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Items: 1 to 20 of 300

1.

Mutations in the β-globin gene from a Saudi population: an update.

Borgio JF, AbdulAzeez S, Naserullah ZA, Al-Jarrash S, Al-Ali RA, Al-Madan MS, Al-Muhanna F, Al-Suliman AM, Al-Nafie A, Steinberg MH, Al-Ali AK.

Int J Lab Hematol. 2016 Jan 29. doi: 10.1111/ijlh.12463. [Epub ahead of print] No abstract available.

PMID:
26822801
2.

The genetic basis of asymptomatic codon 8 frame-shift (HBB:c25_26delAA) β0 -thalassaemia homozygotes.

Jiang Z, Luo HY, Huang S, Farrell JJ, Davis L, Théberge R, Benson KA, Riolueang S, Viprakasit V, Al-Allawi NA, Ünal S, Gümrük F, Akar N, Başak AN, Osorio L, Badens C, Pissard S, Joly P, Campbell AD, Gallagher PG, Steinberg MH, Forget BG, Chui DH.

Br J Haematol. 2016 Jan 13. doi: 10.1111/bjh.13909. [Epub ahead of print]

PMID:
26771086
3.

Eligibility and Disqualification Recommendations for Competitive Athletes With Cardiovascular Abnormalities: Task Force 14: Sickle Cell Trait: A Scientific Statement From the American Heart Association and American College of Cardiology.

Maron BJ, Harris KM, Thompson PD, Eichner ER, Steinberg MH.

J Am Coll Cardiol. 2015 Dec 1;66(21):2444-6. doi: 10.1016/j.jacc.2015.09.046. Epub 2015 Nov 2. No abstract available.

4.

Eligibility and Disqualification Recommendations for Competitive Athletes With Cardiovascular Abnormalities: Task Force 14: Sickle Cell Trait: A Scientific Statement From the American Heart Association and American College of Cardiology.

Maron BJ, Harris KM, Thompson PD, Eichner ER, Steinberg MH; American Heart Association Electrocardiography and Arrhythmias Committee of the Council on Clinical Cardiology, Council on Cardiovascular Disease in the Young, Council on Cardiovascular and Stroke Nursing, Council on Functional Genomics and Translational Biology, and the American College of Cardiology.

Circulation. 2015 Dec 1;132(22):e343-5. doi: 10.1161/CIR.0000000000000250. Epub 2015 Nov 2. No abstract available.

PMID:
26527715
5.

Hereditary Persistence of Fetal Hemoglobin Caused by Single Nucleotide Promoter Mutations in Sickle Cell Trait and Hb SC Disease.

Akinbami AO, Campbell AD, Han ZJ, Luo HY, Chui DH, Steinberg MH.

Hemoglobin. 2016;40(1):64-5. doi: 10.3109/03630269.2015.1080725. Epub 2015 Sep 15.

PMID:
26372199
6.

Genomic approaches to identifying targets for treating β hemoglobinopathies.

Ngo DA, Steinberg MH.

BMC Med Genomics. 2015 Jul 29;8:44. doi: 10.1186/s12920-015-0120-2.

7.

HbA2 : biology, clinical relevance and a possible target for ameliorating sickle cell disease.

Steinberg MH, Rodgers GP.

Br J Haematol. 2015 Sep;170(6):781-7. doi: 10.1111/bjh.13570. Epub 2015 Jun 24. Review.

PMID:
26104837
8.

Genetic polymorphism of APOB is associated with diabetes mellitus in sickle cell disease.

Zhang X, Zhang W, Saraf SL, Nouraie M, Han J, Gowhari M, Hassan J, Miasnikova G, Sergueeva A, Nekhai S, Kittles R, Machado RF, Garcia JG, Gladwin MT, Steinberg MH, Sebastiani P, McClain DA, Gordeuk VR.

Hum Genet. 2015 Aug;134(8):895-904. doi: 10.1007/s00439-015-1572-3. Epub 2015 May 30.

9.

Co-inheritance of novel ATRX gene mutation and globin (α & β) gene mutations in transfusion dependent beta-thalassemia patients.

Al-Nafie AN, Borgio JF, AbdulAzeez S, Al-Suliman AM, Qaw FS, Naserullah ZA, Al-Jarrash S, Al-Madan MS, Al-Ali RA, AlKhalifah MA, Al-Muhanna F, Steinberg MH, Al-Ali AK.

Blood Cells Mol Dis. 2015 Jun;55(1):27-9. doi: 10.1016/j.bcmd.2015.03.008. Epub 2015 Mar 30.

PMID:
25976463
10.

BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia.

Sebastiani P, Farrell JJ, Alsultan A, Wang S, Edward HL, Shappell H, Bae H, Milton JN, Baldwin CT, Al-Rubaish AM, Naserullah Z, Al-Muhanna F, Alsuliman A, Patra PK, Farrer LA, Ngo D, Vathipadiekal V, Chui DH, Al-Ali AK, Steinberg MH.

