Skip to main content

Articles

Page 15 of 15

  1. Graves' disease is a thyroid-specific autoimmune disorder in which the body makes antibodies to the thyroid-stimulating hormone receptor leading to hyperthyroidism. Therapeutic options for the treatment of Gra...

    Authors: Phuong Tran, Shane DeSimone, Mark Barrett and Bert Bachrach
    Citation: International Journal of Pediatric Endocrinology 2010 2010:858359
  2. Objective. Graves' disease is the most common cause of hyperthyroidism in the pediatric population. Antithyroid medications used in children and adults include propylthiouracil (PTU) and methimazole (MMI). At our...

    Authors: Scott A Rivkees, Kerry Stephenson and Catherine Dinauer
    Citation: International Journal of Pediatric Endocrinology 2010 2010:176970
  3. In 2002 a consensus statement pertaining to the management of classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency was jointly produced by the Lawson Wilkins Pediatric Endocrine Society an...

    Authors: Traci L Schaeffer, Jeanie B Tryggestad, Ashwini Mallappa, Adam E Hanna, Sowmya Krishnan, Steven D Chernausek, Laura J Chalmers, William G Reiner, Brad P Kropp and Amy B Wisniewski
    Citation: International Journal of Pediatric Endocrinology 2010 2010:692439
  4. High steroid doses are often necessary in congenital adrenal hyperplasia (CAH) to suppress androgens and may increase blood pressure (BP). We evaluated 24-hour BP profile (ambBP), BP during exercise (excBP), a...

    Authors: Graziamaria Ubertini, Carla Bizzarri, Armando Grossi, Fabrizio Gimigliano, Lucilla Ravà, Danilo Fintini and Marco Cappa
    Citation: International Journal of Pediatric Endocrinology 2010 2009:383610
  5. Objective. To evaluate the effectiveness of oxandrolone in improving the nutritional status and linear growth of pediatric patients with cystic fibrosis (CF). Methods. Medical records of patients with CF treated ...

    Authors: Todd Varness, Erin E. Seffrood, Ellen L. Connor, Michael J. Rock and David B. Allen
    Citation: International Journal of Pediatric Endocrinology 2010 2009:826895
  6. The treatment of congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency is complex. In addition to disease control, important therapeutic goals are the maintenance of normal growth and the acqui...

    Authors: Todd D. Nebesio and Erica A. Eugster
    Citation: International Journal of Pediatric Endocrinology 2010 2010:298937
  7. We report a familial case of the nephrogenic syndrome of inappropriate antidiuresis (NSIAD), including 30-year followup data on two patients. The proband and one maternal uncle presented in their infancy with ...

    Authors: Yoon Hi Cho, Stephen Gitelman, Stephen Rosenthal and Geoffrey Ambler
    Citation: International Journal of Pediatric Endocrinology 2009 2009:431527
  8. Three infants with ambiguous genitalia and suspected ovotestes were given recombinant FSH to induce ovarian follicular development. The development of follicles in the gonadal tissue suggested the presence of ...

    Authors: Shannon French, Luisa Rodriguez, Alan Schlesinger, Laurence McCullough, Jennifer Dietrich, John Hicks and Lefkothea Karaviti
    Citation: International Journal of Pediatric Endocrinology 2009 2009:507964
  9. Objective. To assess the growth and control of adrenal androgen secretion in children with virilizing congenital adrenal hyperplasia (CAH) treated with dexamethasone. Method. We examined doses used, control of ad...

    Authors: Scott A. Rivkees and Kerry Stephenson
    Citation: International Journal of Pediatric Endocrinology 2009 2009:274682
  10. We report an interesting case of a 17-year-old normal-statured female who was diagnosed with congenital panhypopituitarism due to pituitary hypoplasia at the presentation of bilateral slipped capital femoral e...

    Authors: Sasigarn A. Bowden and Kevin E. Klingele
    Citation: International Journal of Pediatric Endocrinology 2009 2009:609131
  11. The choice of therapeutic strategies for hyperthyroidism during pregnancy is limited. Surgery and radioiodine are typically avoided, leaving propylthiouracil and methimazole in the US. Carbimazole, a metabolic...

    Authors: Albert R. Cunningham, C. Alex Carrasquer and Donald R. Mattison
    Citation: International Journal of Pediatric Endocrinology 2009 2009:936154
  12. Data accumulated over recent years have significantly advanced our understanding of growth factors, cytokines, and hormones in breast milk. Here we deal with leptin, adiponectin, IGF-I, ghrelin, and the more r...

    Authors: Francesco Savino, Stefania A. Liguori, Maria F. Fissore and Roberto Oggero
    Citation: International Journal of Pediatric Endocrinology 2009 2009:327505
  13. Cushing syndrome is rare in infancy and usually due to an adrenocortical tumor (ACT). We report an infant with Cushing syndrome due to adrenocortical carcinoma. The patient presented at six months of age with ...

    Authors: ElizabethB Fudge, Daniel von Allmen, KeithE Volmar and AliS Calikoglu
    Citation: International Journal of Pediatric Endocrinology 2009 2009:168749
  14. The incidence of overweight and obesity is rising at an alarming pace in the pediatric population, just as in the adult population. The adult comorbidities associated with this risk factor are well-recognized ...

    Authors: Darren M. Allcock, Michael J. Gardner and James R. Sowers
    Citation: International Journal of Pediatric Endocrinology 2009 2009:108187
  15. Objectives. We investigate whether parents complaining of their children's short stature have misconception of their height. Methods. Parents were asked to report their own height and were then measured. We compa...

