Bibliografía Recomendada sobre Eritropatías Los artículos están ...

Bibliografía Recomendada sobre Eritropatías 

Los artículos están ordenados por mes de publicación y luego por el número de 

identificación en PubMed (PMID). Los artículos más destacados están 

marcados en rojo. 

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2011 Abril 

Galesloot TE, Vermeulen SH, Geurts-Moespot AJ, Klaver SM, Kroot JJ, van 

Tienoven D, Wetzels JF, Kiemeney LA, Sweep FC, den Heijer M, Swinkels 

DW. Serum hepcidin: reference ranges and biochemical correlates in the 

general population. Blood. 2011 Apr 28. [Epub ahead of print] PubMed PMID: 

21527524. 

Narla A, Dutt S, McAuley JR, Al-Shahrour F, Hurst S, McConkey M, Neuberg D, 

Ebert BL. Dexamethasone and lenalidomide have distinct functional effects on 

erythropoiesis. Blood. 2011 Apr 28. [Epub ahead of print] PubMed PMID: 

21527522. 

Zheng Y, Qin H, Frank SJ, Deng L, Litchfield DW, Tefferi A, Pardanani A, Lin FT, 

Li J, Sha B, Benveniste EN. A CK2-dependent mechanism for activation of the 

JAK-STAT signaling pathway. Blood. 2011 Apr 28. [Epub ahead of print] 

PubMed PMID: 21527517. 

Persijn L, Bonroy C, Mondelaers V, Vantilborgh A, Philippé J, Stove V. Screening 

for hereditary spherocytosis in routine practice: evaluation of a diagnostic 

algorithm with focus on non-splenectomised patients. Ann Hematol. 2011 Apr 

27. [Epub ahead of print] PubMed PMID: 21523379. 

Green L, De Lord C, Clark B, Cadet E, Rochette J, Thein SL. Transient aplastic 

crisis as presentation of a previously unknown G6PD deficiency with iron 

overload. Br J Haematol. 2011 Apr 27. doi: 10.1111/j.1365- 

2141.2011.08666.x. [Epub ahead of print] PubMed PMID: 21521183. 

Silver RT, Vandris K, Goldman JJ. Recombinant interferon alpha may retard 

progression of early primary myelofibrosis: a preliminary report. Blood. 2011 

Apr 25. [Epub ahead of print] PubMed PMID: 21518929. 

Smith J, Rahilly M, Davidson K. Extramedullary haematopoiesis secondary to 

hereditary spherocytosis. Br J Haematol. 2011 Apr 22. doi: 10.1111/j.1365- 


Luzzatto L, Gianfaldoni G, Notaro R. Management of Paroxysmal Nocturnal 

Haemoglobinuria: a personal view. Br J Haematol. 2011 Apr 22. doi: 

10.1111/j.1365-2141.2011.08690.x. [Epub ahead of print] PubMed PMID: 

21517820.

Driss F, Moh-Klaren J, Pela AM, Tertian G. Regular automated 

erythrocytapheresis in sickle cell patients. Br J Haematol. 2011 Apr 22. doi: 


21517812. 

Flanagan JM, Frohlich DM, Howard TA, Schultz WH, Driscoll C, 

Nagasubramanian R, Mortier NA, Kimble AC, Aygun B, Adams RJ, Helms 

RW, Ware RE. Genetic predictors for stroke in children with sickle cell anemia. 

Blood. 2011 Apr 22. [Epub ahead of print] PubMed PMID: 21515823. 

Manshouri T, Estrov Z, Quintas-Cardama A, Burger J, Zhang Y, Livun A, Knez L, 

Harris DT, Creighton CJ, Kantarjian HM, Verstovsek S. BONE MARROW 

STROMA SECRETED CYTOKINES PROTECT JAK2V617F-MUTATED 

CELLS FROM THE EFFECTS OF A JAK2 INHIBITOR. Cancer Res. 2011 Apr 


Sankaran VG, Menne J, Heller R. Heterozygous disruption of human SOX6 is 

insufficient to impair erythropoiesis or silencing of fetal hemoglobin. Blood. 

2011 Apr 21;117(16):4396-7. PubMed PMID: 21511965. 

Uaprasert N, Rojnuckarin P, Settapiboon R, Amornsiriwat S, Sutcharitchan P. 

Hematological characteristics and effective screening for compound 

heterozygosity for Hb constant spring and deletional α(+) -thalassemia. Am J 

Hematol. 2011 Mar 21. doi: 10.1002/ajh.22033. [Epub ahead of print] PubMed 

PMID: 21509802. 

