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Oncotarget
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June 26, 2018
A pilot study of circulating microRNAs as potential biomarkers of Fabry disease
Giuseppe Cammarata, Simone Scalia, Paolo Colomba, et al.
Haematologica
|
May 10, 2007
Loss of heterozygosity in acute leukemia: evidence of frequent submicroscopic deletions
Cecilia Agueli, Rosaria Basiricò, Francesco Fabbiano, et al.
Oncotarget
|
March 1, 2018
Fabry disease and multiple sclerosis misdiagnosis: the role of family history and neurological signs
Paolo Colomba, Carmela Zizzo, Riccardo Alessandro, et al.
Biomed Research International
|
May 16, 2015
High variability of Fabry disease manifestations in an extended Italian family
Giuseppe Cammarata, Pasquale Fatuzzo, Margherita Stefania Rodolico, et al.
Kidney & Blood Pressure Research
|
August 13, 2018
Systematic DNA Study for Fabry Disease in the End Stage Renal Disease Patients from a Southern Italy Area
Carmela Zizzo, Alessandra Testa, Paolo Colomba, et al.
Gene
|
December 23, 2015
Molecular and clinical studies in five index cases with novel mutations in the GLA gene
Carmela Zizzo, Ines Monte, Antonio Pisani, et al.
Biomedicines
|
August 26, 2022
Generation and Characterization of Novel iPSC Lines from a Portuguese Family Bearing Heterozygous and Homozygous <i>GRN</i> Mutations
Ana Rafaela Oliveira, Solange Martins, Giuseppe Cammarata, et al.
American Journal of Hematology
|
June 26, 2010
14q32/miRNA clusters loss of heterozygosity in acute lymphoblastic leukemia is associated with up-regulation of BCL11a
Cecilia Agueli, Giuseppe Cammarata, Domenico Salemi, et al.
Leukemia Research
|
June 10, 2015
miR-155 regulative network in FLT3 mutated acute myeloid leukemia
Domenico Salemi, Giuseppe Cammarata, Cecilia Agueli, et al.
Aging
|
August 4, 2020
Pompe disease: pathogenesis, molecular genetics and diagnosis
Simona Taverna, Giuseppe Cammarata, Paolo Colomba, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 28) with videos related to
Sort By:
Page
of 3
Oncotarget
|
June 26, 2018
A pilot study of circulating microRNAs as potential biomarkers of Fabry disease
Giuseppe Cammarata, Simone Scalia, Paolo Colomba, et al.
Haematologica
|
May 10, 2007
Loss of heterozygosity in acute leukemia: evidence of frequent submicroscopic deletions
Cecilia Agueli, Rosaria Basiricò, Francesco Fabbiano, et al.
Oncotarget
|
March 1, 2018
Fabry disease and multiple sclerosis misdiagnosis: the role of family history and neurological signs
Paolo Colomba, Carmela Zizzo, Riccardo Alessandro, et al.
Biomed Research International
|
May 16, 2015
High variability of Fabry disease manifestations in an extended Italian family
Giuseppe Cammarata, Pasquale Fatuzzo, Margherita Stefania Rodolico, et al.
Kidney & Blood Pressure Research
|
August 13, 2018
Systematic DNA Study for Fabry Disease in the End Stage Renal Disease Patients from a Southern Italy Area
Carmela Zizzo, Alessandra Testa, Paolo Colomba, et al.
Gene
|
December 23, 2015
Molecular and clinical studies in five index cases with novel mutations in the GLA gene
Carmela Zizzo, Ines Monte, Antonio Pisani, et al.
Biomedicines
|
August 26, 2022
Generation and Characterization of Novel iPSC Lines from a Portuguese Family Bearing Heterozygous and Homozygous <i>GRN</i> Mutations
Ana Rafaela Oliveira, Solange Martins, Giuseppe Cammarata, et al.
American Journal of Hematology
|
June 26, 2010
14q32/miRNA clusters loss of heterozygosity in acute lymphoblastic leukemia is associated with up-regulation of BCL11a
Cecilia Agueli, Giuseppe Cammarata, Domenico Salemi, et al.
Leukemia Research
|
June 10, 2015
miR-155 regulative network in FLT3 mutated acute myeloid leukemia
Domenico Salemi, Giuseppe Cammarata, Cecilia Agueli, et al.
Aging
|
August 4, 2020
Pompe disease: pathogenesis, molecular genetics and diagnosis
Simona Taverna, Giuseppe Cammarata, Paolo Colomba, et al.
Page
of 3