Afify, Ghada M.: search on Z-Library

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1

Another n -Dimensional Generalization of Pompeiu’s Theorem

Al-Afifi, Ghada, Hajja, Mowaffaq, Hamdan, Ahmad

Journal:

American Mathematical Monthly

Year:

2018

Language:

english

File:

PDF, 609 KB

english, 2018

2

[IEEE 2015 Tenth International Conference on Computer Engineering & Systems (ICCES) - Cairo, Egypt (2015.12.23-2015.12.24)] 2015 Tenth International Conference on Computer Engineering & Systems (ICCES) - A ZigBee-based industrial WLAN

Afifi, Ghada, Halawa, Hassan H., Daoud, Ramez M., Amer, Hassanein H.

Year:

2015

Language:

english

File:

PDF, 438 KB

english, 2015

3

The supposed tumor suppressor geneWWOXis mutated in an early lethal microcephaly syndrome with epilepsy, growth retardation and retinal degeneration

Abdel-Salam, Ghada, Thoenes, Michaela, Afifi, Hanan H, Körber, Friederike, Swan, Daniel, Bolz, Hanno

Journal:

Orphanet Journal of Rare Diseases

Year:

2014

Language:

english

File:

PDF, 324 KB

english, 2014

4

[IEEE 2016 24th Mediterranean Conference on Control and Automation (MED) - Athens, Greece (2016.6.21-2016.6.24)] 2016 24th Mediterranean Conference on Control and Automation (MED) - Dual protocol performance using WiFi and Zigbee for industrial WLAN

Afifi, Ghada, Halawa, Hassan H., Daoud, Ramez M., Amer, Hassanein H.

Year:

2016

Language:

english

File:

PDF, 1.62 MB

english, 2016

5

Facile synthesis of novel nanocomposite prepared from spinel copper ferrite and reduced graphene oxide in the presence of anti-fouling agent diethyl ammonium acid sulphate for ultrasensitive detection of rosuvastatin in human plasma

El-Wekil, Mohamed M., Afify, Khaled K., Abdel Salam, Randa A., Hadad, Ghada M., Ali, Ramadan

Journal:

Microchemical Journal

Year:

2019

Language:

english

File:

PDF, 1.11 MB

english, 2019

6

Fatal burn injuries: A five year retrospective autopsy study in Cairo city, Egypt

Mostafa M. Afify, Naglaa F. Mahmoud, Ghada M. Abd El Azzim, Nevein A. El Desouky

Journal:

Egyptian Journal of Forensic Sciences

Year:

2012

Language:

english

File:

PDF, 636 KB

english, 2012

7

De Novo 17q24.2-q24.3 microdeletion presenting with generalized hypertrichosis terminalis, gingival fibromatous hyperplasia, and distinctive facial features

Afifi, Hanan H., Fukai, Ryoko, Miyake, Noriko, Gamal el Din, Amina A., Eid, Maha M., Eid, Ola M., Thomas, Manal M., El-Badry, Tarek H., Tosson, Angie M. S., Abdel-Salam, Ghada M. H., Matsumoto, Naomic

Journal:

American Journal of Medical Genetics Part A

Year:

2015

Language:

english

File:

PDF, 2.12 MB

english, 2015

8

Magnetic resonance imaging of developmental facial paresis: a spectrum of complex anomalies

Mohammad, Shaimaa Abdelsattar, Abdelaziz, Tougan Taha, Gadelhak, Mohamed I., Afifi, Hanan H., Abdel-Salam, Ghada M. H.

Journal:

Year:

2018

Language:

english

File:

PDF, 4.03 MB

english, 2018

9

Plastic Surgery Secrets Plus || Contributors

Afifi, Ghada Y.

Year:

2010

File:

PDF, 106 KB

2010

10

Lipoid proteinosis: A clinical and molecular study in Egyptian patients

Afifi, Hanan H., Amr, Khalda S., Tosson, Angie M.S., Hassan, Tarak A., Mehrez, Mennat I., El-Kamah, Ghada Y.

