A
-
Abdelfattah, Maha I
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]
-
Abdel-Hamid, Mohamed S.
A novel missense variant in CYP1B1 in an Egyptian patient with Primary Congenital Glaucoma [Volume 11, Issue 2, 2022, Pages 54-57]
-
Abd El-Massieh, Phoebe M.
Fanconi and Non-Fanconi anemia: A Single Center Experience of A Large Egyptian Cohort [Volume 11, Issue 1, 2022, Pages 19-28]
-
Abd El-Massieh, Phoebe M.
Health-related quality of life in Egyptian patients with familial Mediterranean fever [Volume 11, Issue 1, 2022, Pages 38-45]
-
Abdel-Salam, Ghada M.H.
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]
-
Abozid, Heba E.
Prenatal Screening of Sialic Acid-Storage Disease in Nonimmune Hydrops Fetalis [Volume 11, Issue 2, 2022, Pages 65-72]
-
Agadi, Soumya
The Need for Continuous Genomic Surveillance for Early Diagnosis of Novel Virus Infection [Volume 11, Issue 2, 2022, Pages 73-74]
-
Amer, Mahmoud A.
A novel missense variant in CYP1B1 in an Egyptian patient with Primary Congenital Glaucoma [Volume 11, Issue 2, 2022, Pages 54-57]
-
Amr, Khalda S.
Trials for Implementing Cost-effective Fanconi Anemia (FA) Molecular Diagnosis [Volume 11, Issue 2, 2022, Pages 58-64]
-
Ashaat, Engy A.
Mild phenotype of Molybdenum cofactor (MoCo) deficiency Type B among Egyptian patients [Volume 11, Issue 1, 2022, Pages 29-37]
-
Ashaat, Engy A.
Phelan–McDermid Syndrome: Expanding the Phenotype [Volume 11, Issue 2, 2022, Pages 46-53]
-
Ashaat, Neveen A.
Mild phenotype of Molybdenum cofactor (MoCo) deficiency Type B among Egyptian patients [Volume 11, Issue 1, 2022, Pages 29-37]
B
-
Baiomy, Ahmed A.
A novel missense variant in CYP1B1 in an Egyptian patient with Primary Congenital Glaucoma [Volume 11, Issue 2, 2022, Pages 54-57]
C
-
Cantagrel, Vincent
Mild phenotype of Molybdenum cofactor (MoCo) deficiency Type B among Egyptian patients [Volume 11, Issue 1, 2022, Pages 29-37]
E
-
Eid, Maha M.
Fanconi and Non-Fanconi anemia: A Single Center Experience of A Large Egyptian Cohort [Volume 11, Issue 1, 2022, Pages 19-28]
-
Eid, Maha M.
Trials for Implementing Cost-effective Fanconi Anemia (FA) Molecular Diagnosis [Volume 11, Issue 2, 2022, Pages 58-64]
-
Eid, Ola M.
Phelan–McDermid Syndrome: Expanding the Phenotype [Volume 11, Issue 2, 2022, Pages 46-53]
-
Eissa, Noura R.
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]
-
El-Bassyouni, Hala T.
Health-related quality of life in Egyptian patients with familial Mediterranean fever [Volume 11, Issue 1, 2022, Pages 38-45]
-
El-Bassyouni, Hala T.
Phelan–McDermid Syndrome: Expanding the Phenotype [Volume 11, Issue 2, 2022, Pages 46-53]
-
El-Kamah, Ghada Y.
Fanconi and Non-Fanconi anemia: A Single Center Experience of A Large Egyptian Cohort [Volume 11, Issue 1, 2022, Pages 19-28]
-
El-Kamah, Ghada Y.
Trials for Implementing Cost-effective Fanconi Anemia (FA) Molecular Diagnosis [Volume 11, Issue 2, 2022, Pages 58-64]
-
Elkhouly, Asmaa E.
A novel missense variant in CYP1B1 in an Egyptian patient with Primary Congenital Glaucoma [Volume 11, Issue 2, 2022, Pages 54-57]
-
El Noury, Mohamed A.
Prenatal Screening of Sialic Acid-Storage Disease in Nonimmune Hydrops Fetalis [Volume 11, Issue 2, 2022, Pages 65-72]
-
El Ruby, Mona O.
Mild phenotype of Molybdenum cofactor (MoCo) deficiency Type B among Egyptian patients [Volume 11, Issue 1, 2022, Pages 29-37]
-
El-Ruby, Mona O.
Phelan–McDermid Syndrome: Expanding the Phenotype [Volume 11, Issue 2, 2022, Pages 46-53]
-
Erian, Peter SF
Fanconi and Non-Fanconi anemia: A Single Center Experience of A Large Egyptian Cohort [Volume 11, Issue 1, 2022, Pages 19-28]
-
Essawi, Mona L.
