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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.
Clinical Genetics
|
January 15, 2008
Skewed X chromosome inactivation failed to explain the normal phenotype of a carrier female with MECP2 mutation resulting in Rett syndrome
S Takahashi, J Ohinata, Y Makita, et al.
Endocrine Journal
|
October 1, 1996
Spontaneous growth in growth hormone-treated short children
T Tanaka, K Takano, K Hanew, et al.
Clinical Genetics
|
April 24, 2010
Partial paternal uniparental disomy of chromosome 6 in monozygotic twins with transient neonatal diabetes mellitus and macroglossia
S Suzuki, D Fujisawa, K Hashimoto, et al.
Nihon Hinyokika Gakkai Zasshi. the Japanese Journal of Urology
|
March 1, 1990
[A study on sex chromosome mosaicism--endocrinological and immunohistochemical findings with glutathion S-transferase in the gonads]
K Nonomura, T Koyama, K Toyota, et al.
Endocrine Journal
|
June 13, 2002
Height responses in complete idiopathic growth hormone deficient children less than three years of age during growth hormone therapy. Executive Committee of the International Cooperative Growth Study in Japan
T Hirano, K Takano, T Tanaka, et al.
Endocrine Journal
|
October 28, 1998
Slipped capital femoral epiphysis, Perthes' disease and scoliosis in children with growth hormone deficiency
Y Nishi, T Tanaka, K Fujieda, et al.
Lancet (London, England)
|
January 2, 1988
TSH-receptor antibodies in mothers with Graves' disease and outcome in their offspring
N Matsuura, J Konishi, K Fujieda, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 14, 1997
Three novel mutations and a de novo deletion mutation of the DAX-1 gene in patients with X-linked adrenal hypoplasia congenita
J Nakae, S Abe, T Tajima, et al.
Endocrinologia Japonica
|
February 1, 1989
Hyperglucagonemia of insulin autoimmune syndrome induced by methimazole in a patient with Graves' disease
H Yoshikawa, K Kawai, S Inoue, et al.
Page
of 14
Search research articles
Search
Showing results (101-110 of 135) with videos related to
Sort By:
Page
of 14
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.
Clinical Genetics
|
January 15, 2008
Skewed X chromosome inactivation failed to explain the normal phenotype of a carrier female with MECP2 mutation resulting in Rett syndrome
S Takahashi, J Ohinata, Y Makita, et al.
Endocrine Journal
|
October 1, 1996
Spontaneous growth in growth hormone-treated short children
T Tanaka, K Takano, K Hanew, et al.
Clinical Genetics
|
April 24, 2010
Partial paternal uniparental disomy of chromosome 6 in monozygotic twins with transient neonatal diabetes mellitus and macroglossia
S Suzuki, D Fujisawa, K Hashimoto, et al.
Nihon Hinyokika Gakkai Zasshi. the Japanese Journal of Urology
|
March 1, 1990
[A study on sex chromosome mosaicism--endocrinological and immunohistochemical findings with glutathion S-transferase in the gonads]
K Nonomura, T Koyama, K Toyota, et al.
Endocrine Journal
|
June 13, 2002
Height responses in complete idiopathic growth hormone deficient children less than three years of age during growth hormone therapy. Executive Committee of the International Cooperative Growth Study in Japan
T Hirano, K Takano, T Tanaka, et al.
Endocrine Journal
|
October 28, 1998
Slipped capital femoral epiphysis, Perthes' disease and scoliosis in children with growth hormone deficiency
Y Nishi, T Tanaka, K Fujieda, et al.
Lancet (London, England)
|
January 2, 1988
TSH-receptor antibodies in mothers with Graves' disease and outcome in their offspring
N Matsuura, J Konishi, K Fujieda, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 14, 1997
Three novel mutations and a de novo deletion mutation of the DAX-1 gene in patients with X-linked adrenal hypoplasia congenita
J Nakae, S Abe, T Tajima, et al.
Endocrinologia Japonica
|
February 1, 1989
Hyperglucagonemia of insulin autoimmune syndrome induced by methimazole in a patient with Graves' disease
H Yoshikawa, K Kawai, S Inoue, et al.
Page
of 14