Lista de obras -

A family with red cell pyrimidine 5'-nucleotidase deficiency ⬇️

artículo científico publicado el 1 de junio de 1976

A search for bcl1, bcl2, and c-myc oncogene rearrangements in chronic lymphocytic leukemia

scientific article published on 01 January 1989

Absence of p53 mutations in malignant mesotheliomas

artículo científico publicado en 1997

Activated macrophages for treating skin ulceration: gene expression in human monocytes after hypo-osmotic shock.

artículo científico publicado en 2002

Activation of human monocytes/macrophages by hypo-osmotic shock

artículo científico publicado en 2001

Acute lymphoblastic leukemia subtypes in Israel: the Sheba medical center experience

artículo científico publicado en 1982

Adenosine deaminase (ADA) activity in lymphocytes of normal individuals and patients with chronic lymphatic leukaemia

artículo científico publicado el 1 de mayo de 1977

Advances in reverse genetics: jump, don't run

artículo científico publicado el 15 de enero de 1992

Amplification of immunological functions by subcutaneous injection of intermediate-high dose interleukin-2 for 2 years after autologous stem cell transplantation in children with stage IV neuroblastoma

artículo científico publicado en 2000

Analysis of microsatellite repeats in pediatric brain tumors.

artículo científico publicado en 1995

Analysis of rearranged immunoglobulin genes indicating a process of clonal evolution in chronic lymphocytic leukaemia

scientific article published on 01 July 1993

Aplastic crisis due to human B19 parvovirus infection in red cell pyrimidine-5'-nucleotidase deficiency

artículo científico publicado en 1989

Artifactual p53 point mutations: possible effect of gene secondary structure on PCR and direct sequence analysis

artículo científico publicado el 14 de noviembre de 1992

Assessment of the response to imatinib in chronic myeloid leukemia patients--comparison between the FISH, multiplex and RT-PCR methods.

artículo científico publicado en 2004

Autosomal-dominant giant platelet syndromes: a hint of the same genetic defect as in Fechtner syndrome owing to a similar genetic linkage to chromosome 22q11-13.

artículo científico publicado en 2000

Biased representation of immunoglobulin heavy chain variable region subgroups in chronic lymphocytic leukemia.

artículo científico publicado en 1994

Blood leucocyte enzymes. II. Activities at 8-9 a.m. in cells of normal subjects, chronic lymphatic leukaemia and chronic myeloid leukaemia patients

artículo científico publicado el 1 de febrero de 1975

Blood leucocyte enzymes. III. Diurnal rhythm of activity in isolated lymphocytes of normal subjects and chronic lymphatic leukaemia patients

artículo científico publicado en 1976

Bone marrow cell populations mimicking common acute lymphoblastic leukemia in infants with stage IV-S neuroblastoma

scientific article published on 01 January 1991

CD10+ cell population in the bone marrow of patients with advanced neuroblastoma

scientific article published on 01 January 1994

Central nervous system involvement at diagnosis in a case of pediatric CD30+ anaplastic large cell lymphoma

artículo científico publicado en 1997

Chimerism testing and detection of minimal residual disease after allogeneic hematopoietic transplantation using the bioView (Duet) combined morphological and cytogenetical analysis

artículo científico publicado en 2002

Chronic lymphocytic leukaemia in twin sisters: monozygous but not identical

scientific article published on 01 February 1987

Clinical and epidemiological observations on acute lymphoblastic leukemia subtypes at the Sheba Medical Center, Israel.

artículo científico publicado en 1983

Coexistence of several unbalanced translocations in a case of neuroblastoma: the contribution of multicolor spectral karyotyping

artículo científico

Coinheritance of BRCA1 and BRCA2 mutations with Fanconi anemia and Bloom syndrome mutations in Ashkenazi Jewish population: possible role in risk modification for cancer development.

