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Hannah Tamary

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TOP 3
Vered Shkalim-Zemer; Orly Dgany; Tanya Krasnov; Joanne Yacobovich; Hannah Tamary
MPL Baltimore mutation and thrombocytosis: case report and literature review.
Hanna Shalev; Arnon Broides; Orly Dgany; Oded Gilad; Joseph Kapelushnik; Tatyana Krasnov; Daniela Landau; Serge Pissard; Hannah Tamary
A novel epsilon gamma delta beta thalassemia presenting with pregnancy complications and severe neonatal anemia.
Joanne Yacobovich; Shoshana Revel-Vilk; Hannah Tamary
Childhood immune thrombocytopenia-who will spontaneously recover?

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All Publications

2013: Vered Shkalim-Zemer; Orly Dgany; Tanya Krasnov; Joanne Yacobovich; Hannah Tamary
MPL Baltimore mutation and thrombocytosis: case report and literature review.
Journal of pediatric hematology/oncology 2013;35(3):e112-4.
2013: Hanna Shalev; Arnon Broides; Orly Dgany; Oded Gilad; Joseph Kapelushnik; Tatyana Krasnov; Daniela Landau; Serge Pissard; Hannah Tamary
A novel epsilon gamma delta beta thalassemia presenting with pregnancy complications and severe neonatal anemia.
European journal of haematology 2013;90(2):127-33.
2013: Joanne Yacobovich; Shoshana Revel-Vilk; Hannah Tamary
Childhood immune thrombocytopenia-who will spontaneously recover?
Seminars in hematology 2013;50 Suppl 1():S71-4.
2013: Ami Ballin; Yona Avni; Aeed Hussein; Letizia Schreiber; Yehuda Senecky; Hannah Tamary; Hananya Vaknine; Mona Boaz
Anemia associated with acute infection in children: an animal model.
Journal of pediatric hematology/oncology 2013;35(1):14-7.
2013: Hanna Shalev; Dorine W Swinkels; Carole Brasse-Lagnel; Joseph Kapelushnik; Itai Levi; Galit Perez-Avraham; Anat Rabinovich; Hannah Tamary
High levels of soluble serum hemojuvelin in patients with congenital dyserythropoietic anemia type I.
European journal of haematology 2013;90(1):31-6.
2012: Shraga Aviner; Ehud Even-Or; Hannah Tamary
Spontaneous resolution of extreme thrombocytosis in 2 children.
Pediatric hematology and oncology 2012;29(4):372-7.
2011: Thomas Kühne; Lisa A Michaels; Johannes Rischewski; Francesco Rodeghiero; Hannah Tamary; Runhui Wu; Willi Berchtold; Meera Chitlur; Hugo Donato; Bibiana Espina; Paul Imbach
Newly diagnosed immune thrombocytopenia in children and adults: a comparative prospective observational registry of the Intercontinental Cooperative Immune Thrombocytopenia Study Group.
Haematologica 2011;96(12):1831-7.
2011: Roberta Russo; Maria Luisa Serra; Hannah Tamary; Annaelena Troiano; Mario Capasso; Ilaria De Maggio; Jean Delaunay; Maria Rosaria Esposito; Antonella Gambale; Lucio Luzzatto; Achille Iolascon
Two founder mutations in the SEC23B gene account for the relatively high frequency of CDA II in the Italian population.
American journal of hematology 2011;86(9):727-32.
2011: Philip S Rosenberg; Hannah Tamary; BLANCHE ALTER
How high are carrier frequencies of rare recessive syndromes? Contemporary estimates for Fanconi Anemia in the United States and Israel.
American journal of medical genetics. Part A 2011;155A(8):1877-83.
2011: Ami Ballin; Shlomit Barzilai-Birenbaum; Hitam Saab; Orit Waisbourd-Zinman; Joanne Yacobovich; Isaac Yaniv; Meirah Zoldan; Hannah Tamary
Steroid therapy may be effective in augmenting hemoglobin levels during hemolytic crises in children with hereditary spherocytosis.
Pediatric blood & cancer 2011;57(2):303-5.
2011: Ofer Schiller; Shifra Ash; Tommy Schonfeld; Gili Kadmon; Elhanan Nahum; Joanne Yacobovich; Hannah Tamary; Miriam Davidovits
Postoperative thrombotic thrombocytopenic purpura in an infant: case report and literature review.
