Maria Marsella

ORCID: 0000-0003-0334-8785
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About
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Research Areas
  • Hemoglobinopathies and Related Disorders
  • Iron Metabolism and Disorders
  • Blood groups and transfusion
  • Viral gastroenteritis research and epidemiology
  • Obesity and Health Practices
  • Child and Adolescent Health
  • Erythrocyte Function and Pathophysiology
  • Obesity, Physical Activity, Diet
  • Infectious Diseases and Tuberculosis
  • Bone and Joint Diseases
  • Sarcoma Diagnosis and Treatment
  • Sexual Differentiation and Disorders
  • Hepatitis Viruses Studies and Epidemiology
  • Testicular diseases and treatments
  • Myeloproliferative Neoplasms: Diagnosis and Treatment
  • Viral Infections and Immunology Research
  • Healthcare cost, quality, practices
  • Congenital Anomalies and Fetal Surgery
  • Trace Elements in Health
  • Cerebral Palsy and Movement Disorders
  • Parasitic Diseases Research and Treatment
  • Infectious Diseases and Mycology
  • Medical Imaging and Pathology Studies
  • Spondyloarthritis Studies and Treatments
  • Pericarditis and Cardiac Tamponade

Azienda Ospedaliera S.Giuseppe Moscati
2017-2024

Ospedale Antonio Cardarelli
2016

Azienda Ospedaliera G.Rummo
2015

University of Ferrara
2009-2014

Clínica Santa María
2010

Istituto Nazionale per le Malattie Infettive Lazzaro Spallanzani
2008

Background It has been repeatedly reported that female patients with thalassemia major survive longer than males and the difference is due to a lower rate of cardiac disease in females.Design Methods We compared iron load as measured by T2* magnetic resonance imaging 776 (370 males) examined at National Research Council part an Italian cooperative study. also established normal left ventricular ejection fraction values for our population.Results The prevalence was higher females (105 versus...

10.3324/haematol.2010.025510 article EN cc-by-nc Haematologica 2011-01-12

The severity of thalassemia intermedia depends on the degree imbalance between alpha and non-alpha chains as well other genetic environmental factors that modify natural history disease. By definition, patients spontaneously maintain hemoglobin at or above 7 g/dL, sometimes price intense hyperplasia bone marrow is in turn responsible for deformities, osteoporosis, extramedullary erythropoietic masses often characterize intermedia. Transfusion may become necessary with advancing age, during...

10.1111/j.1749-6632.2010.05550.x article EN Annals of the New York Academy of Sciences 2010-08-01

Sickle cell disease is the commonest haemoglobinopathy in Africa, Middle East and India. In recent years, its incidence has increased dramatically also Europe North America because of high rate migration people from endemic areas. From January 2009 to 2010 number foreign residents province Ferrara (Italy) by 12.2%: most immigrants were countries at risk sickle disease. Since neonatal screening prophylactic penicillin early childhood could reduce mortality 10 years age less than 2%, aim this...

10.2450/2012.0030-12 article EN PubMed 2013-04-01

Abstract Classical Poland Syndrome (PS) is characterized by unilateral, partial or complete absence of the sternocostal head major pectoral muscle and brachysyndactyly fingers on same side. We report case a newborn infant with dextrocardia PS located left This association very rare: to date only 19 cases have been described in scientific literature. In all reported cases, as present, defect involved side was associated rib defects, whereas most are right few defects. supports view that...

10.1186/1824-7288-36-21 article EN cc-by ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics 2010-02-20

Non-transfusion-dependent thalassemia includes a variety of phenotypes and genotypes that rarely require regular transfusions. However, these patients can experience wide range complications. The objective this retrospective study was to verify whether there is significant difference in non-transfusion-dependent thalassemia-related complications treatment among males females.We performed re-analysis samples evaluated previously published cross-sectional study, regarding 96 followed at the...

