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Béatrice Parfait

Showing results (1-10 of 70) with videos related to

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Human Genetics|October 21, 2010
Gene symbol: MAP2K2. Disease: Cardio-Facio-Cutaneous syndromeNadine Hanna, Béatrice Parfait
Medecine Sciences : M/S|November 9, 2005
[Mutation mechanisms and their consequences]Nadine Hanna, Béatrice Parfait, Dominique Vidaud, et al.
American Journal of Medical Genetics. Part A|January 17, 2013
Neurofibromatosis type 2 in the elderly population: clinical and molecular featuresStéphane Goutagny, Alpha B Bah, Béatrice Parfait, et al.
Journal of Neuro-Oncology|June 29, 2013
Relevance of MPNST cell lines as models for NF1 associated-tumorsEric Pasmant, Armelle Luscan, Jennifer Varin, et al.
American Journal of Medical Genetics. Part A|August 1, 2012
Two independent de novo mutations as a cause for neurofibromatosis type 1 and Noonan syndrome in a single familyEric Pasmant, Jeanne Amiel, Diana Rodriguez, et al.
Neurosurgery|January 13, 2023
Surgical Management of Peripheral Nerve Pathology in Patients With Neurofibromatosis Type 2Matthieu Peyre, Suzanne Tran, Béatrice Parfait, et al.
Journal of Neurosurgery|May 23, 2020
Validation of a scoring system to evaluate the risk of rapid growth of intracranial meningiomas in neurofibromatosis type 2 patientsSamiya Abi Jaoude, Matthieu Peyre, Vincent Degos, et al.
Medecine Sciences : M/S|July 13, 2010
[The amazing story of ANRIL, a long non-coding RNA]Eric Pasmant, Ingrid Laurendeau, Audrey Sabbagh, et al.
Operative Neurosurgery (Hagerstown, Md.)|April 28, 2025
Surgical Management of Peripheral Nerve Schwannomas in Non-Neurofibromatosis Type 2 SchwannomatosisMatthieu Peyre, Alix Addi, Béatrice Parfait, et al.
Human Genetics|March 13, 2026
High frequency of mosaic NF2-related schwannomatosis diagnosed after somatic analysis of multi-nodular schwannomas in schwannomatosis patientsMatthieu Peyre, Cécile Barbance, Suzanne Tran, et al.
Pageof 7

Showing results (1-10 of 70) with videos related to

Sort By:
Pageof 7
Human Genetics|October 21, 2010
Gene symbol: MAP2K2. Disease: Cardio-Facio-Cutaneous syndromeNadine Hanna, Béatrice Parfait
Medecine Sciences : M/S|November 9, 2005
[Mutation mechanisms and their consequences]Nadine Hanna, Béatrice Parfait, Dominique Vidaud, et al.
American Journal of Medical Genetics. Part A|January 17, 2013
Neurofibromatosis type 2 in the elderly population: clinical and molecular featuresStéphane Goutagny, Alpha B Bah, Béatrice Parfait, et al.
Journal of Neuro-Oncology|June 29, 2013
Relevance of MPNST cell lines as models for NF1 associated-tumorsEric Pasmant, Armelle Luscan, Jennifer Varin, et al.
American Journal of Medical Genetics. Part A|August 1, 2012
Two independent de novo mutations as a cause for neurofibromatosis type 1 and Noonan syndrome in a single familyEric Pasmant, Jeanne Amiel, Diana Rodriguez, et al.
Neurosurgery|January 13, 2023
Surgical Management of Peripheral Nerve Pathology in Patients With Neurofibromatosis Type 2Matthieu Peyre, Suzanne Tran, Béatrice Parfait, et al.
Journal of Neurosurgery|May 23, 2020
Validation of a scoring system to evaluate the risk of rapid growth of intracranial meningiomas in neurofibromatosis type 2 patientsSamiya Abi Jaoude, Matthieu Peyre, Vincent Degos, et al.
Medecine Sciences : M/S|July 13, 2010
[The amazing story of ANRIL, a long non-coding RNA]Eric Pasmant, Ingrid Laurendeau, Audrey Sabbagh, et al.
Operative Neurosurgery (Hagerstown, Md.)|April 28, 2025
Surgical Management of Peripheral Nerve Schwannomas in Non-Neurofibromatosis Type 2 SchwannomatosisMatthieu Peyre, Alix Addi, Béatrice Parfait, et al.
Human Genetics|March 13, 2026
High frequency of mosaic NF2-related schwannomatosis diagnosed after somatic analysis of multi-nodular schwannomas in schwannomatosis patientsMatthieu Peyre, Cécile Barbance, Suzanne Tran, et al.
Pageof 7