These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

91 related articles for article (PubMed ID: 25246255)

  • 1. [Hemoglobin H disease combined with hemoglobin Q-thailand and β-thalassemia: one case report and literature review].
    Xie J; Wang G; Xiao Q; Zhang Y; Zhou Y; Hu L
    Zhonghua Xue Ye Xue Za Zhi; 2014 Sep; 35(9):840-1. PubMed ID: 25246255
    [No Abstract]   [Full Text] [Related]  

  • 2. Mild hemoglobin H-constant spring disease with β-thalassemia-a case report.
    Li DZ; Liao C; Zhou JY; Xie XM; Li J
    Ann Hematol; 2011 Jan; 90(1):123-4. PubMed ID: 20383502
    [No Abstract]   [Full Text] [Related]  

  • 3. Biophysical changes of red cells with thalassemia-like abnormal hemoglobin.
    Bunyaratvej A; Fucharoen S; Tatsumi N
    Southeast Asian J Trop Med Public Health; 1992; 23 Suppl 2():86-90. PubMed ID: 1299000
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Hypochromic microcytic anemia with a variant hemoglobin.
    Bain BJ
    Am J Hematol; 2009 Jan; 84(1):59. PubMed ID: 19006231
    [No Abstract]   [Full Text] [Related]  

  • 5. Haemoglobin Q-alpha-thalassaemia.
    DORMANDY KM; LOCK SP; LEHMANN H
    Br Med J; 1961 Jun; 1(5239):1582-5. PubMed ID: 13723916
    [No Abstract]   [Full Text] [Related]  

  • 6. [Drepanocytosis with alpha and beta(o) thalassemia: a case report].
    Désidéri-Vaillant C; Olivro J; Valéro E; Kerdoncuff C; Lafontaine Y; Laborde JP
    Ann Biol Clin (Paris); 2009; 67(3):349-52. PubMed ID: 19411239
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Thalassemia, hemoglobin H disease and persistent Bart's hemoglobin in a Jewish family from Iraq].
    RAMOTH B; SHEBA C; FISHER S
    Harefuah; 1960 Jan; 58():1-3. PubMed ID: 14436103
    [No Abstract]   [Full Text] [Related]  

  • 8. A first report on Hb Q-Iran in association with alpha-thalassemia in a case of spinal ischemia.
    Zur B; Hildesheim A; Ludwig M; Stoffel-Wagner B
    Clin Lab; 2011; 57(3-4):221-4. PubMed ID: 21500730
    [TBL] [Abstract][Full Text] [Related]  

  • 9. THE FIRST OBSERVATION OF HOMOZYGOUS HEMOGLOBIN S-ALPHA THALASSEMIA DISEASE AND TWO TYPES OF SICKLE CELL THALASSEMIA DISEASE: (A) SICKLE CELL-ALPHA THALASSEMIA DISEASE, (B) SICKLE CELL-BETA THALASSEMIA DISEASE.
    AKSOY M
    Blood; 1963 Dec; 22():757-69. PubMed ID: 14084634
    [No Abstract]   [Full Text] [Related]  

  • 10. Hemoglobin Q-Thailand related disorders: origin, molecular, hematological and diagnostic aspects.
    Singsanan S; Karnpean R; Fucharoen G; Sanchaisuriya K; Sae-Ung N; Fucharoen S
    Blood Cells Mol Dis; 2010 Oct; 45(3):210-4. PubMed ID: 20615730
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Cord blood screening for alpha-thalassemia and hemoglobin variants by isoelectric focusing in northern Thai neonates: correlation with genotypes and hematologic parameters.
    Charoenkwan P; Taweephol R; Sirichotiyakul S; Tantiprabha W; Sae-Tung R; Suanta S; Sakdasirisathaporn P; Sanguansermsri T
    Blood Cells Mol Dis; 2010 Jun; 45(1):53-7. PubMed ID: 20299254
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Four cases of Hb Q-H disease found in Southern China.
    Li D; Liao C; Xie X; Zhong H; Li J
    Hemoglobin; 2007; 31(1):109-11. PubMed ID: 17365013
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Diagnosis of concurrent hemoglobin H disease and heterozygous beta-thalassemia.
    Ma ES; Chan AY; Au WY; Yeung YM; Chan LC
    Haematologica; 2001 Apr; 86(4):432-3. PubMed ID: 11325652
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Pregnancy outcomes in women complicated by thalassemia syndrome at Maharaj Nakorn Chiang Mai Hospital.
    Traisrisilp K; Luewan S; Tongsong T
    Arch Gynecol Obstet; 2009 May; 279(5):685-9. PubMed ID: 18815801
    [TBL] [Abstract][Full Text] [Related]  

  • 15. THE COEXISTENCE OF THE GENES FOR HEMOGLOBIN E AND ALPHA-THALASSEMIA IN THAIS, WITH RESULTANT SUPPRESSION OF HEMOGLOBIN E SYNTHESIS.
    TUCHINDA S; RUCKNAGEL DL; MINNICH V; BOONYAPRAKOB U; BALANKURA K; SUVATEE V
    Am J Hum Genet; 1964 Sep; 16(3):311-35. PubMed ID: 14207548
    [No Abstract]   [Full Text] [Related]  

  • 16. [Screening Abnormal Hemoglobin Diseases for Couples of Childbearing Age in Guangzhou City by HPLC].
    Chen GL; Qu YX; Jiang F; Tang Y; Tang F; Zuo LD
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2017 Dec; 25(6):1768-1771. PubMed ID: 29262913
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [CONCERNING A CASE OF TYPICAL REGIONAL PATHOLOGY: THE FIRST CASE IN SARDINIA OF COMBINED HEMOGLOBIN H DISEASE AND THALASSEMIA].
    FIASCHI E; CAMPANACCI L; NACCARATO R
    Minerva Med; 1964 May; 55():1717-24. PubMed ID: 14175655
    [No Abstract]   [Full Text] [Related]  

  • 18. Alpha-chain thalassemia and hydrops fetalis in Malaya: report of five cases.
    LIE-INJO LE
    Blood; 1962 Nov; 20():581-90. PubMed ID: 13930509
    [No Abstract]   [Full Text] [Related]  

  • 19. HAEMOGLOBIN H DISEASE IN THAILAND: A GENETICAL STUDY.
    WASI P; NA-NAKORN S; SUINGDUMRONG A
    Nature; 1964 Nov; 204():907-8. PubMed ID: 14235731
    [No Abstract]   [Full Text] [Related]  

  • 20. The correlation of α-globin gene mutations and the XmnI polymorphism with clinical severity of Hb E/β-thalassemia.
    Charoenkwan P; Teerachaimahit P; Sanguansermsri T
    Hemoglobin; 2014; 38(5):335-8. PubMed ID: 25238043
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.