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Dirlewanger, Mijam
Dirlewanger, Mijam
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Elements: 13
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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
;
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