Published in Neurology on September 15, 2009
The changing concept of sudden infant death syndrome: diagnostic coding shifts, controversies regarding the sleeping environment, and new variables to consider in reducing risk. Pediatrics (2005) 6.87
Defining the sudden infant death syndrome (SIDS): deliberations of an expert panel convened by the National Institute of Child Health and Human Development. Pediatr Pathol (1992) 3.92
How common is repeat sudden infant death syndrome? Arch Dis Child (2007) 1.51
Neuroimaging of mitochondrial disease. Mitochondrion (2008) 1.43
Epidemiology of apparent life threatening events. Arch Dis Child (2005) 1.05
Microduplications of 16p11.2 are associated with schizophrenia. Nat Genet (2009) 6.13
Neurologic complications in children hospitalized with influenza: characteristics, incidence, and risk factors. J Pediatr (2007) 2.75
Fasting c-peptide and insulin-like growth factor-binding protein-1 levels help to distinguish childhood type 1 and type 2 diabetes at diagnosis. Pediatr Diabetes (2007) 2.30
Pediatric perfusion imaging using pulsed arterial spin labeling. J Magn Reson Imaging (2003) 2.07
Molecular and clinical genetics of mitochondrial diseases due to POLG mutations. Hum Mutat (2008) 2.04
Preoperative brain injury in transposition of the great arteries is associated with oxygenation and time to surgery, not balloon atrial septostomy. Circulation (2009) 1.99
Reference range for cerebrospinal fluid opening pressure in children. N Engl J Med (2010) 1.89
Very long-chain acyl-CoA dehydrogenase deficiency in a patient with normal newborn screening by tandem mass spectrometry. J Pediatr (2010) 1.75
Optical measurement of cerebral hemodynamics and oxygen metabolism in neonates with congenital heart defects. J Biomed Opt (2010) 1.75
Neurological and neuromuscular disease as a risk factor for respiratory failure in children hospitalized with influenza infection. JAMA (2005) 1.67
Cerebral hemodynamics in preterm infants during positional intervention measured with diffuse correlation spectroscopy and transcranial Doppler ultrasound. Opt Express (2009) 1.58
Predictors of outcome in childhood intracerebral hemorrhage: a prospective consecutive cohort study. Stroke (2009) 1.56
Mitochondrial tRNA(Phe) mutation as a cause of end-stage renal disease in childhood. Pediatr Nephrol (2012) 1.56
Pediatric intracerebral hemorrhage: acute symptomatic seizures and epilepsy. JAMA Neurol (2013) 1.55
Mitochondrial DNA depletion syndrome due to mutations in the RRM2B gene. Neuromuscul Disord (2008) 1.39
Predicting outcome in children with hypoxic ischemic encephalopathy. Pediatr Crit Care Med (2008) 1.38
Clinical neonatal brain MRI segmentation using adaptive nonparametric data models and intensity-based Markov priors. Med Image Comput Comput Assist Interv (2007) 1.36
Mimics of childhood stroke: characteristics of a prospective cohort. Pediatrics (2006) 1.27
Risk of later seizure after perinatal arterial ischemic stroke: a prospective cohort study. Pediatrics (2011) 1.25
Pediatric perfusion MR imaging using arterial spin labeling. Neuroimaging Clin N Am (2006) 1.24
Variant non ketotic hyperglycinemia is caused by mutations in LIAS, BOLA3 and the novel gene GLRX5. Brain (2013) 1.22
An X-linked cobalamin disorder caused by mutations in transcriptional coregulator HCFC1. Am J Hum Genet (2013) 1.20
Association of impaired linear growth and worse neurodevelopmental outcome in infants with single ventricle physiology: a report from the pediatric heart network infant single ventricle trial. J Pediatr (2012) 1.17
Arterial spin labeling perfusion MRI in pediatric arterial ischemic stroke: initial experiences. J Magn Reson Imaging (2009) 1.14
Validation of diffuse correlation spectroscopic measurement of cerebral blood flow using phase-encoded velocity mapping magnetic resonance imaging. J Biomed Opt (2012) 1.14
ABC/XYZ estimates intracerebral hemorrhage volume as a percent of total brain volume in children. Stroke (2010) 1.13
The cerebral vasculopathy of PHACES syndrome. Stroke (2008) 1.12
