Raffaele Renella

Publications | Mémoires et thèses

La recherche avancée est accessible via Serval

Les publications peuvent être gérées en accédant à Serval via MyUnil


78 publications

En préparation
 
Modelling erythropoiesis in congenital dyserythropoietic anaemia type I (CDA-I)
Scott Caroline, Downes Damien J., Brown Jill M., Babbs Christian, Olijnik Aude-Anais, Gosden Matthew, Beagrie Robert, Schwessinger Ron, Fisher Christopher A., Rose Anna et al..
[DOI][serval:BIB_40F5982ECB5F]
Sous presse
Residential exposure to solar ultraviolet radiation and risk of childhood hematological malignancies in Switzerland: A census-based cohort study.
Coste A., Kreis C., Backes C., Bulliard J.L., Folly C., Brack E., Renella R., Vernez D., Spycher B.D., SNC study group International journal of cancer. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_8731CE3456C6]
2024
EWS-WT1 fusion isoforms establish oncogenic programs and therapeutic vulnerabilities in desmoplastic small round cell tumors.
Boulay G., Broye L.C., Dong R., Iyer S., Sanalkumar R., Xing Y.H., Buisson R., Rengarajan S., Naigles B., Duc B. et al., 2024/08/28. Nature communications, 15 (1) p. 7460. Peer-reviewed.
[URN][DOI][Pmid][serval:BIB_C8226720A9A3]
 
An atypical form of 60S ribosomal subunit in Diamond-Blackfan anemia linked to RPL17 variants.
Fellmann F., Saunders C., O'Donohue M.F., Reid D.W., McFadden K.A., Montel-Lehry N., Yu C., Fang M., Zhang J., Royer-Bertrand B. et al., 2024/08/01. JCI insight, 9 (17). Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_AF432CACC4A3]
Preclinical spheroid models identify BMX as a therapeutic target for metastatic MYCN nonamplified neuroblastoma.
Sundaramoorthy S., Colombo D.F., Sanalkumar R., Broye L., Balmas Bourloud K., Boulay G., Cironi L., Stamenkovic I., Renella R., Kuttler F. et al., 2024/07/22. JCI insight, 9 (14) pp. e169647. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_4CD788654EA8]
 
Assessment of Dietary Iron Intake and Sources in Early Childhood in a Nationally Representative Cross-Sectional Survey.
Chouraqui J.P., Renella R., Turck D., 2024/07. Journal of the Academy of Nutrition and Dietetics, 124 (7) pp. 823-832.e1. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_7356E59A976B]
Characteristics and treatment of acute myeloid neoplasms with cutaneous involvement in infants up to 6 months of age: A retrospective study.
Renaud J., Goemans B.F., Locatelli F., Pigazzi M., Redmond S., Kuehni C.E., Destaillats A., Alonzo T.A., Gerbing R.B., Gamis A. et al., 2024/07. Pediatric blood & cancer, 71 (7) pp. e31006. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_CCB2557653E6]
CIC-DUX4 Chromatin Profiling Reveals New Epigenetic Dependencies and Actionable Therapeutic Targets in CIC-Rearranged Sarcomas.
Bakaric A., Cironi L., Praz V., Sanalkumar R., Broye L.C., Favre-Bulle K., Letovanec I., Digklia A., Renella R., Stamenkovic I. et al., 2024/01/21. Cancers, 16 (2) p. 457. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_6DD2EB3D2A00]
2023
 
The Association of SEPTIN6 Mutations with Pediatric Myelodysplasia.
Mohamad Safa F, McGuinness Meaghan, Casirati Gabriele, Harris Chad Everett, Renella Raffaele, Genovese Pietro, Allenspach Eric, Williams David A., 2023/11/02., 65th ASH Annual Meeting December 9-12, 2023 pp. 1846-1846 dans Blood.
[DOI][WoS][serval:BIB_D0EE733437AA]
PSTPIP1-Associated Myeloid-Related Proteinemia Inflammatory (PAMI) Syndrome: A Systematic Review.
Mejbri M., Renella R., Candotti F., Jaques C., Holzinger D., Hofer M., Theodoropoulou K., 2023/08/19. Genes, 14 (8) p. 1655. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_E4AFB0AA68AA]
 