Journal of pediatric surgery 2011;46(4):764-6.
2011: Uri Pollak; Joanne Yacobobich; Hannah Tamary; Ovdi Dagan; Orit Manor-Shulman
Heparin-induced thrombocytopenia and extracorporeal membrane oxygenation: a case report and review of the literature.
The Journal of extra-corporeal technology 2011;43(1):5-12.
2011: Achiya Amir; Orly Dgany; Tanya Krasnov; Peretz Resnitzky; Ronit Mor-Cohen; Michael Bennett; Alain Berrebi; Hannah Tamary
E109K is a SEC23B founder mutation among Israeli Moroccan Jewish patients with congenital dyserythropoietic anemia type II.
Acta haematologica 2011;125(4):202-7.
2010: Lillian McMahon; Hannah Tamary; Melissa Askin; Patricia Adams-Graves; Robert T Eberhardt; Millicent Sutton; Elizabeth C Wright; Serguei A Castaneda; Douglas V Faller; Susan P Perrine
A randomized phase II trial of Arginine Butyrate with standard local therapy in refractory sickle cell leg ulcers.
British journal of haematology 2010;151(5):516-24.
2010: Lionel Arnaud; Carole Saison; Virginie Helias; Nicole Lucien; Dominique Steschenko; Marie-Catherine Giarratana; Claude Prehu; Bernard Foliguet; Lory Montout; Alexandre G de Brevern; Alain Francina; Pierre Ripoche; Odile Fenneteau; Lydie Da Costa; Thierry Peyrard; Gail Coghlan; Niels Illum; Henrik Birgens; Hannah Tamary; Achille Iolascon; Jean Delaunay; Gil Tchernia; Jean-Pierre Cartron
A dominant mutation in the gene encoding the erythroid transcription factor KLF1 causes a congenital dyserythropoietic anemia.
American journal of human genetics 2010;87(5):721-7.
2010: Lutfi Jaber; Shmuel Rigler; Ahmad Taya; Fadel Tebi; Mohamad Baloum; Isaac Yaniv; Mohamad Haj Yehia; Hannah Tamary
Iron polymaltose versus ferrous gluconate in the prevention of iron deficiency anemia of infancy.
Journal of pediatric hematology/oncology 2010;32(8):585-8.
2010: Joanne Yacobovich; Pinhas Stark; Shlomit Barzilai-Birenbaum; Irit Krause; Idit Pazgal; Isaac Yaniv; Hannah Tamary
Acquired proximal renal tubular dysfunction in β-thalassemia patients treated with deferasirox.
Journal of pediatric hematology/oncology 2010;32(7):564-7.
2010: Achiya Amir; Oded Gilad; Joanne Yacobovich; Oded Scheuerman; Hannah Tamary; Ben-Zion Garty
Post-varicella thrombocytopenic purpura.
Acta paediatrica (Oslo, Norway : 1992) 2010;99(9):1385-8.
2010: Hannah Tamary; Daniella Nishri; Joanne Yacobovich; Rama Zilber; Orly Dgany; Tatyana Krasnov; Shraga Aviner; Polina Stepensky; Shoshana Ravel-Vilk; Menachem Bitan; Chaim Kaplinsky; Ayelet Ben-Barak; Ronit Elhasid; Joseph Kapelusnik; Ariel Koren; Carina Levin; Dina Attias; Ruth Laor; Isaac Yaniv; Philip S Rosenberg; BLANCHE ALTER
Frequency and natural history of inherited bone marrow failure syndromes: the Israeli Inherited Bone Marrow Failure Registry.
Haematologica 2010;95(8):1300-7.
2010: Dror Kraus; Joanne Yacobovich; Vered Hoffer; Oded Scheuerman; Hannah Tamary; Ben-Zion Garty
Infantile pyknocytosis: a rare form of neonatal anemia.
The Israel Medical Association journal : IMAJ 2010;12(3):188-9.
2010: Mira Malcov; Adi Reches; Dalit Ben-Yosef; Tania Cohen; Ami Amit; Orly Dgany; Hannah Tamary; Yuval Yaron
Resolving a genetic paradox throughout preimplantation genetic diagnosis for autosomal dominant severe congenital neutropenia.
Prenatal diagnosis 2010;30(3):207-11.
