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Diagnosis and management of iron deficiency in children with or without anemia: consensus recommendations of the SPOG Pediatric Hematology Working Group
Author / Creator:Mattiello Veneranda ; Schmugge, Markus ; Hengartner Heinz ; von der Weid Nicolas ; Renella Raffaele
Publisher:Berlin: Springer Nature B.V
Journal title:European journal of pediatrics, 2020-04, Vol.179 (4), p.527-545
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The landscape of pediatric Diamond-Blackfan anemia in Switzerland: genotype and phenotype characteristics
Author / Creator:Vogel, Nicole ; Schmugge, Markus ; Renella Raffaele ; Waespe Nicolas ; Hengartner Heinz
Publisher:Berlin: Springer Nature B.V
Journal title:European journal of pediatrics, 2021-12, Vol.180 (12), p.3581-3585
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Parental occupational exposure to pesticides and risk of childhood cancer in Switzerland: a census-based cohort study
Author / Creator:Coste, Astrid ; Bailey, Helen D. ; Kartal-Kaess, Mutlu ; Renella, Raffaele ; Berthet, Aurélie ; Spycher, Ben D.
Publisher:England: BioMed Central Ltd
Journal title:BMC cancer, 2020-08, Vol.20 (1), p.819-11, Article 819
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Multiple neonicotinoids in children’s cerebro-spinal fluid, plasma, and urine
Author / Creator:Laubscher, Bernard ; Diezi, Manuel ; Renella, Raffaele ; Mitchell, Edward A. D. ; Aebi, Alexandre ; Mulot, Matthieu ; Glauser, Gaëtan
Publisher:England: BioMed Central Ltd
Journal title:Environmental health, 2022-01, Vol.21 (1), p.10-9, Article 10
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EWS-WT1 fusion isoforms establish oncogenic programs and therapeutic vulnerabilities in desmoplastic small round cell tumors
Author / Creator:Boulay, Gaylor ; Broye, Liliane C. ; Dong, Rui ; Iyer, Sowmya ; Sanalkumar, Rajendran ; Xing, Yu-Hang ; Buisson, Rémi ; Rengarajan, Shruthi ; Naigles, Beverly ; Duc, Benoît ; Volorio, Angela ; Awad, Mary E. ; Renella, Raffaele ; Chebib, Ivan ; Nielsen, G. Petur ; Choy, Edwin ; Cote, Gregory M. ; Zou, Lee ; Letovanec, Igor ; Stamenkovic, Ivan ; Rivera, Miguel N. ; Riggi, Nicolò
Publisher:London: Nature Publishing Group UK
Journal title:Nature communications, 2024-08, Vol.15 (1), p.7460-17, Article 7460
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CIC-DUX4 Chromatin Profiling Reveals New Epigenetic Dependencies and Actionable Therapeutic Targets in CIC-Rearranged Sarcomas
Author / Creator:Bakaric, Arnaud ; Cironi, Luisa ; Praz, Viviane ; Sanalkumar, Rajendran ; Broye, Liliane C. ; Favre-Bulle, Kerria ; Letovanec, Igor ; Digklia, Antonia ; Renella, Raffaele ; Stamenkovic, Ivan ; Ott, Christopher J. ; Nakamura, Takuro ; Antonescu, Cristina R. ; Rivera, Miguel N. ; Riggi, Nicolò
Publisher:Switzerland: MDPI AG
Journal title:Cancers, 2024-01, Vol.16 (2), p.457
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TWIST1 expression is associated with high-risk neuroblastoma and promotes primary and metastatic tumor growth
Author / Creator:Sepporta, Maria-Vittoria ; Praz, Viviane ; Balmas Bourloud, Katia ; Joseph, Jean-Marc ; Jauquier, Nicolas ; Riggi, Nicolò ; Nardou-Auderset, Katya ; Petit, Audrey ; Scoazec, Jean-Yves ; Sartelet, Hervé ; Renella, Raffaele ; Mühlethaler-Mottet, Annick
Publisher:London: Nature Publishing Group UK
Journal title:Communications biology, 2022-01, Vol.5 (1), p.42-17, Article 42
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Generation of bivalent chromatin domains during cell fate decisions
Author / Creator:De Gobbi, Marco ; Garrick, David ; Lynch, Magnus ; Vernimmen, Douglas ; Hughes, Jim R ; Goardon, Nicolas ; Luc, Sidinh ; Lower, Karen M ; Sloane-Stanley, Jacqueline A ; Pina, Cristina ; Soneji, Shamit ; Renella, Raffaele ; Enver, Tariq ; Taylor, Stephen ; Jacobsen, Sten Eirik W ; Vyas, Paresh ; Gibbons, Richard J ; Higgs, Douglas R
Publisher:England: BioMed Central Ltd
Journal title:Epigenetics & chromatin, 2011-06, Vol.4 (1), p.9-9, Article 9
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Risk of cancer in patients with polycystic kidney disease
Author / Creator:Cachat, Francois ; Renella, Raffaele
Publisher:England: Elsevier Ltd
Journal title:The lancet oncology, 2016-11, Vol.17 (11), p.e474-e474
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Lineage-specific BCL11A knockdown circumvents toxicities and reverses sickle phenotype
Author / Creator:Brendel, Christian ; Guda, Swaroopa ; Renella, Raffaele ; Bauer, Daniel E. ; Canver, Matthew C. ; Kim, Young-Jo ; Heeney, Matthew M. ; Klatt, Denise ; Fogel, Jonathan ; Milsom, Michael D. ; Orkin, Stuart H. ; Gregory, Richard I. ; Williams, David A.
Publisher:United States: American Society for Clinical Investigation
Journal title:The Journal of clinical investigation, 2016-10, Vol.126 (10), p.3868-3878
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PSTPIP1-Associated Myeloid-Related Proteinemia Inflammatory (PAMI) Syndrome: A Systematic Review
Author / Creator:Mejbri, Manel ; Renella, Raffaele ; Candotti, Fabio ; Jaques, Cecile ; Holzinger, Dirk ; Hofer, Michael ; Theodoropoulou, Katerina
Publisher:Switzerland: MDPI AG