artículo científico publicado en 2005

Complement-sensitive red cells in aplastic anemia ⬇️

artículo científico publicado el 1 de septiembre de 1975

Congenital haemolytic anaemia associated with adenylate kinase deficiency

scientific article published on 01 June 1994

Congenital inclusion body hemolytic anemia: study of a family

artículo científico

Contribution of fragiligrams to the differential diagnosis of thalessemia and iron deficiency anemia

scientific article published on 01 January 1970

Demonstration of Thymopoietin Transcripts in Different Hematopoietic Cell Lines ⬇️

artículo científico publicado el 1 de enero de 1995

Detection and clinical relevance of genetic abnormalities in pediatric acute lymphoblastic leukemia: a comparison between cytogenetic and polymerase chain reaction analyses.

artículo científico publicado en 1993

Detection of adeno-associated virus type 2 in human peripheral blood cells

artículo científico publicado el 1 de abril de 1992

Detection of unidentified chromosome abnormalities in human neuroblastoma by spectral karyotyping (SKY).

artículo científico

EBV genome and immunoglobulin gene rearrangement in the differential diagnosis of nasopharyngeal carcinoma and lymphoma

artículo científico publicado en 1991

Engraftment-associated hypophosphatemia--the role of cytokine release and steep leukocyte rise post stem cell transplantation

scientific article published on 01 February 2001

Enzyme activities in human red blood cells of different age groups

artículo científico publicado en 1966

Erythrocyte glutathione and tumour response to chemotherapy

artículo científico publicado el 2 de mayo de 1992

Familial leukemia: description of two kindreds and a review of the genetic aspects of the disease

artículo científico publicado en 1994

Fast-FISH detection and semi-automated image analysis of numerical chromosome aberrations in hematological malignancies.

artículo científico publicado en 1998

GLI3 is not mutated commonly in sporadic medulloblastomas.

artículo científico publicado en 2002

Genetic linkage of autosomal-dominant Alport syndrome with leukocyte inclusions and macrothrombocytopenia (Fechtner syndrome) to chromosome 22q11-13

artículo científico publicado en 1999

Glucose 6-phosphate dehydrogenase, hexokinase activities and ATP levels as a function of cell density in thalassemia and iron deficiency anemia

scientific article published on 01 November 1969

Glucose phosphate isomerase deficiency with congenital nonspherocytic hemolytic anemia

artículo científico publicado en 1994

Hexasomy of chromosome 8 and trisomy of chromosome 11 characterize two karyotypically independent clones in a case of acute non-lymphocytic leukemia. Conventional cytogenetic and FISH investigation.

artículo científico publicado en 1995

High prevalences of vitamin B12 and folic acid deficiency in elderly subjects in Israel ⬇️

artículo científico publicado el 1 de noviembre de 2003

Identity of rearranged LINE/c-MYC junction sequences specific for the canine transmissible venereal tumor ⬇️

artículo científico publicado el 15 de septiembre de 1991

Immunoglobulin VH3-positive AIDS-related Burkitt's lymphoma: a possible role for the HIV gp120 superantigen

artículo científico publicado en 1994

Immunoglobulin heavy chain gene rearrangements in chronic lymphocytic leukaemia: correlation with clinical stage

artículo científico publicado en 1989

In vitro proliferative advantage of bone marrow cells with tetrasomy 8 in Ewing sarcoma

artículo científico publicado en 1996

In vivo clonal evolution of pre-B to B-cell acute lymphoblastic leukemia in childhood

artículo científico publicado en 1994

Instability of dinucleotide repeats in Hodgkin's disease.

artículo científico publicado en 1998

Interphase fluorescence in situ hybridization detection of chromosome 17 and 17q region gains in neuroblastoma: are they secondary events?

scientific article published on 01 September 2002

Lack of N-myc-amplification and normal karyotype in stage IV-N neuroblastoma

artículo científico publicado en 1996

Lack ofbcr rearrangement in juvenile chronic myeloid leukemia ⬇️

artículo científico publicado el 1 de enero de 1991

MAP kinase activation by mu opioid receptor in cord blood CD34(+)CD38(-) cells

artículo científico publicado en 2002

MYH9 spectrum of autosomal-dominant giant platelet syndromes: Unexpected association with fibulin-1 variant-D inactivation

artículo científico publicado en 2003

Molecular analysis of Burkitt's leukemia in two hemophilic brothers with AIDS.

