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Items: 1 to 50 of 567

1.

Mendelian Susceptibility to Mycobacterial Disease Caused by a Novel Founder IL12B Mutation in Saudi Arabia.

Alodayani AN, Al-Otaibi AM, Deswarte C, Frayha HH, Bouaziz M, AlHelale M, Le Voyer T, Nieto-Patlan A, Rattina V, AlZahrani M, Halwani R, Al Sohime F, Al-Mousa H, Al-Muhsen S, Alhajjar SH, Dhayhi NS, Abel L, Casanova JL, Bin-Hussain I, AlBarrak MS, Al-Jumaah SA, Bustamante J.

J Clin Immunol. 2018 Mar 27. doi: 10.1007/s10875-018-0490-2. [Epub ahead of print]

PMID:
29589181
2.

Preference-based measures to obtain health state utility values for use in economic evaluations with child-based populations: a review and UK-based focus group assessment of patient and parent choices.

Wolstenholme JL, Bargo D, Wang K, Harnden A, Räisänen U, Abel L.

Qual Life Res. 2018 Mar 21. doi: 10.1007/s11136-018-1831-6. [Epub ahead of print] Review.

PMID:
29564713
3.

Saccades under Mental Load in Infantile Nystagmus Syndrome and Controls.

Salehi Fadardi M, Abel LA.

Optom Vis Sci. 2018 Apr;95(4):373-383. doi: 10.1097/OPX.0000000000001194.

PMID:
29561505
4.

A novel genetic architecture of infectious diseases.

Abel L.

Nat Rev Immunol. 2018 Apr;18(4):224. doi: 10.1038/nri.2018.19. Epub 2018 Mar 16. No abstract available.

PMID:
29545642
5.

IRF4 haploinsufficiency in a family with Whipple's disease.

Guérin A, Kerner G, Marr N, Markle JG, Fenollar F, Wong N, Boughorbel S, Avery DT, Ma CS, Bougarn S, Bouaziz M, Beziat V, Della Mina E, Oleaga-Quintas C, Lazarovt T, Worley L, Nguyen T, Patin E, Deswarte C, Martinez-Barricarte R, Boucherit S, Ayral X, Edouard S, Boisson-Dupuis S, Rattina V, Bigio B, Vogt G, Geissmann F, Quintana-Murci L, Chaussabel D, Tangye SG, Raoult D, Abel L, Bustamante J, Casanova JL.

Elife. 2018 Mar 14;7. pii: e32340. doi: 10.7554/eLife.32340. [Epub ahead of print]

6.

Congenital achiasma and see-saw nystagmus in VATER syndrome association with hydrocephalus.

Nguyen CT, Goh C, Desmond P, Abel LA, Lim CHL, Andrew Symons RC, Hardy TG.

J Clin Neurosci. 2018 May;51:63-65. doi: 10.1016/j.jocn.2018.02.008. Epub 2018 Feb 23. No abstract available.

PMID:
29483009
7.

Inborn Errors of RNA Lariat Metabolism in Humans with Brainstem Viral Infection.

Zhang SY, Clark NE, Freije CA, Pauwels E, Taggart AJ, Okada S, Mandel H, Garcia P, Ciancanelli MJ, Biran A, Lafaille FG, Tsumura M, Cobat A, Luo J, Volpi S, Zimmer B, Sakata S, Dinis A, Ohara O, Garcia Reino EJ, Dobbs K, Hasek M, Holloway SP, McCammon K, Hussong SA, DeRosa N, Van Skike CE, Katolik A, Lorenzo L, Hyodo M, Faria E, Halwani R, Fukuhara R, Smith GA, Galvan V, Damha MJ, Al-Muhsen S, Itan Y, Boeke JD, Notarangelo LD, Studer L, Kobayashi M, Diogo L, Fairbrother WG, Abel L, Rosenberg BR, Hart PJ, Etzioni A, Casanova JL.

Cell. 2018 Feb 22;172(5):952-965.e18. doi: 10.1016/j.cell.2018.02.019.

PMID:
29474921
8.

Review and critical appraisal of studies mapping from quality of life or clinical measures to EQ-5D: an online database and application of the MAPS statement.

Dakin H, Abel L, Burns R, Yang Y.

Health Qual Life Outcomes. 2018 Feb 12;16(1):31. doi: 10.1186/s12955-018-0857-3.

9.

The Suspected CANcer (SCAN) pathway: protocol for evaluating a new standard of care for patients with non-specific symptoms of cancer.

