Mehaney, Dina: search on Z-Library

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1

Biochemical and genetic analysis of Leigh syndrome with complex I deficiency

Dina A. Mehaney⁎, Fayza A. Hassan, Laila A. Selim, Sawsn A. Hassan, Enrico Bertini, Fillipo Santorelli, Fabiana Fattori, Randa Sabry, Reham Zeyada

Journal:

Year:

2011

Language:

english

File:

PDF, 68 KB

english, 2011

2

Clinical, biochemical and genetic spectrum of mitochondrial disorders in Egyptian children: A study of 17 cases

Selim, Laila, Mehaney, Dina, Van Coster, Rudy, Hadi, Sawsan Abdel, Gamal, Iman, Youssry, Mariane, El Badawya, Amira, Vanlander, Arnaud, Smét, Joel, De Latter, Elien, Vandemeulebroecke, Katrien, Abdo,

Journal:

Year:

2015

Language:

english

File:

PDF, 53 KB

english, 2015

3

Lysosomal Storage Disorders in Egyptian Children

Elmonem, Mohamed A., Mahmoud, Iman G., Mehaney, Dina A., Sharaf, Sahar A., Hassan, Sawsan A., Orabi, Azza, Salem, Fadia, Girgis, Marian Y., El-Badawy, Amira, Abdelwahab, Magy, Salah, Zeinab, Soliman,

Journal:

Indian Journal of Pediatrics

Year:

2016

Language:

english

File:

PDF, 363 KB

english, 2016

4

Mitochondrial encephalopathy with lactic acidosis and stroke-like episodes in a Japanese child: Clinical, radiological and molecular genetic analysis

Selim, Laila, Mehaney, Dina

Journal:

Egyptian Journal of Medical Human Genetics

Year:

2013

Language:

english

File:

PDF, 824 KB

english, 2013

5

Serum Vitamin D and Vitamin D Receptor Gene Polymorphism in Mycosis Fungoides Patients: A Case Control Study

Rasheed, Hoda, Hegazy, Rehab A., Gawdat, Heba I., Mehaney, Dina A., Kamel, Marwa M., Fawzy, Marwa M., Nooh, Mohammed M., Darwish, Hebatallah A., Zmijewski, Michal

Journal:

Year:

2016

Language:

english

File:

PDF, 192 KB

english, 2016

6

Profile of cystic fibrosis in a single referral center in Egypt

El-Falaki, Mona M., Shahin, Walaa A., El-Basha, Noussa R., Ali, Aliaa A., Mehaney, Dina A., El-Attar, Mona M.

Journal:

Journal of Advanced Research

Year:

2014

Language:

english

File:

PDF, 453 KB

english, 2014

7

Interleukins 17 and 10 in a sample of Egyptian relapsing remitting multiple sclerosis patients

Tawfik, Tarek Z., Gad, Adel H., Mehaney, Dina A., El Nahrery, Eslam, Shehata, Hatem S., Hashem, Hebatalla, Ghaffar, Nawal F. Abdel, Shalaby, Nevin

Journal:

Journal of the Neurological Sciences

Year:

2016

Language:

english

File:

PDF, 324 KB

english, 2016

8

New Insights on Iron Study in Myelodysplasia

El Husseiny, Noha M., Mehaney, Dina Ahmed, Morad, Mohamed Abd El Kader

Journal:

Turkish Journal of Hematology

Year:

2014

File:

PDF, 229 KB

2014

9

Mitochondrial DNA depletion syndrome presenting with ataxia and external ophthalmoplegia: Case report

Selim, Laila, Mehaney, Dina, Hassan, Fayza, Sabry, Randa, Zeyada, Reham, Hassan, Sawsan, Eldin, Iman Gamal, Bertini, Enrico

Journal:

Egyptian Journal of Medical Human Genetics

Year:

2012

Language:

english

File:

PDF, 771 KB

english, 2012

10

The status of BRAFV600E mutation among Egyptian patients with papillary thyroid carcinoma

El Tawil, Ahmed, Mehaney, Dina, Anis, Shady, Salama, Asmaa, Khattab, Hany, El-Refaei, Sherif

Journal:

Comparative Clinical Pathology

Year:

2015

Language:

english

File:

PDF, 291 KB

english, 2015

11

Merosin deficient congenital muscular dystrophy: Clinical, neuroimaging and immunohistochemical study of 8 Egyptian pediatric patients

Selim, Laila Abdel moteleb, Mehaney, Dina Ahmed, Hassan, Fayza Abdel Hamid, Hassan, Sawsan Abdel Hady, Gamaleldin, Iman, Sabry, Randa, Bertini, Enrico

Journal:

Journal of Genetic Engineering and Biotechnology

Year:

2013

Language:

english

File:

PDF, 1.12 MB

english, 2013

12

Obituary

Selim, Laila Abdel moteleb, Mehaney, Dina Ahmed, Hassan, Fayza Abdel Hamid, Hassan, Sawsan Abdel Hady, Gamaleldin, Iman, Sabry, Randa, Bertini, Enrico

Journal:

Year:

1953

Language:

english

File:

PDF, 200 KB

english, 1953

13

The effect of CYP3A5 polymorphism on cyclosporine plasma level in Egyptian renal transplant recipients

Zayed, Bahaa Eldin Mostafa, Mehaney, Dina

Journal:

Comparative Clinical Pathology

Year:

2015

Language:

english

File:

PDF, 193 KB

english, 2015

14

Concerning the article “Interleukins 17 and 10 in a sample of Egyptian relapsing remitting multiple sclerosis patients”

Tawfik, Tarek Z., Gad, Adel H., Mehaney, Dina A., El Nahrery, Eslam, Shehata, Hatem S., Hashem, Hebatalla, Abdel Ghaffar, Nawal F., Shalaby, Nevin

Journal:

Journal of the Neurological Sciences

Year:

2017

Language:

english

File:

PDF, 324 KB

english, 2017

15

Mutation spectrum of Egyptian children with cystic fibrosis

Shahin, Walaa Aboulkasem, Mehaney, Dina Ahmed, El-Falaki, Mona Mostafa

Journal:

Year:

2016

Language:

english

File:

PDF, 1.04 MB

english, 2016

16

Genetic study of pediatric hypertrophic cardiomyopathy in Egypt

Darwish, Rania K., Haghighi, Alireza, Seliem, Zeinab S., El-Saiedi, Sonia A., Radwan, Nora H., El-Gayar, Dina F., Elfeel, Nesrine S., Abouelhoda, Mohamed, Mehaney, Dina A.

Journal:

Cardiology in the Young

Year:

2020

File:

PDF, 297 KB

2020

17

Triple Test Screening for Down Syndrome: An Egyptian-Tailored Study

Abou-Youssef, Hazem S., Kamal, Manal M., Mehaney, Dina A., Cai, Tao

Journal:

Year:

2014

Language:

english

File:

PDF, 828 KB

english, 2014

18

Association of vitamin D deficiency with severe pneumonia in hospitalized children under 5 years

El Basha, Noussa, Mohsen, Mona, Kamal, Marwa, Mehaney, Dina

Journal:

Comparative Clinical Pathology

Year:

2014

Language:

english

File:

PDF, 137 KB

english, 2014

19

Association of chitotriosidase enzyme activity and genotype with the risk of nephropathy in type 2 diabetes

Elmonem, Mohamed A., Amin, Hanan S., El-Essawy, Riham A., Mehaney, Dina A., Nabil, Malak, Kamel, Laila N., Farid, Ibtisam M.

Journal:

Clinical Biochemistry

Year:

2015

Language:

english

File:

PDF, 403 KB

english, 2015

20

Mitochondrial encephalopathy with lactic acidosis and stroke-like episodes (MELAS) in a Japanese child: Clinical, radiological and molecular genetic analysis

Laila Selim, Fayza Hassan, Dina Mehaney

Journal:

Year:

2012

Language:

english

File:

PDF, 71 KB

english, 2012

21

Screening of the most common mitochondrial DNA mutations among Egyptian pediatric patients with mitochondrial disorders: A one year study

Dina Mehaney, Laila Selim, Fayza Hassan

Journal:

Year:

2012

Language:

english

File:

PDF, 57 KB

english, 2012

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