Search research articles
Contact Us
Filters
Showing results (41-50 of 54) with videos related to
Page
of 6
Sort By:
Journal of Cutaneous Pathology
|
October 23, 1997
CD56-positive (nasal-type T/NK cell) lymphoma arising on the skin. Report of two cases and review of the literature
S Ansai, K Maeda, M Yamakawa, et al.
The Journal of Clinical Endocrinology and Metabolism
|
January 3, 2001
A novel missense mutation of mineralocorticoid receptor gene in one Japanese family with a renal form of pseudohypoaldosteronism type 1
T Tajima, H Kitagawa, S Yokoya, et al.
Acta Endocrinologica
|
February 1, 1990
Isolated human growth hormone deficiency due to the hGH-I gene deletion with (type IA) and without (the Israeli-type) hGH antibody formation during hGH therapy
Y Nishi, H Masuda, S Nishimura, et al.
Endocrinologia Japonica
|
April 1, 1987
Treatment of pituitary dwarfism with authentic recombinant human growth hormone (SM-9500)
K Takano, K Shizume, I Hibi, et al.
Acta Paediatrica Scandinavica. Supplement
|
January 1, 1988
Treatment of hypopituitarism with recombinant somatropin for 1 year
K Takano, K Shizume, I Hibi, et al.
Gan No Rinsho. Japan Journal of Cancer Clinics
|
June 1, 1986
[Clinical investigation of indications in proton therapy]
T Kitagawa, T Inada, T Arimoto, et al.
Nihon Naibunpi Gakkai Zasshi
|
December 20, 1994
[Serum levels of intact molecular osteocalcin in children with growth hormone (GH) deficiency during GH therapy: an early predictor of GH therapy]
Y Seino, S Kanzaki, T Kubo, et al.
European Journal of Pediatrics
|
August 1, 1984
Follow-up study of a nation-wide neonatal metabolic screening program in Japan. A collaborative study group of neonatal screening for inborn errors of metabolism in Japan
K Tada, H Tateda, S Arashima, et al.
Acta Paediatrica Scandinavica. Supplement
|
January 1, 1987
Clinical trial with authentic recombinant somatropin in Japan
K Takano, K Shizume, I Hibi, et al.
European Journal of Pediatrics
|
February 14, 1998
Clinical characteristics of children with hypoparathyroidism due to 22q11.2 microdeletion
M Adachi, K Tachibana, M Masuno, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 54) with videos related to
Sort By:
Page
of 6
Journal of Cutaneous Pathology
|
October 23, 1997
CD56-positive (nasal-type T/NK cell) lymphoma arising on the skin. Report of two cases and review of the literature
S Ansai, K Maeda, M Yamakawa, et al.
The Journal of Clinical Endocrinology and Metabolism
|
January 3, 2001
A novel missense mutation of mineralocorticoid receptor gene in one Japanese family with a renal form of pseudohypoaldosteronism type 1
T Tajima, H Kitagawa, S Yokoya, et al.
Acta Endocrinologica
|
February 1, 1990
Isolated human growth hormone deficiency due to the hGH-I gene deletion with (type IA) and without (the Israeli-type) hGH antibody formation during hGH therapy
Y Nishi, H Masuda, S Nishimura, et al.
Endocrinologia Japonica
|
April 1, 1987
Treatment of pituitary dwarfism with authentic recombinant human growth hormone (SM-9500)
K Takano, K Shizume, I Hibi, et al.
Acta Paediatrica Scandinavica. Supplement
|
January 1, 1988
Treatment of hypopituitarism with recombinant somatropin for 1 year
K Takano, K Shizume, I Hibi, et al.
Gan No Rinsho. Japan Journal of Cancer Clinics
|
June 1, 1986
[Clinical investigation of indications in proton therapy]
T Kitagawa, T Inada, T Arimoto, et al.
Nihon Naibunpi Gakkai Zasshi
|
December 20, 1994
[Serum levels of intact molecular osteocalcin in children with growth hormone (GH) deficiency during GH therapy: an early predictor of GH therapy]
Y Seino, S Kanzaki, T Kubo, et al.
European Journal of Pediatrics
|
August 1, 1984
Follow-up study of a nation-wide neonatal metabolic screening program in Japan. A collaborative study group of neonatal screening for inborn errors of metabolism in Japan
K Tada, H Tateda, S Arashima, et al.
Acta Paediatrica Scandinavica. Supplement
|
January 1, 1987
Clinical trial with authentic recombinant somatropin in Japan
K Takano, K Shizume, I Hibi, et al.
European Journal of Pediatrics
|
February 14, 1998
Clinical characteristics of children with hypoparathyroidism due to 22q11.2 microdeletion
M Adachi, K Tachibana, M Masuno, et al.
Page
of 6