In vitro-transfusional model for red-blood-cell study: the advantage of lowering hematocrit.
Längst E., Crettaz D., Delobel J., Renella R., Bardyn M., Turcatti G., Tissot J.D., Prudent M., 2023/07. Blood transfusion = Trasfusione del sangue, 21 (4) pp. 277-288. Peer-reviewed.
[DOI][Pmid][serval:BIB_D2AB61FF2462]
Hematological variations in healthy participants exposed 2 h to propylene glycol ethers under controlled conditions.
Borgatta M., Wild P., Delobel J., Renella R., Hopf N.B., 2023/06/25. The Science of the total environment, 879 p. 162865. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_1E48EC62F766]
 
Predictive Factors for the Occurrence of Perioperative Complications in Pediatric Posterior Fossa Tumors.
Anetsberger S., Mellal A., Garvayo M., Diezi M., Perez M.H., Beck Popovic M., Renella R., Cossu G., Daniel R.T., Starnoni D. et al., 2023/04. World neurosurgery, 172 pp. e508-e516. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_5AC13C65A34A]
Highly connected 3D chromatin networks established by an oncogenic fusion protein shape tumor cell identity.
Sanalkumar R., Dong R., Lee L., Xing Y.H., Iyer S., Letovanec I., La Rosa S., Finzi G., Musolino E., Papait R. et al., 2023/03/31. Science advances, 9 (13) pp. eabo3789. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_5B801BAF4F3B]
2022
 
Mitapivat in adult patients with pyruvate kinase deficiency receiving regular transfusions (ACTIVATE-T): a multicentre, open-label, single-arm, phase 3 trial.
Glenthøj A., van Beers E.J., Al-Samkari H., Viprakasit V., Kuo KHM, Galactéros F., Chonat S., Porter J., Zagadailov E., Xu R. et al., 2022/10. The Lancet. Haematology, 9 (10) pp. e724-e732. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_F5567A16F49E]
 
Blood cells molecules and diseases in 2022: A fountain of youth.
Blanc L., Renella R., 2022/07. Blood cells, molecules & diseases, 95 p. 102665. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_5FEBF792AF55]
 
Functional impairment of erythropoiesis in Congenital Dyserythropoietic Anaemia type I arises at the progenitor level.
Scott C., Bartolovic K., Clark S.A., Waithe D., Hill Q.A., Okoli S., Renella R., Ryan K., Cahill M.R., Higgs D.R. et al., 2022/07. British journal of haematology, 198 (1) pp. e10-e14. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_5DA75C953320]
 
PASTEC - a prospective, single-center, randomized, cross-over trial of pure physical versus physical plus attentional training in children with cancer.
Fontana A., Matthey S., Mayor C., Dufour C., Destaillats A., Ballabeni P., Maeder S., Newman C.J., Beck Popovic M., Renella R. et al., 2022/05. Pediatric hematology and oncology, 39 (4) pp. 329-342. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_88C22ABD5AEF]
 
Mitapivat versus Placebo for Pyruvate Kinase Deficiency.
Al-Samkari H., Galactéros F., Glenthøj A., Rothman J.A., Andres O., Grace R.F., Morado-Arias M., Layton D.M., Onodera K., Verhovsek M. et al., 2022/04/14. The New England journal of medicine, 386 (15) pp. 1432-1442. Peer-reviewed.
[DOI][Pmid][serval:BIB_C3CD4D20DDE8]
TWIST1 expression is associated with high-risk neuroblastoma and promotes primary and metastatic tumor growth.
Sepporta M.V., Praz V., Balmas Bourloud K., Joseph J.M., Jauquier N., Riggi N., Nardou-Auderset K., Petit A., Scoazec J.Y., Sartelet H. et al., 2022/01/12. Communications biology, 5 (1) p. 42. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_2625E45392D6]
 
Multiple neonicotinoids in children's cerebro-spinal fluid, plasma, and urine.
Laubscher B., Diezi M., Renella R., Mitchell EAD, Aebi A., Mulot M., Glauser G., 2022/01/11. Environmental health, 21 (1) p. 10. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_B71E0F102843]
 
Congenital X-linked neutropenia with myelodysplasia and somatic tetraploidy due to a germline mutation in SEPT6.
Renella R., Gagne K., Beauchamp E., Fogel J., Perlov A., Sola M., Schlaeger T., Hofmann I., Shimamura A., Ebert B.L. et al., 2022/01/01. American journal of hematology, 97 (1) pp. 18-29. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_8C68E388AD85]
2021
 
