Robinson IC - Search Results

1

Isolated autosomal dominant growth hormone deficiency: an evolving pituitary deficit? A multicenter follow-up study.

Mullis PE, Robinson IC, Salemi S, Eblé A, Besson A, Vuissoz JM, Deladoey J, Simon D, Czernichow P, Binder G. Mullis PE, et al. Among authors: robinson ic. J Clin Endocrinol Metab. 2005 Apr;90(4):2089-96. doi: 10.1210/jc.2004-1280. Epub 2005 Jan 25. J Clin Endocrinol Metab. 2005. PMID: 15671105

2

Exon splice enhancer mutation (GH-E32A) causes autosomal dominant growth hormone deficiency.

Petkovic V, Lochmatter D, Turton J, Clayton PE, Trainer PJ, Dattani MT, Eblé A, Robinson IC, Flück CE, Mullis PE. Petkovic V, et al. Among authors: robinson ic. J Clin Endocrinol Metab. 2007 Nov;92(11):4427-35. doi: 10.1210/jc.2007-0857. Epub 2007 Aug 28. J Clin Endocrinol Metab. 2007. PMID: 17726075

3

Growth hormone (GH)-releasing hormone increases the expression of the dominant-negative GH isoform in cases of isolated GH deficiency due to GH splice-site mutations.

Petkovic V, Godi M, Lochmatter D, Eblé A, Flück CE, Robinson IC, Mullis PE. Petkovic V, et al. Among authors: robinson ic. Endocrinology. 2010 Jun;151(6):2650-8. doi: 10.1210/en.2009-1280. Epub 2010 Mar 29. Endocrinology. 2010. PMID: 20351314

4

Isolated GH deficiency type II: knockdown of the harmful Delta3GH recovers wt-GH secretion in rat tumor pituitary cells.

Lochmatter D, Strom M, Eblé A, Petkovic V, Flück CE, Bidlingmaier M, Robinson IC, Mullis PE. Lochmatter D, et al. Among authors: robinson ic. Endocrinology. 2010 Sep;151(9):4400-9. doi: 10.1210/en.2010-0196. Epub 2010 Jun 30. Endocrinology. 2010. PMID: 20591972

5

Variability of isolated autosomal dominant GH deficiency (IGHD II): impact of the P89L GH mutation on clinical follow-up and GH secretion.

Salemi S, Yousefi S, Baltensperger K, Robinson IC, Eblé A, Simon D, Czernichow P, Binder G, Sonnet E, Mullis PE. Salemi S, et al. Among authors: robinson ic. Eur J Endocrinol. 2005 Dec;153(6):791-802. doi: 10.1530/eje.1.02041. Eur J Endocrinol. 2005. PMID: 16322384

6

Isolated autosomal dominant growth hormone deficiency: stimulating mutant GH-1 gene expression drives GH-1 splice-site selection, cell proliferation, and apoptosis.

Salemi S, Yousefi S, Lochmatter D, Eblé A, Deladoëy J, Robinson IC, Simon HU, Mullis PE. Salemi S, et al. Among authors: robinson ic. Endocrinology. 2007 Jan;148(1):45-53. doi: 10.1210/en.2006-0772. Epub 2006 Oct 12. Endocrinology. 2007. PMID: 17038549

7

Evolution of gonadotropin deficiency in a patient with type II autosomal dominant GH deficiency.

Turton JP, Buchanan CR, Robinson IC, Aylwin SJ, Dattani MT. Turton JP, et al. Among authors: robinson ic. Eur J Endocrinol. 2006 Dec;155(6):793-9. doi: 10.1530/eje.1.02293. Eur J Endocrinol. 2006. PMID: 17132747

8

Rescue of pituitary function in a mouse model of isolated growth hormone deficiency type II by RNA interference.

Shariat N, Ryther RC, Phillips JA 3rd, Robinson IC, Patton JG. Shariat N, et al. Among authors: robinson ic. Endocrinology. 2008 Feb;149(2):580-6. doi: 10.1210/en.2007-1360. Epub 2007 Nov 15. Endocrinology. 2008. PMID: 18006625 Free PMC article.

9

Autosomal dominant growth hormone deficiency disrupts secretory vesicles in vitro and in vivo in transgenic mice.

McGuinness L, Magoulas C, Sesay AK, Mathers K, Carmignac D, Manneville JB, Christian H, Phillips JA 3rd, Robinson IC. McGuinness L, et al. Among authors: robinson ic. Endocrinology. 2003 Feb;144(2):720-31. doi: 10.1210/en.2002-220847. Endocrinology. 2003. PMID: 12538635

10

Growth hormone replacement therapy for adults: into the new millennium.

Simpson H, Savine R, Sönksen P, Bengtsson BA, Carlsson L, Christiansen JS, Clemmons D, Cohen P, Hintz R, Ho K, Mullis P, Robinson I, Strasburger C, Tanaka T, Thorner M; GRS Council. Simpson H, et al. Growth Horm IGF Res. 2002 Feb;12(1):1-33. doi: 10.1054/ghir.2001.0263. Growth Horm IGF Res. 2002. PMID: 12127299 Review. No abstract available.

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