Report for Hamajima N

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References (3)

Title : Highly prevalent LIPH founder mutations causing autosomal recessive woolly hair\/hypotrichosis in Japan and the genotype\/phenotype correlations - Tanahashi_2014_PLoS.One_9_e89261
Author(s) : Tanahashi K , Sugiura K , Kono M , Takama H , Hamajima N , Akiyama M
Ref : PLoS ONE , 9 :e89261 , 2014
Abstract : Tanahashi_2014_PLoS.One_9_e89261
ESTHER : Tanahashi_2014_PLoS.One_9_e89261
PubMedSearch : Tanahashi_2014_PLoS.One_9_e89261
PubMedID: 24586639
Gene_locus related to this paper: human-LIPH

Title : Polymorphisms of Nrf2, an antioxidative gene, are associated with blood pressure in Japanese - Shimoyama_2014_Nagoya.J.Med.Sci_76_113
Author(s) : Shimoyama Y , Mitsuda Y , Hamajima N , Niwa T
Ref : Nagoya J Med Sci , 76 :113 , 2014
Abstract : Shimoyama_2014_Nagoya.J.Med.Sci_76_113
ESTHER : Shimoyama_2014_Nagoya.J.Med.Sci_76_113
PubMedSearch : Shimoyama_2014_Nagoya.J.Med.Sci_76_113
PubMedID: 25129997

Title : Elevated serum lipase levels in patients with dyspepsia of unknown cause in general practice - Okada_2009_Med.Princ.Pract_18_130
Author(s) : Okada R , Okada A , Okada T , Hamajima N
Ref : Med Princ Pract , 18 :130 , 2009
Abstract : Okada_2009_Med.Princ.Pract_18_130
ESTHER : Okada_2009_Med.Princ.Pract_18_130
PubMedSearch : Okada_2009_Med.Princ.Pract_18_130
PubMedID: 19204432