Pasricha SR, McQuilten ZK, Westerman M, Keller A, Nemeth E, Ganz T, Wood 

EM. Serum hepcidin as a diagnostic test of iron deficiency in premenopausal 

female blood donors. Haematologica. 2011 Apr 20. [Epub ahead of print] 


Sardina JL, López-Ruano G, Sánchez-Sánchez B, Llanillo M, Hernández- 

Hernández A. Reactive oxygen species: Are they important for 

haematopoiesis? Crit Rev Oncol Hematol. 2011 Apr 18. [Epub ahead of print] 


Lucarelli G, Gaziev J, Isgrò A, Sodani P, Paciaroni K, Alfieri C, De Angelis G, 

Marziali M, Simone MD, Gallucci C, Roveda A, Saltarelli F, Torelli F, Andreani 

M. Allogeneic cellular gene therapy in hemoglobinopathies-evaluation of 

hematopoietic SCT in sickle cell anemia. Bone Marrow Transplant. 2011 Apr 


Singer ST, Vichinsky EP, Sweeters N, Rachmilewitz E. Darbepoetin alfa for the 

treatment of anaemia in alpha- or betathalassaemia intermedia syndromes.

Br J Haematol. 2011 Apr 18. doi: 10.1111/j.1365-2141.2011.08617.x. [Epub 

ahead of print] PubMed PMID: 21496003. 

Chen W, Huang FW, Barrientos de Renshaw T, Andrews NC. Skeletal muscle 

hemojuvelin is dispensable for systemic iron homeostasis. Blood. 2011 Apr 


Akinsheye I, Alsultan A, Solovieff N, Ngo D, Baldwin CT, Sebastiani P, Chui DH, 

Steinberg MH. Fetal hemoglobin in sickle cell anemia. Blood. 2011 Apr 13. 

[Epub ahead of print] PubMed PMID: 21490337. 

Luzzatto L. Somatic mutations in cancer development. Environ Health. 2011 Apr 

5;10 Suppl 1:S12. PubMed PMID: 21489208; PubMed Central PMCID: 

PMC3073190. 

Solomon LR. Iron-chelating therapy for transfusional iron overload. N Engl J Med. 

2011 Apr 14;364(15):1475-6; author reply 1477. PubMed PMID: 21488788. 

Musallam KM, Taher AT. Iron-chelating therapy for transfusional iron overload. N 

Engl J Med. 2011 Apr 14;364(15):1476; author reply 1477. PubMed PMID: 

21488787. 

Taccone-Gallucci M, Manca-di-Villahermosa S, Noce A. Iron-chelating therapy for 

transfusional iron overload. N Engl J Med. 2011 Apr 14;364(15):1476-7; 

author reply 1477. PubMed PMID: 21488786. 

Heimpel H. Vitamin B(12)-Responsive Pancytopenia Mimicking Myelodysplastic 

Syndrome. Acta Haematol. 2011 Apr 11;126(2):68. [Epub ahead of print] 


Lawrence C. Blood. Lancet. 2011 Apr 9;377(9773):1231. PubMed PMID: 

21481693. 

Musallam KM, Khoury B, Abi-Habib R, Bazzi L, Succar J, Halawi R, Hankir A, 

Koussa S, Taher AT. Health-related quality of life in adults with transfusionindependent 

thalassemia intermedia compared to regularly-transfused 

thalassemia major: New insights. Eur J Haematol. 2011 Apr 11. doi: 


21480999. 

Ramos E, Kautz L, Rodriguez R, Hansen M, Gabayan V, Ginzburg Y, Roth MP, 

Nemeth E, Ganz T. Evidence for distinct pathways of hepcidin regulation by 

acute and chronic iron loading in mice. Hepatology. 2011 Apr;53(4):1333-41. 

doi: 10.1002/hep.24178. PubMed PMID: 21480335; PubMed Central PMCID: 

PMC3074982.

Saad GS, Musallam KM, Taher AT. The surgeon and the patient with βthalassaemia 

intermedia. Br J Surg. 2011 Jun;98(6):751-60. doi: 

10.1002/bjs.7533. Epub 2011 Apr 8. PubMed PMID: 21480198. 

Gill BS, Aragon-Ching JB, Perlin E. Hematuria in sickle cell trait: the importance 

of ruling out occult cancer. Ann Hematol. 2011 Apr 9. [Epub ahead of print] 


Kirwan M, Beswick R, Walne AJ, Hossain U, Casimir C, Vulliamy T, Dokal I. 

Dyskeratosis congenita and the DNA damage response. Br J Haematol. 2011 

Jun;153(5):634-43. doi: 10.1111/j.1365-2141.2011.08679.x. Epub 2011 Apr 8. 


