339 results on '"Mendonca, B."'
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2. Voluntary sustainability initiatives and ESG certifications in lithium-ion battery material supply chains: a thematic analysis of key drivers, barriers, and agents.
3. Malignant testicular germ cell tumors in postpubertal individuals with androgen insensitivity: prevalence, pathology and relevance of single nucleotide polymorphism-based susceptibility profiling
4. Growth hormone pharmacogenetics: the interactive effect of a microsatellite in the IGF1 promoter region with the GHR-exon 3 and −202 A/C IGFBP3 variants on treatment outcomes of children with severe GH deficiency
5. Ectopic ACTH syndrome caused by pheochromocytoma: Computed tomography-guided percutaneous ethanol injection as an alternative treatment
6. Height and bone mineral density in androgen insensitivity syndrome with mutations in the androgen receptor gene
7. Adverse outcomes and economic burden of congenital adrenal hyperplasia late diagnosis in the newborn screening absence
8. Low-concentration ethanol stove for rural areas in India
9. Genealogy of the nuclear [beta]-fibrinogen locus in a highly structured lizard species: Comparison with mtDNA and evidence for intragenic recombination in the hybrid zone
10. The effect of fetal androgen metabolism-related gene variants on external genitalia virilization in congenital adrenal hyperplasia
11. Novel Mutations (p.R511W and P.G6R) inIGF1RGene in Children Born Small for Gestational Age (SGA) without Catch-Up Growth.
12. The Presence of Clitoromegaly in Nonclassical Form of 21-Hydroxylase Deficiency Is Modulated by the CAG Polymorphic Tract of Androgen Receptor Gene.
13. Association ofCYP3A7, POR,SRD5A2andHSD17B5Gene Polymorphisms with the Prader Score in Females with Classical Form of CAH.
14. Novel Mutations in the Growth Hormone Secretagogue Receptor Gene (GHSR) Associated with Constitutional Delay in Growth and Puberty (CDGP).
15. Lack of reduction in body fat after treatment with insulin-like growth factor-I in two children with growth hormone gene deletions
16. Growth hormone pharmacogenetics: the interactive effect of a microsatellite in the IGF1 promoter region with the GHR-exon 3 and -202 A/C IGFBP3 variants on treatment outcomes of children with severe GH deficiency
17. Mutations of the KISS1 Gene in Disorders of Puberty
18. Molecular analysis of CYP21A2 can optimize the follow-up of positive results in newborn screening for congenital adrenal hyperplasia
19. Psychosexual Aspects, Effects of Prenatal Androgen Exposure, and Gender Change in 46,XY Disorders of Sex Development
20. Global practice of glucocorticoid and mineralocorticoid treatment in children and adults with congenital adrenal hyperplasia - insight from the I-CAH registry
21. Reproductive Outcome of Women with 21-Hydroxylase-Deficient Nonclassic Adrenal Hyperplasia
22. Combined pituitary hormone deficiency (CPHD) due to a complete PROP1 deletion
23. Inhibin α-subunit (INHA) gene and locus changes in paediatric adrenocortical tumours from TP53 R337H mutation heterozygote carriers
24. Laparoscopic management of intersex patients: the preferred approach
25. Glucocorticoid receptor gene polymorphisms in ACTH-secreting pituitary tumours
26. Two Novel Mutations in the Gonadotropin-Releasing Hormone Receptor Gene in Brazilian Patients with Hypogonadotropic Hypogonadism and Normal Olfaction*
27. Mutations in the type II 3β-hydroxysteroid dehydrogenase (HSD3B2) gene can cause premature pubarche in girls
28. A novel missense mutation (S18N) in the 5′ non-HMG box region of the SRY gene in a patient with partial gonadal dysgenesis and his normal male relatives
29. Diagnostic Value of Fluorometric Assays in the Evaluation of Precocious Puberty*
30. Mutation analysis of the 2 kb 5' to SRY in XY females and XY intersex subjects
31. Defining the dose, type and timing of glucocorticoid and mineralocorticoid replacement in 256 children and adults with congenital adrenal hyperplasia (CAH) in the I-CAH registry
32. Spontaneous fertility in a male patient with testotoxicosis despite suppression of FSH levels
33. Ice Nuclei, Total Aerosol, and Climatology at Mauna Loa, Hawaii
34. The Proportion of Volatile Aerosols on the Island of Hawaii
35. Discriminating between virilizing ovary tumors and ovary hyperthecosis in postmenopausal women: clinical data, hormonal profiles and image studies
36. Effects of Type 1 Insulin-Like Growth Factor Receptor Silencing in a Human Adrenocortical Cell Line
37. Identification of the first homozygous 1‐bp deletion in <italic>GDF9</italic> gene leading to primary ovarian insufficiency by using targeted massively parallel sequencing.
38. DAX1 Overexpression in Pediatric Adrenocortical Tumors: A Synergic Role with SF1 in Tumorigenesis
39. Gonadotropin-independent precocious puberty due to luteinizing hormone receptor mutations in Brazilian boys: a novel constitutively activating mutation in the first transmembrane helix
40. CYP21A2 Genotypes do not Predict the Severity of Hyperandrogenic Manifestations in the Nonclassical Form of Congenital Adrenal Hyperplasia
41. 2153 ORAL Impact of Electronic Treatment Scheduling and Web Based Communication Technology on Systemic Therapy Delivery at the Sunnybrook Odette Cancer Center, Toronto, Canada
42. Effects of electronic chemotherapy scheduling and communication tools on chemotherapy delivery.
43. Growth hormone pharmacogenetics: the interactive effect of a microsatellite in the IGF1 promoter region with the GHR-exon 3 and −202 A/C IGFBP3 variants on treatment outcomes of children with severe GH deficiency
44. Mutations of the KISS1 Gene Associated with Central Precocious Puberty
45. Measurements of stratospheric aerosols over Mauna Loa, Hawaii and Boulder, Colorado
46. Regional rearrangements in chromosome 15q21 cause formation of cryptic promoters for the CYP19 (aromatase) gene
47. Reproductive Outcome of Women With 21-Hydroxylase-Deficient Nonclassic Adrenal Hyperplasia
48. Height and bone mineral density in androgen insensitivity syndrome with mutations in the androgen receptor gene
49. Use of simulation in support of analysis and improvement of blood collection process.
50. Mutations in the Type II 3β-Hydroxysteroid Dehydrogenase (HSD3B2) Gene Can Cause Premature Pubarche in Girls
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