Results 131 to 140 of about 2,414 (178)
New England Journal of Medicine, 1970 Abstract The conversion of vitamin D3 to 25-hydroxycholecalciferol (25-HCC) is quantitatively decreased in some patients with familial hypophosphatemia and vitamin-D-resistant rickets.
H S, Earp +4 more
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Familial Hypophosphatemia (Familial Hypophosphatemic Rickets)
, 1979 W.G. BEAMER, E.M. EICHER, L.D. COWGILL
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Intestinal Defect in Familial Hypophosphatemia
New England Journal of Medicine, 1976 openaire +2 more sources
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Familial Hypophosphatemia: Report of Two Cases
The Journal of Clinical Endocrinology & Metabolism, 1966Two cases of hypophosphatemic vitamin D refractory rickets occurring in Negro children are reported. They presented with vitamin D refractory rickets, had hypophosphatemia, exhibited a familial pattern of inheritance, and responded to large doses of vitamin D. As in most reported cases, the male was more seriously affected.
M J, Fratkin, A R, Sharpe
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Ankylosing Spondylosis in Familial Hypophosphatemia.
Annals of Internal Medicine, 1970Excerpt A large group of adults, including several family groups, with vitamin-D-resistant hypophosphatemic rickets have been studied.
Rahel K. Steinhauser +3 more
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Low Breast Milk Phosphorus Concentration in Familial Hypophosphatemia
Journal of Pediatric Gastroenterology and Nutrition, 1989SummaryWe report breast milk mineral concentrations in a mother with familial hypophosphatemia that was untreated due to poor compliance with medical advice. Milk phosphorus content was extremely low despite normal maternal serum phosphorus concentrations.
A J, Jonas, B, Dominguez
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Wiener klinische Wochenschrift, 1990
The main features of X-linked dominant renal hypophosphatemic rickets are illustrated in this study of two patients who presented with rickets, deformities of the lower limbs, and small stature. Hypophosphatemia secondary to a reduction in renal tubular reabsorption of phosphate and a defect of vitamin D hydroxylation are the hallmarks of the disease ...
E, Ring, G, Zobel, M, Riccabona
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The main features of X-linked dominant renal hypophosphatemic rickets are illustrated in this study of two patients who presented with rickets, deformities of the lower limbs, and small stature. Hypophosphatemia secondary to a reduction in renal tubular reabsorption of phosphate and a defect of vitamin D hydroxylation are the hallmarks of the disease ...
E, Ring, G, Zobel, M, Riccabona
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Metabolism of tritiated vitamin D3 in familial vitamin D-resistant rickets with hypophosphatemia
The Journal of Pediatrics, 1967The metabolism of tritiated vitamin D 3 in two control subjects and two with familial vitamin D-resistant rickets was studied. Sixteen hours after a 0.25 mg. intravenous dose of H 3 vitamin D 3 was given, blood samples were taken, extracted, and chromatographed.
H F, DeLuca +3 more
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The Journal of Bone & Joint Surgery, 1964
The regulation of vitamin-D dosage in resistant rickets (familial or essential hypophosphatemia) is best accomplished by measuring the twenty-four-hour urinary calcium output against the curve of normal excretion. For such comparison the subject's weight and a fairly close estimate of calcium intake are also necessary.
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The regulation of vitamin-D dosage in resistant rickets (familial or essential hypophosphatemia) is best accomplished by measuring the twenty-four-hour urinary calcium output against the curve of normal excretion. For such comparison the subject's weight and a fairly close estimate of calcium intake are also necessary.
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