artículo científico publicado en 1987

More than two immunoglobulin heavy chain J region genes in the majority of infant leukemia

scientific article published on 01 June 1988

Mutation analysis of the FAS and TNFR apoptotic cascade genes in hematological malignancies.

artículo científico publicado en 2001

Nuclear membrane protein LAP2beta mediates transcriptional repression alone and together with its binding partner GCL (germ-cell-less)

scientific journal article

Nucleoside phosphorylase activity in normal and leukemic cells

artículo científico publicado en 1981

Oxygen Delivery at Marathon ⬇️

artículo científico publicado el 28 de junio de 1973

PGI*3(Israel), a new, unstable allele in the phosphoglucose isomerase system

scientific article published on 01 September 1987

Paroxysmal nocturnal hemoglobinuria. Diagnosis by acetylcholinesterase and Ham's test in different cell populations

artículo científico publicado el 1 de enero de 1976

Pediatric small cell variant of Ki-1 (CD30) + T-cell lymphoma with germ-line configuration of the T-cell receptor gene

scientific article published on 01 January 1996

Philadelphia-chromosome-positive T-lymphoblastic leukemia: acute leukemia or chronic myelogenous leukemia blastic crisis

artículo científico publicado en 2005

Phosphofructokinase deficiency (Tarui disease) associated with hepatic glucuronyltransferase deficiency (Gilbert's syndrome): a case and family study

artículo científico publicado en 1990

Plasma glutathione peroxidase deficiency and platelet insensitivity to nitric oxide in children with familial stroke

artículo científico publicado en 1999

Preferred usage of specific immunoglobulin gene segments in chronic lymphocytic leukaemia cells of three HLA-identical sisters

artículo científico publicado en 1995

Primary central nervous system Burkitt's lymphoma presenting as Guillain-Barré syndrome

artículo científico publicado en 1994

Rearrangement of the immunoglobulin heavy chain gene in juvenile chronic myeloid leukaemia

scientific article published on 01 June 1995

Reduced expression of plakoglobin correlates with adverse outcome in patients with neuroblastoma.

artículo científico publicado en 2001

Spontaneous regression of congenital leukaemia with an 8;16 translocation

artículo científico publicado en 2000

Spurious haemoglobinopathy

artículo científico publicado en 1986

Standardization criteria for the detection of BCR/ABL fusion in interphase nuclei of chronic myelogenous leukemia patients by fluorescence in situ hybridization

artículo científico publicado en 2000

Subgroup of patients with Philadelphia-positive chronic myelogenous leukemia characterized by a deletion of 9q proximal to ABL gene: expression profiling, resistance to interferon therapy, and poor prognosis.

artículo científico publicado en 2001

Successful human umbilical cord blood stem cell transplantation without conditioning in severe combined immune deficiency

scientific article published on 01 February 1999

The characterization and localization of the mouse thymopoietin/lamina-associated polypeptide 2 gene and its alternatively spliced products

artículo científico publicado en 1996

The diurnal rhythm of enzymes in human red cells

artículo científico publicado en 1976

Transformation of chronic lymphocytic leukemia to multiple myeloma: clonal evolution of second malignancy?

scientific article published on 01 November 1995

Translocation t(2;8) in AIDS-associated Burkitt leukemia

scientific article published on 01 March 1989

Viral hepatitis with extreme hyperbilirubinemia, massive hemolysis and encephalopathy in a patient with a new G6PD variant

artículo científico publicado en 1980

Lista de obras de

A family with red cell pyrimidine 5'-nucleotidase deficiency ⬇️

A search for bcl1, bcl2, and c-myc oncogene rearrangements in chronic lymphocytic leukemia

Absence of p53 mutations in malignant mesotheliomas

Activated macrophages for treating skin ulceration: gene expression in human monocytes after hypo-osmotic shock.

