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1

Genomic and phenotypic delineation of congenital microcephaly

Shaheen, Ranad, Maddirevula, Sateesh, Ewida, Nour, Alsahli, Saud, Abdel-Salam, Ghada M. H., Zaki, Maha S., Tala, Saeed Al, Alhashem, Amal, Softah, Ameen, Al-Owain, Mohammed, Alazami, Anas M., Abadel,

Journal:

Genetics in Medicine

Year:

2018

Language:

english

File:

PDF, 3.95 MB

english, 2018

2

Sulfasalazine and pentoxifylline in psoriasis: A possible safe alternative

El-Mofty, Medhat, El-Darouti, Mohamed, Rasheed, Hoda, Bassiouny, Dalia Ahmed, Abdel-Halim, Mona, Zaki, Naglaa Sameh, El-Hanafy, Ghada, El-Hadidi, Heba, Azzam, Omar, El-Ramly, Amany, Fawzy, Marwa

Journal:

Journal of Dermatological Treatment

Year:

2011

Language:

english

File:

PDF, 148 KB

english, 2011

3

Molecular and phenotypic spectrum of ASPM -related primary microcephaly: Identification of eight novel mutations

Abdel-Hamid, Mohamed S., Ismail, Manal F., Darwish, Hebatallh A., Effat, Laila K., Zaki, Maha S., Abdel-Salam, Ghada M. H.

Journal:

American Journal of Medical Genetics Part A

Year:

2016

Language:

english

File:

PDF, 341 KB

english, 2016

4

Concentrations of several phthalates contaminants in Egyptian bottled water: Effects of storage conditions and estimate of human exposure

Zaki, Ghada, Shoeib, Tamer

Journal:

Science of The Total Environment

Year:

2018

Language:

english

File:

PDF, 852 KB

english, 2018

5

Neuroectodermal stem cells: A remyelinating potential in acute compressed spinal cord injury in rat model

Ramadan, Wafaa S, Abdel-Hamid, Ghada A, Al-Karim, Saleh, Zakar, Noor Ahmed Mubarak Ben, Elassouli, M-Zaki

Journal:

Journal of Biosciences

Year:

2018

Language:

english

File:

PDF, 3.53 MB

english, 2018

6

Sensitive/stable complementary fault identification scheme for overhead transmission lines

Zaki, Mohamed I., El Sehiemy, Ragab A., Amer, Ghada M., Abo El Enin, Fathy M.

Journal:

IET Generation Transmission & Distribution

Year:

2019

Language:

english

File:

PDF, 3.30 MB

english, 2019

7

Blepharophimosisâptosisâintellectual disability syndrome: A report of nine Egyptian patients with further expansion of phenotypic and mutational spectrum

Zaki, Maha S., Otaify, Ghada A., Ismail, Samira, Issa, Mahmoud Y., ElâRuby, Mona O., Sadek, Abdelrahim A., Ashaat, Engy A., El Saeidi, Sonia A., Aglan, Mona S., Temtamy, Samia, AbdelâHamid, Mohame

Journal:

American Journal of Medical Genetics Part A

Year:

2020

File:

PDF, 2.07 MB

2020

8

Identification of a novel recessive RELN mutation using a homozygous balanced reciprocal translocation

Maha Zaki, Marwa Shehab, Alice Abd El-Aleem, Ghada Abdel-Salam, Hajira B. Koeller, Yesim Ilkin, M. Elizabeth Ross, William B. Dobyns, Joseph G. Gleeson

Journal:

American Journal of Medical Genetics Part A

Year:

2007

Language:

english

File:

PDF, 253 KB

english, 2007

9

Microcephaly, malformation of brain development and intracranial calcification in sibs: Pseudo-TORCH or a new syndrome

Ghada M.H. Abdel-Salam, Maha S. Zaki, Sahar N. Saleem, Khaled R. Gaber

Journal:

American Journal of Medical Genetics Part A

Year:

2008

Language:

english

File:

PDF, 181 KB

english, 2008

10

Band-like intracranial calcification (BIC), microcephaly and malformation of brain development: A distinctive form of congenital infection like syndromes

Ghada M.H. Abdel-Salam, Maha S. Zaki

Journal:

American Journal of Medical Genetics Part A

Year:

2009

Language:

english

File:

PDF, 109 KB

english, 2009

11

New recessive syndrome of microcephaly, cerebellar hypoplasia, and congenital heart conduction defect

