Gamal, Radwa: search on Z-Library

The world's largest scientific articles store. 70,000,000+ articles for free.

1

Kabuki make-up syndrome with genitourinary anomalies, ophthalmologic features and hyperpigmentation in an Egyptian child

Shawky, Rabah M., Gamal, Radwa, Mostafa, Nayera

Journal:

Egyptian Journal of Medical Human Genetics

Year:

2016

Language:

english

File:

PDF, 2.01 MB

english, 2016

2

Removal notice to “An Egyptian patient with Schwartz-Jampel syndrome type I and new ocular findings” [Egypt J Med Hum Genet 18 (2017) 393–396]

Elsayed, Solaf M., Gamal, Radwa

Journal:

Egyptian Journal of Medical Human Genetics

Year:

2018

File:

PDF, 238 KB

2018

3

Blepharophimosis, ptosis, epicanthus inversus syndrome type 2 with red hair, lymphedema of lower limbs and kidney stones in an Egyptian patient

Shawky, Rabah M., Gamal, Radwa, Seifeldin, Neveen S.

Journal:

Egyptian Journal of Medical Human Genetics

Year:

2015

Language:

english

File:

PDF, 1.30 MB

english, 2015

4

Berardinelli–Seip syndrome type 2 – An Egyptian child

Shawky, Rabah M., Gamal, Radwa, Seifeldin, Neveen S

Journal:

Egyptian Journal of Medical Human Genetics

Year:

2015

Language:

english

File:

PDF, 1.02 MB

english, 2015

5

Repressing PU.1 by miR-29a∗ in NK cells of HCV patients, diminishes its cytolytic effect on HCV infected cell models

Elemam, Noha Mousaad, Mekky, Radwa Yehia, El-Ekiaby, Nada Magdy, El Sobky, Shereen Ahmed, El Din, Mohammad Ahmad Mohey, Esmat, Gamal, Abdelaziz, Ahmed Ihab

Journal:

Human Immunology

Year:

2015

Language:

english

File:

PDF, 1002 KB

english, 2015

6

Baraitser–Winter syndrome: An additional Egyptian patient with skeletal anomalies, bilateral iris and choroid colobomas, retinal hypoplasia and hypoplastic scrotum

Shawky, Rabah M., Gamal, Radwa, Mohammad, Shaimaa Abdelsattar

Journal:

Egyptian Journal of Medical Human Genetics

Year:

2016

Language:

english

File:

PDF, 1.42 MB

english, 2016

7

Genotype-phenotype correlation in 18 Egyptian patients with glutaric acidemia type I

Mosaeilhy, Ahmed, Mohamed, Magdy M., C, George Priya Doss, El Abd, Heba S. A., Gamal, Radwa, Zaki, Osama K., Zayed, Hatem

Journal:

Metabolic Brain Disease

Year:

2017

Language:

english

File:

PDF, 738 KB

english, 2017

8

Predictive prognostic role of miR‑181a with discrepancy in the liver and serum of genotype 4 hepatitis C virus patients

Elhelw, Dalia, Mekky, Radwa, El‑Ekiaby, Nada, Ahmed, Rasha, Mohey Eldin, Mohammad, El‑Sayed, Mohammad, Abouelkhair, Mahmoud, Salah, Ayman, Zekri, Abdel, Esmat, Gamal, Abdelaziz, Ahmed

Journal:

Biomedical Reports

Year:

2014

Language:

english

File:

PDF, 361 KB

english, 2014

9

miR-148a and miR-30a limit HCV-dependent suppression of the lipid droplet protein, ADRP, in HCV infected cell models

El-Ekiaby, Nada M., Mekky, Radwa Y., Riad, Sarah E., Elhelw, Dalia S., El-Sayed, Mohammed, Esmat, Gamal, Abdelaziz, Ahmed I.

Journal:

Journal of Medical Virology

Year:

2016

Language:

english

File:

PDF, 949 KB

english, 2016

10

Contradicting Roles of miR-182 in Both NK Cells and Their Host Target Hepatocytes in HCV

El Sobky, Shereen A., El-Ekiaby, Nada M., Mekky, Radwa Y., Elemam, Noha M., Eldin, Mohammad A. Mohey, El-sayed, Mohammed, Esmat, Gamal, Abdelaziz, Ahmed I.

Journal:

Immunology Letters

Year:

2015

Language:

english

File:

PDF, 644 KB

english, 2015

11

Challenges in diagnosis and counseling of a family with two recessive neurometabolic disorders

Abd-Elkhalek, Heba S., Gamal, Radwa, Zaki, Osama K., Elsayed, Solaf M.

