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1

Antiviral screening of forty-two Egyptian medicinal plants

Maha Mohamed Soltan, Adel Kamal Zaki

Journal:

Journal of Ethnopharmacology

Year:

2009

Language:

english

File:

PDF, 197 KB

english, 2009

2

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

3

Syndrome of Hepatic Cirrhosis, Dystonia, Polycythemia, and Hypermanganesemia Caused by Mutations in SLC30A10, a Manganese Transporter in Man

Karin Tuschl, Peter T. Clayton, Sidney M. Gospe Jr., Shamshad Gulab, Shahnaz Ibrahim, Pratibha Singhi, Roosy Aulakh, Reinaldo T. Ribeiro, Orlando G. Barsottini, Maha S. Zaki, Maria Luz Del Rosario, Sa

Journal:

The American Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 1.09 MB

english, 2012

4

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

5

Identification of a novel homozygous ALX4 mutation in two unrelated patients with frontonasal dysplasia type-2

El-Ruby, Mona, El-Din Fayez, Alaa, El-Dessouky, Sara H., Aglan, Mona S., Mazen, Inas, Ismail, Nora, Afifi, Hanan H., Eid, Maha M., Mostafa, Mostafa I., Mehrez, Mennat I., Khalil, Yasmin, Zaki, Maha S.

Journal:

American Journal of Medical Genetics Part A

Year:

2018

Language:

english

File:

PDF, 563 KB

english, 2018

6

Prognosis of Bell Palsy

Zaki, Maha A., Elkholy, Saly H., Abokrysha, Noha T., Khalil, Alshaimaa Sobhi, Nawito, Amani M., Magharef, Nagween W., Kishk, Nirmeen A.

Journal:

Journal of Clinical Neurophysiology

Year:

2018

Language:

english

File:

PDF, 253 KB

english, 2018

7

Recessive mutations in muscle-specific isoforms of FXR1 cause congenital multi-minicore myopathy

Estañ, María Cristina, Fernández-Núñez, Elisa, Zaki, Maha S., Esteban, María Isabel, Donkervoort, Sandra, Hawkins, Cynthia, Caparros-Martin, José A., Saade, Dimah, Hu, Ying, Bolduc, Véronique, Chao, K

Journal:

Nature Communications

Year:

2019

Language:

english

File:

PDF, 10.56 MB

english, 2019

8

Bi-allelic Loss of Human APC2, Encoding Adenomatous Polyposis Coli Protein 2, Leads to Lissencephaly, Subcortical Heterotopia, and Global Developmental Delay

Lee, Sangmoon, Chen, Dillon Y., Zaki, Maha S., Maroofian, Reza, Houlden, Henry, Di Donato, Nataliya, Abdin, Dalia, Morsy, Heba, Mirzaa, Ghayda M., Dobyns, William B., McEvoy-Venneri, Jennifer, Stanley

Journal:

The American Journal of Human Genetics

Year:

2019

Language:

english

File:

PDF, 1.71 MB

english, 2019

9

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

10

Flow cytometric DNA analysis of fresh prostatic resections: Correlation with conventional prognostic parameters in patients with prostate cancer

Maha H. Hussain, Isaac Powell, Nagi Zaki, Zocia Maciorowski, Wael Sakr, Mark Kukuruga, Daniel Visscher, Gabriel P. Haas, J. Edson Pontes, John F. Ensley

Journal:

Year:

1993

Language:

english

File:

PDF, 721 KB

english, 1993

11

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

12

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

13

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

14

Familial congenital unilateral cerebral ventriculomegaly: Delineation of a distinct genetic disorder

Maha S. Zaki, Hanan H. Afifi, AJ. Barkovich, Joseph G. Gleeson

Journal:

American Journal of Medical Genetics Part A

Year:

2009

Language:

english

File:

PDF, 224 KB

english, 2009

15

Congenital isolated leukonychia totalis in three Egyptian sibs

Hanan H. Afifi, Mahmoud F. Abdel-Hamid, Maha S. Zaki

Journal:

