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[Early manifestations of Tangier disease].
Lachaux A, Sassolas A, Bouvier R, Le Gall C, Loras I, Regnier F, Plauchu H, Froelich P, Hermier M. Lachaux A, et al. Among authors: sassolas a. Arch Pediatr. 1995 May;2(5):447-51. doi: 10.1016/0929-693x(96)81180-8. Arch Pediatr. 1995. PMID: 7640737 French.
Molecular spectrum of autosomal dominant hypercholesterolemia in France.
Marduel M, Carrié A, Sassolas A, Devillers M, Carreau V, Di Filippo M, Erlich D, Abifadel M, Marques-Pinheiro A, Munnich A, Junien C; French ADH Research Network; Boileau C, Varret M, Rabès JP. Marduel M, et al. Among authors: sassolas a. Hum Mutat. 2010 Nov;31(11):E1811-24. doi: 10.1002/humu.21348. Hum Mutat. 2010. PMID: 20809525 Free PMC article.
Digestive tract involvement in an infant and a child with Tangier disease.
Lachaux A, Sassolas A, Loras-Duclaux I, Le Gall C, Bouvier R. Lachaux A, et al. Among authors: sassolas a. J Pediatr Gastroenterol Nutr. 1998 Aug;27(2):234-6. doi: 10.1097/00005176-199808000-00022. J Pediatr Gastroenterol Nutr. 1998. PMID: 9702662 No abstract available.
Homozygous MTTP and APOB mutations may lead to hepatic steatosis and fibrosis despite metabolic differences in congenital hypocholesterolemia.
Di Filippo M, Moulin P, Roy P, Samson-Bouma ME, Collardeau-Frachon S, Chebel-Dumont S, Peretti N, Dumortier J, Zoulim F, Fontanges T, Parini R, Rigoldi M, Furlan F, Mancini G, Bonnefont-Rousselot D, Bruckert E, Schmitz J, Scoazec JY, Charrière S, Villar-Fimbel S, Gottrand F, Dubern B, Doummar D, Joly F, Liard-Meillon ME, Lachaux A, Sassolas A. Di Filippo M, et al. Among authors: sassolas a. J Hepatol. 2014 Oct;61(4):891-902. doi: 10.1016/j.jhep.2014.05.023. Epub 2014 May 16. J Hepatol. 2014. PMID: 24842304
Chylomicron retention disease: a long term study of two cohorts.
Peretti N, Roy CC, Sassolas A, Deslandres C, Drouin E, Rasquin A, Seidman E, Brochu P, Vohl MC, Labarge S, Bouvier R, Samson-Bouma ME, Charcosset M, Lachaux A, Levy E. Peretti N, et al. Among authors: sassolas a. Mol Genet Metab. 2009 Jun;97(2):136-42. doi: 10.1016/j.ymgme.2009.02.003. Epub 2009 Feb 20. Mol Genet Metab. 2009. PMID: 19285442
Apolipoprotein B48 glycosylation in abetalipoproteinemia and Anderson's disease.
Berriot-Varoqueaux N, Dannoura AH, Moreau A, Verthier N, Sassolas A, Cadiot G, Lachaux A, Munck A, Schmitz J, Aggerbeck LP, Samson-Bouma ME. Berriot-Varoqueaux N, et al. Among authors: sassolas a. Gastroenterology. 2001 Nov;121(5):1101-8. doi: 10.1053/gast.2001.29331. Gastroenterology. 2001. PMID: 11677202
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