Author Index

A

  • Abd Allah, Saly G. Phenotypic correlation and molecular cytogenomic study of a patient with 9p duplication and 14q terminal deletion [Volume 8, Issue 2, 2020]
  • AbdelAzeem, Amira A. A study on the association between − 31T/C and − 511C/T polymorphisms in interleukin-1β gene in Egyptian patients with keratoconus [Volume 8, Issue 2, 2020]
  • Abd El-Fattah, Abeer I. Beta-glucocerebrosidase gene mutation in a sample of Egyptian patients with Gaucher disease [Volume 8, Issue 2, 2020]
  • Abdelhamid, Ismail A. A study on the association between − 31T/C and − 511C/T polymorphisms in interleukin-1β gene in Egyptian patients with keratoconus [Volume 8, Issue 2, 2020]
  • Abdel-Kader, Mohmed Genetic syndromes with premature loss of teeth: A retrospective study and a suggested classification [Volume 8, Issue 2, 2020]
  • AbdelKader, Mohamed A. A report of four patients with Moebius syndrome: New oral anomalies and challenges in dental management [Volume 8, Issue 2, 2020]
  • Aboul-Ezz, Eman Genetic syndromes with premature loss of teeth: A retrospective study and a suggested classification [Volume 8, Issue 2, 2020]
  • Aboulnasr, Ahmed L. Prenatal counseling and diagnosis of Gaucher disease in Egypt: an 18-year experience [Volume 8, Issue 1, 2019]
  • AbulEzz, Eman A. A report of four patients with Moebius syndrome: New oral anomalies and challenges in dental management [Volume 8, Issue 2, 2020]
  • Aglan, Mona Genetic syndromes with premature loss of teeth: A retrospective study and a suggested classification [Volume 8, Issue 2, 2020]
  • Aglan, Mona S. Chromosomal aberrations and chromosomal heteromorphisms among young couples with recurrent spontaneous abortion [Volume 8, Issue 1, 2019]
  • Aglan, Mona S. A novel matrix metalloproteinase-2 mutation in two Egyptian siblings with Winchester syndrome [Volume 8, Issue 1, 2019]
  • Aglan, Mona S. A report of four patients with Moebius syndrome: New oral anomalies and challenges in dental management [Volume 8, Issue 2, 2020]
  • Ahmed Kamel, Inas E. M. Osteoarthritis in patients with familial Mediterranean fever: genetic basis and anti-inflammatory effect of laser acupuncture [Volume 8, Issue 1, 2019]
  • Alassi, Hoda H. Clinical, biochemical, and molecular characterization of an Egyptian group of patients with phenylketonuria and hyperphenylalaninemia: A pilot study [Volume 8, Issue 2, 2020]
  • Ammar, Shaimaa S. Clinical, biochemical, and molecular characterization of an Egyptian group of patients with phenylketonuria and hyperphenylalaninemia: A pilot study [Volume 8, Issue 2, 2020]
  • Amr, Khalda A novel frameshift mutation of in an Egyptian patient with autosomal recessive dystrophic epidermolysis bullosa [Volume 8, Issue 2, 2020]
  • Anwar, Shaimaa A. Clinical, biochemical, and molecular characterization of an Egyptian group of patients with phenylketonuria and hyperphenylalaninemia: A pilot study [Volume 8, Issue 2, 2020]
  • Ashaat, Engy A. Phenotypic correlation and molecular cytogenomic study of a patient with 9p duplication and 14q terminal deletion [Volume 8, Issue 2, 2020]
  • Ashaat, Engy A. Cytogenetic study of a large cohort of patients with corpus callosum abnormalities [Volume 8, Issue 2, 2020]
  • Ashaat, Engy A. Chromosomal aberrations and chromosomal heteromorphisms among young couples with recurrent spontaneous abortion [Volume 8, Issue 1, 2019]

B

  • Bellah, Nermeen El Moataz Genetic syndromes with premature loss of teeth: A retrospective study and a suggested classification [Volume 8, Issue 2, 2020]

