Submissions from 2003
Cognitive decline with immunologic and virologic stability in four children with human immunodeficiency virus disease, M. A. T. Tamula, P. L. Wolters, C. Walsek, and S. Zeichner
Mutation in GPIb beta impairs assembly of the platelet von Willebrand factor receptor and causes Bernard-Souller syndrome, J. Tang, S. Stern-Nezer, P. Liu, L. Matyakhina, and N. Luban
Novel mutations in the CLN6 gene causing a variant late infantile neuronal ceroid lipofuscinosis, C. A. Teixeira, J. Espinola, L. Huo, J. Kohlschutter, and D. A. P. Sawin
Rapid genotyping of common MeCP2 mutations with an electronic DNA microchip using serial differential hybridization, W. A. Thistlethwaite, L. M. Moses, K. C. Hoffbuhr, J. M. Devaney, and E. P. Hoffman
Paracetamol and metabolite pharmacokinetics in infants, C. D. van der Marel, B. J. Anderson, R. A. van Lingen, N. H. G. Holford, and M. A. L. Pluim
Oral health status of children and adolescents by rural residence, US, 1988-1994, C.M. Vargas, C.R. Ronzio, and K. Hayes
Ketamine and midazolam is an inappropriate preinduction combination in uncooperative children undergoing brief ambulatory procedures, S. T. Verghese, R. S. Hannallah, R. I. Patel, and K. M. Patel
Prolonged cannulation of the left internal mammary artery (LIMA) for blood pressure monitoring in a child after cardiopulmonary bypass, S. T. Verghese, J. E. Sell, F. M. Midgley, M. Margolis, and G. R. Martin
Health insurance coverage for oral diseases - Toward a more sophisticated model, H. S. Weiss, L. Hecht, and B. Friedland
Inhibition of melanoma tumor growth by a novel inhibitor of glucosylceramide synthase, M. Weiss, S. Hettmer, P. Smith, and S. Ladisch
ADHD treatment with once-daily OROS methylphenidate: Interim 12-month results from a long-term open-label study, T. Wilens, W. Pelham, M. Stein, C. K. Conners, and H. Abikoff
Expression profiling of FSHD muscle supports a defect in specific stages of myogenic differentiation, S. T. Winokur, Y. W. Chen, P. S. Masny, J. H. Martin, and J. T. Ehmsen
A case of congenitally protected d-transposition of the great arteries in a very low-birth-weight infant, K. E. Woodson, C. A. Sable, J. T. Berger, M. C. Slack, and G. Wernovsky
Acculturation and the health and well-being of US immigrant adolescents, S. M. Yu, Z. J. Huang, R. H. Schwalberg, M. Overpeck, and M. D. Kogan
In vivo filtering of in vitro expression data reveals MyoD targets, P. Zhao, J. W. Seo, Z. Y. Wang, Y. Wang, and B. Shneiderman
Submissions from 2002
Bone marrow failure syndromes in children, B.P Alter
Radiosensitivity in Fanconi?s anemia patients, BP Alter
Development of a human muscle expression data warehouse, M.A. Bakay, J. Chen, and E.P. Hoffman
Sources of variability and effect of experimental approach on expression profiling data interpretation., M. Bakay, Y.W. Chen, R. Borup, P. Zhao, and K. Nagaraju
A web-accessible complete transcriptome of normal human and DMD muscle., M. Bakay, P. Zhao, J. Chen, and E.P. Hoffman
The utility of functional magnetic resonance imaging in epilepsy and language., L.M. Balsamo and W.D. Gaillard
A functional magnetic resonance imaging study of left hemisphere language dominance in children., L.M. Balsamo, B. Xu, C.B. Grandin, J.R. Petrella, and S.H. Braniecki
The time to certify pediatric urologists has arrived, A.B. Belman
Gene expression changes during early anterior ischemic optic neuropathy, S.L. Bernstein, M. Mintz, D. Stephan, and Y. Guo
Development and production of an oligonucleotide MuscleChip: use for validation of ambiguous ESTs, R.H.A. Borup, S. Toppo, Y.W. Chen, T.M. Teslovich, and G. Lanfranchi
