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Showing 1 to 12 of 637 entries
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Fertility preservation options for prepubertal boys facing gonadotoxic therapies

STEM and boys

Hussein AA.
GSID: v1Whb-JgdKcJ
AA Hussein, P Yango, Y Ezz, JF Smith… - Minerva …, 2016 - europepmc.org

Infertility is a common disease affecting 10-15% of reproductive couples with significant psychological and financial impacts to both patients and society. Approximately 80 million people worldwide are infertile, with an increasing incidence of male infertility. Semen cryopreservation in adults...

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Hussein, A. A., Yango, P., Ezz, Y., Smith, J. F., & Tran, N. D. (2016). Fertility preservation options for prepubertal boys facing gonadotoxic therapies. Minerva Ginecologica, 68(6), 668-674.
Hussein, Ahmed A., et al. "Fertility preservation options for prepubertal boys facing gonadotoxic therapies." Minerva Ginecologica 68.6 (2016): 668-674.
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Hepatobiliary Tumors: Update on Diagnosis and Management.

Journal of clinical and translational hepatology

Kabbach G, Assi HA, Bolotin G, Schuster M, Lee HJ, Tadros M.
PMID: 26623263
J Clin Transl Hepatol. 2015 Sep 28;3(3):169-81. doi: 10.14218/JCTH.2015.00012. Epub 2015 Sep 15.

Tumors of the liver and biliary tree, mainly hepatocellular carcinoma and cholangiocarcinoma, are the second leading cause of cancer related death worldwide and the sixth leading cause of cancer related death among men in developed countries. Recent developments in...

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Kabbach G, Assi HA, Bolotin G, et al. Hepatobiliary Tumors: Update on Diagnosis and Management. J Clin Transl Hepatol. 2015;3(3):169-81doi: 10.14218/JCTH.2015.00012.
Kabbach, G., Assi, H. A., Bolotin, G., Schuster, M., Lee, H. J., & Tadros, M. (2015). Hepatobiliary Tumors: Update on Diagnosis and Management. Journal of clinical and translational hepatology, 3(3), 169-81. https://doi.org/10.14218/JCTH.2015.00012
Kabbach, Ghassan, et al. "Hepatobiliary Tumors: Update on Diagnosis and Management." Journal of clinical and translational hepatology vol. 3,3 (2015): 169-81. doi: https://doi.org/10.14218/JCTH.2015.00012
Kabbach G, Assi HA, Bolotin G, Schuster M, Lee HJ, Tadros M. Hepatobiliary Tumors: Update on Diagnosis and Management. J Clin Transl Hepatol. 2015 Sep 28;3(3):169-81. doi: 10.14218/JCTH.2015.00012. Epub 2015 Sep 15. PMID: 26623263; PMCID: PMC4663198.
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Safety and esthetic outcomes of therapeutic mammoplasty using medial pedicle for early breast cancer.

Breast cancer (Dove Medical Press)

Roshdy S, Hussein O, Khater A, Zuhdy M, El-Hadaad HA, Farouk O, Senbel A, Fathi A, Hamed E, Denewer A.
PMID: 26185469
Breast Cancer (Dove Med Press). 2015 Jul 07;7:173-8. doi: 10.2147/BCTT.S83725. eCollection 2015.

BACKGROUND: Although therapeutic mammoplasty (TM) was introduced for treatment of localized ductal carcinoma in situ and invasive breast carcinoma (stages I and II) in females with large breast size, the suitability of medial pedicle TM for treatment of breast...

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Roshdy S, Hussein O, Khater A, et al. Safety and esthetic outcomes of therapeutic mammoplasty using medial pedicle for early breast cancer. Breast Cancer (Dove Med Press). 2015;7:173-8doi: 10.2147/BCTT.S83725.
Roshdy, S., Hussein, O., Khater, A., Zuhdy, M., El-Hadaad, H. A., Farouk, O., Senbel, A., Fathi, A., Hamed, E., & Denewer, A. (2015). Safety and esthetic outcomes of therapeutic mammoplasty using medial pedicle for early breast cancer. Breast cancer (Dove Medical Press), 7173-8. https://doi.org/10.2147/BCTT.S83725
Roshdy, Sameh, et al. "Safety and esthetic outcomes of therapeutic mammoplasty using medial pedicle for early breast cancer." Breast cancer (Dove Medical Press) vol. 7 (2015): 173-8. doi: https://doi.org/10.2147/BCTT.S83725
Roshdy S, Hussein O, Khater A, Zuhdy M, El-Hadaad HA, Farouk O, Senbel A, Fathi A, Hamed E, Denewer A. Safety and esthetic outcomes of therapeutic mammoplasty using medial pedicle for early breast cancer. Breast Cancer (Dove Med Press). 2015 Jul 07;7:173-8. doi: 10.2147/BCTT.S83725. eCollection 2015. PMID: 26185469; PMCID: PMC4500603.
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Selection of Novel Cowpea Genotypes Derived through Gamma Irradiation.