Cerebral cortical folding analysis with multivariate modeling and testing: Studies on gender differences and neonatal development. Neuroimage (2010) 1.10
Hepatocerebral form of mitochondrial DNA depletion syndrome: novel MPV17 mutations. Arch Neurol (2008) 1.04
Seizures as a presenting symptom of acute arterial ischemic stroke in childhood. J Pediatr (2011) 1.00
Evidence for a recurrent microdeletion at chromosome 16p11.2 associated with congenital anomalies of the kidney and urinary tract (CAKUT) and Hirschsprung disease. Am J Med Genet A (2010) 0.99
COL4A2 mutation associated with familial porencephaly and small-vessel disease. Eur J Hum Genet (2012) 0.98
Quantification issues in arterial spin labeling perfusion magnetic resonance imaging. Top Magn Reson Imaging (2010) 0.96
Younger gestational age is associated with worse neurodevelopmental outcomes after cardiac surgery in infancy. J Thorac Cardiovasc Surg (2012) 0.96
Prediction of periventricular leukomalacia. Part I: Selection of hemodynamic features using logistic regression and decision tree algorithms. Artif Intell Med (2009) 0.94
A novel mutation in the mitochondrial DNA cytochrome b gene (MTCYB) in a patient with mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes syndrome. J Child Neurol (2012) 0.94
Novel inborn error of folate metabolism: identification by exome capture and sequencing of mutations in the MTHFD1 gene in a single proband. J Med Genet (2011) 0.94
Early postoperative changes in cerebral oxygen metabolism following neonatal cardiac surgery: effects of surgical duration. J Thorac Cardiovasc Surg (2012) 0.94
Lupus anticoagulant and thrombosis following Henoch-Schonlein purpura. Pediatr Neurol (2007) 0.94
Lysine restricted diet for pyridoxine-dependent epilepsy: first evidence and future trials. Mol Genet Metab (2012) 0.93
Noninvasive cerebral perfusion imaging in high-risk neonates. Semin Perinatol (2010) 0.93
Pediatric palliative, end-of-life, and bereavement care. Pediatr Clin North Am (2005) 0.92
Intravenous levetiracetam in critically ill children with status epilepticus or acute repetitive seizures. Pediatr Crit Care Med (2009) 0.92
Effects of congenital heart disease on brain development. Prog Pediatr Cardiol (2010) 0.92
International Paediatric Stroke Study: stroke associated with cardiac disorders. Int J Stroke (2012) 0.91
Why perfusion in neonates with congenital heart defects is negative--technical issues related to pulsed arterial spin labeling. Magn Reson Imaging (2005) 0.90
The G13513A mutation in the ND5 gene of mitochondrial DNA as a common cause of MELAS or Leigh syndrome: evidence from 12 cases. Arch Neurol (2008) 0.90
Patient position during lumbar puncture has no meaningful effect on cerebrospinal fluid opening pressure in children. J Child Neurol (2010) 0.88
De novo heterozygous mutations in SMC3 cause a range of Cornelia de Lange syndrome-overlapping phenotypes. Hum Mutat (2015) 0.87
Medical staff attitudes toward family presence during pediatric procedures. Pediatr Emerg Care (2004) 0.87
Significant liver disease in a patient with Y116H mutation in the MVK gene. Am J Med Genet A (2011) 0.87
Intravenous levetiracetam terminates refractory focal status epilepticus. Neurocrit Care (2009) 0.87
Protecting the infant brain during cardiac surgery: a systematic review. Ann Thorac Surg (2012) 0.86
Prediction of periventricular leukomalacia. Part II: Selection of hemodynamic features using computational intelligence. Artif Intell Med (2009) 0.86
Practice patterns of mitochondrial disease physicians in North America. Part 1: diagnostic and clinical challenges. Mitochondrion (2013) 0.86
Hemorrhagic transformation of childhood arterial ischemic stroke. Stroke (2011) 0.86
Sodium bicarbonate causes dose-dependent increases in cerebral blood flow in infants and children with single-ventricle physiology. Pediatr Res (2013) 0.85
Application of decision tree in the prediction of periventricular leukomalacia (PVL) occurrence in neonates after heart surgery. Conf Proc IEEE Eng Med Biol Soc (2012) 0.84
Complex management of a patient with a contiguous Xp11.4 gene deletion involving ornithine transcarbamylase: a role for detailed molecular analysis in complex presentations of classical diseases. Mol Genet Metab (2008) 0.84
