Zobrazeno 1 - 10
of 266
pro vyhledávání: '"Marfans Syndrome"'
Publikováno v:
Annals of Pathology and Laboratory Medicine. 7:C10-12
The Bombay Blood Group (Oh) is characterized by absence of normal ABH antigens and presence of corresponding antibodies in serum. This blood group is suspected when a sample doesn’t show any reaction to anti-A and anti-B antibodies just like a norm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f82dbd8db3d47f213cbf923d011b757e
https://doi.org/10.21276/apalm.2588
https://doi.org/10.21276/apalm.2588
Publikováno v:
Paediatrics and Child Health. 28:50-56
Hypermobility can be a normal variant in children but it is also found in a group of children presenting with musculoskeletal pain. A smaller group of children will have hypermobility associated with a more concerning syndrome. The clinical challenge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c5307f1231f7487b9893e5e74fd45c32
https://doi.org/10.1016/j.paed.2017.12.001
https://doi.org/10.1016/j.paed.2017.12.001
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
International Surgery Journal. 7:4241
This case describes 13-year-old female with Marfans syndrome who presented recurrent small intestinal obstruction which was later diagnosed as acute midgut volvulus due to malrotation after extensive workup. Laparoscopic Ladd’s procedure was perfor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6418f97377b6c9325ed8a01c0d0c4f2c
https://doi.org/10.18203/2349-2902.isj20205393
https://doi.org/10.18203/2349-2902.isj20205393
Autor:
Venkatesh Kode, Meghana Mukund
Publikováno v:
ISACON KARNATAKA 2017 33rd Annual Conference of Indian Society of Anaesthesiologists (ISA), Karnataka State Chapter.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b3c67fe88c0d975e57be1761dee82bca
https://doi.org/10.18311/isacon-karnataka/2017/ep119
https://doi.org/10.18311/isacon-karnataka/2017/ep119
Publikováno v:
Çağdaş Tıp Dergisi, Vol 2, Iss 1, Pp 33-37 (2014)
Volume: 2, Issue: 1 33-37
Çağdaş Tıp Dergisi
Volume: 2, Issue: 1 33-37
Çağdaş Tıp Dergisi
Marfans syndrome is a disorder of the connective tissue inherited as an autosomal dominant condition of variable expression and its classical form comprises of skeletal, cardiovascular and ocular abnormalities. It is attributed as a defect in the mut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::e4c626f54082f045f5fd029954019c2a
http://dergipark.gov.tr/gopctd/issue/7307/95615?publisher=selcuk
http://dergipark.gov.tr/gopctd/issue/7307/95615?publisher=selcuk
Autor:
Abu Siddique, Nandita Paul, Sajal Krishna Banerjee, Mohammad Ferdous Ur Rahaman, Reehum Haque, Mahbubur Rahman, Mohammad Mainul Hasan Chowdhury
Publikováno v:
University Heart Journal. 10:39-41
Marfans Syndrome patients with aortic root aneurysm or dissection may present with shortness of breath and chest pain and may be missed during clinical evaluation. Subsequently, sudden aortic rupture may occur in these groups of patients and give r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84c47e1bbec628c0823f72181cecce3d
https://doi.org/10.3329/uhj.v10i1.24598
https://doi.org/10.3329/uhj.v10i1.24598
Publikováno v:
Çağdaş Tıp Dergisi, Vol 2, Iss 1, Pp 33-37 (2012)
Marfans syndrome is a disorder of the connective tissue inherited as an autosomal dominant condition of variable expression and its classical form comprises of skeletal, cardiovascular and ocular abnormalities. It is attributed as a defect in the mut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::fb75a68cb15ecb4ef765d53bc9bd00a6
http://www.scopemed.org/fulltextpdf.php?mno=18996
http://www.scopemed.org/fulltextpdf.php?mno=18996
Autor:
Seth A. Hollander, James R. Priest, Daniel Bernstein, John C. Dykes, Beth D. Kaufman, Katsuhide Maeda, David Liang, Olaf Reinhartz, S.E. Tierney, Shuping Chen, David N. Rosenthal, Christopher S. Almond
Publikováno v:
The Journal of Heart and Lung Transplantation. 36:S393-S394
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9ebe8189dd2424856ff8bdceb3d8809a
https://doi.org/10.1016/j.healun.2017.01.1123
https://doi.org/10.1016/j.healun.2017.01.1123
Publikováno v:
Indian Heart Journal, Vol 67, Iss S1, p S93 (2015)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07232b6b6ce97dab730186f865c2b634