Görgen-Pauly, U <br/><br/>
Familial pontocerebellar hypoplasia type I with anterior horn cell disease.  [electronic resource] 

 -  European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society  1999 
 - 33-8 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1090-3798 
<br/><br/><label>Standard No.: </label>10.1053/ejpn.1999.0177  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Atrophy--pathology<br/>Cerebellum--abnormalities<br/>Diagnosis, Differential<br/>Fatal Outcome<br/>Female<br/>Humans<br/>Infant, Newborn<br/>Magnetic Resonance Imaging<br/>Motor Neuron Disease--complications<br/>Olivopontocerebellar Atrophies--complications<br/>Pedigree<br/>Pons--abnormalities<br/>Pregnancy