Nicholson BD, Oke J, Friedemann Smith C, Phillips JA, Lee J, Abel L, Kelly S, Gould I, Mackay T, Kaveney Z, Anthony S, Hayles S, Lasserson D, Gleeson F.

BMJ Open. 2018 Jan 21;8(1):e018168. doi: 10.1136/bmjopen-2017-018168.

10.

Fostering Spontaneous Visual Attention in Children on the Autism Spectrum: A Proof-of-Concept Study Comparing Singing and Speech.

Thompson GA, Abel LA.

Autism Res. 2018 Jan 22. doi: 10.1002/aur.1930. [Epub ahead of print]

PMID:
29356417
11.

Human genetics of infectious diseases: Unique insights into immunological redundancy.

Casanova JL, Abel L.

Semin Immunol. 2018 Apr;36:1-12. doi: 10.1016/j.smim.2017.12.008. Epub 2017 Dec 16. Review.

PMID:
29254755
12.

Differences in regional grey matter volumes in currently ill patients with anorexia nervosa.

Phillipou A, Rossell SL, Gurvich C, Castle DJ, Abel LA, Nibbs RG, Hughes ME.

Eur J Neurosci. 2018 Jan;47(2):177-183. doi: 10.1111/ejn.13793. Epub 2018 Jan 10.

PMID:
29244231
13.

Point-of-care Helicobacter pylori testing: primary care technology update.

Nicholson BD, Abel LM, Turner PJ, Price CP, Heneghan C, Hayward G, Plüddemann A.

Br J Gen Pract. 2017 Dec;67(665):576-577. doi: 10.3399/bjgp17X693881. No abstract available.

PMID:
29192118
14.

Genetics of human susceptibility to active and latent tuberculosis: present knowledge and future perspectives.

Abel L, Fellay J, Haas DW, Schurr E, Srikrishna G, Urbanowski M, Chaturvedi N, Srinivasan S, Johnson DH, Bishai WR.

Lancet Infect Dis. 2018 Mar;18(3):e64-e75. doi: 10.1016/S1473-3099(17)30623-0. Epub 2017 Oct 27. Review.

PMID:
29111156
15.

Spontaneous blink rate in anorexia nervosa: Implications for dopaminergic activity in anorexia nervosa.

Phillipou A, Woods W, Abel LA, Rossell SL, Hughes ME, Castle DJ, Gurvich C.

Aust N Z J Psychiatry. 2017 Oct 1:4867417739692. doi: 10.1177/0004867417739692. [Epub ahead of print] No abstract available.

PMID:
29081234
16.

An eQTL variant of ZXDC is associated with IFN-γ production following Mycobacterium tuberculosis antigen-specific stimulation.

Jabot-Hanin F, Cobat A, Feinberg J, Orlova M, Niay J, Deswarte C, Poirier C, Theodorou I, Bustamante J, Boisson-Dupuis S, Casanova JL, Alcaïs A, Hoal EG, Delacourt C, Schurr E, Abel L.

Sci Rep. 2017 Oct 9;7(1):12800. doi: 10.1038/s41598-017-13017-8.

17.

An in vitro diagnostic certified point of care single nucleotide test for IL28B polymorphisms.

Duffy D, Mottez E, Ainsworth S, Buivan TP, Baudin A, Vray M, Reed B, Fontanet A, Rohel A, Petrov-Sanchez V, Abel L, Theodorou I, Miele G, Pol S, Albert ML.

PLoS One. 2017 Sep 6;12(9):e0183084. doi: 10.1371/journal.pone.0183084. eCollection 2017.

18.

Inborn errors in RNA polymerase III underlie severe varicella zoster virus infections.

Ogunjimi B, Zhang SY, Sørensen KB, Skipper KA, Carter-Timofte M, Kerner G, Luecke S, Prabakaran T, Cai Y, Meester J, Bartholomeus E, Bolar NA, Vandeweyer G, Claes C, Sillis Y, Lorenzo L, Fiorenza RA, Boucherit S, Dielman C, Heynderickx S, Elias G, Kurotova A, Auwera AV, Verstraete L, Lagae L, Verhelst H, Jansen A, Ramet J, Suls A, Smits E, Ceulemans B, Van Laer L, Plat Wilson G, Kreth J, Picard C, Von Bernuth H, Fluss J, Chabrier S, Abel L, Mortier G, Fribourg S, Mikkelsen JG, Casanova JL, Paludan SR, Mogensen TH.

