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acetazolamide
acid maltase deficiency
advances in neurology
adverse drug reaction
airway obstruction
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
anesthesia, general
antiarrhythmic drugs
antibodies to voltage-gated calcium channels
anticonvulsants
antihistamines
arrhythmia, cardiac
arthrogryposis multiplex
ataxia
ataxia, paroxysmal
autoimmune disease
baldness
botulism
brainstem, lesion of
calcium antagonist
calcium channel dysfunction
carbamazepine
carcinoma
cardiac surgery, neurologic complications with
cardiac transplantation
cardiomyopathy
CAT scan
CAT scan, muscle
cataracts
central core disease
central nervous system, infection of
Charcot-Marie-Tooth
chewing, impaired
children
chloride channel dysfunction
chronic progressive external ophthalmoplegia
clubfoot as related to neurologic disease
complications
congenital birth defects
congenital heart disease
congenital myopathy
controversies in neurology
corpus callosum
corpus callosum, thinning
creatine phosphokinase(CPK)elevated
degenerative diseases of CNS
differential diagnosis
dilantin
dropped head syndrome
drug induced neurologic disorders
electrocardiogram, abnormal
electromyogram
electron microscopy
encephalopathy
encephalopathy, anoxic
encephalopathy, neonatal
epidemiology of neurology
eye closure
facial appearance, abnormal
facial nerve palsy
facial nerve palsy, bilateral
facial nerve, lesion of
facial weakness
facial weakness, bilateral
falling
familial
familial hemiplegic migraine
Fazio-Londe's disease
floppy infant
frontal balding
gene mutation
genetic neurologic disorders
genetic testing
heavy metal intoxication
high arched feet
high arched palate
Huntington's chorea
hydrocephalus
hyperkalemic periodic paralysis
hypokalemia
hypokalemic periodic paralysis
hypotonia
hypotonia, causes of
hypotonia, infants
hypoxic encephalopathy
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion body myositis
kaliuresis
Kearns-Sayre syndrome
Kugelberg-Welander syndrome
lid closure, weakness of
lordosis
malignant hyperpyrexia
Melkersson's syndrome
metabolic acidosis
mexiletine
micrognathia
migraine
mitochondrial disease
mitochondrial encephalomyopathy
molecular genetics
motor neuron disease
MRI
MRI, abnormal
MRI, muscle
muscle biopsy
muscle cramp
muscle hypertrophy
muscle pain
muscle stiffness
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, congenital
muscular dystrophy, Duchenne
myasthenia gravis
myoglobinuria
myopathy
myopathy, drug-induced
myopathy, mitochondrial
myotonia
myotonia congenita
myotonia dystrophica
myotonia dystrophica, classification
myotonia, treatment of
neck weakness
neoplasm, metastatic to CNS
neoplasm, primary of CNS
neurofibrillary degeneration
neurologic disease, diagnoses of
neurologic evaluation
newborn, evaluation of
nifedipine
ocular myopathy
orbicularis oculi muscle
paramyotonia congenita
paresthesias
paroxysmal neurologic deficits
percussion induced muscle contraction
periodic paralysis
poison, mercury
poison, neurologic problems with
polymerase chain reaction
polymerase chain reaction, false negative
polymerase chain reaction, false positive
polymyositis
postoperative neurologic complications
potassium channel antibodies
potassium channel dysfunction
procainamide
prognosis
respiratory failure
review article
rhabdomyolysis
seizure
sodium channel dysfunction
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 6
temporalis muscle wasting
term infant
tocainide
treatment of neurologic disorder
tricresylphosphate
trinucleotide repeats
tubular aggregates, muscle
viral infection, CNS
weakness
weaning from respirator, failure to
Werdnig-Hoffman disease
workup
Showing articles 100 to 150 of 1186 << Previous Next >>

Ptosis as Partial Oculomotor Nerve Palsy Due to Compression by Infundibular Dilatation of Posterior Communicating Artery, Visualized with Three-Dimensional Computer Graphics:Case Report
Neurol Med Chir (Tokyo) 54:214-218, Fukushima,Y.,et al, 2024

A 22-Year-Old Woman with Episodic Weakness and Jaundice
Neurol 103:e210018, Rathinasbapathi,M.,et al, 2024

Clinical Neurologic Features and Evaluation of PTEN Hamartoma Tumor Syndrome, A Systematic Review
Neurol 103:e209844, Dhawan,A.,et al, 2024

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

Congenital and Acquired Chiari Syndrome
NEJM 390:2191-2198, Friedlander,R.M., 2024

Infective Endocarditis
Lancet 404:377-392, Li,M.,et al, 2024

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

Adult Patient Presenting with Spine Pain Following a Motor Vehicle Accident
Neurol 100:1025-1031, Sharma,V. & Soto,O, 2023

Tersons Syndrome
NEJM 388:e79, Sherman,S.V., 2023

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

Subarachnoid Hemmorhage During Pregnancy and Puerperium:A Population-Based Study
Stroke 54:198-207, Korhonen,A., et al, 2023

Progressive Camptocormia with Head Drop and Dysphagia
JAMA Neurol 80:209-210, El-Wahsh,S., et al, 2023

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

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

Case Report of Lambl Excrescences in a Pediatric Patient with Multifocal Strokes
Neurol 99:73-76, Robertson, D.M.,et al, 2022

Spina Bifida
NEJM 387:444-450, Iskandar, B.J. & Finnell, R.H., 2022

Bilateral Hearing Loss and Constricted Visual Fields
BMJ 378:e070672, Sachdeva, G. & Shafquat, S., 2022

Spontaneous Subarachnoid Haemorrhage
Lancet 400:846-862, Claassen, J. & Park, S., 2022

A 31-year-Old Man with Bilateral Limited Mobility of Joints
JAMA Neurol 79:1083-1084, Wang, Z.,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

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

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 6-Year-Old Boy with Muscle Twitching
Neurol 96:e301-e304, Lewis, H.S.,et al, 2021

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

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

Clenched Fists as an Unusual Presentation of Focal Neuromyotonia
Neurol 97:e429-e430, Dhanapalaratnam, R.,et al, 2021

A 59-Year-Old Man with Progressive Proximal Weakness Since Childhood
Neurol 97:958-963, Davalos, L.,et al, 2021

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

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

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

Morvan Syndrome and Diffuse Large B-Cell Lymphoma in the Central Nervous System
Neurologist 25:73-77, Jiang, C.,et al, 2020

CASPR2 Autoimmunity in Children Expanding to Mild Encephalopathy with Hypertension
Neurol 94:e2290-e2301,953, Syrbe, S.,et al, 2020

A 10-Year-Old Girl with Muscle Stiffness
Neurol 95:e773-e778, Prior, D.E. & Ghosh, P.S., 2020

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

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

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 Case of Muscle Twitching with Psoriasis
JAMA Neurol 76:1119-1120, Qian, M.,et al, 2019

Muscular Dystrophies
Lancet 394:2025-2038, Mercuri, E.,et al, 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

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

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



Showing articles 100 to 150 of 1186 << Previous Next >>