Ohcanbohtosat - Immacolata Andolfo

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  1. 1
    Advances in understanding the pathogenesis of red cell membrane disorders

    Advances in understanding the pathogenesis of red cell membrane disorders Dahkki Achille Iolascon, Immacolata Andolfo, Roberta Russo

    Almmustuhtton 2019
    Viečča ollesdeavstta Viečča ollesdeavstta
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  2. 2
    Congenital dyserythropoietic anemias

    Congenital dyserythropoietic anemias Dahkki Achille Iolascon, Immacolata Andolfo, Roberta Russo

    Almmustuhtton 2020
    Viečča ollesdeavstta Viečča ollesdeavstta
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  3. 3
    New insights on hereditary erythrocyte membrane defects

    New insights on hereditary erythrocyte membrane defects Dahkki Immacolata Andolfo, Roberta Russo, Antonella Gambale, Achille Iolascon

    Almmustuhtton 2016
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  4. 4
    Hereditary stomatocytosis: An underdiagnosed condition

    Hereditary stomatocytosis: An underdiagnosed condition Dahkki Immacolata Andolfo, Roberta Russo, Antonella Gambale, Achille Iolascon

    Almmustuhtton 2017
    Viečča ollesdeavstta Viečča ollesdeavstta
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  5. 5
    Genetic Analysis of the Coronavirus SARS-CoV-2 Host Protease TMPRSS2 in Different Populations

    Genetic Analysis of the Coronavirus SARS-CoV-2 Host Protease TMPRSS2 in Different Populations Dahkki Roberta Russo, Immacolata Andolfo, Vito Alessandro Lasorsa, Achille Iolascon, Mario Capasso

    Almmustuhtton 2020
    Viečča ollesdeavstta Viečča ollesdeavstta
    Artigo
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  6. 6
    Genetics and Genomics Approaches for Diagnosis and Research Into Hereditary Anemias

    Genetics and Genomics Approaches for Diagnosis and Research Into Hereditary Anemias Dahkki Roberta Russo, Roberta Marra, Barbara Eleni Rosato, Achille Iolascon, Immacolata Andolfo

    Almmustuhtton 2020
    Viečča ollesdeavstta Viečča ollesdeavstta
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  7. 7
    Genotype-phenotype correlation and risk stratification in a cohort of 123 hereditary stomatocytosis patients

    Genotype-phenotype correlation and risk stratification in a cohort of 123 hereditary stomatocytosis patients Dahkki Immacolata Andolfo, Roberta Russo, Barbara Eleni Rosato, Francesco Manna, Antonella Gambale, Carlo Brugnara, Achille Iolascon

    Almmustuhtton 2018
    Viečča ollesdeavstta Viečča ollesdeavstta
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  8. 8
    Regulation of divalent metal transporter 1 (DMT1) non-IRE isoform by the microRNA Let-7d in erythroid cells

    Regulation of divalent metal transporter 1 (DMT1) non-IRE isoform by the microRNA Let-7d in erythroid cells Dahkki Immacolata Andolfo, Luigia De Falco, Ramazan Aşçı, Roberta Russo, Simona Colucci, Marisa Gorrese, Massimo Zollo, Achille Iolascon

    Almmustuhtton 2010
    Viečča ollesdeavstta Viečča ollesdeavstta
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  9. 9
    Gain‐of‐function mutations in PIEZO1 directly impair hepatic iron metabolism via the inhibition of the BMP/SMADs pathway

    Gain‐of‐function mutations in PIEZO1 directly impair hepatic iron metabolism via the inhibition of the BMP/SMADs pathway Dahkki Immacolata Andolfo, Barbara Eleni Rosato, Francesco Manna, Gianluca De Rosa, Roberta Marra, Antonella Gambale, Domenico Girelli, Roberta Russo, Achille Iolascon

    Almmustuhtton 2019
    Viečča ollesdeavstta Viečča ollesdeavstta
    Artigo
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  10. 10
    A role of PIEZO1 in iron metabolism in mice and humans

    A role of PIEZO1 in iron metabolism in mice and humans Dahkki Shang Ma, Adrienne E. Dubin, Yunxiao Zhang, Seyed Ali Reza Mousavi, Yu Wang, Adam Coombs, Meaghan Loud, Immacolata Andolfo, Ardem Patapoutian

    Almmustuhtton 2021
    Viečča ollesdeavstta
    Artigo
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  11. 11
    Novel Gardos channel mutations linked to dehydrated hereditary stomatocytosis (xerocytosis)

    Novel Gardos channel mutations linked to dehydrated hereditary stomatocytosis (xerocytosis) Dahkki Immacolata Andolfo, Roberta Russo, Francesco Manna, Boris E. Shmukler, Antonella Gambale, Giuseppina Vitiello, Gianluca De Rosa, Carlo Brugnara, Seth L. Alper, L. Michael Snyder, Achille Iolascon

    Almmustuhtton 2015
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  12. 12
    Dietary -3 fatty acids protect against vasculopathy in a transgenic mouse model of sickle cell disease

    Dietary -3 fatty acids protect against vasculopathy in a transgenic mouse model of sickle cell disease Dahkki Brian T. Kalish, Alessandro Mattè, Immacolata Andolfo, Achille Iolascon, Olga K. Weinberg, Alessandra Ghigo, James Cimino, Angela Siciliano, Emilio Hirsch, Enrica Federti, Mark Puder, Carlo Brugnara, Lucia De Franceschi

    Almmustuhtton 2015
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  13. 13
    Missense mutations in the ABCB6 transporter cause dominant familialpseudohyperkalemia