Journal:

Year:

2017

Language:

english

File:

PDF, 1.23 MB

english, 2017

11

Ectodermal Abnormalities in Patients with Kabuki Syndrome

Ghada M.H. Abdel-Salam, Hanan H. Afifi, Maha M. Eid, Tarek H. El-Badry, Naglaa Kholoussi

Journal:

Pediatric Dermatology

Year:

2011

Language:

english

File:

PDF, 153 KB

english, 2011

12

The Implementation of an Integrated Management System at Qatar Biobank

Hannigan, Linda, Deyab, Ghada, Al Thani, Asmaa, Al Marri, Ajayeb, Afifi, Nahla

Journal:

Biopreservation and Biobanking

Year:

2019

File:

PDF, 1.20 MB

2019

13

De Novo Mutation in ABCC9 Causes Hypertrichosis Acromegaloid Facial Features Disorder

Afifi, Hanan H., Abdel-Hamid, Mohamed S., Eid, Maha M., Mostafa, Inas S., Abdel-Salam, Ghada M.H.

Journal:

Pediatric Dermatology

Year:

2016

Language:

english

File:

PDF, 441 KB

english, 2016

14

Erratum: Clinical Variability of PallisterâKillian Syndrome in Two Egyptian Patients

Eid, Maha M., Eid, Ola M., Abdel-Hadi, Sawsan, Hassib, Nehal, Madian, Abdelrahman, Afifi, Hanan H., Abdel-Salam, Ghada M.H.

Journal:

Journal of Pediatric Genetics

Year:

2019

File:

PDF, 34 KB

2019

15

Mutation in WDR4 impairs tRNA m7G46 methylation and causes a distinct form of microcephalic primordial dwarfism

Shaheen, Ranad, Abdel-Salam, Ghada M H, Guy, Michael P., Alomar, Rana, Abdel-Hamid, Mohamed S., Afifi, Hanan H., Ismail, Samira I., Emam, Bayoumi A., Phizicky, Eric M., Alkuraya, Fowzan S.

Journal:

Year:

2015

Language:

english

File:

PDF, 1.64 MB

english, 2015

16

Child homicide in Cairo from 2006 to 2010: Characteristics and trends

Alsaif, Dalia, Alsowayigh, Kholoud, Alfaraidy, Maram, Albayat, Marwa, Alshamsi, Ghada, Aldosary, Mohammed, Madadin, Mohammed, Afify, Mostafa, Kharoshah, Magdy

Journal:

Journal of Forensic and Legal Medicine

Year:

2013

Language:

english

File:

PDF, 466 KB

english, 2013

17

A Comprehensive Study of the Effect of Spatial Resolution and Color of Digital Images on Vehicle Classification

Hussain, Khaled F., Afifi, Mahmoud, Moussa, Ghada

Journal:

IEEE Transactions on Intelligent Transportation Systems

Year:

2018

Language:

english

File:

PDF, 6.18 MB

english, 2018

18

Phenotypic and molecular insights into PQBP1 -related intellectual disability

Abdel-Salam, Ghada M. H., Miyake, Noriko, Abdel-Hamid, Mohamed S., Sayed, Inas S. M., Gadelhak, Mohamed I., Ismail, Samira I., Aglan, Mona S., Afifi, Hanan H., Temtamy, Samia A., Matsumoto, Naomichi

Journal:

American Journal of Medical Genetics Part A

Year:

2018

Language:

english

File:

PDF, 2.49 MB

english, 2018

19

Further delineation of the oculoauricular syndrome phenotype: A new family with a novel truncating HMX1 mutation

Abdel-Salam, Ghada M.H., Abdel-Hamid, Mohamed S., Mehrez, Mennat I., Kamal, Ahmad M., Taher, Mohamed B., Afifi, Hanan H.

Journal:

Ophthalmic Genetics

Year:

2017

Language:

english

File:

PDF, 1.02 MB

english, 2017

20

Controlled release of injectable liposomal in situ gel loaded with recombinant human bone morphogenetic protein-2 for the repair of alveolar bone clefts in rabbits

Hassan, Ali H., Hosny, Khaled M., Murshid, Zuahir A., Alhadlaq, Adel, Yamani, Ahmed, Naguib, Ghada, Alkhalidi, Hala M., Afify, Ahmed R.

Journal:

Journal of Liposome Research

Year:

2015

Language:

english

File:

PDF, 442 KB

english, 2015

21

A hybrid filtering approach for storage optimization in main-memory cloud database

Afify, Ghada M., El Bastawissy, Ali, Hegazy, Osman M.

