MD
Publications
20
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Title Published in Access level OA Policy Year Views Downloads
Prevalence of Differences of Sex Development Among Pediatric Endocrine Care Centers in Switzerland From 2000 to 2019Journal of the Endocrine Society
accessLevelPublic
2025 11 10
Maladies thyroïdiennes auto-immunes de l’enfant et de l’adolescentRevue médicale suisse
accessLevelRestricted
2025 10 0
Diabète monogénique : pionnier dans la prise en charge par la médecine de précisionRevue médicale suisse
accessLevelPublic
2023 69 58
Aktuelle Herausforderungen in der Therapie des Typ-1-Diabetes beim KindSwiss medical forum
accessLevelPublic
2023 93 77
Predictors of surgical complications in boys with hypospadias : data from an internationa registryWorld journal of pediatric surgery
accessLevelPublic
2023 81 56
NOS1 mutations cause hypogonadotropic hypogonadism with sensory and cognitive deficits that can be reversed in infantile miceScience translational medicine
accessLevelPublic
2022 83 47
Hepatic non-parenchymal S100A9-TLR4-mTORC1 axis normalizes diabetic ketogenesisNature communications
accessLevelPublic
2022 378 113
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 421 612
Global Inequality in Type 1 Diabetes: a Comparison of Switzerland and Low-and Middle-Income CountriesPediatric endocrinology reviews : PER
accessLevelPrivate
2020 380 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 332 210
Combined Pancreatic Islet-Lung-Liver Transplantation in a Pediatric Patient with Cystic Fibrosis-Related DiabetesHormone Research in Paediatrics
accessLevelRestricted
2018 556 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 460 0
KLB, encoding β-Klotho, is mutated in patients with congenital hypogonadotropic hypogonadismEMBO Molecular Medicine
accessLevelPublic
2017 553 273
Transition en diabétologieRevue médicale suisse
accessLevelRestricted
2015 560 1
A novel SRY mutation leads to asymmetric SOX9 activation and is responsible for mixed 46,XY gonadal dysgenesisHormone research in paediatrics
accessLevelRestricted
2012 670 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 612 0
Drug-eluting versus bare-metal stents in saphenous vein graft lesions (ISAR-CABG): a randomised controlled superiority trialLancet
accessLevelRestricted
2011 567 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 632 0
L'enfant diabétique et les spécificités de son traitement insuliniqueRevue médicale suisse
accessLevelRestricted
2007 523 2
Traitement par hormone de croissance : phase de transition de l'enfance à l'âge adulteRevue médicale suisse
accessLevelRestricted
2005 513 0
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