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مقالات الدوريات
0
0
Congenital anomalies in infant with congenital hypothyroidism.
Razavi, Zahra.
Oman Medical Specialty Board.
2012-09
Congenital anomalies in infant with congenital hypothyroidism.
مقالات الدوريات
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.
مقالات الدوريات
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.
مقالات الدوريات
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.
مقالات الدوريات
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.
مقالات الدوريات
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.
مقالات الدوريات
0
0
Fetal amelia : a case report.
Al-Riyamiyah, Nihal.
Oman Medical Specialty Board.
2012-01
Fetal amelia : a case report.
مقالات الدوريات
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?.
مقالات الدوريات
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.
مقالات الدوريات
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.
مقالات الدوريات
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.
مقالات الدوريات
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.
مقالات الدوريات
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.
مقالات الدوريات
0
0
Transposition of the great arteries and coarctation of the aorta in an infant presenting with bronchiolitis : an incidental finding.
Al-Mukhainiyah, Khaloud S.
College of Medicine, Sultan Qaboos University.
2017-10
Transposition of the great arteries and coarctation of the aorta in an infant presenting with bronchiolitis : an incidental finding.
مقالات الدوريات
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.
مقالات الدوريات
0
0
A case of congenital syndromic hydrocephalus : a subtype of 'Game-Friedman- Paradice syndrome'.
Jana, Tapan Kumar.
Oman Medical Specialty Board.
2013-01
A case of congenital syndromic hydrocephalus : a subtype of 'Game-Friedman- Paradice syndrome'.
مقالات الدوريات
0
0
Health consequences of iodine deficiency.
Kapil, Umesh.
College of Medicine, Sultan Qaboos University.
2007-09
Health consequences of iodine deficiency.
مقالات الدوريات
0
0
Uncommon presentation of congenital lacrimal duct obstruction : a case report of congenital amniontocele.
Bhatia, Jagdish.
Oman Medical Specialty Board.
2007-10
Uncommon presentation of congenital lacrimal duct obstruction : a case report of congenital amniontocele.
مقالات الدوريات
0
0
Congenital hypothyroidism in preterm newborns : a retrospective study arising from a screening program in Fars Province, Southwestern Iran.
Hemmati, Fariba.
Oman Medical Specialty Board.
2019-05
Congenital hypothyroidism in preterm newborns : a retrospective study arising from a screening program in Fars Province, Southwestern Iran.
مقالات الدوريات
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.
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Oman
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Adolescents--Oman
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Botulinum toxin type A
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CGGM (Congenital Glucose Galactose Malabsorption)
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Congenital anomalies.
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Congenital generalized
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Congenital hyperinsulinism
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Congenital nasal pyriform aperture stenosis.
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Consanguineous marriages.
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Consanguinity.
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المؤلف
Al-Balushi, Asim.
(2)
Al-Abri, Rashid.
(1)
Al-Azmi, Fayez.
(1)
Al-Balushiyah, Zainab.
(1)
Al-Jafari, Mohammed.
(1)
Al-Lawati, Tawfiq
(1)
Al-Mukhainiyah, Khaloud S.
(1)
Al-Riyamiyah, Nihal.
(1)
Al-Sinaniyah, Siham.
(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)
Razavi, Zahra.
(1)
Shatla, Emad Sadek.
(1)
Tayebi, Naeimeh.
(1)
Zakaria, Ossama M.
(1)
الناشر
Oman Medical Specialty Board
(22)
College of Medicine Sultan Qaboos University
(3)
Medquest Communications LLC
(1)
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