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Journal of Inherited Metabolic Disease
|
January 1, 1991
A four-nucleotide insertion at the E1 alpha gene in a patient with pyruvate dehydrogenase deficiency
H Endo, S Miyabayashi, K Tada, et al.
Journal of Orthopaedic Surgery (Hong Kong)
|
August 30, 2008
Acute plastic bowing of the forearm in adults: a report of two cases
K Tada, K Ikeda, H Tsubouchi, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1990
Genomic analysis of non-ketotic hyperglycinaemia: a partial deletion of P-protein gene
K Tada, S Kure, A Kume, et al.
Journal of Inherited Metabolic Disease
|
July 10, 1999
An 84 bp insertion found in a propionic acidaemia patient is not a disease-causing mutation but a product of cryptic mRNA
T Ohura, K Narisawa, K Tada, et al.
European Journal of Pediatrics
|
May 4, 1976
Hyperalaninemia hyperpyruvicemia and lactic acidosis due to pyruvate carboxylase deficiency of the liver; treatment with thiamine and lipoic acid
H Maesaka, K Komiya, K Misugi, et al.
Nihon Rinsho. Japanese Journal of Clinical Medicine
|
December 1, 1979
[Screening of G6PD deficiency using the blood collected on filter paper]
K Tada, Y Ogasawara, K Narisawa, et al.
Progress in Neuro-Psychopharmacology & Biological Psychiatry
|
January 1, 1984
A therapeutic trial of caerulein to a long-term heavy marihuana user with amotivational syndrome
N Watanabe, T Moroji, K Tada, et al.
Journal of Hand Surgery (Edinburgh, Scotland)
|
June 1, 1987
A new treatment of painful amputation neuroma: a preliminary report
K Tada, H Nakashima, T Yoshida, et al.
The Tohoku Journal of Experimental Medicine
|
June 1, 1974
Free amino acid levels in amniotic fluid of fetuses affected with Lowe's syndrome or Phenylketonuria
K Tada, S Higami, A Fujimoto, et al.
The Tohoku Journal of Experimental Medicine
|
August 1, 1971
Urocanic aciduria: a defect in the urocanase activity in the liver of a mentally retarded
T Yoshida, K Tada, Y Honda, et al.
Page
of 63
Search research articles
Search
Showing results (121-130 of 623) with videos related to
Sort By:
Page
of 63
Journal of Inherited Metabolic Disease
|
January 1, 1991
A four-nucleotide insertion at the E1 alpha gene in a patient with pyruvate dehydrogenase deficiency
H Endo, S Miyabayashi, K Tada, et al.
Journal of Orthopaedic Surgery (Hong Kong)
|
August 30, 2008
Acute plastic bowing of the forearm in adults: a report of two cases
K Tada, K Ikeda, H Tsubouchi, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1990
Genomic analysis of non-ketotic hyperglycinaemia: a partial deletion of P-protein gene
K Tada, S Kure, A Kume, et al.
Journal of Inherited Metabolic Disease
|
July 10, 1999
An 84 bp insertion found in a propionic acidaemia patient is not a disease-causing mutation but a product of cryptic mRNA
T Ohura, K Narisawa, K Tada, et al.
European Journal of Pediatrics
|
May 4, 1976
Hyperalaninemia hyperpyruvicemia and lactic acidosis due to pyruvate carboxylase deficiency of the liver; treatment with thiamine and lipoic acid
H Maesaka, K Komiya, K Misugi, et al.
Nihon Rinsho. Japanese Journal of Clinical Medicine
|
December 1, 1979
[Screening of G6PD deficiency using the blood collected on filter paper]
K Tada, Y Ogasawara, K Narisawa, et al.
Progress in Neuro-Psychopharmacology & Biological Psychiatry
|
January 1, 1984
A therapeutic trial of caerulein to a long-term heavy marihuana user with amotivational syndrome
N Watanabe, T Moroji, K Tada, et al.
Journal of Hand Surgery (Edinburgh, Scotland)
|
June 1, 1987
A new treatment of painful amputation neuroma: a preliminary report
K Tada, H Nakashima, T Yoshida, et al.
The Tohoku Journal of Experimental Medicine
|
June 1, 1974
Free amino acid levels in amniotic fluid of fetuses affected with Lowe's syndrome or Phenylketonuria
K Tada, S Higami, A Fujimoto, et al.
The Tohoku Journal of Experimental Medicine
|
August 1, 1971
Urocanic aciduria: a defect in the urocanase activity in the liver of a mentally retarded
T Yoshida, K Tada, Y Honda, et al.
Page
of 63