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Items: 3

1.

Thyroid Disorders in Homozygous β-Thalassemia: Current Knowledge, Emerging Issues and Open Problems.

De Sanctis V, Soliman AT, Canatan D, Yassin MA, Daar S, Elsedfy H, Di Maio S, Raiola G, Corrons JV, Kattamis C.

Mediterr J Hematol Infect Dis. 2019 May 1;11(1):e2019029. doi: 10.4084/MJHID.2019.029. eCollection 2019. Review.

2.

Density, heterogeneity and deformability of red cells as markers of clinical severity in hereditary spherocytosis.

Huisjes R, Makhro A, Llaudet-Planas E, Hertz L, Petkova-Kirova P, Verhagen LP, Pignatelli S, Rab MAE, Schiffelers RM, Seiler E, van Solinge WW, Corrons JV, Kaestner L, Mañú-Pereira M, Bogdanov A, van Wijk R.

Haematologica. 2020 Jan 31;105(2):338-347. doi: 10.3324/haematol.2018.188151. Print 2020.

3.

Meeting Report: The Equality Project on Endocrine Complications in Thalassemia: Selected Highlights from the First Turkish Congress, Antalya, 10th-11th December 2018.

Canatan D, De Sanctis V, Corrons JV, Gorar S, Turkkahraman D, Baran RT, Kurtoglu E, Aslan V, Kupesiz FT, Tamburaci Uslu ZD, Ozdemir Z, Erinekci O.

Pediatr Endocrinol Rev. 2019 Mar;16(3):401-411. doi: 10.17458/per.vol16.2019.csc.mr.thalassemia.

PMID:
30888129

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