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2: Lien R, Lin YF, Lai MW, Weng HY, Wu RC, Jaing TH, Huang JL, Tsai SF, Lee WI. Novel Mutations of the Tetratricopeptide Repeat Domain 7A Gene and Phenotype/Genotype Comparison. Front Immunol. 2017 Sep 7;8:1066. doi: 10.3389/fimmu.2017.01066. eCollection 2017. PubMed PMID: 28936210; PubMed Central
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9: Pecoraro A, Nigro E, Polito R, Monaco ML, Scudiero O, Mormile I, Cesoni Marcelli A, Capasso M, Habetswallner F, Genovese A, Daniele A, Spadaro G. Total and High Molecular Weight Adiponectin Expression Is Decreased in Patients with Common Variable Immunodeficiency: Correlation with Ig Replacement Therapy. Front Immunol. 2017 Jul 31;8:895. doi: 10.3389/fimmu.2017.00895. eCollection 2017. PubMed PMID: 28824624; PubMed Central PMCID: PMC5534466.

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12: Seleman M, Hoyos-Bachiloglu R, Geha RS, Chou J. Uses of Next-Generation Sequencing Technologies for the Diagnosis of Primary Immunodeficiencies. Front Immunol. 2017 Jul 24;8:847. doi: 10.3389/fimmu.2017.00847. eCollection 2017. Review. PubMed PMID: 28791010; PubMed Central PMCID: PMC5522848.

13: Deripapa E, Balashov D, Rodina Y, Laberko A, Myakova N, Davydova NV, Gordukova MA, Abramov DS, Pay GV, Shelikhova L, Prodeus AP, Maschan MA, Maschan AA, Shcherbina A. Prospective Study of a Cohort of Russian Nijmegen Breakage Syndrome Patients Demonstrating Predictive Value of Low Kappa-Deleting Recombination Excision Circle (KREC) Numbers and Beneficial Effect of Hematopoietic Stem Cell Transplantation (HSCT). Front Immunol. 2017 Jul 24;8:807. doi: 10.3389/fimmu.2017.00807. eCollection 2017. PubMed PMID: 28791007; PubMed Central PMCID: PMC5523727.

14: Rios X, Chinn IK, Orange JS, Hanson CI, Rider NL. T-Cell Lymphopenia Detected by Newborn Screening in Two Siblings with an Xq13.1 Duplication. Front Pediatr. 2017 Jul 18;5:156. doi: 10.3389/fped.2017.00156. eCollection 2017. PubMed PMID: 28770187; PubMed Central PMCID: PMC5513981.

15: Zimmerman O, Rosen LB, Swamydas M, Ferre EMN, Natarajan M, van de Veerdonk F, Holland SM, Lionakis MS. Autoimmune Regulator Deficiency Results in a ecrease in STAT1 Levels in Human Monocytes. Front Immunol. 2017 Jul 14;8:820. doi: 10.3389/fimmu.2017.00820. eCollection 2017. PubMed PMID: 28769929; ubMed Central PMCID: PMC5509791.

16: Tan Q, Ren FL, Wang H. Pyoderma Gangrenosum in a Patient with X-Linked Agammaglobulinemia. Ann Dermatol. 2017 Aug;29(4):476-478. doi: 10.5021/ad.2017.29.4.476. Epub 2017 Jun 21. PubMed PMID: 28761297; PubMed Central PMCID: PMC5500714.

17: Borte M, Melamed IR, Pulka G, Pyringer B, Knutsen AP, Ochs HD, Kobayashi RH, Kobayashi AL, Gupta S, Strach M, Smits W, Pituch-Noworolska A, Moy JN. Efficacy and Safety of Human Intravenous Immunoglobulin 10% (Panzyga®) in Patients with Primary Immunodeficiency Diseases: a Two-Stage, Multicenter, rospective, Open-Label Study. J Clin Immunol. 2017 Jul 29. doi: 10.1007/s10875-017-0424-4. [Epub ahead of print] PubMed PMID: 28755067; PubMed Central PMCID: PMC5554470.

18: Luk ADW, Lee PP, Mao H, Chan KW, Chen XY, Chen TX, He JX, Kechout N, Suri D, Tao YB, Xu YB, Jiang LP, Liew WK, Jirapongsananuruk O, Daengsuwan T, Gupta A, Singh S, Rawat A, Abdul Latiff AH, Lee ACW, Shek LP, Nguyen TVA, Chin TJ, Chien YH, Latiff ZA, Le TMH, Le NNQ, Lee BW, Li Q, Raj D, Barbouche MR, Thong MK, Ang MCD, Wang XC, Xu CG, Yu HG, Yu HH, Lee TL, Yau FYS, Wong WH, Tu W, Yang W, Chong PCY, Ho MHK, Lau YL. Family History of Early Infant Death Correlates with Earlier Age at Diagnosis But Not Shorter Time to Diagnosis for Severe Combined Immunodeficiency. Front Immunol. 2017 Jul 12;8:808. doi: 10.3389/fimmu.2017.00808. eCollection 2017. PubMed PMID: 28747913; PubMed Central PMCID: PMC5506088.

19: Ruiz-García R, Rodríguez-Vigil C, Marco FM, Gallego-Bustos F, Castro-Panete MJ, Diez-Alonso L, Muñoz-Ruiz C, Ruiz-Contreras J, Paz-Artal E, González-Granado LI, Allende LM. Acquired Senescent T-Cell Phenotype Correlates with Clinical Severity in GATA Binding Protein 2-Deficient Patients. Front Immunol. 2017 Jul 12;8:802. doi: 10.3389/fimmu.2017.00802. eCollection 2017. PubMed PMID: 28747912; PubMed Central PMCID: PMC5506090.