Frontiers in plant science

Horn LN, Ghebrehiwot HM, Shimelis HA.
PMID: 27148275
Front Plant Sci. 2016 Mar 10;7:262. doi: 10.3389/fpls.2016.00262. eCollection 2016.

Cowpea (Vigna unguiculata [L.] Walp.) yields are considerably low in Namibia due to lack of improved varieties and biotic and abiotic stresses, notably, recurrent drought. Thus, genetic improvement in cowpea aims to develop cultivars with improved grain yield and...

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Horn LN, Ghebrehiwot HM, Shimelis HA. Selection of Novel Cowpea Genotypes Derived through Gamma Irradiation. Front Plant Sci. 2016;7:262doi: 10.3389/fpls.2016.00262.
Horn, L. N., Ghebrehiwot, H. M., & Shimelis, H. A. (2016). Selection of Novel Cowpea Genotypes Derived through Gamma Irradiation. Frontiers in plant science, 7262. https://doi.org/10.3389/fpls.2016.00262
Horn, Lydia N, et al. "Selection of Novel Cowpea Genotypes Derived through Gamma Irradiation." Frontiers in plant science vol. 7 (2016): 262. doi: https://doi.org/10.3389/fpls.2016.00262
Horn LN, Ghebrehiwot HM, Shimelis HA. Selection of Novel Cowpea Genotypes Derived through Gamma Irradiation. Front Plant Sci. 2016 Mar 10;7:262. doi: 10.3389/fpls.2016.00262. eCollection 2016. PMID: 27148275; PMCID: PMC4834446.
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Subcellular fractionation method to study endosomal trafficking of Kaposi's sarcoma-associated herpesvirus.

Cell & bioscience

Walker LR, Hussein HA, Akula SM.
PMID: 26779333
Cell Biosci. 2016 Jan 15;6:1. doi: 10.1186/s13578-015-0066-2. eCollection 2016.

BACKGROUND: Virus entry involves multiple steps and is a highly orchestrated process on which successful infection collectively depends. Entry processes are commonly analyzed by monitoring internalized virus particles via Western blotting, polymerase chain reaction, and imaging techniques that allow...

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Walker LR, Hussein HA, Akula SM. Subcellular fractionation method to study endosomal trafficking of Kaposi's sarcoma-associated herpesvirus. Cell Biosci. 2016;6:1doi: 10.1186/s13578-015-0066-2.
Walker, L. R., Hussein, H. A., & Akula, S. M. (2016). Subcellular fractionation method to study endosomal trafficking of Kaposi's sarcoma-associated herpesvirus. Cell & bioscience, 61. https://doi.org/10.1186/s13578-015-0066-2
Walker, Lia R, et al. "Subcellular fractionation method to study endosomal trafficking of Kaposi's sarcoma-associated herpesvirus." Cell & bioscience vol. 6 (2016): 1. doi: https://doi.org/10.1186/s13578-015-0066-2
Walker LR, Hussein HA, Akula SM. Subcellular fractionation method to study endosomal trafficking of Kaposi's sarcoma-associated herpesvirus. Cell Biosci. 2016 Jan 15;6:1. doi: 10.1186/s13578-015-0066-2. eCollection 2016. PMID: 26779333; PMCID: PMC4714431.
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Effect of Polymers on the Physicochemical Properties and Biological Performance of Fenoprofen Calcium Dihydrate-Triacetyl-β-Cyclodextrin Complex.

