Skip to main content
Toggle menu
Browse By
Authors
Collections
Subjects
Contact Us
Tools
Release notes
Submit content
A-
A
A+
English
العربية
Log in
Log in
Voice search
×
Start
Stop
Loading ...
Fulltext search
Media uses External URI
Sort by
Relevance
Views
Title
Author
Date Issued
Order
Asc
Desc
Items per page
20
40
60
80
Advanced Search
56 results found
Select all
Search tools
Export to CSV
Save search
Items per page
20
40
60
80
Sort Options
Relevance
Views
Title
Author
Date Issued
Sort Order
ASC
DESC
Grid
List
Select all
Journal articles
0
0
A case report of basal ganglia calcification : a rare finding of hypoparathyroidism.
Basak, Ramen C.
Oman Medical Specialty Board.
2009-07
A case report of basal ganglia calcification : a rare finding of hypoparathyroidism.
Journal articles
0
0
Congenital anomalies in infant with congenital hypothyroidism.
Razavi, Zahra.
Oman Medical Specialty Board.
2012-09
Congenital anomalies in infant with congenital hypothyroidism.
Theses and Dissertations
0
0
Assessment of folate and vitamin B12 status among newly diagnosed Omani autistic children
Al-Khalili, Maha Ali Abdullah.
Sultan Qaboos University
2012
Assessment of folate and vitamin B12 status among newly diagnosed Omani autistic children
Journal articles
0
0
Neonatal stridor in familial congenital laryngeal paralysis (Plott syndrome) : a case study in an Omani family.
Shatla, Emad Sadek.
Oman Medical Specialty Board.
2017-11
Neonatal stridor in familial congenital laryngeal paralysis (Plott syndrome) : a case study in an Omani family.
Journal articles
0
0
Familial ectrodactyly syndrome in a Nigerian child : a case report.
Durowaye, Mathew.
Oman Medical Specialty Board.
2011-07
Familial ectrodactyly syndrome in a Nigerian child : a case report.
Journal articles
3
0
Genetic analysis and outcomes of Omani children with steroid-resistant nephrotic syndrome.
Al-Riyami, Mohamed S.
John Wiley and Sons Inc.
2023-09-01
Genetic analysis and outcomes of Omani children with steroid-resistant nephrotic syndrome.
Theses and Dissertations
0
0
Mutation analysis of KI13B as a candidate gene for autosomal recessive hereditary spastic paraplegia.
Al-Barwaniyah, Hamida Sarhan.
Sultan Qaboos University
2006
Mutation analysis of KI13B as a candidate gene for autosomal recessive hereditary spastic paraplegia.
Journal articles
0
0
Berardinelli-Seip syndrome and essential thrombocytosis : an unusual association.
Alzu'bi, Ali A.
Oman Medical Specialty Board.
2020-05
Berardinelli-Seip syndrome and essential thrombocytosis : an unusual association.
Journal articles
0
0
Scapular bronchogenic cyst : a case report and literature review.
Al-Balushiyah, Zainab.
Oman Medical Specialty Board.
2012-03
Scapular bronchogenic cyst : a case report and literature review.
Journal articles
0
0
Adolescents and adults with congenital heart diseases in Oman.
Al-Balushi, Asim.
Oman Medical Specialty Board.
2015-01
Adolescents and adults with congenital heart diseases in Oman.
Journal articles
0
0
Fetal amelia : a case report.
Al-Riyamiyah, Nihal.
Oman Medical Specialty Board.
2012-01
Fetal amelia : a case report.
Journal articles
0
0
Patent contralateral processus vaginalis in infants and children : Is herniotomy justified?.
Zakaria, Ossama M.
Oman Medical Specialty Board.
2018-11
Patent contralateral processus vaginalis in infants and children : Is herniotomy justified?.
Journal articles
0
0
Coarctation of the aorta, known yet can be missed.
Al-Balushi, Asim.
Oman Medical Specialty Board.
2013-05
Coarctation of the aorta, known yet can be missed.
Journal articles
0
0
The prevalence of congenital malformations and its correlation with consanguineous marriages.
Tayebi, Naeimeh.
Oman Medical Specialty Board.
2010-01
The prevalence of congenital malformations and its correlation with consanguineous marriages.
Journal articles
19
0
A rare case of familial methemoglobinemia with congenital heart disease.
Nayak, Jhasaketan.
Oman Medical Specialty Board.
2024-05-01
A rare case of familial methemoglobinemia with congenital heart disease.
Journal articles
0
0
Oculocutaneous albinism associated with Axenfeld's anomaly : three case reports.
Keshav, B. R.
College of Medicine, Sultan Qaboos University.
2010-04
Oculocutaneous albinism associated with Axenfeld's anomaly : three case reports.
Journal articles
0
0
Nutritional status and cognitive impairment in elderly.
Daradkeh, Ghazi.
Asian Network for Scientific Information.
2014-10
Nutritional status and cognitive impairment in elderly.
Journal articles
0
0
Profile difference between male and female psychiatric patients seeking certificate of disability.
Balhara, Yatan Pal Singh.
Oman Medical Specialty Board.
2011-11
Profile difference between male and female psychiatric patients seeking certificate of disability.