J Clin Invest. 2017 Sep 1;127(9):3543-3556. doi: 10.1172/JCI92280. Epub 2017 Aug 7.

19.

[Management of a Port Catheter-Related Superior Vena Cava Thrombosis in the Setting of Active Crohn's Disease: A Case Report].

Abel L, Uhde B, Dembinski R, Schraepler K.

Dtsch Med Wochenschr. 2017 Aug;142(15):1155-1157. doi: 10.1055/s-0043-112231. Epub 2017 Aug 1. German.

PMID:
28763827
20.

Recurrent rhinovirus infections in a child with inherited MDA5 deficiency.

Lamborn IT, Jing H, Zhang Y, Drutman SB, Abbott JK, Munir S, Bade S, Murdock HM, Santos CP, Brock LG, Masutani E, Fordjour EY, McElwee JJ, Hughes JD, Nichols DP, Belkadi A, Oler AJ, Happel CS, Matthews HF, Abel L, Collins PL, Subbarao K, Gelfand EW, Ciancanelli MJ, Casanova JL, Su HC.

J Exp Med. 2017 Jul 3;214(7):1949-1972. doi: 10.1084/jem.20161759. Epub 2017 Jun 12.

21.

Effects of drinking desalinated seawater on cell viability and proliferation.

Macarrão CL, Bachi ALL, Mariano M, Abel LJ.

J Water Health. 2017 Jun;15(3):360-366. doi: 10.2166/wh.2017.252.

PMID:
28598340
22.

Kaposi sarcoma, oral malformations, mitral dysplasia, and scoliosis associated with 7q34-q36.3 heterozygous terminal deletion.

Jackson CC, Lefèvre-Utile A, Guimier A, Malan V, Bruneau J, Gessain A, Cassar O, Amiel J, Cobat A, Rattina V, Abel L, Casanova JL, Blanche S.

Am J Med Genet A. 2017 May 9. doi: 10.1002/ajmg.a.38275. [Epub ahead of print]

PMID:
28488400
23.

Inherited GINS1 deficiency underlies growth retardation along with neutropenia and NK cell deficiency.

Cottineau J, Kottemann MC, Lach FP, Kang YH, Vély F, Deenick EK, Lazarov T, Gineau L, Wang Y, Farina A, Chansel M, Lorenzo L, Piperoglou C, Ma CS, Nitschke P, Belkadi A, Itan Y, Boisson B, Jabot-Hanin F, Picard C, Bustamante J, Eidenschenk C, Boucherit S, Aladjidi N, Lacombe D, Barat P, Qasim W, Hurst JA, Pollard AJ, Uhlig HH, Fieschi C, Michon J, Bermudez VP, Abel L, de Villartay JP, Geissmann F, Tangye SG, Hurwitz J, Vivier E, Casanova JL, Smogorzewska A, Jouanguy E.

J Clin Invest. 2017 May 1;127(5):1991-2006. doi: 10.1172/JCI90727. Epub 2017 Apr 17.

24.

Evidence synthesis to inform model-based cost-effectiveness evaluations of diagnostic tests: a methodological review of health technology assessments.

Shinkins B, Yang Y, Abel L, Fanshawe TR.

BMC Med Res Methodol. 2017 Apr 14;17(1):56. doi: 10.1186/s12874-017-0331-7. Review.

25.

Autosomal Recessive Cardiomyopathy Presenting as Acute Myocarditis.

Belkaya S, Kontorovich AR, Byun M, Mulero-Navarro S, Bajolle F, Cobat A, Josowitz R, Itan Y, Quint R, Lorenzo L, Boucherit S, Stoven C, Di Filippo S, Abel L, Zhang SY, Bonnet D, Gelb BD, Casanova JL.

J Am Coll Cardiol. 2017 Apr 4;69(13):1653-1665. doi: 10.1016/j.jacc.2017.01.043.

26.

Task-induced Changes in Idiopathic Infantile Nystagmus Vary with Gaze.

Salehi Fadardi M, Bathke AC, Harrar SW, Abel LA.

Optom Vis Sci. 2017 May;94(5):606-615. doi: 10.1097/OPX.0000000000001060.

PMID:
28288017
27.

A Meta-Analysis of Single-Subject Research on Behavioral Momentum to Enhance Success in Students with Autism.

Cowan RJ, Abel L, Candel L.

J Autism Dev Disord. 2017 May;47(5):1464-1477. doi: 10.1007/s10803-017-3076-6. Review.

PMID:
28236099
28.

Human Adaptive Immunity Rescues an Inborn Error of Innate Immunity.

