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Pediatrics
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June 1, 1988
Worldwide experience in newborn screening for classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency
S Y Pang, M A Wallace, L Hofman, et al.
Pediatric Research
|
September 27, 2000
Three novel PHEX gene mutations in Japanese patients with X-linked hypophosphatemic rickets
K Sato, T Tajima, J Nakae, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD
|
January 1, 2018
Long-term clinical impact of serum albumin in coronary artery disease patients with preserved renal function
H Wada, T Dohi, K Miyauchi, et al.
Frontiers in Rehabilitation Sciences
|
December 26, 2022
Hopes and fears regarding care robots: Content analysis of newspapers in East Asia and Western Europe, 2001-2020
N Kodate, Y Maeda, B Hauray, et al.
Page
of 6
Search research articles
Search
Showing results (51-60 of 54) with videos related to
Sort By:
Page
of 6
You have reached the last page of results.
This site can display upto 54 results.
Pediatrics
|
June 1, 1988
Worldwide experience in newborn screening for classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency
S Y Pang, M A Wallace, L Hofman, et al.
Pediatric Research
|
September 27, 2000
Three novel PHEX gene mutations in Japanese patients with X-linked hypophosphatemic rickets
K Sato, T Tajima, J Nakae, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD
|
January 1, 2018
Long-term clinical impact of serum albumin in coronary artery disease patients with preserved renal function
H Wada, T Dohi, K Miyauchi, et al.
Frontiers in Rehabilitation Sciences
|
December 26, 2022
Hopes and fears regarding care robots: Content analysis of newspapers in East Asia and Western Europe, 2001-2020
N Kodate, Y Maeda, B Hauray, et al.
Page
of 6