    Authors: Paulo F. Collett-Solberg and Pedro R. Collett-Solberg
    Citation: International Journal of Pediatric Endocrinology 2009 2009:919405
  16. Objectives. (1) Determine the predictive value of a school-based test of cardiovascular fitness (CVF) for insulin resistance (IR); (2) compare a "school-based" prediction of IR to a "laboratory-based" prediction,...

    Authors: Todd Varness, Aaron L. Carrel, Jens C. Eickhoff and David B. Allen
    Citation: International Journal of Pediatric Endocrinology 2009 2009:487804
  17. The most common monogenic cause of neonatal diabetes is mutation in KCNJ11, which encodes a potassium channel in pancreatic beta cells. Some mutations in this gene, including Q52R, have been described in assoc...

    Authors: Natalie D. Shaw and Joseph A. Majzoub
    Citation: International Journal of Pediatric Endocrinology 2009 2009:453240
  18. Objectives. To determine if the low iron state described in obese children is associated with the chronic inflammatory state seen in obesity. Study Design. Obese children age from 2 to 19 years seen at a weight m...

    Authors: MatthewW Richardson, Leybie Ang, PaulF Visintainer and ChrystalA Wittcopp
    Citation: International Journal of Pediatric Endocrinology 2009 2009:713269
  19. Disorders of sex development refer to a collection of congenital conditions in which atypical development of chromosomal, gonadal, or anatomic sex occurs. Studies of 46,XY DSD have focused largely on gender id...

    Authors: Amy B. Wisniewski and Tom Mazur
    Citation: International Journal of Pediatric Endocrinology 2009 2009:567430
  20. The effect of intracerebroventricular (ICV) antileptin antibody on the onset of puberty in the female rat and the relationship between serum leptin, luteinizing hormone (LH), and body weight were investigated....

    Authors: Ruimin Chen, Gail J. Mick, Rongxian Xu, Daoxin Zheng, Yanfeng Fan, Xiangquan Lin and Kenneth L. McCormick
    Citation: International Journal of Pediatric Endocrinology 2009 2009:194807
  21. As the first wave of biopharmaceuticals is set to expire, biosimilars or follow-on protein products (FOPPs) have emerged. The regulatory foundation for these products is more advanced and better codified in Eu...

    Authors: Paul Saenger
    Citation: International Journal of Pediatric Endocrinology 2009 2009:370329
  22. Hyponatremia with hyperkalemia in infancy is an uncommon but life-threatening occurrence. In the first weeks of life, this scenario is often associated with aldosterone deficiency due to salt-wasting congenita...

    Authors: Radha Nandagopal, Priya Vaidyanathan and Paul Kaplowitz
    Citation: International Journal of Pediatric Endocrinology 2009 2009:195728
  23. This study examined changes in insulin resistance (IR) in 120 youth over two years. IR was quantified via homeostatic model (HOMA-IR), and weight status changes were quantified via body mass index (BMI). When ...

    Authors: Kristin S. Ondrak, Robert G. McMurray, Claudio L. Battaglini, Kelly R. Evenson and Joanne S. Harrell
    Citation: International Journal of Pediatric Endocrinology 2009 2009:862061
  24. Propylthiouracil (PTU) was introduced for clinical use in July 1947 for Graves' disease (GD) treatment. Over the 60 years that this medication has been used, reports of PTU-related liver failure and death have...

    Authors: Scott A. Rivkees and Donald R. Mattison
    Citation: International Journal of Pediatric Endocrinology 2009 2009:132041
  25. Severe iodine deficiency results in impaired thyroid hormone synthesis and thyroid enlargement. In the United States, adequate iodine intake is a concern for women of childbearing age and pregnant women. Beyon...

    Authors: Stefanie Leniszewski and Richard Mauseth
    Citation: International Journal of Pediatric Endocrinology 2009 2009:628034
  26. Background. Gonadotropin releasing hormone analogs (GnRHas) are standard of care for central precocious puberty (CPP). The histrelin subcutaneous implant is safe and effective in the treatment of CPP for one year...

    Authors: Samar Rahhal, William L. Clarke, Gad B. Kletter, Peter A. Lee, E. Kirk Neely, Edward O. Reiter, Paul Saenger, Dorothy Shulman, Lawrence Silverman and Erica A. Eugster
    Citation: International Journal of Pediatric Endocrinology 2009 2009:812517
  27. Galactocele is a benign breast lesion, usually occurring in nursing women. This lesion is a rare cause of breast enlargement in children. In this paper we describe the case of an infant with hyperprolactinemia...

    Authors: Paolo A. Tomasi, Giuseppe Fanciulli, Tiziana Casti and Giuseppe Delitala
    Citation: International Journal of Pediatric Endocrinology 2009 2009:578610
  28. In adult patients with congenital adrenal hyperplasia (CAH), the presence of testicular adrenal rest tumours (TART) is an important complication leading to gonadal dysfunction and infertility. These tumours ca...

    Authors: H. L. Claahsen-van der Grinten, A. R. M. M. Hermus and B. J. Otten
    Citation: International Journal of Pediatric Endocrinology 2009 2009:624823
  29. The Constant Carbohydrate diet, based entirely on carbohydrate exchanges, is now widely used in the dietary treatment of diabetes mellitus. Being based on sound scientific principles and simple in design, the ...

    Authors: Charles Herbert Read Jr.
    Citation: International Journal of Pediatric Endocrinology 2008 2009:469623
  30. Obesity is a significant cause of morbidity and mortality worldwide. There has been a significant worsening of the obesity epidemic mainly due to alterations in dietary intake and energy expenditure. Alternati...

    Authors: Juliana Austin and Daniel Marks
    Citation: International Journal of Pediatric Endocrinology 2008 2009:141753