Journal title:Genes, 2023-08, Vol.14 (8), p.1655
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miRNA-embedded shRNAs for Lineage-specific BCL11A Knockdown and Hemoglobin F Induction
Author / Creator:Guda, Swaroopa ; Brendel, Christian ; Renella, Raffaele ; Du, Peng ; Bauer, Daniel E ; Canver, Matthew C ; Grenier, Jennifer K ; Grimson, Andrew W ; Kamran, Sophia C ; Thornton, James ; de Boer, Helen ; Root, David E ; Milsom, Michael D ; Orkin, Stuart H ; Gregory, Richard I ; Williams, David A
Publisher:United States: Elsevier Inc
Journal title:Molecular therapy, 2015-09, Vol.23 (9), p.1465-1474
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Opportunities and challenges in the immunological therapy of pediatric malignancy: a concise snapshot
Author / Creator:Ceppi, Francesco ; Beck-Popovic, Maja ; Bourquin, Jean-Pierre ; Renella, Raffaele
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:European journal of pediatrics, 2017-09, Vol.176 (9), p.1163-1172
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Aldehyde dehydrogenase activity plays a Key role in the aggressive phenotype of neuroblastoma
Author / Creator:Flahaut, Marjorie ; Jauquier, Nicolas ; Chevalier, Nadja ; Nardou, Katya ; Balmas Bourloud, Katia ; Joseph, Jean-Marc ; Barras, David ; Widmann, Christian ; Gross, Nicole ; Renella, Raffaele ; Mühlethaler-Mottet, Annick
Publisher:England: BioMed Central Ltd
Journal title:BMC cancer, 2016-10, Vol.16 (1), p.781-781, Article 781
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Genetic deficiency of tartrate-resistant acid phosphatase associated with skeletal dysplasia, cerebral calcifications and autoimmunity
Author / Creator:Lausch, Ekkehart ; Janecke, Andreas ; Bros, Matthias ; Trojandt, Stefanie ; Alanay, Yasemin ; De Laet, Corinne ; Hübner, Christian A ; Meinecke, Peter ; Nishimura, Gen ; Matsuo, Mari ; Hirano, Yoshiko ; Tenoutasse, Sylvie ; Kiss, Andrea ; Machado Rosa, Rafael Fabiano ; Unger, Sharon L ; Renella, Raffaele ; Bonafé, Luisa ; Spranger, Jürgen ; Unger, Sheila ; Zabel, Bernhard ; Superti-Furga, Andrea
Publisher:New York: Nature Publishing Group US
Journal title:Nature genetics, 2011-02, Vol.43 (2), p.132-137
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314. Mathematical Modeling of Erythrocyte Chimerism Informs Clinical Strategies for Sickle Cell Disease
Author / Creator:Altrock, Philipp M. ; Brendel, Christian ; Renella, Raffaele ; Orkin, Stuart H. ; Williams, David A. ; Michor, Franziska
Publisher:Elsevier Inc
Journal title:Molecular therapy, 2016-05, Vol.24, p.S126-S127
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Genetic and functional insights into CDA-I prevalence and pathogenesis
Author / Creator:Olijnik, Aude-Anais ; Roy, Noémi B A ; Scott, Caroline ; Marsh, Joseph A ; Brown, Jill ; Lauschke, Karin ; Ask, Katrine ; Roberts, Nigel ; Downes, Damien J ; Brolih, Sanja ; Johnson, Errin ; Xella, Barbara ; Proven, Melanie ; Hipkiss, Ria ; Ryan, Kate ; Frisk, Per ; Mäkk, Johan ; Stattin, Eva-Lena Maria ; Sadasivam, Nandini ; McIlwaine, Louisa ; Hill, Quentin A ; Renella, Raffaele ; Hughes, Jim R ; Gibbons, Richard J ; Groth, Anja ; McHugh, Peter J ; Higgs, Douglas R ; Buckle, Veronica J ; Babbs, Christian
Publisher:England: BMJ Publishing Group LTD
Journal title:Journal of medical genetics, 2021-03, Vol.58 (3), p.185-195
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282. Circumventing Hematopoietic Toxicities and Reversing Sickle Phenotype by Lineage-Specific BCL11A Knock Down and γ-Globin Induction
Author / Creator:Brendel, Christian ; Guda, Swaroopa ; Renella, Raffaele ; Bauer, Daniel E. ; Canver, Matthew C. ; Kim, Young-Jo ; Heeney, Matthew M. ; Klatt, Denise ; Fogel, Jonathan ; Milsom, Michael D. ; Orkin, Stuart H. ; Gregory, Richard I. ; Williams, David A.
Publisher:Elsevier Inc
Journal title:Molecular therapy, 2016-05, Vol.24, p.S113-S113
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Stem Cell Gene Therapy for Fanconi Anemia: Report from the 1st International Fanconi Anemia Gene Therapy Working Group Meeting
Author / Creator:Tolar, Jakub ; Adair, Jennifer E ; Antoniou, Michael ; Bartholomae, Cynthia C ; Becker, Pamela S ; Blazar, Bruce R ; Bueren, Juan ; Carroll, Thomas ; Cavazzana-Calvo, Marina ; Clapp, D Wade ; Dalgleish, Robert ; Galy, Anne ; Gaspar, H Bobby ; Hanenberg, Helmut ; Von Kalle, Christof ; Kiem, Hans-Peter ; Lindeman, Dirk ; Naldini, Luigi ; Navarro, Susana ; Renella, Raffaele ; Rio, Paula ; Sevilla, Julián ; Schmidt, Manfred ; Verhoeyen, Els ; Wagner, John E ; Williams, David A ; Thrasher, Adrian J
Publisher:United States: Elsevier Inc
Journal title:Molecular therapy, 2011-07, Vol.19 (7), p.1193-1198
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Childhood extraordinary daytime urinary frequency—a case series and a systematic literature review
Author / Creator:Bergmann, Manuela ; Corigliano, Teresa ; Ataia, Iris ; Renella, Raffaele ; Simonetti, Giacomo D. ; Bianchetti, Mario G. ; von Vigier, Rodo O.
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Pediatric nephrology (Berlin, West), 2009-04, Vol.24 (4), p.789-795
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Showing 1 to 20 of 25 results

