Search Results - "Hercent, Agathe"

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    Clinical vs. molecular diagnosis of Gorlin syndrome: relevance of diagnostic criteria depends on the age of the patients by Hercent, Agathe, Bennani, Rizk, Lafitte, Philippe, Mary, Mickael, Lamoril, Jerôme, Bourrat, Emmanuelle, Kannengiesser, Caroline, Tchernitchko, Dimitri

    Published in Clinical and experimental dermatology (20-05-2024)
    “…Abstract Background Gorlin syndrome (GS) is an autosomal dominant disorder characterized by a predisposition to basal cell carcinoma and developmental defects…”
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    Journal Article
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    Pancreatic Neuroendocrine Tumors in French VHL Mutation Carriers by Muller, Marie, Hammel, Pascal, Couvelard, Anne, Védie, Anne-Laure, Cros, Jérôme, Burnichon, Nelly, Hercent, Agathe, Sauvanet, Alain, Richard, Stéphane, de Mestier, Louis

    “…Abstract Context Von Hippel-Lindau disease (VHL) is a rare, autosomal-dominant hereditary cancer-predisposition syndrome caused by germline pathogenic variants…”
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    Journal Article
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    Clinical versus molecular diagnosis of Gorlin syndrome: Relevance of diagnostic criteria depends on the age of patients by Hercent, Agathe, Bennani, Rizk, Lafitte, Philippe, Mary, Mickael, Lamoril, Jerôme, Bourrat, Emmanuelle, Kannengiesser, Caroline, Tchernitchko, Dimitri

    Published in Clinical and experimental dermatology (20-05-2024)
    “…Gorlin Syndrome (GS) is an autosomal dominant disorder characterised by a predisposition to basal cell carcinoma and developmental defects, and caused by…”
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    Journal Article
  6. 6

    Pancreatic neuroendocrine tumors in French VHL mutation carriers: a multicentric retrospective study by Muller, Marie, Hammel, Pascal, Couvelard, Anne, Védie, Anne-Laure, Cros, Jérôme, Burnichon, Nelly, Hercent, Agathe, Sauvanet, Alain, Richard, Stéphane, de Mestier, Louis

    “…Von Hippel-Lindau disease (VHL) is a rare autosomal dominant hereditary cancer-predisposition syndrome caused by germline pathogenic variants (PV) in VHL gene…”
    Get full text
    Journal Article