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الرسائل والأطروحات الجامعية
0
0
A prospective study of antiretroviral drug adherence in HIV-infected patients in Oman.
Al-Bimaniyah, Zamzam Mohanna Hamed.
Sultan Qaboos University
2005
A prospective study of antiretroviral drug adherence in HIV-infected patients in Oman.
الرسائل والأطروحات الجامعية
0
0
Single nucleotide polymorphisms in toll-like receptors -4, -7 and -9 and their association with AIDS pathogenesis among Omani patients.
Al-Yafeiyah, Fawziya Ahmed Ali.
2013
Single nucleotide polymorphisms in toll-like receptors -4, -7 and -9 and their association with AIDS pathogenesis among Omani patients.
الرسائل والأطروحات الجامعية
0
0
Genetic variation and diversity of the CCR5 gene and its relation to HIV.
Al-Mahruqiyah, Samira Hamed Mohamed.
2014
Genetic variation and diversity of the CCR5 gene and its relation to HIV.
مقالات الدوريات
0
0
Epidemiological and clinical characteristics of HIV infected patients at a tertiary care hospital in Oman.
Khamis, Faryal.
Oman Medical Specialty Board.
2018-07
Epidemiological and clinical characteristics of HIV infected patients at a tertiary care hospital in Oman.
مقالات الدوريات
0
0
Histomorphometric survey of placentas of HIV-positive mothers in relation to their clinical stage in a teaching Hospital in Uyo, South-South Nigeria.
Eziagu, Uchechukwu Brian.
Oman Medical Specialty Board.
2022-11
Histomorphometric survey of placentas of HIV-positive mothers in relation to their clinical stage in a teaching Hospital in Uyo, South-South Nigeria.
مقالات الدوريات
6
0
An inframe perforin gene deletion in familial hemophagocytic lymphohistiocytosis is associated with perforin expression.
Muralitharan, Shanmugakonar.
Wiley-Liss, Inc.
2005-01-01
An inframe perforin gene deletion in familial hemophagocytic lymphohistiocytosis is associated with perforin expression.
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
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
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.
مقالات الدوريات
0
0
Infectious complications reporting in common variable Immunodeficiency : a systematic review and meta-analysis.
Zainaldain, Hamed.
Oman Medical Specialty Board.
2020-07
Infectious complications reporting in common variable Immunodeficiency : a systematic review and meta-analysis.
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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Al-Raaie, Faiza
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Eteiwi, Suzan.
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Khamis, Faryal.
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Soundaram, V.
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(7)
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WileyLiss Inc
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Blackwell
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Elsevier Ltd
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Tehran University of Medical Sciences
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W B Saunders Ltd
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