Development and production of an oligonucleotide MuscleChip: use for validation of ambiguous ESTs., R.H. Borup, S. Toppo, Y.W. Chen, T.M. Teslovich, and G. Lanfranchi
Injury surveillance in emergency departments: design, implementation and analysis., R. Brenner, P. Scheidt, M. Rossi, T. Cheng, and M. Overpeck
Skateboard and scooter injuries, M. Bull, P. Agran, H. Gardner, D. Laraque, and S. Pollack
Selecting and using the most appropriate car safety seats for growing children: guidelines for counseling parents, M. Bull, P. Aran, G. Gardner, D. Laraque, and S. Pollack
National Marrow Donor Program Working Group. Unrelated marrow transplantation for children with acute lymphoblastic leukemia in second remission, N. Bunin, M. Carston, D. Wall, R. Adams, and J. Casper
Marriage after cure: life after childhood cancer, J. Byrne
Excess risk for Mullerian Duct anomalies in girls with Wilms tumor, J. Byrne and H.S. Nicholson
Cloning and expression of the human N-acetylglutamate synthase gene., L. Caldovic, H. Morizono, M. Gracia Panglao, R. Gallegos, and X. Yu
Identification, cloning and expression of the mouse N-acetylglutamate synthase gene, L. Caldovic, H. Morizono, X. Yu, M. Thompson, and D. Shi
Diagnosis of infectious diseases with point-of-care assays, J. M. Campos
Serologic testing, J.M. Campos
Quantitative structure-activity relationships for a series of symmetrical bisquaternary anticancer compound., J.M. Campos, M.C. Nunez, R.M. Sanchez, J.A. Gomez-Vidal, and A. Rodriguez-Gonzalez
Germline mutations in the ribonuclease L gene in families showing linkage with HPC1Germline mutations in the ribonuclease L gene in families showing linkage with HPC1, J. Carpten, N. Nupponen, S. Isaacs, R. Sood, and C. Robbins
The INK locus in relapsed childhood acute lymphoblastic leukemia, T.L. Carter, P.M. Watt, G.H. Reaman, and U.R. Kees
Feeding disorders in infants and toddlers: diagnosis and treatment, I. Chatoor
Temporal expression profiling in a disease, Duchenne muscular dystrophy, Y. W. Chen, M. Bakay, R. Borup, S. Toppo, and G. Valle
Disease-specific changes in facioscapulohumeral muscular dystrophy by expression profiling, Y. W. Chen, P. Masny, K. M. Flanigan, J. Martin, and H. Qian
Response of rat muscle to acute resistance exercise defined by transcriptional and translational profiling., Y.W. Chen, G.A. Nader, K.R. Baar, M.J. Fedele, and E.P. Hoffman
An aberrant umbilical vein draining into the coronary sinus., A. Chi, C. Sable, S. Cummings, and G. Martin
Can a clinical decision rule decrease antibiotic use in viral meningitis?, M.B. Chitkara, L.M. Ryan, D. Stockwell, and B.L. Wiedermann
Youth Targeting by Tobacco Manufacturers Since the Master Settlement Agreement., P.J. Chung, C.F. Garfield, P.J. Rathouz, D.S. Lauderdale, and D. Best
Propofol or midazolam do not reduce the incidence of emergence agitation associated with desflurane anaesthesia in children undergoing adenotonsillectomy, I.T. Cohen, S. Drewsen, and R.S. Hannallah
The effect of fentanyl on the emergence characteristics after desflurane or sevoflurane anesthesia in children, I.T. Cohen, J.C. Finkel, R.S. Hannallah, K.A. Hummer, and K.M. Patel
Progresive myoclonic epilepsies, J.A. Conry
Pediatric brain death, N. Crain
Topical treatment of sclerodermoid chronic graft vs. host disease., D.M. Currie, G.K. Ludvigsdottir, C.A. Diaz, and N. Kamani
Association between conformational mutations in neuroserpin and onset and severity of dementia., R.L. Davis, A.E. Shrimpton, R.W. Carrell, D.A. Lomas, and L. Gerhard
Analysis of pediatric hospitalizations after emergency department release as a quality improvement tool, A.D. Depiero, D.W. Ochsenschlager, and J.M. Chamberlain