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]
F
-
Farid, Marwa
Fanconi and Non-Fanconi anemia: A Single Center Experience of A Large Egyptian Cohort [Volume 11, Issue 1, 2022, Pages 19-28]
-
Fateen, Ekram M.
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]
G
-
Gaber, Khaled R.
Prenatal Screening of Sialic Acid-Storage Disease in Nonimmune Hydrops Fetalis [Volume 11, Issue 2, 2022, Pages 65-72]
-
Gamal El Din, Heba M.
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]
-
Gouda, Amr S.
Prenatal Screening of Sialic Acid-Storage Disease in Nonimmune Hydrops Fetalis [Volume 11, Issue 2, 2022, Pages 65-72]
H
-
Hamed, Khaled
Health-related quality of life in Egyptian patients with familial Mediterranean fever [Volume 11, Issue 1, 2022, Pages 38-45]
-
Hamed, Khaled
Phelan–McDermid Syndrome: Expanding the Phenotype [Volume 11, Issue 2, 2022, Pages 46-53]
-
Hamed, Khaled
A novel missense variant in CYP1B1 in an Egyptian patient with Primary Congenital Glaucoma [Volume 11, Issue 2, 2022, Pages 54-57]
-
Hamed, Khaled
Trials for Implementing Cost-effective Fanconi Anemia (FA) Molecular Diagnosis [Volume 11, Issue 2, 2022, Pages 58-64]
-
Hassan, Heba A.
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]
-
Hussein, Shymaa H.
Phelan–McDermid Syndrome: Expanding the Phenotype [Volume 11, Issue 2, 2022, Pages 46-53]
I
-
Ismail, Samira
Mild phenotype of Molybdenum cofactor (MoCo) deficiency Type B among Egyptian patients [Volume 11, Issue 1, 2022, Pages 29-37]
-
Ismail, Samira
Phelan–McDermid Syndrome: Expanding the Phenotype [Volume 11, Issue 2, 2022, Pages 46-53]
-
Ismail, Somaia
A novel missense variant in CYP1B1 in an Egyptian patient with Primary Congenital Glaucoma [Volume 11, Issue 2, 2022, Pages 54-57]
-
Issa, Mahmoud Y.
A novel missense variant in CYP1B1 in an Egyptian patient with Primary Congenital Glaucoma [Volume 11, Issue 2, 2022, Pages 54-57]
K
-
Kamel, Alaa K.
Phelan–McDermid Syndrome: Expanding the Phenotype [Volume 11, Issue 2, 2022, Pages 46-53]
M
-
Mahrous, Rana
Phelan–McDermid Syndrome: Expanding the Phenotype [Volume 11, Issue 2, 2022, Pages 46-53]
-
Megahed, Hisham
Mild phenotype of Molybdenum cofactor (MoCo) deficiency Type B among Egyptian patients [Volume 11, Issue 1, 2022, Pages 29-37]
-
Mohamed, Amal M.
Phelan–McDermid Syndrome: Expanding the Phenotype [Volume 11, Issue 2, 2022, Pages 46-53]
-
Mohamed, Ramy
Phelan–McDermid Syndrome: Expanding the Phenotype [Volume 11, Issue 2, 2022, Pages 46-53]
-
Mosaad, Rehab M.
Trials for Implementing Cost-effective Fanconi Anemia (FA) Molecular Diagnosis [Volume 11, Issue 2, 2022, Pages 58-64]
N
-
Nazim, Walaa S.
Prenatal Screening of Sialic Acid-Storage Disease in Nonimmune Hydrops Fetalis [Volume 11, Issue 2, 2022, Pages 65-72]
R
-
Ravichandhiran, Gowthamkarthic
The Need for Continuous Genomic Surveillance for Early Diagnosis of Novel Virus Infection [Volume 11, Issue 2, 2022, Pages 73-74]
S
-
Sabry, Sahar
Trials for Implementing Cost-effective Fanconi Anemia (FA) Molecular Diagnosis [Volume 11, Issue 2, 2022, Pages 58-64]
-
Sharnoubi, Jehan A.
Prenatal Screening of Sialic Acid-Storage Disease in Nonimmune Hydrops Fetalis [Volume 11, Issue 2, 2022, Pages 65-72]
-
Soliman, Doaa R.
Phelan–McDermid Syndrome: Expanding the Phenotype [Volume 11, Issue 2, 2022, Pages 46-53]
T
-
Temtamy, Samia A.
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]
-
Thomas, Manal M.
Fanconi and Non-Fanconi anemia: A Single Center Experience of A Large Egyptian Cohort [Volume 11, Issue 1, 2022, Pages 19-28]
-
Thomas, Manal M.
Health-related quality of life in Egyptian patients with familial Mediterranean fever [Volume 11, Issue 1, 2022, Pages 38-45]
Z
-
Zaki, Maha S.
Phelan–McDermid Syndrome: Expanding the Phenotype [Volume 11, Issue 2, 2022, Pages 46-53]
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