Published in Pediatr Diabetes on April 01, 2007
The clinical utility of C-peptide measurement in the care of patients with diabetes. Diabet Med (2013) 1.50
Retracted Epidemiological pattern of newly diagnosed children with type 1 diabetes mellitus, Taif, Saudi Arabia. ScientificWorldJournal (2013) 1.41
Proteomic profiling of amniotic fluid in preterm labor using two-dimensional liquid separation and mass spectrometry. J Matern Fetal Neonatal Med (2008) 0.94
Approach to the obese adolescent with new-onset diabetes. J Clin Endocrinol Metab (2010) 0.83
Fasting serum C-peptide is useful for initial classification of diabetes mellitus in children and adolescents. Ann Pediatr Endocrinol Metab (2014) 0.81
Epigenetic analyses of the insulin-like growth factor binding protein 1 gene in type 1 diabetes and diabetic nephropathy. Clin Epigenetics (2014) 0.80
Elevated C-peptide and insulin predict increased risk of colorectal adenomas in normal mucosa. BMC Cancer (2012) 0.80
Distinguishing type 1 and type 2 diabetes at diagnosis. What is the problem? Pediatr Diabetes (2007) 0.79
Randomized, controlled, parallel-group prospective study to investigate the clinical effectiveness of early insulin treatment in patients with latent autoimmune diabetes in adults. BMC Endocr Disord (2008) 0.75
Clinical and Laboratory Characteristics of Childhood Diabetes Mellitus: A Single-Center Study from 2000 to 2013. Chonnam Med J (2016) 0.75
Can biochemical markers discriminate between new-onset type 1 and type 2 diabetes mellitus in children? Nat Clin Pract Endocrinol Metab (2007) 0.75
Microduplications of 16p11.2 are associated with schizophrenia. Nat Genet (2009) 6.13
The Children's Hospital of Philadelphia modification of the Furlow double-opposing Z-palatoplasty: 30-year experience and long-term speech outcomes. Plast Reconstr Surg (2013) 2.60
Computer-assisted segmentation of white matter lesions in 3D MR images using support vector machine. Acad Radiol (2008) 2.25
Molecular and clinical genetics of mitochondrial diseases due to POLG mutations. Hum Mutat (2008) 2.04
A family-school intervention for children with ADHD: results of a randomized clinical trial. J Consult Clin Psychol (2012) 1.64
Coping, self-management, and adaptation in adolescents with type 1 diabetes. Ann Behav Med (2012) 1.60
Mitochondrial tRNA(Phe) mutation as a cause of end-stage renal disease in childhood. Pediatr Nephrol (2012) 1.56
Persistent hypercholesterolemia is associated with the development of obesity among girls: the Bogalusa Heart Study. Am J Clin Nutr (2002) 1.48
Effect of osmotic-release oral system methylphenidate on different domains of attention and executive functioning in children with attention-deficit-hyperactivity disorder. Dev Med Child Neurol (2011) 1.44
Effects of a functional COMT polymorphism on prefrontal cognitive function in patients with 22q11.2 deletion syndrome. Am J Psychiatry (2004) 1.43
Mitochondrial DNA depletion syndrome due to mutations in the RRM2B gene. Neuromuscul Disord (2008) 1.39
MRI diffusion coefficients in spinal cord correlate with axon morphometry. Neuroreport (2005) 1.25
Social cognition in context: validating a cartoon-based attributional measure for urban girls. Child Dev (2006) 1.25
Education and telephone case management for children with type 1 diabetes: a randomized controlled trial. J Pediatr Nurs (2005) 1.23
Influence of decorin on the mechanical, compositional, and structural properties of the mouse patellar tendon. J Biomech Eng (2012) 1.20
A new self-report measure of self-management of type 1 diabetes for adolescents. Nurs Res (2009) 1.20
An initial evaluation of a culturally adapted social problem-solving and relational aggression prevention program for urban African-American relationally aggressive girls. J Prev Interv Community (2009) 1.17
Regenerative properties of fetal sheep tendon are not adversely affected by transplantation into an adult environment. J Orthop Res (2006) 1.17
Housing strain, mortgage foreclosure, and health. Nurs Outlook (2011) 1.14
Investigating tendon fascicle structure-function relationships in a transgenic-age mouse model using multiple regression models. Ann Biomed Eng (2004) 1.13
Interrater reliability of the Pediatric National Institutes of Health Stroke Scale (PedNIHSS) in a multicenter study. Stroke (2011) 1.09
