Case Report: Rhabdomyolysis in Glutaric Aciduria Type I

By Chow S. L.   Rohan C.   Morris A. A. M.   Morris A. A. M.  

Journal of Inherited Metabolic Disease, Vol. 26, Iss. 7, 2003-01 ,pp. : 711-712

Springer Publishing Company

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Case Report: 3-Methyglutaconic Aciduria in a Chinese Patient with Glycogen Storage Disease Ib

By Law L. K.   Law L. K.   Tang N. L. S.   Hui J.   Lam C. W. K.   Fok T. F.  

Journal of Inherited Metabolic Disease, Vol. 26, Iss. 7, 2003-01 ,pp. : 705-709

Springer Publishing Company

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Case Report: Severe phenotype despite high residual glutaryl-CoA dehydrogenase activity: A novel mutation in a Turkish patient with glutaric aciduria type I

By Mühlhausen C.   Mühlhausen C.   Christensen E.   Schwartz M.   Muschol N.   Ullrich K.   Lukacs Z.  

Journal of Inherited Metabolic Disease, Vol. 26, Iss. 7, 2003-01 ,pp. : 713-714

Springer Publishing Company

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L-2-Hydroxyglutaric Aciduria: Report of Two Indian Families

By Kamate Mahesh   Prashanth Gowda   Hattiholi Virupaxi  

The Indian Journal of Pediatrics, Vol. 81, Iss. 3, 2014-03 ,pp. : 296-298

Springer Publishing Company

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Novel Cathepsin C Mutation in a Brazilian Family with Papillon-Lefèvre Syndrome: Case Report and Mutation Update

By Pallos Debora   Acevedo Ana Carolina   Mestrinho Heliana Dantas   Cordeiro Ilia   Hart Thomas C.   Hart P. Suzanne  

Journal of Dentistry for Children, Vol. 77, Iss. 1, 2010-01 ,pp. : 36-41

American Academy of Pediatric Dentistry

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