2010: Aurore Crétien; Alexis Proust; Jean Delaunay; Patricia Rincé; Thierry Leblanc; Rolande Ducrocq; Maud Simansour; Isabelle Marie; Hannah Tamary; Joerg Meerpohl; Charlotte Niemeyer; Hanna Gazda; Colin Sieff; Sarah Ball; Gil Tchernia; Narla Mohandas; Lydie Da Costa
Genetic variants in the noncoding region of RPS19 gene in Diamond-Blackfan anemia: potential implications for phenotypic heterogeneity.
American journal of hematology 2010;85(2):111-6.
2009: Anke K Bergmann; Hannah Tamary; Ellis J Neufeld
Remission from transfusion-dependence in a patient with congenital dyserythropoietic anemia (CDA) and increased intensity of iron chelation.
Pediatric blood & cancer 2009;53(6):1167-8.
2009: Sharon Noy-Lotan; Orly Dgany; Roxane Lahmi; Nathaly Marcoux; Tanya Krasnov; Nissan Yissachar; Doron Ginsberg; Benny Motro; Peretz Resnitzky; Isaac Yaniv; Gary M Kupfer; Hannah Tamary
Codanin-1, the protein encoded by the gene mutated in congenital dyserythropoietic anemia type I (CDAN1), is cell cycle-regulated.
Haematologica 2009;94(5):629-37.
2008: Hannah Tamary; Hanna Shalev; Galit Perez-Avraham; Meira Zoldan; Itai Levi; Dorine W Swinkels; Toshihiko TANNO; Jeffery L Miller
Elevated growth differentiation factor 15 expression in patients with congenital dyserythropoietic anemia type I.
Blood 2008;112(13):5241-4.
2008: David Shitrit; Hannah Tamary; Ariel Koren; Carina Levin; Ariella Bargil-Shitrit; Jaqueline Sulkes; mordechai kramer
Correlation of vascular endothelial growth factor with the severity of thalassemia intermedia.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2008;19(7):611-4.
2008: Hanna Shalev; Galit Perez Avraham; Reli Hershkovitz; Amalia Levy; Eyal Sheiner; Itai Levi; Hannah Tamary
Pregnancy outcome in congenital dyserythropoietic anemia type I.
European journal of haematology 2008;81(4):317-21.
2008: Lina Basel-Vanagaite; Inderjeet Dokal; Hannah Tamary; Abraham Avigdor; Ben Zion Garty; Alexander Volkov; Tom Vulliamy
Expanding the clinical phenotype of autosomal dominant dyskeratosis congenita caused by TERT mutations.
Haematologica 2008;93(6):943-4.
2008: Moshe Mittelman; Gilles Lugassy; Drorit Merkel; Hannah Tamary; Nadav Sarid; Eliezer Rachmilewitz; Chaim Hershko
Iron chelation therapy in patients with myelodysplastic syndromes: consensus conference guidelines.
The Israel Medical Association journal : IMAJ 2008;10(5):374-6.
2008: Ariel Koren; Carina Levin; Orly Dgany; Tatyan Kransnov; Ronit Elhasid; Lucia Zalman; Haya Palmor; Hannah Tamary
Response to hydroxyurea therapy in beta-thalassemia.
American journal of hematology 2008;83(5):366-70.
2008: Hannah Tamary; H Offret; Orly Dgany; B Foliguet; Sunitha N Wickramasinghe; Tatyana Krasnov; F Rumilly; C Goujard; M Fénéant-Thibault; Thérèse Cynober; Jean Delaunay
Congenital dyserythropoietic anaemia, type I, in a Caucasian patient with retinal angioid streaks (homozygous Arg1042Trp mutation in codanin-1).
European journal of haematology 2008;80(3):271-4.
2007: Anna Marrone; Amanda Walne; Hannah Tamary; Yuka Masunari; Michael Kirwan; Richard Beswick; Tom Vulliamy; Inderjeet Dokal
Telomerase reverse-transcriptase homozygous mutations in autosomal recessive dyskeratosis congenita and Hoyeraal-Hreidarsson syndrome.
Blood 2007;110(13):4198-205.
2007: Orna Steinberg; Gil Gilad; Orly Dgany; Tatyana Krasnov; Meira Zoldan; Ruth Laor; Joseph Kapelushnik; Herzel Gabriel; Chaim Churi; Jerry Stein; Isaac Yaniv; Hannah Tamary
Congenital amegakaryocytic thrombocytopenia-3 novel c-MPL mutations and their phenotypic correlations.
