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1Management of Sickle Cell Disease Pain among Adolescent and Pediatric Patients
Samar Abdo,Khawla Q. Nuseir,Ahmad A. Altarifi,Moussa Barqawi,Nehad M. Ayoub,Tareq L. Mukkatash
Brain Sciences.2019;9(8)182
[DOI]
2Homozygosity for a haplotype in theHBG2-OR51B4region is exclusive to Arab-Indian haplotype sickle cell anemia
Vinod Vathipadiekal,Abdulrahman Alsultan,Kristin Baltrusaitis,John J. Farrell,Abdullah M. Al-Rubaish,Fahad Al-Muhanna,Zaki Naserullah,Ahmed Suliman,P.K. Patra,Jacqueline N. Milton,Lindsay A. Farrer,David H.K. Chui,Amein K. Al-Ali,Paola Sebastiani,Martin. H. Steinberg
American Journal of Hematology.2016;91(6)E308
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3A telephonic mindfulness-based intervention for persons with sickle cell disease: study protocol for a randomized controlled trial
Hants Williams,Susan Silva,Leigh Ann Simmons,Paula Tanabe
Trials.2017;18(1)E308
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4Enhancing Effect of Hydroxyurea on Hb F in Sickle Cell Disease: Ten-Year Egyptian Experience
Ilham Youssry,Amina Abdel-Salam,Rania Ismail,Rayan Bou-Fakhredin,Rania Mohamed Samy,Fatma Ezz El-Deen,Ali T. Taher
Hemoglobin.2017;41(4-6)267
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5Enhancing Effect of Hydroxyurea on Hb F in Sickle Cell Disease: Ten-Year Egyptian Experience
Robert W. Snow,Punam Amratia,Ghasem Zamani,Clara W. Mundia,Abdisalan M. Noor,Ziad A. Memish,Mohammad H. Al Zahrani,Adel Al Jasari,Mahmoud Fikri,Hoda Atta
Hemoglobin.2013;82(4-6)205
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6The role of epigenetics in human evolution
Alexander Osborne
Bioscience Horizons: The International Journal of Student Research.2017;10(4-6)205
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7Retinal changes in children and adolescents with sickle cell disease attending a paediatric hospital in Cairo, Egypt: risk factors and relation to ophthalmic and cerebral blood flow
A. A. G. Tantawy,N. G. Andrawes,A. A. M. Adly,B. A. El Kady,A. S. Shalash
Transactions of the Royal Society of Tropical Medicine and Hygiene.2013;107(4)205
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8Effect of Health Education Programme on the Knowledge of and Attitude about Sickle Cell Anaemia among Male Secondary School Students in the Jazan Region of Saudi Arabia: Health Policy Implications
Mohammed Mahmoud Kotb,Mohammed J. Almalki,Yasser Hassan,Anwar Al Sharif,Maseer Khan,Kamaludin Sheikh
BioMed Research International.2019;2019(4)1
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9Sharing sensitive health information through social media in the Arab world
Eman Asiri,Mohamed Khalifa,Syed-Abdul Shabir,Md Nassif Hossain,Usman Iqbal,Mowafa Househ
International Journal for Quality in Health Care.2016;2019(4)1
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10Quantifying the Levels of Knowledge, Attitude, and Practice Associated with Sickle Cell Disease and Premarital Genetic Counseling in 350 Saudi Adults
Heba M. Al-Qattan,Dana F. Amlih,Fatima S. Sirajuddin,Dalal I. Alhuzaimi,Mai S. Alageel,Reema M. Bin Tuwaim,Farjah H. Al Qahtani
Advances in Hematology.2019;2019(4)1
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11The Development of Genetic Counseling Services and Training Program in Saudi Arabia
Alya A. Qari,Ameera S. Balobaid,Rifaat R. Rawashdeh,Moeenaldeen D. Al-Sayed
