Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Louis Hofmeyr"'
Autor:
Louis Hofmeyr, Gerrida Herbst, Elias Pretorius, Brian Sarembock, Kathryn Taylor, David Roytowski
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
IntroductionPrimary IgG4-related disease (IgG4-RD) of the temporal bone is a rare condition. Unlike typical petrous apicitis or Gradenigo syndrome, our patient presented exclusively with unilateral cranial nerve VI palsy and symptoms of diplopia. Sku
Externí odkaz:
https://doaj.org/article/973af1948a3d4fbd855a590db2142369
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Externí odkaz:
https://doaj.org/article/5a6187e80893435cb605c77f2e128603
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::682e594d265d44665173fc8f9baa2c87
https://doi.org/10.3389/fneur.2021.740690
https://doi.org/10.3389/fneur.2021.740690
Publikováno v:
Echocardiography (Mount Kisco, N.Y.). 26(4)
Article Title: Association between Left Atrium Enlargement and Intradialytic Hypotension: Role of Diastolic Dysfunction in the Hemodynamic Complications during Hemodialysis.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30f583f69907af499a692999bb937495
https://pubmed.ncbi.nlm.nih.gov/19054023
https://pubmed.ncbi.nlm.nih.gov/19054023
Publikováno v:
Echocardiography (Mount Kisco, N.Y.). 26(4)
We describe a 29-year-old male, previously in good health, with no history of angina pectoris and no risk factors for ischemic heart disease presenting with biventricular failure and severe mitral valve regurgitation. There were no signs or serologic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::feebb5871b1cbeea83a126950e63e8d2
https://pubmed.ncbi.nlm.nih.gov/19382946
https://pubmed.ncbi.nlm.nih.gov/19382946
Autor:
Herman, Hamersma, Louis, Hofmeyr
Publikováno v:
Advances in oto-rhino-laryngology. 65
The middle ear changes in Sclerosteosis and Van Buchem disease are described. Reduced bone resorption occurs due to faulty activity of the sclerostin molecule, a product of the recently discovered SOST gene in chromosome 17. Syndactyly draws attentio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::60f6e10c5e82d3f22992325a51b28771
https://pubmed.ncbi.nlm.nih.gov/17245025
https://pubmed.ncbi.nlm.nih.gov/17245025