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A Fiumara

Showing results (51-60 of 73) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|May 1, 1997
In situ evidence of neoplastic cell phagocytosis by macrophages in papillary thyroid cancerA Fiumara, A Belfiore, G Russo, et al.
Journal of Inherited Metabolic Disease|May 19, 1998
Lysosomal enzyme activities in serum and leukocytes from patients with carbohydrate-deficient glycoprotein syndrome type IA (phosphomannomutase deficiency)R Barone, H Carchon, E Jansen, et al.
Acta Endocrinologica|August 1, 1989
High frequency of cancer in cold thyroid nodules occurring at young ageA Belfiore, D Giuffrida, G L La Rosa, et al.
Acta Neurologica Belgica|September 6, 2022
Dandy-Walker malformation and variants: clinical features and associated anomalies in 28 affected children-a single retrospective study and a review of the literatureA Di Nora, G Costanza, F Pizzo, et al.
European Journal of Neurology|May 28, 2019
Hyperkinetic movement disorders in congenital disorders of glycosylationG Mostile, R Barone, A Nicoletti, et al.
Neurogenetics|May 17, 2001
Autism: evidence of association with adenosine deaminase genetic polymorphismN Bottini, D De Luca, P Saccucci, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 14, 2000
beta-hexosaminidase, alpha-D-mannosidase, and beta-mannosidase expression in serum from patients with carbohydrate-deficient glycoprotein syndrome type IT Beccari, F Mancuso, E Costanzi, et al.
American Journal of Medical Genetics. Part A|March 3, 2009
A novel mutation in the X-linked cyclin-dependent kinase-like 5 (CDKL5) gene associated with a severe Rett phenotypeT Sprovieri, F L Conforti, A Fiumara, et al.
Neuropediatrics|October 9, 2002
Aromatic L-amino acid decarboxylase deficiency with hyperdopaminuria. Clinical and laboratory findings in response to different therapiesA Fiumara, C Bräutigam, K Hyland, et al.
Journal of Inherited Metabolic Disease|September 16, 2003
Dihydropyrimidine dehydrogenase deficiency and acute neurological presentationA Fiumara, A B P van Kuilenburg, U Caruso, et al.
Pageof 8

Showing results (51-60 of 73) with videos related to

Sort By:
Pageof 8
The Journal of Clinical Endocrinology and Metabolism|May 1, 1997
In situ evidence of neoplastic cell phagocytosis by macrophages in papillary thyroid cancerA Fiumara, A Belfiore, G Russo, et al.
Journal of Inherited Metabolic Disease|May 19, 1998
Lysosomal enzyme activities in serum and leukocytes from patients with carbohydrate-deficient glycoprotein syndrome type IA (phosphomannomutase deficiency)R Barone, H Carchon, E Jansen, et al.
Acta Endocrinologica|August 1, 1989
High frequency of cancer in cold thyroid nodules occurring at young ageA Belfiore, D Giuffrida, G L La Rosa, et al.
Acta Neurologica Belgica|September 6, 2022
Dandy-Walker malformation and variants: clinical features and associated anomalies in 28 affected children-a single retrospective study and a review of the literatureA Di Nora, G Costanza, F Pizzo, et al.
European Journal of Neurology|May 28, 2019
Hyperkinetic movement disorders in congenital disorders of glycosylationG Mostile, R Barone, A Nicoletti, et al.
Neurogenetics|May 17, 2001
Autism: evidence of association with adenosine deaminase genetic polymorphismN Bottini, D De Luca, P Saccucci, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 14, 2000
beta-hexosaminidase, alpha-D-mannosidase, and beta-mannosidase expression in serum from patients with carbohydrate-deficient glycoprotein syndrome type IT Beccari, F Mancuso, E Costanzi, et al.
American Journal of Medical Genetics. Part A|March 3, 2009
A novel mutation in the X-linked cyclin-dependent kinase-like 5 (CDKL5) gene associated with a severe Rett phenotypeT Sprovieri, F L Conforti, A Fiumara, et al.
Neuropediatrics|October 9, 2002
Aromatic L-amino acid decarboxylase deficiency with hyperdopaminuria. Clinical and laboratory findings in response to different therapiesA Fiumara, C Bräutigam, K Hyland, et al.
Journal of Inherited Metabolic Disease|September 16, 2003
Dihydropyrimidine dehydrogenase deficiency and acute neurological presentationA Fiumara, A B P van Kuilenburg, U Caruso, et al.
Pageof 8