Hoppe C, Kuypers F, Larkin S, Hagar W, Vichinsky E, Styles L. A pilot study of 

the short-term use of simvastatin in sickle cell disease: effects on markers of 

vascular dysfunction. Br J Haematol. 2011 Jun;153(5):655-63. doi: 

10.1111/j.1365-2141.2010.08480.x. Epub 2011 Apr 8. PubMed PMID: 

21477202. 

Howes RE, Patil AP, Piel FB, Nyangiri OA, Kabaria CW, Gething PW, 

Zimmerman PA, Barnadas C, Beall CM, Gebremedhin A, Ménard D, Williams 

TN, Weatherall DJ, Hay SI. The global distribution of the Duffy blood group. 

Nat Commun. 2011 Apr;2:266. PubMed PMID: 21468018; PubMed Central 

PMCID: PMC3074097. 

Macari ER, Lowrey CH. Induction of human fetal hemoglobin via the NRF2 

antioxidant response signaling pathway. Blood. 2011 Apr 4. [Epub ahead of 

print] PubMed PMID: 21464371. 

Franceschi LD, Cappellini MD, Olivieri O. Thrombosis and sickle cell disease. 

Semin Thromb Hemost. 2011 Apr;37(3):226-36. Epub 2011 Mar 31. PubMed 

PMID: 21455857. 

Bond J, Gale DP, Connor T, Adams S, de Boer J, Gascoyne DM, Williams O, 

Maxwell PH, Ancliff PJ. Dysregulation of the HIF pathway due to VHL mutation 

causing severe erythrocytosis and pulmonary arterial hypertension. Blood. 

2011 Mar 31;117(13):3699-701. PubMed PMID: 21454469. 

Modesti PA, Rapi S, Paniccia R, Bilo G, Revera M, Agostoni P, Piperno A, Cambi 

GE, Rogolino A, Biggeri A, Mancia G, Gensini GF, Abbate R, Parati G. Index 

measured at an intermediate altitude to predict impending Acute Mountain 

Sickness. Med Sci Sports Exerc. 2011 Mar 25. [Epub ahead of print] PubMed 

PMID: 21448078.

Schödel J, Oikonomopoulos S, Ragoussis J, Pugh CW, Ratcliffe PJ, Mole DR. 

High-resolution genome-wide mapping of HIF-binding sites by ChIP-seq. 

Blood. 2011 Mar 29. [Epub ahead of print] PubMed PMID: 21447827. 

JJ, Mukhina G, Wang H, Savage WJ, Brodsky RA. Natural history of paroxysmal 

nocturnal hemoglobinuria clones in patients presenting as aplastic anemia. 

Eur J Haematol. 2011 Mar 29. doi: 10.1111/j.1600-0609.2011.01615.x. [Epub 


Carpenter JP, He T, Kirk P, Roughton M, Anderson LJ, de Noronha SV, 

Sheppard MN, Porter JB, Walker JM, Wood JC, Galanello R, Forni G, Catani 

G, Matta G, Fucharoen S, Fleming A, House MJ, Black G, Firmin DN, St 

Pierre TG, Pennell DJ. On t2* magnetic resonance and cardiac iron. 

Circulation. 2011 Apr 12;123(14):1519-28. Epub 2011 Mar 28. PubMed PMID: 

21444881. 

Fung EB, Vichinsky EP, Kwiatkowski JL, Huang J, Bachrach LK, Sawyer AJ, 

Zemel BS. Characterization of low bone mass in young patients with 

thalassemia by DXA, pQCT and markers of bone turnover. Bone. 2011 Apr 5. 


Padate B, Bain BJ, de la Fuente J. Ineffective hemopoietic in beta thalassemia 

major visualised. Am J Hematol. 2011 Apr;86(4):372. doi: 10.1002/ajh.21953. 


Greenway A, Ware RE, Thornburg CD. Long-term results using 

hydroxyurea/phlebotomy for reducing secondary stroke risk in children with 

sickle cell anemia and iron overload. Am J Hematol. 2011 Apr;86(4):357-61. 

doi: 10.1002/ajh.21986. PubMed PMID: 21442640. 

Clark RJ, Tan CC, Preza GC, Nemeth E, Ganz T, Craik DJ. Understanding the 

structure/activity relationships of the iron regulatory peptide hepcidin. Chem 

Biol. 2011 Mar 25;18(3):336-43. PubMed PMID: 21439478; PubMed Central 


Rourke K, Fairbairn DJ, Jackson KA, Morris KL, Tey SK, Kennedy GA. A novel 

mutation of the erythropoietin receptor gene associated with primary familial 

and congenital polycythaemia. Int J Hematol. 2011 Apr;93(4):542-4. Epub 

2011 Mar 25. PubMed PMID: 21437635. 

Narla A, Vlachos A, Nathan DG. Diamond Blackfan anemia treatment: past, 

present, and future. Semin Hematol. 2011 Apr;48(2):117-23. PubMed PMID: 

21435508; PubMed Central PMCID: PMC3073777.

