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  1. Article ; Online: Effect of Oropharyngeal Administration of Mother's Milk Prior to Gavage Feeding on Gastrin, Motilin, Secretin, and Cholecystokinin Hormones in Preterm Infants: A Pilot Crossover Study.

    Mohammed, Abdel-Rahman / Eid, Abdel-Rahman / Elzehery, Rasha / Al-Harrass, Mohammad / Shouman, Basma / Nasef, Nehad

    JPEN. Journal of parenteral and enteral nutrition

    2020  Volume 45, Issue 4, Page(s) 777–783

    Abstract: Background: Oropharyngeal administration of milk prior to gavage feeding has been shown to improve feeding tolerance in preterm infants.: Objectives: The aim is to study the effect of oropharyngeal administration of mother's milk (OPAMM), prior to ... ...

    Abstract Background: Oropharyngeal administration of milk prior to gavage feeding has been shown to improve feeding tolerance in preterm infants.
    Objectives: The aim is to study the effect of oropharyngeal administration of mother's milk (OPAMM), prior to gavage feeding, on the levels of gastrin, motilin, secretin, and cholecystokinin hormones.
    Methods: Preterm infants (<32 weeks' gestation) were randomized at a corrected gestational age of 33-34 weeks, in a crossover design, to receive 1 of 2 protocols: 24 hours of OPAMM practice (applying 0.2 mL of mother's milk prior to each gavage feeding) followed by 24 hours of regular gavage-feeding practice in the first protocol or vice versa in the second protocol. The levels of gastrin, motilin, secretin, and cholecystokinin hormones were measured at the end of 24 hours of both practices.
    Results: The data of 40 preterm infants (20 in each protocol) were analyzed. OPAMM was associated with a significant increase in the levels of motilin (median, 233; interquartile range [IQR], 196-296 vs median, 196; IQR, 128-233; P < .01), secretin (median, 401; IQR, 353-458 vs median, 370; IQR, 331-407; P = .04), and cholecystokinin (median, 21.4; IQR, 16-27.1 vs median, 14.9; IQR, 11-20.5; P <.01) but not gastrin (median, 202; IQR, 125-238 vs median, 175; IQR, 128-227; P = .7), compared with regular gavage-feeding practice.
    Conclusion: Oro-pharyngeal stimulation by OPAMM, prior to gavage feeding, significantly increased motilin hormone and possibly increased secretin and cholecystokinin hormones.
    MeSH term(s) Cholecystokinin ; Cross-Over Studies ; Female ; Gastrins ; Humans ; Infant ; Infant, Newborn ; Infant, Premature ; Milk, Human ; Mothers ; Motilin ; Secretin
    Chemical Substances Gastrins ; Secretin (1393-25-5) ; Motilin (52906-92-0) ; Cholecystokinin (9011-97-6)
    Language English
    Publishing date 2020-06-25
    Publishing country United States
    Document type Journal Article
    ZDB-ID 800861-9
    ISSN 1941-2444 ; 0148-6071
    ISSN (online) 1941-2444
    ISSN 0148-6071
    DOI 10.1002/jpen.1935
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    In stock of ZB MED Cologne/Königswinter

    Zs.A 1524: Show issues Location:
    Je nach Verfügbarkeit (siehe Angabe bei Bestand)
    bis Jg. 1994: Bestellungen von Artikeln über das Online-Bestellformular
    Jg. 1995 - 2021: Lesesall (1.OG)
    ab Jg. 2022: Lesesaal (EG)

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  2. Article: Screening for the Most Common Mutations of

    Al-Haggar, Mohammad / Osman, Engy / Eid, Abdel-Rahman / Barakat, Tarek / El-Morsi, Samar

    Journal of pediatric genetics

    2020  Volume 9, Issue 3, Page(s) 164–170

    Abstract: Cystic fibrosis (CF) is panethnic autosomal recessive disease that affects the exocrine glands of pancreas, lungs, and intestine. It is often misdiagnosed in developing countries as difficult-to-treat asthma. We enrolled 150 Egyptian families with one or ...