Maha S. Zaki, Ghada M. H. Abdel Salam, Sahar N. Saleem, William B. Dobyns, Mahmoud Y. Issa, Shifteh Sattar, Joseph G. Gleeson

Journal:

American Journal of Medical Genetics Part A

Year:

2011

Language:

english

File:

PDF, 14.95 MB

english, 2011

12

AHI1 gene mutations cause specific forms of Joubert syndrome–related disorders

Enza Maria Valente, Francesco Brancati, Jennifer L. Silhavy, Marco Castori, Sarah E. Marsh, Giuseppe Barrano, Enrico Bertini, Eugen Boltshauser, Maha S. Zaki, Alice Abdel-Aleem, Ghada M. H. Abdel-Sala

Journal:

Annals of Neurology

Year:

2006

Language:

english

File:

PDF, 431 KB

english, 2006

13

Rapid Detection of Oculopathogenic Adenovirus in Conjunctivitis

Maysaa El-Sayed Zaki, Ghada A. Abd-El Fatah

Journal:

Current Microbiology

Year:

2008

Language:

english

File:

PDF, 163 KB

english, 2008

14

Profound microcephaly, primordial dwarfism with developmental brain malformations: A new syndrome

Ghada M.H. Abdel-Salam, Mohamed S. Abdel-Hamid, Sahar N. Saleem, Mahmoud K.H. Ahmed, Mahmoud Issa, Laila K. Effat, Hisham F. Kayed, Maha S. Zaki, Khaled R. Gaber

Journal:

American Journal of Medical Genetics Part A

Year:

2012

Language:

english

File:

PDF, 511 KB

english, 2012

15

Recessive Mutations in the Gene Encoding the Tight Junction Protein Occludin Cause Band-like Calcification with Simplified Gyration and Polymicrogyria

Mary C. O'Driscoll, Sarah B. Daly, Jill E. Urquhart, Graeme C.M. Black, Daniela T. Pilz, Knut Brockmann, Meriel McEntagart, Ghada Abdel-Salam, Maha Zaki, Nicole I. Wolf, Roger L. Ladda, Susan Sell, St

Journal:

The American Journal of Human Genetics

Year:

2010

Language:

english

File:

PDF, 1.36 MB

english, 2010

16

Isolated Dandy–Walker malformation associated with brain stem dysgenesis in male sibs

Ghada M.H. Abdel-Salam, Marwa Shehab, Maha S. Zaki

Journal:

Brain and Development

Year:

2006

Language:

english

File:

PDF, 197 KB

english, 2006

17

Anthropometric measurements in Egyptian patients with osteogenesis imperfecta

Mona S. Aglan, Moushira E. Zaki, Laila Hosny, Rasha El-Houssini, Ghada Oteify, Samia A. Temtamy

Journal:

American Journal of Medical Genetics Part A

Year:

2012

Language:

english

File:

PDF, 230 KB

english, 2012

18

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

19

Finite-Element Model Tuning of Global Modes of a Grandstand Structure Using Ambient Vibration Testing

Saudi, Ghada, Reynolds, Paul, Zaki, Mohammed, Hodhod, Hossam

Journal:

Journal of Performance of Constructed Facilities

Year:

2009

Language:

english

File:

PDF, 2.89 MB

english, 2009

20

Clinical and molecular findings in eight Egyptian patients with suspected mitochondrial disorders and optic atrophy

Al-Ettribi, Ghada M.M., Effat, Laila K., El-Bassyouni, Hala T., Zaki, Maha S., Shanab, Gamila, Karim, Amr M.

Journal:

Egyptian Journal of Medical Human Genetics

Year:

2013

Language:

english

File:

PDF, 1.38 MB

english, 2013

21

Mutations in EOGT Confirm the Genetic Heterogeneity of Autosomal-Recessive Adams-Oliver Syndrome

Shaheen, Ranad, Aglan, Mona, Keppler-Noreuil, Kim, Faqeih, Eissa, Ansari, Shinu, Horton, Kim, Ashour, Adel, Zaki, Maha S., Al-Zahrani, Fatema, Cueto-González, Anna M., Abdel-Salam, Ghada, Temtamy, Sam

Journal:

The American Journal of Human Genetics

Year:

2013

Language:

english

File:

PDF, 956 KB

english, 2013

22

HYGIENE.

ElBaz, Farida M., Zaki, Mona M., Youssef, Azza M., ElDorry, Ghada F., Elalfy, Dina Y.