The landscape of pediatric Diamond-Blackfan anemia in Switzerland: genotype and phenotype characteristics.
Vogel N., Schmugge M., Renella R., Waespe N., Hengartner H., Swiss Paediatric Oncology Group (SPOG) Hematology Working Group, 2021/12. European journal of pediatrics, 180 (12) pp. 3581-3585. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_1E57E07E08DE]
Recapitulation of erythropoiesis in congenital dyserythropoietic anaemia type I (CDA-I) identifies defects in differentiation and nucleolar abnormalities.
Scott C., Downes D.J., Brown J.M., Beagrie R., Olijnik A.A., Gosden M., Schwessinger R., Fisher C.A., Rose A., Ferguson DJP et al., 2021/11/01. Haematologica, 106 (11) pp. 2960-2970. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_C1E9ACEBC1DA]
 
Biomarkers for the central nervous system complications of sickle cell disease: are we there yet?
Renella R., 2021/09. Proteomics. Clinical applications, 15 (5) pp. e2100026. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_854A4A200CEA]
A live single-cell reporter assay links intratumor heterogeneity to metastatic proclivity in Ewing sarcoma.
Keskin T., Rucci B., Cornaz-Buros S., Martin P., Fusco C., Broye L., Cisarova K., Perez E.M., Letovanec I., La Rosa S. et al., 2021/07. Science advances, 7 (27) pp. eabf9394. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_16E18D416FE5]
 
Pediatric cranial osteoblastoma: Technical note of surgical treatment and review of the literature.
Garvayo M., Cossu G., Broome M., Maeder P., Renella R., Maduri R., Daniel R.T., Messerer M., 2021/07. Neuro-Chirurgie, 67 (4) pp. 383-390. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_04FD8998EC98]
 
Spontaneous Partial Remission in a Child With B-Lineage Acute Lymphoblastic Leukemia and Chickenpox: A Role For Acyclovir?
Chtioui H., Ceppi F., Renella R., Diezi M., 2021/07/01. Journal of pediatric hematology/oncology, 43 (5) pp. e711-e714. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_4886CE725DDF]
 
Immune deficiency, autoimmune disease and intellectual disability: A pleiotropic disorder caused by biallelic variants in the TPP2 gene.
Atallah I., Quinodoz M., Campos-Xavier B., Peter V.G., Fouriki A., Bonvin C., Bottani A., Kumps C., Angelini F., Bellutti Enders F. et al., 2021/06. Clinical genetics, 99 (6) pp. 780-788. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_ED69F497CA09]
 
Multiple Neonicotinoids in Children's Cerebro-Spinal Fluid, Plasma, and Urine
Laubscher Bernard, Diezi Manuel, Renella Raffaele, Mitchell Edward AD, Aebi Alexandre, Glauser Gaëtan, 2021/04/14. SSRN Electronic Journal.
[DOI][serval:BIB_5D5DF49185E0]
 
Cancer surveillance in children with Ollier Disease and Maffucci Syndrome.
Diezi M., Zambelli P.Y., Superti-Furga A., Unger S., Renella R., 2021/04. American journal of medical genetics. Part A, 185 (4) pp. 1338-1340. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_856FB220C691]
 
Comment on: Intravenous ferric carboxymaltose for iron deficiency anemia or iron deficiency without anemia after poor response to oral iron treatment: Benefits and risks in a cohort of 144 children and adolescents.
Schmugge M., Mattiello V., Hengartner H., von der Weid N., Renella R., SPOG Pediatric Hematology Working Group, 2021/03. Pediatric blood & cancer, 68 (3) pp. e28726. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_E4C27BBC82AD]
 
Genetic and functional insights into CDA-I prevalence and pathogenesis.
Olijnik A.A., Roy NBA, Scott C., Marsh J.A., Brown J., Lauschke K., Ask K., Roberts N., Downes D.J., Brolih S. et al., 2021/03. Journal of medical genetics, 58 (3) pp. 185-195. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_2D6024C777F7]
Cancer Care of Children, Adolescents and Adults With Autism Spectrum Disorders: Key Information and Strategies for Oncology Teams
Vuattoux Delphine, Colomer-Lahiguera Sara, Fernandez Pierre-Alain, Jequier Gygax Marine, Choucair Marie-Louise, Beck-Popovic Maja, Diezi Manuel, Manificat Sabine, Latifyan Sofiya, Ramelet Anne-Sylvie et al., 2021/01/19. Frontiers in Oncology, 10.
[URN][DOI][serval:BIB_E72708EF0DF5]
2020
 
