HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Multiple acyl-CoA dehydrogenation deficiency (glutaric aciduria type II), congenital polycystic kidneys, and symmetric warty dysplasia of the cerebral cortex in two newborn brothers. II. Morphology and pathogenesis.

AuthorsN Böhm, J Uy, M Kiessling, W Lehnert
JournalEuropean journal of pediatrics (Eur J Pediatr) Vol. 139 Issue 1 Pg. 60-5 (Sep 1982) ISSN: 0340-6199 [Print] Germany
PMID7173260 (Publication Type: Case Reports, Journal Article)
Chemical References
  • Glutarates
Topics
  • Abnormalities, Multiple (pathology)
  • Cerebral Cortex (abnormalities)
  • Glutarates (urine)
  • Humans
  • Infant, Newborn
  • Male
  • Metabolism, Inborn Errors (genetics, pathology)
  • Polycystic Kidney Diseases (genetics, pathology)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: