Author Index

A

  • Abdallah, Zeinab Y. Biochemical evaluations at two time points in 15 patients with nephropathic cystinosis under cysteamine treatment [Volume 10, Issue 2, 2022]
  • Abdelfattah, Maha I. Frequent genetic disorders associated with missing teeth and revisiting classification of anodontia: a retrospective study [Volume 10, Issue 2, 2022]
  • Abd El-Hamid, Mahmoud F. Clinical implementation of sperm DNA fragmentation studies in the assessment of male unexplained infertility [Volume 10, Issue 1, 2021]
  • Abdelkader, Mohamed A. Frequent genetic disorders associated with missing teeth and revisiting classification of anodontia: a retrospective study [Volume 10, Issue 2, 2022]
  • Abdel Kader, Rania M. A. Clinical implementation of sperm DNA fragmentation studies in the assessment of male unexplained infertility [Volume 10, Issue 1, 2021]
  • Abdelkawy, Rania F. M. Association of epidermal growth factor genotype with angiogenesis in Egyptian hepatocellular carcinoma and cirrhotic patients [Volume 10, Issue 1, 2021]
  • Abdelrahman, Moustapha A. Frequent genetic disorders associated with missing teeth and revisiting classification of anodontia: a retrospective study [Volume 10, Issue 2, 2022]
  • AboulEzz, Eman Craniofacial anomalies and three-dimensional imaging modalities with reference to the Egyptian experience [Volume 10, Issue 1, 2021]
  • Abouzaid, Maha R. Frequent genetic disorders associated with missing teeth and revisiting classification of anodontia: a retrospective study [Volume 10, Issue 2, 2022]
  • Ahmed, Nermeen El.Moataz B. Frequent genetic disorders associated with missing teeth and revisiting classification of anodontia: a retrospective study [Volume 10, Issue 2, 2022]
  • Akhavan-Niaki, Haleh Genotype–phenotype association in alpha-thalassemia cohort in a population with high prevalence of alpha and beta-thalassemia: importance of genetic screening [Volume 10, Issue 1, 2021]
  • Ashaat, Engy A. Cytokine profile in a cohort of Egyptian patients with autism spectrum disorders [Volume 10, Issue 2, 2022]
  • Azizi, Mandana Genotype–phenotype association in alpha-thalassemia cohort in a population with high prevalence of alpha and beta-thalassemia: importance of genetic screening [Volume 10, Issue 1, 2021]

B

  • Banihashemi, Ali Genotype–phenotype association in alpha-thalassemia cohort in a population with high prevalence of alpha and beta-thalassemia: importance of genetic screening [Volume 10, Issue 1, 2021]

D

  • Dawoud, Heba Case of autosomal-recessive spinal muscular atrophy with respiratory distress type 1 caused by compound heterozygous mutations in immunoglobulin-binding protein 2 gene: expansion in clinical features [Volume 10, Issue 2, 2022]
  • Dhillon, Gurpreet Black Immunity: Racial discrimination or genetic susceptibility? [Volume 10, Issue 1, 2021]
  • Dhillon, Harpreet S. Black Immunity: Racial discrimination or genetic susceptibility? [Volume 10, Issue 1, 2021]

E

  • Eid, Maha M. Clinical implementation of sperm DNA fragmentation studies in the assessment of male unexplained infertility [Volume 10, Issue 1, 2021]
  • El-Badry, Tarek H. Frequent genetic disorders associated with missing teeth and revisiting classification of anodontia: a retrospective study [Volume 10, Issue 2, 2022]
  • ElBadry, Tarek Craniofacial anomalies and three-dimensional imaging modalities with reference to the Egyptian experience [Volume 10, Issue 1, 2021]
  • El Batran, Mona Craniofacial anomalies and three-dimensional imaging modalities with reference to the Egyptian experience [Volume 10, Issue 1, 2021]
  • Eltoukhy, Safinaz E. Clinical implementation of sperm DNA fragmentation studies in the assessment of male unexplained infertility [Volume 10, Issue 1, 2021]
  • Esmaiel, Nora N. Association of epidermal growth factor genotype with angiogenesis in Egyptian hepatocellular carcinoma and cirrhotic patients [Volume 10, Issue 1, 2021]

