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Claudia De Toma

Research Profile

Chemicals & Drugs

Physiology

Concepts & Ideas

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Genes & Molecular Sequences

Disorders

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Publications

TOP 3
Emmanuelle Jeannot; Karine Poussin; Laurence Chiche; Yannick Bacq; Nathalie Sturm; Jean-Yves Scoazec; Catherine Buffet; Jeanne Tran Van Nhieu; Christine Bellanné-Chantelot; Claudia De Toma; Pierre Laurent-Puig; Paulette Bioulac-Sage; Jessica Zucman-Rossi
Association of CYP1B1 germ line mutations with hepatocyte nuclear factor 1alpha-mutated hepatocellular adenoma.
Emmanuelle Jeannot; Dominique Wendum; François Paye; Najat Mourra; Claudia De Toma; Jean-François Fléjou; Jessica Zucman-Rossi
Hepatocellular adenoma displaying a HNF1alpha inactivation in a patient with familial adenomatous polyposis coli.
Christine Bellanné-Chantelot; Isabelle Chaumarel; Myriam Labopin; Florence Bellanger; Véronique Barbu; Claudia De Toma; François Delhommeau; Nicole Casadevall; William Vainchenker; Gilles Thomas; Albert Najman
Genetic and clinical implications of the Val617Phe JAK2 mutation in 72 families with myeloproliferative disorders.

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All Publications

2007: Emmanuelle Jeannot; Karine Poussin; Laurence Chiche; Yannick Bacq; Nathalie Sturm; Jean-Yves Scoazec; Catherine Buffet; Jeanne Tran Van Nhieu; Christine Bellanné-Chantelot; Claudia De Toma; Pierre Laurent-Puig; Paulette Bioulac-Sage; Jessica Zucman-Rossi
Association of CYP1B1 germ line mutations with hepatocyte nuclear factor 1alpha-mutated hepatocellular adenoma.
Cancer research 2007;67(6):2611-6.
2006: Emmanuelle Jeannot; Dominique Wendum; François Paye; Najat Mourra; Claudia De Toma; Jean-François Fléjou; Jessica Zucman-Rossi
Hepatocellular adenoma displaying a HNF1alpha inactivation in a patient with familial adenomatous polyposis coli.
Journal of hepatology 2006;45(6):883-6.
2006: Christine Bellanné-Chantelot; Isabelle Chaumarel; Myriam Labopin; Florence Bellanger; Véronique Barbu; Claudia De Toma; François Delhommeau; Nicole Casadevall; William Vainchenker; Gilles Thomas; Albert Najman
Genetic and clinical implications of the Val617Phe JAK2 mutation in 72 families with myeloproliferative disorders.
Blood 2006;108(1):346-52.

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