Journal of Genetic Counseling.2013;22(6)835
[DOI]
12Expression pattern of CD55 and CD59 on red blood cells in sickle cell disease
Lama Al-Faris,Monera Al-Rukhayes,Salah Al-Humood
Hematology.2017;22(2)105
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13Current status of newborn screening worldwide: 2015
Bradford L. Therrell,Carmencita David Padilla,J. Gerard Loeber,Issam Kneisser,Amal Saadallah,Gustavo J.C. Borrajo,John Adams
Seminars in Perinatology.2015;39(3)171
[DOI]
14Current status of newborn screening worldwide: 2015
Gwyn Campbell
Seminars in Perinatology.2016;39(3)275
[DOI]
15Frequencies and phenotypic consequences of association of a- and ß-thalassemia alleles with sickle-cell disease in Bahrain
S. Abuamer,D. K. Shome,A. Jaradat,A. Radhi,J. P. Bapat,K. A. Sharif,J. Al-Touq,A. Al-Asheeri,A. Al-Ajami
International Journal of Laboratory Hematology.2017;39(1)76
[DOI]
16ßS globin gene haplotype and the stroke risk among Egyptian children with sickle cell disease
Heba H. Abou-Elew,Ilham Youssry,Shireen Hefny,Rania H. Hashem,Nevine Fouad,Rania A. Zayed
Hematology.2018;23(6)362
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17The origin of sickle cell disease in Thailand
Julia Z. Xu,Suchada Riolueang,Waraporn Glomglao,Kalaya Tachavanich,Thidarat Suksangpleng,Supachai Ekwattanakit,Vip Viprakasit
International Journal of Laboratory Hematology.2019;41(1)e13
[DOI]
18Differential Artery–Vein Analysis Improves the Performance of OCTA Staging of Sickle Cell Retinopathy
Minhaj Alam,Jennifer I. Lim,Devrim Toslak,Xincheng Yao
Translational Vision Science & Technology.2019;8(2)3
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19Novel G6B gene variant causes familial autosomal recessive thrombocytopenia and anemia
Motasem Melhem,Mohamed Abu-Farha,Dinu Antony,Ashraf Al Madhoun,Chiara Bacchelli,Fadi Alkayal,Irina AlKhairi,Sumi John,Mohamad Alomari,Phillip L. Beales,Osama Alsmadi
European Journal of Haematology.2017;98(3)218
[DOI]
20The Daily Experiences of Adolescents in Lebanon With Sickle Cell Disease
Mia Atoui,Lina Kurdahi Badr,Tamara Drenttel Brand,Ruby Khoury,Randa Shahine,Miguel Abboud
Journal of Pediatric Health Care.2015;29(5)424
[DOI]
21Allogenic hematopoietic stem cell transplantation in sickle cell disease
Ahmed Galal,Mona Asslan
Current Opinion in Hematology.2019;26(6)399
[DOI]
22Distribution of hemoglobinopathy disorders in Saudi Arabia based on data from the premarital screening and genetic counseling program, 2011–2015
Eman S. Alsaeed,Ghada N. Farhat,Abdullah M. Assiri,Ziad Memish,Elawad M. Ahmed,Mohammad Y. Saeedi,Mishal F. Al-Dossary,Hisham Bashawri
Journal of Epidemiology and Global Health.2018;7(6)S41
[DOI]
23Individualized medicine enabled by genomics in Saudi Arabia
Muhammad Abu-Elmagd,Mourad Assidi,Hans-Juergen Schulten,Ashraf Dallol,Peter Natesan Pushparaj,Farid Ahmed,Stephen W Scherer,Mohammed Al-Qahtani
BMC Medical Genomics.2015;8(S1)S41
[DOI]
24Prenatal Molecular Diagnosis of ß-Thalassemia and Sickle Cell Anemia in the Syrian Population
Hossam Murad,Faten Moassas,Rami Jarjour,Yasser Mukhalalaty,Walid Al-Achkar
Hemoglobin.2014;38(6)390
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25Prenatal Molecular Diagnosis of ß-Thalassemia and Sickle Cell Anemia in the Syrian Population
Adekunle Adekile,Julie Makani
Hemoglobin.2016;38(6)339
[DOI]
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