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Human Parechovirus Meningoencephalitis: Neuroimaging in the Era of Polymerase Chain Reaction-Based Testing
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Molybdenum Cofactor Deficiency
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Distinctive Pattern of White Matter Injury in Neonates with Rotavirus Infection
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Sturge-Weber Syndrome
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Extending the KCNQ2 encephalopathy Spectrum
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Sturge-Weber Syndrome
MedLink Neurology, July, Comi, A.M., 2013
Neonatal Cerebral Sinovenous Thrombosis From Symptom to Outcome
Stroke 41:1382-1388, Berfelo,F.J., et al, 2010
Clinicopath Conf, Severe Acute Chorioamnionitis With Umbilical-Cord Phlebitis and Intense Chorionic-Plate Vasculitis
NEJM 358:1713-1723, Case 12-2008, 2008
Neonatal Brain Injury
NEJM 351:1985-1995, Ferriero,D.M., 2004
Mutations in the Molybdenum Cofactor Biosynthetic Genes MOCS1, MOCS2, and GEPH
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Early Prognostic Indicators of Outcome in Infants with Neonatal Cerebral Infarction:A Clinical,Electroencephalogram,and Magnetic Resonance Imaging Study
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Electrographic Seizures in Preterm & Full-Term Neonates:Clin Corr Brain Lesions, Risk for Sequelae
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Neonatal Idiopathic Cerebral Venous Thrombosis:An Unrecognized Cause of Transient Seizures or Lethargy
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Prospective Observations of 100 High-Risk Neonates by High-Field MRI of CNS:II. Hypoxic-Ischemic Encephalopathy
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Tentorial Hemorrhage Associated with Vacuum Extraction
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Intracranial Hemorrhage in the Term Newborn
Arch Neurol 41:30-34, Fenichel,G.M.,et al, 1984
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Clinical Manifestations and Diagnosis of Listeria Monocytogenes Infection
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Congenital Cytomegalovirus Infection
BMJ 373:m1212, Pesch, M.H.,et al, 2021
Human Parechovirus: An Increasingly Recognized Cause of Sepsis-Like Illness in Young Infants
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Drug Treatment of Epilepsy in Adults
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Inherited Metabolic Diseases of the Nervous System, Pyridoxine Dependent Seizures
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Inherited Metabolic Diseases of the Nervous System, Biopterine Deficiency
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Inherited Metabolic Diseases of the Nervous System, Inherited Hypeammonemia
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Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
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Unexplained Seizures in an Infant
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The Expanding Phenotype of GLUT1-Deficiency Syndrome
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Long-Term Prognosis in Children With Neonatal Seizures: A Population-Based Study
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Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies
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Natural History of Nonketotic Hyperglycinemia in 65 Patients
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Clinical Correlations of Mutations in the SCN1A Gene: From Febrile Seizures to Severe Myoclonic Epilepsy in Infancy
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Neonatal Epileptic Encephalopathy
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Cerebral Infarctin in the Term Newborn: Clinical Presentation and Long-Term Outcome
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Lethal Cytomegalovirus Infection in Preterm Infants:Clinical, Radiological, and Neuropathological Findings
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Twinning and Neurologic Morbisity
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Benign Familial Neonatal Convulsions:Evidence for Clinical and Genetic Heterogeneity
Ann Neurol 29:469-473, Ryan,S.G.,et al, 1991
Neurologic Outcome after Electroencephalographically Proven Neonatal Seizures
Pediatrics 88:583-596, Legido,A.,et al, 1991
Neonatal Seizures
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One-Year Follow-up of Infants with Abstinence-Associated Seizures
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Surgical Treatment of Intractable Neonatal-Onset Seizures:The Role of Positron Emission Tomography
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The Peroxisome:Nervous System Role of a Previously Underrated Organelle, The 1987 Robert Wartenberg Lecture
Neurol 38:1617-1627, Moser,H.W., 1988
Characterization & Classification of Neonatal Seizures
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Biotinidase Deficiency:Initial Clinical Features & Rapid Diagnosis
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