MMG PUBLICATIONS

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Results: 2278  publications found.

Fultang, L.  et al. 2019

Macrophage-Derived IL1 beta and TNF alpha Regulate Arginine Metabolism in Neuroblastoma

Neuroblastoma is the most common childhood solid tumor, yet the prognosis for high-risk disease remains poor. We demonstrate here that arginase 2 (ARG2) drives neuroblastoma cell proliferation via...
- issue: 3 - volume: 79 - pages: 611-624.


Romanet, P.  et al. 2019

Using Digital Droplet Polymerase Chain Reaction to Detect the Mosaic GNAS Mutations in Whole Blood DNA or Circulating Cell-Free DNA in Fibrous Dysplasia and McCune-Albright Syndrome

The GNAS postzygotic mosaic activating mutations involved in fibrous dysplasia and McCune-Albright syndrome (MAS) are not detectable in leukocytes by Sanger sequencing. Digital droplet polymerase...
- issue: - volume: 205 - pages: 281+.


Castinetti, F.  et al. 2019

French Endocrine Society Guidance on endocrine side effects of immunotherapy

The management of cancer patients has changed due to the considerably more frequent use of immune checkpoint inhibitors (ICPIs). However, the use of ICPI has a risk of side effects, particularly...
- issue: 2 - volume: 26 - pages: G1-G18.


Jullien, N.  et al. 2019

Heterozygous LHX3 mutations may lead to a mild phenotype of combined pituitary hormone deficiency

LHX3 is an LIM domain transcription factor involved in the early steps of pituitary ontogenesis. We report here functional studies of three allelic variants, including the first heterozygous variant...
Eur. J. Hum. Genet. - issue: 2 - volume: 27 - pages: 216-225.


Vergier, J.  et al. 2019

Evaluation of flash glucose monitoring after long-term use: A pediatric survey

Aims: To understand the opinions of children with type 1 diabetes about their everyday use of flash glucose monitoring. (FGM). Methods: Children with type 1 diabetes using the FreeStyle Libre (R) FGM...
- issue: 1 - volume: 13 - pages: 63-70.


Jullien, N.  et al. 2019

Heterozygous LHX3 mutations may lead to a mild phenotype of combined pituitary hormone deficiency

LHX3 is an LIM domain transcription factor involved in the early steps of pituitary ontogenesis. We report here functional ;studies of three allelic variants, including the first heterozygous variant...
- issue: 2 - volume: 27 - pages: 216-225.


Grapperon, A.  et al. 2019

Guillain-Barre syndrome subtypes: A clinical electrophysiological study of 100 patients

Introduction. - A retrospective analysis was performed to document the clinical and electrophysiological features of Guillain-Barre syndrome (GBS) subtypes using different diagnostic criteria....
- issue: 1-2 - volume: 175 - pages: 73-80.


Romanet, P.  et al. 2019

Using Digital Droplet Polymerase Chain Reaction to Detect the Mosaic GNAS Mutations in Whole Blood DNA or Circulating Cell-Free DNA in Fibrous Dysplasia and McCune-Albright Syndrome

The GNAS postzygotic mosaic activating mutations involved in fibrous dysplasia and McCune-Albright syndrome (MAS) are not detectable in leukocytes by Sanger sequencing. Digital droplet polymerase...
J. Pediatr. - issue: - volume: 205 - pages: 281-285.e4.


Macagno, N.  et al. 2019

Grading of Meningeal Solitary Fibrous Tumors/Hemangiopericytomas: Prognostic Value of the Marseille Grading System in a Cohort of 132 Patients in correlation with molecular data

- issue: 1, SI - volume: 29 - pages: 35-36.


Valdeolivas, A.  et al. 2019

Random walk with restart on multiplex and heterogeneous biological networks

- issue: 3 - volume: 35 - pages: 497-505.


Giovannini-Chami, L.  et al. 2019

STAT3 gain of function: a new aetiology of severe rheumatic disease

- issue: 2 - volume: 58 - pages: 365-367.


Fultang, L.  et al. 2019

Macrophage-Derived IL1 beta and TNF alpha Regulate Arginine Metabolism in Neuroblastoma

- issue: 3 - volume: 79 - pages: 611-624.


Romanet, P.  et al. 2019

Using Digital Droplet Polymerase Chain Reaction to Detect the Mosaic GNAS Mutations in Whole Blood DNA or Circulating Cell-Free DNA in Fibrous Dysplasia and McCune-Albright Syndrome

- issue: - volume: 205 - pages: 281+.


Castinetti, F.  et al. 2019

French Endocrine Society Guidance on endocrine side effects of immunotherapy

- issue: 2 - volume: 26 - pages: G1-G18.


Vergier, J.  et al. 2019

Evaluation of flash glucose monitoring after long-term use: A pediatric survey

- issue: 1 - volume: 13 - pages: 63-70.


Jullien, N.  et al. 2019

Heterozygous LHX3 mutations may lead to a mild phenotype of combined pituitary hormone deficiency

- issue: 2 - volume: 27 - pages: 216-225.


Grapperon, A.  et al. 2019

Guillain-Barre syndrome subtypes: A clinical electrophysiological study of 100 patients

- issue: 1-2 - volume: 175 - pages: 73-80.


Grigioni, F.  et al. 2019

Long-Term Implications of Atrial Fibrillation in Patients With Degenerative Mitral Regurgitation

BACKGROUND Scientific guidelines consider atrial fibrillation (AF) complicating degenerative mitral regurgitation (DMR) a debated indication for surgery. OBJECTIVES This study analyzed the...
- issue: 3 - volume: 73 - pages: 264-274.


Grigioni, F.  et al. 2019

Long-Term Implications of Atrial Fibrillation in Patients With Degenerative Mitral Regurgitation

- issue: 3 - volume: 73 - pages: 264-274.


Jalkh, N.  et al. 2019

The added value of WES reanalysis in the field of genetic diagnosis: lessons learned from 200 exomes in the Lebanese population

The past few decades have witnessed a tremendous development in the field of genetics. The implementation of next generation sequencing (NGS) technologies revolutionized the field of molecular biology...
- issue: - volume: 12 - pages: .