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Journal Articles

Genotype-phenotype correlations in chronic granulomatous disease: insights from a large national cohort

Blood (2024) 144 (12): 1300–1313.

https://doi.org/10.1182/blood.2023022590

Published: 2024

Includes: Supplemental data

Journal Articles

Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype

Blood (2016) 127 (25): 3154–3164.

https://doi.org/10.1182/blood-2015-11-679902

Published: 2016

Includes: Supplemental data

Journal Articles

Deficiency Of JAGN1 Causes Severe Congenital Neutropenia Associated With Defective Secretory Pathway and Aberrant Myeloid Cell Homeostasis

Blood (2013) 122 (21): 439.

https://doi.org/10.1182/blood.V122.21.439.439

Published: 2013

Journal Articles

Kindlin-3 is required for the stabilization of TCR-stimulated LFA-1:ICAM-1 bonds critical for lymphocyte arrest and spreading on dendritic cells

Sara W. Feigelson, Valentin Grabovsky, Eugenia Manevich-Mendelson, Ronit Pasvolsky, Ziv Shulman, Vera Shinder, Eugenia Klein, Amos Etzioni, Memet Aker, Ronen Alon

Blood (2011) 117 (26): 7042–7052.

https://doi.org/10.1182/blood-2010-12-322859

Published: 2011

Includes: Multimedia, Supplemental data

Journal Articles

Loss of Kindlin-3 in LAD-III eliminates LFA-1 but not VLA-4 adhesiveness developed under shear flow conditions

Eugenia Manevich-Mendelson, Sara W. Feigelson, Ronit Pasvolsky, Memet Aker, Valentin Grabovsky, Ziv Shulman, Sara Sebnem Kilic, Maria Alessandra Rosenthal-Allieri, Shifra Ben-Dor, Adi Mory, Alain Bernard, Markus Moser, Amos Etzioni, Ronen Alon

Blood (2009) 114 (11): 2344–2353.

https://doi.org/10.1182/blood-2009-04-218636

Published: 2009

Includes: Supplemental data

Journal Articles

Kindlin-3: a new gene involved in the pathogenesis of LAD-III

Adi Mory, Sara W. Feigelson, Nese Yarali, Sara S. Kilic, Gulsum I. Bayhan, Ruth Gershoni-Baruch, Amos Etzioni, Ronen Alon

Blood (2008) 112 (6): 2591.

https://doi.org/10.1182/blood-2008-06-163162

Published: 2008

Includes: Supplemental data

Journal Articles

LAD III versus LAD I variant

Amos Etzioni, Ronen Alon

Blood (2007) 110 (12): 4129.

https://doi.org/10.1182/blood-2007-05-089227

Published: 2007

Journal Articles

LAD-III, a leukocyte adhesion deficiency syndrome associated with defective Rap1 activation and impaired stabilization of integrin bonds

Tatsuo Kinashi, Memet Aker, Maya Sokolovsky-Eisenberg, Valentin Grabovsky, Chisato Tanaka, Revital Shamri, Sara Feigelson, Amos Etzioni, Ronen Alon

Blood (2004) 103 (3): 1033–1036.

https://doi.org/10.1182/blood-2003-07-2499

Published: 2004

Journal Articles

A novel genetic leukocyte adhesion deficiency in subsecond triggering of integrin avidity by endothelial chemokines results in impaired leukocyte arrest on vascular endothelium under shear flow

Ronen Alon, Memet Aker, Sara Feigelson, Maya Sokolovsky-Eisenberg, Donald E. Staunton, Guy Cinamon, Valentin Grabovsky, Revital Shamri, Amos Etzioni

Blood (2003) 101 (11): 4437–4445.

https://doi.org/10.1182/blood-2002-11-3427

Published: 2003

Journal Articles

Autoimmunity in severe combined immunodeficiency (SCID)

Ronit Elhasid, Reuven Bergman, Amos Etzioni

Blood (2002) 100 (7): 2677–2678.

https://doi.org/10.1182/blood-2002-05-1583

Published: 2002

Journal Articles

Alterations of the X-linked lymphoproliferative disease gene SH2D1A in common variable immunodeficiency syndrome

Massimo Morra, Olin Silander, Silvia Calpe, Michelle Choi, Hans Oettgen, Laurie Myers, Amos Etzioni, Rebecca Buckley, Cox Terhorst

Blood (2001) 98 (5): 1321–1325.

https://doi.org/10.1182/blood.V98.5.1321

Published: 2001

Journal Articles

Fucose supplementation in leukocyte adhesion deficiency type II

Amos Etzioni, Michela Tonetti

Blood (2000) 95 (11): 3641–3643.

https://doi.org/10.1182/blood.V95.11.3641

Published: 2000

Journal Articles

Loss of Endothelial Surface Expression of E-Selectin—A Third LAD Syndrome?

Amos Etzioni

Blood (1999) 94 (11): 3956–3957.

https://doi.org/10.1182/blood.V94.11.3956

Published: 1999

Journal Articles

Of Man and Mouse: Leukocyte and Endothelial Adhesion Molecule Deficiencies

Amos Etzioni, Claire M. Doerschuk, John M. Harlan

Blood (1999) 94 (10): 3281–3288.

https://doi.org/10.1182/blood.V94.10.3281.422k37_3281_3288

Published: 1999

NARROW

Genotype-phenotype correlations in chronic granulomatous disease: insights from a large national cohort

Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype

Deficiency Of JAGN1 Causes Severe Congenital Neutropenia Associated With Defective Secretory Pathway and Aberrant Myeloid Cell Homeostasis

Kindlin-3 is required for the stabilization of TCR-stimulated LFA-1:ICAM-1 bonds critical for lymphocyte arrest and spreading on dendritic cells

Loss of Kindlin-3 in LAD-III eliminates LFA-1 but not VLA-4 adhesiveness developed under shear flow conditions

Kindlin-3: a new gene involved in the pathogenesis of LAD-III

LAD III versus LAD I variant

LAD-III, a leukocyte adhesion deficiency syndrome associated with defective Rap1 activation and impaired stabilization of integrin bonds

A novel genetic leukocyte adhesion deficiency in subsecond triggering of integrin avidity by endothelial chemokines results in impaired leukocyte arrest on vascular endothelium under shear flow

Autoimmunity in severe combined immunodeficiency (SCID)

Alterations of the X-linked lymphoproliferative disease gene SH2D1A in common variable immunodeficiency syndrome

Fucose supplementation in leukocyte adhesion deficiency type II

Loss of Endothelial Surface Expression of E-Selectin—A Third LAD Syndrome?

Of Man and Mouse: Leukocyte and Endothelial Adhesion Molecule Deficiencies

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American Society of Hematology

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ASH Publications

American Society of Hematology

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