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JCO Precision Oncology
|
June 7, 2024
Efficacy and Safety of Immune Checkpoint Blockade in Patients With Li-Fraumeni Syndrome
Michele Bottosso, Benjamin Verret, Olivier Caron, et al.
British Journal of Cancer
|
May 13, 2016
Prognostic value of a newly identified MALAT1 alternatively spliced transcript in breast cancer
Didier Meseure, Sophie Vacher, François Lallemand, et al.
Journal of Medical Genetics
|
October 25, 2018
Chemoresistant pleomorphic rhabdomyosarcoma: whole exome sequencing reveals underlying cancer predisposition and therapeutic options
Camille Tlemsani, Karen Leroy, Anne-Paule Gimenez-Roqueplo, et al.
Blood Cells, Molecules & Diseases
|
November 9, 2021
Malignant histiocytosis with a Langerhans cell subtype: A report on the diagnostic and therapeutic challenge
Amel Kime, Claire Bréal, Anne-Ségolène Cottereau, et al.
Human Mutation
|
August 6, 2013
NF1 molecular characterization and neurofibromatosis type I genotype-phenotype correlation: the French experience
Audrey Sabbagh, Eric Pasmant, Apolline Imbard, et al.
Familial Cancer
|
May 19, 2024
A de novo germline pathogenic BRCA1 variant identified following an osteosarcoma pangenomic molecular analysis
Adrien Mouren, Albain Chansavang, Nadim Hamzaoui, et al.
Journal of Neuropathology and Experimental Neurology
|
December 17, 2009
Differential expression of CCN1/CYR61, CCN3/NOV, CCN4/WISP1, and CCN5/WISP2 in neurofibromatosis type 1 tumorigenesis
Eric Pasmant, Nicolas Ortonne, Laure Rittié, et al.
Human Mutation
|
March 15, 2019
Proposition of adjustments to the ACMG-AMP framework for the interpretation of MEN1 missense variants
Pauline Romanet, Marie-Françoise Odou, Marie-Odile North, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 20, 2018
UMD-MEN1 Database: An Overview of the 370 MEN1 Variants Present in 1676 Patients From the French Population
Pauline Romanet, Amira Mohamed, Sophie Giraud, et al.
Human Molecular Genetics
|
September 11, 2012
Somatic NF1 inactivation is a frequent event in sporadic pheochromocytoma
Nelly Burnichon, Alexandre Buffet, Béatrice Parfait, et al.
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of 13
Search research articles
Search
Showing results (61-70 of 124) with videos related to
Sort By:
Page
of 13
JCO Precision Oncology
|
June 7, 2024
Efficacy and Safety of Immune Checkpoint Blockade in Patients With Li-Fraumeni Syndrome
Michele Bottosso, Benjamin Verret, Olivier Caron, et al.
British Journal of Cancer
|
May 13, 2016
Prognostic value of a newly identified MALAT1 alternatively spliced transcript in breast cancer
Didier Meseure, Sophie Vacher, François Lallemand, et al.
Journal of Medical Genetics
|
October 25, 2018
Chemoresistant pleomorphic rhabdomyosarcoma: whole exome sequencing reveals underlying cancer predisposition and therapeutic options
Camille Tlemsani, Karen Leroy, Anne-Paule Gimenez-Roqueplo, et al.
Blood Cells, Molecules & Diseases
|
November 9, 2021
Malignant histiocytosis with a Langerhans cell subtype: A report on the diagnostic and therapeutic challenge
Amel Kime, Claire Bréal, Anne-Ségolène Cottereau, et al.
Human Mutation
|
August 6, 2013
NF1 molecular characterization and neurofibromatosis type I genotype-phenotype correlation: the French experience
Audrey Sabbagh, Eric Pasmant, Apolline Imbard, et al.
Familial Cancer
|
May 19, 2024
A de novo germline pathogenic BRCA1 variant identified following an osteosarcoma pangenomic molecular analysis
Adrien Mouren, Albain Chansavang, Nadim Hamzaoui, et al.
Journal of Neuropathology and Experimental Neurology
|
December 17, 2009
Differential expression of CCN1/CYR61, CCN3/NOV, CCN4/WISP1, and CCN5/WISP2 in neurofibromatosis type 1 tumorigenesis
Eric Pasmant, Nicolas Ortonne, Laure Rittié, et al.
Human Mutation
|
March 15, 2019
Proposition of adjustments to the ACMG-AMP framework for the interpretation of MEN1 missense variants
Pauline Romanet, Marie-Françoise Odou, Marie-Odile North, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 20, 2018
UMD-MEN1 Database: An Overview of the 370 MEN1 Variants Present in 1676 Patients From the French Population
Pauline Romanet, Amira Mohamed, Sophie Giraud, et al.
Human Molecular Genetics
|
September 11, 2012
Somatic NF1 inactivation is a frequent event in sporadic pheochromocytoma
Nelly Burnichon, Alexandre Buffet, Béatrice Parfait, et al.
Page
of 13