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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 cancer
A 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 age
A 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 literature
A Di Nora, G Costanza, F Pizzo, et al.
European Journal of Neurology
|
May 28, 2019
Hyperkinetic movement disorders in congenital disorders of glycosylation
G Mostile, R Barone, A Nicoletti, et al.
Neurogenetics
|
May 17, 2001
Autism: evidence of association with adenosine deaminase genetic polymorphism
N 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 I
T 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 phenotype
T 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 therapies
A Fiumara, C Bräutigam, K Hyland, et al.
Journal of Inherited Metabolic Disease
|
September 16, 2003
Dihydropyrimidine dehydrogenase deficiency and acute neurological presentation
A Fiumara, A B P van Kuilenburg, U Caruso, et al.
Page
of 8
Search research articles
Search
Showing results (51-60 of 73) with videos related to
Sort By:
Page
of 8
The Journal of Clinical Endocrinology and Metabolism
|
May 1, 1997
In situ evidence of neoplastic cell phagocytosis by macrophages in papillary thyroid cancer
A 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 age
A 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 literature
A Di Nora, G Costanza, F Pizzo, et al.
European Journal of Neurology
|
May 28, 2019
Hyperkinetic movement disorders in congenital disorders of glycosylation
G Mostile, R Barone, A Nicoletti, et al.
Neurogenetics
|
May 17, 2001
Autism: evidence of association with adenosine deaminase genetic polymorphism
N 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 I
T 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 phenotype
T 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 therapies
A Fiumara, C Bräutigam, K Hyland, et al.
Journal of Inherited Metabolic Disease
|
September 16, 2003
Dihydropyrimidine dehydrogenase deficiency and acute neurological presentation
A Fiumara, A B P van Kuilenburg, U Caruso, et al.
Page
of 8