F

  • Fateen, Ekram Biochemical evaluations at two time points in 15 patients with nephropathic cystinosis under cysteamine treatment [Volume 10, Issue 2, 2022]

H

  • Hamza, Hala Fragile X syndrome clinical and associated comorbidities [Volume 10, Issue 1, 2021]
  • Harkan, Ahmed I. Case of autosomal-recessive spinal muscular atrophy with respiratory distress type 1 caused by compound heterozygous mutations in immunoglobulin-binding protein 2 gene: expansion in clinical features [Volume 10, Issue 2, 2022]
  • Hassib, Nehal F. Frequent genetic disorders associated with missing teeth and revisiting classification of anodontia: a retrospective study [Volume 10, Issue 2, 2022]
  • Helmy, Nivine A. Clinical implementation of sperm DNA fragmentation studies in the assessment of male unexplained infertility [Volume 10, Issue 1, 2021]
  • Helwa, Iman Association of epidermal growth factor genotype with angiogenesis in Egyptian hepatocellular carcinoma and cirrhotic patients [Volume 10, Issue 1, 2021]
  • Helwa, Iman Cytokine profile in a cohort of Egyptian patients with autism spectrum disorders [Volume 10, Issue 2, 2022]
  • Hindawy, Amina Autism spectrum disorder and achondroplasia in an Egyptian patient [Volume 10, Issue 2, 2022]

I

  • Ismail, Samira Autism spectrum disorder and achondroplasia in an Egyptian patient [Volume 10, Issue 2, 2022]
  • Ismail, Somaya Autism spectrum disorder and achondroplasia in an Egyptian patient [Volume 10, Issue 2, 2022]

K

  • Kamangari, Reza Youssefi Genotype–phenotype association in alpha-thalassemia cohort in a population with high prevalence of alpha and beta-thalassemia: importance of genetic screening [Volume 10, Issue 1, 2021]
  • Kayed, Hesham F. Clinical implementation of sperm DNA fragmentation studies in the assessment of male unexplained infertility [Volume 10, Issue 1, 2021]
  • Khairat, Rabab Case of autosomal-recessive spinal muscular atrophy with respiratory distress type 1 caused by compound heterozygous mutations in immunoglobulin-binding protein 2 gene: expansion in clinical features [Volume 10, Issue 2, 2022]
  • Khalil, Yasmin M. Frequent genetic disorders associated with missing teeth and revisiting classification of anodontia: a retrospective study [Volume 10, Issue 2, 2022]
  • Kholoussi, Naglaa Association of epidermal growth factor genotype with angiogenesis in Egyptian hepatocellular carcinoma and cirrhotic patients [Volume 10, Issue 1, 2021]
  • Kholoussi, Naglaa Cytokine profile in a cohort of Egyptian patients with autism spectrum disorders [Volume 10, Issue 2, 2022]
  • Kholoussi, Shams Cytokine profile in a cohort of Egyptian patients with autism spectrum disorders [Volume 10, Issue 2, 2022]

M

  • Manalikuzhiyil, Babitha Black Immunity: Racial discrimination or genetic susceptibility? [Volume 10, Issue 1, 2021]
  • Megahed, Hisham Autism spectrum disorder and achondroplasia in an Egyptian patient [Volume 10, Issue 2, 2022]
  • Megahed, Hisham Fragile X syndrome clinical and associated comorbidities [Volume 10, Issue 1, 2021]
  • Mehrez, Mennat Craniofacial anomalies and three-dimensional imaging modalities with reference to the Egyptian experience [Volume 10, Issue 1, 2021]
  • Mehrez, Mennatahllah I. Frequent genetic disorders associated with missing teeth and revisiting classification of anodontia: a retrospective study [Volume 10, Issue 2, 2022]
  • Mohamed, Magdy M. Clinical implementation of sperm DNA fragmentation studies in the assessment of male unexplained infertility [Volume 10, Issue 1, 2021]
  • Morcos, Botros Cytokine profile in a cohort of Egyptian patients with autism spectrum disorders [Volume 10, Issue 2, 2022]
  • Mostafa, Mostafa I. Frequent genetic disorders associated with missing teeth and revisiting classification of anodontia: a retrospective study [Volume 10, Issue 2, 2022]
  • MostafaSayed, Inas S. Frequent genetic disorders associated with missing teeth and revisiting classification of anodontia: a retrospective study [Volume 10, Issue 2, 2022]