Journal articles
0
0
Glucose galactose malabsorption complicated with rickets and nephrogenic diabetes insipidus.
Al-Lawati, Tawfiq
Oman Medical Specialty Board.
2008-07
Glucose galactose malabsorption complicated with rickets and nephrogenic diabetes insipidus.
Journal articles
0
0
Congenital nasal pyriform aperture Stenosis : first case report in Oman.
Al-Abri, Rashid.
Oman Medical Specialty Board.
2008-07
Congenital nasal pyriform aperture Stenosis : first case report in Oman.
Pagination
Current page
1
Page
2
Page
3
Next page
›
Last page
››
Filters
x
Fulltext only
Language
English
(56)
Category
Journal articles
(48)
Theses and Dissertations
(8)
Publication Date
Collection
Journal articles
(45)
Theses and Dissertations
(8)
Subject
Congenital
(4)
Congenital hypothyroidism
(4)
Substance-related disorders
(4)
Genetic disorders
(3)
Autism spectrum disorders
(2)
Congenital heart disease
(2)
Diseases
(2)
Infants
(2)
Magnetic Resonance Imaging
(2)
Neonatal screening
(2)
Oman
(2)
Psychiatric disorders
(2)
Saudi Arabia
(2)
Stridor, Congenital abnormalities
(2)
Vision disorders in children--Diagnosis--Oman
(2)
Adolescents
(1)
Anxiety
(1)
Children
(1)
Congenital anomalies.
(1)
Congenital generalized
(1)
Consanguineous marriages.
(1)
Consanguinity.
(1)
COVID-19--Oman
(1)
Cross-sectional studies
(1)
Cross-sectional studies--Oman
(1)
Decision trees
(1)
Depression
(1)
Doping in sports
(1)
Drug misuse--Oman
(1)
Epidemiology--Iran
(1)
Genes
(1)
Genetic testing
(1)
Hypoparathyroidism
(1)
Infant, Newborn
(1)
Iran
(1)
Laparoscopy
(1)
Lipodystrophy
(1)
Methadone
(1)
Methemoglobinemia
(1)
Phenotype
(1)
Polycystic ovary syndrome
(1)
Polymyalgia rheumatica
(1)
Prevalence
(1)
Sleep
(1)
Steroids
(1)
Thrombocytosis
(1)
Tobacco use--Oman
(1)
Tracheostomy
(1)
Universities and Colleges--Students--Oman
(1)
Weight lifting
(1)
Author
Al-Balushi, Asim.
(2)
, .Omar AbdulazizAl-Farsi
(1)
Al-Abri, Rashid.
(1)
Al-Azmi, Fayez.
(1)
Al-Balushiyah, Zainab.
(1)
Al-Barwaniyah, Hamida Sarhan.
(1)
Al-Busaidi, Saoud.
(1)
Al-Harbi, Fares F.
(1)
Al-Harby, Saleh.
(1)
Al-Harthiyah, Hasina Ahmed Suliman.
(1)
Al-Hinaai, Hazaa.
(1)
Al-Jafari, Mohammed.
(1)
Al-Kaabi, Juma.
(1)
Al-Khalili, Maha Ali Abdullah.
(1)
Al-Lawati, Tawfiq
(1)
Al-Mukhaini, Yahya Khamis Hamed.
(1)
Al-Mukhainiyah, Khaloud S.
(1)
Al-Saidiyah, Iman Khalfan.
(1)
Al-Sharbati, Marwan M.
(1)
Al-Sinaniyah, Siham.
(1)
Al-Sultiyah, Ahlam Salim Ali.
(1)
Al-Zidiyah, Ward Al-Muna Ali Rashid.
(1)
Alzu'bi, Ali A.
(1)
Ashrafi, Mahnaz.
(1)
Bait Amer, Ahmed.
(1)
Balhara, Yatan Pal Singh.
(1)
Basak, Ramen C.
(1)
Bhatia, Jagdish.
(1)
Chitme, Havagiray R.
(1)
Durowaye, Mathew.
(1)
Gogri, Urmi.
(1)
Hemmati, Fariba.
(1)
Jana, Tapan Kumar.
(1)
Jesmin, Akhter.
(1)
Juibari, Toraj Ahmadi.
(1)
Kapil, Umesh.
(1)
Keshav, B. R.
(1)
Khalid, Saifullah.
(1)
Khandekar, Rajiv B.
(1)
Manzar, Md. Dilshad.
(1)
Moradinazar, Mehdi.
(1)
Mshelbwala, M.
(1)
Mula-Abed, Waad-Allah S.
(1)
Razavi, Zahra.
(1)
Saadat, Payam.
(1)
Shatla, Emad Sadek.
(1)
Shetty, Shibani.
(1)
Tayebi, Naeimeh.
(1)
Toghae, Mansoureh.
(1)
Zakaria, Ossama M.
(1)
Publisher
Oman Medical Specialty Board
(36)
Sultan Qaboos University
(8)
College of Medicine Sultan Qaboos University
(5)
Asian Network for Scientific Information
(1)
Elsevier
(1)
John Wiley and Sons Inc
(1)
Medknow Publications
(1)
Medquest Communications LLC
(1)
Wolters Kluwer Medknow Publications
(1)
sfy39587stp18