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Items: 1 to 50 of 333

1.

Long term outcome of WHIM syndrome in 18 patients: high risk of lung disease and HPV-related malignancies.

Dotta L, Notarangelo LD, Moratto D, Kumar R, Porta F, Soresina A, Lougaris V, Plebani A, Smith CIE, Norlin AC, Gòmez Raccio AC, Bubanska E, Bertolini P, Amendola G, Visentini M, Fiorilli M, Venuti A, Badolato R.

J Allergy Clin Immunol Pract. 2019 Feb 1. pii: S2213-2198(19)30117-5. doi: 10.1016/j.jaip.2019.01.045. [Epub ahead of print]

PMID:
30716504
2.

A monoallelic activating mutation in RAC2 resulting in a combined immunodeficiency.

Lougaris V, Chou J, Beano A, Wallace JG, Baronio M, Gazzurelli L, Lorenzini T, Moratto D, Tabellini G, Parolini S, Seleman M, Stafstrom K, Xu H, Harris C, Geha RS, Plebani A.

J Allergy Clin Immunol. 2019 Jan 14. pii: S0091-6749(19)30011-9. doi: 10.1016/j.jaci.2019.01.001. [Epub ahead of print] No abstract available.

PMID:
30654050
3.

A novel monoallelic gain of function mutation in p110δ causing atypical activated phosphoinositide 3-kinase δ syndrome (APDS-1).

Lougaris V, Baronio M, Moratto D, Tampella G, Gazzurelli L, Facchetti M, Martire B, Cardinale F, Lanzarotto F, Bondioni MP, Villanacci V, Grimbacher B, Plebani A.

Clin Immunol. 2019 Jan 9;200:31-34. doi: 10.1016/j.clim.2019.01.003. [Epub ahead of print]

PMID:
30639166
4.

Imaging of Bronchial Pathology in Antibody Deficiency: Data from the European Chest CT Group.

Schütz K, Alecsandru D, Grimbacher B, Haddock J, Bruining A, Driessen G, de Vries E, van Hagen PM, Hartmann I, Fraioli F, Milito C, Mitrevski M, Quinti I, Serra G, Kelleher P, Loebinger M, Litzman J, Postranecka V, Thon V, Babar J, Condliffe AM, Exley A, Kumararatne D, Screaton N, Jones A, Bondioni MP, Lougaris V, Plebani A, Soresina A, Sirignano C, Spadaro G, Galal N, Gonzalez-Granado LI, Dettmer S, Stirling R, Chapel H, Lucas M, Patel S, Farber CM, Meyts I, Banerjee AK, Hackett S, Hurst JR, Warnatz K, Gathmann B, Baumann U; Chest CT in Antibody Deficiency Group.

J Clin Immunol. 2018 Dec 13. doi: 10.1007/s10875-018-0577-9. [Epub ahead of print]

PMID:
30547383
5.

Early B cell developmental impairment with progressive B cell deficiency in NFKB2 mutated CVID disease without autoimmunity.

Lougaris V, Moratto D, Baronio M, Lorenzini T, Rossi S, Gazzurelli L, Bondioni MP, Plebani A.

Clin Immunol. 2018 Nov 27. pii: S1521-6616(18)30641-7. doi: 10.1016/j.clim.2018.11.014. [Epub ahead of print]

PMID:
30500415
6.

A de novo monoallelic CTLA-4 deletion causing pediatric onset CVID with recurrent autoimmune cytopenias and severe enteropathy.

Lougaris V, Baronio M, Gazzurelli L, Lorenzini T, Fuoti M, Moratto D, Bozzola A, Ricci C, Bondioni MP, Ravelli A, Villanacci V, Plebani A.

Clin Immunol. 2018 Dec;197:186-188. doi: 10.1016/j.clim.2018.10.007. Epub 2018 Oct 13. No abstract available.

PMID:
30326257
7.

Comparison of Common Monogenic Defects in a Large Predominantly Antibody Deficiency Cohort.

