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Clinical Immunology (Orlando, Fla.)
|
January 7, 2016
Clinical heterogeneity of dominant chronic mucocutaneous candidiasis disease: presenting as treatment-resistant candidiasis and chronic lung disease
Laura Dotta, Omar Scomodon, Rita Padoan, et al.
Data in Brief
|
March 17, 2016
Clinical and immunological data of nine patients with chronic mucocutaneous candidiasis disease
Laura Dotta, Omar Scomodon, Rita Padoan, et al.
Journal of Biological Regulators and Homeostatic Agents
|
October 1, 2020
Dilated cardiomyopathy in mucolipidosis type 2
E Carboni, S Sestito, M Lucente, et al.
Oncotarget
|
November 9, 2016
Genetic variants associated with gastrointestinal symptoms in Fabry disease
Maria Teresa Di Martino, Francesca Scionti, Simona Sestito, et al.
Journal of Medical Genetics
|
September 17, 2025
GAPO syndrome: a comprehensive examination and review of 105 clinical cases
Clarissa Modafferi, Pino D'Ambrosio, Silvia Andaloro, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
March 5, 2017
Early diagnosis of mucopolysaccharidoses in developing countries: A low cost and easy execution approach
Orazio Gabrielli, Lucia Zampini, Chiara Monachesi, et al.
Genes
|
June 26, 2026
Expanding the Mutational Spectrum of <i>ACADVL</i>: Integrative Characterization of the p.Ser72Phe Variant in Very Long-Chain Acyl-CoA Dehydrogenase Deficiency
Francesca Dinatolo, Lucia D'Antona, Radha Procopio, et al.
Journal of Endocrinological Investigation
|
June 6, 2009
17beta-Hydroxysteroid dehydrogenase-3 deficiency: from pregnancy to adolescence
S Bertelloni, A Balsamo, L Giordani, et al.
AJNR. American Journal of Neuroradiology
|
October 21, 2017
Redefining the Pulvinar Sign in Fabry Disease
S Cocozza, C Russo, A Pisani, et al.
Tumori
|
August 1, 1981
Results of the Italian interlaboratory quality control program for estradiol receptor assay
S Fumero, G P Berruto, D Pelizzola, et al.
Page
of 35
Search research articles
Search
Showing results (311-320 of 347) with videos related to
Sort By:
Page
of 35
Clinical Immunology (Orlando, Fla.)
|
January 7, 2016
Clinical heterogeneity of dominant chronic mucocutaneous candidiasis disease: presenting as treatment-resistant candidiasis and chronic lung disease
Laura Dotta, Omar Scomodon, Rita Padoan, et al.
Data in Brief
|
March 17, 2016
Clinical and immunological data of nine patients with chronic mucocutaneous candidiasis disease
Laura Dotta, Omar Scomodon, Rita Padoan, et al.
Journal of Biological Regulators and Homeostatic Agents
|
October 1, 2020
Dilated cardiomyopathy in mucolipidosis type 2
E Carboni, S Sestito, M Lucente, et al.
Oncotarget
|
November 9, 2016
Genetic variants associated with gastrointestinal symptoms in Fabry disease
Maria Teresa Di Martino, Francesca Scionti, Simona Sestito, et al.
Journal of Medical Genetics
|
September 17, 2025
GAPO syndrome: a comprehensive examination and review of 105 clinical cases
Clarissa Modafferi, Pino D'Ambrosio, Silvia Andaloro, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
March 5, 2017
Early diagnosis of mucopolysaccharidoses in developing countries: A low cost and easy execution approach
Orazio Gabrielli, Lucia Zampini, Chiara Monachesi, et al.
Genes
|
June 26, 2026
Expanding the Mutational Spectrum of <i>ACADVL</i>: Integrative Characterization of the p.Ser72Phe Variant in Very Long-Chain Acyl-CoA Dehydrogenase Deficiency
Francesca Dinatolo, Lucia D'Antona, Radha Procopio, et al.
Journal of Endocrinological Investigation
|
June 6, 2009
17beta-Hydroxysteroid dehydrogenase-3 deficiency: from pregnancy to adolescence
S Bertelloni, A Balsamo, L Giordani, et al.
AJNR. American Journal of Neuroradiology
|
October 21, 2017
Redefining the Pulvinar Sign in Fabry Disease
S Cocozza, C Russo, A Pisani, et al.
Tumori
|
August 1, 1981
Results of the Italian interlaboratory quality control program for estradiol receptor assay
S Fumero, G P Berruto, D Pelizzola, et al.
Page
of 35