Journal of pediatric hematology/oncology 2007;29(12):822-5.
2007: Micky Osovsky; Hannah Tamary; Paul Merlob
Neonatal thrombocytosis following G-CSF treatment.
Clinical toxicology (Philadelphia, Pa.) 2007;45(7):801-2.
2007: Alexis Proust; Benoît Guillet; Capucine Picard; Geneviève de Saint Basile; Corinne Pondarré; Hannah Tamary; Marie Dreyfus; Gil Tchernia; Alain Fischer; Jean Delaunay
Detection of 28 novel mutations in the Wiskott-Aldrich syndrome and X-linked thrombocytopenia based on multiplex PCR.
Blood cells, molecules & diseases 2007;39(1):102-6.
2007: Hannah Tamary; BLANCHE ALTER
Current diagnosis of inherited bone marrow failure syndromes.
Pediatric hematology and oncology 2007;24(2):87-99.
2007: Hanna Shalev; Joseph Kapelushnik; Asher Moser; Haim Y Knobler; Hannah Tamary
Hypocholesterolemia in chronic anemias with increased erythropoietic activity.
American journal of hematology 2007;82(3):199-202.
2006: Orna Steinberg; Joanne Yacobovich; Orly Dgany; Yona Kodman; Gilat Livni; Avinoam Rachmel; Jerry Stein; Isaac Yaniv; Hannah Tamary
Prolonged course of familial hemophagocytic lymphohistiocytosis.
Journal of pediatric hematology/oncology 2006;28(12):831-3.
2006: Rawi Hazzan; Mashaand Mukamel; Joanne Yacobovich; Isaac Yaniv; Hannah Tamary
Risk factors for future development of systemic lupus erythematosus in children with idiopathic thrombocytopenic purpura.
Pediatric blood & cancer 2006;47(5 Suppl):657-9.
2006: Momin R Ahmed; Aref Chehal; Laila Zahed; Ali Taher; Joud H Haidar; Ali Shamseddine; Anne-Marie O'Hea; Nicola Bienz; Orly Dgany; Nili Avidan; Jacques Beckmann; Hannah Tamary; Douglas Higgs; Paresh Vyas; William G Wood; Sunitha N Wickramasinghe
Linkage and mutational analysis of the CDAN1 gene reveals genetic heterogeneity in congenital dyserythropoietic anemia type I.
Blood 2006;107(12):4968-9.
2006: Hermann Heimpel; Klaus Schwarz; Monika Ebnöther; Jeroen S Goede; Detlev Heydrich; Torsten Kamp; Lothar Plaumann; Bettina Rath; Jochen Roessler; Otto Schildknecht; Mathias Schmid; Walter A Wuillemin; Beate Einsiedler; Rosi Leichtle; Hannah Tamary; Elisabeth Kohne
Congenital dyserythropoietic anemia type I (CDA I): molecular genetics, clinical appearance, and prognosis based on long-term observation.
Blood 2006;107(1):334-40.
2005: Hannah Tamary; Orly Dgany; Alexis Proust; Tatyana Krasnov; Nili Avidan; Tal Eidelitz-Markus; Gil Tchernia; David Geneviève; Valérie Cormier-Daire; Brigitte Bader-Meunier; Corinne Ferrero-Vacher; Martine Munzer; Ralph A Gruppo; Eitan Fibach; Osnat Konen; Isaac Yaniv; Jean Delaunay
Clinical and molecular variability in congenital dyserythropoietic anaemia type I.
British journal of haematology 2005;130(4):628-34.
2005: Shlomit Shalitin; Doron Carmi; Naomi Weintrob; Moshe Phillip; Hagit Miskin; Liora Kornreich; Rama Zilber; Isaac Yaniv; Hannah Tamary
Serum ferritin level as a predictor of impaired growth and puberty in thalassemia major patients.
European journal of haematology 2005;74(2):93-100.
2004: Hanna Shalev; Joseph Kapelushnik; Asher Moser; Orly Dgany; Tatyana Krasnov; Hannah Tamary
A comprehensive study of the neonatal manifestations of congenital dyserythropoietic anemia type I.
Journal of pediatric hematology/oncology 2004;26(11):746-8.
2004: Gili Kenet; Dalia Waldman; Aharon Lubetsky; Nurit Kornbrut; Abdalla Khalil; Ariel Koren; Baruch Wolach; Aviva Fattal; Joseph Kapelushnik; Hannah Tamary; Joanne Yacobovitch; Eyal Raveh; Shoshana Revel-Vilk; Amos Toren; Benjamin Brenner
Paediatric cerebral sinus vein thrombosis. A multi-center, case-controlled study.