Yazdani R, Abolhassani H, Kiaee F, Habibi S, Azizi G, Tavakol M, Chavoshzadeh Z, Mahdaviani SA, Momen T, Gharagozlou M, Movahedi M, Hamidieh AA, Behniafard N, Nabavi M, Bemanian MH, Arshi S, Molatefi R, Sherkat R, Shirkani A, Amin R, Aleyasin S, Faridhosseini R, Jabbari-Azad F, Mohammadzadeh I, Ghaffari J, Shafiei A, Kalantari A, Mansouri M, Mesdaghi M, Babaie D, Ahanchian H, Khoshkhui M, Soheili H, Eslamian MH, Cheraghi T, Dabbaghzadeh A, Tavassoli M, Kalmarzi RN, Mortazavi SH, Kashef S, Esmaeilzadeh H, Tafaroji J, Khalili A, Zandieh F, Sadeghi-Shabestari M, Darougar S, Behmanesh F, Akbari H, Zandkarimi M, Abolnezhadian F, Fayezi A, Moghtaderi M, Ahmadiafshar A, Shakerian B, Sajedi V, Taghvaei B, Safari M, Heidarzadeh M, Ghalebaghi B, Fathi SM, Darabi B, Bazregari S, Bazargan N, Fallahpour M, Khayatzadeh A, Javahertrash N, Bashardoust B, Zamani M, Mohsenzadeh A, Ebrahimi S, Sharafian S, Vosughimotlagh A, Tafakoridelbari M, Rahim M, Ashournia P, Razaghian A, Rezaei A, Samavat A, Mamishi S, Khazaei HA, Mohammadi J, Negahdari B, Parvaneh N, Rezaei N, Lougaris V, Giliani S, Plebani A, Ochs HD, Hammarström L, Aghamohammadi A.

J Allergy Clin Immunol Pract. 2018 Sep 19. pii: S2213-2198(18)30579-8. doi: 10.1016/j.jaip.2018.09.004. [Epub ahead of print]

PMID:
30240888
8.

Circulating Follicular Helper and Follicular Regulatory T Cells Are Severely Compromised in Human CD40 Deficiency: A Case Report.

Cicalese MP, Gerosa J, Baronio M, Montin D, Licciardi F, Soresina A, Dellepiane RM, Miano M, Baselli LA, Volpi S, Dufour C, Plebani A, Aiuti A, Lougaris V, Fousteri G.

Front Immunol. 2018 Aug 6;9:1761. doi: 10.3389/fimmu.2018.01761. eCollection 2018.

9.

CTLA-4 regulates human Natural Killer cell effector functions.

Lougaris V, Tabellini G, Baronio M, Patrizi O, Gazzurelli L, Mitsuiki N, Pozzi MR, Grimbacher B, Parolini S, Plebani A.

Clin Immunol. 2018 Sep;194:43-45. doi: 10.1016/j.clim.2018.06.010. Epub 2018 Jun 30. No abstract available.

PMID:
29966715
10.

Response to the Letter to the Editor Regarding "Functional evaluation of natural killer cell cytotoxic activity in NFKB-2 mutated patients".

Lougaris V, Tabellini G, Baronio M, Patrizi O, Parolini S, Plebani A.

Immunol Lett. 2018 Aug;200:16-17. doi: 10.1016/j.imlet.2018.05.004. Epub 2018 May 30. No abstract available.

PMID:
29859209
11.

Recurrent Bleedings in Newborn: A Factor VII Deficiency Case Report.

Cattivelli K, Distefano C, Bonetti L, Testa S, Siboni SM, Plebani A, Poggiani C.

Transfus Med Hemother. 2018 Apr;45(2):104-106. doi: 10.1159/000481993. Epub 2018 Mar 8.

12.