    Abstract Cystic fibrosis (CF) is panethnic autosomal recessive disease that affects the exocrine glands of pancreas, lungs, and intestine. It is often misdiagnosed in developing countries as difficult-to-treat asthma. We enrolled 150 Egyptian families with one or more probands who were complaining of difficult-to-treat asthma, and 112 cases were studied extensively through history taking including pedigree construction and clinical examination. In addition, spirometry and computed tomography of the chest were done in selected cases. All cases were subjected to quantitative sweat chloride test and molecular screening for the three most common mutations of cystic fibrosis transconductance regulator (
    Language English
    Publishing date 2020-02-03
    Publishing country Germany
    Document type Journal Article
    ISSN 2146-4596
    ISSN 2146-4596
    DOI 10.1055/s-0040-1701446
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Molecular characterization of

    Zaki, Maysaa / Galeb, Sara / Eid, Abdel-Rahman / Ahmed, Doaa / Mabrouk, Amna / Latif, Radwa Abdel

    Germs

    2020  Volume 10, Issue 4, Page(s) 295–302

    Abstract: Introduction: The objective of this study was to determine the prevalence of antibiotic resistance genes : Methods: The study was a retrospective cross-sectional study, including 250 unique isolates of : Results: Methicillin resistant : ... ...

    Abstract Introduction: The objective of this study was to determine the prevalence of antibiotic resistance genes
    Methods: The study was a retrospective cross-sectional study, including 250 unique isolates of
    Results: Methicillin resistant
    Conclusions: The present study highlights that major
    Language English
    Publishing date 2020-12-28
    Publishing country Romania
    Document type Journal Article
    ZDB-ID 2649305-6
    ISSN 2248-2997
    ISSN 2248-2997
    DOI 10.18683/germs.2020.1221
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: Screening for the Most Common Mutations of CFTR Gene among Egyptian Children with Difficult-to-Treat Asthma

    Al-Haggar, Mohammad / Osman, Engy / Eid, Abdel-Rahman / Barakat, Tarek / El-Morsi, Samar

    Journal of Pediatric Genetics

    2020  Volume 09, Issue 03, Page(s) 164–170

    Abstract: Cystic fibrosis (CF) is panethnic autosomal recessive disease that affects the exocrine glands of pancreas, lungs, and intestine. It is often misdiagnosed in developing countries as difficult-to-treat asthma. We enrolled 150 Egyptian families with one or ...

    Abstract Cystic fibrosis (CF) is panethnic autosomal recessive disease that affects the exocrine glands of pancreas, lungs, and intestine. It is often misdiagnosed in developing countries as difficult-to-treat asthma. We enrolled 150 Egyptian families with one or more probands who were complaining of difficult-to-treat asthma, and 112 cases were studied extensively through history taking including pedigree construction and clinical examination. In addition, spirometry and computed tomography of the chest were done in selected cases. All cases were subjected to quantitative sweat chloride test and molecular screening for the three most common mutations of cystic fibrosis transconductance regulator ( CFTR ) gene ( ΔF508 G542X W1282X ) using amplification refractory mutation system (ARMS) technique. Probands of difficult-to-treat asthma comprised 66 males and 46 females; their age range was 1 to 14 years. Sixty-one probands (54.5%) were carriers of one or more of the studied mutations (36 cases and 25 carriers). Six carriers of single mutations had mild respiratory symptoms and negative sweat test. The most common allele was ΔF508, 60 alleles in 56 individuals (4 were homozygous ΔF508 ΔF508 ) followed by W1282X in 25 individuals and G542X in 12 individuals. Allele W1282X had an increased risk of recurrent chest infection and bronchiectasis. Moreover, cases with two mutations had more severe symptoms compared with those with a single mutation. CFTR mutations and CF-related syndromes are not rare as thought in Egypt, especially among the high-risk difficult-to-treat asthma. The readily available ARMS technique is recommended for ΔF508 and/or W1282X screening on priority basis among these children.
    Keywords cystic fibrosis ; CFTR ; difficult-to-treat asthma
    Language English
    Publishing date 2020-02-03
    Publisher Georg Thieme Verlag KG
    Publishing place Stuttgart ; New York
    Document type Article
    ISSN 2146-460X ; 2146-4596
    ISSN (online) 2146-460X
    ISSN 2146-4596
    DOI 10.1055/s-0040-1701446
    Database Thieme publisher's database

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  5. Article ; Online: Beta Thalassemia Carrier Rate: Problem Burden among High School Children.

