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Publications by Renata C. Scalco
Growth Hormone Insensitivity With Immune Dysfunction Caused by a STAT5B Mutation in the South of Brazil: Evidence for a Founder Effect
Genetics and Molecular Biology
Genetics
Molecular Biology
Related publications
Dominant-Negative STAT5B Mutations Cause Growth Hormone Insensitivity With Short Stature and Mild Immune Dysregulation
Nature Communications
Astronomy
Genetics
Molecular Biology
Biochemistry
Chemistry
Physics
A Novel Mutation of Exon 7 in Growth Hormone Receptor mRNA in a Patient With Growth Hormone Insensitivity Syndrome and Neurofibromatosis Type I
International Journal of Molecular Medicine
Medicine
Genetics
Growth Hormone Insensitivity Syndrome
Growth Hormone Insensitivity: Mexican Case Report
Endocrinology, Diabetes and Metabolism Case Reports
Internal Medicine
Endocrinology
Metabolism
Diabetes
The D152H Mutation Found in Growth Hormone Insensitivity Syndrome Impairs Expression and Function of Human Growth Hormone Receptor but Is Silent in Rat Receptor
Journal of Molecular Endocrinology
Endocrinology
Molecular Biology
Mapping the Growth Hormone–Stat5b–IGF-I Transcriptional Circuit
Trends in Endocrinology and Metabolism
Endocrinology
Metabolism
Diabetes
Effect of Parathyroid Hormone Administration in a Patient With Severe Hypoparathyroidism Caused by Gain-Of-Function Mutation of Calcium-Sensing Receptor
Endocrine Journal
Endocrinology
Metabolism
Diabetes
A Founder Effect for the HGD G360R Mutation in Italy: Implications for a Regional Screening of Alkaptonuria
JIMD Reports
Internal Medicine
Genetics
Molecular Biology
Biochemistry
Endocrinology
Metabolism
Diabetes
The 752delG26 Mutation in the RFXANK Gene Associated With Major Histocompatibility Complex Class II Deficiency: Evidence for a Founder Effect in the Moroccan Population
BMC Proceedings
Biochemistry
Medicine
Genetics
Molecular Biology