No missense mutation of WKL1 in a subgroup of probands with schizophrenia., J.M. Devaney, E.A. Donarum, K.M. Brown, J. Meyer, and G. Stober
Discovery of single nucleotide polymorphisms in eleven genes involved in muscle function: efficiency of a systematic sequencing approach compared to bioinformatic extraction with five SNP databases, J. M. Devaney, B. T. Harmon, and E. P. Hoffman
Ikaros, a lymphoid-cell-specific transcription factor, contributes to the leukemogenic phenotype of a mink cell focus-inducing murine leukemia virus, N.L. DiFronzo, C.T. Leung, M.K. Mammel, K. Georgopoulos, and B.J. Taylor
Experimental spinal cord injury temporal profiling identifies cell cycle genes associated with neuronal damage: possible SNP candidates, S. Di Giovanni, S. Knoblach, A. I. Faden, and E. P. Hoffman
Alpha- and beta-sarcoglycan delivery by AAV: Efficient rescue of muscle, but differential peristence of gene expression, D. Dressman, K. Araishi, M. Imamura, T. Sasaoka, and L. Liu
Delivery of alpha- and beta-sarcoglycan by recombinant adeno-associated virus: efficient rescue of muscle, but differential toxicity., D. Dressman, K. Araishi, M. Imamura, T. Sasaoka, and L.A. Liu
Bilateral occurrence of congenital middle ear cholesteatoma., M.A. El-Bitar and S.S. Choi
Retained ventilation tubes: should they be removed at 2 years?, M.A. El-Bitar, M.T. Pena, S.S. Choi, and G.H. Zalzal
Powered instrumentation in the treatment of recurrent respiratory papillomatosis: an alternative to the carbon dioxide laser, M.A. El-Bitar and G.H. Zalzal
p53 protein overexpression in bone marrows of patients with Shwachman-Diamond Syndrome has a prevalence similar to that of patients with refractory anemia, M.T. Elghetany and B.P Alter
Fetal MRI evaluation of an intracranial mass: in utero evolution of hemorrhage., S.A. Emamian, D.I. Bulas, G.L. Vezina, E.C. Dubovsky, and P. Cogan
Collaborative translational research leading to multicenter clinical trials in Duchenne muscular dystrophy: the Cooperative International Neuromuscular Research Group (CINRG)., D.M. Escolar, E.K. Henricson, L. Pasquali, K. Gorni, and E.P. Hoffman
Chronic inflammatory demyelinating polyradiculoneuropathy in children, D. M. Escolar, C. Tesi-Rocha, and L. Pasquali
CT dose parameters and their limitations, T. Fearon
Admission troponin I, cardiac dysfunction and disease severity in pediatric patients with septic shock, K. E. Fenton, C. A. Sable, M. J. Bell, K. M. Patel, and J. T. Berger
Infectious complications of intensive chemotherapy on children's cancer group protocol CCG-2961 for pediatric acute myeloid leukemia, J. H. Feusner, T. A. Alonzo, P. Dinndorf, F. O. Smith, and R. Arceci
The effect of baricity of intrathecal morphine in children receiving tetracaine spinal anaesthesia for cardiac surgery: a preliminary report, J.C. Finkel, M.G. Boltz, and A.M. Conran
An evaluation of the efficacy and tolerability of oral tramadol hydrochloride tablets for the treatment of postsurgical pain in children, J.C. Finkel, J.B. Rose, M.L. Schmitz, P.K. Birmingham, and G.A. Ulma
Neuroselective sensory electrodiagnostic evaluation of 4% liposomal topical lidocaine., J.C. Finkel, C.I. Yang, J.L. Yarvitz, and K.M. Patel
Expression profiling reveals metabolic and structural components of extraocular muscles, M. D. Fischer, J. R. Gorospe, E. Felder, S. Bogdanovich, and F. Pedrosa-Domellof
Adolescent Risk and Vulnerability: Concepts and Measurement, B. Fischhoff, E.O. Nightingale, and J.G. Iannotta
Malignant myeloid transformation in congenital forms of neutropenia, M.H. Freedman and B.P Alter
Risk of myelodysplastic syndrome and acute myeloid leukemia in congenital neutropenias, M.H. Freedman and B.P Alter
