Karla Melo
0000-0003-0096-2325
17 papers found
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Onde os brasileiros obtiveram os medicamentos para o diabetes na pandemia de COVID-19? Resultados da DIABETESvid
Where did Brazilians get their diabetes drugs during the COVID-19 pandemic? DIABETESvid results
Short-acting insulin analogues versus regular human insulin on postprandial glucose and hypoglycemia in type 1 diabetes mellitus: a systematic review and meta-analysis
Functional Impact of Novel Androgen Receptor Mutations on the Clinical Manifestation of Androgen Insensitivity Syndrome
Intensive insulin treatment induces insulin resistance in diabetic rats by impairing glucose metabolism-related mechanisms in muscle and liver
46,XY Disorders of Sex Development (46,XY DSD) due to Androgen Receptor Defects: Androgen Insensitivity Syndrome
Study of association of polymorphisms in the glutamate-cysteine ligase catalytic subunit gene (GCLC) and gluthatione peroxidase 1 (GPX1) gene with chronic kidney disease (CKD) in type 1 diabetes mellitus (T1DM)
Na + -Glucose Transporter-2 Messenger Ribonucleic Acid Expression in Kidney of Diabetic Rats Correlates with Glycemic Levels: Involvement of Hepatocyte Nuclear Factor-1α Expression and Activity
The degree of external genitalia virilization in girls with 21-hydroxylase deficiency appears to be influenced by the CAG repeats in the androgen receptor gene
Frequency of molecular diagnosis in Brazilian patients with 46, XY disorders of sexual development (DSD)
Height and bone mineral density in androgen insensitivity syndrome with mutations in the androgen receptor gene
Types of prandial bolus and self-monitoring (SM) on glycemic control in type 1 diabetes (DM1)
Height and bone mineral apparent density (BMAD) in patients with androgen insensitivity syndrome (AIS) with mutations in the androgen receptor (AR) gene
Clinical, Hormonal, Behavioral, and Genetic Characteristics of Androgen Insensitivity Syndrome in a Brazilian Cohort: Five Novel Mutations in the Androgen Receptor Gene
An unusual phenotype of Frasier syndrome due to IVS9+4C > T mutation in the WT1 gene: Predominantly male ambiguous genitalia and absence of gonadal dysgenesis
Adrenal Nodules in Patients with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency: Regression after Adequate Hormonal Control
Analysis of Exon 5 Of the Androgen Receptor (AR) Gene in Patients with Male Pseudohermaphroditism (MPH) Due to Androgen Insensitivity or Undetermined Cause
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