N

  • Nemat, Amany Craniofacial anomalies and three-dimensional imaging modalities with reference to the Egyptian experience [Volume 10, Issue 1, 2021]
  • Nesheli, Hassan Mahmoudi Genotype–phenotype association in alpha-thalassemia cohort in a population with high prevalence of alpha and beta-thalassemia: importance of genetic screening [Volume 10, Issue 1, 2021]
  • Nosier, Soha S. Biochemical evaluations at two time points in 15 patients with nephropathic cystinosis under cysteamine treatment [Volume 10, Issue 2, 2022]

O

  • Omar, Ahmed M. Clinical implementation of sperm DNA fragmentation studies in the assessment of male unexplained infertility [Volume 10, Issue 1, 2021]

P

  • Paniri, Alireza Genotype–phenotype association in alpha-thalassemia cohort in a population with high prevalence of alpha and beta-thalassemia: importance of genetic screening [Volume 10, Issue 1, 2021]
  • Patrick, Reeba Clinical report of Roifman syndrome with vitamin D-dependent rickets – an undocumented association [Volume 10, Issue 1, 2021]

R

  • Raouf, Haiam A. Association of epidermal growth factor genotype with angiogenesis in Egyptian hepatocellular carcinoma and cirrhotic patients [Volume 10, Issue 1, 2021]
  • Raouf, Haiam A. Cytokine profile in a cohort of Egyptian patients with autism spectrum disorders [Volume 10, Issue 2, 2022]
  • Reddy, Srivathsa T. Clinical report of Roifman syndrome with vitamin D-dependent rickets – an undocumented association [Volume 10, Issue 1, 2021]
  • Reddy, Srivathsa T. Professor Samia Temtamy: the founder of human genetics at the National Research Centre, Egypt [Volume 10, Issue 2, 2022]
  • Reddy, Srivathsa T. Molecular and cytogenetic diagnosis of disorders/differences of sex development: molecular update of genes controlling sexual differentiation [Volume 10, Issue 2, 2022]
  • Refeat, Miral M. Fragile X syndrome clinical and associated comorbidities [Volume 10, Issue 1, 2021]

S

  • Sasidharan, Shibu Black Immunity: Racial discrimination or genetic susceptibility? [Volume 10, Issue 1, 2021]
  • Shaheen, Ola Fragile X syndrome clinical and associated comorbidities [Volume 10, Issue 1, 2021]
  • Sherif, Naglaa S. Clinical implementation of sperm DNA fragmentation studies in the assessment of male unexplained infertility [Volume 10, Issue 1, 2021]
  • Singh, Shalendra Black Immunity: Racial discrimination or genetic susceptibility? [Volume 10, Issue 1, 2021]
  • Soliman, Nadia Craniofacial anomalies and three-dimensional imaging modalities with reference to the Egyptian experience [Volume 10, Issue 1, 2021]
  • Soliman, Neveen A. Biochemical evaluations at two time points in 15 patients with nephropathic cystinosis under cysteamine treatment [Volume 10, Issue 2, 2022]

T

  • Tamaddoni, Ahmad Genotype–phenotype association in alpha-thalassemia cohort in a population with high prevalence of alpha and beta-thalassemia: importance of genetic screening [Volume 10, Issue 1, 2021]
  • Thirumalesh, Parimala V. Clinical report of Roifman syndrome with vitamin D-dependent rickets – an undocumented association [Volume 10, Issue 1, 2021]

Z

  • Zaki, Maha S. Case of autosomal-recessive spinal muscular atrophy with respiratory distress type 1 caused by compound heterozygous mutations in immunoglobulin-binding protein 2 gene: expansion in clinical features [Volume 10, Issue 2, 2022]