Author Index

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]