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عدد العناصر المسترجعة: 114
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مقالات الدوريات
0
0
Dyskeratosis congenita- management and review of complications : a case report.
Sinha, Shivam.
2013-07
Dyskeratosis congenita- management and review of complications : a case report.
مقالات الدوريات
0
0
Avascular necrosis of the hip in sickle cell disease in Oman : is it serious enough to warrant bone marrow transplantation?.
Wali, Yasser.
College of Medicine, Sultan Qaboos University.
2011-02
Avascular necrosis of the hip in sickle cell disease in Oman : is it serious enough to warrant bone marrow transplantation?.
مقالات الدوريات
0
0
Comparative study of the therapeutic potential of mesenchymal stem cells derived from adipose tissue and bone marrow on acute myocardial infarction model.
Omar, Amira M.
Oman Medical Specialty Board.
2019-11
Comparative study of the therapeutic potential of mesenchymal stem cells derived from adipose tissue and bone marrow on acute myocardial infarction model.
مقالات الدوريات
1
0
A retrospective study of osteogenesis imperfecta in Dakhliya Region, Sultanate of Oman.
Johnson, Samuel Ceaser.
Oman Medical Specialty Board.
2008-01
A retrospective study of osteogenesis imperfecta in Dakhliya Region, Sultanate of Oman.
مقالات الدوريات
0
0
Acute renal failure in a patient with both leptospirosis and dengue fever.
Mohammad, Ehab.
Oman Medical Specialty Board.
2008-04
Acute renal failure in a patient with both leptospirosis and dengue fever.
مقالات الدوريات
0
0
Use of recombinant human parathyroid hormone to treat hungry bone syndrome in hemodialysis patient. Use of recombinant human parathyroid hormone to treat hungry bone syndrome in hemodialysis patient. Oman Medical Journal
Ahmed, Chaaban.
Oman Medical Specialty Board.
2020-07
Use of recombinant human parathyroid hormone to treat hungry bone syndrome in hemodialysis patient. Use of recombinant human parathyroid hormone to treat hungry bone syndrome in hemodialysis patient. Oman Medical Journal
مقالات الدوريات
0
0
No more milk in milk-alkali syndrome : a case report.
Al-Musawi, Ali.
Oman Medical Specialty Board.
2012-09
No more milk in milk-alkali syndrome : a case report.
مقالات الدوريات
3
0
Allelic heterogeneity in the COH1 gene explains clinical variability in Cohen syndrome.
Hennies, Hans Christian.
American Society of Human Genetics.
2004-07-28
Allelic heterogeneity in the COH1 gene explains clinical variability in Cohen syndrome.
مقالات الدوريات
0
0
Refractory seizure in childhood : Dyke-Davidoff-Masson syndrome revisited.
Dutta, Abhijit.
Oman Medical Specialty Board.
2016-07
Refractory seizure in childhood : Dyke-Davidoff-Masson syndrome revisited.
مقالات الدوريات
4
0
Spectrum of MKS1 and MKS3 mutations in Meckel syndrome : a genotype-phenotype correlation. mutation in brief #960. online.
Khaddour, Rana.
Wiley-Liss, Inc.
2007-05-01
Spectrum of MKS1 and MKS3 mutations in Meckel syndrome : a genotype-phenotype correlation. mutation in brief #960. online.
مقالات الدوريات
0
0
The effect of intradialytic aerobic exercise on dialysis efficacy in hemodialysis patients : a randomized controlled trial.
Mohseni, Raheleh.
Oman Medical Specialty Board.
2013-09
The effect of intradialytic aerobic exercise on dialysis efficacy in hemodialysis patients : a randomized controlled trial.
مقالات الدوريات
0
0
Coronary artery fistula with heart failure in early infancy.
Al-Maskari, Salim.
Oman Medical Specialty Board.
2010-07
Coronary artery fistula with heart failure in early infancy.
مقالات الدوريات
0
0
Concurrent mastoid cellulitis and langerhans cells histiocytosis : a challenging diagnosis.
Ong, Hui Yan.
Oman Medical Specialty Board.
2018-03
Concurrent mastoid cellulitis and langerhans cells histiocytosis : a challenging diagnosis.
مقالات الدوريات
0
0
An uncommon presentation of giant cell tumor.
Al-Kindiyah, Hunaina.
Oman Medical Specialty Board.
2011-09
An uncommon presentation of giant cell tumor.
مقالات الدوريات
0
0
Systolic function and intraventricular mechanical dyssynchrony assessed by advanced speckle tracking imaging with N-terminal prohormone of brain natriuretic peptide for outcome prediction in chronic heart failure patients.
Obaid, Faida A.
College of Medicine, Sultan Qaboos University.
2013-11
Systolic function and intraventricular mechanical dyssynchrony assessed by advanced speckle tracking imaging with N-terminal prohormone of brain natriuretic peptide for outcome prediction in chronic heart failure patients.
مقالات الدوريات
1
0
Factors contributing to school failure among school children in a very fast developing Arabian society.
Kamal, Madeeha.
Oman Medical Specialty Board.
2009-07
Factors contributing to school failure among school children in a very fast developing Arabian society.
مقالات الدوريات
6
0
Recurrent mutations in kindlin-1, a novel keratinocyte focal contact protein, in the autosomal recessive skin fragility and photosensitivity disorder, kindler syndrome.
Ashton, Gabrielle H. S.
Blackwell
2004-01-01
Recurrent mutations in kindlin-1, a novel keratinocyte focal contact protein, in the autosomal recessive skin fragility and photosensitivity disorder, kindler syndrome.
مقالات الدوريات
0
0
One in three : congenital bent bone disease and intermittent hyperthermia in three siblings with Stuve-Wiedemann syndrome.
Koul, Roshan.
College of Medicine, Sultan Qaboos University.
2013-05
One in three : congenital bent bone disease and intermittent hyperthermia in three siblings with Stuve-Wiedemann syndrome.
مقالات الدوريات
0
0
Pearson's Marrow-pancreas syndrome.
Al-Tamemi, Salem H.
College of Medicine, Sultan Qaboos University.
2009-08
Pearson's Marrow-pancreas syndrome.
مقالات الدوريات
4
0
Aberrant splicing is a common mutational mechanism in MKS1, a key player in Meckel-Gruber syndrome.
Frank, Valeska.
Wiley-Liss, Inc.
2007-07-01
Aberrant splicing is a common mutational mechanism in MKS1, a key player in Meckel-Gruber syndrome.
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