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Items: 1 to 20 of 29

1.

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 25;672:45-49. doi: 10.1016/j.gene.2018.05.097. Epub 2018 Jun 1.

PMID:
29864493
2.

Low-dose sirolimus in two cousins with autoimmune lymphoproliferative syndrome-associated infection.

Nocerino A, Valencic E, Loganes C, Pelos G, Tommasini A.

Pediatr Int. 2018 Mar;60(3):315-317. doi: 10.1111/ped.13494. Epub 2018 Feb 26. No abstract available.

PMID:
29480551
3.

Stabilized β-Catenin Ameliorates ALPS-Like Symptoms of B6/lpr Mice.

Xu X, Huang J, Zhao M, Chen H, Mo J, Zhou X, Su Q, Yu B, Huang Z.

J Immunol Res. 2017;2017:3469108. doi: 10.1155/2017/3469108. Epub 2017 Nov 9.

4.

Autoimmune and medication-induced lymphadenopathies.

Gru AA, O'Malley DP.

Semin Diagn Pathol. 2018 Jan;35(1):34-43. doi: 10.1053/j.semdp.2017.11.015. Epub 2017 Nov 28. Review.

PMID:
29208331
5.

STAT5B: A Differential Regulator of the Life and Death of CD4+ Effector Memory T Cells.

Majri SS, Fritz JM, Villarino AV, Zheng L, Kanellopoulou C, Chaigne-Delalande B, Grönholm J, Niemela JE, Afzali B, Biancalana M, Pittaluga S, Sun A, Cohen JL, Holland SM, O'Shea JJ, Uzel G, Lenardo MJ.

J Immunol. 2018 Jan 1;200(1):110-118. doi: 10.4049/jimmunol.1701133. Epub 2017 Nov 29.

6.

Eruption of lymphocyte recovery with atypical lymphocytes mimicking a primary cutaneous T-cell lymphoma: a series of 12 patients.

Hurabielle C, Sbidian E, Beltraminelli H, Bouchindhomme B, Chassagne-Clément C, Balme B, Bossard C, Delfau-Larue MH, Wolkenstein P, Chosidow O, Cordonnier C, Toma A, Pautas C, Ortonne N.

Hum Pathol. 2018 Jan;71:100-108. doi: 10.1016/j.humpath.2017.10.018. Epub 2017 Oct 28.

PMID:
29107664
7.

What's up in the ALPS.

Rieux-Laucat F.

Curr Opin Immunol. 2017 Dec;49:79-86. doi: 10.1016/j.coi.2017.10.001. Epub 2017 Oct 23. Review.

PMID:
29073495
8.

Flow Cytometry Assays in Primary Immunodeficiency Diseases.

O'Gorman MRG.

Methods Mol Biol. 2018;1678:321-345. doi: 10.1007/978-1-4939-7346-0_14.

PMID:
29071685
9.

Nonapoptotic functions of Fas/CD95 in the immune response.

Guégan JP, Legembre P.

FEBS J. 2018 Mar;285(5):809-827. doi: 10.1111/febs.14292. Epub 2017 Nov 16. Review.

10.

Genetic heterogeneity of uncharacterized childhood autoimmune diseases with lymphoproliferation.

Takagi M, Hoshino A, Yoshida K, Ueno H, Imai K, Piao J, Kanegane H, Yamashita M, Okano T, Muramatsu H, Okuno Y, Shiraishi Y, Chiba K, Tanaka H, Miyano S, Ogawa S, Hayashi Y, Kojima S, Morio T.

Pediatr Blood Cancer. 2018 Feb;65(2). doi: 10.1002/pbc.26831. Epub 2017 Sep 29.

PMID:
28960754
11.

Evans Syndrome as First Manifestation of Primary Immunodeficiency in Clinical Practice.

Martínez-Valdez L, Deyà-Martínez A, Giner MT, Berrueco R, Esteve-Solé A, Juan M, Plaza-Martín AM, Alsina L.

