Shimozawa N - Search Results

1

Clinical, biochemical and molecular characterization of peroxisomal diseases in Arabs.

Shaheen R, Al-Dirbashi OY, Al-Hassnan ZN, Al-Owain M, Makhsheed N, Basheeri F, Seidahmed MZ, Salih MA, Faqih E, Zaidan H, Al-Sayed M, Rahbeeni Z, Al-Sheddi T, Hashem M, Kurdi W, Shimozawa N, Alkuraya FS. Shaheen R, et al. Among authors: shimozawa n. Clin Genet. 2011 Jan;79(1):60-70. doi: 10.1111/j.1399-0004.2010.01498.x. Clin Genet. 2011. PMID: 20681997

2

Zellweger syndrome caused by PEX13 deficiency: report of two novel mutations.

Al-Dirbashi OY, Shaheen R, Al-Sayed M, Al-Dosari M, Makhseed N, Abu Safieh L, Santa T, Meyer BF, Shimozawa N, Alkuraya FS. Al-Dirbashi OY, et al. Among authors: shimozawa n. Am J Med Genet A. 2009 Jun;149A(6):1219-23. doi: 10.1002/ajmg.a.32874. Am J Med Genet A. 2009. PMID: 19449432

3

The peroxin Pex6p gene is impaired in peroxisomal biogenesis disorders of complementation group 6.

Matsumoto N, Tamura S, Moser A, Moser HW, Braverman N, Suzuki Y, Shimozawa N, Kondo N, Fujiki Y. Matsumoto N, et al. Among authors: shimozawa n. J Hum Genet. 2001;46(5):273-7. doi: 10.1007/s100380170078. J Hum Genet. 2001. PMID: 11355018

4

Molecular and clinical aspects of peroxisomal diseases.

Shimozawa N. Shimozawa N. J Inherit Metab Dis. 2007 Apr;30(2):193-7. doi: 10.1007/s10545-007-0516-z. Epub 2007 Mar 8. J Inherit Metab Dis. 2007. PMID: 17347916 Review.

5

Peroxisomal disorders: clinical aspects.

Suzuki Y, Shimozawa N, Takahashi Y, Imamura A, Kondo N, Orii T. Suzuki Y, et al. Among authors: shimozawa n. Ann N Y Acad Sci. 1996 Dec 27;804:442-9. doi: 10.1111/j.1749-6632.1996.tb18635.x. Ann N Y Acad Sci. 1996. PMID: 8993563

6

Incidence of peroxisomal disorders in Japan.

Suzuki Y, Shimozawa N, Yajima S, Inoue K, Orii T, Kondo N. Suzuki Y, et al. Among authors: shimozawa n. Jpn J Hum Genet. 1996 Mar;41(1):167-75. doi: 10.1007/BF01892624. Jpn J Hum Genet. 1996. PMID: 8914632

7

Defective PEX gene products correlate with the protein import, biochemical abnormalities, and phenotypic heterogeneity in peroxisome biogenesis disorders.

Shimozawa N, Imamura A, Zhang Z, Suzuki Y, Orii T, Tsukamoto T, Osumi T, Fujiki Y, Wanders RJ, Besley G, Kondo N. Shimozawa N, et al. J Med Genet. 1999 Oct;36(10):779-81. doi: 10.1136/jmg.36.10.779. J Med Genet. 1999. PMID: 10528859 Free PMC article.

8

Prenatal diagnosis of peroxisome biogenesis disorders by means of immunofluorescence staining of cultured chorionic villous cells.

Zhang Z, Suzuki Y, Shimozawa N, Kawabata I, Tamaya T, Sato K, Kondo N. Zhang Z, et al. Among authors: shimozawa n. Clin Genet. 1999 Dec;56(6):467-8. doi: 10.1034/j.1399-0004.1999.560612.x. Clin Genet. 1999. PMID: 10665669 No abstract available.

9

[Molecular analysis of peroxisomal disorders].

Shimozawa N. Shimozawa N. No To Hattatsu. 1998 Mar;30(2):128-33. No To Hattatsu. 1998. PMID: 9545777 Japanese.

10

Identification of PEX3 as the gene mutated in a Zellweger syndrome patient lacking peroxisomal remnant structures.

Shimozawa N, Suzuki Y, Zhang Z, Imamura A, Ghaedi K, Fujiki Y, Kondo N. Shimozawa N, et al. Hum Mol Genet. 2000 Aug 12;9(13):1995-9. doi: 10.1093/hmg/9.13.1995. Hum Mol Genet. 2000. PMID: 10942428

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