    El-Shanshory, Mohamed R / Sherief, Laila M / Yahia, Sohier / Ragab, Seham M / Mansour, Ahmed K / Hassab, Hoda M / Hesham, Mervat A / Ahmed, Adel S / Beshir, Mohamed R / El Fotoh, Wafaa M Abo / El Naby, Sameh A Abd / Alllah, Ahmed M Gad / Khalifa, Naglaa A / Soliman, Mohamed A / El-Dahtory, Faeza / El-Farahaty, Reham M / Osman, Engy / Elhabyan, Abdelazeem / El-Lateef, Amal E Abd /
    Kamal, Naglaa M / Kabbash, Ibrahim A / Saied, Shimaa M / Eid, Abdel-Rahman

    Current pediatric reviews

    2022  Volume 19, Issue 2, Page(s) 203–209

    Abstract: Background & Aim of the Work: β-Thalassemia (βT) is highly prevalent in some countries like Egypt. Accurate data about actual disease prevalence and heavily prevalent geographic locations are essential to help in early detection and in setting up ... ...

    Abstract Background & Aim of the Work: β-Thalassemia (βT) is highly prevalent in some countries like Egypt. Accurate data about actual disease prevalence and heavily prevalent geographic locations are essential to help in early detection and in setting up effective preventive programs. We aim for screening βT carriers among Egyptian high school students in the Delta region.
    Subjects and methods: A cross-sectional multicenter study was carried out on 4320 randomly selected students from four governorates of the Nile Delta region, Egypt. All patients were to be tested for their complete blood count. Those with microcytic hypochromic anemia not caused by iron deficiency were tested for βT carrier status using high-performance liquid chromatography.
    Results: The total prevalence of βT carrier rate was 6.13%. The highest prevalence was detected in Al-Sharkia Governorate, reaching 7.89%, followed by 6.90% in Al-Gharbia Governorate. Al- Dakahilia and Al-Menoufia showed lower rates of 4.86% and 3.73%, respectively.
    Conclusion: Despite the premarital national screening program for βT in Egypt, the carrier rate is still high. More effort should be done into the proper implementation of national prevention programs.
    MeSH term(s) Humans ; Child ; beta-Thalassemia/diagnosis ; beta-Thalassemia/epidemiology ; Cross-Sectional Studies ; Anemia, Hypochromic ; Prevalence ; Egypt/epidemiology
    Language English
    Publishing date 2022-07-12
    Publishing country United Arab Emirates
    Document type Multicenter Study ; Journal Article
    ISSN 1875-6336
    ISSN (online) 1875-6336
    DOI 10.2174/1573396318666220624142349
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: A novel fibrillin-1 mutation in an egyptian marfan family: A proband showing nephrotic syndrome due to focal segmental glomerulosclerosis.

    Al-Haggar, Mohammad / Bakr, Ashraf / Wahba, Yahya / Coucke, Paul J / El-Hussini, Fatma / Hafez, Mona / Eid, Riham / Eid, Abdel-Rahman / Sarhan, Amr / Shaltout, Ali / Hammad, Ayman / Yahia, Sohier / El-Rifaie, Ahmad / Abdel-Hadi, Dina

    Saudi journal of kidney diseases and transplantation : an official publication of the Saudi Center for Organ Transplantation, Saudi Arabia

    2017  Volume 28, Issue 1, Page(s) 141–148

    Abstract: Marfan syndrome (MFS), the founding member of connective tissue disorder, is an autosomal dominant disease; it is caused by a deficiency of the microfibrillar protein fibrillin-1 (FBN1) and characterized by involvement of three main systems; skeletal, ... ...

    Abstract Marfan syndrome (MFS), the founding member of connective tissue disorder, is an autosomal dominant disease; it is caused by a deficiency of the microfibrillar protein fibrillin-1 (FBN1) and characterized by involvement of three main systems; skeletal, ocular, and cardiovascular. More than one thousand mutations in FBN1 gene on chromosome 15 were found to cause MFS. Nephrotic syndrome (NS) had been described in very few patients with MFS being attributed to membranoproliferative glomerulonephritis secondary to infective endocarditis. Focal segmental glomerulosclerosis (FSGS) had been reported in NS in conjunction with MFS without confirming the diagnosis by mutational analysis of FBN1. We hereby present an Egyptian family with MFS documented at the molecular level; it showed a male proband with NS secondary to FSGS, unfortunately, we failed to make any causal link between FBN dysfunction and FSGS. In this context, we review the spectrum of renal involvements occurring in MFS patients.
    MeSH term(s) Adolescent ; Child ; Child, Preschool ; DNA Mutational Analysis ; Female ; Fibrillin-1/genetics ; Genetic Predisposition to Disease ; Glomerulosclerosis, Focal Segmental/complications ; Glomerulosclerosis, Focal Segmental/diagnosis ; Heredity ; Humans ; Male ; Marfan Syndrome/complications ; Marfan Syndrome/diagnosis ; Marfan Syndrome/genetics ; Middle Aged ; Mutation ; Nephrotic Syndrome/diagnosis ; Nephrotic Syndrome/etiology ; Pedigree ; Phenotype ; Risk Factors ; Young Adult
    Chemical Substances FBN1 protein, human ; Fibrillin-1
    Language English
    Publishing date 2017-01-17
    Publishing country Saudi Arabia
    Document type Case Reports ; Journal Article ; Review
    ZDB-ID 1379955-1
    ISSN 1319-2442
    ISSN 1319-2442
    DOI 10.4103/1319-2442.198166
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    In stock of ZB MED Cologne/Königswinter