D

E

  • Eid, Ola M. Phenotypic correlation and molecular cytogenomic study of a patient with 9p duplication and 14q terminal deletion [Volume 8, Issue 2, 2020]
  • Elbagoury, Nagham M. Beta-glucocerebrosidase gene mutation in a sample of Egyptian patients with Gaucher disease [Volume 8, Issue 2, 2020]
  • El-Bassyouni, Hala T Osteoarthritis in patients with familial Mediterranean fever: genetic basis and anti-inflammatory effect of laser acupuncture [Volume 8, Issue 1, 2019]
  • El-Bassyouni, Hala T. Body image, Anxiety, Depression and DNA damage in Obese Egyptian Women [Volume 8, Issue 1, 2019]
  • El-Bassyouni, Hala T. Chromosomal aberrations and chromosomal heteromorphisms among young couples with recurrent spontaneous abortion [Volume 8, Issue 1, 2019]
  • El-Bassyouni, Hala T. Multiple cytokine analysis in familial Mediterranean fever Egyptian cases using multiplex assay (Luminex technology) as a new inflammatory biomarker for disease activity [Volume 8, Issue 2, 2020]
  • El Darouti, Mohamed A novel frameshift mutation of in an Egyptian patient with autosomal recessive dystrophic epidermolysis bullosa [Volume 8, Issue 2, 2020]
  • Eldeen, Ghada N. Multiple cytokine analysis in familial Mediterranean fever Egyptian cases using multiplex assay (Luminex technology) as a new inflammatory biomarker for disease activity [Volume 8, Issue 2, 2020]
  • El-Desouky, Dina Genetic syndromes with premature loss of teeth: A retrospective study and a suggested classification [Volume 8, Issue 2, 2020]
  • El-Fattha, Aliaa A. A study on the association between − 31T/C and − 511C/T polymorphisms in interleukin-1β gene in Egyptian patients with keratoconus [Volume 8, Issue 2, 2020]
  • Elgerzawy, Assad M. S. Phenotypic correlation and molecular cytogenomic study of a patient with 9p duplication and 14q terminal deletion [Volume 8, Issue 2, 2020]
  • El Ghor, Mohammed Akmal Biochemical diagnosis of Wolman disease among patients with suspected lysosomal storage diseases [Volume 8, Issue 2, 2020]
  • El-Hadidi, Saher M. Genetic syndromes with premature loss of teeth: A retrospective study and a suggested classification [Volume 8, Issue 2, 2020]
  • El-Husseini, Rasha Genetic syndromes with premature loss of teeth: A retrospective study and a suggested classification [Volume 8, Issue 2, 2020]
  • El-Kamah, Ghada A novel frameshift mutation of in an Egyptian patient with autosomal recessive dystrophic epidermolysis bullosa [Volume 8, Issue 2, 2020]
  • Elnady, Hala Multiple cytokine analysis in familial Mediterranean fever Egyptian cases using multiplex assay (Luminex technology) as a new inflammatory biomarker for disease activity [Volume 8, Issue 2, 2020]
  • El Ruby, Mona O. Phenotypic correlation and molecular cytogenomic study of a patient with 9p duplication and 14q terminal deletion [Volume 8, Issue 2, 2020]
  • El Ruby, Mona O. Cytogenetic study of a large cohort of patients with corpus callosum abnormalities [Volume 8, Issue 2, 2020]
  • El Toukhy, Safinaz Body image, Anxiety, Depression and DNA damage in Obese Egyptian Women [Volume 8, Issue 1, 2019]
  • Esmail, Asmaa M. Genetic syndromes with premature loss of teeth: A retrospective study and a suggested classification [Volume 8, Issue 2, 2020]
  • Essawi, Mona L. Beta-glucocerebrosidase gene mutation in a sample of Egyptian patients with Gaucher disease [Volume 8, Issue 2, 2020]
  • Essawi, Mona L. A novel matrix metalloproteinase-2 mutation in two Egyptian siblings with Winchester syndrome [Volume 8, Issue 1, 2019]

F

  • Fateen, Ekram Biochemical diagnosis of Wolman disease among patients with suspected lysosomal storage diseases [Volume 8, Issue 2, 2020]
  • Fateen, Ekram M. Beta-glucocerebrosidase gene mutation in a sample of Egyptian patients with Gaucher disease [Volume 8, Issue 2, 2020]
  • Fateen, Ekram M. A rare mutation in an Egyptian family with Sanfilippo B syndrome [Volume 8, Issue 2, 2020]
  • Fateen, Ekram M. Prenatal counseling and diagnosis of Gaucher disease in Egypt: an 18-year experience [Volume 8, Issue 1, 2019]
  • Fathy, Heba M. Beta-glucocerebrosidase gene mutation in a sample of Egyptian patients with Gaucher disease [Volume 8, Issue 2, 2020]

G

  • Gadelhak, Mohamed I. Multiple cytokine analysis in familial Mediterranean fever Egyptian cases using multiplex assay (Luminex technology) as a new inflammatory biomarker for disease activity [Volume 8, Issue 2, 2020]

