurrent Fever
Neurol 102:e209358, Barbosa,A.R.,et al, 2024

A 24-Year-Old Man with Spastic Ataxia and Hypodontia
JAMA Neurol 81:658-659, Marien,L.,et al, 2024

Rationale for Screening Children with Hereditary Hemorrhagic Telangiectasis for Brain Vascular Malformations
AJNR 45:1177-1184, Beslow,L.A.,et al, 2024

Newborn Screening and Presymptomatic Treatment of Metachromatic Leukodystrophy
NEJM 391:1256-1258, Laugwitz,L.,et al, 2024

Seizures When Exiting a Bath, A Rare Type of Reflex Epilepsy
Neurol 103:e210025, Pascarella,A.,et al, 2024

Clinical Features, Diagnosis and Management of Klinefelter Syndrome
www.UptoDaate.com, Matsumoto,A.M. & Anawals,B.D., 2024

Reversible Cerebral Atrophy and Substantia Nigra Changes after Vitamin B12 Treatment in Infantile Tremor Syndrome
Neurol 103:e210076, Singh,R.,et al, 2024

Slowly Expanding Lesions Differentiate Pediatric Multiple Sclerosis from Myelin Oligodendrocyte Glycoprotein Antibody Disease
Ann Neurol 96:1086-1091, Fadda,G.,et al, 2024

Neurocysticercosis School Outbreak in Belgium
Lancet 404:2415-2416, Vanden Driessche,K., et al, 2024

Genome Sequencing in the NICU and PICU is Here to Stay
Neurol 104:e210267, Hoffman,E.P. and Kesari,A., 2024

Clinicopathologic Conference, Nutritional Optic Neuropathy Due to Multiple Nutritional Deficits, Including Vitamin A, Copper, and Zinc Deficiencies
NEJM 391:641-650, Gaier,E.D.,et al, 2024

Hyperventilation-Induced Alternating Hemiplegia with Concomitant Hemispheric EEG Slowing in a 7-Year-Old Girl with Headache
Neurol 103:e209759, Proietti,J.,et al, 2024

A Teenager With Right-Sides Headache and Periorbital Changes
Neurol 100:144-150, Lax,D.M.,et al, 2023

Brain Calcification in a Young Woman With Seizures, Explore the Rare Differentials
Neurol 100:397-398, Menon,B.,et al, 2023

Neuroimaging Features of Biotinidase Deficiency
AJNR 44:328-333, Biswas,A.,et al, 2023

Salt and Pepper Sign, PLNTY for Drug-Resistant Epilepsy
Neurol 100:791-795, Paredes-Aragon,E.M.,et al, 2023

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

A Teenager with Chronic Meningitis-Does Occams Razor Apply?
Neurol 100:828-835, Havuluri,H.,et al, 2023

Neonatal Seizures
NEJM 388:1692-1700, Ropper.A.H., 2023

Brain Abscess and Stroke in Children and Adults with Hereditary Hemorrhagic Telangiectasia
Neurol 100:e2324-e2330, White,A.J.,et al, 2023

A 17-Year-Old Girl with Progressive Cognitive Impairment
Neurol 101:e1466-e1472, Zhao,B.,et al, 2023

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

Pediatric and Adult Brain Death/Death by Neurologic Criteria Consensus Guidelines
Neurol 101:1112-1132, Greer,D.M.,et al, 2023

Extracranial Etiology of Acute Onset Ataxia and Weakness
Neurol 99:898-899, Nordli,D.,et al, 2022

New Onset Focal Tremor in Patient with Human Immunodeficienccy Virus
Clin Infect Dis 75:1861-1863, Finelli,P.F., 2022

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

Infantile and Childhood Hydrocephalus
NEJM 387:2067-2073, Whitehead,W.E.&Weiner,J.L., 2022

Imaging Findings in Children Presenting with CNS Nelarabine Toxicity
AJNR 43:1802-1809, Serrallach,B.L.,et al, 2022

Mild Encephalitis/Encephalopathy with a Reversible Splenial Lesion Associated with Systemic Mycoplasma Pneumoniae Infection in North America: A Case Report
J Med Case Reports doi:10.1186/s13256-022-03299-6, Talukder,N.T.,et al, 2022

Carbon Monoxide Poisoning During Major U.S. Power Outages
NEJM 386:191, Worsham, C.M., et al, 2022

Spectrum of Neuroradiologic Findings Associated with Monogenic Interferonopathies
AJNR 43:2-10, Benjamin, P.,et al, 2022

Multiple Cranial Nerve Gadolinium Enhancement in Norrie Disease
Ann Neurol 91:158-159, Jokela, M.,et al, 2022

Leptomeningeal Enhancement Associated with Cerebral Venous Thrombosis
JAMA Neurol 79:195-196, Lozano-Chinga, M.,et al, 2022

A 6-Year-Old Girl with Progressive Toe Walking
Neurol 98:e769-e773, Libdeh, A.A. & Ibrahim, A., 2022

Efficacy and Safety of Selumetinib in Pediatric Patients with Neurofibromatosis Type 1
Neurol 98:e938-e946, Hwang, J.,et al, 2022

Recent Advances in the Diagnosis and Management of Cluster Headache
BMJ 376:e059577, Schindler, E. & Burish, M.J., 2022

Multicenter Consensus Approach to Evaluation of Neonatal Hypotonia in the Genomic Era
JAMA Neurol 79:405-413, Morton, S.U.,et al, 2022



Showing articles 0 to 50 of 1516 Next >>