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Journal articles
0
0
Sanjad-Sakati Syndrome in Omani children.
Rafique, Bushra.
Oman Medical Specialty Board.
2010-07
Sanjad-Sakati Syndrome in Omani children.
Theses and Dissertations
0
0
Genomic studies of autosomal recessive epilepsies in three Omani consanguineous families
Basak, Saroma.
Sultan Qaboos University
2016
Genomic studies of autosomal recessive epilepsies in three Omani consanguineous families
Journal articles
0
0
A novel mutation of PARK-2 gene in a patient with early-onset Parkinson's disease.
Alafifi, Tariq.
Oman Medical Specialty Board.
2020-05
A novel mutation of PARK-2 gene in a patient with early-onset Parkinson's disease.
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
0
0
Treatable neuropsychiatric syndrome of catatonia : a case review from Oman.
Al-Sinawi, Hamed.
Oman Medical Specialty Board.
2013-09
Treatable neuropsychiatric syndrome of catatonia : a case review from Oman.
Theses and Dissertations
0
0
Assessment of social and economic burden of autism spectrum disorder in the Sultanate of Oman: a cross-sectional study.
Al-Fahdiyah, Samiya Sulaiman Sailm.
Sultan Qaboos University
2012
Assessment of social and economic burden of autism spectrum disorder in the Sultanate of Oman: a cross-sectional study.
Journal articles
0
0
Measurement of impairment among children with attention deficit hyperactivity disorder as part of evaluating treatment outcome.
Al-Ansari, Ahmed M.
College of Medicine, Sultan Qaboos University.
2013-05
Measurement of impairment among children with attention deficit hyperactivity disorder as part of evaluating treatment outcome.
Journal articles
0
0
Psychological morbidity in primary health care in Oman : a preliminary study.
Al-Lawatiyah, Jalila.
College of Medicine, Sultan Qaboos University.
2000
Psychological morbidity in primary health care in Oman : a preliminary study.
Journal articles
0
0
Autosomal dominant polycystic kidney disease and pericardial effusion.
Fernandez, Guillermo Alberto Perez.
Oman Medical Specialty Board.
2018-09
Autosomal dominant polycystic kidney disease and pericardial effusion.
Journal articles
0
0
Genetic biomarkers in association with depressive disorder in UAE residents : a pilot case study.
Mahmood, Nailah.
Oman Medical Specialty Board.
2021-07
Genetic biomarkers in association with depressive disorder in UAE residents : a pilot case study.
Theses and Dissertations
1
0
The quality of life among parents of children with autism spectrum disorder in Oman : a case-control study
, .Omar AbdulazizAl-Farsi
Sultan Qaboos University
2016
The quality of life among parents of children with autism spectrum disorder in Oman : a case-control study
Journal articles
0
0
Autologous peripheral blood stem cell transplantation among lymphoproliferative disease patiets : factors influencing engraftment.
Hassan, Mohd. Nazri.
Oman Medical Specialty Board.
2019
Autologous peripheral blood stem cell transplantation among lymphoproliferative disease patiets : factors influencing engraftment.
Journal articles
0
0
Autologous Peripheral blood stem cell transplantation among lymphoproliferative disease patients : factors Influencing engraftment.
Hassan, Mohd Nazri.
Oman Medical Specialty Board.
2019-01
Autologous Peripheral blood stem cell transplantation among lymphoproliferative disease patients : factors Influencing engraftment.
Journal articles
0
0
Quality of life in patients with coronary artery disease and panic disorder : a comparative study.
Srivastava, Shruti.
Oman Medical Specialty Board.
2017-01
Quality of life in patients with coronary artery disease and panic disorder : a comparative study.
Journal articles
0
0
Hypertelorism in Charcot-Marie-Tooth disease 1A from the common PMP22 duplication : a case report.
Finsterer, Josef.
Oman Medical Specialty Board.
2012-03
Hypertelorism in Charcot-Marie-Tooth disease 1A from the common PMP22 duplication : a case report.