Thrombosis and haemostasis 2004;92(4):713-8.
2004: Yonit Fromovich-Amit; Ariella Zivelin; Nurit Rosenberg; Hannah Tamary; meytal landau; Uri Seligsohn
Characterization of mutations causing factor VII deficiency in 61 unrelated Israeli patients.
Journal of thrombosis and haemostasis : JTH 2004;2(10):1774-81.
2004: Shmuel Arnon; Hannah Tamary; Orly Dgany; Ita Litmanovitz; Rivka Regev; Sofia Bauer; Tzipora Dolfin; Joanne Yacobovich; Baruch Wolach; Lutfi Jaber
Hydrops fetalis associated with homozygosity for hemoglobin Taybe (alpha 38/39 THR deletion) in newborn triplets.
American journal of hematology 2004;76(3):263-6.
2004: Yaron Finkelstein; Isaac Yaniv; Michael Berant; Rama Zilber; Ben-Zion Garty; Orit Epstein; Judith Lahav; Hannah Tamary
Central venous line thrombosis in children and young adults with thalassemia major.
Pediatric hematology and oncology 2004;21(5):375-81.
2004: Hannah Tamary; Orly Dgany; Helen Toledano; Zvi Shalev; Tatyana Krasnov; Lea Shalmon; Tali Schechter; Dani Bercovich; Dina Attias; Ruth Laor; Ariel Koren; Isaac Yaniv
Molecular characterization of three novel Fanconi anemia mutations in Israeli Arabs.
European journal of haematology 2004;72(5):330-5.
2004: Yael Oestreicher-Kedem; Eyal Raveh; Liora Kornreich; Isaac Yaniv; Hannah Tamary
Prothrombotic factors in children with otitis media and sinus thrombosis.
The Laryngoscope 2004;114(1):90-5.
2003: Hannah Tamary; Shraga Aviner; Enrique Freud; Hagit Miskin; Tatyana Krasnov; Michael Schwarz; Isaac Yaniv
High incidence of early cholelithiasis detected by ultrasonography in children and young adults with hereditary spherocytosis.
Journal of pediatric hematology/oncology 2003;25(12):952-4.
2003: Jérôme Feldmann; Isabelle Callebaut; Graça Raposo; Stéphanie Certain; Delphine Bacq; Cécile Dumont; Nathalie Lambert; Marie Ouachée-Chardin; Gaëlle Chedeville; Hannah Tamary; Véronique Minard-Colin; Etienne Vilmer; Stéphane Blanche; Françoise Le Deist; Alain Fischer; Geneviève de Saint Basile
Munc13-4 is essential for cytolytic granules fusion and is mutated in a form of familial hemophagocytic lymphohistiocytosis (FHL3).
Cell 2003;115(4):461-73.
2003: Hannah Tamary; Isaac Yaniv; J Stein; Orly Dgany; Z Shalev; T Shechter; Peretz Resnitzky; Dina Shaft; Meira Zoldan; Liora Kornreich; R Levy; A Cohen; R A Moser; Joseph Kapelushnik; Hanna Shalev
A clinical and molecular study of a Bedouin family with dysmegakaryopoiesis, mild anemia, and neutropenia cured by bone marrow transplantation.
European journal of haematology 2003;71(3):196-203.
2003: Amir Asher Kuperman; Isaac Yaniv; Bracha Stahl; Hannah Tamary
Methylphenidate as a possible cause of thrombocytopenia.
The Annals of pharmacotherapy 2003;37(7-8):1146.
2003: Nili Avidan; Hannah Tamary; Orly Dgany; Daniel Cattan; Alexandre Pariente; Michel Thulliez; Nicolas Borot; Lucien Moati; Alain Barthelme; Lea Shalmon; Tatyana Krasnov; Edna Ben-Asher; Tsviya Olender; Miriam Khen; Isaac Yaniv; Rina Zaizov; Hanna Shalev; Jean Delaunay; Marc Fellous; Doron Lancet; Jacques Beckmann
CATSPER2, a human autosomal nonsyndromic male infertility gene.
European journal of human genetics : EJHG 2003;11(7):497-502.