Journal:

Year:

1894

Language:

english

File:

PDF, 449 KB

english, 1894

23

Study of plasma amino acid levels in children with autism: An Egyptian sample

ElBaz, Farida M., Zaki, Mona M., Youssef, Azza M., ElDorry, Ghada F., Elalfy, Dina Y.

Journal:

Egyptian Journal of Medical Human Genetics

Year:

2014

Language:

english

File:

PDF, 419 KB

english, 2014

24

Further delineation of the clinical spectrum in RNU 4 ATAC related microcephalic osteodysplastic primordial dwarfism type I

Abdel-Salam, Ghada M.H., Abdel-Hamid, Mohamed S., Hassan, Nihal A., Issa, Mahmoud Y., Effat, Laila, Ismail, Samira, Aglan, Mona S., Zaki, Maha S.

Journal:

American Journal of Medical Genetics Part A

Year:

2013

Language:

english

File:

PDF, 1.70 MB

english, 2013

25

Screening seven common mitochondrial mutations in 28 Egyptian patients with suspected mitochondrial disease

Al-Ettribi, Ghada M.M., Effat, Laila K., El-Bassyouni, Hala T., Zaki, Maha S., Shanab, Gamila, Karim, Amr M.

Journal:

Middle East Journal of Medical Genetics

Year:

2013

Language:

english

File:

PDF, 697 KB

english, 2013

26

Prevalence of Parkinsonism and Parkinson's disease in Qena governorate/Egypt: a cross-sectional community-based survey

Khedr, Eman M., Fawi, Gharib, Abbas, Mohammed Abd Allah, Mohammed, Talal A., El-Fetoh, Noha Abo, Attar, Ghada Al, Zaki, Ahmed F.

Journal:

Neurological Research

Year:

2015

Language:

english

File:

PDF, 229 KB

english, 2015

27

Prevalence of Diabetes and Diabetic Neuropathy in Qena Governorate: Population-Based Survey

Khedr, Eman M., Fawi, Gharib, Allah Abbas, Mohammed Abd, El-Fetoh, Noha Abo, Al Attar, Ghada, Zaki, Ahmed F., Gamea, Ayman

Journal:

Neuroepidemiology

Year:

2016

Language:

english

File:

PDF, 110 KB

english, 2016

28

Extending the mutation spectrum for Galloway-Mowat syndrome to include homozygous missense mutations in the WDR73 gene

Rosti, Rasim O., Dikoglu, Esra, Zaki, Maha S., Abdel-Salam, Ghada, Makhseed, Nawal, Sese, Jordan C., Musaev, Damir, Rosti, Basak, Harbert, Mary J., Jones, Marilyn C., Vaux, Keith K., Gleeson, Joseph G

Journal:

American Journal of Medical Genetics Part A

Year:

2016

Language:

english

File:

PDF, 930 KB

english, 2016

29

PYCR2 Mutations cause a lethal syndrome of microcephaly and failure to thrive

Zaki, Maha S., Bhat, Gifty, Sultan, Tipu, Issa, Mahmoud, Jung, Hea-Jin, Dikoglu, Esra, Selim, Laila, G. Mahmoud, Imam, Abdel-Hamid, Mohamed S., Abdel-Salam, Ghada, Marin-Valencia, Isaac, Gleeson, Jose

Journal:

Annals of Neurology

Year:

2016

Language:

english

File:

PDF, 662 KB

english, 2016

30

Megalencephalic leukoencephalopathy with cysts in twelve Egyptian patients: novel mutations inMLC1andHEPACAMand a founder effect

Abdel-Salam, Ghada M. H., Abdel-Hamid, Mohamed S., Ismail, Samira I., Hosny, Heba, Omar, Tarek, Effat, Laila, Aglan, Mona S., Temtamy, Samia A., Zaki, Maha S.

