Otaify, G.: search on Z-Library

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1

Size dependence of ultrafast charge dynamics in monodisperse Au nanoparticles supported on TiO2 colloidal spheres

Al-Otaify, Ali, Leontiadou, Marina A., dos Reis, Flavia V. E., Damato, Tatiana C., Camargo, Pedro H. C., Binks, David J.

Journal:

Physical Chemistry Chemical Physics

Year:

2014

Language:

english

File:

PDF, 1.96 MB

english, 2014

2

Ultrafast Exciton Dynamics in CdxHg(1−x)Te alloy Quantum Dots

Leontiadou, Marina A., Al-Otaify, Ali, Kershaw, Stephen V., Zhovtiuk, Olga, Kalytchuk, Sergii, Mott, Derrick, Maenosono, Shinya, Rogach, Andrey L., Binks, David J.

Journal:

Chemical Physics

Year:

2016

Language:

english

File:

PDF, 1.04 MB

english, 2016

3

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

4

Diffusion from a point source in an urban atmosphere

Khaled S. M. Essa, Maha S. El-Otaify

Journal:

Meteorology and Atmospheric Physics

Year:

2006

Language:

english

File:

PDF, 106 KB

english, 2006

5

Mathematical model for hermitized atmospheric dispersion in low winds with eddy diffusivities as linear functions of down wind distance

K. S. M. Essa, M. S. El-Otaify

Journal:

Meteorology and Atmospheric Physics

Year:

2007

Language:

english

File:

PDF, 141 KB

english, 2007

6

Multiple exciton generation and ultrafast exciton dynamics in HgTe colloidal quantum dots

Al-Otaify, Ali, Kershaw, Stephen V., Gupta, Shuchi, Rogach, Andrey L., Allan, Guy, Delerue, Christophe, Binks, David. J.

Journal:

Physical Chemistry Chemical Physics

Year:

2013

Language:

english

File:

PDF, 990 KB

english, 2013

7

A Novel Homozygous Mutation in FGFR3 Causes Tall Stature, Severe Lateral Tibial Deviation, Scoliosis, Hearing Impairment, Camptodactyly, and Arachnodactyly

Makrythanasis, Periklis, Temtamy, Samia, Aglan, Mona S., Otaify, Ghada A., Hamamy, Hanan, Antonarakis, Stylianos E.

Journal:

Year:

2014

Language:

english

File:

PDF, 811 KB

english, 2014

8

Exome sequencing in the diagnosis of an atypical phenotype of infantile hyalinosis

Temtamy, Samia A., Aglan, Mona S., Otaify, Ghada A., Abdel-Hamid, Mohamed, Ismail, Somaia, Makrythanasis, Periklis, Hamamy, Hanan, Antonarakis, Stylianos E.

Journal:

Middle East Journal of Medical Genetics

Year:

2015

Language:

english

File:

PDF, 435 KB

english, 2015

9

Mutational spectrum of COL1A1 and COL1A2 in Egyptian patients with autosomal dominant osteogenesis imperfecta with clinical severity score and genotype/phenotype correlation

Aglan, Mona S., Abdel-Hamid, Mohamed S., Otaify, Ghada A., Ismail, Somaia M., Effat, Laila K., Temtamy, Samia A.

Journal:

Middle East Journal of Medical Genetics

Year:

2015

Language:

english

File:

PDF, 537 KB

english, 2015

10

Specific variants in WDR35 cause a distinctive form of Ellis-van Creveld syndrome by disrupting the recruitment of the EvC complex and SMO into the cilium

Caparros-Martin, J. A., De Luca, A., Cartault, F., Aglan, M., Temtamy, S., Otaify, G. A., Mehrez, M., Valencia, M., Vazquez, L., Alessandri, J.-L., Nevado, J., Rueda-Arenas, I., Heath, K. E., Digilio,

Journal:

Human Molecular Genetics

Year:

2015

Language:

english

File:

PDF, 1.19 MB

english, 2015

11

Zoledronic acid in children with osteogenesis imperfecta and Bruck syndrome: a 2-year prospective observational study

Otaify, G. A., Aglan, M. S., Ibrahim, M. M., Elnashar, M., El Banna, R. A. S., Temtamy, S. A.

Journal:

Osteoporosis International

Year:

2016

Language:

english

File:

PDF, 759 KB

english, 2016

12

Atmospheric vertical dispersion in moderate winds with eddy diffusivities as power law functions

Essa, Khaled S. M., El-Otaify, Maha S.

Journal:

Meteorologische Zeitschrift

Year:

2008

Language:

english

File:

PDF, 149 KB

english, 2008

13

Clinical and molecular characterization of seven Egyptian families with autosomal recessive robinow syndrome: Identification of four novel ROR2 gene mutations

Aglan, Mona, Amr, Khalda, Ismail, Samira, Ashour, Adel, Otaify, Ghada A., Mehrez, Mennat Allah I., Aboul-Ezz, Eman H. A., El-Ruby, Mona, Mazen, Inas, Abdel-Hamid, Mohamed S., Temtamy, Samia A.