Type 1 diabetes eHealth psychoeducation: youth recruitment, participation, and satisfaction. J Med Internet Res (2013) 1.09
Internet psycho-education programs improve outcomes in youth with type 1 diabetes. Diabetes Care (2013) 1.06
The Preventing Relational Aggression in Schools Everyday Program: A Preliminary Evaluation of Acceptability and Impact. School Psych Rev (2010) 1.05
Apparent diffusion coefficients in spinal cord transplants and surrounding white matter correlate with degree of axonal dieback after injury in rats. AJNR Am J Neuroradiol (2005) 1.05
The epidemiology of type 1 diabetes in children. Endocrinol Metab Clin North Am (2012) 1.05
Hepatocerebral form of mitochondrial DNA depletion syndrome: novel MPV17 mutations. Arch Neurol (2008) 1.04
Effects of limb exercise after spinal cord injury on motor neuron dendrite structure. J Comp Neurol (2004) 1.04
Patterns of complementary and alternative medicine use in a population of pediatric patients with inflammatory bowel disease. Inflamm Bowel Dis (2004) 1.00
The relationship between nurse staffing and patient outcomes. J Nurs Adm (2003) 1.00
A comparison of two internet programs for adolescents with type 1 diabetes: design and methods. Contemp Clin Trials (2012) 0.98
Rethinking growth failure in Alagille syndrome: the role of dietary intake and steatorrhea. J Pediatr Gastroenterol Nutr (2002) 0.97
Free and total insulin-like growth factor (IGF)-I levels decline during fasting: relationships with insulin and IGF-binding protein-1. J Clin Endocrinol Metab (2002) 0.96
Disordered eating behaviors in youth with type 1 diabetes. Diabetes Educ (2005) 0.96
Chromosome 22q11 deletion in patients with ventricular septal defect: frequency and associated cardiovascular anomalies. Pediatrics (2003) 0.96
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
Parents' perceptions of factors that affect successful diabetes management for their children. Pediatrics (2005) 0.94
Effects of COMT genotype on behavioral symptomatology in the 22q11.2 Deletion Syndrome. Child Neuropsychol (2005) 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
Parent attendance and homework adherence predict response to a family-school intervention for children with ADHD. J Clin Child Adolesc Psychol (2013) 0.93
Incidence of type 1 diabetes in Philadelphia is higher in black than white children from 1995 to 1999: epidemic or misclassification? Diabetes Care (2006) 0.93
Rituximab-treated patients have a poor response to influenza vaccination. J Clin Immunol (2012) 0.92
Calcium and dairy intake and measures of obesity in hyper- and normocholesterolemic children. Obes Res (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
Mechanical, compositional, and structural properties of the mouse patellar tendon with changes in biglycan gene expression. J Orthop Res (2013) 0.90
Weight-related concerns and behaviors in children and adolescents with type 1 diabetes. J Am Psychiatr Nurses Assoc (2008) 0.90
Mechanical property changes during neonatal development and healing using a multiple regression model. J Biomech (2012) 0.90
Respiratory inductance plethysmography in healthy 3- to 5-year-old children. Chest (2003) 0.89
Non-invasive measurements of carboxyhemoglobin and methemoglobin in children with sickle cell disease. Pediatr Pulmonol (2012) 0.89
Adoptive transfer of autologous T cells improves T-cell repertoire diversity and long-term B-cell function in pediatric patients with neuroblastoma. Clin Cancer Res (2012) 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
Neuropsychiatric disorders at the presentation of type 2 diabetes mellitus in children. Pediatr Diabetes (2005) 0.87
Brief daily periods of binocular vision prevent deprivation-induced acuity loss. Curr Biol (2003) 0.87
Significant liver disease in a patient with Y116H mutation in the MVK gene. Am J Med Genet A (2011) 0.87
Needle anxiety in children with type 1 diabetes and their mothers. MCN Am J Matern Child Nurs (2010) 0.87
The efficacy of influenza vaccination in a pediatric oncology population. J Pediatr Hematol Oncol (2010) 0.87
Evaluation of pulmonary embolism in a pediatric population with high clinical suspicion. Pediatr Radiol (2008) 0.87
Practice patterns of mitochondrial disease physicians in North America. Part 1: diagnostic and clinical challenges. Mitochondrion (2013) 0.86