Burwick N, Shimamura A, Liu JM. Non-Diamond Blackfan anemia disorders of 

ribosome function: Shwachman Diamond syndrome and 5q- syndrome. Semin 

Hematol. 2011 Apr;48(2):136-43. PubMed PMID: 21435510. 

Farrar JE, Dahl N. Untangling the phenotypic heterogeneity of Diamond Blackfan 

anemia. Semin Hematol. 2011 Apr;48(2):124-35. PubMed PMID: 21435509; 

PubMed Central PMCID: PMC3078697. 

McGowan KA, Mason PJ. Animal models of Diamond Blackfan anemia. Semin 


Fumagalli S, Thomas G. The role of p53 in ribosomopathies. Semin Hematol. 

2011 Apr;48(2):97-105. PubMed PMID: 21435506. 

Ellis SR, Gleizes PE. Diamond Blackfan anemia: ribosomal proteins going rogue. 

Semin Hematol. 2011 Apr;48(2):89-96. PubMed PMID: 21435505. 

Taylor AM, Zon LI. Modeling Diamond Blackfan anemia in the zebrafish. Semin 


Arturi MC. Patient advocacy in Diamond Blackfan anemia: facilitating translational 

research and progress towards the cure of a rare disease. Semin Hematol. 

2011 Apr;48(2):75-80. PubMed PMID: 21435503. 

Ebert B, Lipton JM. Diamond Blackfan anemia and ribosome biogenesis: 

introduction. Semin Hematol. 2011 Apr;48(2):73-4. PubMed PMID: 21435502. 

Field JJ, Nathan DG, Linden J. Targeting iNKT cells for the treatment of sickle cell 

disease. Clin Immunol. 2011 Mar 21. [Epub ahead of print] PubMed PMID: 

21429807. 

Williams TN, Obaro SK. Sickle cell disease and malaria morbidity: a tale with two 

tails. Trends Parasitol. 2011 Mar 21. [Epub ahead of print] PubMed PMID: 

21429801. 

Lee SJ, Park SY, Jung MY, Bae SM, Kim IS. Mechanism for phosphatidylserinedependent 

erythrophagocytosis in mouse liver. Blood. 2011 Mar 22. [Epub 


Giardine B, Borg J, Higgs DR, Peterson KR, Philipsen S, Maglott D, Singleton BK, 

Anstee DJ, Basak AN, Clark B, Costa FC, Faustino P, Fedosyuk H, Felice AE, 

Francina A, Galanello R, Gallivan MV, Georgitsi M, Gibbons RJ, Giordano PC, 

Harteveld CL, Hoyer JD, Jarvis M, Joly P, Kanavakis E, Kollia P, Menzel S, 

Miller W, Moradkhani K, Old J, Papachatzopoulou A, Papadakis MN, 

Papadopoulos P, Pavlovic S, Perseu L, Radmilovic M, Riemer C, Satta S, 

Schrijver I, Stojiljkovic M, Thein SL, Traeger-Synodinos J, Tully R, Wada T,

Waye JS, Wiemann C, Zukic B, Chui DH, Wajcman H, Hardison RC, Patrinos 

GP. Systematic documentation and analysis of human genetic variation in 

hemoglobinopathies using the microattribution approach. Nat Genet. 2011 Mar 

20;43(4):295-301. PubMed PMID: 21423179. 

Singbrant S, Russell MR, Jovic T, Liddicoat B, Izon DJ, Purton LE, Sims NA, 

Martin TJ, Sankaran VG, Walkley CR. Erythropoietin couples erythropoiesis, B 

lymphopoiesis, and bone homeostasis within the bone marrow 

microenvironment. Blood. 2011 Mar 18. [Epub ahead of print] PubMed PMID: 

21421837. 

Saraf S, Farooqui M, Infusino G, Oza B, Sidhwani S, Gowhari M, Vara S, Gao W, 

Krauz L, Lavelle D, Desimone J, Molokie R, Saunthararajah Y. Standard 

clinical practice underestimates the role and significance of erythropoietin 

deficiency in sickle cell disease. Br J Haematol. 2011 May;153(3):386-92. doi: 

10.1111/j.1365-2141.2010.08479.x. Epub 2011 Mar 21. PubMed PMID: 

21418176. 

fer A, Howell JP, Lange AP, Yamamoto R, Heuscher J, Gregor M, Wuillemin WA. 