Issues in children's hospital disaster preparedness., R. Frieshtat, J. Wright, and P. Holbrook
Language dominance in partial epilepsy patients identified with an fMRI reading task, W.D. Gaillard, L. Balsamo, B. Xu, C.B. Grandin, and S.H. Braniecki
Low incidence of abnormal (18) FDG-PET in children with new-onset partial epilepsy: a prospective study, W.D. Gaillard, L. Kopylev, S. Weinstein, J. Conry, and P.L. Pearl
IMx tacrolimus II assay: is it reliable at low blood concentrations? A comparison with tandem MS/MS., A.K. Ghoshal and S.J. Soldin
Citation of randomized evidence in support of guidelines of therapeutic and preventive interventions, I.A. Giannakakis, A.B. Haidich, D.G. Contopoulos-Ioannidis, G.N. Papanikolaou, and M.S. Baltogianni
Abnormal GABA/glutamine metabolism in succinic semialdehyde dehydrogenase (SSADH) deficiency, an epilepsy syndrome with elevated CNS GABA, K. M. Gibson, M. Gupta, M. Callan, H. Senephansiri, and M. Polinsky
Adaptive skills and executive function in autism spectrum disorders, L. Gilotty, L. Kenworthy, L. Sirian, D. Black, and A. Wagner
Profiles of everyday executive function in acquired and developmental disorders, G. A. Gioia, P. K. Isquith, L. Kenworthy, and R. M. Barton
Profiles of everyday executive function in acquired and developmental disorders., G.A. Gioia, P.K. Isquith, L. Kenworthy, and R.M. Barton
Confirmatory factor analysis of the Behavior Rating Inventory of Executive Function (BRIEF) in a clinical sample, G. Gioia, P. Isquith, P. Retzlaff, and K. Espy
Parvovirus B19 quiescence during the course of human immunodeficiency virus infection in persons with hemophilia, J.J. Goedert, D.D. Erdman, B.A. Konkle, T.J. Torok, and M.M. Lederman
End-stage liver disease in persons with hemophilia and transfusion-associated infections., J.J. Goedert, M.E. Eyster, M.M. Lederman, T. Mandalaki, and P. Moerloose
Routine MRI evaluation of low imperforate anus reveals unexpected high incidence of tethered spinal cord., N.R. Golonka, L.J. Haga, R.P. Keating, M.R. Eichelberger, and J.C. Gilbert
Effects of non-disease genetic information on the self-concept of individuals in the FAMuSS study, E. S. Gordon, J. M. Devaney, B. T. Harmon, M. J. Hubal, and P. M. Clarkson
The FKRP l2761 change: High allele frequency and common cause of LGMD, K. Gorni, M. Bakay, J. Devaney, and E. Hoffman
Peripheral neuropathies in childhood, K. Gorni, C. Tesi-Rocha, and D. M. Escolar
Molecular findings in symptomatic and pre-symptomatic Alexander disease patients, J.R. Gorospe, S. Naidu, A.B. Johnson, V. Puri, and G.V. Raymond
A complete ascertainment haplotyping in a SNP-Intensive gene: Clear population-specific haplotypes in the Cardiac Ankyrin Repeat Protein (CARP) gene, B. T. Harmon, J. M. Devaney, and E. P. Hoffman
The effect of genetic modifiers on phenotypic variation in cystic fibrosis-associated pulmonary disease, S. C. Hilmer, C. A. Merlo, R. A. Enke, M. E. Couch, and E. P. Hoffman
Longitudinal expression profiling and analysis of exercise-responsive genes in type-2 diabetics, D. S. Hittel, W. F. Kraus, and E. P. Hoffman
Associations between MeCP2 mutations, X-chromosome inactivation, and phenotype., K.C. Hoffbuhr, L.M. Moses, M.A. Jerdonek, S. Naidu, and E.P. Hoffman
Downstream of an RNA regulatory protein causing a common human disease: Expression-profiling human SMN-deficient muscle, E. Hoffman, C. Brandoli, and S. Servidei
Genetic medicine and the muscular dystrophies: triumphs and tribulations, E.P. Hoffman and Y.W. Chen
Immunostimulatory properties of dystrophic muscle alter persistence of transgenes, E. P. Hoffman, H. Gordish, K. Araishi, M. Imamura, and T. Sasaoka