Search research articles
Contact Us
Filters
Showing results (41-50 of 84) with videos related to
Page
of 9
Sort By:
Acta Paediatrica (Oslo, Norway : 1992)
|
November 8, 2001
Pancreatic beta-cell stimulation tests in transient and persistent congenital hyperinsulinism
H B Christesen, N Feilberg-Jørgensen, B B Jacobsen
Acta Paediatrica Scandinavica
|
July 1, 1983
Primary hyperparathyroidism in infancy associated with familial hypocalciuric hypercalcemia
K Lillquist, N Illum, B B Jacobsen, et al.
European Journal of Pediatrics
|
October 1, 1992
Mediastinal germ cell tumour associated with Klinefelter syndrome. A report of case and review of the literature
H Hasle, B B Jacobsen, P Asschenfeldt, et al.
Acta Paediatrica Scandinavica
|
January 1, 1979
Serum concentrations of thyroxine-binding globulin, prealbumin and albumin in healthy fullterm, small-for-gestational age and preterm newborn infants
B B Jacobsen, B Peitersen, H J Andersen, et al.
Acta Paediatrica Scandinavica
|
September 1, 1977
Pituitary-thyroid responsiveness to thyrotropin-releasing hormone in preterm and small-for-gestational age newborns
B B Jacobsen, H Andersen, H Dige-Petersen, et al.
Acta Paediatrica Scandinavica
|
November 1, 1982
X-linked congenital adrenal hypoplasia. A study of five generations of a Greenlandic Family
K E Petersen, T Bille, B B Jacobsen, et al.
Archives of Disease in Childhood
|
April 1, 1978
Neonatal hypocalcaemia associated with maternal hyperparathyroidism. New pathogenetic observations
B B Jacobsen, E Terslev, B Lund, et al.
Acta Paediatrica Scandinavica
|
July 1, 1976
Thyrotropin response to thyrotropin-releasing hormone in fullterm, euthyroid and hypothyroid newborns
B B Jacobsen, H Andersen, H Dige-Petersen, et al.
Acta Paediatrica Scandinavica
|
November 1, 1986
Fatal familial cholestatic syndrome in Greenland Eskimo children
I M Nielsen, K Ornvold, B B Jacobsen, et al.
Genes, Chromosomes & Cancer
|
August 1, 1993
Clonal karyotypic evolution in an embryonal rhabdomyosarcoma with trisomy 8 as the primary chromosomal abnormality
C U Dietrich, B B Jacobsen, H Starklint, et al.
Page
of 9
Search research articles
Search
Showing results (41-50 of 84) with videos related to
Sort By:
Page
of 9
Acta Paediatrica (Oslo, Norway : 1992)
|
November 8, 2001
Pancreatic beta-cell stimulation tests in transient and persistent congenital hyperinsulinism
H B Christesen, N Feilberg-Jørgensen, B B Jacobsen
Acta Paediatrica Scandinavica
|
July 1, 1983
Primary hyperparathyroidism in infancy associated with familial hypocalciuric hypercalcemia
K Lillquist, N Illum, B B Jacobsen, et al.
European Journal of Pediatrics
|
October 1, 1992
Mediastinal germ cell tumour associated with Klinefelter syndrome. A report of case and review of the literature
H Hasle, B B Jacobsen, P Asschenfeldt, et al.
Acta Paediatrica Scandinavica
|
January 1, 1979
Serum concentrations of thyroxine-binding globulin, prealbumin and albumin in healthy fullterm, small-for-gestational age and preterm newborn infants
B B Jacobsen, B Peitersen, H J Andersen, et al.
Acta Paediatrica Scandinavica
|
September 1, 1977
Pituitary-thyroid responsiveness to thyrotropin-releasing hormone in preterm and small-for-gestational age newborns
B B Jacobsen, H Andersen, H Dige-Petersen, et al.
Acta Paediatrica Scandinavica
|
November 1, 1982
X-linked congenital adrenal hypoplasia. A study of five generations of a Greenlandic Family
K E Petersen, T Bille, B B Jacobsen, et al.
Archives of Disease in Childhood
|
April 1, 1978
Neonatal hypocalcaemia associated with maternal hyperparathyroidism. New pathogenetic observations
B B Jacobsen, E Terslev, B Lund, et al.
Acta Paediatrica Scandinavica
|
July 1, 1976
Thyrotropin response to thyrotropin-releasing hormone in fullterm, euthyroid and hypothyroid newborns
B B Jacobsen, H Andersen, H Dige-Petersen, et al.
Acta Paediatrica Scandinavica
|
November 1, 1986
Fatal familial cholestatic syndrome in Greenland Eskimo children
I M Nielsen, K Ornvold, B B Jacobsen, et al.
Genes, Chromosomes & Cancer
|
August 1, 1993
Clonal karyotypic evolution in an embryonal rhabdomyosarcoma with trisomy 8 as the primary chromosomal abnormality
C U Dietrich, B B Jacobsen, H Starklint, et al.
Page
of 9