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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
[DOI]
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
[DOI]
4Hematopoietic stem cell transplantation for patients with sickle cell disease in the Eastern Mediterranean
Ali D. Alahmari,M. Aljurf,A. Alseraihy,A.A. Hamidieh,S. Alkindi,R. Rihani,T. Satti,H. Alsaedi,F. Almohareb,A. Al-Jefri,W. Rasheed
Hematology/Oncology and Stem Cell Therapy.2020;18(1)E308
[DOI]
5Acute Soft Skull Syndrome in an Adult Male with Sickle Cell Anemia in Sudan: A Case Report
Ziryab Imad Taha,Sulafa Eisa Mohammed,Mohammed Elmujtba Adam Essa,Walaa Mohamed Elsid,Mustafa Mohamed Ali Hussein,Sherihan Mohammed Elkundi Osman,Hussein Osman Ahmed,Mutwaly Defealla Yousif,Abdelkareem A. Ahmed
Exploratory Research and Hypothesis in Medicine.2019;4(4)90
[DOI]
6Enhancing 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
[DOI]
7Prevalence of Hemoglobinopathies (ß-Thalassemia and Sickle Cell Trait) in the Adult Population of Al Majma’ah, Saudi Arabia
Shabir A. Mir,Bader M. Alshehri,Mohammed Alaidarous,Saeed S. Banawas,Abdul Aziz A. Bin Dukhyil,Mohammad K. Alturki
Hemoglobin.2020;41(4-6)1
[DOI]
8Prevalence of Hemoglobinopathies (ß-Thalassemia and Sickle Cell Trait) in the Adult Population of Al Majma’ah, Saudi Arabia
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
[DOI]
9The role of epigenetics in human evolution
Alexander Osborne
Bioscience Horizons: The International Journal of Student Research.2017;10(4-6)205
[DOI]
10Distribution of sickle cell disease and assessment of risk factors based on transcranial Doppler values in the Gulf region
Yasser Wali,Vishwanatha Kini,Mohamed A. Yassin
Hematology.2020;25(1)55
[DOI]
11Retinal 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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12Effect 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
[DOI]
13Sharing 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
[DOI]
14Quantifying 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
[DOI]
15The 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]
16Expression 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
[DOI]
17Clinical and laboratory parameters, risk factors predisposing to the development of priapism in sickle cell patients
Salam Alkindi,Said S Almufargi,Anil Pathare
Experimental Biology and Medicine.2020;245(1)79
[DOI]
18Current 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]
19Current status of newborn screening worldwide: 2015
Gwyn Campbell
Seminars in Perinatology.2016;39(3)275
[DOI]
20Frequencies 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]
21ßS 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
[DOI]
22The 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]
23Differential 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
[DOI]
24Novel 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]
25The 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]
26Allogenic hematopoietic stem cell transplantation in sickle cell disease
Ahmed Galal,Mona Asslan
Current Opinion in Hematology.2019;26(6)399
[DOI]
27Distribution 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.2017;7(S1)S41
[DOI]
28Individualized 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]
29Prenatal 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
[DOI]
30Glucose 6 phosphate dehydrogenase deficiency and hemoglobinopathy in South Western Region Nepal: a boon or burden
Narayan Gautam,Bhagwati Gaire,Trishna Manandhar,Bishnu P. Marasini,Niranjan Parajuli,Sunil P. Lekhak,Monica Nepal
BMC Research Notes.2019;12(1)390
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31Effectiveness of Nurse Led Intervention on Health Related Quality of Life among Children with Sickle Cell Disease in Oman: A Pilot Study
Suthan Pandarakutty,Kamala Murali,Judie Arulappan,Deepa Shaji Thomas
Advances in Hematology.2019;2019(1)1
[DOI]
32Effectiveness of Nurse Led Intervention on Health Related Quality of Life among Children with Sickle Cell Disease in Oman: A Pilot Study
Adekunle Adekile,Julie Makani
Advances in Hematology.2016;2019(1)339
[DOI]
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