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Philippe Halimi

Showing results (11-20 of 16) with videos related to

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BMC Medical Genetics|December 1, 2006
Identification of the first intragenic deletion of the PITX2 gene causing an Axenfeld-Rieger Syndrome: case reportGuillaume de la Houssaye, Ivan Bieche, Olivier Roche, et al.
European Radiology|October 3, 2015
The value of a rapid contrast-enhanced angio-MRI protocol in the detection of head and neck paragangliomas in SDHx mutations carriers: a retrospective study on behalf of the PGL.EVA investigatorsGuillaume Gravel, Patricia Niccoli, Vincent Rohmer, et al.
Molecular Vision|April 10, 2007
Three new PAX6 mutations including one causing an unusual ophthalmic phenotype associated with neurodevelopmental abnormalitiesAnouk Dansault, Gabriel David, Claire Schwartz, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|October 23, 2015
In Vivo Detection of Succinate by Magnetic Resonance Spectroscopy as a Hallmark of SDHx Mutations in ParagangliomaCharlotte Lussey-Lepoutre, Alexandre Bellucci, Aurélie Morin, et al.
Injury|September 1, 2016
Terrorist attacks in Paris: Surgical trauma experience in a referral centerThomas M Gregory, Thomas Bihel, Pierre Guigui, et al.
The Journal of Clinical Endocrinology and Metabolism|November 20, 2012
Imaging work-up for screening of paraganglioma and pheochromocytoma in SDHx mutation carriers: a multicenter prospective study from the PGL.EVA InvestigatorsAnne-Paule Gimenez-Roqueplo, Aurore Caumont-Prim, Claire Houzard, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
BMC Medical Genetics|December 1, 2006
Identification of the first intragenic deletion of the PITX2 gene causing an Axenfeld-Rieger Syndrome: case reportGuillaume de la Houssaye, Ivan Bieche, Olivier Roche, et al.
European Radiology|October 3, 2015
The value of a rapid contrast-enhanced angio-MRI protocol in the detection of head and neck paragangliomas in SDHx mutations carriers: a retrospective study on behalf of the PGL.EVA investigatorsGuillaume Gravel, Patricia Niccoli, Vincent Rohmer, et al.
Molecular Vision|April 10, 2007
Three new PAX6 mutations including one causing an unusual ophthalmic phenotype associated with neurodevelopmental abnormalitiesAnouk Dansault, Gabriel David, Claire Schwartz, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|October 23, 2015
In Vivo Detection of Succinate by Magnetic Resonance Spectroscopy as a Hallmark of SDHx Mutations in ParagangliomaCharlotte Lussey-Lepoutre, Alexandre Bellucci, Aurélie Morin, et al.
Injury|September 1, 2016
Terrorist attacks in Paris: Surgical trauma experience in a referral centerThomas M Gregory, Thomas Bihel, Pierre Guigui, et al.
The Journal of Clinical Endocrinology and Metabolism|November 20, 2012
Imaging work-up for screening of paraganglioma and pheochromocytoma in SDHx mutation carriers: a multicenter prospective study from the PGL.EVA InvestigatorsAnne-Paule Gimenez-Roqueplo, Aurore Caumont-Prim, Claire Houzard, et al.
Pageof 2