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K. Tada

Prevalence of K329E mutation in medium-chain acyl-CoA dehydrogenase gene determined from Guthrie cards
1991 · Y. Matsubara, K. Narisawa, et al. · The Lancet · 112
Identification of a common mutation in Finnish patients with nonketotic hyperglycinemia.
1992 · S Kure, M Takayanagi, et al. · Journal of Clinical Investigation · 91
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Non‐ketotic hyperglycinaemia: Molecular lesion, diagnosis and pathophysiology
1993 · K. Tada, S. Kure · Journal of Inherited Metabolic Disease · 88
Non-ketotic hyperglycinaemia: clinical and biochemical aspects
1987 · K. Tada, K. Hayasaka · European Journal of Pediatrics · 78
Biochemical study in 28 children with lactic acidosis, in relation to Leigh's encephalomyelopathy
1985 · S. Miyabayashi, T. Ito, et al. · European Journal of Pediatrics · 77
Defective gene in lactic acidosis: abnormal pyruvate dehydrogenase E1 alpha-subunit caused by a frame shift.
1989 · H Endo, K Hasegawa, et al. · Europe PMC (PubMed Central) · 68
Retrospective survey of urea cycle disorders: Part 1. Clinical and laboratory observations of thirty‐two Japanese male patients with ornithine transcarbamylase deficiency
1991 · I. Matsuda, N. Nagata, et al. · American Journal of Medical Genetics · 54
Gyrate atrophy with hyperornithinaemia: different types of responsiveness to vitamin B6.
1981 · S Hayasaka, T Saito, et al. · British Journal of Ophthalmology · 52
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Two siblings with cytochromec oxidase deficiency
1983 · S. Miyabayashi, K. Narisawa, et al. · Journal of Inherited Metabolic Disease · 51
Nonketotic Hyperglycinemia: Clinical and Metabolic Aspects
2017 · K. Tada · Enzyme · 49
Follow-up study of a nation-wide neonatal metabolic screening program in Japan
1984 · K. Tada, H. Tateda, et al. · European Journal of Pediatrics · 49
Retrospective survey of urea cycle disorders: Part 2. Neurological outcome in forty‐nine Japanese patients with urea cycle enzymopathies
1991 · N. Nagata, I. Matsuda, et al. · American Journal of Medical Genetics · 47
Ultrastructural study of the childhood mitochondrial myopathic syndrome associated with lactic acidosis
1982 · Y. Kobayashi, S. Miyabayashi, et al. · European Journal of Pediatrics · 43
Pilot study of screening for Wilson disease using dried blood spots obtained from children seen at outpatient clinics
1999 · T. Ohura, D. Abukawa, et al. · Journal of Inherited Metabolic Disease · 41
Clinical trials of vitamin B6 and proline supplementation for gyrate atrophy of the choroid and retina.
1985 · S. Hayasaka, T. Saito, et al. · British Journal of Ophthalmology · 41
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Human glycine decarboxylase gene ( GLDC) and its highly conserved processed pseudogene ( ψ GLDC) : their structure and expression, and the identification of a large deletion in a family with nonketotic hyperglycinemia
2000 · M. Takayanagi, S. Kure, et al. · Human Genetics · 39
Chronic pancreatitis in a child with glycogen storage disease type 1
1991 · M. Kikuchi, K. Hasegawa, et al. · European Journal of Pediatrics · 38
Medium-chain acyl-CoA dehydrogenase deficiency: Molecular aspects
1992 · Y. Matsubara, K. Narisawa, et al. · European Journal of Pediatrics · 35
Indicanuria in phenylketonuria.
1960 · S P BESSMAN, K TADA · PubMed · 35
Hyperamino-acidaemia and hyperammonaemia in epileptic children treated with valproic acid
1988 · K. Iinuma, K. Hayasaka, et al. · European Journal of Pediatrics · 31
Immunochemical study in three patients with cytochromec oxidase deficiency presenting leigh's encephalomyelopathy
1987 · S. Miyabayashi, T. Ito, et al. · Journal of Inherited Metabolic Disease · 30
Clinical and biochemical findings on a child with multiple biotin‐responsive carboxylase deficiencies
1982 · K. Narisawa, N. Arai, et al. · Journal of Inherited Metabolic Disease · 30
A new variant of glycogen storage disease type 1: Probably due to a defect in the glucose‐6‐phosphate transport system
1979 · Y. Igarashi, H. Otomo, et al. · Journal of Inherited Metabolic Disease · 30
Direct evidence for the absence of active Na+ reabsorption in hamster ascending thin limb of Henle's loop.
1993 · Y Kondo, K Abe, et al. · Journal of Clinical Investigation · 26
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Successful transplantation of soy bean agglutinin-fractionated, histoincompatible, maternal marrow in a patient with severe combined immunodeficiency and BCG infection
1985 · M. Minegishi, S. Tsuchiya, et al. · European Journal of Pediatrics · 25
Works count: 125
Citation count: 1,947
H-index: 25
I10-index: 55
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