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Dominique Vidaud

Showing results (71-80 of 90) with videos related to

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The British Journal of Dermatology|October 13, 2023
Identification of potential common genetic modifiers of neurofibromas: a genome-wide association study in 1333 patients with neurofibromatosis type 1Laurence Pacot, Audrey Sabbagh, Pierre Sohier, et al.
American Journal of Medical Genetics. Part A|April 20, 2017
Moyamoya syndrome in children with neurofibromatosis type 1: Italian-French experienceClaudia Santoro, Federico Di Rocco, Manoelle Kossorotoff, et al.
Orphanet Journal of Rare Diseases|April 27, 2025
Neurofibromatosis-Noonan syndrome: a prospective monocentric study of 26 patients and literature reviewDidier Bessis, Dominique Vidaud, Pierre Meyer, et al.
Hepatology (Baltimore, Md.)|October 13, 2009
Acute portal vein thrombosis unrelated to cirrhosis: a prospective multicenter follow-up studyAurelie Plessier, Sarwa Darwish-Murad, Manuel Hernandez-Guerra, et al.
Journal of Hepatology|September 29, 2011
IL28B polymorphism is associated with treatment response in patients with genotype 4 chronic hepatitis CTarik Asselah, Simon De Muynck, Philippe Broët, et al.
Science Translational Medicine|June 26, 2024
MEK-SHP2 inhibition prevents tibial pseudarthrosis caused by <i>NF1</i> loss in Schwann cells and skeletal stem/progenitor cellsSimon Perrin, Sanela Protic, Vincent Bretegnier, et al.
Genes|August 25, 2019
One <i>NF1</i> Mutation may Conceal AnotherLaurence Pacot, Cyril Burin des Roziers, Ingrid Laurendeau, et al.
Human Genetics|August 8, 2022
Contribution of whole genome sequencing in the molecular diagnosis of mosaic partial deletion of the NF1 gene in neurofibromatosis type 1Laurence Pacot, Valerie Pelletier, Albain Chansavang, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|November 13, 2013
The activation of the WNT signaling pathway is a Hallmark in neurofibromatosis type 1 tumorigenesisArmelle Luscan, Ghjuvan'ghjacumu Shackleford, Julien Masliah-Planchon, et al.
Cancer Medicine|June 15, 2019
NF1 mutations identify molecular and clinical subtypes of lung adenocarcinomasCamille Tlemsani, Nicolas Pécuchet, Aurelia Gruber, et al.
Pageof 9

Showing results (71-80 of 90) with videos related to

Sort By:
Pageof 9
The British Journal of Dermatology|October 13, 2023
Identification of potential common genetic modifiers of neurofibromas: a genome-wide association study in 1333 patients with neurofibromatosis type 1Laurence Pacot, Audrey Sabbagh, Pierre Sohier, et al.
American Journal of Medical Genetics. Part A|April 20, 2017
Moyamoya syndrome in children with neurofibromatosis type 1: Italian-French experienceClaudia Santoro, Federico Di Rocco, Manoelle Kossorotoff, et al.
Orphanet Journal of Rare Diseases|April 27, 2025
Neurofibromatosis-Noonan syndrome: a prospective monocentric study of 26 patients and literature reviewDidier Bessis, Dominique Vidaud, Pierre Meyer, et al.
Hepatology (Baltimore, Md.)|October 13, 2009
Acute portal vein thrombosis unrelated to cirrhosis: a prospective multicenter follow-up studyAurelie Plessier, Sarwa Darwish-Murad, Manuel Hernandez-Guerra, et al.
Journal of Hepatology|September 29, 2011
IL28B polymorphism is associated with treatment response in patients with genotype 4 chronic hepatitis CTarik Asselah, Simon De Muynck, Philippe Broët, et al.
Science Translational Medicine|June 26, 2024
MEK-SHP2 inhibition prevents tibial pseudarthrosis caused by <i>NF1</i> loss in Schwann cells and skeletal stem/progenitor cellsSimon Perrin, Sanela Protic, Vincent Bretegnier, et al.
Genes|August 25, 2019
One <i>NF1</i> Mutation may Conceal AnotherLaurence Pacot, Cyril Burin des Roziers, Ingrid Laurendeau, et al.
Human Genetics|August 8, 2022
Contribution of whole genome sequencing in the molecular diagnosis of mosaic partial deletion of the NF1 gene in neurofibromatosis type 1Laurence Pacot, Valerie Pelletier, Albain Chansavang, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|November 13, 2013
The activation of the WNT signaling pathway is a Hallmark in neurofibromatosis type 1 tumorigenesisArmelle Luscan, Ghjuvan'ghjacumu Shackleford, Julien Masliah-Planchon, et al.
Cancer Medicine|June 15, 2019
NF1 mutations identify molecular and clinical subtypes of lung adenocarcinomasCamille Tlemsani, Nicolas Pécuchet, Aurelia Gruber, et al.
Pageof 9