Periodic limb movements and disrupted sleep in children with sickle cell disease. Sleep (2011) 0.86
Fostering health equity: clinical and research training strategies from nursing education. Kaohsiung J Med Sci (2009) 0.86
Upper airway lymphoid tissue size in children with sickle cell disease. Chest (2012) 0.85
Detection of electrographic seizures by critical care providers using color density spectral array after cardiac arrest is feasible. Pediatr Crit Care Med (2015) 0.85
Effects of hypoglycemia on developmental outcome in children with congenital hyperinsulinism. J Pediatr Nurs (2005) 0.85
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
Sickle cell disease: ratio of blood flow velocity of intracranial to extracranial cerebral arteries--initial experience. Radiology (2009) 0.83
Modeling clinical outcome of children with autistic spectrum disorders. Pediatrics (2005) 0.83
Lung function in 3-5-year-old children with cystic fibrosis. Pediatr Pulmonol (2008) 0.83
Concept analysis: self-monitoring in type 2 diabetes mellitus. Int J Nurs Stud (2008) 0.82
Severe combined immunodeficiency resulting from mutations in MTHFD1. Pediatrics (2013) 0.82
Parental expectations in the care of their children and adolescents with diabetes. J Pediatr Nurs (2010) 0.82
Expanded molecular features of carnitine acyl-carnitine translocase (CACT) deficiency by comprehensive molecular analysis. Mol Genet Metab (2011) 0.82
Age-dependent closure of bony defects after frontal orbital advancement. Plast Reconstr Surg (2006) 0.82
Immunologic consequences of chemotherapy for acute myeloid leukemia. J Pediatr Hematol Oncol (2013) 0.82
Concurrent validity and reliability of retrospective scoring of the Pediatric National Institutes of Health Stroke Scale. Stroke (2011) 0.82
Upper airway genioglossal activity in children with sickle cell disease. Sleep (2011) 0.81
The evaluation of peripheral neuropathy in youth with type 1 diabetes. Diabetes Res Clin Pract (2013) 0.81
Visual analytical tool for evaluation of 10-year perioperative transfusion practice at a children's hospital. J Am Med Inform Assoc (2013) 0.81
Relationship of youth involvement in diabetes-related decisions to treatment adherence. J Clin Psychol Med Settings (2014) 0.81
A prospective study of chemotherapy immunologic effects and predictors of humoral influenza vaccine responses in a pediatric oncology cohort. Influenza Other Respir Viruses (2012) 0.80
Racial differences in parents' perceptions of factors important for children to live well with diabetes. Diabetes Educ (2011) 0.80
Infraspinatus and supraspinatus tendon strain explained using multiple regression models. Ann Biomed Eng (2010) 0.80
Artificial multiple sclerosis lesions on simulated FLAIR brain MR images: echo time and observer performance in detection. Radiology (2006) 0.80
Diminished T cell numbers in patients with chronic granulomatous disease. Clin Immunol (2002) 0.80
Somatic mosaicism for PDHA1 mutation in a male with pyruvate dehydrogenase complex deficiency. Mol Genet Metab (2010) 0.79
Unusual cardiac "masses" in a newborn with infantile pompe disease. JIMD Rep (2011) 0.79
Outcomes associated with 12 years of grant funding: the Pediatric Endocrinology Nursing Society grant program. J Pediatr Nurs (2007) 0.79
Short periods of concordant binocular vision prevent the development of deprivation amblyopia. Eur J Neurosci (2006) 0.79
Executive Functioning in Children, Adolescents, and Young Adults with Chronic Kidney Disease. J Dev Behav Pediatr (2015) 0.78
A cluster randomized trial to evaluate external support for the implementation of positive behavioral interventions and supports by school personnel. Implement Sci (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
Preliminary examination of a cartoon-based hostile attributional bias measure for urban African American boys. Am J Community Psychol (2012) 0.77
Implementation of a clinical practice guideline for identification of microalbuminuria in the pediatric patient with type 1 diabetes. Nurs Clin North Am (2013) 0.77
Developing and Validating a New Classroom Climate Observation Assessment Tool. J Sch Violence (2011) 0.77
Assessing the regression to the mean for non-normal populations via kernel estimators. N Am J Med Sci (2010) 0.77
Liver pathology in infantile mitochondrial DNA depletion syndrome. Pediatr Dev Pathol (2013) 0.76