Journal:

Metabolic Brain Disease

Year:

2016

Language:

english

File:

PDF, 4.48 MB

english, 2016

31

Evaluation of CT perfusion parameters for assessment of split renal function in healthy donors

El-Diasty, Mohamed Tarek, Gaballa, Ghada, Gad, Hossam Mostafa, Borg, Mohamed Abdelghaffar, Abou-Elghar, Mohamed Ebrahem, Sheir, Khaled Zaki, El-Diasty, Tarek Abdelmoneim

Journal:

The Egyptian Journal of Radiology and Nuclear Medicine

Year:

2016

Language:

english

File:

PDF, 1.83 MB

english, 2016

32

Prevalence of neuromuscular disorders in Qena governorate/Egypt: population-based survey

Khedr, Eman M., Fawi, Gharib, Abbas, Mohammed Abd-Allah, Abo El-Fetoh, Noha, Zaki, Ahmed F., Gamea, Ayman, Al Attar, Ghada

Journal:

Neurological Research

Year:

2016

Language:

english

File:

PDF, 558 KB

english, 2016

33

A novel frameshift mutation in the sterol 27-hydroxylase gene in an Egyptian family with cerebrotendinous xanthomatosis without cataract

Abdel-Hamid, Mohamed S., Issa, Mahmoud Y., Otaify, Ghada A., Zaki, Maha S.

Journal:

Metabolic Brain Disease

Year:

2017

Language:

english

File:

PDF, 2.44 MB

english, 2017

34

Band-like calcification with simplified gyration and polymicrogyria: report of 10 new families and identification of five novel OCLN mutations

Abdel-Hamid, Mohamed S, Abdel-Salam, Ghada M H, Issa, Mahmoud Y, Emam, Bayoumi A, Zaki, Maha S

Journal:

Journal of Human Genetics

Year:

2017

Language:

english

File:

PDF, 1.29 MB

english, 2017

35

Sitagliptin and liraglutide reversed nigrostriatal degeneration of rodent brain in rotenone-induced Parkinson’s disease

Badawi, Ghada A., Abd El Fattah, Mai A., Zaki, Hala F., El Sayed, Moushira I.

Journal:

Inflammopharmacology

Year:

2017

Language:

english

File:

PDF, 3.11 MB

english, 2017

36

Double Logarithmic Arithmetic Technique for Low-Power 3-D Graphics Applications

Ellaithy, Dina M., El-Moursy, Magdy A., Ibrahim, Ghada H., Zaki, Amal, Zekry, Abdelhalim

Journal:

IEEE Transactions on Very Large Scale Integration (VLSI) Systems

Year:

2017

Language:

english

File:

PDF, 2.36 MB

english, 2017

37

Aicardi-Goutières syndrome: unusual neuro-radiological manifestations

Abdel-Salam, Ghada M. H., Abdel-Hamid, Mohamed S., Mohammad, Shaimaa A., Abdel-Ghafar, Sherif F., Soliman, Doaa R., EL-Bassyouni, Hala T., Effat, Laila, Zaki, Maha S.

Journal:

Metabolic Brain Disease

Year:

2017

Language:

english

File:

PDF, 746 KB

english, 2017

38

[IEEE 2017 29th International Conference on Microelectronics (ICM) - Beirut, Lebanon (2017.12.10-2017.12.13)] 2017 29th International Conference on Microelectronics (ICM) - Accurate piecewise uniform approximation logarithmic/antilogarithmic converters for GPU applications

Ellaithy, Dina M., El-Moursy, Magdy A., Hamdy, Ghada, Zaki, Amal, Zekry, Abdelhalim

Year:

2017

Language:

english

File:

PDF, 219 KB

english, 2017

39

[IEEE 2017 12th International Conference on Computer Engineering and Systems (ICCES) - Cairo, Egypt (2017.12.19-2017.12.20)] 2017 12th International Conference on Computer Engineering and Systems (ICCES) - Double logarithmic arithmetic technique for GPU

Ellaithy, Dina M., El-Moursy, Magdy A., Ibrahim, Ghada H., Zaki, Amal, Zekry, Abdelhalim

Year:

2017

Language:

english

File:

PDF, 290 KB

english, 2017

40

[IEEE 2017 Nineteenth International Middle East Power Systems Conference (MEPCON) - Cairo, Egypt (2017.12.19-2017.12.21)] 2017 Nineteenth International Middle East Power Systems Conference (MEPCON) - Integrated discrete wavelet transform-based faulted phase identification for multi-terminals power systems

Zaki, Mohamed I., Sehiemy, Ragab A. El, Amer, Ghada M., Enin, Fathy M. Abo El

Year:

2017

Language:

english

File:

PDF, 618 KB

english, 2017

41

[IEEE 2017 Intl Conf on Advanced Control Circuits Systems (ACCS) Systems & 2017 Intl Conf on New Paradigms in Electronics & Information Technology (PEIT) - Alexandria (2017.11.5-2017.11.8)] 2017 Intl Conf on Advanced Control Circuits Systems (ACCS) Systems & 2017 Intl Conf on New Paradigms in Electronics & Information Technology (PEIT) - Efficient piecewise non-uniform approximation logarithmic and antilogarithmic converters

