Matsuda J - Search Results

1

Matsuda J, Kuroda Y. Matsuda J, et al. Nihon Rinsho. 2002 Apr;60 Suppl 4:126-9. Nihon Rinsho. 2002. PMID: 12013833 Review. Japanese. No abstract available.

2

Ghrelin concentration in cord and neonatal blood: relation to fetal growth and energy balance.

Kitamura S, Yokota I, Hosoda H, Kotani Y, Matsuda J, Naito E, Ito M, Kangawa K, Kuroda Y. Kitamura S, et al. Among authors: matsuda j. J Clin Endocrinol Metab. 2003 Nov;88(11):5473-7. doi: 10.1210/jc.2002-021350. J Clin Endocrinol Metab. 2003. PMID: 14602792

3

Plasma adiponectin levels in newborns are higher than those in adults and positively correlated with birth weight.

Kotani Y, Yokota I, Kitamura S, Matsuda J, Naito E, Kuroda Y. Kotani Y, et al. Among authors: matsuda j. Clin Endocrinol (Oxf). 2004 Oct;61(4):418-23. doi: 10.1111/j.1365-2265.2004.02041.x. Clin Endocrinol (Oxf). 2004. PMID: 15473872

4

Thiamine-responsive pyruvate dehydrogenase deficiency in two patients caused by a point mutation (F205L and L216F) within the thiamine pyrophosphate binding region.

Naito E, Ito M, Yokota I, Saijo T, Matsuda J, Ogawa Y, Kitamura S, Takada E, Horii Y, Kuroda Y. Naito E, et al. Among authors: matsuda j. Biochim Biophys Acta. 2002 Oct 9;1588(1):79-84. doi: 10.1016/s0925-4439(02)00142-4. Biochim Biophys Acta. 2002. PMID: 12379317 Free article.

5

Genetic background markedly influences vulnerability of the hippocampal neuronal organization in the "twitcher" mouse model of globoid cell leukodystrophy.

Tominaga K, Matsuda J, Kido M, Naito E, Yokota I, Toida K, Ishimura K, Suzuki K, Kuroda Y. Tominaga K, et al. Among authors: matsuda j. J Neurosci Res. 2004 Aug 15;77(4):507-16. doi: 10.1002/jnr.20190. J Neurosci Res. 2004. PMID: 15264220

6

Mutation in saposin D domain of sphingolipid activator protein gene causes urinary system defects and cerebellar Purkinje cell degeneration with accumulation of hydroxy fatty acid-containing ceramide in mouse.

Matsuda J, Kido M, Tadano-Aritomi K, Ishizuka I, Tominaga K, Toida K, Takeda E, Suzuki K, Kuroda Y. Matsuda J, et al. Hum Mol Genet. 2004 Nov 1;13(21):2709-23. doi: 10.1093/hmg/ddh281. Epub 2004 Sep 2. Hum Mol Genet. 2004. PMID: 15345707

7

Pyruvate dehydrogenase deficiency caused by a four-nucleotide insertion in the E1 alpha subunit gene.

Naito E, Ito M, Yokota I, Matsuda J, Yara A, Kuroda Y. Naito E, et al. Among authors: matsuda j. Hum Mol Genet. 1994 Jul;3(7):1193-4. doi: 10.1093/hmg/3.7.1193. Hum Mol Genet. 1994. PMID: 7981697 No abstract available.

8

DNA diagnosis of pyruvate dehydrogenase deficiency in female patients with congenital lactic acidaemia.

Matsuda J, Ito M, Naito E, Yokota I, Kuroda Y. Matsuda J, et al. J Inherit Metab Dis. 1995;18(5):534-46. doi: 10.1007/BF02435998. J Inherit Metab Dis. 1995. PMID: 8598634

9

Molecular genetic analysis of a female patient with pyruvate dehydrogenase deficiency: detection of a new mutation and differential expression of mutant gene product in cultured cells.

Ito M, Naito E, Yokota I, Takeda E, Matsuda J, Hirose M, Sejima H, Aiba H, Hojo H, Kuroda Y. Ito M, et al. Among authors: matsuda j. J Inherit Metab Dis. 1995;18(5):547-57. doi: 10.1007/BF02435999. J Inherit Metab Dis. 1995. PMID: 8598635

10

Relationship between GAD antibody and residual beta-cell function in children after overt onset of IDDM.

Yokota I, Shirakawa N, Shima K, Matsuda J, Naito E, Ito M, Kuroda Y. Yokota I, et al. Among authors: matsuda j. Diabetes Care. 1996 Jan;19(1):74-5. doi: 10.2337/diacare.19.1.74. Diabetes Care. 1996. PMID: 8720540 No abstract available.

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