Israel L, Wang Y, Bulek K, Della Mina E, Zhang Z, Pedergnana V, Chrabieh M, Lemmens NA, Sancho-Shimizu V, Descatoire M, Lasseau T, Israelsson E, Lorenzo L, Yun L, Belkadi A, Moran A, Weisman LE, Vandenesch F, Batteux F, Weller S, Levin M, Herberg J, Abhyankar A, Prando C, Itan Y, van Wamel WJB, Picard C, Abel L, Chaussabel D, Li X, Beutler B, Arkwright PD, Casanova JL, Puel A.

Cell. 2017 Feb 23;168(5):789-800.e10. doi: 10.1016/j.cell.2017.01.039.

29.

A genome wide association study identifies a lncRna as risk factor for pathological inflammatory responses in leprosy.

Fava VM, Manry J, Cobat A, Orlova M, Van Thuc N, Moraes MO, Sales-Marques C, Stefani MM, Latini AC, Belone AF, Thai VH, Abel L, Alcaïs A, Schurr E.

PLoS Genet. 2017 Feb 21;13(2):e1006637. doi: 10.1371/journal.pgen.1006637. eCollection 2017 Feb.

30.

Treatment of Horizontal Nystagmus Using Myectomy Without Reattachment.

Hertle RW, DellOsso LF, Granet D, Abel LA, Jacobs JB.

J Pediatr Ophthalmol Strabismus. 2017 Jan 1;54(1):59. doi: 10.3928/01913913-20161109-01. No abstract available.

PMID:
28128845
31.

Trichodysplasia Spinulosa Polyomavirus Infection Occurs during Early Childhood with Intrafamilial Transmission, Especially from Mother to Child.

Pedergnana V, Martel-Jantin C, Nicol JTJ, Leblond V, Tortevoye P, Coursaget P, Touzé A, Abel L, Gessain A.

J Invest Dermatol. 2017 May;137(5):1181-1183. doi: 10.1016/j.jid.2016.12.017. Epub 2017 Jan 17. No abstract available.

PMID:
28108298
32.

Inherited human IRAK-1 deficiency selectively impairs TLR signaling in fibroblasts.

Della Mina E, Borghesi A, Zhou H, Bougarn S, Boughorbel S, Israel L, Meloni I, Chrabieh M, Ling Y, Itan Y, Renieri A, Mazzucchelli I, Basso S, Pavone P, Falsaperla R, Ciccone R, Cerbo RM, Stronati M, Picard C, Zuffardi O, Abel L, Chaussabel D, Marr N, Li X, Casanova JL, Puel A.

Proc Natl Acad Sci U S A. 2017 Jan 24;114(4):E514-E523. doi: 10.1073/pnas.1620139114. Epub 2017 Jan 9.

33.

The influence of action video game playing on eye movement behaviour during visual search in abstract, in-game and natural scenes.

Azizi E, Abel LA, Stainer MJ.

Atten Percept Psychophys. 2017 Feb;79(2):484-497. doi: 10.3758/s13414-016-1256-7.

PMID:
27981521
34.

Utility of the QuantiFERON-TB Gold In-Tube assay for the diagnosis of tuberculosis in Moroccan children.

El Azbaoui S, Sabri A, Ouraini S, Hassani A, Asermouh A, Agadr A, Abilkassem R, Dini N, Kmari M, Akhaddar A, Laktati Z, Aieche S, El Hafidi N, Ben Brahim F, Bousfiha AA, Ailal F, Deswarte C, Schurr E, Amar L, Bustamante J, Boisson-Dupuis S, Casanova JL, Abel L, El Baghdadi J.

Int J Tuberc Lung Dis. 2016 Dec;20(12):1639-1646.

PMID:
27931340
35.

Genetic, immunological, and clinical features of patients with bacterial and fungal infections due to inherited IL-17RA deficiency.

Lévy R, Okada S, Béziat V, Moriya K, Liu C, Chai LY, Migaud M, Hauck F, Al Ali A, Cyrus C, Vatte C, Patiroglu T, Unal E, Ferneiny M, Hyakuna N, Nepesov S, Oleastro M, Ikinciogullari A, Dogu F, Asano T, Ohara O, Yun L, Della Mina E, Bronnimann D, Itan Y, Gothe F, Bustamante J, Boisson-Dupuis S, Tahuil N, Aytekin C, Salhi A, Al Muhsen S, Kobayashi M, Toubiana J, Abel L, Li X, Camcioglu Y, Celmeli F, Klein C, AlKhater SA, Casanova JL, Puel A.