H

  • Hammad, Saida A. Chromosomal aberrations and chromosomal heteromorphisms among young couples with recurrent spontaneous abortion [Volume 8, Issue 1, 2019]
  • Hammad, Sayda Phenotypic correlation and molecular cytogenomic study of a patient with 9p duplication and 14q terminal deletion [Volume 8, Issue 2, 2020]
  • Hassan, Heba A. A novel matrix metalloproteinase-2 mutation in two Egyptian siblings with Winchester syndrome [Volume 8, Issue 1, 2019]
  • Hassib, Nehal Genetic syndromes with premature loss of teeth: A retrospective study and a suggested classification [Volume 8, Issue 2, 2020]
  • Hassib, Nehal F. A report of four patients with Moebius syndrome: New oral anomalies and challenges in dental management [Volume 8, Issue 2, 2020]
  • Helmy, Nivine A. Cytogenetic study of a large cohort of patients with corpus callosum abnormalities [Volume 8, Issue 2, 2020]
  • Helwa, Iman Multiple cytokine analysis in familial Mediterranean fever Egyptian cases using multiplex assay (Luminex technology) as a new inflammatory biomarker for disease activity [Volume 8, Issue 2, 2020]
  • Hosny, Laila Genetic syndromes with premature loss of teeth: A retrospective study and a suggested classification [Volume 8, Issue 2, 2020]
  • Hussein, Shymaa H. Phenotypic correlation and molecular cytogenomic study of a patient with 9p duplication and 14q terminal deletion [Volume 8, Issue 2, 2020]
  • Hussen, Dalia F. Cytogenetic study of a large cohort of patients with corpus callosum abnormalities [Volume 8, Issue 2, 2020]
  • Hussen, Dalia F. Chromosomal aberrations and chromosomal heteromorphisms among young couples with recurrent spontaneous abortion [Volume 8, Issue 1, 2019]

I

  • Ismail, Samira Genetic syndromes with premature loss of teeth: A retrospective study and a suggested classification [Volume 8, Issue 2, 2020]
  • Ismail, Samira Cytogenetic study of a large cohort of patients with corpus callosum abnormalities [Volume 8, Issue 2, 2020]
  • Ismail, Samira Body image, Anxiety, Depression and DNA damage in Obese Egyptian Women [Volume 8, Issue 1, 2019]
  • Ismail, Samira A novel matrix metalloproteinase-2 mutation in two Egyptian siblings with Winchester syndrome [Volume 8, Issue 1, 2019]
  • Ismail, Somaia M. A study on the association between − 31T/C and − 511C/T polymorphisms in interleukin-1β gene in Egyptian patients with keratoconus [Volume 8, Issue 2, 2020]
  • Issa, Mahmoud Y. Cytogenetic study of a large cohort of patients with corpus callosum abnormalities [Volume 8, Issue 2, 2020]

K

  • Kamel, Alaa K. Phenotypic correlation and molecular cytogenomic study of a patient with 9p duplication and 14q terminal deletion [Volume 8, Issue 2, 2020]
  • Kamel, Alaa K. Cytogenetic study of a large cohort of patients with corpus callosum abnormalities [Volume 8, Issue 2, 2020]
  • Kassem, Heba S. Clinical, biochemical, and molecular characterization of an Egyptian group of patients with phenylketonuria and hyperphenylalaninemia: A pilot study [Volume 8, Issue 2, 2020]
  • Kholoussi, Naglaa Multiple cytokine analysis in familial Mediterranean fever Egyptian cases using multiplex assay (Luminex technology) as a new inflammatory biomarker for disease activity [Volume 8, Issue 2, 2020]
  • Kholoussi, Shams Multiple cytokine analysis in familial Mediterranean fever Egyptian cases using multiplex assay (Luminex technology) as a new inflammatory biomarker for disease activity [Volume 8, Issue 2, 2020]

M

  • Mahmoud, Enas A novel frameshift mutation of in an Egyptian patient with autosomal recessive dystrophic epidermolysis bullosa [Volume 8, Issue 2, 2020]
  • Mansour, Lamia A novel frameshift mutation of in an Egyptian patient with autosomal recessive dystrophic epidermolysis bullosa [Volume 8, Issue 2, 2020]
  • Mehrez, Mennat I. Genetic syndromes with premature loss of teeth: A retrospective study and a suggested classification [Volume 8, Issue 2, 2020]
  • Mekkawy, Mona Cytogenetic study of a large cohort of patients with corpus callosum abnormalities [Volume 8, Issue 2, 2020]
  • Mohamed, Amal M. Phenotypic correlation and molecular cytogenomic study of a patient with 9p duplication and 14q terminal deletion [Volume 8, Issue 2, 2020]
  • Mohamed, Amal M. Cytogenetic study of a large cohort of patients with corpus callosum abnormalities [Volume 8, Issue 2, 2020]
  • Mohamed, Nagwa H. Osteoarthritis in patients with familial Mediterranean fever: genetic basis and anti-inflammatory effect of laser acupuncture [Volume 8, Issue 1, 2019]
  • Mohamed, Ramy Body image, Anxiety, Depression and DNA damage in Obese Egyptian Women [Volume 8, Issue 1, 2019]
  • Mohammed, Eman E. A. A rare mutation in an Egyptian family with Sanfilippo B syndrome [Volume 8, Issue 2, 2020]