Ellaithy, Dina M., El-Moursy, Magdy A., Hamdy, Ghada, Zaki, Amal, Zekry, Abdelhalim

Year:

2017

Language:

english

File:

PDF, 393 KB

english, 2017

42

Assessment of physical growth, some oxidative stress biomarkers and vitamin D status in children with Familial Mediterranean Fever

Zaki, Moushira, El-Bassyouni,, Reyad, Hanaa, Yousef, Walaa, Youness, Eman, Mohamed, Ghada, Ramadan, Abeer

Journal:

Year:

2018

Language:

english

File:

PDF, 433 KB

english, 2018

43

GAPO syndrome in seven new patients: Identification of five novel ANTXR1 mutations including the first large intragenic deletion

Abdel-Hamid, Mohamed S., Ismail, Samira, Zaki, Maha S., Abdel-Salam, Ghada M. H., Otaify, Ghada A., Issa, Mahmoud Y., Abdel-Kader, Mohamed, Girgis, Marian, Aboul-Ezz, Eman, Mazen, Inas, Aglan, Mona S.

Journal:

American Journal of Medical Genetics Part A

Year:

2018

Language:

english

File:

PDF, 1.11 MB

english, 2018

44

An investigated reactive power measurements-based fault-identification scheme for teed transmission lines

Zaki, Mohamed I., El Sehiemy, Ragab A., Amer, Ghada M., El Enin, Fathy M. Abo

Journal:

Year:

2018

Language:

english

File:

PDF, 883 KB

english, 2018

45

Interaction between 12p chromosomal abnormalities and Lnc‐HOTAIR mediated pathway in acute myeloid leukemia

El‐Khazragy, Nashwa, Ghozy, Sherief, Matbouly, Safa, Zaki, Walid, Safwat, Gehan, Hussien, Ghada, Khalifa, Omar

Journal:

Journal of Cellular Biochemistry

Year:

2019

Language:

english

File:

PDF, 614 KB

english, 2019

46

Comparison between multi-spot laser and conventional laser in treatment of diabetic clinically signifcant macular edema

Elsawah, Kareem Mohsen, El-lkwa, Amin Faisal, El-Abedin, Ghada Zein, Zaky, Marwa Aly

Journal:

Revista Brasileira de Oftalmologia

Year:

2017

File:

PDF, 650 KB

2017

47

Interaction between 12p chromosomal abnormalities and Lnc‐HOTAIR mediated pathway in acute myeloid leukemia

El‐Khazragy, Nashwa, Ghozy, Sherief, Matbouly, Safa, Zaki, Walid, Safwat, Gehan, Hussien, Ghada, Khalifa, Omar

Journal:

Journal of Cellular Biochemistry

Year:

2019

File:

PDF, 614 KB

2019

48

Phenotypic and mutational spectrum of thirty-five patients with Sjögren–Larsson syndrome: identification of eleven novel ALDH3A2 mutations and founder effects

Abdel-Hamid, Mohamed S., Issa, Mahmoud Y., Elbendary, Hasnaa M., Abdel-Ghafar, Sherif F., Rafaat, Karima, Hosny, Heba, Girgis, Marian, Abdel-Salam, Ghada M. H., Zaki, Maha S.

Journal:

Journal of Human Genetics

Year:

2019

Language:

english

File:

PDF, 1.14 MB

english, 2019

49

Pulmonary deregulation of expression of miR-155 and two of its putative target genes; PROS1 and TP53INP1 associated with gold nanoparticles (AuNPs) administration in rat

Ali, Ghada E., Ibrahim, Marwa A., El-Deeb, Ayman H., Amer, Hassan, Zaki, Said M.

Journal:

International Journal of Nanomedicine

Year:

2019

Language:

english

File:

PDF, 2.39 MB

english, 2019

50

Bilateral Calcification of Basal Ganglia in a Patient with Duplication of Both 11q13.1q22.1 and 4q35.2 with New Phenotypic Features

Zaki, Maha S., Eid, Ola M., Eid, Maha M., Mohamed, Amal M., Sayed, Inas S.M., Abdel-Hamid, Mohamed S., Abdel-Salam, Ghada M.H.

Journal:

Cytogenetic and Genome Research

Year:

2019

Language:

english

File:

PDF, 967 KB

english, 2019