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European Journal of Pediatrics
|
October 1, 1983
Circulating immune complex in the mucocutaneous lymph node syndrome
A Furuse, I Matsuda
Archives of Disease in Childhood
|
November 1, 1988
Incidence of zinc and copper deficiency in Japan
I Matsuda, A Higashi
Rinsho Byori. the Japanese Journal of Clinical Pathology
|
August 1, 1971
[Tests of acid-base controlling function of the kidney]
N Shida, I Matsuda
Biology of the Neonate
|
January 1, 1973
Microsomal desaturation of linoleic into -linolenic acid in livers of fetal, suckling and pregnant rats
S Satomi, I Matsuda
Ryoikibetsu Shokogun Shirizu
|
May 20, 1998
[Ornithine transcarbamylase deficiency (OTCD)]
T Matsuura, I Matsuda
Ryoikibetsu Shokogun Shirizu
|
May 20, 1998
[Maple syrup urine disease]
Y Indo, I Matsuda
Human Genetics
|
January 1, 1981
Screening method for prolidase deficiency
F Endo, I Matsuda
Nihon Rinsho. Japanese Journal of Clinical Medicine
|
December 1, 1992
[Recent progress in molecular biology of inherited tubular transport abnormalities]
Y Indo, I Matsuda
Pediatric Neurology
|
March 1, 1986
Carnitine status in Reye and Reye-like syndromes
I Matsuda, Y Ohtani
Acta Paediatrica Japonica : Overseas Edition
|
April 1, 1996
Gene therapy for ornithine transcarbamylase deficiency
K Kiwaki, I Matsuda
Page
of 61
Search research articles
Search
Showing results (31-40 of 603) with videos related to
Sort By:
Page
of 61
European Journal of Pediatrics
|
October 1, 1983
Circulating immune complex in the mucocutaneous lymph node syndrome
A Furuse, I Matsuda
Archives of Disease in Childhood
|
November 1, 1988
Incidence of zinc and copper deficiency in Japan
I Matsuda, A Higashi
Rinsho Byori. the Japanese Journal of Clinical Pathology
|
August 1, 1971
[Tests of acid-base controlling function of the kidney]
N Shida, I Matsuda
Biology of the Neonate
|
January 1, 1973
Microsomal desaturation of linoleic into -linolenic acid in livers of fetal, suckling and pregnant rats
S Satomi, I Matsuda
Ryoikibetsu Shokogun Shirizu
|
May 20, 1998
[Ornithine transcarbamylase deficiency (OTCD)]
T Matsuura, I Matsuda
Ryoikibetsu Shokogun Shirizu
|
May 20, 1998
[Maple syrup urine disease]
Y Indo, I Matsuda
Human Genetics
|
January 1, 1981
Screening method for prolidase deficiency
F Endo, I Matsuda
Nihon Rinsho. Japanese Journal of Clinical Medicine
|
December 1, 1992
[Recent progress in molecular biology of inherited tubular transport abnormalities]
Y Indo, I Matsuda
Pediatric Neurology
|
March 1, 1986
Carnitine status in Reye and Reye-like syndromes
I Matsuda, Y Ohtani
Acta Paediatrica Japonica : Overseas Edition
|
April 1, 1996
Gene therapy for ornithine transcarbamylase deficiency
K Kiwaki, I Matsuda
Page
of 61