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The design of an information system on thalassemia
Rossi-Mori, Angelo; Ricci, Fabrizio L.; Zambon, Giulio
Follow Informatics for Health and Social Care , Volume 9 (1)
Informa Healthcare – Jan 1, 1984 -
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ThalInd , a β‐thalassemia and hemoglobinopathies database for India: defining a model country‐specific and disease‐centric bioinformatics resource
Sinha, Sujata; Black, Michael L.; Agarwal, Sarita; Das, Reena; Bittles, Alan H.; Bellgard, Matthew
Follow Human Mutation , Volume 32 (8)
Wiley – Aug 1, 2011be accommodated within the purview of a national health system. Disease‐specific national resources can accommodate the requirements of information on disease burden, treatment options, and existing facilities ...
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New Strategies in the Treatment of the Thalassemias
Schrier, Stanley L.; Angelucci, Emanuele
Follow Annual Review of Medicine , Volume 56
Annual Reviews – Feb 18, 2005as iron overload. The TREATMENT OF THALASSEMIAS thalassemias are likely to beneï¬t in the future from speciï¬c gene therapy designed to overcome the block in the synthesis of a speciï¬c globin chain ...
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Cognitive function and event related potentials in children with beta-thalassemia
Shehata, Ghaydaa A.; Elsayh, Khaled I.; Mohamed, Amany O.; Rageh, Tarek A.; Rafet, Nafisa H.
Follow Journal of Pediatric Neurology , Volume 8 (2)
IOS Press – Jan 1, 2010Over the years, several reports have demonstrated the involvement of the nervous system in patients with beta-thalassemia. In most cases, neurological involvement does not initially present ...
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The Natural Progression of Symptomatic Humeral Head Osteonecrosis in Adults with Sickle Cell Disease
Poignard, Alexandre; Flouzat-Lachaniette, Charles-Henri; Amzallag, Julien; Galacteros, Frederic; Hernigou, Philippe
Follow Journal of Bone and Joint Surgery , Volume 94 (2)
JB&JS – Jan 18, 2012had hemoglobin S/beta-thalassemia (S/T). Shoulder osteonecrosis was graded with the method of Cruess with an adaptation for MRI as proposed by Steinberg et al. for hip osteonecrosis. Annual radiographs ...
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Population programs for the detection of couples at risk for severe monogenic genetic diseases
Joël, Zlotogora
Follow Human Genetics , Volume 126 (2)
Springer Journals – Aug 1, 2009an increasing number of young couples are not being screened since they are unaware of the disease. This observation led to design a pilot study implementing education on thalassemia early at school and to oVer ...
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Phenylbutyrate Mouthwash Mitigates Oral Mucositis During Radiotherapy or Chemoradiotherapy in Patients With Head-and-Neck Cancer
Yen, Sang-Hue; Wang, Ling-Wei; Lin, Yi-Hsien; Jen, Yee-Min; Chung, Yih-Lin
Follow International Journal of Radiation Oncology Biology Physics , Volume 82 (4)
Elsevier – Mar 15, 2012the quality of life and can greatly limit the success of antineoplastic therapy by reducing the tolerance to optimal tumoricidal treatment (3) . Systemic and topical approaches, including the use ...
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"The Most Important Test You’ll Ever Take"?: Attitudes toward confidential carrier matching and open individual testing among modern-religious Jews in Israel
Frumkin, Ayala; Raz, Aviad E.; Plesser-Duvdevani, Morasha; Lieberman, Sari
Follow Social Science & Medicine , Volume 73 (12)
Elsevier – Dec 1, 2011organization) and open individual carrier testing (through a medical center), examining how this important choice is being informed, communicated, made, and reflected on. Qualitative analysis of semi-structured ...
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Gene susceptibility to oxidative damage: From single nucleotide polymorphisms to function
Simonelli, Valeria; Mazzei, Filomena; D’Errico, Mariarosaria; Dogliotti, Eugenia
Follow Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis , Volume 731 (1)
Elsevier – Mar 1, 2012to be much milder. Further slowing down progress are the paucity of accurate and reproducible functional assays and poor epidemiological design of many studies. This review will focus on the most common ...
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β-Thalassemia Microelectronic Chip: A Fast and Accurate Method for Mutation Detection
Foglieni, Barbara; Cremonesi, Laura; Travi, Maurizio; Ravani, Anna; Giambona, Antonino; Rosatelli, Maria Cristina; Perra, Chiara; Fortina, Paolo; Ferrari, Maurizio
Follow Clinical Chemistry , Volume 50 (1): 73
American Association for Clinical Chemistry – Jan 1, 2004accounting for >95% of the β-thalassemia alleles in the Mediterranean area. Our final goal will be the development of a system that covers all or most of the common β-thalassemia-associated mutations that can ...
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