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ICSH recommendations for the standardization of nomenclature and grading of peripheral blood cell morphological features

International journal of laboratory hematology, 2015-06, Vol.37 (3), p.287-303

2015

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Bone marrow evaluation for pediatric patients

International journal of laboratory hematology, 2013-06, Vol.35 (3), p.283-289

Proytcheva, M.

2013

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Assembly and evaluation of an inventory of guidelines that are available to support clinical hematology laboratory practice

International journal of laboratory hematology, 2015-05, Vol.37 (S1), p.36-45

2015

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Report on the International Society for Laboratory Hematology Survey on guidelines to support clinical hematology laboratory practice

International journal of laboratory hematology, 2016-05, Vol.38 (S1), p.133-138

2016

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Monosomy 7 associated with pediatric acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS): successful management by allogeneic hematopoietic stem cell transplant (HSCT)

Bone marrow transplantation (Basingstoke), 2005-01, Vol.35 (2), p.143-149

2005

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Case-control study of risk factors for the development of post-transplant lymphoproliferative disease in a pediatric heart transplant cohort

Pediatric transplantation, 2007-02, Vol.11 (1), p.58-65

2007

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BLM, the Bloom's syndrome protein, varies during the cell cycle in its amount, distribution, and co-localization with other nuclear proteins

Cytogenetic and genome research, 2000-01, Vol.91 (1-4), p.217-223

2000

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The Bloom's syndrome gene product is homologous to RecQ helicases

Cell, 1995-11, Vol.83 (4), p.655-666

1995

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The DNA helicase activity of BLM is necessary for the correction of the genomic instability of bloom syndrome cells

Molecular biology of the cell, 1999-03, Vol.10 (3), p.665-676

1999

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Linkage disequilibrium between the FES, D15S127, and BLM loci in Ashkenazi Jews with Bloom syndrome

American journal of human genetics, 1994-09, Vol.55 (3), p.453-460

1994

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Juvenile myelomonocytic leukemia

Seminars in diagnostic pathology, 2011-11, Vol.28 (4), p.298-303

Proytcheva, Maria, MD

2011

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Somatic intragenic recombination within the mutated locus BLM can correct the high sister-chromatid exchange phenotype of Bloom syndrome cells

American journal of human genetics, 1995-11, Vol.57 (5), p.1019-1027

1995

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Eosinophilic angiocentric fibrosis

Journal of laryngology and otology, 2003-05, Vol.117 (5), p.410-413

2003

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Transfection of BLM into Cultured Bloom Syndrome Cells Reduces the Sister-Chromatid Exchange Rate toward Normal

American journal of human genetics, 1999-11, Vol.65 (5), p.1368-1374

1999

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A 17-month-old boy with fever of unknown origin

Pediatric annals, 2006-03, Vol.35 (3), p.152, 154, 156-158

Listernick, Robert

2006

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Bloom's syndrome. XIX. Cytogenetic and population evidence for genetic heterogeneity

Clinical genetics, 1996-05, Vol.49 (5), p.223-231

1996

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A rapid method for detecting the predominant Ashkenazi Jewish mutation in the Bloom's syndrome gene

Human mutation, 1998, Vol.11 (2), p.175-178

1998

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The Ashkenazic Jewish bloom syndrome mutation blmAsh is present in non-Jewish Americans of Spanish ancestry

American journal of human genetics, 1998-12, Vol.63 (6), p.1685-1693

1998

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Physical Mapping of the Bloom Syndrome Region by the Identification of YAC and P1 Clones from Human Chromosome 15 Band q26.1

Genomics (San Diego, Calif.), 1996-07, Vol.35 (1), p.118-128

1996

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Linkage disequilibrium between the FES, DI5SI27, and BLM Loci in Ashkenazi jews with bloom syndrome

American journal of human genetics, 1994, Vol.55 (3), p.453-460

1994

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Basophilic blast phase of chronic myelogenous leukemia

Blood, 2014-10, Vol.124 (15), p.2464-2464

2014

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Serum Neopterin Levels as a Diagnostic Marker of Hemophagocytic Lymphohistiocytosis Syndrome

Clinical and Vaccine Immunology, 2011-04, Vol.18 (4), p.609-614

2011

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Mesenteric Castleman Disease Detected by Capsule Endoscopy

Journal of pediatric gastroenterology and nutrition, 2013-07, Vol.57 (1), p.e3-e5-e3-e5

2013

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ICSH recommendations for the standardization of nomenclature and grading of peripheral blood cell morphological features

Bone marrow evaluation for pediatric patients

Assembly and evaluation of an inventory of guidelines that are available to support clinical hematology laboratory practice

Report on the International Society for Laboratory Hematology Survey on guidelines to support clinical hematology laboratory practice

Monosomy 7 associated with pediatric acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS): successful management by allogeneic hematopoietic stem cell transplant (HSCT)

Case-control study of risk factors for the development of post-transplant lymphoproliferative disease in a pediatric heart transplant cohort

BLM, the Bloom's syndrome protein, varies during the cell cycle in its amount, distribution, and co-localization with other nuclear proteins

The Bloom's syndrome gene product is homologous to RecQ helicases

The DNA helicase activity of BLM is necessary for the correction of the genomic instability of bloom syndrome cells

Linkage disequilibrium between the FES, D15S127, and BLM loci in Ashkenazi Jews with Bloom syndrome

Juvenile myelomonocytic leukemia

Somatic intragenic recombination within the mutated locus BLM can correct the high sister-chromatid exchange phenotype of Bloom syndrome cells

Eosinophilic angiocentric fibrosis

Transfection of BLM into Cultured Bloom Syndrome Cells Reduces the Sister-Chromatid Exchange Rate toward Normal

A 17-month-old boy with fever of unknown origin

Bloom's syndrome. XIX. Cytogenetic and population evidence for genetic heterogeneity

A rapid method for detecting the predominant Ashkenazi Jewish mutation in the Bloom's syndrome gene

The Ashkenazic Jewish bloom syndrome mutation blmAsh is present in non-Jewish Americans of Spanish ancestry

Physical Mapping of the Bloom Syndrome Region by the Identification of YAC and P1 Clones from Human Chromosome 15 Band q26.1

Linkage disequilibrium between the FES, DI5SI27, and BLM Loci in Ashkenazi jews with bloom syndrome

Basophilic blast phase of chronic myelogenous leukemia

Serum Neopterin Levels as a Diagnostic Marker of Hemophagocytic Lymphohistiocytosis Syndrome

Mesenteric Castleman Disease Detected by Capsule Endoscopy

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