G. Borgström

发表

Culture of bone marrow reveals more cells with chromosomal abnormalities than the direct method in patients with hematologic disorders.

A. de la Chapelle, S. Knuutila, M. Siimes, 1981, Blood.

Outcome of ETV6/RUNX1‐positive childhood acute lymphoblastic leukaemia in the NOPHO‐ALL‐1992 protocol: frequent late relapses but good overall survival

B. Johansson, A. Nordgren, E. Blennow, 2008, British journal of haematology.

High incidence of the ETV6/RUNX1 fusion gene in paediatric precursor B‐cell acute lymphoblastic leukaemias with trisomy 21 as the sole cytogenetic change: a Nordic series of cases diagnosed 1989–2005

B. Johansson, M. Andersen, R. Hovland, 2006, British journal of haematology.

Clinical and cytogenetic features of a population‐based consecutive series of 285 pediatric T‐cell acute lymphoblastic leukemias: Rare T‐cell receptor gene rearrangements are associated with poor outcome

B. Johansson, A. Nordgren, E. Blennow, 2009, Genes, chromosomes & cancer.

Clodronate for osteolytic metastases due to breast cancer.

C. Blomqvist, C. Lamberg-Allardt, I. Elomaa, 1988, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.

DIPHOSPHONATES FOR OSTEOLYTIC METASTASES

C. Blomqvist, I. Elomaa, G. Borgström, 1985, The Lancet.

Paediatric B‐cell precursor acute lymphoblastic leukaemia with t(1;19)(q23;p13): clinical and cytogenetic characteristics of 47 cases from the Nordic countries treated according to NOPHO protocols

B. Johansson, A. Nordgren, L. Cavelier, 2011, British journal of haematology.

Cytogenetic abnormalities in childhood acute myeloid leukaemia: a Nordic series comprising all children enrolled in the NOPHO‐93‐AML trial between 1993 and 2001

B. Johansson, A. Nordgren, E. Blennow, 2003, British journal of haematology.

Platelet function in preleukaemia.

E. Ikkala, V. Rasi, P. Vuopio, 2009, Scandinavian journal of haematology.

Cytogenetics of the myelodysplastic syndromes.

G. Borgström, 2009, Scandinavian journal of haematology. Supplementum.

Abnormalities of chromosome No. 17 in myeloproliferative disorders.

A. de la Chapelle, P. Vuopio, G. Borgström, 1982, Cancer genetics and cytogenetics.

Cytogenetic findings in a population‐based series of 787 childhood acute lymphoblastic leukemias from the Nordic countries

B. Johansson, S. Heim, G. Borgström, 2000, European journal of haematology.

Additional aberrations of the ETV6 and RUNX1 genes have no prognostic impact in 229 t(12;21)(p13;q22)-positive B-cell precursor acute lymphoblastic leukaemias treated according to the NOPHO-ALL-2000 protocol.

B. Johansson, A. Nordgren, E. Kjeldsen, 2012, Leukemia research.

Treatment of skeletal disease in breast cancer: a controlled clodronate trial.

C. Blomqvist, C. Lamberg-Allardt, I. Elomaa, 1987, Bone.

High modal number and triple trisomies are highly correlated favorable factors in childhood B-cell precursor high hyperdiploid acute lymphoblastic leukemia treated according to the NOPHO ALL 1992/2000 protocols

B. Johansson, A. Nordgren, L. Cavelier, 2013, Haematologica.

The origin of bone marrow fibroblasts.

A. de la Chapelle, P. Vuopio, G. Borgström, 1973, Blood.

A method for simultaneous study of the karyotype, morphology, and immunologic phenotype of mitotic cells in hematologic malignancies.

A. de la Chapelle, S. Knuutila, L. Andersson, 1984, Blood.

Massive cutaneous hyalinosis. A newly recognized disease.

J. Viikari, G. Borgström, S. Stenman, 1980, Archives of dermatology.

Change in cellular phenotype from lymphoid to erythroid in a case of ALL.

C. Gahmberg, L. Andersson, G. Borgström, 2009 .

A case of pure monocytic leukaemia in a child - characterization of cellular morphology, membrane markers, surface glycoproteins and karyotype.

C. Gahmberg, L. Andersson, G. Borgström, 2009, Scandinavian journal of haematology.

Chromosomes in leukemia

A. Chapelle, F. Mitelman, J. Lindsten, 1977 .

Higher frequency of 51--clone in bone marrow mitoses after culture than by a direct method.

