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مقالات الدوريات
0
0
Multiple autoimmune syndromes associated with psoriasis : a rare clinical presentation.
Masood, Sadia.
Oman Medical Specialty Board.
2014-03
Multiple autoimmune syndromes associated with psoriasis : a rare clinical presentation.
مقالات الدوريات
0
0
Autoimmune polyglandular syndrome Type II presenting as an endocrine emergency : a case report.
Ray, Sayantan.
Oman Medical Specialty Board.
2013-05
Autoimmune polyglandular syndrome Type II presenting as an endocrine emergency : a case report.
مقالات الدوريات
4
0
Latent autoimmune diabetes in adults : a case report.
Shaikh, Khalid.
Oman Medical Specialty Board.
2024-01-01
Latent autoimmune diabetes in adults : a case report.
مقالات الدوريات
0
0
Ulcerative stomatitis as the sole manifestation of progesterone hypersensitivity.
Al-Amad, Suhail H.
Oman Medical Specialty Board.
2020-11
Ulcerative stomatitis as the sole manifestation of progesterone hypersensitivity.
الرسائل والأطروحات الجامعية
0
0
Machine learning for identifying severity clusters in Omani patients with systemic lupus erythematosus.
AL-Sawafiyah, Sumaya Khalifa Aamir.
Sultan Qaboos University.
2021
Machine learning for identifying severity clusters in Omani patients with systemic lupus erythematosus.
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
Genetic association between interleukin genes and alopecia areata in Jordanian patients.
Al-Eitan, Laith N.
Oman Medical Specialty Board.
2022-09
Genetic association between interleukin genes and alopecia areata in Jordanian patients.
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
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.
مقالات الدوريات
0
0
Neuroleptic malignant syndrome associated with lithium toxicity.
Patil, Vaibhav.
Oman Medical Specialty Board.
2016-07
Neuroleptic malignant syndrome associated with lithium toxicity.
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