I agree that this site is using cookies. You can find further informations here.
X
Le Collen, Lauriane
31  results:
Search for persons X
?
1

Dominant PDX1 deficiency causes highly penetrant diabetes a..:

Kouidrat, Youssef ; Le Collen, Lauriane ; Vaxillaire, Martine...
Diabetes & Metabolism.  50 (2024)  1 - p. 101507 , 2024
Link: https://doi.org/10.1016/..
 
?
2

Towards the recognition of oligogenic forms of type 2 diabe..:

Le Collen, Lauriane ; Froguel, Philippe ; Bonnefond, Amélie
Trends in Endocrinology & Metabolism.  , 2024
Link: https://doi.org/10.1016/..
 
?
3

Heterozygous pathogenic variants in POMC are not responsibl..:

Le Collen, Lauriane ; Delemer, Brigitte ; Poitou, Christine...
Genetics in Medicine.  25 (2023)  7 - p. 100857 , 2023
Link: https://doi.org/10.1016/..
 
?
4

Patients' perspective on the medical pathway from first sym..:

Mosbah, Héléna ; Vatier, Camille ; Andriss, Béatrice...
European Journal of Endocrinology.  190 (2023)  1 - p. 23-33 , 2023
Link: https://doi.org/10.1093/..
 
?
5

Early Detection of Relapse by ctDNA Sequencing in a Patient..:

Lagarde, Arnaud ; Le Collen, Lauriane ; Boulagnon, Camille...
The Journal of Clinical Endocrinology & Metabolism.  107 (2022)  10 - p. e4154-e4158 , 2022
Link: https://doi.org/10.1210/..
 
?
6

Systematic detection of mosaicism by using digital NGS reve..:

Lagarde, Arnaud ; Mougel, Grégory ; Coppin, Lucie...
Endocrine Connections.  11 (2022)  11 - p. , 2022
Link: https://doi.org/10.1530/..
 
?
7

Compound genetic etiology in a patient with a syndrome incl..:

Le Collen, Lauriane ; Delemer, Brigitte ; Spodenkiewicz, Marta...
Orphanet Journal of Rare Diseases.  17 (2022)  1 - p. , 2022
Link: https://doi.org/10.1186/..
 
?
8

A large extended family with hyperparathyroidism-jaw tumor ..:

Le Collen, Lauriane ; Barraud, Sara ; Braconnier, Antoine...
Endocrine.  73 (2021)  3 - p. 693-701 , 2021
Link: https://doi.org/10.1007/..
 
?
9

SDHx mutation and pituitary adenoma: can in vivo (1)H-MR sp..:

Branzoli, Francesca ; Salgues, Betty ; Marjańska, Małgorzata...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9885742/.  , 2023
Link: http://www.ncbi.nlm.nih...
 
?
10

Heterozygous pathogenic variants in POMC are not responsibl..:

Le Collen, Lauriane ; Delemer, Brigitte ; Poitou, Christine...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.gim.2023.100857.  , 2023
Link: https://hal.sorbonne-uni..
 
?
11

Heterozygous pathogenic variants in POMC are not responsibl..:

Le Collen, Lauriane ; Delemer, Brigitte ; Poitou, Christine...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.gim.2023.100857.  , 2023
Link: https://hal.sorbonne-uni..
 
?
12

Systematic detection of mosaicism by using digital NGS reve..:

Lagarde, Arnaud ; Mougel, Grégory ; Coppin, Lucie...
info:eu-repo/semantics/altIdentifier/doi/10.1530/EC-22-0093.  , 2022
Link: https://amu.hal.science/..
 
?
13

Systematic detection of mosaicism by using digital NGS reve..:

Lagarde, Arnaud ; Mougel, Grégory ; Coppin, Lucie...
info:eu-repo/semantics/altIdentifier/doi/10.1530/EC-22-0093.  , 2022
Link: https://amu.hal.science/..
 
?
14

Systematic detection of mosaicism by using digital NGS reve..:

Lagarde, Arnaud ; Mougel, Grégory ; Coppin, Lucie...
info:eu-repo/semantics/altIdentifier/doi/10.1530/EC-22-0093.  , 2022
Link: https://amu.hal.science/..
 
?
15

Early Detection of Relapse by ctDNA Sequencing in a Patient..:

Lagarde, Arnaud ; Le Collen, Lauriane ; Boulagnon, Camille...
info:eu-repo/semantics/altIdentifier/doi/10.1210/clinem/dgac454.  , 2022
Link: https://hal.univ-reims.f..
 
1-15