Activation of human monocytes/macrophages by hypo-osmotic shock

Acute lymphoblastic leukemia subtypes in Israel: the Sheba medical center experience

Adenosine deaminase (ADA) activity in lymphocytes of normal individuals and patients with chronic lymphatic leukaemia

Advances in reverse genetics: jump, don't run

Amplification of immunological functions by subcutaneous injection of intermediate-high dose interleukin-2 for 2 years after autologous stem cell transplantation in children with stage IV neuroblastoma

Analysis of microsatellite repeats in pediatric brain tumors.

Analysis of rearranged immunoglobulin genes indicating a process of clonal evolution in chronic lymphocytic leukaemia

Aplastic crisis due to human B19 parvovirus infection in red cell pyrimidine-5'-nucleotidase deficiency

Artifactual p53 point mutations: possible effect of gene secondary structure on PCR and direct sequence analysis

Assessment of the response to imatinib in chronic myeloid leukemia patients--comparison between the FISH, multiplex and RT-PCR methods.

Autosomal-dominant giant platelet syndromes: a hint of the same genetic defect as in Fechtner syndrome owing to a similar genetic linkage to chromosome 22q11-13.

Biased representation of immunoglobulin heavy chain variable region subgroups in chronic lymphocytic leukemia.

Blood leucocyte enzymes. II. Activities at 8-9 a.m. in cells of normal subjects, chronic lymphatic leukaemia and chronic myeloid leukaemia patients

Blood leucocyte enzymes. III. Diurnal rhythm of activity in isolated lymphocytes of normal subjects and chronic lymphatic leukaemia patients

Bone marrow cell populations mimicking common acute lymphoblastic leukemia in infants with stage IV-S neuroblastoma

CD10+ cell population in the bone marrow of patients with advanced neuroblastoma

Central nervous system involvement at diagnosis in a case of pediatric CD30+ anaplastic large cell lymphoma

Chimerism testing and detection of minimal residual disease after allogeneic hematopoietic transplantation using the bioView (Duet) combined morphological and cytogenetical analysis

Chronic lymphocytic leukaemia in twin sisters: monozygous but not identical

Clinical and epidemiological observations on acute lymphoblastic leukemia subtypes at the Sheba Medical Center, Israel.

Coexistence of several unbalanced translocations in a case of neuroblastoma: the contribution of multicolor spectral karyotyping

Coinheritance of BRCA1 and BRCA2 mutations with Fanconi anemia and Bloom syndrome mutations in Ashkenazi Jewish population: possible role in risk modification for cancer development.

Complement-sensitive red cells in aplastic anemia ⬇️

Congenital haemolytic anaemia associated with adenylate kinase deficiency

Congenital inclusion body hemolytic anemia: study of a family

Contribution of fragiligrams to the differential diagnosis of thalessemia and iron deficiency anemia

Demonstration of Thymopoietin Transcripts in Different Hematopoietic Cell Lines ⬇️

Detection and clinical relevance of genetic abnormalities in pediatric acute lymphoblastic leukemia: a comparison between cytogenetic and polymerase chain reaction analyses.

Detection of adeno-associated virus type 2 in human peripheral blood cells

Detection of unidentified chromosome abnormalities in human neuroblastoma by spectral karyotyping (SKY).

EBV genome and immunoglobulin gene rearrangement in the differential diagnosis of nasopharyngeal carcinoma and lymphoma

Engraftment-associated hypophosphatemia--the role of cytokine release and steep leukocyte rise post stem cell transplantation

Enzyme activities in human red blood cells of different age groups

Erythrocyte glutathione and tumour response to chemotherapy

Familial leukemia: description of two kindreds and a review of the genetic aspects of the disease

Fast-FISH detection and semi-automated image analysis of numerical chromosome aberrations in hematological malignancies.

GLI3 is not mutated commonly in sporadic medulloblastomas.