Hereditary hyperferritinemia-cataract syndrome (HHCS) presenting with iron 

deficiency anemia associated with a new mutation in the iron responsive 

element of the L ferritin gene in a swiss family. Eur J Haematol. 2011 Mar 15. 

doi: 10.1111/j.1600-0609.2011.01607.x. [Epub ahead of print] PubMed PMID: 

21410535. 

Frede S, Freitag P, Geuting L, Konietzny R, Fandrey J. Oxygen-regulated 

expression of the erythropoietin gene in the human renal cell line REPC. 

Blood. 2011 May 5;117(18):4905-14. Epub 2011 Mar 15. PubMed PMID: 

21406725. 

Miller ST. How I treat acute chest syndrome in children with sickle cell disease. 

Blood. 2011 Mar 15. [Epub ahead of print] PubMed PMID: 21406723. 

Steinbicker AU, Sachidanandan C, Vonner AJ, Yusuf RZ, Deng DY, Lai CS, 

Rauwerdink KM, Winn JC, Saez B, Cook CM, Szekely BA, Roy CN, Seehra 

JS, Cuny GD, Scadden DT, Peterson RT, Bloch KD, Yu PB. Inhibition of bone 

morphogenetic protein signaling attenuates anemia associated with 

inflammation. Blood. 2011 May 5;117(18):4915-23. Epub 2011 Mar 10. 


Ochola LB, Siddondo BR, Ocholla H, Nkya S, Kimani EN, Williams TN, Makale 

JO, Liljander A, Urban BC, Bull PC, Szestak T, Marsh K, Craig AG. Specific 

receptor usage in Plasmodium falciparum cytoadherence is associated with 

disease outcome. PLoS One. 2011 Mar 3;6(3):e14741. PubMed PMID: 


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2011 Marzo 

Pallais JC, Mackool BT, Pitman MB. Case records of the Massachusetts General 

Hospital: Case 7-2011: a 52-year-old man with upper respiratory symptoms 

and low oxygen saturation levels. N Engl J Med. 2011 Mar 10;364(10):957-66. 

Erratum in: N Engl J Med. 2011 Apr 28;364(17):1682. N Engl J Med. 2011 Mar 

31;364(13):1281. PubMed PMID: 21388314. 

Berentsen S. How I manage cold agglutinin disease. Br J Haematol. 2011 

May;153(3):309-17. doi: 10.1111/j.1365-2141.2011.08643.x. Epub 2011 Mar 

8. PubMed PMID: 21385173. 

Inati A, Musallam KM, Cappellini MD, Duca L, Taher AT. Nontransferrin-bound 

iron in transfused patients with sickle cell disease. Int J Lab Hematol. 2011 

Apr;33(2):133-7. doi: 10.1111/j.1751-553X.2010.01224.x. PubMed PMID: 

21382180. 

Gur I, Afshari S, Kilkenny JW. Sudden false oxygen desaturation and factitious 

methemoglobinemia after subcutaneous injection of isosulfan blue 

(lymphazurin). Am Surg. 2011 Mar;77(3):383-5. PubMed PMID: 21375867. 

Koury MJ. Self-renewal in late-stage erythropoiesis. Blood. 2011 Mar 

3;117(9):2562-4. PubMed PMID: 21372160. 

Chatthanawaree W. Biomarkers of cobalamin (vitamin B12) deficiency and its 

application. J Nutr Health Aging. 2011 Mar;15(3):227-31. Review. PubMed 

PMID: 21369672. 

Yoon D, Ponka P, Prchal JT. Hypoxia and Hematopoiesis. Am J Physiol Cell 

Physiol. 2011 Mar 2. [Epub ahead of print] PubMed PMID: 21368293. 

Renella R, Roberts NA, Brown JM, De Gobbi M, Bird LE, Hassanali T, Sharpe JA, 

Sloane-Stanley J, Ferguson DJ, Cordell J, Buckle VJ, Higgs DR, Wood WG. 

Codanin-1 mutations in congenital dyserythropoietic anemia type 1 affect 

HP1α localization in erythroblasts. Blood. 2011 Mar 1. [Epub ahead of 


Gladwin MT, Kato GJ, Weiner D, Onyekwere OC, Dampier C, Hsu L, Hagar RW, 

Howard T, Nuss R, Okam MM, Tremonti CK, Berman B, Villella A, 

Krishnamurti L, Lanzkron S, Castro O, Gordeuk VR, Coles WA, Peters- 

Lawrence M, Nichols J, Hall MK, Hildesheim M, Blackwelder WC, Baldassarre 

J, Casella JF; DeNOVO Investigators. Nitric oxide for inhalation in the acute 

treatment of sickle cell pain crisis: a randomized controlled trial. JAMA. 2011 

Mar 2;305(9):893-902. PubMed PMID: 21364138.

