A
-
Ankylosing spondylitis
Increased LncRNA TUG1 expression level impacted ankylosing spondylitis risk, association with disability, and patients’ quality of life [(Articles in Press)]
-
Aplastic anemia
Fanconi and Non-Fanconi anemia: A Single Center Experience of A Large Egyptian Cohort [Volume 11, Issue 1, 2022, Pages 19-28]
C
-
CMA
Phelan–McDermid Syndrome: Expanding the Phenotype [Volume 11, Issue 2, 2022, Pages 46-53]
-
CYP1B1 gene
A novel missense variant in CYP1B1 in an Egyptian patient with Primary Congenital Glaucoma [Volume 11, Issue 2, 2022, Pages 54-57]
D
-
Disability
Increased LncRNA TUG1 expression level impacted ankylosing spondylitis risk, association with disability, and patients’ quality of life [(Articles in Press)]
E
-
Egyptian
Fanconi and Non-Fanconi anemia: A Single Center Experience of A Large Egyptian Cohort [Volume 11, Issue 1, 2022, Pages 19-28]
-
Egyptian patient
A novel missense variant in CYP1B1 in an Egyptian patient with Primary Congenital Glaucoma [Volume 11, Issue 2, 2022, Pages 54-57]
-
Emotional functioning
Health-related quality of life in Egyptian patients with familial Mediterranean fever [Volume 11, Issue 1, 2022, Pages 38-45]
F
-
Familial Mediterranean fever
Health-related quality of life in Egyptian patients with familial Mediterranean fever [Volume 11, Issue 1, 2022, Pages 38-45]
-
FANCA
Trials for Implementing Cost-effective Fanconi Anemia (FA) Molecular Diagnosis [Volume 11, Issue 2, 2022, Pages 58-64]
-
FANCL
Trials for Implementing Cost-effective Fanconi Anemia (FA) Molecular Diagnosis [Volume 11, Issue 2, 2022, Pages 58-64]
-
Fanconi anemia
Fanconi and Non-Fanconi anemia: A Single Center Experience of A Large Egyptian Cohort [Volume 11, Issue 1, 2022, Pages 19-28]
-
Fanconi anemia
Trials for Implementing Cost-effective Fanconi Anemia (FA) Molecular Diagnosis [Volume 11, Issue 2, 2022, Pages 58-64]
-
Fanconi anemia
Exploring Telomere Length in Progeroid Syndromes through Quantitative Fluorescence In-Situ Hybridization (QFISH) [(Articles in Press)]
-
Fetal bovine serum
Influence of Different Concentrations of Human Platelet Rich Plasma Versus Fetal Bovine Serum on Periodontal Ligament Derived Stem Cells [Volume 11, Issue 1, 2022, Pages 12-18]
G
-
Genetics
Expanding the genetic spectrum of Mucolipidosis in Egyptian patients: Recurrent and novel GNPTAB and GNPTG genes variants [Volume 11, Issue 1, 2022, Pages 1-11]
-
GNPTAB gene
Expanding the genetic spectrum of Mucolipidosis in Egyptian patients: Recurrent and novel GNPTAB and GNPTG genes variants [Volume 11, Issue 1, 2022, Pages 1-11]
-
GNPTG gene
Expanding the genetic spectrum of Mucolipidosis in Egyptian patients: Recurrent and novel GNPTAB and GNPTG genes variants [Volume 11, Issue 1, 2022, Pages 1-11]
-
GPHN
Mild phenotype of Molybdenum cofactor (MoCo) deficiency Type B among Egyptian patients [Volume 11, Issue 1, 2022, Pages 29-37]
H
-
Health-Related Quality of Life
Health-related quality of life in Egyptian patients with familial Mediterranean fever [Volume 11, Issue 1, 2022, Pages 38-45]
I
-
Infection
Development of mRNA vaccine against Measles virus globally [(Articles in Press)]
K
-
Key words: Antibodies
Association of anti-thyroid peroxidase antibody among Euthyroid women with adverse pregnancy outcomes [(Articles in Press)]