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, Bulashevska A, Salzer U, Schubert D, Hayakawa S, Okada S, Kanariou M, Kucuk ZY, Chapdelaine H, Petruzelkova L, Sumnik Z, Sediva A, Slatter M, Arkwright PD, Cant A, Lorenz HM, Giese T, Lougaris V, Plebani A, Price C, Sullivan KE, Moutschen M, Litzman J, Freiberger T, van de Veerdonk FL, Recher M, Albert MH, Hauck F, Seneviratne S, Pachlopnik Schmid J, Kolios A, Unglik G, Klemann C, Speckmann C, Ehl S, Leichtner A, Blumberg R, Franke A, Snapper S, Zeissig S, Cunningham-Rundles C, Giulino-Roth L, Elemento O, Dückers G, Niehues T, Fronkova E, Kanderová V, Platt CD, Chou J, Chatila TA, Geha R, McDermott E, Bunn S, Kurzai M, Schulz A, Alsina L, Casals F, Deyà-Martinez A, Hambleton S, Kanegane H, Taskén K, Neth O, Grimbacher B.

J Allergy Clin Immunol. 2018 Dec;142(6):1932-1946. doi: 10.1016/j.jaci.2018.02.055. Epub 2018 May 4.

PMID:
29729943
13.

Long term outcome of eight patients with type 1 Leukocyte Adhesion Deficiency (LAD-1): Not only infections, but high risk of autoimmune complications.

De Rose DU, Giliani S, Notarangelo LD, Lougaris V, Lanfranchi A, Moratto D, Martire B, Specchia F, Tommasini A, Plebani A, Badolato R.

Clin Immunol. 2018 Jun;191:75-80. doi: 10.1016/j.clim.2018.03.005. Epub 2018 Mar 13.

PMID:
29548898
14.

Minimum effective betamethasone dosage on the neurological phenotype in patients with ataxia-telangiectasia: a multicenter observer-blind study.

Cirillo E, Del Giudice E, Micheli R, Cappellari AM, Soresina A, Dellepiane RM, Pietrogrande MC, Dell'Era L, Specchia F, Pession A, Plebani A, Pignata C.

Eur J Neurol. 2018 Jun;25(6):833-840. doi: 10.1111/ene.13606. Epub 2018 Mar 26.

PMID:
29489040
15.

Progressive severe B cell and NK cell deficiency with T cell senescence in adult CD40L deficiency.

Lougaris V, Lanzi G, Baronio M, Gazzurelli L, Vairo D, Lorenzini T, Badolato R, Notarangelo LD, Boschi A, Moratto D, Plebani A.

Clin Immunol. 2018 May;190:11-14. doi: 10.1016/j.clim.2018.02.008. Epub 2018 Feb 21. No abstract available.

PMID:
29476811
16.

Chronic Granulomatous Disease in children: a single center experience.

Beghin A, Comini M, Soresina A, Imberti L, Zucchi M, Plebani A, Montanelli A, Porta F, Lanfranchi A.

Clin Immunol. 2018 Mar;188:12-19. doi: 10.1016/j.clim.2017.11.016. Epub 2017 Dec 7.

PMID:
29223406
17.

Electrical impedance tomography in children with community acquired pneumonia: preliminary data.

Mazzoni MB, Perri A, Plebani AM, Ferrari S, Amelio G, Rocchi A, Consonni D, Milani GP, Fossali EF.

Respir Med. 2017 Sep;130:9-12. doi: 10.1016/j.rmed.2017.07.001. Epub 2017 Jul 4.

PMID:
29206639
18.

Novel biallelic TRNT1 mutations resulting in sideroblastic anemia, combined B and T cell defects, hypogammaglobulinemia, recurrent infections, hypertrophic cardiomyopathy and developmental delay.

Lougaris V, Chou J, Baronio M, Gazzurelli L, Lorenzini T, Soresina A, Moratto D, Badolato R, Seleman M, Bellettato M, Geha RS, Plebani A.

Clin Immunol. 2018 Mar;188:20-22. doi: 10.1016/j.clim.2017.11.008. Epub 2017 Nov 21. No abstract available.

PMID:
29170023
19.

Corrigendum: Natural Killer Cells from Patients with Recombinase-Activating Gene and Non-Homologous End Joining Gene Defects Comprise a Higher Frequency of CD56bright NKG2A+++ Cells, and Yet Display Increased Degranulation and Higher Perforin Content.