Masaisa F, Gahutu JB, Mukiibi J, Delanghe J, Philippé J. Anemia in human 

immunodeficiency virus-infected and uninfected women in Rwanda. Am J Trop 

Med Hyg. 2011 Mar;84(3):456-60. PubMed PMID: 21363986; PubMed Central 


DeZern AE, Petri M, Drachman DB, Kerr D, Hammond ER, Kowalski J, Tsai HL, 

Loeb DM, Anhalt G, Wigley F, Jones RJ, Brodsky RA. High-dose 

cyclophosphamide without stem cell rescue in 207 patients with aplastic 

anemia and other autoimmune diseases. Medicine (Baltimore). 2011 

Mar;90(2):89-98. PubMed PMID: 21358440. 

Oosthuizen NM. Undetectable serum alkaline phosphatase activity in a patient 

with fulminant hepatic failure and hemolytic anemia. Clin Chem. 2011 


Finberg KE, Whittlesey RL, Andrews NC. Tmprss6 is a genetic modifier of the 

Hfe-hemochromatosis phenotype in mice. Blood. 2011 Apr 28;117(17):4590-9. 

Epub 2011 Feb 25. PubMed PMID: 21355094. 

Tefferi A. ASH 2010 meeting report-Top 10 clinically-oriented abstracts in 

myeloproliferative neoplasms. Am J Hematol. 2011 Mar;86(3):333-6. doi: 

10.1002/ajh.21969. PubMed PMID: 21351123. 

Tefferi A. Annual Clinical Updates in Hematological Malignancies: a continuing 

medical education series: polycythemia vera and essential thrombocythemia: 

2011 update on diagnosis, risk-stratification, and management. Am J Hematol. 

2011 Mar;86(3):292-301. doi: 10.1002/ajh.21946. Review. PubMed PMID: 

21351120. 

Muscal E, Edwards RM, Kearney DL, Hicks JM, Myones BL, Teruya J. 

Thrombotic microangiopathic hemolytic anemia with reduction of ADAMTS13 

activity: initial manifestation of childhood-onset systemic lupus erythematosus. 

Am J Clin Pathol. 2011 Mar;135(3):406-16. PubMed PMID: 21350095. 

Gurevich I, Luthra R, Konoplev SN, Yin CC, Medeiros LJ, Lin P. Refractory 

anemia with ring sideroblasts associated with marked thrombocytosis: a mixed 

group exhibiting a spectrum of morphologic findings. Am J Clin Pathol. 2011 


Urrechaga E, Borque L, Escanero JF. The role of automated measurement of 

RBC subpopulations in differential diagnosis of microcytic anemia and βthalassemia 

screening. Am J Clin Pathol. 2011 Mar;135(3):374-9. PubMed 

PMID: 21350090. 

Lorenzo FR 5th, Phillips JD, Nussenzveig R, Lingam B, Koul PA, Schrier SL, 

Prchal JT. Molecular basis of two novel mutations found in type I

methemoglobinemia. Blood Cells Mol Dis. 2011 Apr 15;46(4):277-81. Epub 

2011 Feb 24. PubMed PMID: 21349748; PubMed Central PMCID: 

PMC3075332. 

Ganz T. Hepcidin and iron regulation, 10 years later. Blood. 2011 Apr 

28;117(17):4425-33. Epub 2011 Feb 23. PubMed PMID: 21346250. 

Jiang P, Du W, Wang X, Mancuso A, Gao X, Wu M, Yang X. p53 regulates 

biosynthesis through direct inactivation of glucose-6-phosphate 

dehydrogenase. Nat Cell Biol. 2011 Mar;13(3):310-6. Epub 2011 Feb 20. 


Ghoti H, Fibach E, Westerman M, Gordana O, Ganz T, Rachmilewitz EA. 

Increased serum hepcidin levels during treatment with deferasirox in ironoverloaded 

patients with myelodysplastic syndrome. Br J Haematol. 2011 

Apr;153(1):118-20. doi: 10.1111/j.1365-2141.2011.08587.x. Epub 2011 Feb 

20. PubMed PMID: 21332711. 

Moller HJ, Nielsen MJ, Bartram J, Dick MC, Height SE, Moestrup SK, Rees DC. 

