A Missense Mutation Encoding Cys⁶⁷ → Gly in Neurophysin II Is Associated with Early Onset Autosomal Dominant Neurohypophyseal Diabetes Insipidus

By DiMeglio L.A.   Gagliardi P.C.   Browning J.E.   Quigley C.A.   Repaske D.R.  

Molecular Genetics and Metabolism, Vol. 72, Iss. 1, 2001-01 ,pp. : 39-44

Academic Press

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Identification of a Novel Pancreatitis-Associated Missense Mutation, R116C, in the Human Cationic Trypsinogen Gene (PRSS1)

By Le Maréchal C.   Bretagne J-F.   Raguénès O.   Quéré I.   Chen J-M.   Ferec C.  

Molecular Genetics and Metabolism, Vol. 74, Iss. 3, 2001-11 ,pp. : 342-344

Academic Press

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Somatic Mutation as Mechanism for Cyst Formation in Autosomal Dominant Polycystic Kidney Disease

By Qian F.   Watnick T.J.  

Molecular Genetics and Metabolism, Vol. 68, Iss. 2, 1999-10 ,pp. : 237-242

Academic Press

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Risk factors associated with diabetes insipidus in brain dead patients

By Domnguez-Roldan J.M.   Garcia-Alfaro C.   Daz-Parejo P.   Murillo-Cabezas F.   Barrera-Chacon J.M.   Caldera-Gonzalez A.  

Transplantation Proceedings, Vol. 34, Iss. 1, 2002-02 ,pp. : 13-14

Elsevier

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Kidney transplantation in the recipient with autosomal-dominant polycystic kidney disease: a single center experience

By Shiroyanagi Y.   Tanabe K.   Hashimoto Y.   Okuda H.   Oshima T.   Tokumoto T.   Ishikawa N.   Tomq H.  

Transplantation Proceedings, Vol. 32, Iss. 7, 2000-11 ,pp. : 1841-1843

Elsevier

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