J M de Pablos - JoVE Visualize

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Bone Marrow Transplantation|October 1, 1996

Use of rhG-CSF in the collection of peripheral blood stem cells for autologous blood stem cell transplantation in acute myeloblastic leukemiaM Jurado, C Delgado, A Moratalla, et al.

Sangre|June 1, 1990

[Hemoglobin Setif (alpha 94 (G1) Asp----Tyr) in a Spanish family]J M de Pablos, M A de las Nieves, A Romero, et al.

British Journal of Haematology|September 1, 1988

Hb S(C)-beta+-thalassaemia: different mutations are associated with different levels of normal Hb AJ M Gonzalez-Redondo, F Kutlar, A Kutlar, et al.

Cancer Genetics and Cytogenetics|April 1, 1997

Coexistence of tetrasomy 8 and trisomy 8 in a case with myeloid metaplasia with myelofibrosisF Solé, J M de Pablos, S Woessner, et al.

Hemoglobin|January 1, 1995

Hb Anamosa or alpha 2(111)(G18)Ala-->Val beta 2 (alpha 2 mutation) and Hb Mulhacen or alpha 2(123)(H6)Ala-->Ser beta 2 (alpha 1 mutation) are two silent, stable variants detected by sequencing of amplified DNAE G Kazanetz, J Y Leonova, J B Wilson, et al.

Sangre|August 1, 1994

[Frequency of molecular alterations in heterozygous beta-thalassemia in southern Spain and their relation to the hematologic phenotype]M A Molina, M J Romero, E Abril, et al.

Haematologica|February 9, 1999

Adenovirus pneumonitis successfully treated with intravenous ribavirinM Jurado Chacón, F Hernández Mohedo, J M Navarro Marí, et al.

Hemoglobin|September 1, 1994

Hb Fannin-Lubbock in five Spanish families is characterized by two mutations: beta 111 GTC-->CTC (Val-->Leu) and beta 119 GGC-->GAC (Gly-->Asp)W B Qin, D D Pobedimskaya, T P Molchanova, et al.

Blood|May 1, 1990

Hemoglobin Birmingham and hemoglobin Galicia: two unstable beta chain variants characterized by small deletions and insertionsJ B Wilson, B B Webber, H Hu, et al.

Cytometry. Part B, Clinical Cytometry|April 27, 2011

Molecular and flow cytometry characterization during the follow-up of three simultaneous lymphoproliferative disorders: hairy cell leukemia, monoclonal B-cell lymphocytosis, and CD4(++) /CD8(+/- dim) T-large granular lymphocytosis--a case reportP Garrido, P Jiménez, C Sánchez, et al.

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Showing results (1-10 of 11) with videos related to

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Pageof 2

Bone Marrow Transplantation|October 1, 1996

Use of rhG-CSF in the collection of peripheral blood stem cells for autologous blood stem cell transplantation in acute myeloblastic leukemiaM Jurado, C Delgado, A Moratalla, et al.

Sangre|June 1, 1990

[Hemoglobin Setif (alpha 94 (G1) Asp----Tyr) in a Spanish family]J M de Pablos, M A de las Nieves, A Romero, et al.

British Journal of Haematology|September 1, 1988

Hb S(C)-beta+-thalassaemia: different mutations are associated with different levels of normal Hb AJ M Gonzalez-Redondo, F Kutlar, A Kutlar, et al.

Cancer Genetics and Cytogenetics|April 1, 1997

Coexistence of tetrasomy 8 and trisomy 8 in a case with myeloid metaplasia with myelofibrosisF Solé, J M de Pablos, S Woessner, et al.

Hemoglobin|January 1, 1995

Hb Anamosa or alpha 2(111)(G18)Ala-->Val beta 2 (alpha 2 mutation) and Hb Mulhacen or alpha 2(123)(H6)Ala-->Ser beta 2 (alpha 1 mutation) are two silent, stable variants detected by sequencing of amplified DNAE G Kazanetz, J Y Leonova, J B Wilson, et al.

Sangre|August 1, 1994

[Frequency of molecular alterations in heterozygous beta-thalassemia in southern Spain and their relation to the hematologic phenotype]M A Molina, M J Romero, E Abril, et al.

Haematologica|February 9, 1999

Adenovirus pneumonitis successfully treated with intravenous ribavirinM Jurado Chacón, F Hernández Mohedo, J M Navarro Marí, et al.

Hemoglobin|September 1, 1994

Hb Fannin-Lubbock in five Spanish families is characterized by two mutations: beta 111 GTC-->CTC (Val-->Leu) and beta 119 GGC-->GAC (Gly-->Asp)W B Qin, D D Pobedimskaya, T P Molchanova, et al.

Blood|May 1, 1990

Hemoglobin Birmingham and hemoglobin Galicia: two unstable beta chain variants characterized by small deletions and insertionsJ B Wilson, B B Webber, H Hu, et al.

Cytometry. Part B, Clinical Cytometry|April 27, 2011

Molecular and flow cytometry characterization during the follow-up of three simultaneous lymphoproliferative disorders: hairy cell leukemia, monoclonal B-cell lymphocytosis, and CD4(++) /CD8(+/- dim) T-large granular lymphocytosis--a case reportP Garrido, P Jiménez, C Sánchez, et al.

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