Sadewa AH - Search Results

1

Attention Deficit/Hyperactivity Disorder (ADHD): age related change of completion time and error rates of Stroop test.

Thursina C, Ar Rochmah M, Nurputra DK, Harahap IS, Harahap NI, Sa'Adah N, Wibowo S, Sutarni S, Sadewa AH, Nishimura N, Mandai T, Iijima K, Nishio H, Kitayama S. Thursina C, et al. Among authors: sadewa ah. Kobe J Med Sci. 2015 Apr 7;61(1):E19-26. Kobe J Med Sci. 2015. PMID: 25868610 Free article.

2

Novel missense mutation of the UGT1A1 gene in Thai siblings with Gilbert's syndrome.

Sutomo R, Laosombat V, Sadewa AH, Yokoyama N, Nakamura H, Matsuo M, Nishio H. Sutomo R, et al. Among authors: sadewa ah. Pediatr Int. 2002 Aug;44(4):427-32. Pediatr Int. 2002. PMID: 12139570

3

Correlation between SMN2 copy number and clinical phenotype of spinal muscular atrophy: three SMN2 copies fail to rescue some patients from the disease severity.

Harada Y, Sutomo R, Sadewa AH, Akutsu T, Takeshima Y, Wada H, Matsuo M, Nishio H. Harada Y, et al. Among authors: sadewa ah. J Neurol. 2002 Sep;249(9):1211-9. doi: 10.1007/s00415-002-0811-4. J Neurol. 2002. PMID: 12242541

4

The C677T mutation in the methylenetetrahydrofolate reductase gene among the Indonesian Javanese population.

Sadewa AH, Sunarti, Sutomo R, Hayashi C, Lee MJ, Ayaki H, Sofro AS, Matsuo M, Nishio H. Sadewa AH, et al. Kobe J Med Sci. 2002 Dec;48(5-6):137-44. Kobe J Med Sci. 2002. PMID: 12594357 Free article.

5

C677T mutation in the MTHFR gene was not found in patients with frontoethmoidal encephalocele in East Java, Indonesia.

Sadewa AH, Sutomo R, Istiadjid M, Nishiyama K, Shirakawa T, Matsuo M, Nishio H. Sadewa AH, et al. Pediatr Int. 2004 Aug;46(4):409-14. doi: 10.1111/j.1442-200x.2004.01927.x. Pediatr Int. 2004. PMID: 15310304

6

Double fetus-in-fetu: a case report with three-dimensional computed tomography findings.

Wada K, Nishio H, Sadewa AH, Nishimoto K, Suminaga R, Hase M, Ishida A, Hisano K. Wada K, et al. Among authors: sadewa ah. Pediatr Int. 2005 Oct;47(5):598-600. doi: 10.1111/j.1442-200x.2005.02114.x. Pediatr Int. 2005. PMID: 16190975 No abstract available.

7

ACE gene polymorphism in children with nephrotic syndrome in the Indonesian population.

Sasongko TH, Sadewa AH, Kusuma PA, Damanik MP, Lee MJ, Ayaki H, Nozu K, Goto A, Matsuo M, Nishio H. Sasongko TH, et al. Among authors: sadewa ah. Kobe J Med Sci. 2005;51(3-4):41-7. Kobe J Med Sci. 2005. PMID: 16421456 Free article.

8

C117T variant in the SMN1 gene found in the Japanese population.

Sadewa AH, Harada Y, Sasongko TH, Matsuo M, Nishio H. Sadewa AH, et al. Pediatr Int. 2007 Feb;49(1):8-10. doi: 10.1111/j.1442-200X.2007.02301.x. Pediatr Int. 2007. PMID: 17250497

9

A novel mutation at the N-terminal of SMN Tudor domain inhibits its interaction with target proteins.

Kotani T, Sutomo R, Sasongko TH, Sadewa AH, Gunadi, Minato T, Fujii E, Endo S, Lee MJ, Ayaki H, Harada Y, Matsuo M, Nishio H. Kotani T, et al. Among authors: sadewa ah. J Neurol. 2007 May;254(5):624-30. doi: 10.1007/s00415-006-0410-x. Epub 2007 Apr 6. J Neurol. 2007. PMID: 17415510

10

Nonsense mutations of the ZFHX1B gene in two Japanese girls with Mowat-Wilson syndrome.

Sasongko TH, Sadewa AH, Gunadi, Lee MJ, Koterazawa K, Nishio H. Sasongko TH, et al. Among authors: sadewa ah. Kobe J Med Sci. 2007;53(4):157-62. Kobe J Med Sci. 2007. PMID: 17932455 Free article.

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