MD
Publications
18
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1 - 18 of 18
Title Published in Access level OA Policy Year Views Downloads
Diabète monogénique : pionnier dans la prise en charge par la médecine de précisionRevue médicale suisse
accessLevelPublic
2023 20 5
Aktuelle Herausforderungen in der Therapie des Typ-1-Diabetes beim KindSwiss medical forum
accessLevelPublic
2023 56 21
Predictors of surgical complications in boys with hypospadias : data from an internationa registryWorld journal of pediatric surgery
accessLevelPublic
2023 39 12
NOS1 mutations cause hypogonadotropic hypogonadism with sensory and cognitive deficits that can be reversed in infantile miceScience translational medicine
accessLevelPublic
2022 32 19
Hepatic non-parenchymal S100A9-TLR4-mTORC1 axis normalizes diabetic ketogenesisNature communications
accessLevelPublic
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 therapyDiabetes
accessLevelPublic
2020 359 494
Global Inequality in Type 1 Diabetes: a Comparison of Switzerland and Low-and Middle-Income CountriesPediatric endocrinology reviews : PER
accessLevelPrivate
2020 309 0
Transgender youth: implementation of a specialized multidisciplinary team careJoint Annual Meeting Swiss Society of Paediatrics, Swiss Society of Paediatric Surgery and Swiss Society of Child and Adolescent Psychiatry and Psychotherapy
accessLevelPublic
2018 269 126
Combined Pancreatic Islet-Lung-Liver Transplantation in a Pediatric Patient with Cystic Fibrosis-Related DiabetesHormone Research in Paediatrics
accessLevelRestricted
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 StudyDiabetes Technology & Therapeutics
accessLevelRestricted
2018 381 0
KLB, encoding β-Klotho, is mutated in patients with congenital hypogonadotropic hypogonadismEMBO Molecular Medicine
accessLevelPublic
2017 483 217
Transition en diabétologieRevue médicale suisse
accessLevelRestricted
2015 511 1
A novel SRY mutation leads to asymmetric SOX9 activation and is responsible for mixed 46,XY gonadal dysgenesisHormone research in paediatrics
accessLevelRestricted
2012 598 0
Diabète de l'enfant, de l'insulino-vers l'immunothérapie: une prise en charge globale du présent vers le futurRevue médicale suisse
accessLevelRestricted
2011 572 0
Drug-eluting versus bare-metal stents in saphenous vein graft lesions (ISAR-CABG): a randomised controlled superiority trialLancet
accessLevelRestricted
2011 515 0
A homozygous missense mutation in SCNN1A is responsible for a transient neonatal form of pseudohypoaldosteronism type 1American journal of physiology: endocrinology and metabolism
accessLevelRestricted
2011 581 0
L'enfant diabétique et les spécificités de son traitement insuliniqueRevue médicale suisse
accessLevelRestricted
2007 496 2
Traitement par hormone de croissance : phase de transition de l'enfance à l'âge adulteRevue médicale suisse
accessLevelRestricted
2005 481 0
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