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American Journal of Medical Genetics. Part A|July 9, 2017
Diagnosis of Xeroderma pigmentosum variant in a young patient with two novel mutations in the POLH geneArmando De Palma, Marie-Anne Morren, Cécile Ged, et al.
Orphanet Journal of Rare Diseases|May 27, 2017
PIGO deficiency: palmoplantar keratoderma and novel mutationsMarie-Anne Morren, Jaak Jaeken, Gepke Visser, et al.
Revue Medicale Suisse|April 2, 2024
[Autoimmune bullous diseases in children]Laura Bruschi, Frédéric Minisini, Alessia Nidegger, et al.
Orphanet Journal of Rare Diseases|December 15, 2010
Granulomatous skin lesions complicating Varicella infection in a patient with Rothmund-Thomson syndrome and immune deficiency: case reportLien De Somer, Carine Wouters, Marie-Anne Morren, et al.
Pediatric Dermatology|March 2, 2018
Phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha (PIK3CA)-related overgrowth spectrum: A brief reportPieter Denorme, Marie-Anne Morren, Silke Hollants, et al.
European Journal of Pediatrics|April 9, 2015
Overlap between linear scleroderma, progressive facial hemiatrophy and immune-inflammatory encephalitis in a paediatric cohortLien De Somer, Marie-Anne Morren, P C E Hissink Muller, et al.
Dermatology (Basel, Switzerland)|June 6, 2008
Belgian observational drug utilization study of pimecrolimus cream 1% in routine daily practice in atopic dermatitisMarc De Backer, Marie-Anne Morren, Hugo Boonen, et al.
International Journal of Dermatology|June 26, 2018
Scleroderma-like cutaneous lesions during treatment with paclitaxel and gemcitabine in a patient with pancreatic adenocarcinoma. Review of literatureLien Verhulst, Esther Noë, Marie-Anne Morren, et al.
Journal of Medical Genetics|January 30, 2024
Mosaic RASopathies concept: different skin lesions, same systemic manifestations?Marie-Anne Morren, Heidi Fodstad, Hilde Brems, et al.
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