Journal:

American Journal of Medical Genetics Part A

Year:

2015

Language:

english

File:

PDF, 1.56 MB

english, 2015

14

Raine Syndrome (OMIM #259775), Caused by FAM20C Mutation, Is Congenital Sclerosing Osteomalacia With Cerebral Calcification (OMIM 259660)

Whyte, Michael P., McAlister, William H., Fallon, Michael D., Pierpont, Mary Ella, Bijanki, Vinieth N., Duan, Shenghui, Otaify, Ghada A., Sly, William S., Mumm, Steven

Journal:

Journal of Bone and Mineral Research

Year:

2016

Language:

english

File:

PDF, 1.04 MB

english, 2016

15

Molecular spectrum and differential diagnosis in patients referred with sporadic or autosomal recessive osteogenesis imperfecta

Caparros-Martin, Jose A., Aglan, Mona S., Temtamy, Samia, Otaify, Ghada A., Valencia, Maria, Nevado, Julián, Vallespin, Elena, Del Pozo, Angela, Prior de Castro, Carmen, Calatrava-Ferreras, Lucia, Gut

Journal:

Molecular Genetics & Genomic Medicine

Year:

2017

Language:

english

File:

PDF, 126 KB

english, 2017

16

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

17

PGAP3 -related hyperphosphatasia with mental retardation syndrome: Report of 10 new patients and a homozygous founder mutation

Abdel-Hamid, M.S., Issa, M.Y., Otaify, G.A, Abdel-Ghafar, S.F., Elbendary, H.M., Zaki, M.S.

Journal:

Clinical Genetics

Year:

2017

Language:

english

File:

PDF, 1.35 MB

english, 2017

18

Cytoskeleton and nuclear lamina affection in recessive osteogenesis imperfecta: A functional proteomics perspective

Gagliardi, Assunta, Besio, Roberta, Carnemolla, Chiara, Landi, Claudia, Armini, Alessandro, Aglan, Mona, Otaify, Ghada, Temtamy, Samia A., Forlino, Antonella, Bini, Luca, Bianchi, Laura

Journal:

Journal of Proteomics

Year:

2017

Language:

english

File:

PDF, 1.03 MB

english, 2017

19

Nager acrofacial dysostosis with a novel mutation in SF3B4 and developmental retardation in an Egyptian child

Ismail, Samira, Fayez, Alaaeldin, Otaify, Ghada A., Sayed, Inas, El Ruby, Mona O., Aglan, Mona S., Temtamy, Samia A.

Journal:

Middle East Journal of Medical Genetics

Year:

2017

Language:

english

File:

PDF, 328 KB

english, 2017

20

Gnathodiaphyseal dysplasia: Severe atypical presentation with novel heterozygous mutation of the anoctamin gene ( ANO5 )

Otaify, Ghada A., Whyte, Michael P., Gottesman, Gary S., McAlister, William H., Eric Gordon, J., Hollander, Abby, Andrews, Marisa V., El-Mofty, Samir K., Chen, Wei-Shen, Novack, Deborah V., Stolina, M

Journal:

Year:

2017

Language:

english

File:

PDF, 2.17 MB

english, 2017

21

FAM46A mutations are responsible for autosomal recessive osteogenesis imperfecta

Doyard, Mathilde, Bacrot, Séverine, Huber, Céline, Di Rocco, Maja, Goldenberg, Alice, Aglan, Mona S, Brunelle, Perrine, Temtamy, Samia, Michot, Caroline, Otaify, Ghada A, Haudry, Coralie, Castanet, Mi

Journal:

Journal of Medical Genetics

Year:

2018

Language:

english

File:

PDF, 1.43 MB

english, 2018

22

Genetic study of eight Egyptian patients with pycnodysostosis: identification of novel CTSK mutations and founder effect

Otaify, G. A., Abdel-Hamid, M. S., Mehrez, M. I., Aboul-Ezz, E., Zaki, M. S., Aglan, M. S., Temtamy, S. A.

Journal:

Osteoporosis International

Year:

2018

Language:

english

File:

PDF, 6.20 MB

english, 2018

23

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

24

Modelling Volatility of Characteristics-Sorted Portfolios: Evidence from Egyptian Stock Exchange

Otaify, Mahmoud

Journal:

SSRN Electronic Journal

Year:

2018

File:

PDF, 1.10 MB

2018

25

Modelling Volatility of Characteristics-Sorted Portfolios: Evidence from Egyptian Stock Exchange

Otaify, Mahmoud

Journal:

SSRN Electronic Journal

Year:

2018

Language:

english

File:

PDF, 1.10 MB

english, 2018

26

Cellular stress due to impairment of collagen prolyl hydroxylation complex is rescued by the chaperone 4-phenylbutyrate

Besio, Roberta, Garibaldi, Nadia, Leoni, Laura, Cipolla, Lina, Sabbioneda, Simone, Biggiogera, Marco, Mottes, Monica, Aglan, Mona, Otaify, Ghada A., Temtamy, Samia A., Rossi, Antonio, Forlino, Antonel

Journal:

Disease Models & Mechanisms

Year:

2019

Language:

english

File:

PDF, 7.41 MB

english, 2019

27

NEW GENES AND DISEASES

Yoon, G., Estañ, M., Fernandez-Nuñez, E., Zak, M., Esteban, M., Donkervoort, S., Hawkins, C., Caparros-Martin, J., Saade, D., Hu, Y., Bolduc, V., Chao, K., Otaify, G., Temtamy, S., Aglan, M., Issa, M.

Journal:

Neuromuscular Disorders

Year:

2019

Language:

english

File:

PDF, 103 KB

english, 2019

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