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Thyroid : Official Journal of the American Thyroid Association
|
July 25, 2000
A novel V59E missense mutation in the sodium iodide symporter gene in a family with iodide transport defect
H Fujiwara, K Tatsumi, S Tanaka, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 19, 1998
Growth hormone (GH) insensitivity syndrome with high serum GH-binding protein levels caused by a heterozygous splice site mutation of the GH receptor gene producing a lack of intracellular domain
K Iida, Y Takahashi, H Kaji, et al.
Pediatric Neurology
|
January 1, 1988
Does CSF copper level in Wilson disease reflect copper accumulation in the brain?
H Kodama, I Okabe, M Yanagisawa, et al.
Acta Paediatrica Japonica : Overseas Edition
|
December 1, 1989
Prevention of neonatal HBV infection with the combination of HBIG and HBV vaccine and its long-term efficacy in infants born to HBeAg positive HBV carrier mothers
H Tajiri, O Nose, K Shimizu, et al.
The Japanese Journal of Surgery
|
May 1, 1990
Metabolic changes following gastroplasty in Prader-Willi syndrome--a case report
M Miyata, T Dousei, T Harada, et al.
The New England Journal of Medicine
|
July 24, 1980
Increased frequency of HLA-Aw24 in congenital hypothyroidism in Japan
K Miyai, H Mizuta, O Nose, et al.
European Journal of Pediatrics
|
August 17, 1978
Hypothalamic-pituitary functions in patients with idiopathic pituitary dwarfism. Further evidence for hypophysiotropic human deficiencies
O Nose, Y Iida, H Kai, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
August 31, 1983
Study of ammonia metabolism in a patient with ornithine transcarbamylase deficiency using an 15N tracer
H Kodama, K Samukawa, S Okada, et al.
Clinical Chemistry
|
March 1, 1982
Radioimmunoassay of "free thyroxin" in dried blood spots on filter paper - preliminary observations on the effective differentiation of subjects with congenital hypothyroidism from those with subnormal thyroxin-binding globulin and normal subjects
H Mizuta, K Miyai, K Ichihara, et al.
Medical Journal of Osaka University
|
March 1, 1982
Electroencephalographic studies on patients with GH deficiency
S Onoe, J Abe, Y Futagi, et al.
Page
of 7
Search research articles
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Showing results (21-30 of 63) with videos related to
Sort By:
Page
of 7
Thyroid : Official Journal of the American Thyroid Association
|
July 25, 2000
A novel V59E missense mutation in the sodium iodide symporter gene in a family with iodide transport defect
H Fujiwara, K Tatsumi, S Tanaka, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 19, 1998
Growth hormone (GH) insensitivity syndrome with high serum GH-binding protein levels caused by a heterozygous splice site mutation of the GH receptor gene producing a lack of intracellular domain
K Iida, Y Takahashi, H Kaji, et al.
Pediatric Neurology
|
January 1, 1988
Does CSF copper level in Wilson disease reflect copper accumulation in the brain?
H Kodama, I Okabe, M Yanagisawa, et al.
Acta Paediatrica Japonica : Overseas Edition
|
December 1, 1989
Prevention of neonatal HBV infection with the combination of HBIG and HBV vaccine and its long-term efficacy in infants born to HBeAg positive HBV carrier mothers
H Tajiri, O Nose, K Shimizu, et al.
The Japanese Journal of Surgery
|
May 1, 1990
Metabolic changes following gastroplasty in Prader-Willi syndrome--a case report
M Miyata, T Dousei, T Harada, et al.
The New England Journal of Medicine
|
July 24, 1980
Increased frequency of HLA-Aw24 in congenital hypothyroidism in Japan
K Miyai, H Mizuta, O Nose, et al.
European Journal of Pediatrics
|
August 17, 1978
Hypothalamic-pituitary functions in patients with idiopathic pituitary dwarfism. Further evidence for hypophysiotropic human deficiencies
O Nose, Y Iida, H Kai, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
August 31, 1983
Study of ammonia metabolism in a patient with ornithine transcarbamylase deficiency using an 15N tracer
H Kodama, K Samukawa, S Okada, et al.
Clinical Chemistry
|
March 1, 1982
Radioimmunoassay of "free thyroxin" in dried blood spots on filter paper - preliminary observations on the effective differentiation of subjects with congenital hypothyroidism from those with subnormal thyroxin-binding globulin and normal subjects
H Mizuta, K Miyai, K Ichihara, et al.
Medical Journal of Osaka University
|
March 1, 1982
Electroencephalographic studies on patients with GH deficiency
S Onoe, J Abe, Y Futagi, et al.
Page
of 7