Proc Natl Acad Sci U S A. 2016 Dec 20;113(51):E8277-E8285. doi: 10.1073/pnas.1618300114. Epub 2016 Dec 7.

36.

Dual T cell- and B cell-intrinsic deficiency in humans with biallelic RLTPR mutations.

Wang Y, Ma CS, Ling Y, Bousfiha A, Camcioglu Y, Jacquot S, Payne K, Crestani E, Roncagalli R, Belkadi A, Kerner G, Lorenzo L, Deswarte C, Chrabieh M, Patin E, Vincent QB, Müller-Fleckenstein I, Fleckenstein B, Ailal F, Quintana-Murci L, Fraitag S, Alyanakian MA, Leruez-Ville M, Picard C, Puel A, Bustamante J, Boisson-Dupuis S, Malissen M, Malissen B, Abel L, Hovnanian A, Notarangelo LD, Jouanguy E, Tangye SG, Béziat V, Casanova JL.

J Exp Med. 2016 Oct 17;213(11):2413-2435. Epub 2016 Sep 19.

37.

A new 3p25 locus is associated with liver fibrosis progression in human immunodeficiency virus/hepatitis C virus-coinfected patients.

Ulveling D, Le Clerc S, Cobat A, Labib T, Noirel J, Laville V, Coulonges C, Carpentier W, Nalpas B, Heim MH, Poynard T, Cerny A, Pol S, Bochud PY, Dabis F, Theodorou I, Lévy Y, Salmon D, Abel L, Dominguez S, Zagury JF; HEPAVIH ANRS CO13 Cohort Study Group; Swiss Hepatitis C Cohort Study Group; French ANRS HC EP 26 Genoscan Study Group.

Hepatology. 2016 Nov;64(5):1462-1472. doi: 10.1002/hep.28695. Epub 2016 Jul 29.

PMID:
27339598
38.

Exome and genome sequencing for inborn errors of immunity.

Meyts I, Bosch B, Bolze A, Boisson B, Itan Y, Belkadi A, Pedergnana V, Moens L, Picard C, Cobat A, Bossuyt X, Abel L, Casanova JL.

J Allergy Clin Immunol. 2016 Oct;138(4):957-969. doi: 10.1016/j.jaci.2016.08.003. Review.

39.

Self-reported and behavioural impulsivity in anorexia nervosa.

Phillipou A, Abel LA, Castle DJ, Gurvich C, Hughes ME, Rossell SL.

World J Psychiatry. 2016 Sep 22;6(3):345-50. doi: 10.5498/wjp.v6.i3.345. eCollection 2016 Sep 22.

40.

BRIP1 coding variants are associated with a high risk of hepatocellular carcinoma occurrence in patients with HCV- or HBV-related liver disease.

Oussalah A, Avogbe PH, Guyot E, Chery C, Guéant-Rodriguez RM, Ganne-Carrié N, Cobat A, Moradpour D, Nalpas B, Negro F, Poynard T, Pol S, Bochud PY, Abel L, Jeulin H, Schvoerer E, Chabi N, Amouzou E, Sanni A, Barraud H, Rouyer P, Josse T, Goffinet L, Jouve JL, Minello A, Bonithon-Kopp C, Thiefin G, Di Martino V, Doffoël M, Richou C, Raab JJ, Hillon P, Bronowicki JP, Guéant JL; CiRCE Study Group.

Oncotarget. 2016 Aug 17;8(38):62842-62857. doi: 10.18632/oncotarget.11327. eCollection 2017 Sep 8.

41.

Divided visual attention: A comparison of patients with multiple sclerosis and controls, assessed with an optokinetic nystagmus suppression task.

Williams IM, Schofield P, Khade N, Abel LA.

J Clin Neurosci. 2016 Dec;34:187-192. doi: 10.1016/j.jocn.2016.06.015. Epub 2016 Jul 27.

PMID:
27475321
42.

Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery.

Scott EM, Halees A, Itan Y, Spencer EG, He Y, Azab MA, Gabriel SB, Belkadi A, Boisson B, Abel L, Clark AG; Greater Middle East Variome Consortium, Alkuraya FS, Casanova JL, Gleeson JG.

Nat Genet. 2016 Sep;48(9):1071-6. doi: 10.1038/ng.3592. Epub 2016 Jul 18.

43.

The eyes have it: Eye movements and anorexia nervosa.