J Pediatr Hematol Oncol. 2017 Oct;39(7):490-494. doi: 10.1097/MPH.0000000000000880.

PMID:
28937520
12.

Flow cytometry-based diagnosis of primary immunodeficiency diseases.

Kanegane H, Hoshino A, Okano T, Yasumi T, Wada T, Takada H, Okada S, Yamashita M, Yeh TW, Nishikomori R, Takagi M, Imai K, Ochs HD, Morio T.

Allergol Int. 2018 Jan;67(1):43-54. doi: 10.1016/j.alit.2017.06.003. Epub 2017 Jul 3. Review.

13.

Efficacy of mycophenolate on lung disease and autoimmunity in children with immunodeficiency.

Bucciol G, Petrone A, Putti MC.

Pediatr Pulmonol. 2017 Oct;52(10):E73-E76. doi: 10.1002/ppul.23757. Epub 2017 Jul 3.

PMID:
28672090
14.

Rare splicing defects of FAS underly severe recessive autoimmune lymphoproliferative syndrome.

Agrebi N, Ben-Mustapha I, Matoussi N, Dhouib N, Ben-Ali M, Mekki N, Ben-Ahmed M, Larguèche B, Ben Becher S, Béjaoui M, Barbouche MR.

Clin Immunol. 2017 Oct;183:17-23. doi: 10.1016/j.clim.2017.06.009. Epub 2017 Jun 29.

PMID:
28668589
15.

Pearls and pitfalls: Autoimmune lymphoproliferative syndrome and autoimmune lymphoproliferative syndrome-like disease.

Bartels AK, Banks TA, Bay JL.

Allergy Asthma Proc. 2017 Jul 1;38(4):317-321. doi: 10.2500/aap.2017.38.4062.

PMID:
28668112
16.

A case report of septic shock syndrome caused by S. pneumoniae in an immunocompromised patient despite of vaccination.

Singer J, Testori C, Schellongowski P, Handisurya A, Müller C, Reitter EM, Graninger W, Knöbl P, Staudinger T, Winkler S, Thalhammer F.

BMC Infect Dis. 2017 Jun 22;17(1):442. doi: 10.1186/s12879-017-2481-y.

17.

STAT3 gain-of-function mutations associated with autoimmune lymphoproliferative syndrome like disease deregulate lymphocyte apoptosis and can be targeted by BH3 mimetic compounds.

Nabhani S, Schipp C, Miskin H, Levin C, Postovsky S, Dujovny T, Koren A, Harlev D, Bis AM, Auer F, Keller B, Warnatz K, Gombert M, Ginzel S, Borkhardt A, Stepensky P, Fischer U.

Clin Immunol. 2017 Aug;181:32-42. doi: 10.1016/j.clim.2017.05.021. Epub 2017 Jun 1.

PMID:
28579554
18.

T and B cell clonal expansion in Ras-associated lymphoproliferative disease (RALD) as revealed by next-generation sequencing.

Levy-Mendelovich S, Lev A, Rechavi E, Barel O, Golan H, Bielorai B, Neumann Y, Simon AJ, Somech R.

Clin Exp Immunol. 2017 Sep;189(3):310-317. doi: 10.1111/cei.12986. Epub 2017 Jun 5.

19.

IgG4-related disease in autoimmune lymphoproliferative syndrome.

van de Ven AAJM, Seidl M, Drendel V, Schmitt-Graeff A, Voll RE, Rensing-Ehl A, Speckmann C, Ehl S, Warnatz K, Kollert F.

Clin Immunol. 2017 Jul;180:97-99. doi: 10.1016/j.clim.2017.05.003. Epub 2017 May 3.

PMID:
28478106
20.

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. 2017 Aug;66(8):2316-2322. doi: 10.2337/db17-0040. Epub 2017 May 4. Erratum in: Diabetes. 2018 Jan 5;:.

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