Hainmann, I <br/><br/>
Coincidence of 2 severe chronic diseases: presymptomatic diagnosis of Wilson disease in a boy with severe haemophilia A.  [electronic resource] 

 -  Klinische Padiatrie  May 2013 
 - 174-5 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1439-3824 
<br/><br/><label>Standard No.: </label>10.1055/s-0033-1343482  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adenosine Triphosphatases--genetics<br/>Cation Transport Proteins--genetics<br/>Chromosome Deletion<br/>Chromosome Inversion<br/>Copper-Transporting ATPases<br/>DNA Mutational Analysis<br/>Early Diagnosis<br/>Factor VIII--genetics<br/>Genetic Carrier Screening<br/>Hemophilia A--complications<br/>Hepatolenticular Degeneration--complications<br/>Humans<br/>Introns<br/>Liver Function Tests<br/>Male<br/>Penicillamine--therapeutic use<br/>Ultrasonography<br/>Vitamin B 6--therapeutic use