2003: Hagit Miskin; Isaac Yaniv; Michael Berant; C Hershko; Hannah Tamary
Reversal of cardiac complications in thalassemia major by long-term intermittent daily intensive iron chelation.
European journal of haematology 2003;70(6):398-403.
2003: Alexis Proust; Lydie Da Costa; Patricia Rince; Anaely Landois; Hannah Tamary; Rina Zaizov; Gil Tchernia; Jean Delaunay
Ten novel Diamond-Blackfan anemia mutations and three polymorphisms within the rps19 gene.
The hematology journal : the official journal of the European Haematology Association / EHA 2003;4(2):132-6.
2002: Orly Dgany; Nili Avidan; Jean Delaunay; Tatyana Krasnov; Lea Shalmon; Hanna Shalev; Tal Eidelitz-Markus; Joseph Kapelushnik; Daniel Cattan; Alexandre Pariente; Micheline Tulliez; Aurore Crétien; Pierre-Olivier Schischmanoff; Achille Iolascon; Eitan Fibach; Ariel Koren; Jochen Rössler; Martine Le Merrer; Isaac Yaniv; Rina Zaizov; Edna Ben-Asher; Tsviya Olender; Doron Lancet; Jacques Beckmann; Hannah Tamary
Congenital dyserythropoietic anemia type I is caused by mutations in codanin-1.
American journal of human genetics 2002;71(6):1467-74.
2002: Alex Zvulunov; Hannah Tamary; Nathan Gal
Pancytopenia resulting from hemophagocytosis in malaria.
The Pediatric infectious disease journal 2002;21(11):1086-7.
2002: Hannah Tamary; Raanan Bar-Yam; Michal Zemach; Orly Dgany; Lea Shalmon; Isaac Yaniv
The molecular biology of Fanconi anemia.
The Israel Medical Association journal : IMAJ 2002;4(10):819-23.
2002: Corina Hartman; Hannah Tamary; Ada Tamir; Evelyn Shabad; Carina Levine; Ariel Koren; Raanan Shamir
Hypocholesterolemia in children and adolescents with beta-thalassemia intermedia.
The Journal of pediatrics 2002;141(4):543-7.
2002: Laurent Roda; Jérôme Pasche; Alain Fournier; Vaea Terorotua; Sunitha N Wickramasinghe; Hannah Tamary; Pierre-Olivier Schischmanoff; Gil Tchernia; Jean Delaunay
Congenital dyserythropoietic anemia, type 1, in a polynesian patient: response to interferon alpha2b.
Journal of pediatric hematology/oncology 2002;24(6):503-6.
2002: Hanna Shalev; Y Kapleushnik; L Haeskelzon; O Degani; T Kransnov; O Sphilberg; A Moser; I Yaniv; Hannah Tamary
Clinical and laboratory manifestations of congenital dyserythropoietic anemia type I in young adults.
European journal of haematology 2002;68(3):170-4.
2001: Joseph Kapelushnik; Hanna Shalev; H Schulman; A Moser; Hannah Tamary
Upper airway obstruction-related sleep apnea in a child with thalassemia intermedia.
Journal of pediatric hematology/oncology 2001;23(8):525-6.
2001: Ewa Zdebska; E Gołaszewska; J Fabijańska-Mitek; H Schachter; Hanna Shalev; Hannah Tamary; Herbert Sandstrom; Ake Wahlin; J Kościelak
Glycoconjugate abnormalities in patients with congenital dyserythropoietic anaemia type I, II and III.
British journal of haematology 2001;114(4):907-13.
2001: D Marom; I Offer; Hannah Tamary; C L Jaffe; Ben-Zion Garty
Hemophagocytic lymphohistiocytosis associated with visceral leishmaniasis.
Pediatric hematology and oncology 2001;18(1):65-70.
2000: Hannah Tamary; R Bar-Yam; Lea Shalmon; G Rachavi; M Krostichevsky; Ronit Elhasid; Y Barak; Joseph Kapelushnik; Isaac Yaniv; A D Auerbach; Rina Zaizov
Fanconi anaemia group A (FANCA) mutations in Israeli non-Ashkenazi Jewish patients.
British journal of haematology 2000;111(1):338-43.
2000: Shoshana Revel-Vilk; Hannah Tamary; Efrat Broide; Meira Zoldan; Gabriel Dinari; Ilan Zahavi; Isaac Yaniv; Raanan Shamir
Serum transferrin receptor in children and adolescents with inflammatory bowel disease.
