Switching to Weekly Lonapegsomatropin from Daily Somatropin in Children with Growth Hormone Deficiency: The fliGHt Trial von Maniatis, Aristides K., Nadgir, Ulhas, Saenger, Paul, Reifschneider, Kent L., Abuzzahab, Jennifer, Deeb, Larry, Fox, Larry A., Woods, Katie A., Song, Wenjie, Mao, Meng, Chessler, Steven D., Komirenko, Allison S., Shu, Aimee D., Casella, Samuel J., Thornton, Paul S.

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Growth Hormone Insensitivity Associated with a STAT5b Mutation von Kofoed, Eric M, Hwa, Vivian, Little, Brian, Woods, Katie A, Buckway, Caroline K, Tsubaki, Junko, Pratt, Katherine L, Bezrodnik, Liliana, Jasper, Hector, Tepper, Alejandro, Heinrich, Juan J, Rosenfeld, Ron G

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Intrauterine Growth Retardation and Postnatal Growth Failure Associated with Deletion of the Insulin-Like Growth Factor I Gene von Woods, Katie A, Camacho-Hübner, Cecilia, Savage, Martin O, Clark, Adrian J.L

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Cord Blood Leptin Is Associated with Size at Birth and Predicts Infancy Weight Gain in Humans von Ong, Ken K. L, Ahmed, Marion L, Sherriff, Andrea, Woods, Katie A, Watts, Angie, Golding, Jean, Dunger, David B

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Effects of Recombinant Human Insulin-Like Growth Factor I (IGF-I) Therapy on the Growth Hormone-IGF System of a Patient with a Partial IGF-I Gene Deletion von Camacho-Hübner, Cecilia, Woods, Katie A, Miraki-Moud, Farideh, Hindmarsh, Peter C, Clark, Adrian J, Hansson, Yngve, Johnston, Atholl, Baxter, Robert C, Savage, Martin O

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Insulin-like growth factor (IGF)-I gene deletion von Camacho-Hübner, Cecilia, Woods, Katie A, Clark, Adrian J L, Savage, Martin O

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Recombinant Human Growth Hormone Plus Recombinant Human Insulin-Like Growth Factor-1 Coadministration Therapy in Short Children with Low Insulin-Like Growth Factor-1 and Growth Hor... von Backeljauw, Philippe F., Miller, Bradley S., Dutailly, Pascale, Houchard, Aude, Lawson, Elizabeth, Hale, Daniel E., Reiner, Barry, Sperling, Mark A.

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Identification of the first patient with a confirmed mutation of the JAK-STAT system von Rosenfeld, Ron G, Kofoed, Eric, Buckway, Caroline, Little, Brian, Woods, Katie A, Tsubaki, Junko, Pratt, Katherine A, Bezrodnik, Liliana, Jasper, Hector, Tepper, Alejandro, Heinrich, Juan J, Hwa, Vivian

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OR10-05 Phase 3 FliGHt Trial: Experience of Switching from Daily Growth Hormone Therapy to Once-Weekly TransCon HGH in Children with Growth Hormone Deficiency von Maniatis, Aristides K, Nadgir, Ulhas, Saenger, Paul, Mick, Gail, Reifschneider, Kent L, Abuzzahab, Mary Jennifer, Deeb, Larry, Fox, Larry A, Woods, Katie A, Peng, Jessica M, Karpf, David B, Shu, Aimee D, Song, Wenjie, Casella, Samuel J, Thornton, Paul S

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The Broad Spectrum of Inherited Growth Hormone Insensitivity Syndrome von Johnston, Linda B, Woods, Katie A, Rose, Stephen J, Clark, Adrian J.L, Savage, Martin O

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Thyroid cancer susceptibility polymorphisms: confirmation of loci on chromosomes 9q22 and 14q13, validation of a recessive 8q24 locus and failure to replicate a locus on 5q24 von Jones, Angela M, Howarth, Kimberley M, Martin, Lynn, Gorman, Maggie, Mihai, Radu, Moss, Laura, Auton, Adam, Lemon, Catherine, Mehanna, Hisham, Mohan, Hosahalli, Clarke, Susan E M, Wadsley, Jonathan, Macias, Elena, Coatesworth, Andrew, Beasley, Matthew, Roques, Tom, Martin, Craig, Ryan, Paul, Gerrard, Georgina, Power, Danielle, Bremmer, Caroline, Tomlinson, Ian, Carvajal-Carmona, Luis G

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Phenotype: Genotype Relationships in Growth Hormone Insensitivity Syndrome1 von Woods, Katie A, Dastot, Florence, Preece, Michael A, Clark, Adrian J. L, Postel-Vinay, Marie-Catherine, Chatelain, Pierre G, Ranke, Michael B, Rosenfeld, Ron G, Amselem, Serge, Savage, Martin O

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Phenotype: Genotype relationships in growth hormone insensitivity syndrome von WOODS, K. A, DASTOT, F, PREECE, M. A, CLARK, A. J. L, POSTEL-VINAY, M.-C, CHATELAIN, P. G, RANKE, M. B, ROSENFELD, R. G, AMSELEM, S, SAVAGE, M. O

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The somatotropic axis in short children born small for gestational age: Relation to insulin resistance von WOODS, Katie A, VAN HEL VOIRT, Maria, ONG, Ken K. L, MOHN, Angelica, LEVY, Jonathan, DE ZEGHER, Francis, DUNGER, David B

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Establishing a large prospective clinical cohort in people with head and neck cancer as a biomedical resource: head and neck 5000 von Ness, Andrew Robert, Waylen, Andrea, Hurley, Katrina, Jeffreys, Mona, Penfold, Chris, Pring, Miranda, Leary, Sam, Allmark, Christine, Toms, Stu, Ring, Susan, Peters, Tim J, Hollingworth, Will, Worthington, Helen, Nutting, Chris, Fisher, Sheila, Rogers, Simon N, Thomas, Steven J

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A homozygous splice site mutation affecting the intracellular domain of the growth hormone (GH) receptor resulting in Laron syndrome with elevated GH-binding protein von Woods, K A, Fraser, N C, Postel-Vinay, M C, Savage, M O, Clark, A J

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Growth Hormone Insensitivity: Pathophysiology, Diagnosis, Clinical Variation and Future Perspectives von Savage, Martin O., Burren, Christine P., Blair, Joanne C., Woods, Katie A., Metherell, Louise, Clark, Adrian J.L., Camacho-Hübner, Cecilia

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Insulin-like growth factor-I deficiency caused by a partial deletion of the IGF-I gene: Effects of rhIGFmi therapy von Camacho-Hübner, Cecilia, Woods, Katie A., Miraki-Moud, Farideh, Clark, Adrian, Savage, Martin O.

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Spelling in Use: Looking Closely at Spelling in Whole Language Classrooms von Laminack, Lester L, Wood, Katie

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Laron syndrome: typical and atypical forms von Woods, Katie A., Savage, Martin O.

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