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Diagnosis and management of iron deficiency in children with or without anemia: consensus recommendations of the SPOG Pediatric Hematology Working Group

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The landscape of pediatric Diamond-Blackfan anemia in Switzerland: genotype and phenotype characteristics

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Parental occupational exposure to pesticides and risk of childhood cancer in Switzerland: a census-based cohort study

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Multiple neonicotinoids in children’s cerebro-spinal fluid, plasma, and urine

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EWS-WT1 fusion isoforms establish oncogenic programs and therapeutic vulnerabilities in desmoplastic small round cell tumors

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CIC-DUX4 Chromatin Profiling Reveals New Epigenetic Dependencies and Actionable Therapeutic Targets in CIC-Rearranged Sarcomas

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TWIST1 expression is associated with high-risk neuroblastoma and promotes primary and metastatic tumor growth

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Generation of bivalent chromatin domains during cell fate decisions

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Risk of cancer in patients with polycystic kidney disease

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Lineage-specific BCL11A knockdown circumvents toxicities and reverses sickle phenotype

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PSTPIP1-Associated Myeloid-Related Proteinemia Inflammatory (PAMI) Syndrome: A Systematic Review

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miRNA-embedded shRNAs for Lineage-specific BCL11A Knockdown and Hemoglobin F Induction

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Opportunities and challenges in the immunological therapy of pediatric malignancy: a concise snapshot

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Aldehyde dehydrogenase activity plays a Key role in the aggressive phenotype of neuroblastoma

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Genetic deficiency of tartrate-resistant acid phosphatase associated with skeletal dysplasia, cerebral calcifications and autoimmunity

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314. Mathematical Modeling of Erythrocyte Chimerism Informs Clinical Strategies for Sickle Cell Disease

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Genetic and functional insights into CDA-I prevalence and pathogenesis

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282. Circumventing Hematopoietic Toxicities and Reversing Sickle Phenotype by Lineage-Specific BCL11A Knock Down and γ-Globin Induction

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Stem Cell Gene Therapy for Fanconi Anemia: Report from the 1st International Fanconi Anemia Gene Therapy Working Group Meeting

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Childhood extraordinary daytime urinary frequency—a case series and a systematic literature review

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