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Alberto B. Burlina

Progressive neuropathy and recurrent myoglobinuria in a child with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
1991 · Carlo Dionisi Vici, Alberto B. Burlina, et al. · The Journal of Pediatrics · 67
Clinical and biochemical approach to the neonate with a suspected inborn error of amino acid and organic acid metabolism
1999 · Alberto B. Burlina, Luisa Bonafé, et al. · Seminars in Perinatology · 45
Follow-Up of a Child with Hypoacetylaspartia
2004 · E. Boltshauser, B. Schmitt, et al. · Neuropediatrics · 34
Enzymes of Lysosomal Origin in the Cerebrospinal Fluid and Plasma of Patients with Multiple Sclerosis
2008 · G. Goi, D. Caputo, et al. · European Neurology · 7
Levels of some lysosomal activities in newborns
1984 · G. Goi, Felice Achilli, et al. · Institutional Research Information System (Università degli Studi di Brescia) · 2
Quality of life after diet liberalization in individuals with phenylketonuria treated with Pegvaliase
2026 · Chiara Cazzorla, Giacomo Gaiga, et al. · Molecular Genetics and Metabolism Reports · 1
Lyso-Gb3 in a Fabry pediatric cohort diagnosed by newborn screening
2026 · Alessandro P. Burlina, Vincenza Gragnaniello, et al. · Genetics in Medicine Open · 1
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Inflammation and autophagy impairment in presymptomatic pediatric patients with Fabry disease identified by newborn screening
2026 · Vincenza Gragnaniello, Alessandro P. Burlina, et al. · Molecular Genetics and Metabolism
Neonatal screening for Fabry disease and long-term follow-up: The role of plasma globotriaosylsphingosine (LysoGb3) assay
2025 · Alberto B. Burlina, Vincenza Gragnaniello, et al. · Molecular Genetics and Metabolism
Inflammation and impaired autophagy in Gaucher disease type 1 infants diagnosed by newborn screening
2025 · Vincenza Gragnaniello, Daniela Gueraldi, et al. · Molecular Genetics and Metabolism
Heritable and non-heritable uncommon causes of stroke (vol 15, pg 961, 2020)
2020 · Anna Bersano, Markus Kraemer, et al. · Journal of Neurology
PKU in Italy
2012 · M Giovannini, A.B. Burlina, et al.
Lysosomal leukocyte b-D-Glucuronidase during enzyme replacemet therapy in Fabry disease
2002 · A.B. Burlina, C.J. Baquero Herrera, et al.
Study Group on Nutrition and Diet Therapy of the Italian Paediatric Society. Protocol for diet treatment of glycogenosis.
1990 · Riccardo Longhi, A.B. Burlina, et al. · The Italian Journal of Pediatrics/Italian journal of pediatrics
Lysosomal-enzymes in Normal and Pathological Pregnancies
1985 · G. Goi, Alessandra Fabi, et al.
Clinical enzymology of inherited lysosomal diseases
1984 · Guido Tettamanti, Thodhal Yoganandham Suman, et al.
[Blood Transfusion Center; report of the first year's activities].
1955 · A BURLINA · PubMed
Works count: 17
Citation count: 157
H-index: 4
I10-index: 3
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