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Incidence, Survival, and Treatment of Localized and Metastatic Neuroblastoma in Germany 1979–2015

Paediatric drugs, 2017-12, Vol.19 (6), p.577-593

2017

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Pediatric oncology in pakistan experiences of a visiting "senior expert"

Journal of pediatric hematology/oncology, 2009-07, Vol.31 (7), p.500-501

Lampert, Fritz H

2009

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The Human GRAF Gene Is Fused to MLL in a Unique t(5;11)(q31;q23) and Both Alleles Are Disrupted in Three Cases of Myelodysplastic Syndrome/Acute Myeloid Leukemia with a Deletion 5q

Proceedings of the National Academy of Sciences - PNAS, 2000-08, Vol.97 (16), p.9168-9173

2000

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Three Decades Behind the Iron Curtain, Before and After It was Lifted: Notes of a Visiting Pediatric Oncology “Senior Expert”

Journal of pediatric hematology/oncology, 2009-09, Vol.31 (9), p.621-622

Lampert, Fritz H.

2009

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Gene expression of neuronal nitric oxide synthase and adrenomedullin in human neuroblastoma using real‐time PCR

International journal of cancer, 2000-10, Vol.88 (2), p.172-175

2000

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Incidence and Clinical Relevance of TEL/AML1 Fusion Genes in Children With Acute Lymphoblastic Leukemia Enrolled in the German and Italian Multicenter Therapy Trials

Blood, 1997-07, Vol.90 (2), p.571-577

1997

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Chemotherapy in 998 Unselected Childhood Acute Lymphoblastic Leukemia Patients. Results and Conclusions of the Multicenter Trial ALL-BFM 86

Blood, 1994-11, Vol.84 (9), p.3122-3133

1994

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Philadelphia chromosome-positive (Ph+) childhood acute lymphoblastic leukemia : Good initial steroid response allows early prediction of a favorable treatment outcome

Blood, 1998-10, Vol.92 (8), p.2730-2741

1998

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Revisions of the international criteria for neuroblastoma diagnosis, staging, and response to treatment

Journal of clinical oncology, 1993-08, Vol.11 (8), p.1466-1477

1993

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Cloning and characterization of AFX, the gene that fuses to MLL in acute leukemias with a t(X;11)(q13;q23)

Oncogene, 1997-01, Vol.14 (2), p.195-202

1997

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A DNA damage repair mechanism is involved in the origin of chromosomal translocations t(4;11) in primary leukemic cells

Oncogene, 1999-08, Vol.18 (33), p.4663-4671

1999

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Transcription of hepatitis B virus in peripheral blood mononuclear cells from persistently infected patients

Journal of Virology, 1997-07, Vol.71 (7), p.5399-5407

1997

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A new miracle drug in the Caucasus?

Medical and pediatric oncology, 2003-11, Vol.41 (5), p.452-453

Lampert, Fritz H.

2003

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COMPARATIVE GENOMIC HYBRIDIZATION (CGH) ANALYSIS OF NEUROBLASTOMAS-AN IMPORTANT METHODOLOGICAL APPROACH IN PAEDIATRIC TUMOUR PATHOLOGY

The Journal of pathology, 1997-04, Vol.181 (4), p.394-400

1997

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Annals and chronicles: A new miracle drug in the Caucasus?

Medical and pediatric oncology, 2003-11, Vol.41 (5), p.452-453

LAMPERT, Fritz H

2003

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Donald Pinkel: September 7, 1926

European journal of pediatrics, 1995-07, Vol.154 (7), p.503-503

Lampert, Fritz

1995

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Trisomy 21 is a recurrent secondary aberration in childhood acute lymphoblastic leukemia with TEL/AML1 gene fusion

Genes chromosomes & cancer, 1999-03, Vol.24 (3), p.272-277

1999

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LANGERHANS CELL HISTIOCYTOSIS

Hematology/oncology clinics of North America, 1998, Vol.12 (2), p.213-219

Lampert, Fritz

1998

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Favorable outcome of B-cell acute lymphoblastic leukemia in childhood : a report of three consecutive studies of the BFM group

