Literature DB >> 1734988

Homozygous haemoglobin O disease and conjugated hyperbilirubinaemia in a Sudanese family.

S A Ibrahim1, D Mustafa, A O Mohamed, M B Mohed.   

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Year:  1992        PMID： 1734988      PMCID： PMC1880929          DOI： 10.1136/bmj.304.6818.26

Source DB:  PubMed          Journal:  BMJ        ISSN： 0959-8138


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  4 in total

1.  Distribution of sickle-cell hemoglobin in Saudi Arabia.

Authors:  H LEHMANN; G MARANJIAN; A E MOURANT
Journal:  Nature       Date:  1963-05-04       Impact factor: 49.962

2.  Haemoglobin O in An Arab Family.

Authors:  B Ramot; S Fisher; D Remez; R Schneerson; D Kahane; J A Ager; H Lehmann
Journal:  Br Med J       Date:  1960-10-29

3.  [Hemoglobin anomalies and medico-biological data in 10,000 Africans (author's transl)].

Authors:  M L Coquelet; G Jaeger; N Mullender
Journal:  Nouv Rev Fr Hematol       Date:  1978-11-25

4.  Urinary coproporphyrin isomer distribution in the Dubin-Johnson syndrome.

Authors:  P Koskelo; I Toivonen; H Adlercreutz
Journal:  Clin Chem       Date:  1967-11       Impact factor: 8.327
  4 in total
  1 in total

1.  Hemoglobin variants identified in the Uganda Sickle Surveillance Study.

Authors:  Beverly A Schaefer; Charles Kiyaga; Thad A Howard; Grace Ndeezi; Arielle G Hernandez; Isaac Ssewanyana; Mary C Paniagua; Christopher M Ndugwa; Jane R Aceng; Russell E Ware
Journal:  Blood Adv       Date:  2016-11-22
  1 in total

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