Soluble CD163 levels in children with sickle cell disease. Br J Haematol. 2011 

Apr;153(1):105-10. doi: 10.1111/j.1365-2141.2011.08580.x. Epub 2011 Feb 

20. PubMed PMID: 21332709. 

Quinn CT, Johnson VL, Kim HY, Trachtenberg F, Vogiatzi MG, Kwiatkowski JL, 

Neufeld EJ, Fung E, Oliveri N, Kirby M, Giardina PJ; Thalassemia Clinical 

Research Network. Renal dysfunction in patients with thalassaemia. Br J 

Haematol. 2011 Apr;153(1):111-7. doi: 10.1111/j.1365-2141.2010.08477.x. 


Candrilli SD, O'Brien SH, Ware RE, Nahata MC, Seiber EE, Balkrishnan R. 

Hydroxyurea adherence and associated outcomes among Medicaid enrollees 

with sickle cell disease. Am J Hematol. 2011 Mar;86(3):273-7. doi: 

10.1002/ajh.21968. Epub 2011 Feb 15. PubMed PMID: 21328441. 

Miller ST, Milton J, Steinberg MH. G6PD deficiency and stroke in the CSSCD. Am 

J Hematol. 2011 Mar;86(3):331. doi: 10.1002/ajh.21958. Epub 2011 Feb 15. 


Kedar PS, Warang P, Ghosh K, Colah RB. Severe mental retardation and 

recessive congenital methemoglobinemia in three Indian patients: compound 

heterozygous for NADH-cytochrome b5 reductase gene mutations. Am J 

Hematol. 2011 Mar;86(3):327-9. doi: 10.1002/ajh.21956. Epub 2011 Feb 15. 


Dierickx D, Delannoy A, Saja K, Verhoef G, Provan D. Anti-CD20 monoclonal 

antibodies and their use in adult autoimmune hematological disorders. Am J


Review. PubMed PMID: 21328427. 

Samuelson S, Sandmaier BM, Heslop HE, Popat U, Carrum G, Champlin RE, 

Storb R, Prchal JT, Gooley TA, Joachim Deeg H. Allogeneic haematopoietic 

cell transplantation for myelofibrosis in 30 patients 60-78 years of age. Br J 

Haematol. 2011 Apr;153(1):76-82. doi: 10.1111/j.1365-2141.2011.08582.x. 


Thompson AA, Cunningham MJ, Singer ST, Neufeld EJ, Vichinsky E, Yamashita 

R, Giardina P, Kim HY, Trachtenberg F, Kwiatkowski JL; Thalassemia Clinical 

Research Network Investigators. Red cell alloimmunization in a diverse 

population of transfused patients with thalassaemia. Br J Haematol. 2011 

Apr;153(1):121-8. doi: 10.1111/j.1365-2141.2011.08576.x. Epub 2011 Feb 17. 


Saadi AV, Girisha KM, Gopinath PM, Satyamoorthy K. Analysis of cosegregation 

of intragenic DNA sequence variations as markers of maternal cell 

contamination in prenatal diagnosis of β-thalassemia. Transl Res. 2011 

Mar;157(3):150-5. Epub 2011 Jan 12. PubMed PMID: 21316031. 

Horsfall LJ, Zeitlyn D, Tarekegn A, Bekele E, Thomas MG, Bradman N, Swallow 

DM. Prevalence of clinically relevant UGT1A alleles and haplotypes in African 

populations. Ann Hum Genet. 2011 Mar;75(2):236-46. doi: 10.1111/j.1469- 

1809.2010.00638.x. PubMed PMID: 21309756. 

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#################################################################

2011 Enero 

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################################################################# 

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2010 Octubre- Noviembre 

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2010 Septiembre 

Lechner K, Jäger U. How I treat autoimmune hemolytic anemias in adults. Blood. 

2010 Sep 16;116(11):1831-8. PMID: 20548093. 

Perseu L, Giagu N, Satta S, Sollaino MC, Congiu R, Galanello R. Red cell 

pyruvate kinase deficiency in Southern Sardinia. Blood Cells Mol Dis. 2010 

Sep 24. PMID: 20870434. 

Iolascon A, Avvisati RA, Piscopo C. Hereditary spherocytosis. Transfus Clin Biol. 

2010 Sep;17(3):138-142. PMID: 20655264. 

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2010 Agosto 

Dietz HC. New therapeutic approaches to mendelian disorders. N Engl J Med. 

2010 Aug 26;363(9):852-63. PMID: 20818846. 

Cappellini MD, Motta I, Musallam KM, Taher AT. Redefining thalassemia as a 

hypercoagulable state. Ann N Y Acad Sci. 2010 Aug;1202:231-6. PMID: 

20712798. 