Theses and Dissertations
0
0
Prevalence, symptoms and risk factors of diagnosed autistic spectrum disorder in the Sultanate of Oman : a case-control study
, .Omar AbdulazizAl-Farsi
Sultan Qaboos University
2010
Prevalence, symptoms and risk factors of diagnosed autistic spectrum disorder in the Sultanate of Oman : a case-control study
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.
Theses and Dissertations
0
0
Effects of gallic acid and ellagic acid on attention deficit hyperactivity disorder (ADHD) : behavioral, histopathological, molecular and biochemical aspects in a trimethyltin chloride (TMT)-Induced animal model.
Moghadas, Marzieh.
Sultan Qaboos University.
2020
Effects of gallic acid and ellagic acid on attention deficit hyperactivity disorder (ADHD) : behavioral, histopathological, molecular and biochemical aspects in a trimethyltin chloride (TMT)-Induced animal model.
Journal articles
0
0
A novel mutation causing 17-β-hydroxysteroid dehydrogenase Type 3 deficiency in an Omani child : first case report and review of literature.
Al-Sinaniyah, Aisha.
Oman Medical Specialty Board.
2015-03
A novel mutation causing 17-β-hydroxysteroid dehydrogenase Type 3 deficiency in an Omani child : first case report and review of literature.
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English
(19)
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Journal articles
(14)
Theses and Dissertations
(5)
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Journal articles
(14)
Theses and Dissertations
(5)
Subject
Autism in children
(2)
Autistic Disorder
(2)
Autologous transplantation
(2)
Lymphoma
(2)
Lymphoproliferative disorder
(2)
Multiple myeloma
(2)
Stem cell
(2)
17--hydroxysteriod dehydrogenase Type 3 deficiency
(1)
Ambiguous genitalia
(1)
Antioxidants
(1)
Attention deficit disorder with hyperactivity
(1)
Autosomal recessive disorder
(1)
Autosomal recessive Parkinsonism
(1)
Benzodiazepine
(1)
biochemistry
(1)
Biomarkers
(1)
Catatonia
(1)
Chest pain
(1)
Children--Health and hygiene
(1)
Chronic renal diseases
(1)
Codon, Nonsense
(1)
Codon, Terminator
(1)
Congenital diarrheal disorder
(1)
Coronary artery disease
(1)
Delta 4-androstenedione
(1)
Depressive disorder
(1)
Disorder of sex development, 46,XY
(1)
Estrone
(1)
Gene expression
(1)
Genetics
(1)
Hereditary neuropathy
(1)
HSD17B3 gene
(1)
Intestinal transplantation
(1)
Microvillous inclusion disease
(1)
Mood disorder
(1)
Mutation
(1)
Nerve conduction
(1)
Neuro muscular disorder
(1)
PARK 2 protein, Human
(1)
Parkinson's disease
(1)
Pericardial effusion
(1)
Peripheral nervous system
(1)
Polycystic kidney, Autosomal dominant
(1)
Primary Health Care--Oman
(1)
Quality of life
(1)
Sanjad Sakati syndrome
(1)
SLC6A4 protein, Human
(1)
Small intestine biopsy
(1)
Smoking
(1)
Testosterone
(1)
Author
, .Omar AbdulazizAl-Farsi
(2)
Al-Ansari, Ahmed M.
(1)
Al-Fahdiyah, Samiya Sulaiman Sailm.
(1)
Al-Lawatiyah, Jalila.
(1)
Al-Sinaniyah, Aisha.
(1)
Al-Sinaniyah, Siham.
(1)
Al-Sinawi, Hamed.
(1)
Al-Waili, Khalid.
(1)
Alafifi, Tariq.
(1)
Basak, Saroma.
(1)
Fernandez, Guillermo Alberto Perez.
(1)
Finsterer, Josef.
(1)
Hassan, Mohd. Nazri.
(1)
Hassan, Mohd Nazri.
(1)
Mahmood, Nailah.
(1)
Moghadas, Marzieh.
(1)
Rafique, Bushra.
(1)
Srivastava, Shruti.
(1)
Publisher
Oman Medical Specialty Board
(12)
Sultan Qaboos University
(5)
College of Medicine Sultan Qaboos University
(2)
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