Yoshida I - Search Results

1

Sweet syndrome in a child with aplastic anemia receiving recombinant granulocyte colony-stimulating factor.

Shimizu T, Yoshida I, Eguchi H, Takahashi K, Inada H, Kato H. Shimizu T, et al. Among authors: yoshida i. J Pediatr Hematol Oncol. 1996 Aug;18(3):282-4. doi: 10.1097/00043426-199608000-00009. J Pediatr Hematol Oncol. 1996. PMID: 8689342

2

In vitro expansion of human basophils by interleukin-3 from granulocyte colony-stimulating factor-mobilized peripheral blood stem cells.

Takao K, Tanimoto Y, Fujii M, Hamada N, Yoshida I, Ikeda K, Imajo K, Takahashi K, Harada M, Tanimoto M. Takao K, et al. Among authors: yoshida i. Clin Exp Allergy. 2003 Nov;33(11):1561-7. doi: 10.1046/j.1365-2222.2003.01791.x. Clin Exp Allergy. 2003. PMID: 14616869

3

Carbonic anhydrase II deficiency in a Japanese patient produced by a nonsense mutation (TAT-->TAG) at Tyr-40 in exon 2, (Y40X).

Soda H, Yukizane S, Yoshida I, Aramaki S, Kato H. Soda H, et al. Among authors: yoshida i. Hum Mutat. 1995;5(4):348-50. doi: 10.1002/humu.1380050415. Hum Mutat. 1995. PMID: 7627193 No abstract available.

4

Renal handling of methylmalonic acid in a uraemic patient with vitamin B12-unresponsive methylmalonic acidaemia.

Soda H, Yoshida I, Aramaki S, Kuriya N, Aoki K, Inokuchi T, Yoshino M, Kato H. Soda H, et al. Among authors: yoshida i. J Inherit Metab Dis. 1996;19(1):90-1. doi: 10.1007/BF01799356. J Inherit Metab Dis. 1996. PMID: 8830186 No abstract available.

5

A point mutation in exon 3 (His 107-->Tyr) in two unrelated Japanese patients with carbonic anhydrase II deficiency with central nervous system involvement.

Soda H, Yukizane S, Yoshida I, Koga Y, Aramaki S, Kato H. Soda H, et al. Among authors: yoshida i. Hum Genet. 1996 Apr;97(4):435-7. doi: 10.1007/BF02267062. Hum Genet. 1996. PMID: 8834238

6

Maple syrup urine disease: nutritional management by intravenous hyperalimentation and uneventful course after surgical repair of dislocation of the hip.

Koga Y, Iwanaga T, Yoshida I, Yoshino M, Kaneko S, Kato H. Koga Y, et al. Among authors: yoshida i. J Inherit Metab Dis. 1998 Apr;21(2):177-8. doi: 10.1023/a:1005324516186. J Inherit Metab Dis. 1998. PMID: 9584272 No abstract available.

7

Elimination of CO2 in patients with carbonic anhydrase II deficiency, with studies of respiratory function at rest.

Taki K, Kato H, Yoshida I. Taki K, et al. Among authors: yoshida i. Respir Med. 1999 Aug;93(8):536-9. doi: 10.1016/s0954-6111(99)90151-8. Respir Med. 1999. PMID: 10542985 Free article.

8

The effect of furosemide on a patient with hyperkalaemic hypertension and short stature.

Tokunaga Y, Yoshida I, Endo F, Kato H. Tokunaga Y, et al. Among authors: yoshida i. Eur J Pediatr. 1995 Oct;154(10):870. doi: 10.1007/BF01959807. Eur J Pediatr. 1995. PMID: 8529697 No abstract available.

9

The occurrence of intramitochondrial Ca2+ granules in valproate-induced liver injury.

Kimura A, Yoshida I, Yamashita F, Kuriya N, Yamamoto M, Nagayama K. Kimura A, et al. Among authors: yoshida i. J Pediatr Gastroenterol Nutr. 1989 Jan;8(1):13-8. doi: 10.1097/00005176-198901000-00004. J Pediatr Gastroenterol Nutr. 1989. PMID: 2499671

10

[Reye's syndrome].

Yoshida I. Yoshida I. Ryoikibetsu Shokogun Shirizu. 1999;(25 Pt 3):120-3. Ryoikibetsu Shokogun Shirizu. 1999. PMID: 10337754 Review. Japanese. No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

619 results

Search Page

Filters