Rachidi S, Musallam KM, Taher AT. A closer look at paroxysmal nocturnal 

hemoglobinuria. Eur J Intern Med. 2010 Aug;21(4):260-7. PMID: 20603032. 

Pietrangelo A. Hereditary hemochromatosis: pathogenesis, diagnosis, and 

treatment. Gastroenterology. 2010 Aug;139(2):393-408, 408.e1-2. PMID: 

20542038. 

Wang W, Knovich MA, Coffman LG, Torti FM, Torti SV. Serum ferritin: Past, 

present and future. Biochim Biophys Acta. 2010 Aug;1800(8):760-9. PMID: 

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2010 Julio

Garratty G. Immune hemolytic anemia associated with drug therapy. Blood Rev. 

2010 Jul-Sep;24(4-5):143-50. Epub 2010 Jul 21. PubMed PMID: 20650555. 

Adams PC, Barton JC. How I treat hemochromatosis. Blood. 2010 Jul 

22;116(3):317-25. Epub 2010 Mar 22. PMID: 20308595. 

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2010 Junio 

Ye H, Rouault TA. Human iron-sulfur cluster assembly, cellular iron homeostasis, 

and disease. Biochemistry. 2010 Jun 22;49(24):4945-56. PMID: 20481466. 

Weatherall DJ. The inherited diseases of hemoglobin are an emerging global 

health burden. Blood. 2010 Jun 3;115(22):4331-6. PMID: 20233970. 

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2010 Mayo 

Kremastinos DT, Farmakis D, Aessopos A, Hahalis G, Hamodraka E, Tsiapras D, 

Keren A. Beta-thalassemia cardiomyopathy: history, present considerations, 

and future perspectives. Circ Heart Fail. 2010 May;3(3):451-8. PubMed PMID: 

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Prabhakar H, Haywood C Jr, Molokie R. Sickle cell disease in the United States: 

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Cuijpers ML, Raymakers RA, Mackenzie MA, de Witte TJ, Swinkels DW. Recent 

advances in the understanding of iron overload in sideroblastic 

myelodysplastic syndrome. Br J Haematol. 2010 May;149(3):322-33. PMID: 

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2010 Abril 

Benson JM, Therrell BL Jr. History and current status of newborn screening for 

hemoglobinopathies. Semin Perinatol. 2010 Apr;34(2):134-44. PMID: 

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Narla A, Ebert BL. Ribosomopathies: human disorders of ribosome dysfunction. 

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2010 Marzo

Puy H, Gouya L, Deybach JC. Porphyrias. Lancet. 2010 Mar 13;375(9718):924- 

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2010 Febrero 

Kwiatkowski JL. Oral iron chelators. Hematol Oncol Clin North Am. 2010 

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Cao A, Galanello R. Beta-thalassemia. Genet Med. 2010 Feb;12(2):61-76. PMID: 

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Tefferi A, Gotlib J, Pardanani A. Hypereosinophilic syndrome and clonal 

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Mulloy JC, Cancelas JA, Filippi MD, Kalfa TA, Guo F, Zheng Y. Rho GTPases in 

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Boron WF. Evaluating the role of carbonic anhydrases in the transport of HCO3related 

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Belcher JD, Beckman JD, Balla G, Balla J, Vercellotti G. Heme degradation and 

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2010 Enero 

Ganz T, Nemeth E. Hepcidin and Disorders of Iron Metabolism. Annu Rev Med. 


MacMillan ML, Walters MC, Gluckman E. Transplant outcomes in bone marrow 

failure syndromes and hemoglobinopathies. Semin Hematol. 2010 

Jan;47(1):37-45. PMID: 20109610. 

Nemeth E. Targeting the hepcidin-ferroportin axis in the diagnosis and treatment 

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Turbpaiboon C, Wilairat P. Alpha-hemoglobin stabilizing protein: molecular 

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Stover PJ. Vitamin B12 and older adults. Curr Opin Clin Nutr Metab Care. 2010 

Jan;13(1):24-7. PMID: 19904199. 

Ballas SK, Lieff S, Benjamin LJ, Dampier CD, Heeney MM, Hoppe C, Johnson 

CS, Rogers ZR, Smith-Whitley K, Wang WC, Telen MJ; Investigators, 

Comprehensive Sickle Cell Centers. Definitions of the phenotypic 

manifestations of sickle cell disease. Am J Hematol. 2010 Jan;85(1):6-13. 

PMID: 19902523. 

Lankhorst CE, Wish JB. Anemia in renal disease: diagnosis and management. 

Blood Rev. 2010 Jan;24(1):39-47. PMID: 19833421.

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