    Missense mutations in the ABCB6 transporter cause dominant familialpseudohyperkalemia Dahkki Immacolata Andolfo, Seth L. Alper, J. Delaunay, Carla Auriemma, Roberta Russo, Roberta Asci, Maria Rosaria Esposito, Alok K. Sharma, Boris E. Shmukler, Carlo Brugnara, Lucia De Franceschi, Achille Iolascon

    Almmustuhtton 2012
    Viečča ollesdeavstta Viečča ollesdeavstta
    Artigo
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  14. 14
    Increased Red Cell KCNN4 Activity in Sporadic Hereditary Xerocytosis Associated With Enhanced Single Channel Pressure Sensitivity of PIEZO1 Mutant V598M

    Increased Red Cell KCNN4 Activity in Sporadic Hereditary Xerocytosis Associated With Enhanced Single Channel Pressure Sensitivity of PIEZO1 Mutant V598M Dahkki Radhakrishnan Gnanasambandam, Alicia Rivera, David H. Vandorpe, Boris E. Shmukler, Carlo Brugnara, L. Michael Snyder, Immacolata Andolfo, Achille Iolascon, Paulo Augusto Achucarro Silveira, Nelson Hamerschlak, Philip A. Gottlieb, Seth L. Alper

    Almmustuhtton 2018
    Viečča ollesdeavstta
    Carta
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  15. 15
    Multi‐gene panel testing improves diagnosis and management of patients with hereditary anemias

    Multi‐gene panel testing improves diagnosis and management of patients with hereditary anemias Dahkki Roberta Russo, Immacolata Andolfo, Francesco Manna, Antonella Gambale, Roberta Marra, Barbara Eleni Rosato, Paola Caforio, Valeria Maria Pinto, Piero Pignataro, Kottayam Radhakrishnan, Şule Ünal, Giovanna Tomaiuolo, Gian Luca Forni, Achille Iolascon

    Almmustuhtton 2018
    Viečča ollesdeavstta Viečča ollesdeavstta
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  16. 16
    The micro-RNA 199b-5p regulatory circuit involves Hes1, CD15, and epigenetic modifications in medulloblastoma

    The micro-RNA 199b-5p regulatory circuit involves Hes1, CD15, and epigenetic modifications in medulloblastoma Dahkki Immacolata Andolfo, Lucia Liguori, Pasqualino de Antonellis, Emilio Cusanelli, Federica Marinaro, Francesca Pistollato, Livia Garzia, Gennaro De Vita, Giuseppe Petrosino, Benedetta Accordi, Roberta Migliorati, Giuseppe Basso, Achille Iolascon, Giuseppe Cinalli, Massimo Zollo

    Almmustuhtton 2012
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    Artigo
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  17. 17
    Complex Modes of Inheritance in Hereditary Red Blood Cell Disorders: A Case Series Study of 155 Patients

    Complex Modes of Inheritance in Hereditary Red Blood Cell Disorders: A Case Series Study of 155 Patients Dahkki Immacolata Andolfo, Stefania Martone, Barbara Eleni Rosato, Roberta Marra, Antonella Gambale, Gian Luca Forni, Valeria Maria Pinto, Magnus Göransson, Vasiliki Papadopoulou, Mathilde Gavillet, Mohsen Saleh Elalfy, Antonella Panarelli, Giovanna Tomaiuolo, Achille Iolascon, Roberta Russo

    Almmustuhtton 2021
    Viečča ollesdeavstta Viečča ollesdeavstta
    Artigo
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  18. 18
    Erythrocyte ion content and dehydration modulate maximal Gardos channel activity in KCNN4 V282M/+ hereditary xerocytosis red cells

    Erythrocyte ion content and dehydration modulate maximal Gardos channel activity in KCNN4 V282M/+ hereditary xerocytosis red cells Dahkki Alicia Rivera, David H. Vandorpe, Boris E. Shmukler, Immacolata Andolfo, Achille Iolascon, Natasha M. Archer, Estela Shabani, Michael Auerbach, Nelson Hamerschlak, James P. Morton, Jay G. Wohlgemuth, Carlo Brugnara, L. Michael Snyder, Seth L. Alper

    Almmustuhtton 2019
    Viečča ollesdeavstta Viečča ollesdeavstta
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  19. 19
    Hereditary xerocytosis revisited

    Hereditary xerocytosis revisited Dahkki Natasha M. Archer, Boris E. Shmukler, Immacolata Andolfo, David H. Vandorpe, Radhakrishnan Gnanasambandam, John M. Higgins, Alicia Rivera, Mark D. Fleming, Frederick Sachs, Philip A. Gottlieb, Achille Iolascon, Carlo Brugnara, Seth L. Alper, David G. Nathan

    Almmustuhtton 2014
    Viečča ollesdeavstta Viečča ollesdeavstta
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  20. 20
    Recommendations for diagnosis, treatment, and prevention of iron deficiency and iron deficiency anemia

    Recommendations for diagnosis, treatment, and prevention of iron deficiency and iron deficiency anemia Dahkki Achille Iolascon, Immacolata Andolfo, Roberta Russo, Mayka Sánchez, Fabiana Busti, Dorine W. Swinkels, Patricia Martínez, Rayan Bou‐Fakhredin, Martina U. Muckenthaler, Şule Ünal, Graça Porto, Tomas Ganz, Antonis Kattamis, Lucia De Franceschi, Maria Domenica Cappellini, Malcolm G. Munro, Alì Taher

    Almmustuhtton 2024
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    Artigo
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