Genetic linkage of autosomal-dominant Alport syndrome with leukocyte inclusions and macrothrombocytopenia (Fechtner syndrome) to chromosome 22q11-13

Glucose 6-phosphate dehydrogenase, hexokinase activities and ATP levels as a function of cell density in thalassemia and iron deficiency anemia

Glucose phosphate isomerase deficiency with congenital nonspherocytic hemolytic anemia

Hexasomy of chromosome 8 and trisomy of chromosome 11 characterize two karyotypically independent clones in a case of acute non-lymphocytic leukemia. Conventional cytogenetic and FISH investigation.

High prevalences of vitamin B12 and folic acid deficiency in elderly subjects in Israel ⬇️

Identity of rearranged LINE/c-MYC junction sequences specific for the canine transmissible venereal tumor ⬇️

Immunoglobulin VH3-positive AIDS-related Burkitt's lymphoma: a possible role for the HIV gp120 superantigen

Immunoglobulin heavy chain gene rearrangements in chronic lymphocytic leukaemia: correlation with clinical stage

In vitro proliferative advantage of bone marrow cells with tetrasomy 8 in Ewing sarcoma

In vivo clonal evolution of pre-B to B-cell acute lymphoblastic leukemia in childhood

Instability of dinucleotide repeats in Hodgkin's disease.

Interphase fluorescence in situ hybridization detection of chromosome 17 and 17q region gains in neuroblastoma: are they secondary events?

Lack of N-myc-amplification and normal karyotype in stage IV-N neuroblastoma

Lack ofbcr rearrangement in juvenile chronic myeloid leukemia ⬇️

MAP kinase activation by mu opioid receptor in cord blood CD34(+)CD38(-) cells

MYH9 spectrum of autosomal-dominant giant platelet syndromes: Unexpected association with fibulin-1 variant-D inactivation

Molecular analysis of Burkitt's leukemia in two hemophilic brothers with AIDS.

More than two immunoglobulin heavy chain J region genes in the majority of infant leukemia

Mutation analysis of the FAS and TNFR apoptotic cascade genes in hematological malignancies.

Nuclear membrane protein LAP2beta mediates transcriptional repression alone and together with its binding partner GCL (germ-cell-less)

Nucleoside phosphorylase activity in normal and leukemic cells

Oxygen Delivery at Marathon ⬇️

PGI*3(Israel), a new, unstable allele in the phosphoglucose isomerase system

Paroxysmal nocturnal hemoglobinuria. Diagnosis by acetylcholinesterase and Ham's test in different cell populations

Pediatric small cell variant of Ki-1 (CD30) + T-cell lymphoma with germ-line configuration of the T-cell receptor gene

Philadelphia-chromosome-positive T-lymphoblastic leukemia: acute leukemia or chronic myelogenous leukemia blastic crisis

Phosphofructokinase deficiency (Tarui disease) associated with hepatic glucuronyltransferase deficiency (Gilbert's syndrome): a case and family study

Plasma glutathione peroxidase deficiency and platelet insensitivity to nitric oxide in children with familial stroke

Preferred usage of specific immunoglobulin gene segments in chronic lymphocytic leukaemia cells of three HLA-identical sisters

Primary central nervous system Burkitt's lymphoma presenting as Guillain-Barré syndrome

Rearrangement of the immunoglobulin heavy chain gene in juvenile chronic myeloid leukaemia

Reduced expression of plakoglobin correlates with adverse outcome in patients with neuroblastoma.

Spontaneous regression of congenital leukaemia with an 8;16 translocation

Spurious haemoglobinopathy

Standardization criteria for the detection of BCR/ABL fusion in interphase nuclei of chronic myelogenous leukemia patients by fluorescence in situ hybridization

Subgroup of patients with Philadelphia-positive chronic myelogenous leukemia characterized by a deletion of 9q proximal to ABL gene: expression profiling, resistance to interferon therapy, and poor prognosis.

Successful human umbilical cord blood stem cell transplantation without conditioning in severe combined immune deficiency

The characterization and localization of the mouse thymopoietin/lamina-associated polypeptide 2 gene and its alternatively spliced products