Zobrazeno 1 - 10
of 49
pro vyhledávání: '"Ali Hellani"'
Publikováno v:
International Journal of Epidemiologic Research, Vol 7, Iss 2, Pp 63-67 (2020)
Background and aims: Lung cancer is the leading cause of cancer death worldwide. There are no recent data on the lung cancer prevalence in Lebanon, and the available data are based on prediction. Thus, this study aimed to determine the incidence rate
Externí odkaz:
https://doaj.org/article/91eb5738e7d54399903b819eb3c46cf2
Autor:
Ahmad Metwalley, Ali Hellani, Azza A. Abdelrazek, Ahmed El-Damen, Ahmed Al Dawood, Nabeel Brasha, Sandro C. Esteves, Manal El Hamshary, Omaima Khamiss
Publikováno v:
Zygote (Cambridge, England). 30(6)
SummaryThe aim of this study was to assess mitochondrial DNA analysis as a predictor of the pregnancy potential of biopsied preimplantation embryos. The study included 78 blastomeres biopsied from day 4 cleavage stage euploid embryos. The embryo kary
Autor:
Hadiya Brasha, Mohamed Fawzy, Ali Hellani, Ahmad M. Metwalley, Sandro C. Esteves, Omaima Khamiss, Nabeel Brasha, Manal El Hamshary
Publikováno v:
Zygote. 28:519-523
Purpose:To report the utilization of diagnostic intracytoplasmic sperm injection (D-ICSI), an ICSI cycle performed in the natural cycle, to obtain information about embryo development potential after sperm injection into zona pellucida (ZP)-free oocy
Publikováno v:
Annals of Saudi Medicine, Vol 34, Iss 3, Pp 217-221 (2014)
BACKGROUND AND OBJECTIVES: The prevalence of maturity-onset diabetes of the young (MODY) in Saudi population remains unknown, and data on molecular etiology of this condition is limited. Therefore, the present study was undertaken to elucidate clinic
Autor:
Thomas M. Bosley, Darren T. Oystreck, Ibrahim A. Alorainy, Eiman A. Al-Yamani, Mustafa A. Salih, Mohamed Sabry, Mohamed S. Rashed, Ali Hellani, Mohammed Zain Seidahmed, Mohamed Elfaki Osman, Khaled K. Abu-Amero
Publikováno v:
Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 41:42-48
Background:We review clinical, neuroimaging, and genetic information on six individuals with isolated sulfite oxidase deficiency (ISOD).Methods:All patients were examined, and clinical records, biochemistry, neuroimaging, and sulfite oxidase gene (SU
Publikováno v:
Reproductive BioMedicine Online. 38:e47
Introduction Preimplantation Genetic Diagnosis- Aneuploidy Screening (PGD-A) is a technique commonly used in conjunction with IVF treatments. PGD-A is intended to identify those embryos with greater likelihood to implant. It is offered to patients at
Autor:
Arif O. Khan, Darren T. Oystreck, Altaf A. Kondkar, Thomas M. Bosley, Ali Hellani, Khaled K. Abu-Amero
Publikováno v:
Ophthalmic Genetics. 36:99-104
To evaluate possible monogenic and chromosomal anomalies in a patient with unilateral Duane retraction syndrome and modest dysmorphism.Clinical evaluation, sequencing of candidate genes, and array comparative genomic hybridization (array CGH).The pro
Autor:
Thomas M. Bosley, Ibrahim A. Alorainy, Khaled K. Abu-Amero, Abdullah G Al Otaibi, Altaf A. Kondkar, Ali Hellani, Darren T. Oystreck, Arif O. Khan
Publikováno v:
Ophthalmic Genetics. 36:14-20
To evaluate possible monogenic and chromosomal anomalies in a patient with unilateral Duane retraction syndrome, modest dysmorphism, cerebral white matter abnormalities, and normal cognitive function.Performing high-resolution array comparative genom
Publikováno v:
International Ophthalmology. 31:117-120
To carry out an ophthalmological and detailed genetic investigation on a 7-year-old boy with isolated foveal hypoplasia. A full ophthalmological examination and optical coherence tomography (OCT) was performed. We also performed a full genome screen
Autor:
Ali Hellani, Nancy L. Sicotte, Ghassan Zidan, Thomas M. Bosley, Ibrahim A. Alorainy, Khaled K. Abu-Amero, Kyle C. Kern, Mustafa A. Salih
Publikováno v:
Ophthalmic Genetics. 31:147-154
Neuro-ophthalmologic and neuroimaging features of partial chromosome 18p deletion syndromes have not yet been fully described.Careful neuro-ophthalmologic and neuroimaging evaluation of a young woman with a partial 18p deletion, including 3 Tesla MRI