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Lancet (London, England)
|
September 29, 1990
Iodine-induced hypothyroidism in infants treated with continuous cyclic peritoneal dialysis
T Vulsma, D Menzel, F C Abbad, et al.
Acta Endocrinologica
|
August 1, 1993
Thyroxine administration to infants of less than 30 weeks' gestational age does not increase plasma triiodothyronine concentrations
A G van Wassenaer, J H Kok, E Endert, et al.
The Journal of Pediatrics
|
October 13, 1999
Acquired protein S deficiency caused by estrogen treatment of tall stature
C H van Ommen, K Fijnvandraat, T Vulsma, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
April 20, 2000
Neurologic development of the newborn and young child in relation to maternal thyroid function
B J Smit, J H Kok, T Vulsma, et al.
The Journal of Clinical Endocrinology and Metabolism
|
May 8, 2008
Quality of life, developmental milestones, and self-esteem of young adults with congenital hypothyroidism diagnosed by neonatal screening
L van der Sluijs Veer, M J E Kempers, B F Last, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 4, 2000
Two decades of screening for congenital hypothyroidism in The Netherlands: TPO gene mutations in total iodide organification defects (an update)
B Bakker, H Bikker, T Vulsma, et al.
The Journal of Pediatrics
|
June 1, 1994
Motor and cognitive development in children with congenital hypothyroidism: a long-term evaluation of the effects of neonatal treatment
L Kooistra, C Laane, T Vulsma, et al.
The Journal of Clinical Endocrinology and Metabolism
|
July 1, 1994
A 20-basepair duplication in the human thyroid peroxidase gene results in a total iodide organification defect and congenital hypothyroidism
H Bikker, M T den Hartog, F Baas, et al.
Diabetologia
|
November 27, 2010
Successful transfer to sulfonylurea therapy in an infant with developmental delay, epilepsy and neonatal diabetes (DEND) syndrome and a novel ABCC8 gene mutation
N Zwaveling-Soonawala, E E Hagebeuk, A S Slingerland, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
October 23, 1993
[Evaluation of a decade of neonatal screening for congenital hypothyroidism in The Netherlands]
P H Verkerk, G Derksen-Lubsen, T Vulsma, et al.
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Search research articles
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Showing results (21-30 of 62) with videos related to
Sort By:
Page
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Lancet (London, England)
|
September 29, 1990
Iodine-induced hypothyroidism in infants treated with continuous cyclic peritoneal dialysis
T Vulsma, D Menzel, F C Abbad, et al.
Acta Endocrinologica
|
August 1, 1993
Thyroxine administration to infants of less than 30 weeks' gestational age does not increase plasma triiodothyronine concentrations
A G van Wassenaer, J H Kok, E Endert, et al.
The Journal of Pediatrics
|
October 13, 1999
Acquired protein S deficiency caused by estrogen treatment of tall stature
C H van Ommen, K Fijnvandraat, T Vulsma, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
April 20, 2000
Neurologic development of the newborn and young child in relation to maternal thyroid function
B J Smit, J H Kok, T Vulsma, et al.
The Journal of Clinical Endocrinology and Metabolism
|
May 8, 2008
Quality of life, developmental milestones, and self-esteem of young adults with congenital hypothyroidism diagnosed by neonatal screening
L van der Sluijs Veer, M J E Kempers, B F Last, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 4, 2000
Two decades of screening for congenital hypothyroidism in The Netherlands: TPO gene mutations in total iodide organification defects (an update)
B Bakker, H Bikker, T Vulsma, et al.
The Journal of Pediatrics
|
June 1, 1994
Motor and cognitive development in children with congenital hypothyroidism: a long-term evaluation of the effects of neonatal treatment
L Kooistra, C Laane, T Vulsma, et al.
The Journal of Clinical Endocrinology and Metabolism
|
July 1, 1994
A 20-basepair duplication in the human thyroid peroxidase gene results in a total iodide organification defect and congenital hypothyroidism
H Bikker, M T den Hartog, F Baas, et al.
Diabetologia
|
November 27, 2010
Successful transfer to sulfonylurea therapy in an infant with developmental delay, epilepsy and neonatal diabetes (DEND) syndrome and a novel ABCC8 gene mutation
N Zwaveling-Soonawala, E E Hagebeuk, A S Slingerland, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
October 23, 1993
[Evaluation of a decade of neonatal screening for congenital hypothyroidism in The Netherlands]
P H Verkerk, G Derksen-Lubsen, T Vulsma, et al.
Page
of 7