Dobbs K, Tabellini G, Calzoni E, Patrizi O, Martinez P, Giliani SC, Moratto D, Al-Herz W, Cancrini C, Cowan M, Bleesing J, Booth C, Buchbinder D, Burns SO, Chatila TA, Chou J, Daza-Cajigal V, Ott de Bruin LM, de la Morena MT, Di Matteo G, Finocchi A, Geha R, Goyal RK, Hayward A, Holland S, Huang CH, Kanariou MG, King A, Kaplan B, Kleva A, Kuijpers TW, Lee BW, Lougaris V, Massaad M, Meyts I, Morsheimer M, Neven B, Pai SY, Parvaneh N, Plebani A, Prockop S, Reisli I, Soh JY, Somech R, Torgerson TR, Kim YJ, Walter JE, Gennery AR, Keles S, Manis JP, Marcenaro E, Moretta A, Parolini S, Notarangelo LD.

Front Immunol. 2017 Oct 10;8:1244. doi: 10.3389/fimmu.2017.01244. eCollection 2017.

20.

Translation, reliability, and clinical utility of the Melbourne Assessment 2.

Gerber CN, Plebani A, Labruyère R.

Disabil Rehabil. 2019 Jan;41(2):226-234. doi: 10.1080/09638288.2017.1386726. Epub 2017 Oct 12.

PMID:
29025283
21.

Neurovisual Assessment in Children with Ataxia Telangiectasia.

Iodice A, Galli J, Molinaro A, Franzoni A, Micheli R, Pinelli L, Plebani A, Soresina A, Fazzi E.

Neuropediatrics. 2018 Feb;49(1):26-34. doi: 10.1055/s-0037-1607216. Epub 2017 Oct 9.

PMID:
28992644
22.

Response to the Letter to the Editor Regarding "Kinetics of Radiological Response of Thoracic Invasive Fungal Disease in Chronic Granulomatous Disease".

Bondioni MP, Lougaris V, Plebani A.

J Clin Immunol. 2017 Nov;37(8):744-745. doi: 10.1007/s10875-017-0450-2. Epub 2017 Oct 8. No abstract available.

PMID:
28988408
23.

Natural Killer Cells from Patients with Recombinase-Activating Gene and Non-Homologous End Joining Gene Defects Comprise a Higher Frequency of CD56bright NKG2A+++ Cells, and Yet Display Increased Degranulation and Higher Perforin Content.

Dobbs K, Tabellini G, Calzoni E, Patrizi O, Martinez P, Giliani SC, Moratto D, Al-Herz W, Cancrini C, Cowan M, Bleesing J, Booth C, Buchbinder D, Burns SO, Chatila TA, Chou J, Daza-Cajigal V, Ott de Bruin LM, de la Morena M, Di Matteo G, Finocchi A, Geha R, Goyal RK, Hayward A, Holland S, Huang CH, Kanariou MG, King A, Kaplan B, Kleva A, Kuijpers TW, Lee BW, Lougaris V, Massaad M, Meyts I, Morsheimer M, Neven B, Pai SY, Parvaneh N, Plebani A, Prockop S, Reisli I, Soh JY, Somech R, Torgerson TR, Kim YJ, Walter JE, Gennery AR, Keles S, Manis JP, Marcenaro E, Moretta A, Parolini S, Notarangelo LD.

Front Immunol. 2017 Jul 17;8:798. doi: 10.3389/fimmu.2017.00798. eCollection 2017. Erratum in: Front Immunol. 2017 Oct 10;8:1244.

24.

In vivo effects of dexamethasone on blood gene expression in ataxia telangiectasia.

Menotta M, Biagiotti S, Orazi S, Rossi L, Chessa L, Leuzzi V, D'Agnano D, Plebani A, Soresina A, Magnani M.

Mol Cell Biochem. 2018 Jan;438(1-2):153-166. doi: 10.1007/s11010-017-3122-x. Epub 2017 Jul 25.

PMID:
28744812
25.

Beta2 integrins are required for follicular helper T cell differentiation in humans.

Gerosa J, Lougaris V, Baronio M, Plebani A, Cicalese MP, Fousteri G.