    Zs.A 4735: Show issues Location:
    Je nach Verfügbarkeit (siehe Angabe bei Bestand)
    bis Jg. 1994: Bestellungen von Artikeln über das Online-Bestellformular
    Jg. 1995 - 2021: Lesesall (2.OG)
    ab Jg. 2022: Lesesaal (EG)

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  7. Book ; Thesis: Ausbeulen trapezförmiger Platten

    Eid, Abdel-Rahman

    (Mitteilungen aus dem Institut für Baustatik an der Eidgenössischen Technischen Hochschule in Zürich ; 31)

    1957  

    Author's details Dr. sc. techn. Abdel-Rahman Eid
    Series title Mitteilungen aus dem Institut für Baustatik an der Eidgenössischen Technischen Hochschule in Zürich ; 31
    Language German
    Size 96 Seiten, Diagramme, 1 Tafel
    Publisher Verlag Leemann
    Publishing place Zürich
    Document type Book ; Thesis
    Thesis / German Habilitation thesis Techn. Hochsch., Diss.--Zürich, 1957
    Database Former special subject collection: coastal and deep sea fishing

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  8. Book ; Thesis: Ausbeulen trapezförmiger Platten

    Eid, Abdel-Rahman

    (Mitteilungen aus dem Institut für Baustatik an der Eidgenössischen Technischen Hochschule in Zürich ; 31)

    1957  

    Author's details Dr. sc. techn. Abdel-Rahman Eid
    Series title Mitteilungen aus dem Institut für Baustatik an der Eidgenössischen Technischen Hochschule in Zürich ; 31
    Language German
    Size 96 Seiten, Diagramme, 1 Tafel
    Publisher Verlag Leemann
    Publishing place Zürich
    Document type Book ; Thesis
    Thesis / German Habilitation thesis Techn. Hochsch., Diss.--Zürich, 1957
    Database Library catalogue of the German National Library of Science and Technology (TIB), Hannover

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  9. Book ; Online ; Thesis: Ausbeulen trapezförmiger Platten

    Eid, Abdel-Rahman

    (Mitteilungen aus dem Institut für Baustatik an der Eidgenössischen Technischen Hochschule in Zürich ; Nr. 31)

    1957  

    Author's details Abdel-Rahman Eid
    Series title Mitteilungen aus dem Institut für Baustatik an der Eidgenössischen Technischen Hochschule in Zürich ; Nr. 31
    Language German
    Size Online-Ressource (96 S)
    Publisher Leemann
    Publishing place Zürich
    Document type Book ; Online ; Thesis
    Thesis / German Habilitation thesis Diss. Techn. Wiss. ETH Zürich, Nr. 2638. Ref.: Stüssi, F. ; Korref.: Lardy, P--Zürich, 2638
    Database Former special subject collection: coastal and deep sea fishing

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  10. Book ; Online ; Thesis: Ausbeulen trapezförmiger Platten

    Eid, Abdel-Rahman

    (Mitteilungen aus dem Institut für Baustatik an der Eidgenössischen Technischen Hochschule in Zürich ; Nr. 31)

    1957  

    Author's details Abdel-Rahman Eid
    Series title Mitteilungen aus dem Institut für Baustatik an der Eidgenössischen Technischen Hochschule in Zürich ; Nr. 31
    Language German
    Size Online-Ressource (96 S)
    Publisher Leemann
    Publishing place Zürich
    Document type Book ; Online ; Thesis
    Thesis / German Habilitation thesis Diss. Techn. Wiss. ETH Zürich, Nr. 2638. Ref.: Stüssi, F. ; Korref.: Lardy, P--Zürich, 2638
    Database Library catalogue of the German National Library of Science and Technology (TIB), Hannover

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