Anémie hémolytique chronique dépendante de transfusions
Solari Daria, Grandoni Francesco, Alberio Lorenzo, Renella Raffaele, Gavillet Mathilde, 2020/10/20. Swiss Medical Forum ‒ Schweizerisches Medizin-Forum.
[DOI][serval:BIB_69B81D347A33]
Parental occupational exposure to pesticides and risk of childhood cancer in Switzerland: a census-based cohort study.
Coste A., Bailey H.D., Kartal-Kaess M., Renella R., Berthet A., Spycher B.D., 2020/08/28. BMC cancer, 20 (1) p. 819. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_6DEAB4C49276]
Published Erratum: LIN28B Underlies the Pathogenesis of a Subclass of Ewing Sarcoma.
Keskin T., Bakaric A., Waszyk P., Boulay G., Torsello M., Cornaz-Buros S., Chevalier N., Geiser T., Martin P., Volorio A. et al., 2020/04/14. Cell reports, 31 (2) p. 107539. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_69BFEDF2908B]
 
Diagnosis and management of iron deficiency in children with or without anemia: consensus recommendations of the SPOG Pediatric Hematology Working Group.
Mattiello V., Schmugge M., Hengartner H., von der Weid N., Renella R., SPOG Pediatric Hematology Working Group, 2020/04. European journal of pediatrics, 179 (4) pp. 527-545. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_5097C7EF4A64]
 
Erythropoiesis defect observed in STAT3 GOF patients with severe anemia.
Mauracher A.A., Eekels JJM, Woytschak J., van Drogen A., Bosch A., Prader S., Felber M., Heeg M., Opitz L., Trück J. et al., 2020/04. The Journal of allergy and clinical immunology, 145 (4) pp. 1297-1301. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_DD36B0C29E91]
LIN28B Underlies the Pathogenesis of a Subclass of Ewing Sarcoma LIN28B Control of EWS-FLI1 Stability.
Keskin T., Bakaric A., Waszyk P., Boulay G., Torsello M., Cornaz-Buros S., Chevalier N., Geiser T., Martin P., Volorio A. et al., 2020/03/31. Cell reports, 30 (13) pp. 4567-4583.e5. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_EAA705D7C5B5]
 
Perioperative care of children with sickle cell disease: A systematic review and clinical recommendations.
Schyrr F., Dolci M., Nydegger M., Canellini G., Andreu-Ullrich H., Joseph J.M., Diezi M., Cachat F., Rizzi M., Renella R., 2020/01. American journal of hematology, 95 (1) pp. 78-96. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_DDA65BE376E3]
2019
Carence en fer avec et sans anémie chez l’enfant : brève mise à jourpour le praticien [Iron deficiency with and without anemia in children: a brief update for caregivers]
Mattiello V., Sizonenko S., Baleydier F., Bernard F., Diezi M., Renella R., 2019/02/13. Revue medicale suisse, 15 (638) pp. 376-381. Peer-reviewed.
[URN][DOI][Pmid][serval:BIB_A7698B8BA7B8]
 
Progrès récents et orientations futures de la thérapie avec cellules CAR-T en oncologie pédiatrique [Recent advances and future directions in CAR-T cell therapy in pediatric oncology]
Ceppi F., Renella R., Diezi M., Ansari M., Duchosal M.A., Arber C., Kandalaft L., Coukos G., Beck-Popovic M., 2019/01/09. Revue medicale suisse, 15 (N° 632-633) pp. 85-91. Peer-reviewed.
[Pmid][serval:BIB_556228939270]
Expression of the Neuroblastoma-Associated ALK-F1174L Activating Mutation During Embryogenesis Impairs the Differentiation of Neural Crest Progenitors in Sympathetic Ganglia.
Vivancos Stalin L., Gualandi M., Schulte J.H., Renella R., Shakhova O., Mühlethaler-Mottet A., 2019. Frontiers in oncology, 9 p. 275. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_786ADE803D76]
2018
 
