2020

Scientific Articles

unige:143379	Global Inequality in Type 1 Diabetes: a Comparison of Switzerland and Low-and Middle-Income Countries	Almeida Marques, Nilson Jonathan; Lazo Porras, Maria De Los Angeles; Schwitzgebel Luscher, Valérie; Castellsague Perolini, Montserrat; ... Beran, David Henri
unige:131525	Systematic genetic study of diabetic youth in a single country reveals the prevalence of diabetes subtypes, novel candidate genes, and response to precision therapy	Stankute, Ingrida; Verkauskiene, Rasa; Blouin, Jean-Louis; Klee, Philippe; ... Schwitzgebel Luscher, Valérie

2018

Scientific Articles

unige:126950	An Intervention by a Patient-Designed Do-It-Yourself Mobile Device App Reduces HbA1c in Children and Adolescents with Type 1 Diabetes: A Randomized Double-Crossover Study	Klee, Philippe; Bussien, Catherine; Castellsague Perolini, Montserrat; Combescure, Christophe; ... Schwitzgebel Luscher, Valérie
unige:108165	Combined Pancreatic Islet-Lung-Liver Transplantation in a Pediatric Patient with Cystic Fibrosis-Related Diabetes	Klee, Philippe; Dirlewanger, Mijam; Lavallard, Vanessa; Mclin, Valérie Anne; ... Schwitzgebel Luscher, Valérie

Proceedings Chapters

unige:130473

Transgender youth: implementation of a specialized multidisciplinary team care

Dirlewanger, Mijam; Merglen, Arnaud; Edan, Anne; Benard, Julie Gabrielle Anne; ... Schwitzgebel Luscher, Valérie

2017

Scientific Articles

unige:108163

KLB, encoding β-Klotho, is mutated in patients with congenital hypogonadotropic hypogonadism

Xu, Cheng; Messina, Andrea; Somm, Emmanuel; Miraoui, Hichem; ... Pitteloud, Nelly

2015

Scientific Articles

unige:76054

Transition en diabétologie

Hauschild, M; Elowe-Gruau, E; Dwyer, A; Aquarone, M-P; ... Schwitzgebel Luscher, Valérie

2012

Scientific Articles

unige:27579

A novel SRY mutation leads to asymmetric SOX9 activation and is responsible for mixed 46,XY gonadal dysgenesis

Klee, Philippe; Bena, Frédérique; Birraux, Jacques Maurice; Dahoun, Sophie; ... Schwitzgebel Luscher, Valérie

2011

Scientific Articles

unige:25735	A homozygous missense mutation in SCNN1A is responsible for a transient neonatal form of pseudohypoaldosteronism type 1	Dirlewanger, Mijam; Huser, Delphine; Zennaro, Maria-Christina; Girardin, Eric; ... Schwitzgebel Luscher, Valérie
unige:25734	Diabète de l'enfant, de l'insulino-vers l'immunothérapie: une prise en charge globale du présent vers le futur	Dirlewanger, Mijam; Hauschild, Michael; Phan-Hug, Franziska; Schwitzgebel Luscher, Valérie;
unige:25780	Drug-eluting versus bare-metal stents in saphenous vein graft lesions (ISAR-CABG): a randomised controlled superiority trial	Mehilli, Julinda; Pache, Jürgen; Abdel-Wahab, Mohamed; Schulz, Stefanie; ... Dirlewanger, Mijam

2007

Scientific Articles

unige:44737

L'enfant diabétique et les spécificités de son traitement insulinique

Dirlewanger, Mijam; Perrenoud, L; Castellsague Perolini, Montserrat; Schwitzgebel Luscher, Valérie;

2005

Scientific Articles

unige:72872

Traitement par hormone de croissance : phase de transition de l'enfance à l'âge adulte

Fatio, Sandra Agnes; Dirlewanger, Mijam; Meier, Christoph; Schwitzgebel Luscher, Valérie;