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Journal articles
0
0
Persistent hypoglycemia in seven-year-old Saudi child : a case report.
Al-Azmi, Fayez.
Oman Medical Specialty Board.
2020-07
Persistent hypoglycemia in seven-year-old Saudi child : a case report.
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
0
0
Congenital adrenal hyperplasia due to 17-alpha-hydoxylase/17,20-lyase deficiency presenting with hypertension and pseudohermaphroditism : first case report from Oman.
Mula-Abed, Waad-Allah S.
Oman Medical Specialty Board.
2014-01
Congenital adrenal hyperplasia due to 17-alpha-hydoxylase/17,20-lyase deficiency presenting with hypertension and pseudohermaphroditism : first case report from Oman.
Journal articles
0
0
Demographic features and etiology of congenital hypothyroidism at the National Diabetes and Endocrine Center in Oman from 2004 to 2016.
Al-Jafari, Mohammed.
Oman Medical Specialty Board.
2020-09
Demographic features and etiology of congenital hypothyroidism at the National Diabetes and Endocrine Center in Oman from 2004 to 2016.
Journal articles
0
0
Diagnosis of microvillous inclusion disease : a case report and literature review with significance for Oman.
Al-Sinaniyah, Siham.
Oman Medical Specialty Board.
2012-11
Diagnosis of microvillous inclusion disease : a case report and literature review with significance for Oman.
Journal articles
0
0
Fibromatosis colli : a case report.
Khalid, Saifullah.
Oman Medical Specialty Board.
2012-11
Fibromatosis colli : a case report.
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Language
English
(26)
Category
Journal articles
(26)
Publication Date
Collection
Journal articles
(24)
Subject
Congenital
(4)
Congenital hypothyroidism
(4)
Congenital heart disease
(2)
Neonatal screening
(2)
Oman
(2)
Stridor, Congenital abnormalities
(2)
Adolescents--Oman
(1)
Antibiotics
(1)
Basal ganglia
(1)
Birth trauma
(1)
Botulinum toxin type A
(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)
Congenital torticollis
(1)
Consanguineous marriages.
(1)
Consanguinity.
(1)
Endocrine disorders
(1)
Fibromatosis colli
(1)
Hernia, Inguinal
(1)
Hypertension--Oman
(1)
Hypoglycemia
(1)
Hypoparathyroidism
(1)
Infant, Newborn
(1)
Infants
(1)
Insulinoma
(1)
Intestinal transplantation
(1)
Laparoscopy
(1)
Lipodystrophy
(1)
Magnetic Resonance Imaging
(1)
Methemoglobinemia
(1)
Microvillous inclusion disease
(1)
Neonates.
(1)
Pancreatic neoplasm
(1)
Pediatrics
(1)
Premature birth
(1)
Saudi Arabia
(1)
Small intestine biopsy
(1)
Sternomastoid tumor
(1)
Thrombocytosis
(1)
Thyroid-stimulating hormone
(1)
Thyroid dysgenesis
(1)
Thyroxine
(1)
Tracheostomy
(1)
Ultrasonography
(1)
Author
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)
Publisher
Oman Medical Specialty Board
(22)
College of Medicine Sultan Qaboos University
(3)
Medquest Communications LLC
(1)
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