Steward CG - Search Results

1

Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome).

Ostergaard P, Simpson MA, Connell FC, Steward CG, Brice G, Woollard WJ, Dafou D, Kilo T, Smithson S, Lunt P, Murday VA, Hodgson S, Keenan R, Pilz DT, Martinez-Corral I, Makinen T, Mortimer PS, Jeffery S, Trembath RC, Mansour S. Ostergaard P, et al. Among authors: steward cg. Nat Genet. 2011 Sep 4;43(10):929-31. doi: 10.1038/ng.923. Nat Genet. 2011. PMID: 21892158

2

Emberger syndrome-primary lymphedema with myelodysplasia: report of seven new cases.

Mansour S, Connell F, Steward C, Ostergaard P, Brice G, Smithson S, Lunt P, Jeffery S, Dokal I, Vulliamy T, Gibson B, Hodgson S, Cottrell S, Kiely L, Tinworth L, Kalidas K, Mufti G, Cornish J, Keenan R, Mortimer P, Murday V; Lymphoedema Research Consortium. Mansour S, et al. Am J Med Genet A. 2010 Sep;152A(9):2287-96. doi: 10.1002/ajmg.a.33445. Am J Med Genet A. 2010. PMID: 20803646

3

Shwachman-Diamond syndrome: a complex case demonstrating the potential for misdiagnosis as asphyxiating thoracic dystrophy (Jeune syndrome).

Keogh SJ, McKee S, Smithson SF, Grier D, Steward CG. Keogh SJ, et al. Among authors: steward cg. BMC Pediatr. 2012 May 3;12:48. doi: 10.1186/1471-2431-12-48. BMC Pediatr. 2012. PMID: 22554078 Free PMC article.

4

Challenges in long-term control of hypercalcaemia with denosumab after haematopoietic stem cell transplantation for TNFRSF11A osteoclast-poor autosomal recessive osteopetrosis.

Taylor-Miller T, Sivaprakasam P, Smithson SF, Steward CG, Burren CP. Taylor-Miller T, et al. Among authors: steward cg. Bone Rep. 2020 Dec 2;14:100738. doi: 10.1016/j.bonr.2020.100738. eCollection 2021 Jun. Bone Rep. 2020. PMID: 33364264 Free PMC article.

5

Genetic analysis of the G4.5 gene in families with suspected Barth syndrome.

Cantlay AM, Shokrollahi K, Allen JT, Lunt PW, Newbury-Ecob RA, Steward CG. Cantlay AM, et al. Among authors: steward cg. J Pediatr. 1999 Sep;135(3):311-5. doi: 10.1016/s0022-3476(99)70126-5. J Pediatr. 1999. PMID: 10484795

6

Barth syndrome: an X-linked cause of fetal cardiomyopathy and stillbirth.

Steward CG, Newbury-Ecob RA, Hastings R, Smithson SF, Tsai-Goodman B, Quarrell OW, Kulik W, Wanders R, Pennock M, Williams M, Cresswell JL, Gonzalez IL, Brennan P. Steward CG, et al. Prenat Diagn. 2010 Oct;30(10):970-6. doi: 10.1002/pd.2599. Prenat Diagn. 2010. PMID: 20812380 Free PMC article.

7

T cell-depleted unrelated donor bone marrow transplantation for acute myeloid leukemia.

Marks DI, Bird JM, Vettenranta K, Hunt L, Green A, Cornish JM, Goulden N, Pamphilon DH, Steward CG, Oakhill A. Marks DI, et al. Among authors: steward cg. Biol Blood Marrow Transplant. 2000;6(6):646-53. doi: 10.1016/s1083-8791(00)70031-0. Biol Blood Marrow Transplant. 2000. PMID: 11128816 Free article.

8

Hematopoietic stem cell transplantation for osteopetrosis.

Steward CG. Steward CG. Pediatr Clin North Am. 2010 Feb;57(1):171-80. doi: 10.1016/j.pcl.2009.11.006. Pediatr Clin North Am. 2010. PMID: 20307717 Review.

9

Dysmorphology of Barth syndrome.

Hastings R, Steward C, Tsai-Goodman B, Newbury-Ecob R. Hastings R, et al. Clin Dysmorphol. 2009 Oct;18(4):185-7. doi: 10.1097/MCD.0b013e32832a9e62. Clin Dysmorphol. 2009. PMID: 19648820

10

Imaging of malignant infantile osteopetrosis before and after bone marrow transplantation.

Cheow HK, Steward CG, Grier DJ. Cheow HK, et al. Among authors: steward cg. Pediatr Radiol. 2001 Dec;31(12):869-75. doi: 10.1007/s002470100008. Pediatr Radiol. 2001. PMID: 11727023

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