20: Pasquet M, Pellier I, Aladjidi N, Auvrignon A, Cherin P, Clerson P, Cozon GJN, Jaussaud R, Bienvenu B, Hoarau C. A cohort of French pediatric patients with primary immunodeficiencies: are patient preferences regarding replacement immunotherapy fulfilled in real-life conditions? Patient Prefer Adherence. 2017 Jul 10;11:1171-1180. doi: 10.2147/PPA.S123363. eCollection 2017. PubMed PMID: 28744107; PubMed Central PMCID: PMC5513882.

21: Jesenak M, Urbancikova I, Banovcin P. Respiratory Tract Infections and the Role of Biologically Active Polysaccharides in Their Management and Prevention. Nutrients. 2017 Jul 20;9(7). pii: E779. doi: 10.3390/nu9070779. Review. PubMed PMID: 28726737; PubMed Central PMCID: PMC5537893.

22: Bratanič N, Kovač J, Pohar K, Trebušak Podkrajšek K, Ihan A, Battelino T, Avbelj Stefanija M. Multifocal gastric adenocarcinoma in a patient with LRBA deficiency. Orphanet J Rare Dis. 2017 Jul 18;12(1):131. doi: 10.1186/s13023-017-0682-5. PubMed PMID: 28720148; PubMed Central PMCID: PMC5516372.

23: Asgari S, Schlapbach LJ, Anchisi S, Hammer C, Bartha I, Junier T, Mottet-Osman G, Posfay-Barbe KM, Longchamp D, Stocker M, Cordey S, Kaiser L, Riedel T, Kenna T, Long D, Schibler A, Telenti A, Tapparel C, McLaren PJ, Garcin  D, Fellay J. Severe viral respiratory infections in children with IFIH1 loss-of-function mutations. Proc Natl Acad Sci U S A. 2017 Aug 1;114(31):8342-8347. doi: 10.1073/pnas.1704259114. Epub 2017 Jul 17. PubMed PMID: 28716935; PubMed Central PMCID: PMC5547624.

24: Krivan G, Chernyshova L, Kostyuchenko L, Lange A, Nyul Z, Derfalvi B, Musial J, Bellon A, Kappler M, Sadoun A, Bernatowska E. A Multicentre Study on the Efficacy, Safety and Pharmacokinetics of IqYmune®, a Highly Purified 10% Liquid Intravenous Immunoglobulin, in Patients with Primary Immune Deficiency. J Clin Immunol. 2017 Jul 15. doi: 10.1007/s10875-017-0416-4. [Epub ahead of print] PubMed PMID: 28711959; PubMed Central PMCID: PMC5554475.

25: López-Granados L, Torrent M, Sastre A, Gonzalez-Vicent M, Díaz de Heredia C, Argilés B, Pascual A, Pérez-Hurtado JM, Sisinni L, Diaz MÁ, Elorza I, Dasí MA, Badell I. [Reduced-intensity conditioning haematopoietic stem cell transplantation in genetic diseases: Experience of the Spanish Working Group for Bone Marrow ransplantation in Children]. An Pediatr (Barc). 2017 Jul 7. pii: S1695-4033(17)30082-6. doi: 10.1016/j.anpedi.2017.02.015. [Epub ahead of print] Spanish. PubMed PMID: 28694008.

26: 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. Flow cytometry-based diagnosis of primary immunodeficiency diseases. Allergol Int. 2017 Jul 3. pii: S1323-8930(17)30067-9. doi: 10.1016/j.alit.2017.06.003. [Epub ahead of print] Review. PubMed PMID: 28684198.

27: Igarashi Y, Uchiyama T, Minegishi T, Takahashi S, Watanabe N, Kawai T, Yamada M, Ariga T, Onodera M. Single Cell-Based Vector Tracing in Patients with ADA-SCID Treated with Stem Cell Gene Therapy. Mol Ther Methods Clin Dev. 2017 May 25;6:8-16. doi: 10.1016/j.omtm.2017.05.005. eCollection 2017 Sep 15. PubMed PMID: 28626778; PubMed Central PMCID: PMC5466583.

28: Rider NL, Kutac C, Hajjar J, Scalchunes C, Seeborg FO, Boyle M, Orange JS. Health-Related Quality of Life in Adult Patients with Common Variable Immunodeficiency Disorders and Impact of Treatment. J Clin Immunol. 2017 Jul;37(5):461-475. doi: 10.1007/s10875-017-0404-8. Epub 2017 May 23. PubMed PMID: 28536745; PubMed Central PMCID: PMC5489588.

29: Mahlaoui N, Warnatz K, Jones A, Workman S, Cant A. Advances in the Care of Primary Immunodeficiencies (PIDs): from Birth to Adulthood. J Clin Immunol. 2017  Jul;37(5):452-460. doi: 10.1007/s10875-017-0401-y. Epub 2017 May 18. PubMed PMID: 28523402; PubMed Central PMCID: PMC5489581.

30: Heurtier L, Lamrini H, Chentout L, Deau MC, Bouafia A, Rosain J, Plaza JM, Parisot M, Dumont B, Turpin D, Merlin E, Moshous D, Aladjidi N, Neven B, Picard C, Cavazzana M, Fischer A, Durandy A, Stephan JL, Kracker S. Mutations in the adaptor-binding domain and associated linker region of p110δ cause Activated PI3K-δ Syndrome 1 (APDS1). Haematologica. 2017 Jul;102(7):e278-e281. doi: 10.3324/haematol.2017.167601. Epub 2017 Apr 20. PubMed PMID: 28428270; PubMed Central PMCID: PMC5566055.


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