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Oman Medical Specialty Board
Mutation
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Journal articles
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Dystonia in ataxia telangiectasia : a case report with novel mutations.
Zaki-Dizaji, Majid.
Oman Medical Specialty Board.
2020-01
Dystonia in ataxia telangiectasia : a case report with novel mutations.
Journal articles
0
0
Phenotype expression variability in children with GABRB3 heterozygous mutations.
Khair, Abdulhafeez M.
Oman Medical Specialty Board.
2021-03
Phenotype expression variability in children with GABRB3 heterozygous mutations.
Journal articles
0
0
Occurrence of optic neuritis and cervical cord schwannoma with Charcot-Marie-tooth Type 4B1disease.
Scott, Patrick.
Oman Medical Specialty Board.
2016-05
Occurrence of optic neuritis and cervical cord schwannoma with Charcot-Marie-tooth Type 4B1disease.
Journal articles
0
0
Thyroid hormone resistance due to a Novel De Novo mutation in thyroid hormone receptor alpha : first case report from the Middle East and North Africa.
Al Shidhaniyah, Azza.
Oman Medical Specialty Board.
2021-01
Thyroid hormone resistance due to a Novel De Novo mutation in thyroid hormone receptor alpha : first case report from the Middle East and North Africa.
Journal articles
0
0
Genetics and pathophysiology of maturity-onset diabetes of the young (MODY) : a review of current trends.
Yahaya, Tajudeen O.
Oman Medical Specialty Board.
2020-05
Genetics and pathophysiology of maturity-onset diabetes of the young (MODY) : a review of current trends.
Journal articles
0
0
Acrodermatitis enteropathica : a case report.
Al Naamaniyah, Asma.
Oman Medical Specialty Board.
2020-11
Acrodermatitis enteropathica : a case report.
Journal articles
0
0
Mutation in the PCSK9 gene in Omani Arab subjects with autosomal dominant hypercholesterolemia and its effect on PCSK9 protein structure.
Al-Waili, Khalid.
Oman Medical Specialty Board.
2013-01
Mutation in the PCSK9 gene in Omani Arab subjects with autosomal dominant hypercholesterolemia and its effect on PCSK9 protein structure.
Journal articles
1
0
A novel cystic fibrosis gene mutation C.4242+1G>C in an Omani patient : a case Report.
Al-Balushi, Said.
Oman Medical Specialty Board.
2021-03
A novel cystic fibrosis gene mutation C.4242+1G>C in an Omani patient : a case Report.
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Mutation
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English
(8)
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Journal articles
(8)
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(8)
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Mutation
(8)
Oman
(26)
Pregnancy
(19)
Prevalence
(18)
Tuberculosis
(17)
Magnetic Resonance Imaging
(15)
COVID-19--Oman
(14)
Depression
(14)
Incidence
(14)
Children
(13)
Diabetes
(13)
Cesarean section
(11)
Cross-sectional studies
(11)
Diabetes mellitus
(11)
Diabetes mellitus, Type 2
(11)
Infant, Newborn
(10)
Anxiety
(9)
Quality of life
(9)
Surgery
(9)
Surveys and questionnaires
(9)
Antibiotics
(8)
Histopathology
(8)
Hypertension
(8)
Laparoscopy
(8)
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(8)
Primary Health Care--Oman
(8)
Retrospective studies--Oman
(8)
Acute coronary syndrome
(7)
Blood transfusion
(7)
Coronary artery disease
(7)
COVID-19
(7)
HIV
(7)
Immunohistochemistry
(7)
Infants
(7)
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(7)
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(7)
Body mass index
(6)
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(6)
Cross-sectional studies--Oman
(6)
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(6)
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(6)
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(6)
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(6)
Renal dialysis
(6)
Risk factors
(6)
Saudi Arabia
(6)
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(6)
Systemic lupus erythematosus
(6)
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(6)
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(6)
Author
Al-Balushi, Said.
(1)
Al-Waili, Khalid.
(1)
Al Naamaniyah, Asma.
(1)
Al Shidhaniyah, Azza.
(1)
Khair, Abdulhafeez M.
(1)
Scott, Patrick.
(1)
Yahaya, Tajudeen O.
(1)
Zaki-Dizaji, Majid.
(1)
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(-)
Oman Medical Specialty Board
(8)
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