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Journal Articles

Real-Time Quantitative PCR (RQ-PCR) Detection of Minimal Residual Disease (MRD) by Optimized WT1 Assay To Enhance Risk Stratification in Acute Myeloid Leukemia (AML): A European LeukemiaNet Study.

Blood (2007) 110 (11): 542.

https://doi.org/10.1182/blood.V110.11.542.542

Published: 2007

Journal Articles

Sensitive Detection of FIP1L1-PDGFRA Fusion Transcripts by Real-Time Quantitative RT-PCR (RQ-PCR) Reveals Achievement of Molecular Remission in Chronic Eosinophilic Leukemia Treated with Low-Dose Imatinib Therapy.

Blood (2005) 106 (11): 483.

https://doi.org/10.1182/blood.V106.11.483.483

Published: 2005

Journal Articles

Consistent amounts of acute leukemia-associated P190BCR/ABL transcripts are expressed by chronic myelogenous leukemia patients at diagnosis

G Saglio, F Pane, E Gottardi, F Frigeri, MR Buonaiuto, A Guerrasio, D de Micheli, A Parziale, MN Fornaci, G Martinelli, F Salvatore

Blood (1996) 87 (3): 1075–1080.

https://doi.org/10.1182/blood.V87.3.1075.bloodjournal8731075

Published: 1996

Journal Articles

Interaction of rare illegitimate recombination event and a poly A addition site mutation resulting in a severe form of alpha thalassemia

P Fortina, T Parrella, M Sartore, E Gottardi, V Gabutti, K Delgrosso, E Mansfield, E Rappaport, E Schwartz, C Camaschella

Blood (1994) 83 (11): 3356–3362.

https://doi.org/10.1182/blood.V83.11.3356.3356

Published: 1994

Journal Articles

Prenatal diagnosis of fetal hemoglobin Lepore-Boston disease on maternal peripheral blood

C Camaschella, A Alfarano, E Gottardi, M Travi, P Primignani, F Caligaris Cappio, G Saglio

Blood (1990) 75 (11): 2102–2106.

https://doi.org/10.1182/blood.V75.11.2102.2102

Published: 1990

Journal Articles

A new hereditary persistence of fetal hemoglobin deletion has the breakpoint within the 3' beta-globin gene enhancer

C Camaschella, A Serra, E Gottardi, A Alfarano, D Revello, U Mazza, G Saglio

Blood (1990) 75 (4): 1000–1005.

https://doi.org/10.1182/blood.V75.4.1000.1000

Published: 1990

Journal Articles

The homozygous state of G to A--117A gamma hereditary persistence of fetal hemoglobin

C Camaschella, L Oggiano, M Sampietro, E Gottardi, A Alfarano, P Pistidda, F Dore, R Taramelli, S Ottolenghi, M Longinotti

Blood (1989) 73 (7): 1999–2002.

https://doi.org/10.1182/blood.V73.7.1999.1999

Published: 1989

NARROW

Real-Time Quantitative PCR (RQ-PCR) Detection of Minimal Residual Disease (MRD) by Optimized WT1 Assay To Enhance Risk Stratification in Acute Myeloid Leukemia (AML): A European LeukemiaNet Study.

Sensitive Detection of FIP1L1-PDGFRA Fusion Transcripts by Real-Time Quantitative RT-PCR (RQ-PCR) Reveals Achievement of Molecular Remission in Chronic Eosinophilic Leukemia Treated with Low-Dose Imatinib Therapy.

Consistent amounts of acute leukemia-associated P190BCR/ABL transcripts are expressed by chronic myelogenous leukemia patients at diagnosis

Interaction of rare illegitimate recombination event and a poly A addition site mutation resulting in a severe form of alpha thalassemia

Prenatal diagnosis of fetal hemoglobin Lepore-Boston disease on maternal peripheral blood

A new hereditary persistence of fetal hemoglobin deletion has the breakpoint within the 3' beta-globin gene enhancer

The homozygous state of G to A--117A gamma hereditary persistence of fetal hemoglobin

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ASH Publications

American Society of Hematology

Real-Time Quantitative PCR (RQ-PCR) Detection of Minimal Residual Disease (MRD) by Optimized WT1 Assay To Enhance Risk Stratification in Acute Myeloid Leukemia (AML): A European LeukemiaNet Study.

Sensitive Detection of FIP1L1-PDGFRA Fusion Transcripts by Real-Time Quantitative RT-PCR (RQ-PCR) Reveals Achievement of Molecular Remission in Chronic Eosinophilic Leukemia Treated with Low-Dose Imatinib Therapy.

Consistent amounts of acute leukemia-associated P190BCR/ABL transcripts are expressed by chronic myelogenous leukemia patients at diagnosis

Interaction of rare illegitimate recombination event and a poly A addition site mutation resulting in a severe form of alpha thalassemia

Prenatal diagnosis of fetal hemoglobin Lepore-Boston disease on maternal peripheral blood

A new hereditary persistence of fetal hemoglobin deletion has the breakpoint within the 3' beta-globin gene enhancer

The homozygous state of G to A--117A gamma hereditary persistence of fetal hemoglobin

Email alerts

ASH Publications

American Society of Hematology

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