Search Results - "Sabry, M. A."

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  1. 1

    Does the Use of Different Types of Probiotics Possess Detoxification Properties Against Aflatoxins Contamination in Rabbit Diets? by Mohamed, Said I. A., Shehata, Sabry A. M., Bassiony, Sabry M., Mahgoub, Samir A. M., Abd El-Hack, Mohamed E.

    Published in Probiotics and antimicrobial proteins (01-10-2023)
    “…The present work was carried out to study the ability of five probiotics on the in vitro degradation of Aflatoxins B 1 (AFB 1) . The best results of in vitro…”
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    Enzyme profiles and genotyping of Chaetomium globosum isolates from various substrates by Abdel-Azeem, A. M., Gherbawy, Y. A., Sabry, A. M.

    Published in Plant biosystems (03-05-2016)
    “…The genus Chaetomium is a rich source of novel and bioactive secondary metabolites of great importance. To date, a variety of more than 200 secondary…”
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  3. 3

    Dependent Ranked Set Sampling Designs for Parametric Estimation with Applications by Sabry, M. A., Shaaban, M.

    Published in Annals of data science (01-06-2020)
    “…In this paper, we derive the likelihood function of the neoteric ranked set sampling (NRSS) as dependent in sampling method and double neoteric ranked set…”
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    Homozygous mutations in a predicted endonuclease are a novel cause of congenital dyserythropoietic anemia type I by Babbs, C., Roberts, N. A., Sanchez-Pulido, L., McGowan, S. J., Ahmed, M. R., Brown, J. M., Sabry, M. A., Bentley, D. R., McVean, G. A., Donnelly, P., Gileadi, O., Ponting, C. P., Higgs, D. R., Buckle, V. J.

    Published in Haematologica (Roma) (01-09-2013)
    “…The congenital dyserythropoietic anemias are a heterogeneous group of rare disorders primarily affecting erythropoiesis with characteristic morphological…”
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    Successful long‐term treatment of hepatic carnitine palmitoyltransferase I deficiency and a novel mutation by Stoler, J. M., Sabry, M. A., Hanley, C., Hoppel, C. L., Shih, V. E.

    Published in Journal of inherited metabolic disease (01-01-2004)
    “…Individuals with carnitine palmitoyltransferase I (CPT‐I) deficiency cannot metabolize long‐chain fatty acids and can develop life‐threatening hypoglycaemia…”
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  8. 8

    Nuclear-Powered Reverse Osmosis Desalination Unit Performance Improvement Using Six Sigma and Desalination Economic Evaluation Model by Amr M. Sabry, A., Elshahat, Ayah, Nagla, Tarek F., Agamy, Saeed

    Published in Journal of water chemistry and technology (01-12-2022)
    “…Recently, the world faces a serious crisis due to water scarcity and global warming gases. Therefore, in this study, practical and structural sustainable…”
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  9. 9

    Role of Speckle Tracking in the Evaluation of Left Ventricular Remodeling After Streptokinase Infusion in Patients with Acute Anterior Myocardial Infarction by Farag, Sh. I., El-Rabbat, Kh. E., El-Awadi, M. A., Sabry, A. M.

    “…Background . Left ventricular (LV) remodeling is an adverse consequence after acute myocardial infarction. Aim . To assess the role of speckle tracking in the…”
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  10. 10

    Total truncation of the molybdopterin/dimerization domains of SUOX protein in an Arab family with isolated sulfite oxidase deficiency by Seidahmed, M.Z., Alyamani, E.A., Rashed, M.S., Saadallah, A.A., Abdelbasit, O.B., Shaheed, M.M., Rasheed, A., Hamid, F.A., Sabry, M.A.

    “…We ascertained a patient with the full‐blown phenotype of isolated sulfite oxidase deficiency in a consanguineous Arab family. The proband's phenotype included…”
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    Nephrocalcinosis and urolithiasis in carbonic anhydrase II deficiency syndrome by ISMAIL, E. A. R, ABUL SAAD, S, SABRY, M. A

    Published in European journal of pediatrics (01-12-1997)
    “…We report three new Kuwaiti patients with carbonic anhydrase II deficiency (CA II) from two unrelated families. Each patient had osteopetrosis, distal renal…”
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  12. 12

    EFFECT OF GINGER DIETARY SUPPLEMENTATION ON GROWTH PERFORMANCE, IMMUNE RESPONSE AND VACCINE EFFICACY IN Oreochromis niloticus CHALLENGED WITH Aeromonas hydrophila by El-Sebai, Ahmed, El-Murr, Abd El-Hakim, Galal, Azza A. A., Abd El-Motaal, Sabry M. A.

    Published in Slovenski veterinarski zbornik (01-01-2018)
    “…Ginger powder was used in the current study for the improvement of the growth performance and the efficacy of Aeromonas hydrophila (A. hydrophila) vaccination…”
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  13. 13

    Identification of Mediterranean mutation in Egyptian favism patients by Osman, H G, Zahran, F M, El-Sokkary, A M A, El-Said, A, Sabry, A M

    “…Identify and screen the G6PD Mediterranean mutation in favism patients by applying a Amplification Refractory Mutation System Polymerase Chain Reaction…”
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  14. 14

    Kenny-Caffey syndrome is part of the CATCH 22 haploinsufficiency cluster by Sabry, M A, Zaki, M, Abul Hassan, S J, Ramadan, D G, Abdel Rasool, M A, al Awadi, S A, al Saleh, Q

    Published in Journal of medical genetics (01-01-1998)
    “…We report four sibs with Kenny-Caffey syndrome in a consanguineous Bedouin family. The first two died in the neonatal period while the remaining affected…”
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    Kenny-Caffey syndrome: an Arab variant? by Sabry, MA, Farag, TI, Shaltout, AA, Zaki, M, Al-Mazidi, Z, Abulhassan, SJ, Al-Torki, N, Quishawi, A, Al Awadi, SA

    Published in Clinical genetics (01-01-1999)
    “…We describe 2 unrelated Bedouin girls who met the criteria for the diagnosis of Kenny–Caffey syndrome. The girls had some unusual features – microcephaly and…”
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    Oxidative stress and antioxidant defense in Egyptian favism patients by Osman, H G, Zahran, F M, El-Sokkary, A M A, Sabry, A M

    “…Favism occurs as the result of intolerance to the ingesting of fava beans or to the inhalation of pollen from the Vicia faba plant. Patients with favism are…”
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    Femoral hypoplasia-unusual facies syndrome with bifid hallux, absent tibia, and macrophallus: a report of a Bedouin baby by Sabry, M A, Obenbergerova, D, Al-Sawan, R, Saleh, Q A, Farah, S, Al-Awadi, S A, Farag, T I

    Published in Journal of medical genetics (01-02-1996)
    “…A male Bedouin baby with the clinical profile of femoral hypoplasia-unusual facies syndrome is described. The phenotype includes bilateral asymmetrical lower…”
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    Identification and pattern of expression of a developmental isoform of troponin I in chicken and rat cardiac muscle by SABRY, M. A, DHOOT, G. K

    “…A monoclonal antibody that reacts with all known isoforms of troponin I detected a single isoform of cardiac troponin I in both atrial and ventricular chambers…”
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    Triophthalmia and facial clefting: a case report by Tayel, S M, Sabry, M A, Kader, N A, Farah, S, Al-Awadi, S A, Farag, T I

    Published in Journal of medical genetics (01-10-1998)
    “…We describe a Libyan boy with an unusual phenotype of multiple congenital anomalies, including triophthalmia, dolichocephaly, porencephaly, cleft lip/palate,…”
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