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
32 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
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
3
0
Hysterical stridor : a report of two cases.
Nayar, Ravi C.
Medquest Communications LLC.
2003-01-01
Hysterical stridor : a report of two cases.
Journal articles
0
0
Unusual brain changes in tetrasomy X chromosomal anomaly.
Mshelbwala, M.
College of Medicine, Sultan Qaboos University.
2012-11
Unusual brain changes in tetrasomy X chromosomal anomaly.
Journal articles
3
0
Profile of major congenital anomalies in the Dhahira region, Oman.
Patel, Prakash Kurubarahalli.
King Faisal Specialist Hospital and Research Centre.
2007-03-01
Profile of major congenital anomalies in the Dhahira region, Oman.
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.
Journal articles
0
0
Spina bifida and birth outcome before and after fortification of flour with iron and folic acid in Oman.
Al-Asfoor, D.
World Health Organization.
2010-05
Spina bifida and birth outcome before and after fortification of flour with iron and folic acid in Oman.
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
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
Obstructed hemivagina and ipsilateral renal anomaly (OHVIRA) syndrome.
Al-Ghafriyah, Aziza.
Oman Medical Specialty Board.
2018-01
Obstructed hemivagina and ipsilateral renal anomaly (OHVIRA) syndrome.
Journal articles
0
0
Absence of left pulmonary artery : case report.
Sankhla, Dilip.
College of Medicine, Sultan Qaboos University.
2009-08
Absence of left pulmonary artery : case report.
Journal articles
0
0
Prevalence and characteristics of cystic fibrosis in Omani children : a multi-center cross-sectional study.
Al-Oraimiyah, Sumaya.
Oman Medical Specialty Board.
2022-11
Prevalence and characteristics of cystic fibrosis in Omani children : a multi-center cross-sectional study.
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
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
Next page
›
Last page
››
Filters
x
Fulltext only
Language
English
(32)
Category
Journal articles
(32)
Publication Date
Collection
Journal articles
(29)
Subject
Congenital
(4)
Congenital hypothyroidism
(4)
Abnormalities, Human--Oman
(3)
Oman
(3)
Congenital heart disease
(2)
Neonatal screening
(2)
Stridor, Congenital abnormalities
(2)
Acute coronary syndrome
(1)
Antibiotics
(1)
Arabs
(1)
Basal ganglia
(1)
Cardiovascular abnormalities
(1)
CGGM (Congenital Glucose Galactose Malabsorption)
(1)
Coarctation of the aorta
(1)
Congenital anomalies.
(1)
Congenital diarrheal disorder
(1)
Congenital disorders
(1)
Congenital generalized
(1)
Congenital hyperinsulinism
(1)
Congenital nasal pyriform aperture stenosis.
(1)
Consanguineous marriages.
(1)
Consanguinity.
(1)
Diabetes mellitus
(1)
Endocrine disorders
(1)
Hernia, Inguinal
(1)
Hypercholesterolemia
(1)
Hypertension--Oman
(1)
Hypoglycemia
(1)
Hypoparathyroidism
(1)
Infant, Newborn
(1)
Infants
(1)
Insulinoma
(1)
Laparoscopy
(1)
Lipodystrophy
(1)
Magnetic Resonance Imaging
(1)
Methemoglobinemia
(1)
Neonates.
(1)
Pancreatic neoplasm
(1)
Pediatrics
(1)
Premature birth
(1)
Renal agenesis
(1)
Saudi Arabia
(1)
Thrombocytosis
(1)
Thyroid-stimulating hormone
(1)
Thyroid dysgenesis
(1)
Thyroxine
(1)
Tracheostomy
(1)
Ultrasonography
(1)
Urogenital abnormalities
(1)
Uterus didelphys
(1)
Author
Al-Balushi, Asim.
(2)
Al-Abri, Rashid.
(1)
Al-Asfoor, D.
(1)
Al-Azmi, Fayez.
(1)
Al-Balushiyah, Zainab.
(1)
Al-Ghafriyah, Aziza.
(1)
Al-Jafari, Mohammed.
(1)
Al-Lawati, Tawfiq
(1)
Al-Mukhainiyah, Khaloud S.
(1)
Al-Oraimiyah, Sumaya.
(1)
Al-Riyamiyah, Nihal.
(1)
Al-Sinaniyah, Siham.
(1)
Al-Waili, Khalid.
(1)
Alzu'bi, Ali A.
(1)
Basak, Ramen C.
(1)
Bhatia, Jagdish.
(1)
Durowaye, Mathew.
(1)
Hemmati, Fariba.
(1)
Jana, Tapan Kumar.
(1)
Kapil, Umesh.
(1)
Khalid, Saifullah.
(1)
Mshelbwala, M.
(1)
Mula-Abed, Waad-Allah S.
(1)
Nayak, Jhasaketan.
(1)
Nayar, Ravi C.
(1)
Patel, Prakash Kurubarahalli.
(1)
Razavi, Zahra.
(1)
Sankhla, Dilip.
(1)
Shatla, Emad Sadek.
(1)
Tayebi, Naeimeh.
(1)
Zakaria, Ossama M.
(1)
Publisher
Oman Medical Specialty Board
(25)
College of Medicine Sultan Qaboos University
(4)
King Faisal Specialist Hospital and Research…
(1)
Medquest Communications LLC
(1)
World Health Organization
(1)
sfy39587stp18
