Zobrazeno 1 - 10
of 32
pro vyhledávání: '"S. Al Fifi"'
Publikováno v:
Acta Paediatrica. 90:151-153
This paper presents a family case of two brothers and two sisters with congenital lower limb lymphoedema, nail dystrophy, and with esotropia in two of them. They are offspring of healthy parents who are first cousins. This combination of congenital l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::63be169d1dfe441df8c3d8642f651c33
https://doi.org/10.1111/j.1651-2227.2001.tb00276.x
https://doi.org/10.1111/j.1651-2227.2001.tb00276.x
Publikováno v:
Acta Paediatrica. 88:715-717
We evaluated five children with prolonged primary hypothyroidism and noted a significant reduction in renal function (40%), which was reversible with hormonal replacement. This decline was higher than reported in adults and was of sufficient magnitud
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::28e3b204fa4e68b626e73ca95d7a1324
https://doi.org/10.1111/j.1651-2227.1999.tb00030.x
https://doi.org/10.1111/j.1651-2227.1999.tb00030.x
Publikováno v:
Eastern Mediterranean health journal = La revue de sante de la Mediterranee orientale = al-Majallah al-sihhiyah li-sharq al-mutawassit. 16(11)
Mothers of children with bronchial asthma consecutively admitted to Aseer central hospital, Saudi Arabia (n = 171), were interviewed using a questionnaire based on the Chicago Community Asthma Survey to study their knowledge and behaviours concerning
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9c150f6e14a84a30a396a9c51802170c
https://pubmed.ncbi.nlm.nih.gov/21218739
https://pubmed.ncbi.nlm.nih.gov/21218739
Publikováno v:
Journal of pediatric endocrinologymetabolism : JPEM. 14(6)
Objective As multinodular goiter (MNG) is an uncommon pediatric disorder, we decided to evaluate the children with this diagnosis at our center to try to delineate better its etiology, the risk of malignancy and appropriate management strategies. Met
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d744470492206ba408693100f3443851
https://pubmed.ncbi.nlm.nih.gov/11453525
https://pubmed.ncbi.nlm.nih.gov/11453525
Autor:
M A, Alshehri, M A, Abolfotouh, A, Sadeg, Y M, Al Najjar, A A, Asindi, A M, Al Harthi, H, Al Trabulsi, S, Al Fifi, A, Al Frayh
Publikováno v:
Saudi medical journal. 21(11)
The objective of the present study was to measure the prevalence of asthma and asthma-related symptoms among male school children in Abha City and to determine some of the possible risk factors influencing its occurrence.A randomly selected sample of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::80c87bb5c816acbfaafff9081c0131a2
https://pubmed.ncbi.nlm.nih.gov/11360067
https://pubmed.ncbi.nlm.nih.gov/11360067
Publikováno v:
Acta paediatrica (Oslo, Norway : 1992). 90(2)
This paper presents a family case of two brothers and two sisters with congenital lower limb lymphoedema, nail dystrophy, and with esotropia in two of them. They are offspring of healthy parents who are first cousins. This combination of congenital l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::334a5442c229731bcc10bfa97581ca31
https://pubmed.ncbi.nlm.nih.gov/11236043
https://pubmed.ncbi.nlm.nih.gov/11236043
Publikováno v:
American journal of medical genetics. 78(2)
Keutel syndrome is a rare autosomal recessive disorder characterized by diffuse cartilage calcification, characteristic physiognomy, brachytelephalangism, peripheral pulmonary stenosis, hearing loss, and borderline to mild mental retardation. We repo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::70ac6a144ecd0d64f977b1d1ea0f8ec9
https://pubmed.ncbi.nlm.nih.gov/10096599
https://pubmed.ncbi.nlm.nih.gov/10096599
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