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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1995 1
1996 1
1997 2
1998 2
1999 2
2000 1
2001 3
2003 1
2004 2
2005 3
2006 5
2007 5
2008 3
2009 5
2010 5
2011 2
2012 3
2013 2
2014 6
2015 3
2016 3
2017 6
2018 8
2019 4
2020 5
2021 6
2022 3
2023 6
2024 4

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88 results

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Page 1
Biallelic PRKAG2 Truncating Variants Are Associated with Severe Neonatal Cardiomyopathies.
Janin A, Gouy E, Putoux A, Perouse-de-Monclos T, Chevalier P, Faucherre A, Mancilla Abaroa J, Jopling C, Collardeau Frachon S, Radojevic J, El Chehadeh S, Millat G. Janin A, et al. Among authors: millat g. Circ Genom Precis Med. 2023 Jun;16(3):277-279. doi: 10.1161/CIRCGEN.122.003881. Epub 2023 Apr 4. Circ Genom Precis Med. 2023. PMID: 37013823 Free article. No abstract available.
Niemann-Pick disease type C.
Vanier MT, Millat G. Vanier MT, et al. Among authors: millat g. Clin Genet. 2003 Oct;64(4):269-81. doi: 10.1034/j.1399-0004.2003.00147.x. Clin Genet. 2003. PMID: 12974729 Review.
Structure and function of the NPC2 protein.
Vanier MT, Millat G. Vanier MT, et al. Among authors: millat g. Biochim Biophys Acta. 2004 Oct 11;1685(1-3):14-21. doi: 10.1016/j.bbalip.2004.08.007. Biochim Biophys Acta. 2004. PMID: 15465422 Review.
NEXN Gene in Cardiomyopathies and Sudden Cardiac Deaths: Prevalence, Phenotypic Expression, and Prognosis.
Hermida A, Ader F, Millat G, Jedraszak G, Maury P, Cador R, Catalan PA, Clerici G, Combes N, De Groote P, Dupin-Deguine D, Eschalier R, Faivre L, Garcia P, Guillon B, Janin A, Kugener B, Lackmy M, Laredo M, Le Guillou X, Lesaffre F, Lucron H, Milhem A, Nadeau G, Nguyen K, Palmyre A, Perdreau E, Picard F, Rebotier N, Richard P, Rooryck C, Seitz J, Verloes A, Vernier A, Winum P, Yabeta GA, Bouchot O, Chevalier P, Charron P, Gandjbakhch E. Hermida A, et al. Among authors: millat g. Circ Genom Precis Med. 2024 Feb;17(1):e004285. doi: 10.1161/CIRCGEN.123.004285. Epub 2023 Dec 7. Circ Genom Precis Med. 2024. PMID: 38059363 Free article.
Phenotypic Characterization of Timothy Syndrome Caused by the CACNA1C p.Gly402Ser Variant.
Delinière A, Haddad C, Herrera-Siklódy C, Hermida A, Pruvot E, Bressieux-Degueldre S, Millat G, Janin A, Hermida JS, Asatryan B, Chevalier P. Delinière A, et al. Among authors: millat g. Circ Genom Precis Med. 2023 Jun;16(3):280-282. doi: 10.1161/CIRCGEN.122.004010. Epub 2023 Apr 3. Circ Genom Precis Med. 2023. PMID: 37009738 No abstract available.
The adult form of Niemann-Pick disease type C.
Sévin M, Lesca G, Baumann N, Millat G, Lyon-Caen O, Vanier MT, Sedel F. Sévin M, et al. Among authors: millat g. Brain. 2007 Jan;130(Pt 1):120-33. doi: 10.1093/brain/awl260. Epub 2006 Sep 26. Brain. 2007. PMID: 17003072 Review.
Late-onset Fabry disease revealed by ventricular tachycardia: A case report.
Ditac G, Gardey K, Jobbé-Duval A, Fouilhoux A, Millat G, Chevalier P. Ditac G, et al. Among authors: millat g. HeartRhythm Case Rep. 2021 Dec 3;8(2):79-83. doi: 10.1016/j.hrcr.2021.11.025. eCollection 2022 Feb. HeartRhythm Case Rep. 2021. PMID: 35242543 Free PMC article. No abstract available.
88 results