Takusa Y[Author] - Search Results

Year	Number of Results
1995	1
1996	1
1998	2
1999	1
2001	7
2002	7
2003	1
2006	1
2024	0

1

Takusa Y, Yamaguchi S. Takusa Y, et al. Nihon Rinsho. 2002 Apr;60 Suppl 4:743-6. Nihon Rinsho. 2002. PMID: 12013989 Review. Japanese. No abstract available.

2

[Very-long-chain acyl-CoA dehydrogenase deficiency].

Uchiyama A, Takusa Y, Yamaguchi S. Uchiyama A, et al. Among authors: takusa y. Ryoikibetsu Shokogun Shirizu. 2001;(36):65-7. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11596452 Review. Japanese. No abstract available.

3

[Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency].

Takusa Y, Yamaguchi S. Takusa Y, et al. Nihon Rinsho. 2002 Apr;60 Suppl 4:722-5. Nihon Rinsho. 2002. PMID: 12013983 Review. Japanese. No abstract available.

4

[Short-chain 3-hydroxyacyl-CoA dehydrogenase (SCHAD) deficiency].

Takusa Y, Yamaguchi S. Takusa Y, et al. Ryoikibetsu Shokogun Shirizu. 1998;(18 Pt 1):420-1. Ryoikibetsu Shokogun Shirizu. 1998. PMID: 9590089 Review. Japanese. No abstract available.

5

[Mitochondrial trifunctional protein (TP) deficiency].

Takusa Y, Yamaguchi S. Takusa Y, et al. Ryoikibetsu Shokogun Shirizu. 1998;(18 Pt 1):422-5. Ryoikibetsu Shokogun Shirizu. 1998. PMID: 9590090 Review. Japanese. No abstract available.

6

[Short-chain 3-hydroxyacyl-CoA dehydrogenase (SCHAD) deficiency].

Takusa Y, Yamaguchi S. Takusa Y, et al. Ryoikibetsu Shokogun Shirizu. 2001;(36):74-6. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11596455 Review. Japanese. No abstract available.

7

Distal myopathy with rimmed vacuoles is allelic to hereditary inclusion body myopathy.

Nishino I, Noguchi S, Murayama K, Driss A, Sugie K, Oya Y, Nagata T, Chida K, Takahashi T, Takusa Y, Ohi T, Nishimiya J, Sunohara N, Ciafaloni E, Kawai M, Aoki M, Nonaka I. Nishino I, et al. Among authors: takusa y. Neurology. 2002 Dec 10;59(11):1689-93. doi: 10.1212/01.wnl.0000041631.28557.c6. Neurology. 2002. PMID: 12473753

8

Mutation of the doublecortin gene in male patients with double cortex syndrome: somatic mosaicism detected by hair root analysis.

Kato M, Kanai M, Soma O, Takusa Y, Kimura T, Numakura C, Matsuki T, Nakamura S, Hayasaka K. Kato M, et al. Among authors: takusa y. Ann Neurol. 2001 Oct;50(4):547-51. doi: 10.1002/ana.1231. Ann Neurol. 2001. PMID: 11601509

9

[Myopathies with miscellaneous disorders related to mitochondrial fatty acid oxidation: defective synthesis of ketone body, long-chain fatty acid transport defect, and muscular coenzyme Q10 deficiency].

Takusa Y, Yamaguchi S. Takusa Y, et al. Ryoikibetsu Shokogun Shirizu. 2001;(36):90-4. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11596461 Review. Japanese. No abstract available.

10

Molecular study of electron transfer flavoprotein alpha-subunit deficiency in two Japanese children with different phenotypes of glutaric acidemia type II.

Purevjav E, Kimura M, Takusa Y, Ohura T, Tsuchiya M, Hara N, Fukao T, Yamaguchi S. Purevjav E, et al. Among authors: takusa y. Eur J Clin Invest. 2002 Sep;32(9):707-12. doi: 10.1046/j.1365-2362.2002.01045.x. Eur J Clin Invest. 2002. PMID: 12486872

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