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Search life-sciences literature (45,103,477 articles, preprints and more)

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Successful Haematopoietic Stem Cell Transplantation for LRBA Deficiency with Fludarabine, Treosulfan, and Thiotepa-Based Conditioning.
Shadur B, NasserEddin A, Zaidman I, Schejter YD, Even-Or E, Berkun Y, Meyts I, Hmedat H, Sulaiman A, Tangye SG, Stepensky P
J Clin Immunol, 45(1):3, 12 Sep 2024
Cited by: 0 articles | PMID: 39264459 | PMCID: PMC11393013
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An efficient and successful outcome after haematopoietic stem cell transplantation in a patient with an LPS-responsive beige-like anchor gene mutation.
Shen C, Zhang L, Meng Y, Yang L, He W, Lei X, Zhou L, An Y, Dou Y
Front Pediatr, 12:1420118, 23 Jul 2024
Cited by: 0 articles | PMID: 39108694 | PMCID: PMC11300271
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Central nervous system manifestations of LRBA deficiency: case report of two siblings and literature review.
Mangodt TC, Vanden Driessche K, Norga KK, Moes N, De Bruyne M, Haerynck F, Bordon V, Jansen AC, Jonckheere AI
BMC Pediatr, 23(1):353, 13 Jul 2023
Cited by: 3 articles | PMID: 37443020 | PMCID: PMC10339488
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Long-term follow-up of patients with LPS-responsive beige-like anchor protein deficiency after reduced-intensity conditioning for allogeneic hematopoietic stem cell transplantation: report of two cases.
Jafari L, Mohseni R, Barhoom D, Abou Fakher FH, Behfar M, Hamidieh AA
Hematol Transfus Cell Ther, 46(4):481-484, 06 May 2022
Cited by: 0 articles | PMID: 35643917 | PMCID: PMC11451407
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Potential protein-phenotype correlation in three lipopolysaccharide-responsive beige-like anchor protein-deficient patients.
Tang WJ, Hu WH, Huang Y, Wu BB, Peng XM, Zhai XW, Qian XW, Ye ZQ, Xia HJ, Wu J, Shi JR
World J Clin Cases, 9(21):5873-5888, 01 Jul 2021
Cited by: 0 articles | PMID: 34368306 | PMCID: PMC8316938
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Acute Cervical Longitudinally Extensive Transverse Myelitis in a Child With Lipopolysaccharide-Responsive-Beige-Like-Anchor-Protein (LRBA) Deficiency: A New Complication of a Rare Disease.
Chinello M, Mauro M, Cantalupo G, Talenti G, Mariotto S, Balter R, De Bortoli M, Vitale V, Zaccaron A, Bonetti E, Di Carlo D, Barzaghi F, Cesaro S
Front Pediatr, 8:580963, 16 Oct 2020
Cited by: 1 article | PMID: 33178652 | PMCID: PMC7596261
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Hematopoietic Stem Cell Transplantation in Primary Immunodeficiency Diseases: Current Status and Future Perspectives.
Castagnoli R, Delmonte OM, Calzoni E, Notarangelo LD
Front Pediatr, 7:295, 08 Aug 2019
Cited by: 72 articles | PMID: 31440487 | PMCID: PMC6694735
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LRBA Deficiency in a Patient With a Novel Homozygous Mutation Due to Chromosome 4 Segmental Uniparental Isodisomy.
Soler-Palacín P, Garcia-Prat M, Martín-Nalda A, Franco-Jarava C, Rivière JG, Plaja A, Bezdan D, Bosio M, Martínez-Gallo M, Ossowski S, Colobran R
Front Immunol, 9:2397, 16 Oct 2018
Cited by: 21 articles | PMID: 30386343 | PMCID: PMC6198091
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Respiratory manifestations in LPS-responsive beige-like anchor (LRBA) protein-deficient patients.
Shamriz O, Shadur B, NaserEddin A, Zaidman I, Simanovsky N, Elpeleg O, Kerem E, Reiter J, Stepensky P
Eur J Pediatr, 177(8):1163-1172, 18 May 2018
Cited by: 6 articles | PMID: 29777306
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The Treatment of Inflammatory Bowel Disease in Patients with Selected Primary Immunodeficiencies.
Shouval DS, Kowalik M, Snapper SB
J Clin Immunol, 38(5):579-588, 29 Jun 2018
Cited by: 5 articles | PMID: 29956079
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Keeping it in the family: the case for considering late-onset combined immunodeficiency a subset of common variable immunodeficiency disorders.
Ameratunga R, Ahn Y, Jordan A, Lehnert K, Brothers S, Woon ST
Expert Rev Clin Immunol, 14(7):549-556, 26 Jun 2018
Cited by: 13 articles | PMID: 29806948
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Bacille Calmette-Guerin Complications in Newly Described Primary Immunodeficiency Diseases: 2010-2017.
Nunes-Santos CJ, Rosenzweig SD
Front Immunol, 9:1423, 22 Jun 2018
Cited by: 6 articles | PMID: 29988375 | PMCID: PMC6023996
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Novel LRBA Mutation and Possible Germinal Mosaicism in a Slavic Family.
Sharapova SO, Haapaniemi E, Sakovich IS, Rojas J, Gámez-Díaz L, Mareika YE, Guryanova IE, Migas AA, Mikhaleuskaya TM, Grimbacher B, Aleinikova OV