Clin Immunol. 2017 Jul;180:60-62. doi: 10.1016/j.clim.2017.04.002. Epub 2017 Apr 6. No abstract available.

PMID:
28390967
26.

Impaired natural killer cell functions in patients with signal transducer and activator of transcription 1 (STAT1) gain-of-function mutations.

Tabellini G, Vairo D, Scomodon O, Tamassia N, Ferraro RM, Patrizi O, Gasperini S, Soresina A, Giardino G, Pignata C, Lougaris V, Plebani A, Dotta L, Cassatella MA, Parolini S, Badolato R.

J Allergy Clin Immunol. 2017 Aug;140(2):553-564.e4. doi: 10.1016/j.jaci.2016.10.051. Epub 2017 Jan 6.

PMID:
28069426
27.

Shift from intravenous or 16% subcutaneous replacement therapy to 20% subcutaneous immunoglobulin in patients with primary antibody deficiencies.

Canessa C, Iacopelli J, Pecoraro A, Spadaro G, Matucci A, Milito C, Vultaggio A, Agostini C, Cinetto F, Danieli MG, Gambini S, Marasco C, Trizzino A, Vacca A, De Mattia D, Martire B, Plebani A, Di Gioacchino M, Gatta A, Finocchi A, Licciardi F, Martino S, De Carli M, Moschese V, Azzari C.

Int J Immunopathol Pharmacol. 2017 Mar;30(1):73-82. doi: 10.1177/0394632016681577. Epub 2016 Dec 7.

28.

NFKB1 regulates human NK cell maturation and effector functions.

Lougaris V, Patrizi O, Baronio M, Tabellini G, Tampella G, Damiati E, Frede N, van der Meer JWM, Fliegauf M, Grimbacher B, Parolini S, Plebani A.

Clin Immunol. 2017 Feb;175:99-108. doi: 10.1016/j.clim.2016.11.012. Epub 2016 Dec 3.

PMID:
27923702
29.

Diagnostics of Primary Immunodeficiencies through Next-Generation Sequencing.

Gallo V, Dotta L, Giardino G, Cirillo E, Lougaris V, D'Assante R, Prandini A, Consolini R, Farrow EG, Thiffault I, Saunders CJ, Leonardi A, Plebani A, Badolato R, Pignata C.

Front Immunol. 2016 Nov 7;7:466. eCollection 2016.

30.

Novel compound heterozygous mutations in a child with Ataxia-Telangiectasia showing unrelated cerebellar disorders.

Piane M, Molinaro A, Soresina A, Costa S, Maffeis M, Germani A, Pinelli L, Meschini R, Plebani A, Chessa L, Micheli R.

J Neurol Sci. 2016 Dec 15;371:48-53. doi: 10.1016/j.jns.2016.10.014. Epub 2016 Oct 13.

PMID:
27871447
31.

Progressive severe B cell deficiency in pediatric Rubinstein-Taybi syndrome.

Lougaris V, Facchini E, Baronio M, Lorenzini T, Moratto D, Specchia F, Plebani A.

Clin Immunol. 2016 Dec;173:181-183. doi: 10.1016/j.clim.2016.10.019. Epub 2016 Nov 5. No abstract available.

PMID:
27825976
32.

Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency.

Bronson PG, Chang D, Bhangale T, Seldin MF, Ortmann W, Ferreira RC, Urcelay E, Pereira LF, Martin J, Plebani A, Lougaris V, Friman V, Freiberger T, Litzman J, Thon V, Pan-Hammarström Q, Hammarström L, Graham RR, Behrens TW.

Nat Genet. 2016 Nov;48(11):1425-1429. doi: 10.1038/ng.3675. Epub 2016 Oct 10.

33.

Early Identification of Lung Fungal Infections in Chronic Granulomatous Disease (CGD) Using Multidetector Computer Tomography.

Bondioni MP, Lougaris V, Di Gaetano G, Lorenzini T, Soresina A, Laffranchi F, Gatta D, Plebani A.

