References
- McKiernan PJ. Neonatal jaundice. Clin Res Hepatol Gastroenterol 2012;36(3):253–256.
- Yerushalmi B, Sokol RJ, Narkewicz MR, et al. Niemann-pick disease type C in neonatal cholestasis at a North American Center. J Pediatric Gastroenterol Nutr 2002;35(1):44–50.
- Santamaria R, Michelakakis H, Moraitou M, et al. Haplotype analysis suggests a single Balkan origin for the Gaucher disease [D409H;H255Q] double mutant allele. Hum Mutat 2008;29(6):E58–67.
- Mignot C, Gelot A, Bessières B, et al. Perinatal-lethal Gaucher disease. Am J Med Genet A 2003;120A(3):338–44.
- Barbier C, Devisme L, Dobbelaere D, et al. Neonatal cholestasis and infantile Gaucher disease: a case report. Acta Pediatr 2002;91(12):1399–401.
- Elias AF, Johnson MR, Boitnott JK, et al. Neonatal cholestasis as initial manifestation of type 2 Gaucher disease: a continuum in the spectrum of early onset Gaucher disease. JIMD Rep 2012;5:95–8.
- Turkia HB, Tebib N, Kasdallah N, et al. Cholestase néonatale révélatrice d’un phénotype intermédiaire d’une maladie de Gaucher type 2. Arch Pediatr 2009;16(3):255–257.