O

  • Otaify, Ghada Genetic syndromes with premature loss of teeth: A retrospective study and a suggested classification [Volume 8, Issue 2, 2020]
  • Otaify, Ghada A. Chromosomal aberrations and chromosomal heteromorphisms among young couples with recurrent spontaneous abortion [Volume 8, Issue 1, 2019]

R

  • Radwan, Hoda A novel frameshift mutation of in an Egyptian patient with autosomal recessive dystrophic epidermolysis bullosa [Volume 8, Issue 2, 2020]
  • Ramadan, Abeer Osteoarthritis in patients with familial Mediterranean fever: genetic basis and anti-inflammatory effect of laser acupuncture [Volume 8, Issue 1, 2019]
  • Ramzy, Magda I. Genetic syndromes with premature loss of teeth: A retrospective study and a suggested classification [Volume 8, Issue 2, 2020]
  • Raouf, Haiam A. Multiple cytokine analysis in familial Mediterranean fever Egyptian cases using multiplex assay (Luminex technology) as a new inflammatory biomarker for disease activity [Volume 8, Issue 2, 2020]
  • Refaat, Khaled M. Cytogenetic study of a large cohort of patients with corpus callosum abnormalities [Volume 8, Issue 2, 2020]
  • Refaat, Khaled M. Chromosomal aberrations and chromosomal heteromorphisms among young couples with recurrent spontaneous abortion [Volume 8, Issue 1, 2019]

S

  • Sayed, Inas Genetic syndromes with premature loss of teeth: A retrospective study and a suggested classification [Volume 8, Issue 2, 2020]
  • Soliman, Hala N. Beta-glucocerebrosidase gene mutation in a sample of Egyptian patients with Gaucher disease [Volume 8, Issue 2, 2020]

T

  • Temtamy, Samia A. Genetic syndromes with premature loss of teeth: A retrospective study and a suggested classification [Volume 8, Issue 2, 2020]
  • Temtamy, Samia A. Chromosomal aberrations and chromosomal heteromorphisms among young couples with recurrent spontaneous abortion [Volume 8, Issue 1, 2019]
  • Temtamy, Samia A. A novel matrix metalloproteinase-2 mutation in two Egyptian siblings with Winchester syndrome [Volume 8, Issue 1, 2019]
  • Temtamy, Samia A. Frequency of balanced reciprocal translocations from couples with recurrent miscarriages correlates with the density of Alu and L1 repeat elements: literature finding-based study [Volume 8, Issue 1, 2019]
  • Temtamy, Samia A. Bone-specific therapeutic modalities for genetic skeletal diseases [Volume 8, Issue 2, 2020]
  • Temtamy, Samia A. A report of four patients with Moebius syndrome: New oral anomalies and challenges in dental management [Volume 8, Issue 2, 2020]
  • Thomas, Manal M. Osteoarthritis in patients with familial Mediterranean fever: genetic basis and anti-inflammatory effect of laser acupuncture [Volume 8, Issue 1, 2019]

Y

  • Yousef, Walaa Body image, Anxiety, Depression and DNA damage in Obese Egyptian Women [Volume 8, Issue 1, 2019]

Z

  • Zaki, Ahmed A. A study on the association between − 31T/C and − 511C/T polymorphisms in interleukin-1β gene in Egyptian patients with keratoconus [Volume 8, Issue 2, 2020]
  • Zaki, Maha S. Cytogenetic study of a large cohort of patients with corpus callosum abnormalities [Volume 8, Issue 2, 2020]
  • Zaki, Moushira E. A study on the association between − 31T/C and − 511C/T polymorphisms in interleukin-1β gene in Egyptian patients with keratoconus [Volume 8, Issue 2, 2020]
  • Zaki, Moushira E. Body image, Anxiety, Depression and DNA damage in Obese Egyptian Women [Volume 8, Issue 1, 2019]