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Oman Medical Specialty Board
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Journal articles
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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
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.
Journal articles
0
0
Sanjad-Sakati Syndrome in Omani children.
Rafique, Bushra.
Oman Medical Specialty Board.
2010-07
Sanjad-Sakati Syndrome in Omani children.
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.
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.
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
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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Language
English
(9)
Category
Journal articles
(9)
Publication Date
Collection
Journal articles
(9)
Subject
Autologous transplantation
(2)
Lymphoma
(2)
Lymphoproliferative disorder
(2)
Multiple myeloma
(2)
Stem cell
(2)
17--hydroxysteriod dehydrogenase Type 3 deficiency
(1)
Ambiguous genitalia
(1)
Autosomal recessive disorder
(1)
Benzodiazepine
(1)
Biomarkers
(1)
Catatonia
(1)
Chest pain
(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)
Hereditary neuropathy
(1)
HSD17B3 gene
(1)
Intestinal transplantation
(1)
Microvillous inclusion disease
(1)
Mood disorder
(1)
Nerve conduction
(1)
Neuro muscular disorder
(1)
Panic disorder
(1)
Peripheral nervous system
(1)
Quality of life
(1)
Sanjad Sakati syndrome
(1)
SLC6A4 protein, Human
(1)
Small intestine biopsy
(1)
Smoking
(1)
Testosterone
(1)
Author
Al-Sinaniyah, Aisha.
(1)
Al-Sinaniyah, Siham.
(1)
Al-Sinawi, Hamed.
(1)
Finsterer, Josef.
(1)
Hassan, Mohd. Nazri.
(1)
Hassan, Mohd Nazri.
(1)
Mahmood, Nailah.
(1)
Rafique, Bushra.
(1)
Srivastava, Shruti.
(1)
Publisher
(-)
Oman Medical Specialty Board
(9)
Sultan Qaboos University
(4)
College of Medicine Sultan Qaboos University
(3)
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