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Alloimmunization and autoimmunization in adult transfusion-dependent thalassemia patients: a report from a comprehensive center in Israel

Annals of hematology, 2020-12, Vol.99 (12), p.2731-2736

2020

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Thalassemia in Israel: 2012

Thalassemia reports, 2013-03, Vol.3 (11), p.e28

Stark, Pinhas

2013

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High incidence of silent cerebral infarcts in adult patients with Beta thalassemia major

Thrombosis research, 2016-08, Vol.144, p.119-122

2016

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Reduced Number and Function of Endothelial Progenitor Cells in Patients with Beta Thalassemia Major

Blood, 2019-11, Vol.134 (Supplement_1), p.2247-2247

2019

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Splenectomy in childhood for non‐malignant haematologic disorders – long‐term follow‐up shows minimal adverse effects

British journal of haematology, 2020-09, Vol.190 (6), p.909-915

2020

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Alloimmunization and Autoimmunization in Adult Transfusion Dependent Beta Thalassemia Major Patients: Report from a Comprehensive Center in Israel

Blood, 2017-12, Vol.130, p.2408-2408

2017

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Long Term Outcome of Splenectomy in Pediatric Patients with Non-Malignant Hematological Diseases: Four Decades of Follow up

Blood, 2016-12, Vol.128 (22), p.3585-3585

2016

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Cardiac and pancreatic iron overload evaluation of sickle/β-Thalassemia patients utilizing T2 MRI

Journal of cardiovascular magnetic resonance, 2009-01, Vol.11 (S1), p.P112-P112, Article P112

2009

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Acquired proximal renal tubular dysfunction in β-thalassemia patients treated with deferasirox

Journal of pediatric hematology/oncology, 2010-10, Vol.32 (7), p.564-567

2010

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Thalassemia Major and Intermedia in Older Patients – a Single Center Experience

Blood, 2014-12, Vol.124 (21), p.2685-2685

2014

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GFR in Patients with β-Thalassemia Major

Clinical journal of the American Society of Nephrology, 2015-08, Vol.10 (8), p.1350-1356

2015

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Lactose intolerance is not the cause of gastrointestinal adverse effects in beta thalassemia patients treated with deferasirox

American journal of hematology, 2014-09, Vol.89 (9), p.938-939

2014

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Transfusion service management of sickle-cell disease patients

Vox sanguinis, 2016-04, Vol.110 (3), p.288-294

2016

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T2 MRI Provides No Evidence for Myocardial and Pancreatic Iron Overload in Multitransfused Patients with Sickle/β-Thalassemia

Blood, 2008-11, Vol.112 (11), p.1422-1422

2008

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Thrombotic complications in essential thrombocythemia with relatively low platelet counts

American journal of hematology, 1997-11, Vol.56 (3), p.168-172

1997

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Antiphospholipid antibodies may be a new prognostic parameter in aggressive non-Hodgkin's lymphoma

European journal of haematology, 2006-05, Vol.76 (5), p.384-391

2006

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BCR-ABL Transcripts in bone marrow aspirates of Philadelphia-negative essential thrombocythemia patients : Clinical presentation

Blood, 1997-10, Vol.90 (7), p.2768-2771

1997

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B12 deficiency: not an uncommon genetic‐related disorder

British journal of haematology, 2002-12, Vol.119 (3), p.882-883

2002

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Misleading steal phenomenon of Ga-67 uptake by the spleen in a patient with sarcoidosis

Clinical nuclear medicine, 2007-06, Vol.32 (6), p.468-470

2007

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B(12) deficiency: Not an uncommon genetic-related disorder

British journal of haematology, 2002-12, Vol.119 (3), p.882

2002

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Sjögren's syndrome associated T cell large granular lymphocyte leukemia: a possible common etiopathogenesis

Journal of rheumatology, 2001-11, Vol.28 (11), p.2551

2001

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Sublingual therapy for cobalamin deficiency as an alternative to oral and parenteral cobalamin supplementation

The Lancet (British edition), 1999-08, Vol.354 (9180), p.740-741

1999

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Serum CA 125 as a Prognostic Factor in Non-Hodgkin's Lymphoma

Leukemia & lymphoma, 2003-01, Vol.44 (10), p.1733-1738

2003

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Sublingual cobalamin for pernicious anaemia

The Lancet (British edition), 1999-12, Vol.354 (9195), p.2081-2081

1999

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Alloimmunization and autoimmunization in adult transfusion-dependent thalassemia patients: a report from a comprehensive center in Israel

Thalassemia in Israel: 2012

A Phase 3 Trial of Luspatercept in Patients with Transfusion-Dependent β-Thalassemia

High incidence of silent cerebral infarcts in adult patients with Beta thalassemia major

Reduced Number and Function of Endothelial Progenitor Cells in Patients with Beta Thalassemia Major

Splenectomy in childhood for non‐malignant haematologic disorders – long‐term follow‐up shows minimal adverse effects

Alloimmunization and Autoimmunization in Adult Transfusion Dependent Beta Thalassemia Major Patients: Report from a Comprehensive Center in Israel

Long Term Outcome of Splenectomy in Pediatric Patients with Non-Malignant Hematological Diseases: Four Decades of Follow up

Cardiac and pancreatic iron overload evaluation of sickle/β-Thalassemia patients utilizing T2 MRI

Acquired proximal renal tubular dysfunction in β-thalassemia patients treated with deferasirox

Thalassemia Major and Intermedia in Older Patients – a Single Center Experience

GFR in Patients with β-Thalassemia Major

Lactose intolerance is not the cause of gastrointestinal adverse effects in beta thalassemia patients treated with deferasirox

Transfusion service management of sickle-cell disease patients

T2 MRI Provides No Evidence for Myocardial and Pancreatic Iron Overload in Multitransfused Patients with Sickle/β-Thalassemia

Thrombotic complications in essential thrombocythemia with relatively low platelet counts

Antiphospholipid antibodies may be a new prognostic parameter in aggressive non-Hodgkin's lymphoma

BCR-ABL Transcripts in bone marrow aspirates of Philadelphia-negative essential thrombocythemia patients : Clinical presentation

B12 deficiency: not an uncommon genetic‐related disorder

Misleading steal phenomenon of Ga-67 uptake by the spleen in a patient with sarcoidosis

B(12) deficiency: Not an uncommon genetic-related disorder

Sjögren's syndrome associated T cell large granular lymphocyte leukemia: a possible common etiopathogenesis

Sublingual therapy for cobalamin deficiency as an alternative to oral and parenteral cobalamin supplementation

Serum CA 125 as a Prognostic Factor in Non-Hodgkin's Lymphoma

Sublingual cobalamin for pernicious anaemia

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