J Clin Immunol. 2017 Jan;37(1):36-41. doi: 10.1007/s10875-016-0342-x. Epub 2016 Oct 21.

PMID:
27766541
34.

Impaired platelet activation in patients with hereditary deficiency of p47phox.

Carnevale R, Loffredo L, Nocella C, Bartimoccia S, Sanguigni V, Soresina A, Plebani A, Azzari C, Martire B, Pignata C, Violi F.

Br J Haematol. 2018 Feb;180(3):454-456. doi: 10.1111/bjh.14347. Epub 2016 Oct 10. No abstract available.

PMID:
27723093
35.

Early and late B-cell developmental impairment in nuclear factor kappa B, subunit 1-mutated common variable immunodeficiency disease.

Lougaris V, Moratto D, Baronio M, Tampella G, van der Meer JWM, Badolato R, Fliegauf M, Plebani A.

J Allergy Clin Immunol. 2017 Jan;139(1):349-352.e1. doi: 10.1016/j.jaci.2016.05.045. Epub 2016 Jul 16. No abstract available.

PMID:
27555455
36.

Impairment of dendritic cell functions in patients with adaptor protein-3 complex deficiency.

Prandini A, Salvi V, Colombo F, Moratto D, Lorenzi L, Vermi W, De Francesco MA, Notarangelo LD, Porta F, Plebani A, Facchetti F, Sozzani S, Badolato R.

Blood. 2016 Jun 30;127(26):3382-6. doi: 10.1182/blood-2015-06-650689. Epub 2016 May 13.

37.

Using a high-flow nasal cannula provided superior results to low-flow oxygen delivery in moderate to severe bronchiolitis.

Milani GP, Plebani AM, Arturi E, Brusa D, Esposito S, Dell'Era L, Laicini EA, Consonni D, Agostoni C, Fossali EF.

Acta Paediatr. 2016 Aug;105(8):e368-72. doi: 10.1111/apa.13444. Epub 2016 May 16. Erratum in: Acta Paediatr. 2017 Jan;106(1):185.

PMID:
27102726
38.

p85α is an intrinsic regulator of human natural killer cell effector functions.

Lougaris V, Patrizi O, Baronio M, Tabellini G, Tampella G, Lanzi G, Salvini F, Trizzino A, Parolini S, Plebani A.

J Allergy Clin Immunol. 2016 Aug;138(2):605-608.e3. doi: 10.1016/j.jaci.2016.01.026. Epub 2016 Mar 23. No abstract available.

PMID:
27016802
39.

Clinical and immunological data of nine patients with chronic mucocutaneous candidiasis disease.

Dotta L, Scomodon O, Padoan R, Timpano S, Plebani A, Soresina A, Lougaris V, Concolino D, Nicoletti A, Giardino G, Licari A, Marseglia G, Pignata C, Tamassia N, Facchetti F, Vairo D, Badolato R.

Data Brief. 2016 Feb 23;7:311-5. doi: 10.1016/j.dib.2016.02.040. eCollection 2016 Jun.

40.

Exocrine Pancreatic Insufficiency after Roux-en-Y gastric bypass.

Borbély Y, Plebani A, Kröll D, Ghisla S, Nett PC.

Surg Obes Relat Dis. 2016 May;12(4):790-794. doi: 10.1016/j.soard.2015.10.084. Epub 2015 Oct 31.

PMID:
26965152
41.

NOX 5 is expressed in platelets from patients with chronic granulomatous disease.

Bartimoccia S, Carnevale R, Sanguigni V, De Falco E, Frati G, Loffredo L, Plebani A, Soresina A, Pignatelli P, Violi F.

Thromb Haemost. 2016 Jul 4;116(1):198-200. doi: 10.1160/TH15-12-0999. Epub 2016 Mar 10. No abstract available.

PMID:
26963053
42.

Cohort of Iranian Patients with Congenital Agammaglobulinemia: Mutation Analysis and Novel Gene Defects.

