376 related articles for article (PubMed ID: 25931386)
21. Key diagnostic markers for autoimmune lymphoproliferative syndrome with molecular genetic diagnosis.
Molnár E; Radwan N; Kovács G; Andrikovics H; Henriquez F; Zarafov A; Hayman M; Linzner D; Thrasher AJ; Buckland M; Burns SO; Gilmour KC
Blood; 2020 Oct; 136(17):1933-1945. PubMed ID: 32599613
[TBL] [Abstract][Full Text] [Related]
22. Clinical Phenotypes and Immunological Characteristics of 18 Egyptian LRBA Deficiency Patients.
Meshaal S; El Hawary R; Adel R; Abd Elaziz D; Erfan A; Lotfy S; Hafez M; Hassan M; Johnson M; Rojas-Restrepo J; Gamez-Diaz L; Grimbacher B; Shoman W; Abdelmeguid Y; Boutros J; Galal N; El-Guindy N; Elmarsafy A
J Clin Immunol; 2020 Aug; 40(6):820-832. PubMed ID: 32506362
[TBL] [Abstract][Full Text] [Related]
23. Clinical, Immunologic, and Molecular Spectrum of Patients with LPS-Responsive Beige-Like Anchor Protein Deficiency: A Systematic Review.
Habibi S; Zaki-Dizaji M; Rafiemanesh H; Lo B; Jamee M; Gámez-Díaz L; Salami F; Kamali AN; Mohammadi H; Abolhassani H; Yazdani R; Aghamohammadi A; Anaya JM; Azizi G
J Allergy Clin Immunol Pract; 2019; 7(7):2379-2386.e5. PubMed ID: 30995531
[TBL] [Abstract][Full Text] [Related]
24. Autoimmune Lymphoproliferative Syndrome in Children with Nonmalignant Organomegaly, Chronic Immune Cytopenia, and Newly Diagnosed Lymphoma.
Kaya Z; Işık M; Oruklu N; Kirkiz S; Bağrıaçık EÜ; Allende LM; Díaz-Madroñero MJ; Ruiz-García R; Pınarlı FG; Göçün Uyar P; Koçak Ü
Turk J Haematol; 2021 Jun; 38(2):145-150. PubMed ID: 33375216
[TBL] [Abstract][Full Text] [Related]
25. Development of multiple gallstones in a child with lipopolysaccharide-responsive beige-like anchor protein mutation.
Kutluǧ Ş; Boztuǧ K; Yıldıran A
Cent Eur J Immunol; 2019; 44(3):332-335. PubMed ID: 31871423
[TBL] [Abstract][Full Text] [Related]
26. Clinical, immunological, and genetic features in 780 patients with autoimmune lymphoproliferative syndrome (ALPS) and ALPS-like diseases: A systematic review.
Hafezi N; Zaki-Dizaji M; Nirouei M; Asadi G; Sharifinejad N; Jamee M; Erfan Rasouli S; Hamedifar H; Sabzevari A; Chavoshzadeh Z; Yazdani R; Abolhassani H; Aghamohammadi A; Azizi G
Pediatr Allergy Immunol; 2021 Oct; 32(7):1519-1532. PubMed ID: 33963613
[TBL] [Abstract][Full Text] [Related]
27. Autoimmune lymphoproliferative syndrome caused by a homozygous null FAS ligand (FASLG) mutation.
Magerus-Chatinet A; Stolzenberg MC; Lanzarotti N; Neven B; Daussy C; Picard C; Neveux N; Desai M; Rao M; Ghosh K; Madkaikar M; Fischer A; Rieux-Laucat F
J Allergy Clin Immunol; 2013 Feb; 131(2):486-90. PubMed ID: 22857792
[TBL] [Abstract][Full Text] [Related]
28. Pediatric-onset Evans syndrome: Heterogeneous presentation and high frequency of monogenic disorders including LRBA and CTLA4 mutations.
Besnard C; Levy E; Aladjidi N; Stolzenberg MC; Magerus-Chatinet A; Alibeu O; Nitschke P; Blanche S; Hermine O; Jeziorski E; Landman-Parker J; Leverger G; Mahlaoui N; Michel G; Pellier I; Suarez F; Thuret I; de Saint-Basile G; Picard C; Fischer A; Neven B; Rieux-Laucat F; Quartier P;
Clin Immunol; 2018 Mar; 188():52-57. PubMed ID: 29330115
[TBL] [Abstract][Full Text] [Related]
29. A novel homozygous Fas ligand mutation leads to early protein truncation, abrogation of death receptor and reverse signaling and a severe form of the autoimmune lymphoproliferative syndrome.
