Page 1 | Search Results | Blood | American Society of Hematology

1-17 of 17

Sort by

Sort Order Select

Journal Articles

Prospective Controlled Monitoring of Hemlibra Prophylaxis Initiation in a Large Cohort of Hemophilia a Patients- Real World Data

Assaf Arie Barg, Tami Livnat, PhD, Tami Brutman-Barazani, Nurit Rosenberg, Ivan Budnik, MD PhD, Gili Kenet

Blood (2019) 134 (Supplement_1): 2397.

https://doi.org/10.1182/blood-2019-122010

Published: 2019

Journal Articles

Identification and Characterization of a New Mutation in Coagulation Factor VII (Carmel mutation), with Different Reactivity Towards Tissue Factors of Different Origin

Aliza Cassel, PhD, Nurit Rosenberg, PhD, Emad Muhammad, PhD, Rima Dazdik, PhD, Miriam Berl, Meir Preis, MD PhD

Blood (2016) 128 (22): 1396.

https://doi.org/10.1182/blood.V128.22.1396.1396

Published: 2016

Journal Articles

Factor VII Deficiency in the Negev - a 10 Years' Experience of One Tertiary Center

Yariv Fruchtman, MD, Miri Ben harosh, MD, Joseph Kapelushnik, MD, Julia Mazar, PhD, Gili Kenet, Nurit Rosenberg, PhD

Blood (2015) 126 (23): 4695.

https://doi.org/10.1182/blood.V126.23.4695.4695

Published: 2015

Journal Articles

Persistent neonatal thrombocytopenia can be caused by IgA antiplatelet antibodies in breast milk of immune thrombocytopenic mothers

Hagit Hauschner, Nurit Rosenberg, Uri Seligsohn, Rafael Mendelsohn, Aryeh Simmonds, Yakov Shiff, Yaakov Schachter, Shraga Aviner, Nechama Sharon

Blood (2015) 126 (5): 661–664.

https://doi.org/10.1182/blood-2014-12-614446

Published: 2015

Includes: Supplemental data

Journal Articles

Breast Milk from Immune Thrombocytopenic Mothers Can Contain Anti Platelet Antibodies That Are Associated with Persistent Thrombocytopenia in Neonates

Nehama Sharon, MD, Nurit Rosenberg, PhD, Uri Seligsohn, MD, Aryeh Simmonds, MD, Yakov Shiff, MD, Yaakov Schechter, MD, Hagit Hausner, PhD

Blood (2014) 124 (21): 4181.

https://doi.org/10.1182/blood.V124.21.4181.4181

Published: 2014

Journal Articles

A Simple Two Step Approach for Diagnosis of Heparin Induced Thrmbocytopenia Using 4T Score and PaGIA Testing

Aaron Lubetsky, MD, Gili Kenet, MD, Nurit Rosenberg, PhD, Ilia Tamarin

Blood (2014) 124 (21): 1449.

https://doi.org/10.1182/blood.V124.21.1449.1449

Published: 2014

Journal Articles

Essential Thrombocythemia Patients with CALR Mutations Have Increased Platelet Activation Markers Compared to JAK2V617F Mutated Patients

Maya Koren-Michowitz, MD, Hagit Hauschner, PhD, Yulia Shuly, MA, Meital Nagar, PhD, Elena Ribakovsky, MD, Mudi Misgav, MD, Odit Gutwein, MD, Uri Seligsohn, MD, Nurit Rosenberg, PhD, Arnon Nagler, MD

Blood (2014) 124 (21): 3223.

https://doi.org/10.1182/blood.V124.21.3223.3223

Published: 2014

Journal Articles

The Role Of Protein Disulfide Isomerase In The Post-Ligation Phase Of β 3 Integrin-Dependent Cell Adhesion

Avi Leader, MD, Ronit Mor-Cohen, PhD, Nurit Rosenberg, PhD, Ron Ram, MD, Uri Seligsohn, MD, Aida Inbal, MD, Judith Lahav, PhD

Blood (2013) 122 (21): 2307.

https://doi.org/10.1182/blood.V122.21.2307.2307

Published: 2013

Journal Articles

International Consortium for the Study of Clinical and Molecular Aspects of Bernard-Soulier Syndrome

Anna Savoia, PhD, Shinji Kunishima, PhD, Patrizia Noris, MD, Nuria Pujol-Moix, MD, Dermot Kenny, MD, Nurit Rosenberg, Margaret L. Rand, PhD, Barbara Zieger, MD, Ali F. Gargouri, PhD, Miriam P Beltrame, Felisa C. Molinas, MD, PhD, Mehran Karimi, MD, Christopher Ward, MB, CHB, PhD, Philip Kuriakose, MD, Nadia Ewing, MD, Carol Diamond, MD, Alok Srivastava, MD, Carlo Luigi Balduini, MD, Francois Lanza, PhD, MD

Blood (2011) 118 (21): 707.

https://doi.org/10.1182/blood.V118.21.707.707

Published: 2011

Journal Articles

HLADRB30101 Combined with DRB40101 Are Potential Predictor of Neonatal Alloimmune Thrombocytopenia (NAIT) Development

Ophira Salomon, Ron Loewenthal, Rivka Kalt, Nurit Rosenberg, Rima Dardik, Vered Yahalom, Ofelia Avishai, Orit Frenkel, Ephraim Gazit, Shlomon Lipitz

Blood (2011) 118 (21): 2221.

https://doi.org/10.1182/blood.V118.21.2221.2221

Published: 2011

Journal Articles

A unique interaction between αIIb and β3 in the head region is essential for outside-in signaling–related functions of αIIbβ3 integrin

Hagit Hauschner, Meytal Landau, Uri Seligsohn, Nurit Rosenberg

Blood (2010) 115 (22): 4542–4550.

