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Journal articles
0
0
Posterior reversible encephalopathy in undiagnosed systemic lupus erythematous : a case report.
Sulaiman, Wahinuddin.
Oman Medical Specialty Board.
2011-11
Posterior reversible encephalopathy in undiagnosed systemic lupus erythematous : a case report.
Journal articles
0
0
Posterior reversible encephalopathy syndrome in two Omani children with underlying renal diseases.
El-Naggari, Mohamed A.
College of Medicine, Sultan Qaboos University.
2015-08
Posterior reversible encephalopathy syndrome in two Omani children with underlying renal diseases.
Journal articles
0
0
A rare cause of visual efect in a Postpartum Woman
Saifudeen, Abdulrahman.
Oman Medical Specialty Board.
2010-04
A rare cause of visual efect in a Postpartum Woman
Journal articles
0
0
Ossification of posterior longitudinal ligament of cervical spine among Omani patients referred for CT Scan at a tertiary care hospital in Oman.
Sirasanagandla, Srinivasa Rao.
Oman Medical Specialty Board.
2019-09
Ossification of posterior longitudinal ligament of cervical spine among Omani patients referred for CT Scan at a tertiary care hospital in Oman.
Journal articles
0
0
Urinary ascites secondary to bladder perforation in a neonate with posterior urethral valves.
Gupta, Pankaj.
Oman Medical Specialty Board.
2013-07
Urinary ascites secondary to bladder perforation in a neonate with posterior urethral valves.
Journal articles
1
0
Recurrent myonecrosis involving adductor muscle group bilaterally : a rare complication of diabetes mellitus.
Bhat, Manzoor.
Oman Medical Specialty Board.
2014-11
Recurrent myonecrosis involving adductor muscle group bilaterally : a rare complication of diabetes mellitus.
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
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
Mastoiditis causing sinus thrombosis and posterior fossa epidural haematoma : case report.
Kaif, Mohamed.
College of Medicine, Sultan Qaboos University.
2011-02
Mastoiditis causing sinus thrombosis and posterior fossa epidural haematoma : 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
Theses and Dissertations
0
0
Assessment of risk factors related to nutrition and dietary intake among Omani women with polycystic ovarian syndrome.
Al-Fazariyah, Maryam Abdullah Said.
Sultan Qaboos University
2014
Assessment of risk factors related to nutrition and dietary intake among Omani women with polycystic ovarian syndrome.
Journal articles
0
0
Evaluation of the role of postnatal ambroxol in the prevention and treatment of respiratory distress syndrome in preterm neonates.
Elsayed, Hesham F.
College of Medicine, Sultan Qaboos University.
2006-12
Evaluation of the role of postnatal ambroxol in the prevention and treatment of respiratory distress syndrome in preterm neonates.
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Acute coronary syndrome
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Author
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Hui, David S.
(2)
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(2)
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(1)
Al-Duwaikiyah, Suad Marhoon.
(1)
Al-Kathiri, Lutfi.
(1)
Al-Kindi, Salam.
(1)
Al-Naabiyah, Hanan.
(1)
Al-Raaie, Faiza
(1)
Al-Thanoon, Zeina A.
(1)
Al-Waili, Khalid.
(1)
Al-Youbi, Reem A.
(1)
Alam, Mazhar Faiz.
(1)
Al Shidhaniyah, Azza.
(1)
Amiriani, Taghi.
(1)
Benamer, Sufyan.
(1)
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El-Shafieyah, Kawther.
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Eteiwi, Suzan.
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(1)
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(1)
Khamis, Faryal.
(1)
Khan, Amena.
(1)
Kotinatot, Suresh.
(1)
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(1)
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(1)
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(1)
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Masood, Sadia.
(1)
Naik, Sudhir M.
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Orooj, Munazza.
(1)
Panat, Sunil R.
(1)
Rafique, Bushra.
(1)
Ray, Sayantan.
(1)
Razavi, Zahra.
(1)
Roy, Mahua.
(1)
Saifudeen, Abdulrahman.
(1)
Sirasanagandla, Srinivasa Rao.
(1)
Soundaram, V.
(1)
Talari, Hamid Reza.
(1)
Thomson, Viji S.
(1)
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(69)
College of Medicine Sultan Qaboos University
(8)
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American Society of Human Genetics
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Blackwell
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Centers for disease control and prevention CDC
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