Abolhassani H, Vitali M, Lougaris V, Giliani S, Parvaneh N, Parvaneh L, Mirminachi B, Cheraghi T, Khazaei H, Mahdaviani SA, Kiaei F, Tavakolinia N, Mohammadi J, Negahdari B, Rezaei N, Hammarstrom L, Plebani A, Aghamohammadi A.

Expert Rev Clin Immunol. 2016;12(4):479-86. doi: 10.1586/1744666X.2016.1139451. Epub 2016 Feb 24.

PMID:
26910880
43.

Reduction of CRKL expression in patients with partial DiGeorge syndrome is associated with impairment of T-cell functions.

Giacomelli M, Kumar R, Soresina A, Tamassia N, Lorenzini T, Moratto D, Gasperini S, Cassatella M, Plebani A, Lougaris V, Badolato R.

J Allergy Clin Immunol. 2016 Jul;138(1):229-240.e3. doi: 10.1016/j.jaci.2015.10.051. Epub 2016 Feb 11.

PMID:
26875746
44.

Reduced germinal center follicular helper T cells but normal follicular regulatory T cells in the tonsils of a patient with a mutation in the PI3KR1 gene.

Di Fonte R, Baronio M, Plebani A, Lougaris V, Fousteri G.

Clin Immunol. 2016 Mar;164:43-4. doi: 10.1016/j.clim.2016.01.016. Epub 2016 Jan 28. No abstract available.

PMID:
26827886
45.

Proteus syndrome: evaluation of the immunological profile.

Lougaris V, Salpietro V, Cutrupi M, Baronio M, Moratto D, Pizzino MR, Mankad K, Briuglia S, Salpietro C, Plebani A.

Orphanet J Rare Dis. 2016 Jan 13;11:3. doi: 10.1186/s13023-015-0381-z.

46.

Clinical heterogeneity of dominant chronic mucocutaneous candidiasis disease: presenting as treatment-resistant candidiasis and chronic lung disease.

Dotta L, Scomodon O, Padoan R, Timpano S, Plebani A, Soresina A, Lougaris V, Concolino D, Nicoletti A, Giardino G, Licari A, Marseglia G, Pignata C, Tamassia N, Facchetti F, Vairo D, Badolato R.

Clin Immunol. 2016 Mar;164:1-9. doi: 10.1016/j.clim.2015.12.010. Epub 2015 Dec 28.

PMID:
26732859
47.

Burden of Skin Disease in Selective IgA Deficiency and Common Variable Immunodeficiency.

Gualdi G, Lougaris V, Baronio M, Vitali M, Tampella G, Moratto D, Tanghetti P, Monari P, Calzavara-Pinton P, Plebani A.

J Investig Allergol Clin Immunol. 2015;25(5):369-71. No abstract available.

48.

Correlation of bone marrow abnormalities, peripheral lymphocyte subsets and clinical features in uncomplicated common variable immunodeficiency (CVID) patients.

Lougaris V, Baronio M, Masneri S, Lorenzini T, Cattivelli K, Tampella G, Soresina A, Moratto D, Plebani A.

Clin Immunol. 2016 Feb;163:10-3. doi: 10.1016/j.clim.2015.12.006. Epub 2015 Dec 11.

PMID:
26686461
49.

Monoallelic BAFFR P21R/H159Y Mutations and Familiar Primary Antibody Deficiencies.

Lougaris V, Baronio M, Moratto D, Cardinale F, Plebani A.

J Clin Immunol. 2016 Jan;36(1):1-3. doi: 10.1007/s10875-015-0217-6. Epub 2015 Nov 27. No abstract available.

PMID:
26613719
50.

The Tec Kinase-Regulated Phosphoproteome Reveals a Mechanism for the Regulation of Inhibitory Signals in Murine Macrophages.

Tampella G, Kerns HM, Niu D, Singh S, Khim S, Bosch KA, Garrett ME, Moguche A, Evans E, Browning B, Jahan TA, Nacht M, Wolf-Yadlin A, Plebani A, Hamerman JA, Rawlings DJ, James RG.

J Immunol. 2015 Jul 1;195(1):246-56. doi: 10.4049/jimmunol.1403238. Epub 2015 May 29.

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