WordNet

an inherited form of anemia caused by faulty synthesis of hemoglobin (同)thalassaemia, Mediterranean_anemia, Mediterranean anaemia

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1. 造血細胞移植後のサラセミア患者の長期マネージメント long term management of the thalassemic patient after hematopoietic cell transplantation
2. サラセミア症候群の分子病理 molecular pathology of the thalassemic syndromes
3. βサラセミアの病態生理 pathophysiology of beta thalassemia
4. 地域社会の公衆衛生上の問題とサラセミア症候群：他国から得た教訓 community public health issues and the thalassemic syndromes lessons from other countries
5. αサラセミアの病態生理 pathophysiology of alpha thalassemia

Tandem measurements of iron and creatinine by cross injection analysis with application to urine from thalassemic patients.

Choengchan N1, Mantim T2, Inpota P3, Nacapricha D2, Wilairat P2, Jittangprasert P4, Waiyawat W2, Fucharoen S5, Sirankpracha P5, Morales NP6.
Talanta.Talanta.2015 Feb;133:52-8. doi: 10.1016/j.talanta.2014.04.090. Epub 2014 Jul 7.
This work presents development of a method for the dual determination of Fe(III) and creatinine using cross injection analysis (CIA). Two CIA platforms connected in series accommodated sample and reagents plugs aspirated via y-direction channels while water was pumped through the x-direction channel
PMID 25435226

Farra C1, Badra R, Fares F, Muwakkit S, Dbaibo G, Dabbous I, Ashkar H, Mounsef C, Abboud MR.
Pediatric blood & cancer.Pediatr Blood Cancer.2015 Jan;62(1):120-2. doi: 10.1002/pbc.25242. Epub 2014 Oct 4.
BACKGROUND: Hemoglobinopathies are the most common reported monogenic disorders worldwide. It is well established that Mediterranean and Arab countries are high risk areas for thalassemia in general, and for alpha thalassemia in particular. Reports of alpha thalassemia gene mutations from the Lebane
PMID 25284125

Danjou F1, Francavilla M2, Anni F2, Satta S3, Demartis FR2, Perseu L3, Manca M3, Sollaino MC3, Manunza L2, Mereu E2, Marceddu G2, Pissard S4, Joly P5, Thuret I6, Origa R2, Borg J7, Forni GL8, Piga A9, Lai ME3, Badens C10, Moi P2, Galanello R2.
Haematologica.Haematologica.2014 Dec 5. pii: haematol.2014.113886. [Epub ahead of print]
Clinical and hematological characteristics of beta-thalassemia are determined by several factors resulting in a wide spectrum of severity. Phenotype modulators are: HBB mutations, HBA defects and fetal hemoglobin production modulators (HBG2:g.-158C>T polymorphism, HBS1L-MYB intergenic region and
PMID 25480500

The profile of free amino acids in latent fingerprint of healthy and beta-thalassemic volunteers

KHEDR Alaa
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences 878(19), 1576-1582, 2010-06-01
NAID 10028037402

Hepatitis B virus reactivation during combined therapy with deferiprone and desferioxamine in a hepatitis B surface antigen thalassemic carrier

RICCHI Paolo,CINQUE Patrizia,GALEOTA Alfonso Lanza,DI MATOLA Tiziana,AMMIRABILE Massimiliano,PROSSOMARITI Luciano
International journal of hematology 89(2), 135-138, 2009-03-15
NAID 10025159985

Management of Spinal Cord Compression Caused by Extramedullary Hematopoiesis in Beta-thalassemia

Moncef Berhouma,Hafedh Jemel
Internal Medicine 47(12), 1125-1128, 2008
… We present a case of EMH in a thalassemic adolescent boy presenting with a T12 level of compression, treated successfully with blood transfusion, surgical decompression and radiotherapy. …
NAID 130000078862