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Circulating Breast Cancer Cells Are Frequently Apoptotic

The American journal of pathology, 2001-07, Vol.159 (1), p.17-20

2001

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Combined Automatic Immunological and Molecular Cytogenetic Analysis Allows Exact Identification and Quantification of Tumor Cells in the Bone Marrow

Clinical cancer research, 2001-07, Vol.7 (7), p.1969-1975

2001

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Solid and papillary epithelial neoplasm arising in heterotopic pancreatic tissue of the mesocolon

Journal of clinical pathology, 2001-03, Vol.54 (3), p.241-245

2001

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In situ fluorescent visualization of nucleolar organizer region- associated proteins with a thiol reagent

The journal of histochemistry and cytochemistry, 1993-09, Vol.41 (9), p.1413-1417

1993

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Detection of Disseminated Tumor Cells in Neuroblastoma: 3 Log Improvement in Sensitivity by Automatic Immunofluorescence plus FISH (AIPF) Analysis Compared with Classical Bone Marrow Cytology

The American journal of pathology, 2003-08, Vol.163 (2), p.393-399

2003

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Phenotypic and genotypic analyses of blastic cell population suggest that pure B-lymphoblastic leukemia may arise from myelodysplastic syndrome

Leukemia research, 1998, Vol.22 (1), p.13-17

1998

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Multiple constitutional chromosome translocations of familial nature in philadelphia chromosome-positive chronic myeloid leukemia : A report on a unique case

International journal of hematology, 2005-11, Vol.82 (4), p.347-350

2005

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Unequivocal identification of disseminated tumor cells in the bone marrow by combining immunological and genetic approaches - functional and prognostic information

Leukemia, 2001-02, Vol.15 (2), p.275-277

2001

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Karyotype complexity and VH gene status in B-cell chronic lymphocytic leukemia

Haematologica (Roma), 2006-10, Vol.91 (10), p.1430-1431

2006

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Objective analysis of centromere separation

Human genetics, 1996-03, Vol.97 (3), p.365-366

1996

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Cell kinetic analysis in recurrent neuro-epithelial tumours

Acta neurochirurgica, 1996-01, Vol.138 (9), p.1036-1041

1996

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Phenotypic manifestations of the OCTN2 V295X mutation: Sudden infant death and carnitine-responsive cardiomyopathy in Roma families

American journal of medical genetics, 2004-12, Vol.131A (2), p.121-126

2004

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Epithelial Ca2+ channel (ECAC1) in autosomal dominant idiopathic hypercalciuria

Nephrology, dialysis, transplantation, 2002-09, Vol.17 (9), p.1614-1620

2002

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Informative morphogenetic variants in patients with schizophrenia and alcohol-dependent patients: beyond the Waldrop Scale

The American journal of psychiatry, 1997-05, Vol.154 (5), p.691-693

1997

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Elements of Morphology : Standard Terminology for the Nose and Philtrum: Elements of Morphology: Standard Terminology

American journal of medical genetics. Part A, 2009, Vol.149 (1), p.61-76

2009

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Congenital cataract as the first symptom of a neuromuscular disease caused by a novel single large-scale mitochondrial DNA deletion

European journal of human genetics : EJHG, 2003-05, Vol.11 (5), p.375-379

2003

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Muscle carnitine acetyltransferase and carnitine deficiency in a case of mitochondrial encephalomyopathy

Journal of inherited metabolic disease, 1999-10, Vol.22 (7), p.827-838

1999

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Search for Factor V Arg306 Cambridge and Hong Kong Mutations in Mixed Hungarian Population Samples

Acta haematologica, 2003, Vol.110 (4), p.220-222

2003

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Inherited ring chromosomes : an analysis of published cases

Human genetics, 1991-07, Vol.87 (3), p.320-324

1991

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A possible mosaic form of delayed centromere separation and aneuploidy

Human genetics, 1992-02, Vol.88 (4), p.477-478

1992

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Premature centromere division of a translocation-carrier autosome

Human genetics, 1990-08, Vol.85 (3), p.379-380

1990

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Morphologic variants in parents of children with malformation syndromes: are they indicators of somatic mosaicism?

Clinical genetics, 1990-08, Vol.38 (2), p.114-116

1990

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Association of nonsyndromic Wilms tumor with premature centromere division (PCD)

American journal of medical genetics, 2002-10, Vol.112 (2), p.215-216

2002

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Syndrome of arachnodactyly, disturbance of cranial ossification, protruding eyes, feeding difficulties, and mental retardation

American journal of medical genetics, 1995-09, Vol.58 (3), p.213-216

1995

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A nationwide evaluation of multiple congenital abnormalities in Hungary

Genetic epidemiology, 1988, Vol.5 (3), p.183-202

1988

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Circulating Breast Cancer Cells Are Frequently Apoptotic

Combined Automatic Immunological and Molecular Cytogenetic Analysis Allows Exact Identification and Quantification of Tumor Cells in the Bone Marrow

Solid and papillary epithelial neoplasm arising in heterotopic pancreatic tissue of the mesocolon

In situ fluorescent visualization of nucleolar organizer region- associated proteins with a thiol reagent

Detection of Disseminated Tumor Cells in Neuroblastoma: 3 Log Improvement in Sensitivity by Automatic Immunofluorescence plus FISH (AIPF) Analysis Compared with Classical Bone Marrow Cytology

Phenotypic and genotypic analyses of blastic cell population suggest that pure B-lymphoblastic leukemia may arise from myelodysplastic syndrome

Multiple constitutional chromosome translocations of familial nature in philadelphia chromosome-positive chronic myeloid leukemia : A report on a unique case

Unequivocal identification of disseminated tumor cells in the bone marrow by combining immunological and genetic approaches - functional and prognostic information

Karyotype complexity and VH gene status in B-cell chronic lymphocytic leukemia

Objective analysis of centromere separation

Cell kinetic analysis in recurrent neuro-epithelial tumours

Phenotypic manifestations of the OCTN2 V295X mutation: Sudden infant death and carnitine-responsive cardiomyopathy in Roma families

Epithelial Ca2+ channel (ECAC1) in autosomal dominant idiopathic hypercalciuria

Informative morphogenetic variants in patients with schizophrenia and alcohol-dependent patients: beyond the Waldrop Scale

Elements of Morphology : Standard Terminology for the Nose and Philtrum: Elements of Morphology: Standard Terminology

Congenital cataract as the first symptom of a neuromuscular disease caused by a novel single large-scale mitochondrial DNA deletion

Muscle carnitine acetyltransferase and carnitine deficiency in a case of mitochondrial encephalomyopathy

Search for Factor V Arg306 Cambridge and Hong Kong Mutations in Mixed Hungarian Population Samples

Inherited ring chromosomes : an analysis of published cases

A possible mosaic form of delayed centromere separation and aneuploidy

Premature centromere division of a translocation-carrier autosome

Morphologic variants in parents of children with malformation syndromes: are they indicators of somatic mosaicism?

Association of nonsyndromic Wilms tumor with premature centromere division (PCD)

Syndrome of arachnodactyly, disturbance of cranial ossification, protruding eyes, feeding difficulties, and mental retardation

A nationwide evaluation of multiple congenital abnormalities in Hungary

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