J Clin Immunol, 38(4):471-474, 26 May 2018
Cited by: 1 article | PMID: 29804237
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Assessing Disease Severity in Common Variable Immunodeficiency Disorders (CVID) and CVID-Like Disorders.
Ameratunga R
Front Immunol, 9:2130, 28 Sep 2018
Cited by: 23 articles | PMID: 30323807 | PMCID: PMC6172311
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Polyautoimmunity in Patients with LPS-Responsive Beige-Like Anchor (LRBA) Deficiency.
Azizi G, Abolhassani H, Zaki-Dizaji M, Habibi S, Mohammadi H, Shaghaghi M, Yazdani R, Anaya JM, Rezaei N, Hammarström L, Aghamohammadi A
Immunol Invest, 47(5):457-467, 12 Mar 2018
Cited by: 8 articles | PMID: 29528757
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Phenotype, penetrance, and treatment of 133 cytotoxic T-lymphocyte antigen 4-insufficient subjects.
Schwab C, Gabrysch A, Olbrich P, Patiño V, Warnatz K, Wolff D, Hoshino A, Kobayashi M, Imai K, Takagi M, Dybedal I, Haddock JA, Sansom DM, Lucena JM, Seidl M, Schmitt-Graeff A, Reiser V, Emmerich F, Frede N, [...] Grimbacher B
J Allergy Clin Immunol, 142(6):1932-1946, 04 May 2018
Cited by: 202 articles | PMID: 29729943 | PMCID: PMC6215742
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Multiple Presentations of LRBA Deficiency: a Single-Center Experience.
Kostel Bal S, Haskologlu S, Serwas NK, Islamoglu C, Aytekin C, Kendirli T, Kuloglu Z, Yavuz G, Dalgic B, Siklar Z, Kansu A, Ensari A, Boztug K, Dogu F, Ikinciogullari A
J Clin Immunol, 37(8):790-800, 27 Sep 2017
Cited by: 29 articles | PMID: 28956255 | PMCID: PMC7086713
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Multifocal gastric adenocarcinoma in a patient with LRBA deficiency.
Bratanič N, Kovač J, Pohar K, Trebušak Podkrajšek K, Ihan A, Battelino T, Avbelj Stefanija M
Orphanet J Rare Dis, 12(1):131, 18 Jul 2017
Cited by: 16 articles | PMID: 28720148 | PMCID: PMC5516372
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Treatment of severe forms of LPS-responsive beige-like anchor protein deficiency with allogeneic hematopoietic stem cell transplantation.
Seidel MG, Böhm K, Dogu F, Worth A, Thrasher A, Florkin B, İkincioğulları A, Peters A, Bakhtiar S, Meeths M, Stepensky P, Meyts I, Sharapova SO, Gámez-Díaz L, Hammarström L, Ehl S, Grimbacher B, Gennery AR, Inborn Errors Working Party of the European Group for Blood and Marrow Transplantation
J Allergy Clin Immunol, 141(2):770-775.e1, 10 May 2017
Cited by: 28 articles | PMID: 28502825
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Clinical, immunologic, molecular analyses and outcomes of iranian patients with LRBA deficiency: A longitudinal study.
Azizi G, Abolhassani H, Mahdaviani SA, Chavoshzadeh Z, Eshghi P, Yazdani R, Kiaee F, Shaghaghi M, Mohammadi J, Rezaei N, Hammarström L, Aghamohammadi A
Pediatr Allergy Immunol, 28(5):478-484, 19 Jun 2017
Cited by: 28 articles | PMID: 28512785
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Recessively Inherited LRBA Mutations Cause Autoimmunity Presenting as Neonatal Diabetes.
Johnson MB, De Franco E, Lango Allen H, Al Senani A, Elbarbary N, Siklar Z, Berberoglu M, Imane Z, Haghighi A, Razavi Z, Ullah I, Alyaarubi S, Gardner D, Ellard S, Hattersley AT, Flanagan SE
Diabetes, 66(8):2316-2322, 04 May 2017
Cited by: 35 articles | PMID: 28473463 | PMCID: PMC5524180
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Murine LRBA deficiency causes CTLA-4 deficiency in Tregs without progression to immune dysregulation.
Burnett DL, Parish IA, Masle-Farquhar E, Brink R, Goodnow CC
Immunol Cell Biol, 95(9):775-788, 14 Jun 2017
Cited by: 21 articles | PMID: 28611475 | PMCID: PMC5636941
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CHAI and LATAIE: new genetic diseases of CTLA-4 checkpoint insufficiency.
Lo B, Fritz JM, Su HC, Uzel G, Jordan MB, Lenardo MJ
Blood, 128(8):1037-1042, 14 Jul 2016
Cited by: 70 articles | PMID: 27418640 | PMCID: PMC5000841
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LRBA is Essential for Allogeneic Responses in Bone Marrow Transplantation.
Park MY, Sudan R, Srivastava N, Neelam S, Youngs C, Wang JW, Engelman RW, Kerr WG
Sci Rep, 6:36568, 08 Nov 2016
Cited by: 9 articles | PMID: 27824136 | PMCID: PMC5099895
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Atypical Manifestation of LPS-Responsive Beige-Like Anchor Deficiency Syndrome as an Autoimmune Endocrine Disorder without Enteropathy and Immunodeficiency.
Bakhtiar S, Ruemmele F, Charbit-Henrion F, Lévy E, Rieux-Laucat F, Cerf-Bensussan N, Bader P, Paetow U
Front Pediatr, 4:98, 14 Sep 2016
Cited by: 12 articles | PMID: 27683652 | PMCID: PMC5022363
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1-25 of 26 results

