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Carcinoid tumors frequently display genetic abnormalities involving chromosome 11

The journal of clinical endocrinology and metabolism, 1996-09, Vol.81 (9), p.3164-3167

1996

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Increased levels of homocysteine in patients with Crohn's disease are related to folate levels

The American journal of gastroenterology, 2000-12, Vol.95 (12), p.3498-3502

2000

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

Leukemia, 2002-08, Vol.16 (8), p.1413-1418

2002

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

Clinical and experimental immunology, 2002-04, Vol.128 (1), p.59-66

2002

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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

American journal of hematology, 2005-03, Vol.78 (3), p.203-206

2005

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Activation of human monocytes/macrophages by hypo‐osmotic shock

Clinical and experimental immunology, 2001-04, Vol.124 (1), p.103-109

2001

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

Bone marrow transplantation (Basingstoke), 2001-02, Vol.27 (3), p.311-317

2001

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Instability of dinucleotide repeats in Hodgkin's disease

American journal of hematology, 1998-02, Vol.57 (2), p.148-152

1998

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A gene mutated in X-linked myotubular myopathy defines a new putative tyrosine phosphatase family conserved in yeast

Nature genetics, 1996-06, Vol.13 (2), p.175-182

1996

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

Bone marrow transplantation (Basingstoke), 1999-02, Vol.23 (4), p.405-408

1999

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Congenital haemolytic anaemia associated with adenylate kinase deficiency

British journal of haematology, 1994-06, Vol.87 (2), p.376-380

1994

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Erythrocyte glutathione and tumour response to chemotherapy

The Lancet (British edition), 1992-05, Vol.339 (8801), p.1074-1076

1992

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

Leukemia, 1995-11, Vol.9 (11), p.1974-1978

1995

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

Arteriosclerosis, thrombosis, and vascular biology, 1999-08, Vol.19 (8), p.2017-2023

1999

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

British journal of haematology, 1995-12, Vol.91 (4), p.915-917

1995

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GLI3 is not mutated commonly in sporadic medulloblastomas

Cancer, 2002-07, Vol.95 (1), p.28-31

2002

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

Leukemia, 1989, Vol.3 (1), p.57-60

1989

Volltextzugriff (PDF)

Genetic Linkage of Autosomal-Dominant Alport Syndrome with Leukocyte Inclusions and Macrothrombocytopenia (Fechtner Syndrome) to Chromosome 22q11-13

American journal of human genetics, 1999-12, Vol.65 (6), p.1711-1717

1999

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

American journal of hematology, 2003-12, Vol.74 (4), p.254-262

2003

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Lymphomatous T-cell leukemia in two Arab children. Is there a role for an environmental effect ?

Leukemia, 1994-11, Vol.8 (11), p.1995-1998

1994

Volltextzugriff (PDF)

IN VITRO RESTORATION BY LITHIUM OF DEFECTIVE CHEMOTAXIS IN SHWACHMAN‐DIAMOND SYNDROME

British journal of haematology, 1988-12, Vol.70 (4), p.502-503

1988

Volltextzugriff (PDF)

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

Acta haematologica, 1994, Vol.91 (2), p.103-105

1994

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Reduced Expression of Plakoglobin Correlates with Adverse Outcome in Patients with Neuroblastoma

The American journal of pathology, 2001-07, Vol.159 (1), p.43-49

2001

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

Acta haematologica, 1994, Vol.92 (4), p.208-211

1994

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

Leukemia, 1988-06, Vol.2 (6), p.347-350

1988

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Carcinoid tumors frequently display genetic abnormalities involving chromosome 11

Increased levels of homocysteine in patients with Crohn's disease are related to folate levels

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

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

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

Activation of human monocytes/macrophages by hypo‐osmotic shock

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

Instability of dinucleotide repeats in Hodgkin's disease

A gene mutated in X-linked myotubular myopathy defines a new putative tyrosine phosphatase family conserved in yeast

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

Congenital haemolytic anaemia associated with adenylate kinase deficiency

Erythrocyte glutathione and tumour response to chemotherapy

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

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

GLI3 is not mutated commonly in sporadic medulloblastomas

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

Genetic Linkage of Autosomal-Dominant Alport Syndrome with Leukocyte Inclusions and Macrothrombocytopenia (Fechtner Syndrome) to Chromosome 22q11-13

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

Lymphomatous T-cell leukemia in two Arab children. Is there a role for an environmental effect ?

IN VITRO RESTORATION BY LITHIUM OF DEFECTIVE CHEMOTAXIS IN SHWACHMAN‐DIAMOND SYNDROME

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

Reduced Expression of Plakoglobin Correlates with Adverse Outcome in Patients with Neuroblastoma

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

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

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