European journal of pediatrics 2000;159(8):585-9.
2000: Hanna Shalev; A Moser; Joseph Kapelushnik; M Karplus; Nili Zucker; I Yaniv; Hannah Tamary
Congenital dyserythropoietic anemia type I presenting as persistent pulmonary hypertension of the newborn.
The Journal of pediatrics 2000;136(4):553-5.
2000: Hannah Tamary; Yonit Fromovich-Amit; Lea Shalmon; Rina Zaizov; Isaac Yaniv; A Klar; Hava Peretz; B Brenner; Naomi Lanir; Ariella Zivelin; Uri Seligsohn
Molecular characterization of four novel mutations causing factor VII deficiency.
The hematology journal : the official journal of the European Haematology Association / EHA 2000;1(6):382-9.
1999: Irit Krause; Ben-Zion Garty; Miriam Davidovits; Roxana Cleper; Hannah Tamary; Eliezer Rosenmann; Bella Eisenstein
Low serum C3, leukopenia, and thrombocytopenia: unusual features of henoch-schonlein purpura.
European journal of pediatrics 1999;158(11):906-9.
1999: Hannah Tamary; Hanna Shalev; V Pinsk; Meira Zoldan; Rina Zaizov
No response to recombinant human erythropoietin therapy in patients with congenital dyserythropoietic anemia type I.
Pediatric hematology and oncology 1999;16(2):165-8.
1999: Kalman Katz; Hannah Tamary; Judith Lahav; Michael Soudry; Ian J Cohen
Increased operative bleeding during orthopaedic surgery in patients with type I Gaucher disease and bone involvement.
Bulletin (Hospital for Joint Diseases (New York, N.Y.)) 1999;58(4):188-90.
1998: Hannah Tamary; G Klinger; Lea Shalmon; H Kirschmann; Ariel Koren; M Bennet; Rina Zaizov
The diverse molecular basis and mild clinical picture of HbH disease in Israel.
Annals of the New York Academy of Sciences 1998;850():432-5.
1998: Hannah Tamary; Lea Shalmon; Hanna Shalev; A Halil; D Dobrushin; N Ashkenazi; Meira Zoldan; Peretz Resnitzky; Michael Korostishevsky; Batsheva Bonne-Tamir; Rina Zaizov
Localization of the gene for congenital dyserythropoietic anemia type I to a <1-cM interval on chromosome 15q15.1-15.3.
American journal of human genetics 1998;62(5):1062-9.
1998: Romy Zemel; R Dickman; Hannah Tamary; J Bukh; Rina Zaizov; Ran Tur-Kaspa
Viremia, genetic heterogeneity, and immunity to hepatitis G/GB-C virus in multiply transfused patients with thalassemia.
Transfusion 1998;38(3):301-6.
1997: Hannah Tamary; S Surrey; J Augustine; Lea Shalmon; E Schwartz; E F Rappaport
Molecular analysis of a compound heterozygote for hypoprothrombinemia and dysprothrombinemia (-G 7248/7249 and ARG 340 TRP).
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 1997;8(6):337-43.
1997: Hanna Shalev; Hannah Tamary; Dina Shaft; P Reznitsky; Rina Zaizov
Neonatal manifestations of congenital dyserythropoietic anemia type I.
The Journal of pediatrics 1997;131(1 Pt 1):95-7.
1997: Hannah Tamary; G Klinger; Lea Shalmon; Dina Attias; Paolo Fortina; M Kobayashi; Saul Surrey; Rina Zaizov
alpha-thalassemia caused by a 16 bp deletion in the 3' untranslated region of the alpha 2-globin gene including the first nucleotide of the poly A signal sequence.
Hemoglobin 1997;21(2):121-30.
1996: Hannah Tamary; Y Fromovich; Lea Shalmon; Z Reich; O Dym; N Lanir; B Brenner; M Paz; A S Luder; O Blau; Michael Korostishevsky; Rina Zaizov; Uri Seligsohn
Ala244Val is a common, probably ancient mutation causing factor VII deficiency in Moroccan and Iranian Jews.
Thrombosis and haemostasis 1996;76(3):283-91.
1996: Hannah Tamary; Hanna Shalev; David Luria; Dina Shaft; Meira Zoldan; Lea Shalmon; A Gruinspan; B Stark; M Chaison; E Shinar; Peretz Resnitzky; Rina Zaizov
Clinical features and studies of erythropoiesis in Israeli Bedouins with congenital dyserythropoietic anemia type I.
