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Novel erbia-yttria co-doped zirconia fluorescent thermal history sensor

Smart materials and structures, 2017-01, Vol.26 (1), p.15001

2017

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Recurrent Mutations in a Single Exon Encoding the Evolutionarily Conserved Olfactomedin-Homology Domain of TIGR in Familial Open-Angle Glaucoma

Human molecular genetics, 1997-11, Vol.6 (12), p.2091-2097

1997

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A heterozygous variant in MEFV in a familial autoinflammatory syndrome with PAPA-like features

Pediatric rheumatology online journal, 2015-09, Vol.13 (99), p.P68-P68, Article P68

2015

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Association of a single nucleotide polymorphism in the TIGR/MYOCILIN gene promoter with the severity of primary open-angle glaucoma

Clinical genetics, 2001-09, Vol.60 (3), p.220-225

2001

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Sftpa1 Mutation In Familial Idiopathic Interstitial Pneumonia And Lung ă Cancer

American journal of respiratory and critical care medicine, 2016, Vol.193

2016

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B62 THE BIOLOGY OF SCARRING. WHERE ARE WE NOW: Sftpa1 Mutation In Familial Idiopathic Interstitial Pneumonia And Lung Cancer

American journal of respiratory and critical care medicine, 2016-01, Vol.193, p.1

2016

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Mutation en mosaïque de NLRP3 dans des urticaires neutrophiliques avec fièvre: une nouvelle entité

Annales de dermatologie et de vénéréologie, 2019-12, Vol.146 (12), p.A76-A77

2019

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Apolipoprotein E–Promoter Single-Nucleotide Polymorphisms Affect the Phenotype of Primary Open-Angle Glaucoma and Demonstrate Interaction with the Myocilin Gene

American journal of human genetics, 2002-06, Vol.70 (6), p.1575-1581

2002

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L’analyse quantitative du mouvement ciliaire permet d’identifier le phénotype ultra-structural des dyskinésies ciliaires primitives

Revue des maladies respiratoires, 2017-01, Vol.34, p.A34-A34

2017

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PW01-032 – FMF-like state: genetic factors unrelated to MEFV

Pediatric rheumatology online journal, 2013-11, Vol.11 (S1), p.A85-A85, Article A85

2013

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OR13-003 - TNFRSF11A molecular defects cause autoinflammatory disorders

Pediatric rheumatology online journal, 2013-11, Vol.11 (S1), p.A265-A265, Article A265

2013

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P02-014 - Consequences of Arginine 92 mutations in TNFR1

Pediatric rheumatology online journal, 2013-11, Vol.11 (S1), p.A121-A121, Article A121

2013

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Delineation of CCDC39/CCDC40 mutation spectrum and associated phenotypes in primary ciliary dyskinesia

Cilia, 2012-11, Vol.1 (S1), p.P91-P91, Article P91

2012

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A New Start-Up and Loading-Up Turbine System

IFAC Proceedings Volumes, 1979-09, Vol.12 (5), p.309-315

1979

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Alterations in the PI3K Pathway Drive Resistance to MET Inhibitors in NSCLC Harboring MET Exon 14 Skipping Mutations

Journal of thoracic oncology, 2020-05, Vol.15 (5), p.741-751

2020

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The peculiar velocity field up to z ∼ 0.05 by forward-modelling Cosmicflows-3 data

Monthly notices of the Royal Astronomical Society, 2019-10, Vol.488 (4), p.5438-5451

2019

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The multiple paths towards MET receptor addiction in cancer

Oncogene, 2018-06, Vol.37 (24), p.3200-3215

2018

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Immune-checkpoint expression in Epstein-Barr virus positive and negative plasmablastic lymphoma: a clinical and pathological study in 82 patients

Haematologica (Roma), 2016-08, Vol.101 (8), p.976-984

2016

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Dual-Energy CT Perfusion of Invasive Tumor Front in Non-Small Cell Lung Cancers

Radiology, 2022-02, Vol.302 (2), p.448-456

2022

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Nearby Supernova Factory Observations of SN 2007if: First Total Mass Measurement of a Super-Chandrasekhar-Mass Progenitor

The Astrophysical journal, 2010-04, Vol.713 (2), p.1073-1094

2010

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Optimization of Routine Testing for MET Exon 14 Splice Site Mutations in NSCLC Patients

Journal of thoracic oncology, 2018-12, Vol.13 (12), p.1873-1883

2018

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Intratubular amyloid in light chain cast nephropathy is a risk factor for systemic light chain amyloidosis

Modern pathology, 2018-03, Vol.31 (3), p.452-462

2018

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Complete and prolonged response to anti-PD1 therapy in an ALK rearranged lung adenocarcinoma

Lung cancer (Amsterdam, Netherlands), 2020-08, Vol.146, p.366-369

2020

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Novel erbia-yttria co-doped zirconia fluorescent thermal history sensor

Recurrent Mutations in a Single Exon Encoding the Evolutionarily Conserved Olfactomedin-Homology Domain of TIGR in Familial Open-Angle Glaucoma

A heterozygous variant in MEFV in a familial autoinflammatory syndrome with PAPA-like features

Association of a single nucleotide polymorphism in the TIGR/MYOCILIN gene promoter with the severity of primary open-angle glaucoma

Sftpa1 Mutation In Familial Idiopathic Interstitial Pneumonia And Lung ă Cancer

B62 THE BIOLOGY OF SCARRING. WHERE ARE WE NOW: Sftpa1 Mutation In Familial Idiopathic Interstitial Pneumonia And Lung Cancer

Mutation en mosaïque de NLRP3 dans des urticaires neutrophiliques avec fièvre: une nouvelle entité

Apolipoprotein E–Promoter Single-Nucleotide Polymorphisms Affect the Phenotype of Primary Open-Angle Glaucoma and Demonstrate Interaction with the Myocilin Gene

L’analyse quantitative du mouvement ciliaire permet d’identifier le phénotype ultra-structural des dyskinésies ciliaires primitives

PW01-032 – FMF-like state: genetic factors unrelated to MEFV

OR13-003 - TNFRSF11A molecular defects cause autoinflammatory disorders

P02-014 - Consequences of Arginine 92 mutations in TNFR1

Delineation of CCDC39/CCDC40 mutation spectrum and associated phenotypes in primary ciliary dyskinesia

A New Start-Up and Loading-Up Turbine System

Alterations in the PI3K Pathway Drive Resistance to MET Inhibitors in NSCLC Harboring MET Exon 14 Skipping Mutations

The peculiar velocity field up to z ∼ 0.05 by forward-modelling Cosmicflows-3 data

The multiple paths towards MET receptor addiction in cancer

Immune-checkpoint expression in Epstein-Barr virus positive and negative plasmablastic lymphoma: a clinical and pathological study in 82 patients

Dual-Energy CT Perfusion of Invasive Tumor Front in Non-Small Cell Lung Cancers

Nearby Supernova Factory Observations of SN 2007if: First Total Mass Measurement of a Super-Chandrasekhar-Mass Progenitor

Optimization of Routine Testing for MET Exon 14 Splice Site Mutations in NSCLC Patients

MET exon 14 skipping mutation is a hepatocyte growth factor (HGF)-dependent oncogenic driver in vitro and in humanised HGF knock-in mice

Intratubular amyloid in light chain cast nephropathy is a risk factor for systemic light chain amyloidosis

Angioimmunoblastic T-cell lymphoma is the most common T-cell lymphoma in two distinct French information data sets

Complete and prolonged response to anti-PD1 therapy in an ALK rearranged lung adenocarcinoma

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