Gons MH - Search Results

1

The screening for mutations in the thyroglobulin cDNA from six patients with congenital hypothyroidism.

van de Graaf SA, Cammenga M, Ponne NJ, Veenboer GJ, Gons MH, Orgiazzi J, de Vijlder JJ, Ris-Stalpers C. van de Graaf SA, et al. Among authors: gons mh. Biochimie. 1999 May;81(5):425-32. doi: 10.1016/s0300-9084(99)80091-1. Biochimie. 1999. PMID: 10403171

2

The role of serum thyroglobulin concentration and thyroid ultrasound imaging in the detection of iodide transport defects in infants.

Vulsma T, Rammeloo JA, Gons MH, de Vijlder JJ. Vulsma T, et al. Among authors: gons mh. Acta Endocrinol (Copenh). 1991 Apr;124(4):405-10. doi: 10.1530/acta.0.1240405. Acta Endocrinol (Copenh). 1991. PMID: 2031439

3

Maternal-fetal transfer of thyroxine in congenital hypothyroidism due to a total organification defect or thyroid agenesis.

Vulsma T, Gons MH, de Vijlder JJ. Vulsma T, et al. Among authors: gons mh. N Engl J Med. 1989 Jul 6;321(1):13-6. doi: 10.1056/NEJM198907063210103. N Engl J Med. 1989. PMID: 2733742

4

Concentration of plasma thyroglobulin and urinary excretion of iodinated material in the diagnosis of thyroid disorders in congenital hypothyroidism.

Gons MH, Kok JH, Tegelaers WH, de Vijlder JJ. Gons MH, et al. Acta Endocrinol (Copenh). 1983 Sep;104(1):27-34. doi: 10.1530/acta.0.1040027. Acta Endocrinol (Copenh). 1983. PMID: 6624362

5

A 20-basepair duplication in the human thyroid peroxidase gene results in a total iodide organification defect and congenital hypothyroidism.

Bikker H, den Hartog MT, Baas F, Gons MH, Vulsma T, de Vijlder JJ. Bikker H, et al. Among authors: gons mh. J Clin Endocrinol Metab. 1994 Jul;79(1):248-52. doi: 10.1210/jcem.79.1.8027236. J Clin Endocrinol Metab. 1994. PMID: 8027236

6

[Congenital hypothyroidism. Current viewpoints and developments].

Gons MH, Vulsma T, de Vijlder JJ. Gons MH, et al. Tijdschr Kindergeneeskd. 1986 Dec;54(6):164-9. Tijdschr Kindergeneeskd. 1986. PMID: 3103255 Dutch.

7

Prenatal diagnosis of a thyroglobulin synthesis defect in goats.

Kok K, van Dijk JE, Fokkens RH, Gons MH, de Vijlder JJ. Kok K, et al. Among authors: gons mh. Acta Endocrinol (Copenh). 1985 Sep;110(1):83-9. doi: 10.1530/acta.0.1100083. Acta Endocrinol (Copenh). 1985. PMID: 4036507

8

Iodine-induced hypothyroidism in infants treated with continuous cyclic peritoneal dialysis.

Vulsma T, Menzel D, Abbad FC, Gons MH, de Vijlder JJ. Vulsma T, et al. Among authors: gons mh. Lancet. 1990 Sep 29;336(8718):812. doi: 10.1016/0140-6736(90)93276-u. Lancet. 1990. PMID: 1976170 No abstract available.

9

Serum thyroglobulin levels: the physiological decrease in infancy and the absence in athyroidism.

Ket JL, De Vijder JJ, Bikker H, Gons MH, Tegelaers WH. Ket JL, et al. Among authors: gons mh. J Clin Endocrinol Metab. 1981 Dec;53(6):1301-3. doi: 10.1210/jcem-53-6-1301. J Clin Endocrinol Metab. 1981. PMID: 7298806

10

[Screening for raised serum phenylalanine levels in women of reproductive age in Volendam].

Oorthuys JW, Gons MH, Kwakman JV, Schutgens RB, Tegelaers WH. Oorthuys JW, et al. Among authors: gons mh. Ned Tijdschr Geneeskd. 1985 Jan 12;129(2):62-5. Ned Tijdschr Geneeskd. 1985. PMID: 3969173 Dutch. No abstract available.

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