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Journal articles
1
0
Neutrophil-to-lymphocyte ratio as an alternative marker of neonatal sepsis in developing countries.
Sumitro, Khadijah Rizky.
Oman Medical Specialty Board.
2021-01
Neutrophil-to-lymphocyte ratio as an alternative marker of neonatal sepsis in developing countries.
Journal articles
0
0
BRAF V600E and mismatch repair proteins expression in sporadic young-onset colorectal cancer in Kelantan, Malaysia.
Saizul, Zubaidah.
Oman Medical Specialty Board.
2021-07
BRAF V600E and mismatch repair proteins expression in sporadic young-onset colorectal cancer in Kelantan, Malaysia.
Journal articles
0
0
A novel mutation of PARK-2 gene in a patient with early-onset Parkinson's disease.
Alafifi, Tariq.
Oman Medical Specialty Board.
2020-05
A novel mutation of PARK-2 gene in a patient with early-onset Parkinson's disease.
Journal articles
0
0
A novel cystic fibrosis gene mutation C.4242+1G>C in an Omani patient : a case Report.
Al-Balushi, Said.
Oman Medical Specialty Board.
2021-03
A novel cystic fibrosis gene mutation C.4242+1G>C in an Omani patient : a case Report.
Journal articles
0
0
Evaluation of HE4, CA-125, risk of ovarian malignancy algorithm (ROMA) and risk of malignancy index (RMI) in the preoperative assessment of patients with adnexal mass.
Al-Musalhiyah, Khawla.
Oman Medical Specialty Board.
2016-09
Evaluation of HE4, CA-125, risk of ovarian malignancy algorithm (ROMA) and risk of malignancy index (RMI) in the preoperative assessment of patients with adnexal mass.
Journal articles
0
0
Gastrointestinal bleeding in tetralogy of fallot.
Mahajan, Nitin.
Oman Medical Specialty Board.
2008-07
Gastrointestinal bleeding in tetralogy of fallot.
Pagination
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English
(26)
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Journal articles
(24)
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Journal articles
(23)
Theses and Dissertations
(2)
Subject
C-reactive protein
(2)
Gene expression
(2)
Infant, Newborn
(2)
Oxidative stress
(2)
Apgar score
(1)
Autosomal recessive Parkinsonism
(1)
CFTR protein, Human
(1)
Chromosome Xp11.3 deletion
(1)
Codon, Nonsense
(1)
Codon, Terminator
(1)
Cryptogenic cirrhosis
(1)
Cystic fibrosis
(1)
Cystic fibrosis transmembrane conductance…
(1)
Dairy cows
(1)
Diabetes mellitus
(1)
Diabetes mellitus, Type 1
(1)
DNA, Mitochondrial
(1)
Epilepsy
(1)
FTO protein, Human
(1)
Genetic polymorphism
(1)
Genetics
(1)
GSPT2 protein, Human
(1)
HBV surface protein mutations
(1)
Homocysteine
(1)
Hypoacusis
(1)
Hypogonadism
(1)
Intellectual disability
(1)
Intensive care units
(1)
Ki-67 antigen
(1)
Killer cells, Natural
(1)
KLRC3 protein, Human
(1)
Lymphocytes
(1)
MAGED1 protein, Human
(1)
Melanocortin-4 receptor
(1)
Microarray analysis
(1)
Milk
(1)
Mitochondrial diseases
(1)
Multiple sclerosis
(1)
Mutation
(1)
Neonatal
(1)
Neonatal sepsis
(1)
Neoplasms
(1)
Neutrophils
(1)
Obesity
(1)
Occult hepatitis B infection--Iran
(1)
Ovarian neoplasms
(1)
PARK 2 protein, Human
(1)
Parkinson's disease
(1)
productivity
(1)
Wheat
(1)
Author
Al-Balushi, Said.
(1)
Al-Harthiyah, Sheikha Hamed.
(1)
Al-Lawatiyah, Haider Sabah Abdulameer.
(1)
Al-Macki, Nabil.
(1)
Al-Musalhiyah, Khawla.
(1)
Al-Shehhiyah, Halima.
(1)
Al-Zadjaliyah, Shireen I.
(1)
Alafifi, Tariq.
(1)
Anvari, Fatemeh Akhavan.
(1)
Finsterer, Josef.
(1)
Goddard, Stephen.
(1)
Karaarslan, Serap.
(1)
Kiselev, Anton R.
(1)
Lu, C. D.
(1)
Mahajan, Nitin.
(1)
Mahmood, Nailah.
(1)
McCann, Shaun R.
(1)
Mozafarizadeh, Mina.
(1)
Nadaf, S. K.
(1)
Rajendiran, Soundravally.
(1)
Saizul, Zubaidah.
(1)
Shaikh, A. R.
(1)
Shalaby, Dalia.
(1)
Sorkhabi, Rana.
(1)
Sumitro, Khadijah Rizky.
(1)
Thanoon, Imad A-J.
(1)
Publisher
Oman Medical Specialty Board
(16)
Sultan Qaboos University
(3)
College of Medicine Sultan Qaboos University
(2)
Sultan Qaboos university
(2)
BMJ Publishing Group
(1)
Oman Medical Speciality Board
(1)
جامعة السلطان قابوس كلية العلوم الزراعية والبحرية
(1)
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