Moix I - Search Results

1

Periodic fever, aphthous stomatitis, pharyngitis, cervical adenitis syndrome is linked to dysregulated monocyte IL-1β production.

Kolly L, Busso N, von Scheven-Gete A, Bagnoud N, Moix I, Holzinger D, Simon G, Ives A, Guarda G, So A, Morris MA, Hofer M. Kolly L, et al. Among authors: moix i. J Allergy Clin Immunol. 2013 Jun;131(6):1635-43. doi: 10.1016/j.jaci.2012.07.043. Epub 2012 Sep 21. J Allergy Clin Immunol. 2013. PMID: 23006543

2

Increased Prevalence of NLRP3 Q703K Variant Among Patients With Autoinflammatory Diseases: An International Multicentric Study.

Theodoropoulou K, Wittkowski H, Busso N, Von Scheven-Gête A, Moix I, Vanoni F, Hengten V, Horneff G, Haas JP, Fischer N, Palm-Beden K, Berendes R, Heubner G, Jansson A, Lainka E, Leimgruber A, Morris M, Foell D, Hofer M. Theodoropoulou K, et al. Among authors: moix i. Front Immunol. 2020 May 14;11:877. doi: 10.3389/fimmu.2020.00877. eCollection 2020. Front Immunol. 2020. PMID: 32477355 Free PMC article.

3

De novo duplication of MECP2 in a girl with mental retardation and no obvious dysmorphic features.

Makrythanasis P, Moix I, Gimelli S, Fluss J, Aliferis K, Antonarakis SE, Morris MA, Béna F, Bottani A. Makrythanasis P, et al. Among authors: moix i. Clin Genet. 2010 Aug;78(2):175-80. doi: 10.1111/j.1399-0004.2010.01371.x. Epub 2010 Jan 5. Clin Genet. 2010. PMID: 20236124

4

Intermediate and premutation FMR1 alleles in women with occult primary ovarian insufficiency.

Streuli I, Fraisse T, Ibecheole V, Moix I, Morris MA, de Ziegler D. Streuli I, et al. Among authors: moix i. Fertil Steril. 2009 Aug;92(2):464-70. doi: 10.1016/j.fertnstert.2008.07.007. Epub 2008 Oct 29. Fertil Steril. 2009. PMID: 18973899 Free article.

5

MECP2 duplication syndrome in a patient from Cameroon.

Tekendo-Ngongang C, Dahoun S, Nguefack S, Moix I, Gimelli S, Zambo H, Morris MA, Sloan-Béna F, Wonkam A. Tekendo-Ngongang C, et al. Among authors: moix i. Am J Med Genet A. 2020 Apr;182(4):619-622. doi: 10.1002/ajmg.a.61510. Epub 2020 Feb 13. Am J Med Genet A. 2020. PMID: 32052928 Free PMC article.

6

N-acetylcysteine augments adenovirus-mediated gene expression in human endothelial cells by enhancing transgene transcription and virus entry.

Jornot L, Morris MA, Petersen H, Moix I, Rochat T. Jornot L, et al. Among authors: moix i. J Gene Med. 2002 Jan-Feb;4(1):54-65. doi: 10.1002/jgm.232. J Gene Med. 2002. PMID: 11828388

7

Phenotypic heterogeneity of dopa-responsive dystonia in monozygotic twins.

Grötzsch H, Schnorf H, Morris MA, Moix I, Horvath J, Prilipko O, Burkhard PR. Grötzsch H, et al. Among authors: moix i. Neurology. 2004 Feb 24;62(4):637-9. doi: 10.1212/01.wnl.0000110192.27794.e8. Neurology. 2004. PMID: 14981186

8

A Heterozygous ABCB4, RUNDC3B, and ABCB1 Deletion Associated With Severe Cholestatic Liver Disease in Adulthood.

Terziroli Beretta-Piccoli B, Thompson R, Foskett P, Cerny A, Merlo E, Vergani D, Rougemont AL, Moix I, Mieli-Vergani G, Morris M. Terziroli Beretta-Piccoli B, et al. Among authors: moix i. Hepatology. 2019 Oct;70(4):1484-1487. doi: 10.1002/hep.30783. Epub 2019 Jun 26. Hepatology. 2019. PMID: 31127640 No abstract available.

9

Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome (APECED) due to AIRET16M mutation in a consanguineous Greek girl.

Kollios K, Tsolaki A, Antachopoulos C, Moix I, Morris MA, Papadopoulou M, Roilides E. Kollios K, et al. Among authors: moix i. J Pediatr Endocrinol Metab. 2011;24(7-8):599-601. doi: 10.1515/jpem.2011.012. J Pediatr Endocrinol Metab. 2011. PMID: 21932610

10

Expanding the phenotype of fragile X-associated tremor/ataxia syndrome: a new female case.

Horvath J, Burkhard PR, Morris M, Bottani A, Moix I, Delavelle J. Horvath J, et al. Among authors: moix i. Mov Disord. 2007 Aug 15;22(11):1677-8. doi: 10.1002/mds.21571. Mov Disord. 2007. PMID: 17516494 No abstract available.

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