Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 87

1.

Beta-thalassemia minor is associated with IgA nephropathy.

Kang JH, Park BR, Kim KS, Kim DY, Huh HJ, Chae SL, Shin SJ.

Ann Lab Med. 2013 Mar;33(2):153-5. doi: 10.3343/alm.2013.33.2.153. Epub 2013 Feb 21. No abstract available.

2.

68-year-old man with anemia and renal failure.

Chen HH, Shields RC, Bardsley WT.

Mayo Clin Proc. 1996 Feb;71(2):197-200. No abstract available.

PMID:
8577195
3.

Co-inheritance of hemoglobin D and β-thalassemia traits in three Iranian families: clinical relevance.

Taghavi Basmanj M, Karimipoor M, Amirian A, Jafarinejad M, Katouzian L, Valaei A, Bayat F, Kordafshari A, Zeinali S.

Arch Iran Med. 2011 Jan;14(1):61-3. doi: 011141/AIM.0014.

4.

A novel promoter mutation (HBB: c.-75G>T) was identified as a cause of β(+)-thalassemia.

Li Z, Li L, Yao Y, Li N, Li Y, Zhang Z, Yan F, Qiu H, Wu C, Zhang Z.

Hemoglobin. 2015;39(2):115-20. doi: 10.3109/03630269.2014.1002844. Epub 2015 Feb 6.

PMID:
25657036
5.

Hb S/β+-thalassemia due to Hb sickle and a novel deletion of DNase I hypersensitive sites HS3 and HS4 of the β locus control region.

Amid A, Cheong M, Eng B, Hanna M, Hohenadel BA, Nakamura LM, Walker L, Odame I, Kirby-Allen M, Waye JS.

Haematologica. 2015 May;100(5):e166-8. doi: 10.3324/haematol.2014.117408. Epub 2015 Feb 14. No abstract available.

6.

Severe β-thalassemia intermedia in a compound heterozygous patient for the -30 (T>A) β(+)-thalassemia mutation and the δ(0)β(+)-Senegalese deletion.

Griffon C, Joly P, Sénéchal A, Philit F, Francina A.

Hemoglobin. 2010;34(5):505-8. doi: 10.3109/03630269.2010.509230.

PMID:
20854126
7.

[Acute renal insufficiency during an episode of macroscopic hematuria in IgA glomerulonephritis].

Lumbreras Bermejo C, Martínez MA, Praga Terente M, Ruilope Urioste LM, Gutiérrez Rodero F, Rodicio Díaz JL.

Med Clin (Barc). 1987 Feb 7;88(5):195-7. Spanish. No abstract available.

PMID:
3561051
8.

[Clinicopathological study of patients presenting hematuria and proteinuria by renal biopsy].

Shinohara Y, Mitsui H, Nasu T, Hayashida S.

Nihon Hinyokika Gakkai Zasshi. 1991 Jan;82(1):72-9. Japanese.

9.

Association of IgA nephropathy and beta-thalassemia.

Harada T, Ozono Y, Miyazaki M, Yamaguchi K, Kanamoto Y, Hara K, Taguchi T.

Clin Nephrol. 1994 Mar;41(3):181-2. No abstract available.

PMID:
8187364
10.

Screening for thalassemia carriers in populations with a high rate of iron deficiency: revisiting the applicability of the Mentzer Index and the effect of iron deficiency on Hb A2 levels.

Amid A, Haghi-Ashtiani B, Kirby-Allen M, Haghi-Ashtiani MT.

Hemoglobin. 2015;39(2):141-3. doi: 10.3109/03630269.2015.1024321. Epub 2015 Mar 25.

PMID:
25806419
12.

Compromising for carrier detection of beta thalassemia based on measurement of HbA2 levels in unusual cases.

Colaco S, Colah R, Ghosh K, Nadkarni A.

Clin Chim Acta. 2012 Oct 9;413(19-20):1705-7. doi: 10.1016/j.cca.2012.05.019. Epub 2012 May 29.

PMID:
22659060
13.

Coexistence of two β-globin gene deletions in a Chinese girl with β-thalassemia minor.

Huang G, Li P, Li YX, Ye LZ.

Hemoglobin. 2014;38(1):70-2. doi: 10.3109/03630269.2013.853673. Epub 2013 Nov 7.

PMID:
24200214
14.

β-Thalassemia Intermedia Associated with Heterozygous and Isolate β-Globin Gene Mutation [IVS-II-1 (HBB: c.315G>A)].

Poddighe D, Roncoroni L, Comi EV, Bruni P.

Hemoglobin. 2015;39(5):366-7. doi: 10.3109/03630269.2015.1062776. Epub 2015 Jul 21.

PMID:
26193974
15.
16.
17.

Analysis of β/α globin ratio by using relative qRT-PCR for diagnosis of beta-thalassemia carriers.

Ranjbaran R, Okhovat MA, Mobarhanfard A, Aboualizadeh F, Abbasi M, Moezzi L, Golafshan HA, Behzad-Behbahani A, Bagheri M, Sharifzadeh S.

J Clin Lab Anal. 2013 Jul;27(4):267-71. doi: 10.1002/jcla.21594.

PMID:
23852782
18.

Thin-basement-membrane nephropathy in adults with persistent hematuria.

Tiebosch AT, Frederik PM, van Breda Vriesman PJ, Mooy JM, van Rie H, van de Wiel TW, Wolters J, Zeppenfeldt E.

N Engl J Med. 1989 Jan 5;320(1):14-8.

PMID:
2909874
19.

Somatic deletion of the normal beta-globin gene leading to thalassaemia intermedia in heterozygous beta-thalassaemic patients.

Galanello R, Perseu L, Perra C, Maccioni L, Barella S, Longinotti M, Cao A, Cazzola M.

Br J Haematol. 2004 Dec;127(5):604-6.

PMID:
15566365
20.

Absence of macroscopic hematuria in a case of IgA nephropathy and Graves' disease with acute renal failure.

Kogawa K, Ishimura E, Nishitani H, Shoji S, Nishizawa Y, Morii H.

Nephron. 1995;71(2):241-2. No abstract available.

Supplemental Content

Support Center