Pharmaceutics

Ammar HO, Makram TS, Mosallam S.
PMID: 28671624
Pharmaceutics. 2017 Jul 03;9(3). doi: 10.3390/pharmaceutics9030023.

BACKGROUND: Fenoprofen calcium dehydrate (FCD) is counted as a non-steroidal, anti-inflammatory, anti-arthritic drug. FCD is slightly water soluble. It is indicated for mild pain relief, where the suggested dosage is 200 mg orally every 4 to 6 h.AIM: Reduce...

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Ammar HO, Makram TS, Mosallam S. Effect of Polymers on the Physicochemical Properties and Biological Performance of Fenoprofen Calcium Dihydrate-Triacetyl-β-Cyclodextrin Complex. Pharmaceutics. 2017;9(3)doi: 10.3390/pharmaceutics9030023.
Ammar, H. O., Makram, T. S., & Mosallam, S. (2017). Effect of Polymers on the Physicochemical Properties and Biological Performance of Fenoprofen Calcium Dihydrate-Triacetyl-β-Cyclodextrin Complex. Pharmaceutics, 9(3), . https://doi.org/10.3390/pharmaceutics9030023
Ammar, Hussein O, et al. "Effect of Polymers on the Physicochemical Properties and Biological Performance of Fenoprofen Calcium Dihydrate-Triacetyl-β-Cyclodextrin Complex." Pharmaceutics vol. 9,3 (2017). doi: https://doi.org/10.3390/pharmaceutics9030023
Ammar HO, Makram TS, Mosallam S. Effect of Polymers on the Physicochemical Properties and Biological Performance of Fenoprofen Calcium Dihydrate-Triacetyl-β-Cyclodextrin Complex. Pharmaceutics. 2017 Jul 03;9(3). doi: 10.3390/pharmaceutics9030023. PMID: 28671624; PMCID: PMC5620564.
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In vitro effect of glucagon-like peptide-1 (7-36)amide, oxyntomodulin, vasoactive intestinal peptide and somatostatin on gastric acid and pepsinogen secretion.

Inflammation research : official journal of the European Histamine Research Society ... [et al.]

Ben-Hamida A, Houssein AA, Man WK, Spencer J.
PMID: 27518026
Inflamm Res. 1997 Mar;46:105-6. doi: 10.1007/s000110050122.

No abstract available.

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Ben-Hamida A, Houssein AA, Man WK, et al. In vitro effect of glucagon-like peptide-1 (7-36)amide, oxyntomodulin, vasoactive intestinal peptide and somatostatin on gastric acid and pepsinogen secretion. Inflamm Res. 1997;46:105-6doi: 10.1007/s000110050122.
Ben-Hamida, A., Houssein, A. A., Man, W. K., & Spencer, J. (1997). In vitro effect of glucagon-like peptide-1 (7-36)amide, oxyntomodulin, vasoactive intestinal peptide and somatostatin on gastric acid and pepsinogen secretion. Inflammation research : official journal of the European Histamine Research Society ... [et al.], 46105-6. https://doi.org/10.1007/s000110050122
Ben-Hamida, A, et al. "In vitro effect of glucagon-like peptide-1 (7-36)amide, oxyntomodulin, vasoactive intestinal peptide and somatostatin on gastric acid and pepsinogen secretion." Inflammation research : official journal of the European Histamine Research Society ... [et al.] vol. 46 (1997): 105-6. doi: https://doi.org/10.1007/s000110050122
Ben-Hamida A, Houssein AA, Man WK, Spencer J. In vitro effect of glucagon-like peptide-1 (7-36)amide, oxyntomodulin, vasoactive intestinal peptide and somatostatin on gastric acid and pepsinogen secretion. Inflamm Res. 1997 Mar;46:105-6. doi: 10.1007/s000110050122. PMID: 27518026.
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Physical Fitness in Adolescence and Subsequent Inflammatory Bowel Disease Risk.

Clinical and translational gastroenterology

Melinder C, Hiyoshi A, Hussein O, Halfvarson J, Ekbom A, Montgomery S.
PMID: 26540026
Clin Transl Gastroenterol. 2015 Nov 05;6:e121. doi: 10.1038/ctg.2015.49.

