Neves JF - Search Results

1

Recurrent pyogenic infections caused by a novel Gln1420* mutation in the C3 gene.

Coelho PS, Gouveia C, Pinto MV, Neves C, Cordeiro AI, Neves JF. Coelho PS, et al. Among authors: neves jf. Front Pediatr. 2022 Oct 5;10:1017195. doi: 10.3389/fped.2022.1017195. eCollection 2022. Front Pediatr. 2022. PMID: 36299691 Free PMC article.

2

Successful Handling of Disseminated BCG Disease in a Child with Severe Combined Immunodeficiency.

Bacalhau S, Freitas C, Valente R, Barata D, Neves C, Schäfer K, Lubatschofski A, Schulz A, Neves JF. Bacalhau S, et al. Among authors: neves c, neves jf. Case Rep Med. 2011;2011:527569. doi: 10.1155/2011/527569. Epub 2011 Oct 24. Case Rep Med. 2011. PMID: 22110512 Free PMC article.

3

Successful handling of autoimmunity in X-linked thrombocytopenia (XLT) using mycophenolate mofetil.

Casimiro A, Almeida T, Freitas O, Cordeiro AI, Neves C, Neves JF. Casimiro A, et al. Among authors: neves c, neves jf. Pediatr Blood Cancer. 2012 Nov;59(5):961. doi: 10.1002/pbc.24222. Epub 2012 Jun 12. Pediatr Blood Cancer. 2012. PMID: 22692965 No abstract available.

4

Monoclonal IgG kappa gammopathy previous to hematopoietic stem cell transplantation in an infant with severe combined immunodeficiency.

Simão I, Cordeiro AI, Borrego LM, Martins C, Neves C, Neves JF. Simão I, et al. Among authors: neves c, neves jf. Clin Immunol. 2012 Nov;145(2):133-5. doi: 10.1016/j.clim.2012.08.011. Epub 2012 Sep 13. Clin Immunol. 2012. PMID: 23022654 No abstract available.

5

Hemophagocytic lymphohistiocytosis secondary to Falciparum malaria in a 5 year-old boy.

Santos JA, Neves JF, Venâncio P, Gouveia C, Varandas L. Santos JA, et al. Among authors: neves jf. Ann Hematol. 2015 Jan;94(1):161-3. doi: 10.1007/s00277-014-2118-9. Epub 2014 Jun 1. Ann Hematol. 2015. PMID: 24880248 No abstract available.

6

Hemophagocytic lymphohistiocytosis in 2 patients with underlying IFN-γ receptor deficiency.

Tesi B, Sieni E, Neves C, Romano F, Cetica V, Cordeiro AI, Chiang S, Schlums H, Galli L, Avenali S, Tondo A, Canessa C, Henter JI, Nordenskjöld M, Hsu AP, Holland SM, Neves JF, Azzari C, Bryceson YT. Tesi B, et al. Among authors: neves c, neves jf. J Allergy Clin Immunol. 2015 Jun;135(6):1638-41. doi: 10.1016/j.jaci.2014.11.030. Epub 2015 Jan 13. J Allergy Clin Immunol. 2015. PMID: 25592983 No abstract available.

7

Targeted Gene Panel Sequencing for Early-onset Inflammatory Bowel Disease and Chronic Diarrhea.

Petersen BS, August D, Abt R, Alddafari M, Atarod L, Baris S, Bhavsar H, Brinkert F, Buchta M, Bulashevska A, Chee R, Cordeiro AI, Dara N, Dückers G, Elmarsafy A, Frede N, Galal N, Gerner P, Glocker EO, Goldacker S, Hammermann J, Hasselblatt P, Havlicekova Z, Hübscher K, Jesenak M, Karaca NE, Karakoc-Aydiner E, Kharaghani MM, Kilic SS, Kiykim A, Klein C, Klemann C, Kobbe R, Kotlarz D, Laass MW, Leahy TR, Mesdaghi M, Mitton S, Neves JF, Öztürk B, Pereira LF, Rohr J, Restrepo JLR, Ruzaike G, Saleh N, Seneviratne S, Senol E, Speckmann C, Tegtmeyer D, Thankam P, van der Werff Ten Bosch J, von Bernuth H, Zeissig S, Zeissig Y, Franke A, Grimbacher B. Petersen BS, et al. Among authors: neves jf. Inflamm Bowel Dis. 2017 Dec;23(12):2109-2120. doi: 10.1097/MIB.0000000000001235. Inflamm Bowel Dis. 2017. PMID: 28930861

8

Missense mutation of TTC7A mimicking tricho-hepato-enteric (SD/THE) syndrome in a patient with very-early onset inflammatory bowel disease.

Neves JF, Afonso I, Borrego L, Martins C, Cordeiro AI, Neves C, Lacoste C, Badens C, Fabre A. Neves JF, et al. Among authors: neves c. Eur J Med Genet. 2018 Apr;61(4):185-188. doi: 10.1016/j.ejmg.2017.11.014. Epub 2017 Nov 23. Eur J Med Genet. 2018. PMID: 29174094

9

Novel IL2RG Mutation Causes Leaky TLOWB+NK+ SCID With Nodular Regenerative Hyperplasia and Normal IL-15 STAT5 Phosphorylation.

Neves JF, Martins C, Cordeiro AI, Neves C, Plagnol V, Curtis J, Fabre M, Bibi S, Borrego LM, Moshous D, Nejentsev S, Gilmour K. Neves JF, et al. Among authors: neves c. J Pediatr Hematol Oncol. 2019 May;41(4):328-333. doi: 10.1097/MPH.0000000000001232. J Pediatr Hematol Oncol. 2019. PMID: 29939941

10

Fatal Central Nervous System Lymphocytic Vasculitis after Treatment for Burkitt Lymphoma in a Patient with a SH2D1A Mutation.

Neves JF, Raga LT, Chiang SCC, Tesi B, Vieira JP, Cordeiro AI, Borrego L, Bryceson YT. Neves JF, et al. Pediatr Infect Dis J. 2019 Feb;38(2):e29-e31. doi: 10.1097/INF.0000000000002154. Pediatr Infect Dis J. 2019. PMID: 30138256

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