10.1080/10245332.2017.1413789 article EN Hematology 2018-01-05
Joanna Clarke Marguerite Ennis Kathleen R. Lamborn Michael D. Prados Vinay K. Puduvalli and 95 more Marta Penas‐Prado M. R. Gilbert Morris D. Groves Kyle Hess V. A. Levin Joris de Groot HoraceC. Colman Charles A. Conrad Monica Loghin Kylie E Hunter W.K. Alfred Yung C. Chen Denise Damek A. Liu Laurie E. Gaspar Allen Waziri Kevin O. Lillehei B. Kavanagh Jonathan L. Finlay Kristina M. Haley Girish Dhall Sue E. Gardner Jeffrey D. Allen Angela Cornelius Randal Olshefski Jennifer Garvin Keshab C. Pradhan M. Etzl Stephen A. Goldman Michel Atlas Spencer Thompson Andreas Hirt Juliette Hukin Madelyn Comito Salvatore Bertolone Joseph C. Torkildson Meredith Joyce C G Moertel John J. Letterio Gail Kennedy Alice Quinn Walter Laixi Ji Richard Sposto Kathleen Dorris Lis Wagner Theresia Hummel Rachid Drissi Lachlan F. Miles John E. Leach Lillian Shuk-Nga Chow Richard M. Turner M. N. Gragert David W. Pruitt Monica J. Sutton John C. Breneman Kerry R. Crone Maryam Fouladi Bret B. Friday John W Buckner S. K. Anderson Courtney M. Giannini J Kugler M. Mazurczac P Flynn Horst Gross Eduardo R. Pajon Kurt A. Jaeckle Evanthia Galanis Michael Badruddoja Maddalena Pazzi Baldassarre Stea P. Lefferts N. Contreras Michael W. Bishop John D. Seeger Raymond F. Carmody Naomi E. Rance Maria Marsella Knut Schroeder Abhay Sanan L. J. Swinnen Cathryn Rankin Elisabeth J. Rushing Laura F. Hutchins Denise M. Damek Gorana Barger Andrew D. Norden Glenn J. Lesser S. N. Hammond Jan Drappatz Camilo E. Fadul T. T. Batchelor E. C. Quant Rameen Beroukhim Antonio Ciampa

10.1093/neuonc/noq116.s9 article EN Neuro-Oncology 2010-10-21

Abstract: The increased survival and lifespan of thalassemia patients, in the setting better iron overload monitoring chelation, have also however incidence diseases complications, which were less likely to develop. Among these, one most worrying recent years is hepatocellular carcinoma (HCC). Due blood transfusions, many patients with are or been infected hepatitis C virus (HCV) B (HBV), especially those born before 1990s countries universal HBV vaccination safe programs still not...

10.2147/jbm.s186362 article EN cc-by-nc Journal of Blood Medicine 2019-09-01

Abstract Childhood obesity has spread worldwide, it is on the rise, starts earlier and more severe, despite all treatment attempts. According to recent studies, weight stigma a factor that can hinder success of therapies. Healthcare workers, mainly paediatricians, need feel urgency anti-stigma training. The use non-stigmatizing terminologies images in various areas (school, sports clubs, healthcare, media, society general) improve disease management.

10.1186/s13052-020-00821-8 article EN cc-by ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics 2020-05-13

Two premature twins (33 weeks gestation) were born to a woman who had used paroxetine during pregnancy for an anxiety-depression disorder. They admitted the NICU, where they showed prolonged RDS, cardiovascular malformations, and facial dysmorphisms. Soon after birth, also presented abnormal neurobehavioral motor signs, which partially disappeared following weeks, although alterations of tone persisted even at discharge. Selective serotonin reuptake inhibitor (SSRI) antidepressants are...

10.1186/1824-7288-36-27 article EN cc-by ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics 2010-01-01

Transfusion dependency determines iron overload in thalassaemia major, with devastating complications. Significant liver has been observed from early childhood and we aimed to evaluate factors that could predict at the first magnetic resonance imaging (MRI).All transfusion-dependent children who underwent MRI assess were retrospectively studied. Age, weight, height, blood requirement, chelation drug dosage, serum ferritin enzymes evaluated three specific steps: start of transfusion regimen,...

10.2450/2018.0092-18 article EN PubMed 2019-05-01
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