Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Virginia V. Weldon"'
Publikováno v:
Women in Academia Report; 6/10/2024, p1-1, 1p
Autor:
Virginia V. Weldon
Publikováno v:
International Journal of Health Services. 21:561-562
Autor:
Virginia V. Weldon
Publikováno v:
Mayo Clinic Proceedings. 63:821-824
Autor:
Julio V. Santiago, G. Shackelford, Y. Bussman, William H. McAlister, Morey W. Haymond, S. K. Ratzan, Virginia V. Weldon
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 45:845-848
A recent study using the photon absorption technique has revealed a high frequency of significant bone loss in diabetic adults regardless of age or duration of diabetes. In this study 107 diabetic children age 4-18 were studied using cortical bone th
Publikováno v:
American Journal of Medical Genetics. 21:123-129
Although familial forms of hypopituitarism are known, to our knowledge familial septooptic "dysplasia" in association with hypopituitarism has not been reported. We describe two first cousins with panhypopituitarism, one of whom had septooptic dyspla
Autor:
Michael P. Whyte, Virginia V. Weldon
Publikováno v:
The Journal of Pediatrics. 99:608-611
HYPOCAI.CEMIA is most commonly encountered by pediatricians in neonates. ' Early neonatal hypocalcemia presents within the first two days of life and usually affects infants who are premature, are born of diabetic mothers, or have had anoxia, acidosi
Publikováno v:
The Journal of Pediatrics. 101:12-15
Growth failure may be associated with low serum somatomedin concentrations despite normal to increased concentrations of serum growth hormone. We have recognized five patients who responded to GH administration with an increase in serum Sm and an acc
Publikováno v:
The Journal of Pediatrics. 87:58-62
A 14 4/12-year-old white girl, evaluated for progressive virilization and clitoromegaly, was found to have the unusual combination of a 46, XX karyotype, well-developed Mullerian structures, and dysgenetic testes with Leydig cell hyperplasia. Althoug
Autor:
Santosh K. Gupta, Anthony S. Pagliara, Stephen C. Duck, William L. Clarke, Virginia V. Weldon, Morey W. Haymond, Georgeanna Klingensmith
Publikováno v:
The Journal of Pediatrics. 87:540-544
L-Dopa in a dose ranging from 125-500 mg and arginine monochloride in a dose of 0.5 gm/kg were given simultaneously to 56 children with short stature (height less than third percentile). Sixteen of these children were subsequently diagnosed as having
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 47:461-466
Two three-year-old boys with dwarfism (height ages 1–4/12 and 1–11/12 years) and delayed bone ages (1–4/12 and 1–9/12 years) had normal growth hormone (GH) responses after stimulation and low levels of somatomedin. Unlike patients with Laron