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Publications by Maricilda Palandi De Mello
A New Compound Heterozygosis for Inactivating Mutations in the Glucokinase Gene as Cause of Permanent Neonatal Diabetes Mellitus (PNDM) in Double-First Cousins
Diabetology and Metabolic Syndrome
Internal Medicine
Endocrinology
Metabolism
Diabetes
Related publications
Glucokinase Gene Mutations Are Not a Common Cause of Permanent Neonatal Diabetes in France
Diabetologia
Internal Medicine
Endocrinology
Metabolism
Diabetes
A Mutation in the TMD0-L0 Region of Sulfonylurea Receptor-1 (L225P) Causes Permanent Neonatal Diabetes Mellitus (PNDM)
Diabetes
Internal Medicine
Endocrinology
Metabolism
Diabetes
Permanent Neonatal Diabetes Mellitus
Defect in MAPK Signaling as a Cause for Monogenic Obesity Caused by Inactivating Mutations in the Melanocortin-4 Receptor Gene
International Journal of Biological Sciences
Applied Microbiology
Evolution
Ecology
Developmental Biology
Cell Biology
Molecular Biology
Systematics
Behavior
Biotechnology
Recessively Inherited LRBA Mutations Cause Autoimmunity Presenting as Neonatal Diabetes
Diabetes
Internal Medicine
Endocrinology
Metabolism
Diabetes
Recessively Inherited LRBA Mutations Cause Autoimmunity Presenting as Neonatal Diabetes
Yearbook of Paediatric Endocrinology
Permanent Neonatal Diabetes Mellitus: Clinical Presentation and Epidemiology in Oman
Archives of Disease in Childhood: Fetal and Neonatal Edition
Pediatrics
Gynecology
Perinatology
Obstetrics
Medicine
Child Health
Insulin Gene Mutations as Cause of Diabetes in Children Negative for Five Type 1 Diabetes Autoantibodies
Diabetes Care
Internal Medicine
Endocrinology
Advanced
Metabolism
Specialized Nursing
Diabetes
A Glucokinase Gene Mutation in a Young Boy With Diabetes Mellitus, Hyperinsulinemia, and Insulin Resistance
International Medical Case Reports Journal
Medicine