American Journal of Medical Genetics Part A

Year:

2011

Language:

english

File:

PDF, 256 KB

english, 2011

16

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

17

Co-occurrence of distinct ciliopathy diseases in single families suggests genetic modifiers

Maha S. Zaki, Shifteh Sattar, Rustin A. Massoudi, Joseph G. Gleeson

Journal:

American Journal of Medical Genetics Part A

Year:

2011

Language:

english

File:

PDF, 1.62 MB

english, 2011

18

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

19

Fetal MRI in the evaluation of fetuses referred for sonographically suspected neural tube defects (NTDs): impact on diagnosis and management decision

Sahar N. Saleem, Ahmed-Hesham Said, Maged Abdel-Raouf, Eman A. El-Kattan, Maha Saad Zaki, Noha Madkour, Mostafa Shokry

Journal:

Year:

2009

Language:

english

File:

PDF, 355 KB

english, 2009

20

Mutations in INPP5E, encoding inositol polyphosphate-5-phosphatase E, link phosphatidyl inositol signaling to the ciliopathies

Bielas, Stephanie L, Silhavy, Jennifer L, Brancati, Francesco, Kisseleva, Marina V, Al-Gazali, Lihadh, Sztriha, Laszlo, Bayoumi, Riad A, Zaki, Maha S, Abdel-Aleem, Alice, Rosti, Rasim Ozgur

Journal:

Nature Genetics

Year:

2009

Language:

english

File:

PDF, 649 KB

english, 2009

21

Defective Wnt-dependent cerebellar midline fusion in a mouse model of Joubert syndrome

Lancaster, Madeline A, Gopal, Dipika J, Kim, Joon, Saleem, Sahar N, Silhavy, Jennifer L, Louie, Carrie M, Thacker, Bryan E, Williams, Yuko, Zaki, Maha S, Gleeson, Joseph G

Journal:

Nature Medicine

Year:

2011

Language:

english

File:

PDF, 1.61 MB

english, 2011

22

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

23

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

24

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

25

Validity of the distance between mitral leaflets coaptation point and annular plane in differentiation between ischemic and dilated cardiomyopathy

Khalid M. Abd El-Salam, Maha H. El Sebaie, Manar Al Zaky, Ashraf El Saeed

Journal:

The Egyptian Heart Journal

Year:

2011

Language:

english

File:

PDF, 432 KB

english, 2011

26

Diagnosis of intestinal microsporidiosis in pediatric oncology patients in Egypt using modified acid fast trichrome staining versus PCR

Hadir El-Mahallawy, Mayssa Mohamed Zaki, Maha El-Arousy, Lobna Shalabi, Tarek Mansour

Journal:

Acta Parasitologica

Year:

2011

Language:

english

File:

PDF, 295 KB

english, 2011

27

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

28

Expanding the clinical spectrum of SPG11 gene mutations in recessive hereditary spastic paraplegia with thin corpus callosum

Alice Abdel Aleem, Nourhan Abu-Shahba, Dominika Swistun, Jennifer Silhavy, Stephanie L. Bielas, Shifteh Sattar, Joseph G. Gleeson, Maha S. Zaki

Journal:

European Journal of Medical Genetics

Year:

2011

Language:

english

File:

PDF, 432 KB

english, 2011

29

Molecular analysis of MECP2 gene in Egyptian patients with Rett syndrome

Maha S. Zaki, Wessam E. Sharaf El-Din, Germine M. Hamdy, I.H. Kamal, Alice K. Abdel Aleem

Journal:

Egyptian Journal of Medical Human Genetics

Year:

2012

Language:

english

File:

PDF, 764 KB

english, 2012

30

Alteration of Fatty-Acid-Metabolizing Enzymes Affects Mitochondrial Form and Function in Hereditary Spastic Paraplegia

Christelle Tesson, Magdalena Nawara, Mustafa A.M. Salih, Rodrigue Rossignol, Maha S. Zaki, Mohammed Al Balwi, Rebecca Schule, Cyril Mignot, Emilie Obre, Ahmed Bouhouche, Filippo M. Santorelli, Christe

Journal:

The American Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 1.21 MB

english, 2012

31

Efficacy of Some Herbal Feed Additives on Performance and Control of Cecal Coccidiosis in Broilers

Hady, Maha M., Zaki, M.M.