Nabhani S; Hönscheid A; Oommen PT; Fleckenstein B; Schaper J; Kuhlen M; Laws HJ; Borkhardt A; Fischer U
Clin Immunol; 2014 Dec; 155(2):231-7. PubMed ID: 25451160
[TBL] [Abstract][Full Text] [Related]
30. LRBA in the endomembrane system.
Martínez Jaramillo C; Trujillo-Vargas CM
Colomb Med (Cali); 2018 Sep; 49(3):236-243. PubMed ID: 30410199
[TBL] [Abstract][Full Text] [Related]
31. EBV Negative Lymphoma and Autoimmune Lymphoproliferative Syndrome Like Phenotype Extend the Clinical Spectrum of Primary Immunodeficiency Caused by STK4 Deficiency.
Schipp C; Schlütermann D; Hönscheid A; Nabhani S; Höll J; Oommen PT; Ginzel S; Fleckenstein B; Stork B; Borkhardt A; Stepensky P; Fischer U
Front Immunol; 2018; 9():2400. PubMed ID: 30386345
[TBL] [Abstract][Full Text] [Related]
32. Synergistic defects of novo FAS and homozygous UNC13D leading to autoimmune lymphoproliferative syndrome-like disease: A 10-year-old Chinese boy case report.
Gu H; Ma J; Chen Z; Wang J; Zhang R; Wu R
Gene; 2018 Sep; 672():45-49. PubMed ID: 29864493
[TBL] [Abstract][Full Text] [Related]
33. 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; 2017 Nov; 37(8):790-800. PubMed ID: 28956255
[TBL] [Abstract][Full Text] [Related]
34. Spectrum of Phenotypes Associated with Mutations in LRBA.
Alkhairy OK; Abolhassani H; Rezaei N; Fang M; Andersen KK; Chavoshzadeh Z; Mohammadzadeh I; El-Rajab MA; Massaad M; Chou J; Aghamohammadi A; Geha RS; Hammarström L
J Clin Immunol; 2016 Jan; 36(1):33-45. PubMed ID: 26707784
[TBL] [Abstract][Full Text] [Related]
35. 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; 2018 Aug; 177(8):1163-1172. PubMed ID: 29777306
[TBL] [Abstract][Full Text] [Related]
36. Tubulointerstitial nephritis in a patient with probable autoimmune lymphoproliferative syndrome.
Glerup M; Herlin T; Rittig S; Grønbæk K; Hokland M; Hasle H
J Pediatr Hematol Oncol; 2013 Jul; 35(5):e187-9. PubMed ID: 23588339
[TBL] [Abstract][Full Text] [Related]
37. Leishmaniasis and Autoimmunity in Patient with LPS-Responsive Beige-Like Anchor Protein (LRBA) Deficiency.
Salami F; Shirkani A; Shahrooei M; Azizi G; Yazdani R; Abolhassani H; Aghamohammadi A
Endocr Metab Immune Disord Drug Targets; 2020; 20(3):479-484. PubMed ID: 31389321
[TBL] [Abstract][Full Text] [Related]
38. Autoimmune lymphoproliferative syndrome due to FAS mutations outside the signal-transducing death domain: molecular mechanisms and clinical penetrance.
Hsu AP; Dowdell KC; Davis J; Niemela JE; Anderson SM; Shaw PA; Rao VK; Puck JM
Genet Med; 2012 Jan; 14(1):81-9. PubMed ID: 22237435
[TBL] [Abstract][Full Text] [Related]
39. 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; 2023 Jul; 23(1):353. PubMed ID: 37443020
[TBL] [Abstract][Full Text] [Related]
40. Combined germline and somatic human FADD mutations cause autoimmune lymphoproliferative syndrome.
Pellé O; Moreno S; Lorenz MR; Riller Q; Fuehrer M; Stolzenberg MC; Maccari ME; Lenoir C; Cheminant M; Hinze T; Hebart HF; König C; Schvartz A; Schmitt Y; Vinit A; Henry E; Touzart A; Villarese P; Isnard P; Neveux N; Landman-Parker J; Picard C; Fouyssac F; Neven B; Grimbacher B; Speckmann C; Fischer A; Latour S; Schwarz K; Ehl S; Rieux-Laucat F; Rensing-Ehl A; Magérus A
J Allergy Clin Immunol; 2024 Jan; 153(1):203-215. PubMed ID: 37793571
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