Journal:

Egyptian Informatics Journal

Year:

2015

Language:

english

File:

PDF, 1.06 MB

english, 2015

22

Clinical features of SMARCA2 duplication overlap with Coffin-Siris syndrome

Miyake, Noriko, Abdel-Salam, Ghada, Yamagata, Takanori, Eid, Maha M., Osaka, Hitoshi, Okamoto, Nobuhiko, Mohamed, Amal M., Ikeda, Takahiro, Afifi, Hanan H., Piard, Juliette, van Maldergem, Lionel, Miz

Journal:

American Journal of Medical Genetics Part A

Year:

2016

Language:

english

File:

PDF, 3.53 MB

english, 2016

23

Autologous adipose-derived adult stem cells injection versus platelet-rich plasma injection in the treatment of rolling postacne scars

Elkahky, Hanan O., Fathy, Ghada, Abu-Zahra, Fatma A., Afify, Ahmed A.

Journal:

Journal of the Egyptian Womenʼs Dermatologic Society

Year:

2016

Language:

english

File:

PDF, 485 KB

english, 2016

24

Oto-spondylo-megaepiphyseal dysplasia (OSMED): Clinical and radiological findings in sibs homozygous for premature stop codon mutation in the COL11A2 gene

Samia A. Temtamy, Minna Männikkö, Ghada M.H. Abdel-Salam, Nihal A. Hassan, Leena Ala-Kokko, Hanan H. Afifi

Journal:

American Journal of Medical Genetics Part A

Year:

2006

Language:

english

File:

PDF, 272 KB

english, 2006

25

CXCR4 (CD184) expression on stem cell harvest and CD34 + cells post-transplant

Asfour, Inas, Afify, Hanaa, Elkourashy, Shaza, Ayoub, Maryse, Kamal, Gihan, Gamal, Mary, Elgohary, Ghada

Journal:

Hematology/Oncology and Stem Cell Therapy

Year:

2017

Language:

english

File:

PDF, 823 KB

english, 2017

26

Quality of Life Outcomes in a Pediatric Thalassemia Population in Egypt

Adam, Soheir, Afifi, Hanan, Thomas, Manal, Magdy, Phoebe, El-Kamah, Ghada

Journal:

Year:

2017

Language:

english

File:

PDF, 706 KB

english, 2017

27

Microcephalic osteodysplastic primordial dwarfism type II: Additional nine patients with implications on phenotype and genotype correlation

Abdel-Salam, Ghada M. H., Sayed, Inas S. M., Afifi, Hanan H., Abdel-Ghafar, Sherif F., Abouzaid, Maha R., Ismail, Samira I., Aglan, Mona S., Issa, Mahmoud Y., EL-Bassyouni, Hala T., El-Kamah, Ghada, E

Journal:

American Journal of Medical Genetics Part A

Year:

2020

File:

PDF, 3.86 MB

2020

28

Expanding the mutation and clinical spectrum of Roberts syndrome

Afifi, Hanan H., Abdel-Salam, Ghada M.H., Eid, Maha M., Tosson, Angie M.S., Shousha, Wafaa Gh., Abdel Azeem, Amira A., Farag, Mona K., Mehrez, Mennat I., Gaber, Khaled R.

Journal:

Congenital Anomalies

Year:

2016

Language:

english

File:

PDF, 786 KB

english, 2016

29

Increased arterial stiffness in rheumatoid arthritis and Its relation to disease activity: A cross sectional study

Youssef, Ghada, Allam, Nashwa Taher, Gaber, Wafaa, Afifi, Angie, Hesham, Dina

Journal:

The Egyptian Heart Journal

Year:

2017

Language:

english

File:

PDF, 346 KB

english, 2017

30

A homozygous IER3IP1 mutation causes microcephaly with simplified gyral pattern, epilepsy, and permanent neonatal diabetes syndrome (MEDS)

Prof. Ghada M.H. Abdel-Salam, Ashleigh E. Schaffer, Maha S. Zaki, Tracy Dixon-Salazar, Inas S. Mostafa, Hanan H. Afifi, Joseph G. Gleeson

Journal:

American Journal of Medical Genetics Part A

Year:

2012

Language:

english

File:

PDF, 350 KB

english, 2012

31

Gómez-López-hernández syndrome versus rhombencephalosynapsis spectrum: A rare co-occurrence with bipartite parietal bone

Abdel-Salam, Ghada M.H., Abdel-Hadi, Sawsan, Thomas, Manal M., Eid, Ola M., Ali, Manal M., Afifi, Hanan H.

Journal:

American Journal of Medical Genetics Part A

Year:

2014

Language:

english

File:

PDF, 265 KB

english, 2014

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