Nephrogenic diabetes insipidus and Werdnig-Hoffmann disease in a child: an unusual association.

Author:

Bernasconi S,Pezzani C,Balestrazzi P,Marbini A

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference8 articles.

1. Diabete insipido nefrogeno: risposta al DDAVP e trasmissione genetica in due gruppi familiari;Bernasconi, S.; Savi, M.; Giovannelli, G.;Minerva Nefrologica,1976

2. Electromyographic studies in parents of children with spinal muscular atrophy;Emery, A.E.H.; Anderson, A.R.; Noronha, M.J.;Journal ofMedical Genetics,1973

3. On hereditary diabetes insipidus with special reference to a sex linked form;Forsmann, H.;Acta Medica Scandinavica,1956

4. Mendelian Inheritance in Man. Catalogs of Autosomal Dominant, Autosomal Recessive X-linked Phenotypes;McKusick, V.A.,1975

5. Progressive neural muscular atrophy in a case of phenylketonuria;Meier, K.; Lutschg, J.; Vassella, F.;Development Medicine and Child Neurology,1975

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