Marc Fillion

Phenotypic severity of homozygous GCK mutations causing neonatal or childhood-onset diabetes is primarily mediated through effects on protein stability

Anne Raimondo, Ali Chakera, Soren K. Thomsen et al. · Human Molecular Genetics · 2014 · 64 citations · Full text

Pamidronate: Treatment for Severe Hypercalcemia in Neonatal Subcutaneous Fat Necrosis

Nathalie Alos, Dardye Eugène, Marc Fillion et al. · Hormone Research in Paediatrics · 2006 · 55 citations

Retrospective Study of the Potential Benefits and Adverse Events during Growth Hormone Treatment in Children with Prader-Willi Syndrome

Marc Fillion, Cheri Deal, Guy Van Vliet · The Journal of Pediatrics · 2008 · 49 citations

Retrospective Study, Growth Hormone, Human Growth +9

Twenty years later: a reevaluation of the contribution of plasma thyroglobulin to the diagnosis of thyroid dysgenesis in infants with congenital hypothyroidism

Anissa Djemli, Marc Fillion, Jaafar Belgoudi et al. · Clinical Biochemistry · 2004 · 41 citations

Thyroid Disease, Thyroid Disorders, Congenital Hypothyroidism +4

Normal minipuberty of infancy in boys with Prader-Willi syndrome

Marc Fillion, Cheri Deal, Guy Van Vliet · The Journal of Pediatrics · 2006 · 39 citations

Down Syndrome, Developmental Anomaly, Genetic Disorder +7