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References (4)

Title : Deletions of VCX-A and NLGN4: a variable phenotype including normal intellect - Macarov_2007_J.Intellect.Disabil.Res_51_329
Author(s) : Macarov M , Zeigler M , Newman JP , Strich D , Sury V , Tennenbaum A , Meiner V
Ref : J Intellect Disabil Res , 51 :329 , 2007
Abstract : Macarov_2007_J.Intellect.Disabil.Res_51_329
ESTHER : Macarov_2007_J.Intellect.Disabil.Res_51_329
PubMedSearch : Macarov_2007_J.Intellect.Disabil.Res_51_329
PubMedID: 17391250

Title : Successful treatment of Wolman disease by unrelated umbilical cord blood transplantation - Stein_2007_Eur.J.Pediatr_166_663
Author(s) : Stein J , Garty BZ , Dror Y , Fenig E , Zeigler M , Yaniv I
Ref : Eur J Pediatr , 166 :663 , 2007
Abstract : Stein_2007_Eur.J.Pediatr_166_663
ESTHER : Stein_2007_Eur.J.Pediatr_166_663
PubMedSearch : Stein_2007_Eur.J.Pediatr_166_663
PubMedID: 17033804

Title : Characterization of lysosomal acid lipase mutations in the signal peptide and mature polypeptide region causing Wolman disease - Zschenker_2001_J.Lipid.Res_42_1033
Author(s) : Zschenker O , Jung N , Rethmeier J , Trautwein S , Hertel S , Zeigler M , Ameis D
Ref : J Lipid Res , 42 :1033 , 2001
Abstract : Zschenker_2001_J.Lipid.Res_42_1033
ESTHER : Zschenker_2001_J.Lipid.Res_42_1033
PubMedSearch : Zschenker_2001_J.Lipid.Res_42_1033
PubMedID: 11441129
Gene_locus related to this paper: human-LIPA

Title : Hydrops fetalis in four siblings caused by galactosialidosis -
Author(s) : Landau D , Meisner I , Zeigler M , Bargal R , Shinwell ES
Ref : Isr J Med Sci , 31 :321 , 1995
PubMedID: 7759227
Gene_locus related to this paper: human-CTSA