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Results: 1 to 20 of 1681

1.

α-globin as a molecular target in treatment of β-thalassemia.

Mettananda S, Gibbons RJ, Higgs DR.

Blood. 2015 Apr 13. pii: blood-2015-03-633594. [Epub ahead of print]

PMID:
25869286
2.

Pulmonary extramedullary hematopoiesis involving the pulmonary artery.

Monga V, Silverman M.

Hematol Rep. 2015 Mar 24;7(1):5714. doi: 10.4081/hr.2015.5714. eCollection 2015 Feb 24.

3.

Traffic Light: prognosis-based eligibility for clinical trials of hematopoietic SCT in adults with sickle cell anemia.

Rotz SJ, O'Riordan MA, Kim C, de Lima M, Gladwin MT, Little JA.

Bone Marrow Transplant. 2015 Mar 16. doi: 10.1038/bmt.2015.11. [Epub ahead of print]

PMID:
25774596
4.

[When transfusion and hemapheresis are medicine].

Driss F, Saheb S, Garraud O, Heschmati F.

Presse Med. 2015 Feb;44(2):221-6. doi: 10.1016/j.lpm.2014.07.025. Epub 2015 Jan 27. Review. French.

PMID:
25637111
5.

Invasive pulmonary aspergillosis in a haematopoietic stem cell transplant recipient with sickle cell disease: a successful treatment.

Paciaroni K, De Angelis G, Gallucci C, Alfieri C, Ribersani M, Roveda A, Isgrò A, Marziali M, Aloi IP, Inserra A, Gaziev J, Sodani P, Lucarelli G.

Mediterr J Hematol Infect Dis. 2015 Jan 1;7(1):e2015006. doi: 10.4084/MJHID.2015.006. eCollection 2015.

6.

New insights into the pharmacokinetics of intravenous busulfan in children with sickle cell anemia undergoing bone marrow transplantation.

Gaziev J, Isgrò A, Mozzi AF, Petain A, Nguyen L, Ialongo C, Dinallo V, Sodani P, Marziali M, Andreani M, Testi M, Paciaroni K, Gallucci C, De Angelis G, Alfieri C, Ribersani M, Lucarelli G.

Pediatr Blood Cancer. 2015 Apr;62(4):680-6. doi: 10.1002/pbc.25376. Epub 2014 Dec 31.

PMID:
25557687
7.

Mycobacterium avium Complex Infection in a Patient with Sickle Cell Disease and Severe Iron Overload.

Shemisa K, Jafferjee N, Thomas D, Jacobs G, Meyerson HJ.

Case Rep Infect Dis. 2014;2014:405323. doi: 10.1155/2014/405323. Epub 2014 Dec 4.

8.

Type 1 diabetes mellitus in a known sickle cell anaemia patient: a rare combination in Nigeria.

Jarrett OO, Olorundare EI.

Afr J Med Med Sci. 2014 Jun;43(2):177-81.

PMID:
25508774
9.

Type 1 diabetes mellitus in a known sickle cell anaemia patient: a rare combination in Nigeria.

Jarrett OO, Olorundare EI.

Afr J Med Med Sci. 2014 Jun;43(2):177-81.

PMID:
25474995
10.

Peripheral red blood cell split chimerism as a consequence of intramedullary selective apoptosis of recipient red blood cells in a case of sickle cell disease.

Marziali M, Isgrò A, Sodani P, Gaziev J, Fraboni D, Paciaroni K, Gallucci C, Alfieri C, Roveda A, De Angelis G, Cardarelli L, Ribersani M, Andreani M, Lucarelli G.

Mediterr J Hematol Infect Dis. 2014 Nov 1;6(1):e2014066. doi: 10.4084/MJHID.2014.066. eCollection 2014.

11.

Drug development: a complicated path.

Humphries C.

Nature. 2014 Nov 13;515(7526):S4-5. doi: 10.1038/515S4a. No abstract available.

PMID:
25390140
12.

Ectodermal dysplasia associated with sickle cell disease.

Volpato LE, Volpato MC, de Carvalhosa AA, Palma VC, Borges AH.

Case Rep Dent. 2014;2014:314391. doi: 10.1155/2014/314391. Epub 2014 Sep 29.

13.

[Multiorgan failure after sickle cell vaso occlusive attack: integrated clinical and biological emergency].

Cottin L, Rouvet C, Homedan C, Conté M, Mortaza S, Rousselet MC, Corby A, Le Guyader M, Zandecki M, Reynier P.

Ann Biol Clin (Paris). 2014 Sep-Oct;72(5):602-6. doi: 10.1684/abc.2014.0996. French.

PMID:
25336134
14.

Musculoskeletal disorders in sickle cell anaemia--unusual associations.

Umesh S, Ajit NE, Shobha V, Nazuralla S, Ross C, Choudhury R.

J Assoc Physicians India. 2014 Jan;62(1):52-3.

PMID:
25327095
15.

Impairment of bone health in pediatric patients with hemolytic anemia.

Schündeln MM, Goretzki SC, Hauffa PK, Wieland R, Bauer J, Baeder L, Eggert A, Hauffa BP, Grasemann C.

PLoS One. 2014 Oct 9;9(10):e108400. doi: 10.1371/journal.pone.0108400. eCollection 2014.

16.

Thalassemia major and sickle cell disease in adolescents and young adults.

Yacobovich J, Tamary H.

Acta Haematol. 2014;132(3-4):340-7. doi: 10.1159/000360235. Epub 2014 Sep 10. Review.

PMID:
25228560
17.

Sickle cell disease and pulpal necrosis: a review of the literature for the primary care dentist.

Basati MS.

Prim Dent J. 2014 Feb;3(1):76-9. doi: 10.1308/205016814812135922. Review.

PMID:
25198336
18.

BAT2 and BAT3 polymorphisms as novel genetic risk factors for rejection after HLA-related SCT.

Piras IS, Angius A, Andreani M, Testi M, Lucarelli G, Floris M, Marktel S, Ciceri F, La Nasa G, Fleischhauer K, Roncarolo MG, Bulfone A, Gregori S, Bacchetta R.

Bone Marrow Transplant. 2014 Nov;49(11):1400-4. doi: 10.1038/bmt.2014.177. Epub 2014 Aug 11. Erratum in: Bone Marrow Transplant. 2014 Nov;49(11):1452. Nasa, G La [corrected to La Nasa, G].

PMID:
25111513
19.

Prophylactic red blood cell exchange may be beneficial in the management of sickle cell disease in pregnancy.

Asma S, Kozanoglu I, Tarım E, Sarıturk C, Gereklioglu C, Akdeniz A, Kasar M, Turgut NH, Yeral M, Kandemir F, Boga C, Ozdogu H.

Transfusion. 2015 Jan;55(1):36-44. doi: 10.1111/trf.12780. Epub 2014 Jul 29.

PMID:
25070465
20.

Hematopoietic SCT for the Black African and non-Black African variants of sickle cell anemia.

Lucarelli G, Isgrò A, Sodani P, Marziali M, Gaziev J, Paciaroni K, Gallucci C, Cardarelli L, Ribersani M, Alfieri C, De Angelis G, Armiento D, Andreani M, Testi M, Amato A, Akinyanju OO, Wakama TT.

Bone Marrow Transplant. 2014 Nov;49(11):1376-81. doi: 10.1038/bmt.2014.167. Epub 2014 Jul 28.

PMID:
25068420
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