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American Journal of Ophthalmology|December 13, 2006
Blau syndrome associated with a CARD15/NOD2 mutationBernadette Snyers, Karin DahanInternational Ophthalmology|October 9, 2010
Cytomegalovirus retinitis after low-dose intravitreous triamcinolone acetonide in an immunocompetent patient: a warning for the widespread use of intravitreous corticosteroidsDora Vertes, Bernadette Snyers, Patrick De PotterAmerican Journal of Ophthalmology|May 6, 2004
Photodynamic therapy of subfoveal neovascular membrane in type 2A idiopathic juxtafoveolar retinal telangiectasisBernadette Snyers, Claire Verougstraete, Laurence Postelmans, et al.Retina (Philadelphia, Pa.)|December 8, 2006
Susac syndrome in four male patientsBernadette Snyers, Antonella Boschi, Patrick De Potter, et al.Nephrologie & Therapeutique|August 10, 2006
[From Alport syndrome to benign familial hematuria: clinical and genetic aspect]Nicolas Maziers, Karin Dahan, Yves PirsonEuropean Journal of Dermatology : EJD|October 29, 2008
Leg ulcers: a new symptom of Blau syndrome?Veerle Dhondt, Sarah Hofman, Karin Dahan, et al.Case Reports in Nephrology|October 4, 2021
Mutation in the SLC2A9 Gene: A New Family with Familial Renal Hypouricemia Type 2Christian Maalouli, Karin Dahan, Arnaud Devresse, et al.BMJ Case Reports|December 25, 2014
A 'silent', new polymorphism of factor H and apparent de novo atypical haemolytic uraemic syndrome after kidney transplantationEmine N Broeders, Patrick Stordeur, Sandrine Rorive, et al.Clinical Epigenetics|June 19, 2012
Hypermethylation of the 5' CpG island of the p14ARF flanking exon 1β in human colorectal cancer displaying a restricted pattern of p53 overexpression concomitant with increased MDM2 expressionChristine Nyiraneza, Christine Sempoux, Roger Detry, et al.Journal of Medical Genetics|October 4, 2024
K acetyltransferase 2B (KAT2B) variants can be responsible for early onset steroid-resistant nephrotic syndromeOlivier Niel, Ancuta Caliment, Charlotte Hougardy, et al.Pageof 8