Dokal I - Search Results

1

Fludarabine-based stem cell transplantation protocol for Fanconi's anaemia in myelodysplastic transformation.

McCloy M, Almeida A, Daly P, Vulliamy T, Roberts IA, Dokal I. McCloy M, et al. Among authors: dokal i. Br J Haematol. 2001 Feb;112(2):427-9. doi: 10.1046/j.1365-2141.2001.02585.x. Br J Haematol. 2001. PMID: 11167843 Free article.

2

Allogeneic bone marrow transplantation for primary myelofibrosis.

Dokal I, Jones L, Deenmamode M, Lewis SM, Goldman JM. Dokal I, et al. Br J Haematol. 1989 Jan;71(1):158-60. doi: 10.1111/j.1365-2141.1989.tb06292.x. Br J Haematol. 1989. PMID: 2644968 No abstract available.

3

Late onset bone marrow failure associated with proximal fusion of radius and ulna: a new syndrome.

Dokal I, Ganly P, Riebero I, Marsh J, Steed A, Kendra J, Drysdale C, Hows J. Dokal I, et al. Br J Haematol. 1989 Feb;71(2):277-80. doi: 10.1111/j.1365-2141.1989.tb04267.x. Br J Haematol. 1989. PMID: 2923811

4

Positive diepoxybutane test in only one of two brothers found to be compound heterozygotes for Fanconi's anaemia complementation group C mutations.

Dokal I, Chase A, Morgan NV, Coulthard S, Hall G, Mathew CG, Roberts I. Dokal I, et al. Br J Haematol. 1996 Jun;93(4):813-6. doi: 10.1046/j.1365-2141.1996.d01-1726.x. Br J Haematol. 1996. PMID: 8703809

5

Bone marrow transplantation for Fanconi's anaemia: conditioning with reduced doses of cyclophosphamide without radiation.

Dokal IS, Roberts IA. Dokal IS, et al. Br J Haematol. 1996 Aug;94(2):423. Br J Haematol. 1996. PMID: 8759910 No abstract available.

6

Novel mutations and polymorphisms in the Fanconi anemia group C gene.

Gibson RA, Morgan NV, Goldstein LH, Pearson IC, Kesterton IP, Foot NJ, Jansen S, Havenga C, Pearson T, de Ravel TJ, Cohn RJ, Marques IM, Dokal I, Roberts I, Marsh J, Ball S, Milner RD, Llerena JC Jr, Samochatova E, Mohan SP, Vasudevan P, Birjandi F, Hajianpour A, Murer-Orlando M, Mathew CG. Gibson RA, et al. Among authors: dokal i. Hum Mutat. 1996;8(2):140-8. doi: 10.1002/(SICI)1098-1004(1996)8:2<140::AID-HUMU6>3.0.CO;2-F. Hum Mutat. 1996. PMID: 8844212

7

Fine mapping of the dyskeratosis congenita locus in Xq28.

Knight SW, Vulliamy T, Forni GL, Oscier D, Mason PJ, Dokal I. Knight SW, et al. Among authors: dokal i. J Med Genet. 1996 Dec;33(12):993-5. doi: 10.1136/jmg.33.12.993. J Med Genet. 1996. PMID: 9004129 Free PMC article.

8

Somatic mosaicism in Fanconi anemia: molecular basis and clinical significance.

Lo Ten Foe JR, Kwee ML, Rooimans MA, Oostra AB, Veerman AJ, van Weel M, Pauli RM, Shahidi NT, Dokal I, Roberts I, Altay C, Gluckman E, Gibson RA, Mathew CG, Arwert F, Joenje H. Lo Ten Foe JR, et al. Among authors: dokal i. Eur J Hum Genet. 1997 May-Jun;5(3):137-48. Eur J Hum Genet. 1997. PMID: 9272737

9

Skewed X-inactivation in carriers of X-linked dyskeratosis congenita.

Vulliamy TJ, Knight SW, Dokal I, Mason PJ. Vulliamy TJ, et al. Among authors: dokal i. Blood. 1997 Sep 15;90(6):2213-6. Blood. 1997. PMID: 9310472 Free article.

10

Successful second bone marrow transplant for Fanconi's anaemia following escalation of conditioning.

O'Donnell J, Roberts I, De la Fuente J, Daly P, New H, Dokal I. O'Donnell J, et al. Among authors: dokal i. Br J Haematol. 1997 Sep;98(3):772-4. doi: 10.1046/j.1365-2141.1997.2493066.x. Br J Haematol. 1997. PMID: 9332338 Free article.

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