A key role for Rac and Pak signaling in neutrophil extracellular traps (NETs) formation defines a new potential therapeutic target.
Gavillet M., Martinod K., Renella R., Wagner D.D., Williams D.A., 2018/02. American journal of hematology, 93 (2) pp. 269-276. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_D6331230E133]
2017
 
Opportunities and challenges in the immunological therapy of pediatric malignancy: a concise snapshot.
Ceppi F., Beck-Popovic M., Bourquin J. P., Renella R., 2017/08. European journal of pediatrics, 176 (9) pp. 1163-1172.
[DOI][Pmid][serval:BIB_373A5D0422C1]
 
SGPP 17: Glycogen storage disease Ib and hereditary spherocytosis: the diagnostic challenge of concomittant rare diseases
Perez MM, Fodstad H., Nydegger A., Chehade H., Prsa M., Renella R., Ballhausen D., 2017. pp. 74S dans Swiss Medical Weekly.
[WoS][serval:BIB_DF1EE76765AB]
2016
 
Risk of cancer in patients with polycystic kidney disease.
Cachat F., Renella R., 2016/11. The Lancet. Oncology, 17 (11) pp. e474. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_5DED88B9D7F9]
 
Lineage-specific BCL11A knockdown circumvents toxicities and reverses sickle phenotype.
Brendel C., Guda S., Renella R., Bauer D.E., Canver M.C., Kim Y.J., Heeney M.M., Klatt D., Fogel J., Milsom M.D. et al., 2016/10/03. The Journal of clinical investigation, 126 (10) pp. 3868-3878. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_494CBB480254]
 
Mathematical modeling of erythrocyte chimerism informs genetic intervention strategies for sickle cell disease.
Altrock P.M., Brendel C., Renella R., Orkin S.H., Williams D.A., Michor F., 2016/09. American journal of hematology, 91 (9) pp. 931-937. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_F74D9FEBE15C]
Aldehyde dehydrogenase activity plays a Key role in the aggressive phenotype of neuroblastoma.
Flahaut M., Jauquier N., Chevalier N., Nardou K., Balmas Bourloud K., Joseph J.M., Barras D., Widmann C., Gross N., Renella R. et al., 2016. Bmc Cancer, 16 (1) p. 781. Peer-reviewed.
[URN][DOI][Pmid][serval:BIB_8AFB2FAA16EB]
 
Clinically-oriented proteomic investigation of sickle cell disease: Opportunities and challenges.
Renella R., 2016. Proteomics. Clinical Applications, 10 (8) pp. 816-830. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_04909EA2C5E2]
2015
 
miRNA-embedded shRNAs for Lineage-specific BCL11A Knockdown and Hemoglobin F Induction
Guda S., Brendel C., Renella R., Du P., Bauer D. E., Canver M. C., Grenier J. K., Grimson A. W., Kamran S. C., Thornton J. et al., 2015/09. Mol Ther, 23 (9) pp. 1465-74.
[DOI][Pmid][serval:BIB_243CCC0CC5DD]
 
Age-dependent pathophysiology of acute chest syndrome in children with sickle cell disease : ACS in children with SCD
Renella R., 2015/05. Am J Hematol, 90 (5) pp. 367-8.
[DOI][Pmid][serval:BIB_E58545B63B2B]
 
Flow cytometric assay for direct quantification of Neutrophil Extracellular Traps in blood samples. : Flow method for NETs detection
Gavillet Mathilde, Martinod Kimberly, Renella Raffaele, Harris Chad, Shapiro Nate I, Wagner Denisa D, Williams David A, 2015. American Journal of Hematology pp. n/a-n/a.
[DOI][serval:BIB_DAAA202C0A72]
2014
Can smaller-scale comprehensive cancer centers provide outstanding care in abdominal and thoracic pediatric solid tumor surgery? Results of a 14-year retrospective single-center analysis.
Joseph J.M., Farron A.M., Renella R., Gapany C., 2014/05. Annals of surgical oncology, 21 (5) pp. 1726-1731. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_184AFF8098CA]
 
Exploring the association of succinate dehydrogenase complex mutations with lymphoid malignancies
Renella R, Carnevale J, Schneider K A, Hornick J L, Rana H Q, Janeway K A, 2014. Familial Cancer pp. 1-5.
[DOI][serval:BIB_3920B9AF5819]
 