A. de la Chapelle, S. Knuutila, P. Vuopio, 2009, Scandinavian journal of haematology.

Chromosomal abnormalities identify high-risk and low-risk patients with acute lymphoblastic leukemia.

Walker, C. Bloomfield, A. de la Chapelle, 1986, Blood.

Clinical and cytogenetic features of pediatric dic(9;20)(p13.2;q11.2)‐positive B‐cell precursor acute lymphoblastic leukemias: A nordic series of 24 cases and review of the literature

B. Johansson, A. Nordgren, R. Rosenquist, 2008, Genes, chromosomes & cancer.

Clinical and Cytogenetic Features of Pediatric dic ( 9 ; 20 ) ( p 13 . 2 ; q 11 . 2 )-Positive B-Cell Precursor Acute Lymphoblastic Leukemias : A Nordic Series of 24 Cases and Review of the Literature

B. Johansson, R. Rosenquist, M. Andersen, 2007 .

Haem biosynthesis in refractory sideroblastic anaemia associated with the preleukaemic syndrome.

P. Vuopio, G. Borgström, R. Tenhunen, 2009, Scandinavian journal of haematology.

Chromosome abnormalities in 16 Finnish patients with Burkitt's lymphoma or L3 acute lymphocytic leukemia.

K. Franssila, S. Knuutila, E. Elonen, 1984, Cancer genetics and cytogenetics.

Abnormalities of chromosome 13 in myelofibrosis.

A. Chapelle, A. de la Chapelle, S. Knuutila, 2009, Scandinavian journal of haematology.

Chromosome instability is associated with hypodiploid clones in myelodysplastic syndromes.

S. Knuutila, G. Borgström, L. Teerenhovi, 2008, Hereditas.

Erythroid blast crisis in chronic myelogenous leukemia

C. Gahmberg, L. Andersson, P. Vuopio, 1983 .

Erythroid blast crisis in chronic myelogenous leukemia.

C. Gahmberg, L. Andersson, P. Vuopio, 1983, Blood.

UNEVEN GEOGRAPHICAL DISTRIBUTION OF 15;17-TRANSLOCATION IN ACUTE PROMYELOCYTIC LEUKÆMIA

A. Chapelle, F. Mitelman, T. Timonen, 1978, The Lancet.

Clinical implications of monosomy 7 in acute nonlymphocytic leukemia

A. Chapelle, J. Rowley, F. Mitelman, 1980 .

Polyploidy of the bone marrow.

A. Chapelle, A. de la Chapelle, P. Vuopio, 2009 .

New types of unusual and complex Philadelphia chromosome (Ph1) translocations in chronic myeloid leukemia.

G. Borgström, Georg H. Borgström, 1981, Cancer genetics and cytogenetics.

Clinical significance of the del(20q) chromosome in hematologic disorders.

G. Borgström, L. Teerenhovi, E. Armstrong, 1992, Cancer genetics and cytogenetics.

9 CHANGE IN CELLULAR PHENOTYPE FROM LYMPHOID TO ERYTHROID IN A CASE OF ALL

C. Gahmberg, L. Andersson, G. Borgström, 1979, Pediatric Research.

Chromosome studies in acute lymphoblastic leukaemia (ALL).

A. de la Chapelle, S. Knuutila, L. Andersson, 2009, Scandinavian journal of haematology.

Prognostic impact of karyotypic findings in childhood acute lymphoblastic leukaemia: a Nordic series comparing two treatment periods

B. Johansson, G. Gustafsson, S. Heim, 2000, British journal of haematology.

Cytogenetic patterns in ETV6/RUNX1‐positive pediatric B‐cell precursor acute lymphoblastic leukemia: A Nordic series of 245 cases and review of the literature

B. Johansson, A. Nordgren, E. Blennow, 2007, Genes, chromosomes & cancer.

The 5q- chromosome in preleukaemia and acute leukaemia.

A. Chapelle, A. de la Chapelle, P. Vuopio, 2009, Scandinavian journal of haematology.

Familial pericentric inversion (3)(p12q24)

G. Borgström, Laura Lindberg, Kia Pelto, 1992, Human Genetics.

Cytogenetic investigations of patients on clodronate therapy for Paget's disease of bone.

C. Blomqvist, I. Elomaa, G. Borgström, 1987, Bone.