Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Cyril A. L. Abrams"'
Autor:
Ralph David, Ronald L. Bellisario, Marilyn L. Cowger, Pavel Fort, Rosalind S. Brown, Diego Botero, Lawrence Fournier, Cyril A. L. Abrams, Robert A. Richman
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 81:1147-1151
To determine the incidence of transient congenital hypothyroidism due to TSH receptor-blocking antibodies, we screened dried blood specimens obtained from 788 neonates identified as having possible congenital hypothyroidism (from a total population o
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 27:467-472
A 15-yr-old girl with panhypopituitarism, and complete infantilism, was treated with a human menopausal gonadotropin preparation (Pergonal) alone, and in combination with HCG. From the responses obtained the following conclusions have been drawn. 1)
Publikováno v:
The Journal of clinical endocrinology and metabolism. 30(5)
The effect of medroxyprogesterone acetate (MPA) on pituitary-adrenal function was investigated in 10 patients with true precocious puberty. Although the patients receiving MPA responded to exogenously administered ACTH by a rise in the plasma 17-hydr
Publikováno v:
Journal of Adolescent Health Care. 8:305
Autor:
Carol D. Berkowitz, Piers R. Blackett, Cyril A. L. Abrams, Louise L. Phillips, Cedric J. Priebe
Publikováno v:
JAMA. 232:1136
Severe hypertonic dehydration with hyperglycemia developed in a 7-week-old infant girl after she was fed an overconcentrated milk formula for five days. Renal failure, disseminated intravascular coagulation, gangrene of the legs, and coma were added
Publikováno v:
Pediatric Research. 11:430-430
Endocrine disorders are uncommon complications of TBM. They usually occur late and present as sexual precocity or diabetes insipidus. This study concerns a 3 yr old boy with unsuspected anterior pituitary deficiencies 8 months after the onset of TBM.
Publikováno v:
Pediatric Research. 11:429-429
Continuous low-dose insulin infusion was employed in 14 children aged 5 to 18 years with DKA based on the method of Kaufman et al. (J. Pediatr. 87:846, 1975). Regular insulin 0.1 unit/kg was given initially by IV push, followed by 0.1 unit/kg/hr by c
Publikováno v:
Archives of Pediatrics & Adolescent Medicine. 134:93
Sir .—We read with interest the report of Collen et al that detailed a case of primary ovarian failure, juvenile rheumatoid arthritis (JRA), and vitiligo (Journal133:598-600, 1979). We, too, have studied a patient with JRA and an autoimmune polyend
Publikováno v:
Pediatric Research. 12:413-413
The association of DM,HT and JRA has not been previously recorded.The purpose of this communication is to report our preliminary findings in a 14 year old Haitian girl who developed insul in- dependent DM at age 6 yrs, goiter at 9 yrs, and polyarticu
Publikováno v:
Archives of Pediatrics & Adolescent Medicine. 119:267
The syndrome of gonadal dysgenesis, or Turner's syndrome, is essentially a combination of a chromosomal aberration, an endocrine disorder, and a number of congenital somatic malformations. Although coarctation of the aorta is the anomaly most frequen