Genetic deletion of the GATA1‐regulated protein α‐synuclein reduces oxidative stress and nitric oxide synthase levels in mature erythrocytes : α-Synuclein in Murine Erythropoiesis
Renella Raffaele, Schlehe Julia S, Selkoe Dennis J, Williams David A, LaVoie Matthew J, 2014. American Journal of Hematology pp. n/a-n/a.
[DOI][serval:BIB_790BB4978C21]
2012
 
Fulminant thrombotic microangiopathy in Pediatrics: Where diagnostic and therapeutic dilemmas meet.
Renella Raffaele, Stickney Carolyn, Keswani Mahima, Mancuso Thomas, Casavant David, Ferguson Michael, Narla Anupama, 2012/08. American Journal of Hematology, 87 (8) pp. 816-818.
[DOI][serval:BIB_6CE8C7A10AD9]
2011
 
Stem cell gene therapy for fanconi anemia: report from the 1st international Fanconi anemia gene therapy working group meeting
Tolar J., Adair J. E., Antoniou M., Bartholomae C. C., Becker P. S., Blazar B. R., Bueren J., Carroll T., Cavazzana-Calvo M., Clapp D. W. et al., 2011/07. Mol Ther, 19 (7) pp. 1193-8.
[DOI][Pmid][serval:BIB_92790A6675A1]
 
Codanin-1 mutations in congenital dyserythropoietic anemia type 1 affect HP1{alpha} localization in erythroblasts
Renella R., Roberts N. A., Brown J. M., De Gobbi M., Bird L. E., Hassanali T., Sharpe J. A., Sloane-Stanley J., Ferguson D. J., Cordell J. et al., 2011. Blood, 117 (25) pp. 6928-38.
[DOI][Pmid][serval:BIB_2E2AE6437D51]
 
Generation of Bivalent Chromatin Domains During Cell Fate Decisions.
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 et al., 2011. Epigenetics & chromatin, 4 (1) p. 9.
[DOI][serval:BIB_27ACA281FADE]
 
Genetic deficiency of tartrate-resistant acid phosphatase associated with skeletal dysplasia, cerebral calcifications and autoimmunity.
Lausch E., Janecke A., Bros M., Trojandt S., Alanay Y., De Laet C., Hübner C.A., Meinecke P., Nishimura G., Matsuo M. et al., 2011. Nature Genetics, 43 (2) pp. 132-137.
[DOI][WoS][Pmid][serval:BIB_8559E4EB9D44]
2010
 
Progress in the congenital dyserythropoietic anemias: juicy but high-hanging fruits?
Renella R., 2010/12. American journal of hematology, 85 (12) pp. 913-914. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_3A14CD2D9CD7]
 
Frequency of congenital dyserythropoietic anemias in Europe.
Heimpel Hermann, Matuschek Andreas, Ahmed Momin, Bader-Meunier Brigitte, Colita Adriana, Delaunay Jean, Garçon Loïc, Gilsanz Florinda, Goede Jeroen, Högel Josef et al., 2010/07. European journal of haematology, 85 (1) pp. 20-25.
[serval:BIB_101D14CABCC9]
2009
 
Childhood extraordinary daytime urinary frequency-a case series and a systematic literature review.
Bergmann Manuela, Corigliano Teresa, Ataia Iris, Renella Raffaele, Simonetti Giacomo D, Bianchetti Mario G, von Vigier Rodo O, 2009/04. Pediatric nephrology (Berlin, Germany), 24 (4) pp. 789-795.
[DOI][serval:BIB_DDE9DC321DEF]
 
The congenital dyserythropoietic anemias.
Renella Raffaele, Wood William G, 2009/04. Hematology/oncology clinics of North America, 23 (2) pp. 283-306.
[DOI][serval:BIB_B3795DCD9D1A]
2007
 
Isolated extraordinary daytime urinary frequency of childhood: a case series of 26 children in Switzerland.
Corigliano T., Renella R., Robbiani A., Riavis M., Bianchetti M.G., 2007/09. Acta paediatrica, 96 (9) pp. 1347-1349. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_144695FA0217]
 