Blood 1996;87(5):1763-70.
1996: Isaac Yaniv; A Saab; Ian Cohen; Yacov Goshen; D Loven; B Stark; Hannah Tamary; Rina Zaizov
Hodgkin disease in children: reduced tailored chemotherapy for stage I-II disease.
Journal of pediatric hematology/oncology 1996;18(1):76-80.
1994: Hannah Tamary; C Kaplinsky; I Levy; Ian Cohen; Isaac Yaniv; B Stark; Yacov Goshen; Rina Zaizov
Chronic childhood idiopathic thrombocytopenia purpura: long-term follow-up.
Acta paediatrica (Oslo, Norway : 1992) 1994;83(9):931-4.
1994: Hannah Tamary; J Goshen; D Carmi; Isaac Yaniv; C Kaplinsky; Ian J Cohen; Rina Zaizov
Long-term intravenous deferoxamine treatment for noncompliant transfusion-dependent beta-thalassemia patients.
Israel journal of medical sciences 1994;30(8):658-64.
1994: C Kaplinsky; M Drucker; J Goshen; Hannah Tamary; Ian J Cohen; Rina Zaizov
Ambulatory treatment with ceftriaxone in febrile neutropenic children.
Israel journal of medical sciences 1994;30(8):649-51.
1994: Kalman Katz; Gadi Horev; J Goshen; Hannah Tamary
The pattern of bone disease in transfusion-dependent thalassemia major patients.
Israel journal of medical sciences 1994;30(8):577-80.
1994: Hannah Tamary; Yacov Goshen; Isaac Yaniv; Ian Cohen; C Kaplinsky; B Stark; Rina Zaizov
[Chronic immune thrombocytopenic purpura in children].
Harefuah 1994;127(3-4):101-5.
1994: Hannah Tamary; Saul Surrey; H Kirschmann; Lea Shalmon; Rina Zaizov; E Schwartz; Eric F Rappaport
Systematic use of automated fluorescence-based sequence analysis of amplified genomic DNA for rapid detection of point mutations.
American journal of hematology 1994;46(2):127-33.
1994: F Galacteros; Emmanuelle Girodon; A M'Rad; J Martin; Michel Goossens; L Jaber; Ian Cohen; Hannah Tamary; Yacov Goshen; Rina Zaizov
Hb Taybe (alpha 38 or 39 THR deleted): an alpha-globin defect, silent in the heterozygous state and producing severe hemolytic anemia in the homozygous.
Comptes rendus de l'Académie des sciences. Série III, Sciences de la vie 1994;317(5):437-44.
1993: Hannah Tamary; C Kaplinsky; S Shvartzmayer; T Umiel; M Pecht; S Levin; Rina Zaizov
Transient erythroblastopenia of childhood. Evidence for cell-mediated suppression of erythropoiesis.
The American journal of pediatric hematology/oncology 1993;15(4):386-91.
1993: Kazuhiko Adachi; Saul Surrey; Hannah Tamary; J Kim; H S Eck; Eric F Rappaport; Kwaku Ohene-Frempong
Hb Shelby [beta 131(H9)Gln-->Lys] in association with Hb S [beta 6(A3)Glu-->Val]: characterization, stability, and effects on Hb S polymerization.
Hemoglobin 1993;17(4):329-43.
1992: C Kaplinsky; C Mor; Ian J Cohen; Yacov Goshen; Isaac Yaniv; Hannah Tamary; L Jaber; Batia Stark; S Stern; Rina Zaizov
Childhood malignant thymoma: clinical, therapeutic, and immunohistochemical considerations.
Pediatric hematology and oncology 1992;9(3):261-8.
1992: C Kaplinsky; Amos Frisch; Ian J Cohen; Yacov Goshen; L Jaber; Isaac Yaniv; Batia Stark; Hannah Tamary; Rina Zaizov
T-cell acute lymphoblastic leukemia following therapy of rhabdomyosarcoma.
Medical and pediatric oncology 1992;20(3):229-31.
1991: J M Gomori; G Horev; Hannah Tamary; J Zandback; L Kornreich; Rina Zaizov; Enrique Freud; O Krief; J Ben-Meir; H Rotem
Hepatic iron overload: quantitative MR imaging.
Radiology 1991;179(2):367-9.