Burlina AB - Search Results

1

Diagnosis and management of glutaric aciduria type I--revised recommendations.

Kölker S, Christensen E, Leonard JV, Greenberg CR, Boneh A, Burlina AB, Burlina AP, Dixon M, Duran M, García Cazorla A, Goodman SI, Koeller DM, Kyllerman M, Mühlhausen C, Müller E, Okun JG, Wilcken B, Hoffmann GF, Burgard P. Kölker S, et al. Among authors: burlina ab, burlina ap. J Inherit Metab Dis. 2011 Jun;34(3):677-94. doi: 10.1007/s10545-011-9289-5. Epub 2011 Mar 23. J Inherit Metab Dis. 2011. PMID: 21431622 Free PMC article. Review.

2

Acute pancreatitis in propionic acidaemia.

Burlina AB, Dionisi-Vici C, Piovan S, Saponara I, Bartuli A, Sabetta G, Zacchello F. Burlina AB, et al. J Inherit Metab Dis. 1995;18(2):169-72. doi: 10.1007/BF00711758. J Inherit Metab Dis. 1995. PMID: 7564238 No abstract available.

3

Early signs and course of disease of glutaryl-CoA dehydrogenase deficiency.

Hoffmann GF, Böhles HJ, Burlina A, Duran M, Herwig J, Lehnert W, Leonard JV, Muntau A, Plecko-Starting FK, Superti-Furga A, et al. Hoffmann GF, et al. J Inherit Metab Dis. 1995;18(2):173-6. doi: 10.1007/BF00711759. J Inherit Metab Dis. 1995. PMID: 7564239 No abstract available.

4

Secondary 3-hydroxydicarboxylic aciduria mimicking long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.

Bennett MJ, Weinberger MJ, Sherwood WG, Burlina AB. Bennett MJ, et al. Among authors: burlina ab. J Inherit Metab Dis. 1994;17(3):283-6. doi: 10.1007/BF00711808. J Inherit Metab Dis. 1994. PMID: 7807934 No abstract available.

5

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. Hoffmann GF, et al. Among authors: burlina ab. Neuropediatrics. 1996 Jun;27(3):115-23. doi: 10.1055/s-2007-973761. Neuropediatrics. 1996. PMID: 8837070

6

Profound neurological phenotype in a patient presenting with disordered isoleucine and energy metabolism.

Burlina AB, Gibson KM, Ruitenbeek W, Bonafè L, Bennett MJ. Burlina AB, et al. J Inherit Metab Dis. 1998 Dec;21(8):864-6. doi: 10.1023/a:1005426920116. J Inherit Metab Dis. 1998. PMID: 9870212 No abstract available.

7

Improved stable isotope dilution-gas chromatography-mass spectrometry method for serum or plasma free 3-hydroxy-fatty acids and its utility for the study of disorders of mitochondrial fatty acid beta-oxidation.

Jones PM, Quinn R, Fennessey PV, Tjoa S, Goodman SI, Fiore S, Burlina AB, Rinaldo P, Boriack RL, Bennett MJ. Jones PM, et al. Among authors: burlina ab. Clin Chem. 2000 Feb;46(2):149-55. Clin Chem. 2000. PMID: 10657369

8

Measurement of neurotransmitter metabolites in the cerebrospinal fluid of phenylketonuric patients under dietary treatment.

Burlina AB, Bonafé L, Ferrari V, Suppiej A, Zacchello F, Burlina AP. Burlina AB, et al. Among authors: burlina ap. J Inherit Metab Dis. 2000 Jun;23(4):313-6. doi: 10.1023/a:1005694122277. J Inherit Metab Dis. 2000. PMID: 10896282 No abstract available.

9

Propionic acidaemia with basal ganglia stroke: treatment of acute extrapyramidal symptoms with L-DOPA.

Burlina AP, Baracchini C, Carollo C, Burlina AB. Burlina AP, et al. Among authors: burlina ab. J Inherit Metab Dis. 2001 Oct;24(5):596-8. doi: 10.1023/a:1012471928628. J Inherit Metab Dis. 2001. PMID: 11757587

10

Treatment of extrapyramidal symptoms in a patient with homozygous homocystinuria.

Burlina AP, Edini C, Burlina AB. Burlina AP, et al. Among authors: burlina ab. J Inherit Metab Dis. 2002 May;25(2):135-6. doi: 10.1023/a:1015684912709. J Inherit Metab Dis. 2002. PMID: 12118530 No abstract available.

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