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Journal articles
0
0
Late onset central hypoventilation syndrome due to a heterozygous polyalanine repeat expansion mutation in the PHOX2B gene.
Al-Rashdi, Ismail.
Oman Medical Specialty Board.
2011-09
Late onset central hypoventilation syndrome due to a heterozygous polyalanine repeat expansion mutation in the PHOX2B gene.
Journal articles
3
0
Association between reported aetiology of central nervous system infections and the speciality of study investigators-a bias compartmental syndrome?.
Bharucha, Tehmina.
Oxford University Press.
2017-12-01
Association between reported aetiology of central nervous system infections and the speciality of study investigators-a bias compartmental syndrome?.
Journal articles
0
0
Photodynamic therapy with verteporfin for chronic central serous choroidoretinopathy and idiopathic choroidal neovascularization : first report from the Sultanate of Oman.
Wali, Upender Krishen.
Oman Medical Specialty Board.
2008-10
Photodynamic therapy with verteporfin for chronic central serous choroidoretinopathy and idiopathic choroidal neovascularization : first report from the Sultanate of Oman.
Journal articles
0
0
Primary hypothalamic lymphoma in an adult male : a case report and literature review.
Tanki, Humam Nisar.
Oman Medical Specialty Board.
2018-07
Primary hypothalamic lymphoma in an adult male : a case report and literature review.
Journal articles
0
0
Late post traumatic right-sided diaphragmatic hernia presenting with acute intestinal obstruction and strangulation : a rare presentation.
Faridi, Shahbaz Habib.
Oman Medical Specialty Board.
2013-01
Late post traumatic right-sided diaphragmatic hernia presenting with acute intestinal obstruction and strangulation : a rare presentation.
Journal articles
0
0
Central Nervous SystemAspergillosis causing spinal cord compression.
Ahmed, Faraz.
Oman Medical Specialty Board.
2010-07
Central Nervous SystemAspergillosis causing spinal cord compression.
Journal articles
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.
Journal articles
0
0
Retrieval of dislodged central venous pressure catheters early experience with three case presentations.
Al-Hadi, Hafidh.
College of Medicine, Sultan Qaboos University.
2009-08
Retrieval of dislodged central venous pressure catheters early experience with three case presentations.
Journal articles
0
0
Correlation of intraoperative frozen section report and histopathological diagnosis of central nervous system tumors : a six-year retrospective study.
Al-Ajmiyah, Radiya.
Oman Medical Specialty Board.
2016-11
Correlation of intraoperative frozen section report and histopathological diagnosis of central nervous system tumors : a six-year retrospective study.
Journal articles
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.
Journal articles
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.
Journal articles
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.
Journal articles
0
0
Late presentation of congenital diaphragmatic hernia : a case report.
Al-Ghafri, Mohammed.
Oman Medical Specialty Board.
2014-05
Late presentation of congenital diaphragmatic hernia : a case report.
Journal articles
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.
Journal articles
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.
Journal articles
0
0
Pearson's Marrow-pancreas syndrome.
Al-Tamemi, Salem H.
College of Medicine, Sultan Qaboos University.
2009-08
Pearson's Marrow-pancreas syndrome.
Journal articles
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.
Journal articles
5
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.
Journal articles
0
0
Rapunzel syndrome.
Dhinakar, Manjula.
Oman Medical Specialty Board.
2010-10
Rapunzel syndrome.
Theses and Dissertations
0
0
Polycystic ovarian syndrome in Oman: risk factor profile, oxidative stress and psychological burden
Sulaiman, Maha Abdul Hussain Jaffar
Sultan Qaboos University
2018
Polycystic ovarian syndrome in Oman: risk factor profile, oxidative stress and psychological burden
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Acute coronary syndrome
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Ray, Sayantan.
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Shakeer, Shaik Karimulla.
(1)
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Talari, Hamid Reza.
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(1)
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