L
-
LncRNA TUG1 gene expression
Increased LncRNA TUG1 expression level impacted ankylosing spondylitis risk, association with disability, and patients’ quality of life [(Articles in Press)]
M
-
Measles virus
Development of mRNA vaccine against Measles virus globally [(Articles in Press)]
-
MLPA
Phelan–McDermid Syndrome: Expanding the Phenotype [Volume 11, Issue 2, 2022, Pages 46-53]
-
MoCS1
Mild phenotype of Molybdenum cofactor (MoCo) deficiency Type B among Egyptian patients [Volume 11, Issue 1, 2022, Pages 29-37]
-
MoCS2
Mild phenotype of Molybdenum cofactor (MoCo) deficiency Type B among Egyptian patients [Volume 11, Issue 1, 2022, Pages 29-37]
-
MoCS3 genes
Mild phenotype of Molybdenum cofactor (MoCo) deficiency Type B among Egyptian patients [Volume 11, Issue 1, 2022, Pages 29-37]
-
Molecular
Expanding the genetic spectrum of Mucolipidosis in Egyptian patients: Recurrent and novel GNPTAB and GNPTG genes variants [Volume 11, Issue 1, 2022, Pages 1-11]
-
Mucolipidosis
Expanding the genetic spectrum of Mucolipidosis in Egyptian patients: Recurrent and novel GNPTAB and GNPTG genes variants [Volume 11, Issue 1, 2022, Pages 1-11]
N
-
Nonimmune hydrops fetalis
Prenatal Screening of Sialic Acid-Storage Disease in Nonimmune Hydrops Fetalis [Volume 11, Issue 2, 2022, Pages 65-72]
O
-
Outcome
Association of anti-thyroid peroxidase antibody among Euthyroid women with adverse pregnancy outcomes [(Articles in Press)]
P
-
Periodontitis
Influence of Different Concentrations of Human Platelet Rich Plasma Versus Fetal Bovine Serum on Periodontal Ligament Derived Stem Cells [Volume 11, Issue 1, 2022, Pages 12-18]
-
Phelan-McDermid syndrome
Phelan–McDermid Syndrome: Expanding the Phenotype [Volume 11, Issue 2, 2022, Pages 46-53]
-
Pregnancy
Association of anti-thyroid peroxidase antibody among Euthyroid women with adverse pregnancy outcomes [(Articles in Press)]
-
Primary congenital glaucoma
A novel missense variant in CYP1B1 in an Egyptian patient with Primary Congenital Glaucoma [Volume 11, Issue 2, 2022, Pages 54-57]
-
Progeria
Exploring Telomere Length in Progeroid Syndromes through Quantitative Fluorescence In-Situ Hybridization (QFISH) [(Articles in Press)]
-
Progeroid syndromes
Exploring Telomere Length in Progeroid Syndromes through Quantitative Fluorescence In-Situ Hybridization (QFISH) [(Articles in Press)]
-
Prophylaxis
Development of mRNA vaccine against Measles virus globally [(Articles in Press)]
Q
-
QFISH
Exploring Telomere Length in Progeroid Syndromes through Quantitative Fluorescence In-Situ Hybridization (QFISH) [(Articles in Press)]
S
-
SHANK3 gene
Phelan–McDermid Syndrome: Expanding the Phenotype [Volume 11, Issue 2, 2022, Pages 46-53]
-
Social Functioning
Health-related quality of life in Egyptian patients with familial Mediterranean fever [Volume 11, Issue 1, 2022, Pages 38-45]
T
-
Telomere length
Exploring Telomere Length in Progeroid Syndromes through Quantitative Fluorescence In-Situ Hybridization (QFISH) [(Articles in Press)]
-
THYROID
Association of anti-thyroid peroxidase antibody among Euthyroid women with adverse pregnancy outcomes [(Articles in Press)]
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