Phillipou A, Rossell SL, Gurvich C, Castle DJ, Abel LA.

Aust N Z J Psychiatry. 2016 Aug;50(8):806-7. doi: 10.1177/0004867416656260. Epub 2016 Jun 29. No abstract available.

PMID:
27363688
44.

Whole-exome sequencing to analyze population structure, parental inbreeding, and familial linkage.

Belkadi A, Pedergnana V, Cobat A, Itan Y, Vincent QB, Abhyankar A, Shang L, El Baghdadi J, Bousfiha A; Exome/Array Consortium, Alcais A, Boisson B, Casanova JL, Abel L.

Proc Natl Acad Sci U S A. 2016 Jun 14;113(24):6713-8. doi: 10.1073/pnas.1606460113. Epub 2016 May 31.

45.

Pauci- and Multibacillary Leprosy: Two Distinct, Genetically Neglected Diseases.

Gaschignard J, Grant AV, Thuc NV, Orlova M, Cobat A, Huong NT, Ba NN, Thai VH, Abel L, Schurr E, Alcaïs A.

PLoS Negl Trop Dis. 2016 May 24;10(5):e0004345. doi: 10.1371/journal.pntd.0004345. eCollection 2016 May. Review.

46.

Resting state functional connectivity in anorexia nervosa.

Phillipou A, Abel LA, Castle DJ, Hughes ME, Nibbs RG, Gurvich C, Rossell SL.

Psychiatry Res Neuroimaging. 2016 May 30;251:45-52. doi: 10.1016/j.pscychresns.2016.04.008. Epub 2016 Apr 19.

PMID:
27111812
47.

Saccadic Eye Movements in Anorexia Nervosa.

Phillipou A, Rossell SL, Gurvich C, Hughes ME, Castle DJ, Nibbs RG, Abel LA.

PLoS One. 2016 Mar 24;11(3):e0152338. doi: 10.1371/journal.pone.0152338. eCollection 2016.

48.

Mycobacterial disease in patients with chronic granulomatous disease: A retrospective analysis of 71 cases.

Conti F, Lugo-Reyes SO, Blancas Galicia L, He J, Aksu G, Borges de Oliveira E Jr, Deswarte C, Hubeau M, Karaca N, de Suremain M, Guérin A, Baba LA, Prando C, Guerrero GG, Emiroglu M, Öz FN, Yamazaki Nakashimada MA, Gonzalez Serrano E, Espinosa S, Barlan I, Pérez N, Regairaz L, Guidos Morales HE, Bezrodnik L, Di Giovanni D, Dbaibo G, Ailal F, Galicchio M, Oleastro M, Chemli J, Danielian S, Perez L, Ortega MC, Soto Lavin S, Hertecant J, Anal O, Kechout N, Al-Idrissi E, ElGhazali G, Bondarenko A, Chernyshova L, Ciznar P, Herbigneaux RM, Diabate A, Ndaga S, Konte B, Czarna A, Migaud M, Pedraza-Sánchez S, Zaidi MB, Vogt G, Blanche S, Benmustapha I, Mansouri D, Abel L, Boisson-Dupuis S, Mahlaoui N, Bousfiha AA, Picard C, Barbouche R, Al-Muhsen S, Espinosa-Rosales FJ, Kütükçüler N, Condino-Neto A, Casanova JL, Bustamante J.

J Allergy Clin Immunol. 2016 Jul;138(1):241-248.e3. doi: 10.1016/j.jaci.2015.11.041. Epub 2016 Feb 28.

PMID:
26936803
49.

Erratum to: Severe Mycobacterial Diseases in a Patient with GOF IκBα Mutation Without EDA.

Lee AJ, Moncada-Vélez M, Picard C, Llanora G, Huang CH, Abel L, Chan SM, Lee BW, Casanova JL, Bustamante J, Shek LP, Boisson-Dupuis S.

J Clin Immunol. 2016 Apr;36(3):335. doi: 10.1007/s10875-016-0238-9. No abstract available.

PMID:
26888281
50.

A Missense LRRK2 Variant Is a Risk Factor for Excessive Inflammatory Responses in Leprosy.

Fava VM, Manry J, Cobat A, Orlova M, Van Thuc N, Ba NN, Thai VH, Abel L, Alcaïs A, Schurr E; Canadian Lrrk2 in Inflammation Team (CLINT).

PLoS Negl Trop Dis. 2016 Feb 4;10(2):e0004412. doi: 10.1371/journal.pntd.0004412. eCollection 2016 Feb.

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