Prediction of periventricular leukomalacia occurrence in neonates after heart surgery. IEEE J Biomed Health Inform (2013) 0.84
The Pediatric Stroke Recurrence and Recovery Questionnaire: validation in a prospective cohort. Neurology (2012) 0.83
PHACE syndrome: a retrospective review of 23 patients. Pediatr Dermatol (2014) 0.82
Expanded molecular features of carnitine acyl-carnitine translocase (CACT) deficiency by comprehensive molecular analysis. Mol Genet Metab (2011) 0.82
Severe combined immunodeficiency resulting from mutations in MTHFD1. Pediatrics (2013) 0.82
Concurrent validity and reliability of retrospective scoring of the Pediatric National Institutes of Health Stroke Scale. Stroke (2011) 0.82
Haemorrhagic stroke in term and late preterm neonates. Arch Dis Child Fetal Neonatal Ed (2013) 0.81
Management of common neurologic symptoms in pediatric palliative care: seizures, agitation, and spasticity. Pediatr Clin North Am (2007) 0.81
Unusual cardiac "masses" in a newborn with infantile pompe disease. JIMD Rep (2011) 0.79
Somatic mosaicism for PDHA1 mutation in a male with pyruvate dehydrogenase complex deficiency. Mol Genet Metab (2010) 0.79
Development and validation of a semiquantitative brain maturation score on fetal MR images: initial results. Radiology (2013) 0.79
Predictive validity of severity grading for cerebral steno-occlusive arteriopathy in recurrent childhood ischemic stroke. Int J Stroke (2014) 0.78
What new information pediatric autopsies can provide: a retrospective evaluation of 100 consecutive autopsies using family-centered criteria. Arch Pediatr Adolesc Med (2007) 0.78
Neurological complications associated with the treatment of patients with congenital cardiac disease: consensus definitions from the Multi-Societal Database Committee for Pediatric and Congenital Heart Disease. Cardiol Young (2008) 0.78
Discovering hidden relationships in physiological signals for prediction of Periventricular Leukomalacia. Conf Proc IEEE Eng Med Biol Soc (2013) 0.78
Evaluation of intraventricular hemorrhage in pediatric intracerebral hemorrhage. J Child Neurol (2011) 0.78
Penicillamine therapy for pediatric cystinuria: experience from a cohort of American children. J Urol (2008) 0.78
Pediatric intracerebral hemorrhage score: a simple grading scale for intracerebral hemorrhage in children. Stroke (2013) 0.77
Reference range for cerebrospinal fluid protein concentration in children and adolescents. Arch Pediatr Adolesc Med (2011) 0.76
Liver pathology in infantile mitochondrial DNA depletion syndrome. Pediatr Dev Pathol (2013) 0.76
Distinctive pattern of restricted diffusion in a neonate with molybdenum cofactor deficiency. Pediatr Radiol (2012) 0.76
A false-positive newborn screening result: goat's milk acidopathy. Pediatrics (2008) 0.75
Neurodevelopmental Outcomes in Children With Congenital Heart Disease-What Can We Impact? Pediatr Crit Care Med (2016) 0.75
Lysine-Restricted Diet as Adjunct Therapy for Pyridoxine-Dependent Epilepsy: The PDE Consortium Consensus Recommendations. JIMD Rep (2014) 0.75
Neuropsychological status in children after repair of acyanotic congenital heart disease. Pediatrics (2010) 0.75
Electrographic Seizures in Children and Neonates Undergoing Extracorporeal Membrane Oxygenation. Pediatr Crit Care Med (2017) 0.75
Diagnostic challenges in a severely delayed infant with hypersomnolence, failure to thrive and arteriopathy: a unique case of gamma-hydroxybutyric aciduria and Williams syndrome. Am J Med Genet B Neuropsychiatr Genet (2007) 0.75
Modified Pediatric ASPECTS Correlates with Infarct Volume in Childhood Arterial Ischemic Stroke. Front Neurol (2012) 0.75
Pediatric central nervous system infections and inflammatory white matter disease. Pediatr Clin North Am (2005) 0.75
Partial splenic embolization in a child with Gaucher disease, massive splenomegaly and severe thrombocytopenia. Pediatr Radiol (2009) 0.75
Status epilepticus secondary to hypertensive encephalopathy as the presenting manifestation of Guillain-Barré syndrome. Pediatr Emerg Care (2007) 0.75