1 2

Search life-sciences literature (45,103,477 articles, preprints and more)

Search results

Successful Haematopoietic Stem Cell Transplantation for LRBA Deficiency with Fludarabine, Treosulfan, and Thiotepa-Based Conditioning.

An efficient and successful outcome after haematopoietic stem cell transplantation in a patient with an LPS-responsive beige-like anchor gene mutation.

Central nervous system manifestations of LRBA deficiency: case report of two siblings and literature review.

Long-term follow-up of patients with LPS-responsive beige-like anchor protein deficiency after reduced-intensity conditioning for allogeneic hematopoietic stem cell transplantation: report of two cases.

Potential protein-phenotype correlation in three lipopolysaccharide-responsive beige-like anchor protein-deficient patients.

Acute Cervical Longitudinally Extensive Transverse Myelitis in a Child With Lipopolysaccharide-Responsive-Beige-Like-Anchor-Protein (LRBA) Deficiency: A New Complication of a Rare Disease.

Hematopoietic Stem Cell Transplantation in Primary Immunodeficiency Diseases: Current Status and Future Perspectives.

LRBA Deficiency in a Patient With a Novel Homozygous Mutation Due to Chromosome 4 Segmental Uniparental Isodisomy.

Respiratory manifestations in LPS-responsive beige-like anchor (LRBA) protein-deficient patients.

The Treatment of Inflammatory Bowel Disease in Patients with Selected Primary Immunodeficiencies.

Keeping it in the family: the case for considering late-onset combined immunodeficiency a subset of common variable immunodeficiency disorders.

Bacille Calmette-Guerin Complications in Newly Described Primary Immunodeficiency Diseases: 2010-2017.

Novel LRBA Mutation and Possible Germinal Mosaicism in a Slavic Family.

Assessing Disease Severity in Common Variable Immunodeficiency Disorders (CVID) and CVID-Like Disorders.

Polyautoimmunity in Patients with LPS-Responsive Beige-Like Anchor (LRBA) Deficiency.

Phenotype, penetrance, and treatment of 133 cytotoxic T-lymphocyte antigen 4-insufficient subjects.

Multiple Presentations of LRBA Deficiency: a Single-Center Experience.

Multifocal gastric adenocarcinoma in a patient with LRBA deficiency.

Treatment of severe forms of LPS-responsive beige-like anchor protein deficiency with allogeneic hematopoietic stem cell transplantation.

Clinical, immunologic, molecular analyses and outcomes of iranian patients with LRBA deficiency: A longitudinal study.

Recessively Inherited LRBA Mutations Cause Autoimmunity Presenting as Neonatal Diabetes.

Murine LRBA deficiency causes CTLA-4 deficiency in Tregs without progression to immune dysregulation.

CHAI and LATAIE: new genetic diseases of CTLA-4 checkpoint insufficiency.

LRBA is Essential for Allogeneic Responses in Bone Marrow Transplantation.

Atypical Manifestation of LPS-Responsive Beige-Like Anchor Deficiency Syndrome as an Autoimmune Endocrine Disorder without Enteropathy and Immunodeficiency.

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