https://doi.org/10.1182/blood-2009-10-251066

Published: 2010

Includes: Supplemental data

Journal Articles

Major mutations in calf-1 and calf-2 domains of glycoprotein IIb in patients with Glanzmann thrombasthenia enable GPIIb/IIIa complex formation, but impair its transport from the endoplasmic reticulum to the Golgi apparatus

Nurit Rosenberg, Rivka Yatuv, Vladimir Sobolev, Hava Peretz, Ariella Zivelin, Uri Seligsohn

Blood (2003) 101 (12): 4808–4815.

https://doi.org/10.1182/blood-2002-08-2452

Published: 2003

Journal Articles

Factor XI deficiency in French Basques is caused predominantly by an ancestral Cys38Arg mutation in the factor XI gene

Ariella Zivelin, Frederic Bauduer, Louis Ducout, Hava Peretz, Nurit Rosenberg, Rivka Yatuv, Uri Seligsohn

Blood (2002) 99 (7): 2448–2454.

https://doi.org/10.1182/blood.V99.7.2448

Published: 2002

Journal Articles

Identification of a region in glycoprotein IIIa involved in subunit association with glycoprotein IIb: further lessons from Iraqi-Jewish Glanzmann thrombasthenia

Rivka Yatuv, Nurit Rosenberg, Ariella Zivelin, Hava Peretz, Rima Dardik, Luba Trakhtenbrot, Uri Seligsohn

Blood (2001) 98 (4): 1063–1069.

https://doi.org/10.1182/blood.V98.4.1063

Published: 2001

Journal Articles

Synergistic Effects of Prothrombotic Polymorphisms and Atherogenic Factors on the Risk of Myocardial Infarction in Young Males

Aida Inbal, Dov Freimark, Baruch Modan, Angela Chetrit, Shlomi Matetzky, Nurit Rosenberg, Rima Dardik, Zvia Baron, Uri Seligsohn

Blood (1999) 93 (7): 2186–2190.

https://doi.org/10.1182/blood.V93.7.2186

Published: 1999

Journal Articles

A Single Genetic Origin for the Common Prothrombotic G20210A Polymorphism in the Prothrombin Gene

Ariella Zivelin, Nurit Rosenberg, Shlomit Faier, Nurit Kornbrot, Hava Peretz, Christine Mannhalter, Marie Helene Horellou, Uri Seligsohn

Blood (1998) 92 (4): 1119–1124.

https://doi.org/10.1182/blood.V92.4.1119

Published: 1998

Journal Articles

Glanzmann Thrombasthenia Caused by an 11.2-kb Deletion in the Glycoprotein IIIa (β 3 ) Is a Second Mutation in Iraqi Jews That Stemmed From a Distinct Founder

Nurit Rosenberg, Rivka Yatuv, Yael Orion, Ariella Zivelin, Rima Dardik, Hava Peretz, Uri Seligsohn

Blood (1997) 89 (10): 3654–3662.

https://doi.org/10.1182/blood.V89.10.3654

Published: 1997

Update search

NARROW

Publications

Format

Subjects

Article Type

Topics

Date

Availability

Prospective Controlled Monitoring of Hemlibra Prophylaxis Initiation in a Large Cohort of Hemophilia a Patients- Real World Data

Identification and Characterization of a New Mutation in Coagulation Factor VII (Carmel mutation), with Different Reactivity Towards Tissue Factors of Different Origin

Factor VII Deficiency in the Negev - a 10 Years' Experience of One Tertiary Center

Persistent neonatal thrombocytopenia can be caused by IgA antiplatelet antibodies in breast milk of immune thrombocytopenic mothers

Breast Milk from Immune Thrombocytopenic Mothers Can Contain Anti Platelet Antibodies That Are Associated with Persistent Thrombocytopenia in Neonates

A Simple Two Step Approach for Diagnosis of Heparin Induced Thrmbocytopenia Using 4T Score and PaGIA Testing

Essential Thrombocythemia Patients with CALR Mutations Have Increased Platelet Activation Markers Compared to JAK2V617F Mutated Patients

The Role Of Protein Disulfide Isomerase In The Post-Ligation Phase Of β 3 Integrin-Dependent Cell Adhesion

International Consortium for the Study of Clinical and Molecular Aspects of Bernard-Soulier Syndrome

HLADRB30101 Combined with DRB40101 Are Potential Predictor of Neonatal Alloimmune Thrombocytopenia (NAIT) Development

A unique interaction between αIIb and β3 in the head region is essential for outside-in signaling–related functions of αIIbβ3 integrin

Major mutations in calf-1 and calf-2 domains of glycoprotein IIb in patients with Glanzmann thrombasthenia enable GPIIb/IIIa complex formation, but impair its transport from the endoplasmic reticulum to the Golgi apparatus

Factor XI deficiency in French Basques is caused predominantly by an ancestral Cys38Arg mutation in the factor XI gene

Identification of a region in glycoprotein IIIa involved in subunit association with glycoprotein IIb: further lessons from Iraqi-Jewish Glanzmann thrombasthenia

Synergistic Effects of Prothrombotic Polymorphisms and Atherogenic Factors on the Risk of Myocardial Infarction in Young Males

A Single Genetic Origin for the Common Prothrombotic G20210A Polymorphism in the Prothrombin Gene

Glanzmann Thrombasthenia Caused by an 11.2-kb Deletion in the Glycoprotein IIIa (β 3 ) Is a Second Mutation in Iraqi Jews That Stemmed From a Distinct Founder

Email alerts

ASH Publications

American Society of Hematology

Update search

Email alerts

ASH Publications

American Society of Hematology

This Feature Is Available To Subscribers Only