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136 related items for PubMed ID: 9377513
1. Glutaric aciduria type I: a serious pitfall if diagnosed too late. Pfluger T, Weil S, Muntau A, Willemsen UF, Hahn K. Eur Radiol; 1997; 7(8):1264-6. PubMed ID: 9377513 [Abstract] [Full Text] [Related]
12. Glutaric aciduria type I: enzymatic and neuroradiologic investigations of two kindreds. Amir N, Elpeleg ON, Shalev RS, Christensen E. J Pediatr; 1989 Jun; 114(6):983-9. PubMed ID: 2723913 [Abstract] [Full Text] [Related]
14. Dystonia and dyskinesia in glutaric aciduria type I: clinical heterogeneity and therapeutic considerations. Kyllerman M, Skjeldal OH, Lundberg M, Holme I, Jellum E, von Döbeln U, Fossen A, Carlsson G. Mov Disord; 1994 Jan; 9(1):22-30. PubMed ID: 8139602 [Abstract] [Full Text] [Related]
17. Clinical course, early diagnosis, treatment, and prevention of disease in glutaryl-CoA dehydrogenase deficiency. Hoffmann GF, Athanassopoulos S, Burlina AB, Duran M, de Klerk JB, Lehnert W, Leonard JV, Monavari AA, Müller E, Muntau AC, Naughten ER, Plecko-Starting B, Superti-Furga A, Zschocke J, Christensen E. Neuropediatrics; 1996 Jun; 27(3):115-23. PubMed ID: 8837070 [Abstract] [Full Text] [Related]
18. First trimester prenatal exclusion of glutaryl-CoA dehydrogenase deficiency (glutaric aciduria type 1). Christensen E. J Inherit Metab Dis; 1989 Jun; 12 Suppl 2():277-9. PubMed ID: 2512425 [No Abstract] [Full Text] [Related]
20. Severe clinical course with recurrent hyperpyrexia in a patient with glutaric aciduria type I. Hauser SE, Boneh A. Neuropediatrics; 1999 Feb; 30(1):51-2. PubMed ID: 10222465 [No Abstract] [Full Text] [Related] Page: [Next] [New Search]