Blood, 1992-11, Vol.80 (10), p.2471-2478

1992

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Brief report: inherited metabolic myopathy and hemolysis due to a mutation in aldolase A

The New England journal of medicine, 1996-04, Vol.334 (17), p.1100-1104

1996

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Detection of four different 11q23 chromosomal abnormalities by multiplex-PCR and fluorescence-based automatic DNA-fragment analysis

Leukemia, 1995-01, Vol.9 (1), p.210-215

1995

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Detection of fms-oncogene-specific tyrosine kinase activity in human leukemia cells

Journal of cancer research and clinical oncology, 1989-06, Vol.115 (3), p.235-241

1989

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Biology and clinical significance of the TEL/AML1 rearrangement

Current opinion in pediatrics, 1999-02, Vol.11 (1), p.33-38

1999

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Quantitative DNA Fragment Analysis for Detecting Low Amounts of Hepatitis B Virus Deletion Mutants in Highly Viremic Carriers

Hepatology (Baltimore, Md.), 2000-11, Vol.32 (5), p.1096-1105

2000

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Biology and clinical significance of the TEL/AML 1 rearrangement

Current opinion in pediatrics, 1999-02, Vol.11 (1), p.33

1999

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Incidence, Survival, and Treatment of Localized and Metastatic Neuroblastoma in Germany 1979–2015

Pediatric oncology in pakistan experiences of a visiting "senior expert"

The Human GRAF Gene Is Fused to MLL in a Unique t(5;11)(q31;q23) and Both Alleles Are Disrupted in Three Cases of Myelodysplastic Syndrome/Acute Myeloid Leukemia with a Deletion 5q

Three Decades Behind the Iron Curtain, Before and After It was Lifted: Notes of a Visiting Pediatric Oncology “Senior Expert”

Gene expression of neuronal nitric oxide synthase and adrenomedullin in human neuroblastoma using real‐time PCR

Incidence and Clinical Relevance of TEL/AML1 Fusion Genes in Children With Acute Lymphoblastic Leukemia Enrolled in the German and Italian Multicenter Therapy Trials

Chemotherapy in 998 Unselected Childhood Acute Lymphoblastic Leukemia Patients. Results and Conclusions of the Multicenter Trial ALL-BFM 86

Philadelphia chromosome-positive (Ph+) childhood acute lymphoblastic leukemia : Good initial steroid response allows early prediction of a favorable treatment outcome

Revisions of the international criteria for neuroblastoma diagnosis, staging, and response to treatment

Cloning and characterization of AFX, the gene that fuses to MLL in acute leukemias with a t(X;11)(q13;q23)

A DNA damage repair mechanism is involved in the origin of chromosomal translocations t(4;11) in primary leukemic cells

Transcription of hepatitis B virus in peripheral blood mononuclear cells from persistently infected patients

A new miracle drug in the Caucasus?

COMPARATIVE GENOMIC HYBRIDIZATION (CGH) ANALYSIS OF NEUROBLASTOMAS-AN IMPORTANT METHODOLOGICAL APPROACH IN PAEDIATRIC TUMOUR PATHOLOGY

Annals and chronicles: A new miracle drug in the Caucasus?

Donald Pinkel: September 7, 1926

Trisomy 21 is a recurrent secondary aberration in childhood acute lymphoblastic leukemia with TEL/AML1 gene fusion

LANGERHANS CELL HISTIOCYTOSIS

Favorable outcome of B-cell acute lymphoblastic leukemia in childhood : a report of three consecutive studies of the BFM group

Brief report: inherited metabolic myopathy and hemolysis due to a mutation in aldolase A

Detection of four different 11q23 chromosomal abnormalities by multiplex-PCR and fluorescence-based automatic DNA-fragment analysis

Detection of fms-oncogene-specific tyrosine kinase activity in human leukemia cells

Biology and clinical significance of the TEL/AML1 rearrangement

Quantitative DNA Fragment Analysis for Detecting Low Amounts of Hepatitis B Virus Deletion Mutants in Highly Viremic Carriers

Biology and clinical significance of the TEL/AML 1 rearrangement

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