MD
Title | Published in | Access level | OA Policy | Year | Views | Downloads | |
---|---|---|---|---|---|---|---|
Diabète monogénique : pionnier dans la prise en charge par la médecine de précision | Revue médicale suisse | 2023 | 20 | 5 | |||
Aktuelle Herausforderungen in der Therapie des Typ-1-Diabetes beim Kind | Swiss medical forum | 2023 | 56 | 21 | |||
Predictors of surgical complications in boys with hypospadias : data from an internationa registry | World journal of pediatric surgery | 2023 | 39 | 12 | |||
NOS1 mutations cause hypogonadotropic hypogonadism with sensory and cognitive deficits that can be reversed in infantile mice | Science translational medicine | 2022 | 32 | 19 | |||
Hepatic non-parenchymal S100A9-TLR4-mTORC1 axis normalizes diabetic ketogenesis | Nature communications | 2022 | 290 | 66 | |||
Systematic genetic study of diabetic youth in a single country reveals the prevalence of diabetes subtypes, novel candidate genes, and response to precision therapy | Diabetes | 2020 | 359 | 494 | |||
Global Inequality in Type 1 Diabetes: a Comparison of Switzerland and Low-and Middle-Income Countries | Pediatric endocrinology reviews : PER | 2020 | 309 | 0 | |||
Transgender youth: implementation of a specialized multidisciplinary team care | Joint Annual Meeting Swiss Society of Paediatrics, Swiss Society of Paediatric Surgery and Swiss Society of Child and Adolescent Psychiatry and Psychotherapy | 2018 | 269 | 126 | |||
Combined Pancreatic Islet-Lung-Liver Transplantation in a Pediatric Patient with Cystic Fibrosis-Related Diabetes | Hormone Research in Paediatrics | 2018 | 502 | 1 | |||
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 | Diabetes Technology & Therapeutics | 2018 | 381 | 0 | |||
KLB, encoding β-Klotho, is mutated in patients with congenital hypogonadotropic hypogonadism | EMBO Molecular Medicine | 2017 | 483 | 217 | |||
Transition en diabétologie | Revue médicale suisse | 2015 | 511 | 1 | |||
A novel SRY mutation leads to asymmetric SOX9 activation and is responsible for mixed 46,XY gonadal dysgenesis | Hormone research in paediatrics | 2012 | 598 | 0 | |||
Diabète de l'enfant, de l'insulino-vers l'immunothérapie: une prise en charge globale du présent vers le futur | Revue médicale suisse | 2011 | 572 | 0 | |||
Drug-eluting versus bare-metal stents in saphenous vein graft lesions (ISAR-CABG): a randomised controlled superiority trial | Lancet | 2011 | 515 | 0 | |||
A homozygous missense mutation in SCNN1A is responsible for a transient neonatal form of pseudohypoaldosteronism type 1 | American journal of physiology: endocrinology and metabolism | 2011 | 581 | 0 | |||
L'enfant diabétique et les spécificités de son traitement insulinique | Revue médicale suisse | 2007 | 496 | 2 | |||
Traitement par hormone de croissance : phase de transition de l'enfance à l'âge adulte | Revue médicale suisse | 2005 | 481 | 0 |