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Human Molecular Genetics
|
November 1, 1993
Cosegregation of missense mutations of the luteinizing hormone receptor gene with familial male-limited precocious puberty
H Kremer, E Mariman, B J Otten, et al.
European Journal of Endocrinology
|
September 15, 2004
Mutations in the NSD1 gene in patients with Sotos syndrome associate with endocrine and paracrine alterations in the IGF system
L De Boer, H A Van Duyvenvoorde, E C Willemstein-Van Hove, et al.
Early Human Development
|
December 4, 2003
Is hypotension a major risk factor for neurological morbidity at term age in very preterm infants?
S E Martens, M Rijken, G M S J Stoelhorst, et al.
Clinical Endocrinology
|
June 1, 1988
Heterozygotes for 17 alpha-hydroxylase deficiency can be detected with a short ACTH test
J M Wit, H P van Roermund, W Oostdijk, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition
|
May 3, 2008
Antenatal glucocorticoid treatment is not associated with long-term metabolic risks in individuals born before 32 weeks of gestation
M J J Finken, M G Keijzer-Veen, F W Dekker, et al.
Pediatric Research
|
March 10, 2000
Continuing positive secular growth change in The Netherlands 1955-1997
A M Fredriks, S van Buuren, R J Burgmeijer, et al.
Endocrinology
|
September 1, 1979
Serum somatomedin activity and cartilage metabolism in acutely fasted, chronically malnourished, and refed rats
D A Price, J M Wit, S van Buul-Offers, et al.
Archives of Disease in Childhood
|
October 1, 1988
Methionyl human growth hormone in Turner's syndrome
C Rongen-Westerlaken, J M Wit, S L Drop, et al.
Osteoarthritis and Cartilage
|
September 14, 2011
Inhibition of Gsk3β in cartilage induces osteoarthritic features through activation of the canonical Wnt signaling pathway
R L Miclea, M Siebelt, L Finos, et al.
Clinical Endocrinology
|
September 22, 2015
Mild deficits in attentional control in patients with the IGSF1 deficiency syndrome
S D Joustra, C D Andela, W Oostdijk, et al.
Page
of 26
Search research articles
Search
Showing results (211-220 of 259) with videos related to
Sort By:
Page
of 26
Human Molecular Genetics
|
November 1, 1993
Cosegregation of missense mutations of the luteinizing hormone receptor gene with familial male-limited precocious puberty
H Kremer, E Mariman, B J Otten, et al.
European Journal of Endocrinology
|
September 15, 2004
Mutations in the NSD1 gene in patients with Sotos syndrome associate with endocrine and paracrine alterations in the IGF system
L De Boer, H A Van Duyvenvoorde, E C Willemstein-Van Hove, et al.
Early Human Development
|
December 4, 2003
Is hypotension a major risk factor for neurological morbidity at term age in very preterm infants?
S E Martens, M Rijken, G M S J Stoelhorst, et al.
Clinical Endocrinology
|
June 1, 1988
Heterozygotes for 17 alpha-hydroxylase deficiency can be detected with a short ACTH test
J M Wit, H P van Roermund, W Oostdijk, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition
|
May 3, 2008
Antenatal glucocorticoid treatment is not associated with long-term metabolic risks in individuals born before 32 weeks of gestation
M J J Finken, M G Keijzer-Veen, F W Dekker, et al.
Pediatric Research
|
March 10, 2000
Continuing positive secular growth change in The Netherlands 1955-1997
A M Fredriks, S van Buuren, R J Burgmeijer, et al.
Endocrinology
|
September 1, 1979
Serum somatomedin activity and cartilage metabolism in acutely fasted, chronically malnourished, and refed rats
D A Price, J M Wit, S van Buul-Offers, et al.
Archives of Disease in Childhood
|
October 1, 1988
Methionyl human growth hormone in Turner's syndrome
C Rongen-Westerlaken, J M Wit, S L Drop, et al.
Osteoarthritis and Cartilage
|
September 14, 2011
Inhibition of Gsk3β in cartilage induces osteoarthritic features through activation of the canonical Wnt signaling pathway
R L Miclea, M Siebelt, L Finos, et al.
Clinical Endocrinology
|
September 22, 2015
Mild deficits in attentional control in patients with the IGSF1 deficiency syndrome
S D Joustra, C D Andela, W Oostdijk, et al.
Page
of 26