• A familial hypomagnesemia--hypercalciuria (Manz syndrome)
• Addition of the nuclear export inhibitor selinexor to standard intensive treatment for elderly patients with acute myeloid leukemia and high risk myelodysplastic syndrome
• Age and sex associate with outcome in older AML and high risk MDS patients treated with 10-day decitabine
• Antibody response to a third SARS-CoV-2 vaccine dose in recipients of an allogeneic haematopoietic cell transplantation
• Bilateral slipped capital femoral epiphysis in a male adolescent with familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC), chronic renal failure, and severe hyperparathyroidism
• Claudins in Renal Physiology and Pathology
• Complications of Lesser Toe Surgery: How To Avoid Them before Surgery and How To Assess and Treat Them When They Have Occurred
• Diabetes insipidus and Guillain-Barré-like syndrome following CAR-T cell therapy: a case report
• Familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC): report of three cases with a novel mutation in CLDN19 gene
• Fulminant Cardiotoxicity in a Patient With Cardiac Lymphoma Treated With CAR-T Cells
• Generation of a novel fully human non-superagonistic anti-CD28 antibody with efficient and safe T-cell co-stimulation properties
• Hierarchical contribution of individual lifestyle factors and their interactions on adenomatous and serrated polyp risk
• High titers and low fucosylation of early human anti-SARS-CoV-2 IgG promote inflammation by alveolar macrophages
• Identification of the first large deletion in the CLDN16 gene in a patient with FHHNC and late-onset of chronic kidney disease: case report
• Introducing innovative cellular therapies into the clinic: a 2-year retrospective experience of a chimeric antigen receptor T-cell programme at a single centre in Switzerland
• Maternal and neonatal outcomes of pregnancies with COVID-19 after medically assisted reproduction: results from the prospective COVID-19-Related Obstetrical and Neonatal Outcome Study
• Methods to analyze subcellular localization and intracellular trafficking of Claudin-16
• Michaelis-Manz syndrome. A case report
• MIS-C-Implications for the Pediatric Surgeon: An Algorithm for Differential Diagnostic Considerations
• Mutation in the tight-junction gene claudin 19 (CLDN19) and familial hypomagnesemia, hypercalciuria, nephrocalcinosis (FHHNC) and severe ocular disease
• Nerve hyperexcitability in Michaelis-Manz syndrome
• Novel ACE2 fusion protein with adapting activity against SARS-CoV-2 variants <em>in vitro</em>
• Novel compound heterozygous mutations of CLDN16 in a patient with familial hypomagnesemia with hypercalciuria and nephrocalcinosis
• Ocular involvement in a child with medullary nephrocalcinosis
• Renal, ocular, and neuromuscular involvements in patients with CLDN19 mutations
• Severity of Illness Caused by Severe Acute Respiratory Syndrome Coronavirus 2 Variants of Concern in Children: A Single-Center Retrospective Cohort Study
• Severity of Illness Caused by Severe Acute Respiratory Syndrome Coronavirus 2 Variants of Concern in Children: A Single-Center Retrospective Cohort Study