T. Krasnov

发表

Molecular characterization of three novel Fanconi anemia mutations in Israeli Arabs

D. Bercovich, H. Tamary, H. Toledano, 2004, European journal of haematology.

Endoscopic findings and esophageal cancer incidence among Fanconi Anemia patients participating in an endoscopic surveillance program.

H. Tamary, Y. Goldberg, I. Dotan, 2019, Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver.

Frequency and natural history of inherited bone marrow failure syndromes: the Israeli Inherited Bone Marrow Failure Registry

P. Rosenberg, R. Elhasid, H. Tamary, 2008, Haematologica.

MPL Baltimore Mutation and Thrombocytosis: Case Report and Literature Review

H. Tamary, O. Dgany, T. Krasnov, 2013, Journal of pediatric hematology/oncology.

From Blood Smear to Lipid Disorder: A Case Report

H. Tamary, O. Dgany, T. Krasnov, 2013, Journal of pediatric hematology/oncology.

A novel epsilon gamma delta beta thalassemia presenting with pregnancy complications and severe neonatal anemia

H. Tamary, H. Shalev, J. Kapelushnik, 2013, European journal of haematology.

Syndromes predisposing to leukemia are a major cause of inherited cytopenias in children

R. Elhasid, S. Izraeli, H. Tamary, 2022, Haematologica.

Genetic analysis and clinical picture of severe congenital neutropenia in Israel

H. Tamary, N. Giri, B. Alter, 2015, Pediatric blood & cancer.

Diamond Blackfan Anemia: A Nonclassical Patient With Diagnosis Assisted by Genomic Analysis

T. Walsh, M. King, H. Tamary, 2016, Journal of pediatric hematology/oncology.

High Incidence of Early Cholelithiasis Detected by Ultrasonography in Children and Young Adults With Hereditary Spherocytosis

H. Tamary, I. Yaniv, T. Krasnov, 2003, Journal of pediatric hematology/oncology.

Whole-exome sequencing identifies an α-globin cluster triplication resulting in increased clinical severity of β-thalassemia

H. Tamary, J. Ulirsch, V. Sankaran, 2017, Cold Spring Harbor molecular case studies.

Molecular diagnosis of α‐thalassemia in a multiethnic population

S. Ben-Dor, H. Tamary, I. Yaniv, 2017, European journal of haematology.

Morphological features of congenital dyserythropoietic anemia type I: The role of electron microscopy in diagnosis

H. Tamary, H. Shalev, J. Kapelushnik, 2017, European journal of haematology.

Characterization and genotype-phenotype correlation of patients with Fanconi anemia in a multi-ethnic population

A. Toren, H. Tamary, S. Revel-Vilk, 2019, Haematologica.

Targeted next generation sequencing for the diagnosis of patients with rare congenital anemias

H. Tamary, A. Kattamis, O. Dgany, 2018, European journal of haematology.

Congenital dyserythropoietic anemia type I is caused by mutations in codanin-1.

J. Beckmann, D. Lancet, H. Tamary, 2002, American journal of human genetics.

Pediatric myelodysplastic syndrome with inflammatory manifestations: Diagnosis, genetics, treatment, and outcome

S. Izraeli, H. Tamary, I. Geron, 2021, Pediatric blood & cancer.

Incorporation of somatic panels for the detection of haematopoietic transformation in children and young adults with leukaemia predisposition syndromes and with acquired cytopenias

S. Izraeli, H. Tamary, H. Toledano, 2020, British journal of haematology.

Inherited thrombocytopenia associated with mutation of UDP‐galactose‐4‐epimerase (GALE)

T. Walsh, M. King, S. Pierce, 2018, Human molecular genetics.

Syndromes predisposing to leukemia are a major cause of inherited cytopenias in children

R. Elhasid, S. Izraeli, H. Tamary, 2022, Haematologica.

Small‐platelet thrombocytopenia in a family with autosomal recessive inheritance pattern

H. Tamary, M. Khayat, S. Shalev, 2013, Pediatric blood & cancer.

Clinical and molecular variability in congenital dyserythropoietic anaemia type I

H. Tamary, I. Yaniv, B. Bader-Meunier, 2005, British journal of haematology.

CATSPER2, a human autosomal nonsyndromic male infertility gene

J. Beckmann, D. Lancet, H. Tamary, 2003, European Journal of Human Genetics.

Congenital Amegakaryocytic Thrombocytopenia—3 Novel c-MPL Mutations and Their Phenotypic Correlations

H. Tamary, I. Yaniv, J. Kapelushnik, 2007, Journal of pediatric hematology/oncology.

Codanin-1, the protein encoded by the gene mutated in congenital dyserythropoietic anemia type I (CDAN1), is cell cycle-regulated

H. Tamary, G. Kupfer, D. Ginsberg, 2009, Haematologica.

Alpha-Thalassemia Carrier due to –α3.7 Deletion: Not So Silent

H. Tamary, O. Dgany, T. Krasnov, 2020, Acta Haematologica.

Congenital thrombocytopenia associated with a heterozygous variant in the MEIS1 gene encoding a transcription factor essential for megakaryopoiesis

H. Tamary, N. Orenstein, L. Basel-Salmon, 2022, Platelets.

Congenital dyserythropoietic anaemia, type I, in a Caucasian patient with retinal angioid streaks (homozygous arg1042trp mutation in codanin‐1)

H. Offret, H. Tamary, J. Delaunay, 2008, European journal of haematology.

A Comprehensive Study of the Neonatal Manifestations of Congenital Dyserythropoietic Anemia Type I

H. Tamary, H. Shalev, J. Kapelushnik, 2004, Journal of pediatric hematology/oncology.

Molecular Basis of Congenital Dyserythropoietic Anemia Type I in French Patients.

H. Tamary, I. Yaniv, B. Bader-Meunier, 2004 .

E109K Is a SEC23B Founder Mutation among Israeli Moroccan Jewish Patients with Congenital Dyserythropoietic Anemia Type II

A. Berrebi, H. Tamary, O. Dgany, 2011, Acta Haematologica.