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مقالات الدوريات
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.
مقالات الدوريات
2
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.
مقالات الدوريات
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
مقالات الدوريات
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.
مقالات الدوريات
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.
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
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.
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.
مقالات الدوريات
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.
مقالات الدوريات
0
0
Rapunzel syndrome.
Dhinakar, Manjula.
Oman Medical Specialty Board.
2010-10
Rapunzel syndrome.
الرسائل والأطروحات الجامعية
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
الرسائل والأطروحات الجامعية
1
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.
مقالات الدوريات
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.
مقالات الدوريات
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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