Journal:

APCBEE Procedia

Year:

2012

Language:

english

File:

PDF, 193 KB

english, 2012

32

Angiotensin antagonists and renal ischemia/reperfusion: Possible modulation by l-carnitine

Maha A. Rabie, Hala F. Zaki, Ashraf K. Bahgat, Hekma A. Abd El-Latif

Journal:

Bulletin of Faculty of Pharmacy Cairo University

Year:

2012

Language:

english

File:

PDF, 1.48 MB

english, 2012

33

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

34

Hepatoprotective and antioxidant activity of phytic acid and/or catechin against carbon tetrachloride-induced hepatotoxicity in rats

Sohair Hassan, Maha Zaki Rizk, Fathia El-Sharkawi, Osama Badary, Mai Osman Kadry

Journal:

Toxicology Letters

Year:

2009

Language:

english

File:

PDF, 92 KB

english, 2009

35

Poultry rearing and slaughtering practices in rural Egypt: an exploration of risk factors for H5N1 virus human transmission

Lohiniva, Anna-Leena, Dueger, Erica, Talaat, Maha, Refaey, Samir, Zaki, Amal, Chisholm Horton, Katherine, Kandeel, Amr

Journal:

Influenza and Other Respiratory Viruses

Year:

2013

Language:

english

File:

PDF, 92 KB

english, 2013

36

BENEVOLENCE AT CHRISTMAS

El Salam, Khalid Abd, Zaky, Manar Al, Sebaie, Maha El, Akl, Hosneia

Journal:

Year:

1945

Language:

english

File:

PDF, 209 KB

english, 1945

37

Predictive value of D-dimer levels and tissue doppler mitral annular systolic velocity for detection of left atrial appendage thrombi

El Salam, Khalid Abd, Zaky, Manar Al, Sebaie, Maha El, Akl, Hosneia

Journal:

Journal of the Saudi Heart Association (SAUDI ARABIA)

Year:

2013

Language:

english

File:

PDF, 72 KB

english, 2013

38

Protective role of humoral immune responses during an outbreak of hepatitis E in Egypt

Shata, Mohamed T., Daef, Enas A., Zaki, Maysaa E., Abdelwahab, Sayed F., Marzuuk, Naglaa M., Sobhy, Maha, Rafaat, Marwa, Abdelbaki, Liala, Nafeh, Mohamed A., Hashem, Mohamed, El-Kamary, Samer S., Shar

Journal:

Transactions of the Royal Society of Tropical Medicine and Hygiene

Year:

2012

Language:

english

File:

PDF, 309 KB

english, 2012

39

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

40

Mutations in CSPP1 Lead to Classical Joubert Syndrome

Akizu, Naiara, Silhavy, Jennifer L., Rosti, Rasim Ozgur, Scott, Eric, Fenstermaker, Ali G., Schroth, Jana, Zaki, Maha S., Sanchez, Henry, Gupta, Neerja, Kabra, Madhulika, Kara, Majdi, Ben-Omran, Tawfe

Journal:

The American Journal of Human Genetics

Year:

2014

Language:

english

File:

PDF, 1.27 MB

english, 2014

41

Whole-Exome Sequencing Identifies Mutated C12orf57 in Recessive Corpus Callosum Hypoplasia

Akizu, Naiara, Shembesh, Nuri M., Ben-Omran, Tawfeg, Bastaki, Laila, Al-Tawari, Asma, Zaki, Maha S., Koul, Roshan, Spencer, Emily, Rosti, Rasim Ozgur, Scott, Eric, Nickerson, Elizabeth, Gabriel, Stace

Journal:

The American Journal of Human Genetics

Year:

2013

Language:

english

File:

PDF, 954 KB

english, 2013

42

Mutations in ANTXR1 Cause GAPO Syndrome

Stránecký, Viktor, Hoischen, Alexander, Hartmannová, Hana, Zaki, Maha S., Chaudhary, Amit, Zudaire, Enrique, Nosková, Lenka, Barešová, Veronika, Přistoupilová, Anna, Hodaňová, Kateřina, Sovová, Jana,

Journal:

The American Journal of Human Genetics

Year:

2013

Language:

english

File:

PDF, 595 KB

english, 2013

43

Novel mutation in the fukutin gene in an Egyptian family with Fukuyama congenital muscular dystrophy and microcephaly

Ismail, Samira, Schaffer, Ashleigh E., Rosti, Rasim O., Gleeson, Joseph G., Zaki, Maha S.

Journal:

Year:

2014

Language:

english

File:

PDF, 563 KB

english, 2014

44

A comparative study on enteric parasitic infections in immunocompetent and immunosuppressed children in Egypt

El-Mahallawy, Hadir, El Basha, Noussa R., Zaki, Mayssa M., El-Arousy, Maha, Elswaifi, Shaadi F., Abo-hashem, E. M.

Journal:

Comparative Clinical Pathology

Year:

2014

Language:

english

File:

PDF, 195 KB

english, 2014

45

[IEEE 2010 IEEE International Symposium on Signal Processing and Information Technology (ISSPIT) - Luxor, Egypt (2010.12.15-2010.12.18)] The 10th IEEE International Symposium on Signal Processing and Information Technology - SCAMRA: Simulated Context-Aware Meeting Room Application

Zaki, Samah A., Hana, Maha A., Helmy, Yehia K.

Year:

2010

Language:

english

File:

PDF, 657 KB

english, 2010

46

CEP41 is mutated in Joubert syndrome and is required for tubulin glutamylation at the cilium

Lee, Ji Eun, Silhavy, Jennifer L, Zaki, Maha S, Schroth, Jana, Bielas, Stephanie L, Marsh, Sarah E, Olvera, Jesus, Brancati, Francesco, Iannicelli, Miriam, Ikegami, Koji, Schlossman, Andrew M, Merrima

Journal:

Nature Genetics

Year:

2012

Language:

english

File:

PDF, 1.11 MB

english, 2012

47

Functional G1199A ABCB1 Polymorphism May Have an Effect on Cyclosporine Blood Concentration in Renal Transplanted Patients

Mostafa-Hedeab, Gomaa, Saber-Ayad, Maha M., Latif, Inas A., Elkashab, Sahier O., Elshaboney, Tarek H., Mostafa, Magdy Ibrahim, El-Shafy, Sanaa Abd, Zaki, Magda M.

Journal:

Journal of Clinical Pharmacology

Year:

2013

Language:

english

File:

PDF, 258 KB

english, 2013

48

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

49

Biallelic Truncating Mutations in FMN2, Encoding the Actin-Regulatory Protein Formin 2, Cause Nonsyndromic Autosomal-Recessive Intellectual Disability

Law, Rosalind, Dixon-Salazar, Tracy, Jerber, Julie, Cai, Na, Abbasi, Ansar A., Zaki, Maha S., Mittal, Kirti, Gabriel, Stacey B., Rafiq, Muhammad Arshad, Khan, Valeed, Nguyen, Maria, Ali, Ghazanfar, Co

Journal:

The American Journal of Human Genetics

Year:

2014

Language:

english

File:

PDF, 1.03 MB

english, 2014

50

Autosomal dominant SCA5 and autosomal recessive infantile SCA are allelic conditions resulting from SPTBN2 mutations

Elsayed, Solaf M, Heller, Raoul, Thoenes, Michaela, Zaki, Maha S, Swan, Daniel, Elsobky, Ezzat, Zühlke, Christine, Ebermann, Inga, Nürnberg, Gudrun, Nürnberg, Peter, Bolz, Hanno J

Journal:

European Journal of Human Genetics

Year:

2014

Language:

english

File:

PDF, 595 KB

english, 2014

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