A new case of spondyloenchondrodysplasia with immune dysregulation confirms the pleiotropic nature of the disorder: comment on "A syndrome of immunodeficiency, autoimmunity, and spondylometaphyseal dysplasia" by M.L. Kulkarni, K. Baskar, and P.M. Kulkarni [2006].
Renella R., Superti-Furga A., 2007/06/15. American journal of medical genetics. Part A, 143A (12) pp. 1394-1395. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_30078E4E8050]
2006
 
Increased risk of acute myeloid leukaemia after treatment for breast cancer.
Renella R, Verkooijen H M, Fioretta G, Vlastos G, Kurtz J, Sappino A P, Schäfer P, Neyroud-Caspar I, Bouchardy C, 2006/10. Breast (Edinburgh, Scotland), 15 (5) pp. 614-619.
[DOI][serval:BIB_D0F68EC5F540]
 
Human leucocyte antigen-identical haematopoietic stem cell transplantation in major histocompatiblity complex class II immunodeficiency: reduced survival correlates with an increased incidence of acute graft-versus-host disease and pre-existing viral infections.
Renella Raffaele, Picard Capucine, Neven Bénédicte, Ouachée-Chardin Marie, Casanova Jean-Laurent, Le Deist Françoise, Cavazzana-Calvo Marina, Blanche Stéphane, Fischer Alain, 2006/09. British Journal of Haematology, 134 (5) pp. 510-516.
[DOI][serval:BIB_2B0E89154AD6]
Decision-making in pediatrics: a practical algorithm to evaluate complementary and alternative medicine for children.
Renella Raffaele, Fanconi Sergio, 2006/07. European journal of pediatrics, 165 (7) pp. 437-441.
[URN][DOI][serval:BIB_9B73DEE42723]
 
Burkholderia pseudomallei infection in chronic granulomatous disease.
Renella Raffaele, Perez Jean-Marie, Chollet-Martin Sylvie, Sarnacki Sabine, Fischer Alain, Blanche Stéphane, Casanova Jean-Laurent, Picard Capucine, 2006/03. European journal of pediatrics, 165 (3) pp. 175-177.
[DOI][serval:BIB_C926AF391AA2]
 
Spondyloenchondrodysplasia with spasticity, cerebral calcifications, and immune dysregulation: clinical and radiographic delineation of a pleiotropic disorder.
Renella Raffaele, Schaefer Elke, LeMerrer Martine, Alanay Yasemin, Kandemir Nurgun, Eich Georg, Costa Teresa, Ballhausen Diana, Boltshauser Eugen, Bonafé Luisa et al., 2006. American Journal of Medical Genetics Part A, 140 (6) pp. 541-550.
[DOI][serval:BIB_DE90D4D024A9]
2005
 
Le sarcome indifférencié du foie: une tumeur rare chez l'enfant [Undifferentiated sarcoma of the liver: a rare tumor of childhood]
Gonçalves-Matoso V., Renella R., Gudinchet F., Schnyder P., Beck-Popovic M., Lepori D., 2005. Archives de pédiatrie, 12 (11) pp. 1624-1626. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_10F43559B037]
2003
 
Breast-conserving surgery has equivalent effect as mastectomy on stage I breast cancer prognosis only when followed by radiotherapy.
Rapiti E., Fioretta G., Vlastos G., Kurtz J., Schäfer P., Sappino A.P., Spiliopoulos A., Renella R., Neyroud-Caspar I., Bouchardy C., 2003/12. Radiotherapy and oncology, 69 (3) pp. 277-284. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_3B60FC144657]
2002
 
Mon enfant saigne facilement: approche clinique et paraclinique pour le praticien [My child bleeds easily: clinical and paraclinical approach]
Renella R., Nenadov-Beck M., Vienny H., Gehri M., 2002/12. Revue medicale de la Suisse romande, 122 (12) pp. 599-601. Peer-reviewed.
[Pmid][serval:BIB_490926F2377D]
 
Management of women with ductal carcinoma in situ of the breast: a population-based study.
Verkooijen H.M., Fioretta G., De Wolf C., Vlastos G., Kurtz J., Borisch B., Schäfer P., Spiliopoulos A., Sappino A.P., Renella R. et al., 2002/08. Annals of oncology, 13 (8) pp. 1236-1245. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_952ACF49362A]
Partagez:
Unicentre - CH-1015 Lausanne
Suisse
Tél. +41 21 692 11 11
Canton de Vaud
Swiss University