Burlina A - Search Results

1

Oxidative metabolism of dopamine: a colour reaction from human midbrain analysed by mass spectrometry.

De Iuliis A, Arrigoni G, Andersson L, Zambenedetti P, Burlina A, James P, Arslan P, Vianello F. De Iuliis A, et al. Among authors: burlina a. Biochim Biophys Acta. 2008 Nov;1784(11):1687-93. doi: 10.1016/j.bbapap.2008.07.002. Epub 2008 Jul 15. Biochim Biophys Acta. 2008. PMID: 18675943

2

Increased dopamine peroxidation in postmortem Parkinsonian brain.

De Iuliis A, Burlina AP, Boschetto R, Zambenedetti P, Arslan P, Galzigna L. De Iuliis A, et al. Among authors: burlina ap. Biochim Biophys Acta. 2002 Oct 10;1573(1):63-7. doi: 10.1016/s0304-4165(02)00331-8. Biochim Biophys Acta. 2002. PMID: 12383943

3

Lysosomal leukocyte beta-D-glucuronidase during enzyme replacement therapy in Fabry disease.

Goi G, Massaccesi L, Burlina AP, Baquero Herrera CJ, Lombardo A, Tettamanti G, Burlina AB. Goi G, et al. Among authors: burlina ab, burlina ap. Biochim Biophys Acta. 2005 Sep 25;1741(3):300-6. doi: 10.1016/j.bbadis.2005.05.002. Biochim Biophys Acta. 2005. PMID: 15967645 Free article.

4

Newborn screening for lysosomal storage disorders by tandem mass spectrometry in North East Italy.

Burlina AB, Polo G, Salviati L, Duro G, Zizzo C, Dardis A, Bembi B, Cazzorla C, Rubert L, Zordan R, Desnick RJ, Burlina AP. Burlina AB, et al. Among authors: burlina ap. J Inherit Metab Dis. 2018 Mar;41(2):209-219. doi: 10.1007/s10545-017-0098-3. Epub 2017 Nov 15. J Inherit Metab Dis. 2018. PMID: 29143201

5

Wernicke-like encephalopathy during classic maple syrup urine disease decompensation.

Manara R, Del Rizzo M, Burlina AP, Bordugo A, Citton V, Rodriguez-Pombo P, Ugarte M, Burlina AB. Manara R, et al. Among authors: burlina ab, burlina ap. J Inherit Metab Dis. 2012 May;35(3):413-7. doi: 10.1007/s10545-012-9456-3. Epub 2012 Feb 18. J Inherit Metab Dis. 2012. PMID: 22350544

6

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

7

Measurement of melatonin in blood by radioimmunoassay. Analytical considerations and clinical usefulness.

Plebani M, Masiero M, Burlina AP, Chiozza ML, Scanarini M, Burlina A. Plebani M, et al. Among authors: burlina ap, burlina a. Childs Nerv Syst. 1990 Jun;6(4):220-1. doi: 10.1007/BF01850977. Childs Nerv Syst. 1990. PMID: 2383877

8

Whole-blood alpha-D-galactosidase A activity for the identification of Fabry's patients.

Massaccesi L, Burlina A, Baquero CJ, Goi G, Burlina AP, Tettamanti G. Massaccesi L, et al. Among authors: burlina ap, burlina a. Clin Biochem. 2011 Jul;44(10-11):916-21. doi: 10.1016/j.clinbiochem.2011.03.141. Epub 2011 Apr 16. Clin Biochem. 2011. PMID: 21515249

9

The pulvinar sign: frequency and clinical correlations in Fabry disease.

Burlina AP, Manara R, Caillaud C, Laissy JP, Severino M, Klein I, Burlina A, Lidove O. Burlina AP, et al. Among authors: burlina a. J Neurol. 2008 May;255(5):738-44. doi: 10.1007/s00415-008-0786-x. Epub 2008 Feb 26. J Neurol. 2008. PMID: 18297328

10

Maternal germline mosaicism in Fabry disease.

Pianese L, Fortunato A, Silvestri S, Solano FG, Burlina A, Burlina AP, Ragno M. Pianese L, et al. Among authors: burlina ap, burlina a. Neurol Sci. 2019 Jun;40(6):1279-1281. doi: 10.1007/s10072-019-03754-1. Epub 2019 Feb 14. Neurol Sci. 2019. PMID: 30762167

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