Blood Cells Mol Dis. 2015 Mar;54(3):224-30. doi: 10.1016/j.bcmd.2015.01.001. Epub 2015 Jan 30.

PMID:
25703683
11.

Evaluation of an ensemble of genetic models for prediction of a quantitative trait.

Milton JN, Steinberg MH, Sebastiani P.

Front Genet. 2015 Jan 13;5:474. doi: 10.3389/fgene.2014.00474. eCollection 2014.

12.

Hb Youngstown [β101(G3)Glu → Ala; HBB: c.305A > C]: An unstable hemoglobin variant causing severe hemolytic anemia.

Edward HL, Pisani LA, Rodriguez-Romero WE, Chaves-Villalobos J, Garcia-Quesada J, Harris NS, Luo HY, Steinberg MH, Forget BG, Chui DH.

Hemoglobin. 2014;38(6):381-4. doi: 10.3109/03630269.2014.971960. Epub 2014 Oct 27.

PMID:
25347256
13.

More blood for sickle cell anemia?

Steinberg MH.

N Engl J Med. 2014 Aug 21;371(8):775-6. doi: 10.1056/NEJMe1405776. No abstract available.

PMID:
25140964
14.

A novel HBA2 gene conversion in cis or trans: "α12 allele" in a Saudi population.

Borgio JF, AbdulAzeez S, Al-Nafie AN, Naserullah ZA, Al-Jarrash S, Al-Madan MS, Al-Muhanna F, Steinberg MH, Al-Ali AK.

Blood Cells Mol Dis. 2014 Dec;53(4):199-203. doi: 10.1016/j.bcmd.2014.07.001. Epub 2014 Jul 25.

PMID:
25065854
15.

The genetics of hemoglobin A2 regulation in sickle cell anemia.

Griffin PJ, Sebastiani P, Edward H, Baldwin CT, Gladwin MT, Gordeuk VR, Chui DH, Steinberg MH.

Am J Hematol. 2014 Nov;89(11):1019-23. doi: 10.1002/ajh.23811. Epub 2014 Aug 4.

16.

Reply: Practice guideline for pulmonary hypertension in sickle cell: direct evidence needed before universal adoption.

Klings ES, Machado RF, Morris CR, Gordeuk VR, Kato GJ, Ataga KI, Castro O, Hsu L, Telen MJ, Krishnamurti L, Steinberg MH, Gladwin MT; ATS Clinical Guidelines for the Diagnosis and Treatment of Pulmonary Hypertension in Sickle Cell Disease Committee.

Am J Respir Crit Care Med. 2014 Jul 15;190(2):238-40. doi: 10.1164/rccm.201404-0733LE. No abstract available.

17.

Quantitative magnetic resonance imaging analysis of the lacrimal gland in sickle cell disease.

Buch K, Watanabe M, Elias EJ, Liao JH, Jara H, Nadgir RN, Saito N, Steinberg MH, Sakai O.

J Comput Assist Tomogr. 2014 Sep-Oct;38(5):674-80. doi: 10.1097/RCT.0000000000000104.

PMID:
24834886
18.

Deferiprone versus deferoxamine in sickle cell disease: results from a 5-year long-term Italian multi-center randomized clinical trial.

Calvaruso G, Vitrano A, Di Maggio R, Ballas S, Steinberg MH, Rigano P, Sacco M, Telfer P, Renda D, Barone R, Maggio A; Investigators of the Multicenter Randomized Clinical Trial of Deferiprone versus Deferoxamine in Sickle-Cell-Disease.

Blood Cells Mol Dis. 2014 Dec;53(4):265-71. doi: 10.1016/j.bcmd.2014.04.004. Epub 2014 May 9.

PMID:
24814618
19.

An official American Thoracic Society clinical practice guideline: diagnosis, risk stratification, and management of pulmonary hypertension of sickle cell disease.

Klings ES, Machado RF, Barst RJ, Morris CR, Mubarak KK, Gordeuk VR, Kato GJ, Ataga KI, Gibbs JS, Castro O, Rosenzweig EB, Sood N, Hsu L, Wilson KC, Telen MJ, Decastro LM, Krishnamurti L, Steinberg MH, Badesch DB, Gladwin MT; American Thoracic Society Ad Hoc Committee on Pulmonary Hypertension of Sickle Cell Disease.

Am J Respir Crit Care Med. 2014 Mar 15;189(6):727-40. doi: 10.1164/rccm.201401-0065ST.

20.

Prediction of fetal hemoglobin in sickle cell anemia using an ensemble of genetic risk prediction models.

Milton JN, Gordeuk VR, Taylor JG 6th, Gladwin MT, Steinberg MH, Sebastiani P.

Circ Cardiovasc Genet. 2014 Apr;7(2):110-5. doi: 10.1161/CIRCGENETICS.113.000387. Epub 2014 Mar 1.

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