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I Dokal

Showing results (21-30 of 55) with videos related to

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British Journal of Haematology|January 14, 1999
Dyskeratosis Congenita (DC) Registry: identification of new features of DCS Knight, T Vulliamy, A Copplestone, et al.
Bone Marrow Transplantation|August 29, 2007
Late death after unrelated-BMT for dyskeratosis congenita following conditioning with alemtuzumab, fludarabine and melphalanK Amarasinghe, C Dalley, I Dokal, et al.
British Journal of Haematology|February 13, 2001
Fludarabine-based stem cell transplantation protocol for Fanconi's anaemia in myelodysplastic transformationM McCloy, A Almeida, P Daly, et al.
Clinical and Experimental Dermatology|March 19, 2014
X-linked dyskeratosis congenita presenting in adulthood with photodamaged skin and epiphoraJ B Powell, I Dokal, R Carr, et al.
Clinical Genetics|January 5, 2011
Telomere length measurement can distinguish pathogenic from non-pathogenic variants in the shelterin component, TIN2T Vulliamy, R Beswick, M J Kirwan, et al.
British Journal of Haematology|October 23, 1997
Successful second bone marrow transplant for Fanconi's anaemia following escalation of conditioningJ O'Donnell, I Roberts, J De la Fuente, et al.
Leukemia|August 21, 2010
Effects of MSC co-injection on the reconstitution of aplastic anemia patient following hematopoietic stem cell transplantationB G Jaganathan, V Tisato, T Vulliamy, et al.
Journal of Medical Genetics|December 1, 1996
Fine mapping of the dyskeratosis congenita locus in Xq28S W Knight, T Vulliamy, G L Forni, et al.
Nature|September 28, 2001
The RNA component of telomerase is mutated in autosomal dominant dyskeratosis congenitaT Vulliamy, A Marrone, F Goldman, et al.
Human Genetics|May 31, 2001
Identification of novel DKC1 mutations in patients with dyskeratosis congenita: implications for pathophysiology and diagnosisS W Knight, T J Vulliamy, B Morgan, et al.
Pageof 6

Showing results (21-30 of 55) with videos related to

Sort By:
Pageof 6
British Journal of Haematology|January 14, 1999
Dyskeratosis Congenita (DC) Registry: identification of new features of DCS Knight, T Vulliamy, A Copplestone, et al.
Bone Marrow Transplantation|August 29, 2007
Late death after unrelated-BMT for dyskeratosis congenita following conditioning with alemtuzumab, fludarabine and melphalanK Amarasinghe, C Dalley, I Dokal, et al.
British Journal of Haematology|February 13, 2001
Fludarabine-based stem cell transplantation protocol for Fanconi's anaemia in myelodysplastic transformationM McCloy, A Almeida, P Daly, et al.
Clinical and Experimental Dermatology|March 19, 2014
X-linked dyskeratosis congenita presenting in adulthood with photodamaged skin and epiphoraJ B Powell, I Dokal, R Carr, et al.
Clinical Genetics|January 5, 2011
Telomere length measurement can distinguish pathogenic from non-pathogenic variants in the shelterin component, TIN2T Vulliamy, R Beswick, M J Kirwan, et al.
British Journal of Haematology|October 23, 1997
Successful second bone marrow transplant for Fanconi's anaemia following escalation of conditioningJ O'Donnell, I Roberts, J De la Fuente, et al.
Leukemia|August 21, 2010
Effects of MSC co-injection on the reconstitution of aplastic anemia patient following hematopoietic stem cell transplantationB G Jaganathan, V Tisato, T Vulliamy, et al.
Journal of Medical Genetics|December 1, 1996
Fine mapping of the dyskeratosis congenita locus in Xq28S W Knight, T Vulliamy, G L Forni, et al.
Nature|September 28, 2001
The RNA component of telomerase is mutated in autosomal dominant dyskeratosis congenitaT Vulliamy, A Marrone, F Goldman, et al.
Human Genetics|May 31, 2001
Identification of novel DKC1 mutations in patients with dyskeratosis congenita: implications for pathophysiology and diagnosisS W Knight, T J Vulliamy, B Morgan, et al.
Pageof 6