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Research Publications from 2003

Kennedy Krieger’s scientists and researchers are leaders in the worldwide effort to prevent and treat disorders of the brain, spinal cord, and musculoskeletal system. Learn about our innovative research initiatives and latest findings through our faculty research publications, Research Frontiers articles, and research press releases.

Schulze KJ, O'brien KO, Germain-Lee EL, Baer DJ, Leonard AL, Rosenstein BJ. (Dec 2003). Endogenous fecal losses of calcium compromise calcium balance in pancreatic-insufficient girls with cystic fibrosis. J Pediatr. 143(6), 765-71. Abstract
Lancelotta MP, Sheth RN, Meyer RA, Belzberg AJ, Griffin JW, Campbell JN. (Nov 2003). Severity and duration of hyperalgesia in rat varies with type of nerve lesion. Neurosurgery. 53(5), 1200-8; discussion 1208-9. Abstract
Zhang J, Richards LJ, Yarowsky P, Huang H, van Zijl PC, Mori S. (Nov 2003). Three-dimensional anatomical characterization of the developing mouse brain by diffusion tensor microimaging. Neuroimage. 20(3), 1639-48. Abstract
Matsushita H, Johnston MV, Lange MS, Wilson MA. (Sep 2003). Protective effect of erythropoietin in neonatal hypoxic ischemia in mice. Neuroreport. 14(13), 1757-61. Abstract
Germain-Lee EL, Groman J, Crane JL, Jan de Beur SM, Levine MA. (Sep 2003). Growth hormone deficiency in pseudohypoparathyroidism type 1a: another manifestation of multihormone resistance. J Clin Endocrinol Metab. 88(9), 4059-69. Abstract
Pizzini F, Fatemi AS, Barker PB, Nagae-Poetscher LM, Horská A, Zimmerman AW, Moser HW, Bibat G, Naidu S. (Sep 2003). Proton MR spectroscopic imaging in Pelizaeus-Merzbacher disease. AJNR Am J Neuroradiol. 24(8), 1683-9. Abstract
Matsumoto N, Tamura S, Furuki S, Miyata N, Moser A, Shimozawa N, Moser HW, Suzuki Y, Kondo N, Fujiki Y. (Aug 2003). Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation. Am J Hum Genet. 73(2), 233-46. Abstract
Comi AM. (Aug 2003). Pathophysiology of Sturge-Weber syndrome. J Child Neurol. 18(8), 509-16. Abstract



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