Journal:

Egyptian Journal of Medical Human Genetics

Year:

2015

Language:

english

File:

PDF, 433 KB

english, 2015

12

Bilateral iris, choroid, optic nerve colobomas and retinal detachment in an Egyptian patient with mild Baraitser–Winter syndrome

Shawky, Rabah M., Abd-Elkhalek Elabd, Heba Salah, Gamal, Radwa

Journal:

Egyptian Journal of Medical Human Genetics

Year:

2014

Language:

english

File:

PDF, 790 KB

english, 2014

13

Neurofibromatosis type 1 and multiple sclerosis: Genetically related diseases

Elsayed, Solaf M., Fahmy, Nagia, Gamal, Radwa, Wafik, Mohamed, Zamzam, Dina, Fahmy, Mai, Suelam, Mahmoud

Journal:

Egyptian Journal of Medical Human Genetics

Year:

2016

Language:

english

File:

PDF, 1.50 MB

english, 2016

14

Oral–Facial–Digital Syndrome type VI with self mutilations

Shawky, Rabah M., Elabd, Heba Salah Abd-Elkhalek, Gad, Shaimaa, Gamal, Radwa, Mohammad, Shaimaa Abdelsattar

Journal:

Egyptian Journal of Medical Human Genetics

Year:

2014

Language:

english

File:

PDF, 1.46 MB

english, 2014

15

Clinical, biochemical, neuroradiological and molecular characterization of Egyptian patients with glutaric acidemia type 1

Zayed, Hatem, El Khayat, Hamed, Tomoum, Hoda, Khalifa, Ola, Siddiq, Ehab, Mohammad, Shaimaa A., Gamal, Radwa, Shi, Zumin, Mosailhy, Ahmed, Zaki, Osama K.

Journal:

Metabolic Brain Disease

Year:

2019

Language:

english

File:

PDF, 513 KB

english, 2019

16

Clinical, biochemical, neuroradiological and molecular characterization of Egyptian patients with glutaric acidemia type 1

Zayed, Hatem, El Khayat, Hamed, Tomoum, Hoda, Khalifa, Ola, Siddiq, Ehab, Mohammad, Shaimaa A., Gamal, Radwa, Shi, Zumin, Mosailhy, Ahmed, Zaki, Osama K.

Journal:

Metabolic Brain Disease

Year:

2019

File:

PDF, 513 KB

2019

17

Currarino Triad: Importance of Preoperative Magnetic Resonance Imaging

AbouZeid, Amr AbdelHamid, Mohammad, Shaimaa Abdelsattar, Seada, Mohammad, Khiamy, Khaled, Gamal, Radwa

Journal:

European Journal of Pediatric Surgery Reports

Year:

2019

File:

PDF, 214 KB

2019

18

Genotype–phenotype correlation in patients with isovaleric acidaemia: comparative structural modelling and computational analysis of novel variants

Zaki, Osama K., Priya Doss C, George, Ali, Salsabil A., Murad, Ghadeer G., Elashi, Shaima A., Ebnou, Maryam S.A., Kumar D, Thirumal, Khalifa, Ola, Gamal, Radwa, El Abd, Heba S.A., Nasr, Bilal N., Zaye

Journal:

Human Molecular Genetics

Year:

2017

Language:

english

File:

PDF, 717 KB

english, 2017

19

Estrogen-related MxA transcriptional variation in hepatitis C virus-infected patients

Radwa Y. Mekky, Nabila Hamdi, Wafaa El-Akel, Gamal Esmat, Ahmed I. Abdelaziz

Journal:

Translational Research

Year:

2012

Language:

english

File:

PDF, 405 KB

english, 2012

20

Epigenetic harnessing of HCV via modulating the lipid droplet-protein, TIP47, in HCV cell models

El-Ekiaby, Nada M., Mekky, Radwa Y., El Sobky, Shereen A., Elemam, Noha M., El-Sayed, Mohammed, Esmat, Gamal, Abdelaziz, Ahmed I.

Journal:

Year:

2015

Language:

english

File:

PDF, 1.57 MB

english, 2015

21

Pseudoachondroplasia in a child: The role of anthropometric measurements and skeletal imaging in differential diagnosis

Gamal, Radwa, Elsayed, Solaf M., EL-Sobky, Tamer Ahmed, Elabd, Heba Salah

Journal:

The Egyptian Journal of Radiology and Nuclear Medicine

Year:

2017

Language:

english

File:

PDF, 1.26 MB

english, 2017

22

Expression signature of microRNA‑155 inï¿½hepatitis C virus genotype 4 infection

Riad, Sarah, El‑Ekiaby, Nada, Mekky, Radwa, Ahmed, Rasha, Mohey El Din, Mohammad, El‑Sayed, Mohammad, Abouelkhair, Mahmoud, Salah, Ayman, Zekri, Abdel, Esmat, Gamal, Abdelaziz, Ahmed

Journal:

Biomedical Reports

Year:

2014

Language:

english

File:

PDF, 304 KB

english, 2014

23

C syndrome with skeletal anomalies, mental retardation, eyelid chalazion, Bitot’s spots and agenesis of the corpus callosum in an Egyptian child

Shawky, Rabah M., Gamal, Radwa

Journal:

Egyptian Journal of Medical Human Genetics

Year:

2016

Language:

english

File:

PDF, 1.32 MB

english, 2016

24

Moebius syndrome with macular hyperpigmentation, skeletal anomalies, and hypoplasia of pectoralis major muscle in an Egyptian child

Shawky, Rabah M., Gamal, Radwa, Abdelsattar Mohammad, Shaimaa

Journal:

Egyptian Journal of Medical Human Genetics

Year:

2015

Language:

english

File:

PDF, 1.83 MB

english, 2015

25

Cantu syndrome in an Egyptian child

Shawky, Rabah M., Gamal, Radwa

Journal:

Egyptian Journal of Medical Human Genetics

Year:

2018

Language:

english

File:

PDF, 1.61 MB

english, 2018

26

Meier–Gorlin syndrome: An additional Egyptian patient with gastroesophageal reflux, hydronephrosis, renal stones and hypoplastic labia majora and minora with clitromegaly

Shawky, Rabah M., Gamal, Radwa

Journal:

Egyptian Journal of Medical Human Genetics

Year:

2016

Language:

english

File:

PDF, 1.34 MB

english, 2016

27

Cardiomyopathy in Vici syndrome

Elsayed, Solaf M., Gamal, Radwa

Journal:

Egyptian Journal of Medical Human Genetics

Year:

2018

Language:

english

File:

PDF, 456 KB

english, 2018

28

Mir-194 is a hepatocyte gate keeper hindering HCV entry through targeting CD81 receptor

Mekky, Radwa Yehia, El-Ekiaby, Nada Magdy, Hamza, Mohammed Tarif, Elemam, Noha Mousaad, EL-sayed, Mohammed, Esmat, Gamal, Abdelaziz, Ahmed Ihab

Journal:

Journal of Infection

Year:

2015

Language:

english

File:

PDF, 1.45 MB

english, 2015

29

Majewski Osteodysplastic Primordial Dwarfism, Type II with marked loss of subcutaneous fat, severe anemia, clenched hands and skeletal anomalies in an Egyptian patient

Shawky, Rabah M., Gamal, Radwa, Mohammad, Shaimaa Abdelsattar

Journal:

Egyptian Journal of Medical Human Genetics

Year:

2017

Language:

english

File:

PDF, 1.83 MB

english, 2017

30

Preoperative Grading of Glioma Using Dynamic Susceptibility Contrast MRI: Relative Cerebral Blood Volume Analysis of Intra-tumoural and Peri-tumoural Tissue

Soliman, Radwa K., Gamal, Sara A., Essa, Abdel-Hakeem A., Othman, Mostafa H.

Journal:

Clinical Neurology and Neurosurgery

Year:

2018

Language:

english

File:

PDF, 831 KB

english, 2018

31

Interferon-gamma is associated with hepatic dysfunction in fibrosis, cirrhosis, and hepatocellular carcinoma

Attallah, Abdelfattah M., El-Far, Mohamed, Zahran, Faten, Shiha, Gamal E., Farid, Khaled, Omran, Mohamed M., Abdelrazek, Mohamed A., Attallah, Ahmed A., El-Beh, Amira A., El-Hosiny, Radwa M., El-Wasee

Journal:

Journal of Immunoassay and Immunochemistry

Year:

2016

Language:

english

File:

PDF, 9.36 MB

english, 2016

32

Christ-Siemens-Touraine syndrome with cleft palate, absent nipples, gallstones and mild mental retardation in an Egyptian child

Shawky, Rabah M., Gamal, Radwa

Journal:

Egyptian Journal of Medical Human Genetics

Year:

2015

Language:

english

File:

PDF, 1.44 MB

english, 2015

33

An Egyptian patient with Schwartz-Jampel syndrome type I and new ocular findings

Elsayed, Solaf M., Gamal, Radwa

Journal:

Egyptian Journal of Medical Human Genetics

Year:

2017

Language:

english

File:

PDF, 1016 KB

english, 2017

34

Progress in genetics of coronary artery disease

Journal:

Egyptian Journal of Medical Human Genetics

Year:

2017

Language:

english

File:

PDF, 261 KB

english, 2017

35

Microcephalic osteodysplastic primordial dwarfism (MOPD) type I with severe anemia and MRI brain findings of MOPD type II

Shawky, Rabah M., Gamal, Radwa, Mohammad, Shaimaa Abdelsattar

Journal:

Egyptian Journal of Medical Human Genetics

Year:

2017

Language:

english

File:

PDF, 1.82 MB

english, 2017

To build up a library is to create a life. It’s never just a random collection of books.

— Carlos María Domínguez

Official channel

Z-Library Desktop Launcher

Z-Library Since 2009 support@1delivery.pm

EnglishРусскийEspañolItalianoελληνικάاللغة العربيةBahasa IndonesiaBahasa Malaysiaहिन्दीDeutschFrançaisPortuguêsУкраїнськаPolski中文繁體中文日本語Tiếng ViệtAzərbaycan DiliՀայոց լեզուภาษาไทยTürk Diliქართველიবাংলাپښتوతెలుగుاردو한국어SrpskiБългарски