Wada Y - Search Results

1

Identification of a larger than 3 Mb deletion including JAG1 in an Alagille syndrome patient with a translocation t(3;20)(q13.3;p12.2).

Oda T, Elkahloun AG, Meltzer PS, Okajima K, Sugiyama K, Wada Y, Chandrasekharappa SC. Oda T, et al. Among authors: wada y. Hum Mutat. 2000 Jul;16(1):92. doi: 10.1002/1098-1004(200007)16:1<92::AID-HUMU23>3.0.CO;2-4. Hum Mutat. 2000. PMID: 10874319

2

Thymidine kinase activity in individuals with galactokinase deficiency.

Okajima K, Yazaki M, Wada Y. Okajima K, et al. Among authors: wada y. Am J Hum Genet. 1987 Sep;41(3):503-4. Am J Hum Genet. 1987. PMID: 3631083 Free PMC article. No abstract available.

3

[Lipidosis].

Wada Y, Oda T. Wada Y, et al. Nihon Rinsho. 1993 Jan;51 Suppl:317-31. Nihon Rinsho. 1993. PMID: 8459559 Review. Japanese. No abstract available.

4

Molecular cloning of the human UMP synthase gene and characterization of point mutations in two hereditary orotic aciduria families.

Suchi M, Mizuno H, Kawai Y, Tsuboi T, Sumi S, Okajima K, Hodgson ME, Ogawa H, Wada Y. Suchi M, et al. Among authors: wada y. Am J Hum Genet. 1997 Mar;60(3):525-39. Am J Hum Genet. 1997. PMID: 9042911 Free PMC article.

5

Clinical and serological courses of a newborn with post-transfusion hepatitis C.

Maniwa H, Miyake Y, Hamada M, Oda T, Li R, Yokoyama T, Sugiyama K, Wada Y. Maniwa H, et al. Among authors: wada y. J Viral Hepat. 1995;2(6):303-5. doi: 10.1111/j.1365-2893.1995.tb00046.x. J Viral Hepat. 1995. PMID: 8732177

6

Analysis of the hypervariable region of hepatitis C virus E2/NS1 gene in an infant infected by blood transfusion.

Sugiyama K, Goto K, Miyake Y, Ando T, Oda T, Maniwa H, Li R, Kawabe Y, Wada Y. Sugiyama K, et al. Among authors: wada y. Pediatr Res. 1997 Aug;42(2):247-50. doi: 10.1203/00006450-199708000-00020. Pediatr Res. 1997. PMID: 9262231

7

Using polymerase chain reaction to detect the etiological virus of serologically non-A, non-B, non-C fulminant hepatitis in Japanese children.

Miyake Y, Sugiyama K, Goto K, Ando T, Li R, Oda T, Mizutani F, Kawabe Y, Wada Y. Miyake Y, et al. Among authors: wada y. Acta Paediatr Jpn. 1998 Feb;40(1):102-4. doi: 10.1111/j.1442-200x.1998.tb01416.x. Acta Paediatr Jpn. 1998. PMID: 9583215 No abstract available.

8

Antley-Bixler syndrome in a sister and brother.

Suzuki K, Kanda Y, Sugiyama K, Katoh T, Wada Y, Yasui Y. Suzuki K, et al. Among authors: wada y. Jinrui Idengaku Zasshi. 1987 Sep;32(3):247-52. doi: 10.1007/BF01876879. Jinrui Idengaku Zasshi. 1987. PMID: 3448306 No abstract available.

9

The first trimester prenatal diagnosis of Pompe's disease at risk.

Ezaki M, Sugiyama K, Wada Y, Suzumori K. Ezaki M, et al. Among authors: wada y. Jinrui Idengaku Zasshi. 1987 Sep;32(3):267-9. doi: 10.1007/BF01876883. Jinrui Idengaku Zasshi. 1987. PMID: 3329254 No abstract available.

10

Hypomelanosis of Ito associated with benign tumors and chromosomal abnormalities: a neurocutaneous syndrome.

Ishikawa T, Kanayama M, Sugiyama K, Katoh T, Wada Y. Ishikawa T, et al. Among authors: wada y. Brain Dev. 1985;7(1):45-9. doi: 10.1016/s0387-7604(85)80058-9. Brain Dev. 1985. PMID: 4003709

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