47 results on '"Merke Deborah P."'
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2. Androgens correlate with increased erythropoiesis in women with congenital adrenal hyperplasia
3. Diagnosis and Treatment of Primary Adrenal Insufficiency: An Endocrine Society Clinical Practice Guideline
4. Broadening the Spectrum of Ehlers Danlos Syndrome in Patients With Congenital Adrenal Hyperplasia
5. A Phase 2 Study of Chronocort, a Modified-Release Formulation of Hydrocortisone, in the Treatment of Adults With Classic Congenital Adrenal Hyperplasia
6. Cortical bone mineral density in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
7. An oral multiparticulate, modified-release, hydrocortisone replacement therapy that provides physiological cortisol exposure
8. Tenascin-X Haploinsufficiency Associated with Ehlers-Danlos Syndrome in Patients with Congenital Adrenal Hyperplasia
9. Clinical Characteristics of a Cohort of 244 Patients with Congenital Adrenal Hyperplasia
10. Use of PET/CT with Cosyntropin Stimulation to Identify and Localize Adrenal Rest Tissue following Adrenalectomy in a Woman with Congenital Adrenal Hyperplasia
11. Comprehensive Genetic Analysis of 182 Unrelated Families with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
12. Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline
13. A pharmacokinetic and pharmacodynamic study of delayed- and extended-release hydrocortisone (ChronocortTM) vs. conventional hydrocortisone (CortefTM) in the treatment of congenital adrenal hyperplasia
14. Hypoglycemia During Acute Illness in Children With Classic Congenital Adrenal Hyperplasia
15. The Phenotypic Spectrum of Contiguous Deletion of CYP21A2 and Tenascin XB: Quadricuspid Aortic Valve and Other Midline Defects
16. Quality of life in children and adolescents 1-year after cure of Cushing syndrome: a prospective study
17. Cardiovascular Disease Risk in Adult Women with Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
18. Modified-Release Hydrocortisone to Provide Circadian Cortisol Profiles
19. Approach to the Adult with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
20. Oxygen-Uptake Efficiency Slope as a Determinant of Fitness in Overweight Adolescents
21. Patients with Classic Congenital Adrenal Hyperplasia Have Decreased Epinephrine Reserve and Defective Glycemic Control during Prolonged Moderate-Intensity Exercise
22. Amygdala function in adolescents with congenital adrenal hyperplasia: A model for the study of early steroid abnormalities
23. Maternal 21-hydroxylase deficiency and uniparental isodisomy of chromosome 6 and X results in a child with 21-hydroxylase deficiency and Klinefelter syndrome
24. Children Experience Cognitive Decline Despite Reversal of Brain Atrophy One Year After Resolution of Cushing Syndrome
25. Stress Dose of Hydrocortisone Is Not Beneficial in Patients with Classic Congenital Adrenal Hyperplasia Undergoing Short-Term, High-Intensity Exercise
26. Endocrinologic and Psychologic Evaluation of 21-Hydroxylase Deficiency Carriers and Matched Normal Subjects: Evidence for Physical and/or Psychologic Vulnerability to Stress
27. Patients with Classic Congenital Adrenal Hyperplasia Have Decreased Epinephrine Reserve and Defective Glucose Elevation in Response to High-Intensity Exercise
28. In Boys with Abnormal Developmental Tempo, Maturation of the Skeleton and the Hypothalamic-Pituitary-Gonadal Axis Remains Synchronous
29. Effects of Hormones and Sex Chromosomes on Stress-Influenced Regions of the Developing Pediatric Brain
30. Children with Classic Congenital Adrenal Hyperplasia Have Decreased Amygdala Volume: Potential Prenatal and Postnatal Hormonal Effects
31. Pubertal and Gender-Related Changes in the Sympathoadrenal System in Healthy Children
32. Flutamide Decreases Cortisol Clearance in Patients with Congenital Adrenal Hyperplasia
33. Adrenomedullary Function May Predict Phenotype and Genotype in Classic 21-Hydroxylase Deficiency
34. Children with Classic Congenital Adrenal Hyperplasia Have Elevated Serum Leptin Concentrations and Insulin Resistance: Potential Clinical Implications
35. Utility of Plasma Free Metanephrines for Detecting Childhood Pheochromocytoma
36. Future Directions in the Study and Management of Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
37. Novel Basic and Clinical Aspects of Congenital Adrenal Hyperplasia
38. Early Puberty: A Cautionary Tale
39. Adrenomedullary Dysplasia and Hypofunction in Patients with Classic 21-Hydroxylase Deficiency
40. Picture of the Month
41. Flutamide, Testolactone, and Reduced Hydrocortisone Dose Maintain Normal Growth Velocity and Bone Maturation Despite Elevated Androgen Levels in Children with Congenital Adrenal Hyperplasia
42. Early Puberty: A Cautionary Tale
43. Effects of flutamide and testolactone on cortisol clearance in children with congenital adrenal hyperplasia.: 54.
44. Brief Report: Hypogonadotropic Hypogonadism in a Female Caused by an X-Linked Recessive Mutation in the DAX1 Gene
45. Adrenal Lymphocytic Infiltration and Adrenocortical Tumors in a Patient with 21-Hydroxylase Deficiency
46. New Approaches to the Treatment of Congenital Adrenal Hyperplasia
47. Evaluation and management of precocious puberty
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