OBJECTIVES: Physical fitness may reduce systemic inflammation levels relevant to the risk of symptomatic Crohn's disease (CD) and ulcerative colitis (UC); we assessed if fitness in adolescence is associated with subsequent inflammatory bowel disease (IBD) risk, independent of markers...

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Melinder C, Hiyoshi A, Hussein O, et al. Physical Fitness in Adolescence and Subsequent Inflammatory Bowel Disease Risk. Clin Transl Gastroenterol. 2015;6:e121doi: 10.1038/ctg.2015.49.
Melinder, C., Hiyoshi, A., Hussein, O., Halfvarson, J., Ekbom, A., & Montgomery, S. (2015). Physical Fitness in Adolescence and Subsequent Inflammatory Bowel Disease Risk. Clinical and translational gastroenterology, 6e121. https://doi.org/10.1038/ctg.2015.49
Melinder, Carren, et al. "Physical Fitness in Adolescence and Subsequent Inflammatory Bowel Disease Risk." Clinical and translational gastroenterology vol. 6 (2015): e121. doi: https://doi.org/10.1038/ctg.2015.49
Melinder C, Hiyoshi A, Hussein O, Halfvarson J, Ekbom A, Montgomery S. Physical Fitness in Adolescence and Subsequent Inflammatory Bowel Disease Risk. Clin Transl Gastroenterol. 2015 Nov 05;6:e121. doi: 10.1038/ctg.2015.49. PMID: 26540026; PMCID: PMC4816088.
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A case of spontaneous pneumothorax following radiation therapy for non-small cell lung cancer.

Lung India : official organ of Indian Chest Society

Bhardwaj H, Bhardwaj B, Youness HA.
PMID: 24339501
Lung India. 2013 Oct;30(4):360-2. doi: 10.4103/0970-2113.120624.

Spontaneous pneumothorax (SPTX) is a potentially devastating rare complication of the thoracic radiation therapy. Most of the cases in the medical literature, have been described in lymphoma patients receiving radiation therapy. The pathogenesis of this adverse event remains undefined...

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Bhardwaj H, Bhardwaj B, Youness HA. A case of spontaneous pneumothorax following radiation therapy for non-small cell lung cancer. Lung India. 2013;30(4):360-2doi: 10.4103/0970-2113.120624.
Bhardwaj, H., Bhardwaj, B., & Youness, H. A. (2013). A case of spontaneous pneumothorax following radiation therapy for non-small cell lung cancer. Lung India : official organ of Indian Chest Society, 30(4), 360-2. https://doi.org/10.4103/0970-2113.120624
Bhardwaj, Himanshu, et al. "A case of spontaneous pneumothorax following radiation therapy for non-small cell lung cancer." Lung India : official organ of Indian Chest Society vol. 30,4 (2013): 360-2. doi: https://doi.org/10.4103/0970-2113.120624
Bhardwaj H, Bhardwaj B, Youness HA. A case of spontaneous pneumothorax following radiation therapy for non-small cell lung cancer. Lung India. 2013 Oct;30(4):360-2. doi: 10.4103/0970-2113.120624. PMID: 24339501; PMCID: PMC3841700.
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The negative effect of ceria on the propene selectivity for isopropanol decomposition over phosphated and phosphate-free ceria/alumina catalysts.

SpringerPlus

Khalaf HA.
PMID: 24340242
Springerplus. 2013 Nov 20;2:619. doi: 10.1186/2193-1801-2-619. eCollection 2013.

Consequences of loading level of ceria (5, 10 and 20-wt%) on the structural, textural and surface acid-base properties as well as the impacts on catalytic activity towards isopropanol decomposition on pure and phosphated alumina is described. The obtained results...

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Khalaf HA. The negative effect of ceria on the propene selectivity for isopropanol decomposition over phosphated and phosphate-free ceria/alumina catalysts. Springerplus. 2013;2:619doi: 10.1186/2193-1801-2-619.
Khalaf, H. A. (2013). The negative effect of ceria on the propene selectivity for isopropanol decomposition over phosphated and phosphate-free ceria/alumina catalysts. SpringerPlus, 2619. https://doi.org/10.1186/2193-1801-2-619
Khalaf, Hussein A. "The negative effect of ceria on the propene selectivity for isopropanol decomposition over phosphated and phosphate-free ceria/alumina catalysts." SpringerPlus vol. 2 (2013): 619. doi: https://doi.org/10.1186/2193-1801-2-619
Khalaf HA. The negative effect of ceria on the propene selectivity for isopropanol decomposition over phosphated and phosphate-free ceria/alumina catalysts. Springerplus. 2013 Nov 20;2:619. doi: 10.1186/2193-1801-2-619. eCollection 2013. PMID: 24340242; PMCID: PMC3858591.
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Design and synthesis of some substituted thiazolo[3,2-a]pyrimidine derivatives of potential biological activities.

Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society

Abdel Moty SG, Hussein MA, Abdel Aziz SA, Abou-Salim MA.
PMID: 27013904
Saudi Pharm J. 2016 Mar;24(2):119-32. doi: 10.1016/j.jsps.2013.12.016. Epub 2013 Dec 28.

In continuation to our previous work, thiazolopyrimidines 2a-x were synthesized through intramolecular cyclization of 2-phenacylthio-dihydropyrimidine hydrobromides 1a-x using polyphosphoric acid. On the other hand, thiazolo[3,2-a]pyrimidine-3-one 3 was coupled with aryldiazonium salts or condensed with isatin to afford compounds 4a-c...

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Abdel Moty SG, Hussein MA, Abdel Aziz SA, et al. Design and synthesis of some substituted thiazolo[3,2-a]pyrimidine derivatives of potential biological activities. Saudi Pharm J. 2013;24(2):119-32doi: 10.1016/j.jsps.2013.12.016.
Abdel Moty, S. G., Hussein, M. A., Abdel Aziz, S. A., & Abou-Salim, M. A. (2016). Design and synthesis of some substituted thiazolo[3,2-a]pyrimidine derivatives of potential biological activities. Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society, 24(2), 119-32. https://doi.org/10.1016/j.jsps.2013.12.016
Abdel Moty, Samia G, et al. "Design and synthesis of some substituted thiazolo[3,2-a]pyrimidine derivatives of potential biological activities." Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society vol. 24,2 (2016): 119-32. doi: https://doi.org/10.1016/j.jsps.2013.12.016
Abdel Moty SG, Hussein MA, Abdel Aziz SA, Abou-Salim MA. Design and synthesis of some substituted thiazolo[3,2-a]pyrimidine derivatives of potential biological activities. Saudi Pharm J. 2016 Mar;24(2):119-32. doi: 10.1016/j.jsps.2013.12.016. Epub 2013 Dec 28. PMID: 27013904; PMCID: PMC4792894.
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DFT global optimisation of gas-phase and MgO-supported sub-nanometre AuPd clusters.

Physical chemistry chemical physics : PCCP

Hussein HA, Davis JBA, Johnston RL.
PMID: 27711424
Phys Chem Chem Phys. 2016 Sep 21;18(37):26133-26143. doi: 10.1039/c6cp03958h.

The Birmingham Parallel Genetic Algorithm (BPGA) has been adopted for the global optimization of free and MgO(100)-supported Pd, Au and AuPd nanocluster structures, over the size range N = 4-10. Structures were evaluated directly using density functional theory, which...

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Hussein HA, Davis JBA, Johnston RL. DFT global optimisation of gas-phase and MgO-supported sub-nanometre AuPd clusters. Phys Chem Chem Phys. 2016;18(37):26133-26143doi: 10.1039/c6cp03958h.
Hussein, H. A., Davis, J. B. A., & Johnston, R. L. (2016). DFT global optimisation of gas-phase and MgO-supported sub-nanometre AuPd clusters. Physical chemistry chemical physics : PCCP, 18(37), 26133-26143. https://doi.org/10.1039/c6cp03958h
Hussein, Heider A, et al. "DFT global optimisation of gas-phase and MgO-supported sub-nanometre AuPd clusters." Physical chemistry chemical physics : PCCP vol. 18,37 (2016): 26133-26143. doi: https://doi.org/10.1039/c6cp03958h
Hussein HA, Davis JBA, Johnston RL. DFT global optimisation of gas-phase and MgO-supported sub-nanometre AuPd clusters. Phys Chem Chem Phys. 2016 Sep 21;18(37):26133-26143. doi: 10.1039/c6cp03958h. PMID: 27711424.
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Showing 1 to 12 of 637 entries